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Department: Developmental and Stem Cell Biology

All Publications

Stevick RJ, Audrain B, Bedu S, Dray N, Ghigo JM, Pérez-Pascual D, Anti-diarrheal drug loperamide induces dysbiosis in zebrafish microbiota via bacterial inhibition., Microbiome 2023 Nov; 11(1): 252.

Crozet F, Levayer R, Emerging roles and mechanisms of ERK pathway mechanosensing., Cell Mol Life Sci 2023 Nov; 80(12): 355.

Banach-Latapy A, Rincheval V, Briand D, Guénal I, Spéder P, Differential adhesion during development establishes individual neural stem cell niches and shapes adult behaviour in Drosophila., PLoS Biol 2023 Nov; 21(11): e3002352.

Bernheim S, Borgel A, Le Garrec JF, Perthame E, Desgrange A, Michel C, Guillemot L, Sart S, Baroud CN, Krezel W, Raimondi F, Bonnet D, Zaffran S, Houyel L, Meilhac SM, Identification of Greb1l as a genetic determinant of crisscross heart in mice showing torsion of the heart tube by shortage of progenitor cells., Dev Cell 2023 Oct; (): .

Crochemore C, Chica C, Garagnani P, Lattanzi G, Horvath S, Sarasin A, Franceschi C, Bacalini MG, Ricchetti M, Epigenomic signature of accelerated ageing in progeroid Cockayne syndrome., Aging Cell 2023 Sep; (): e13959.

Caro H, Dollin S, Biton A, Brancotte B, Desvillechabrol D, Dufresne Y, Li B, Kornobis E, Lemoine F, Maillet N, Perrin A, Traut N, Néron B, Cokelaer T, BioConvert: a comprehensive format converter for life sciences., NAR Genom Bioinform 2023 Sep; 5(3): lqad074.

Laure Mancini, Boris Guirao, Sara Ortica, Miriam Labusch, Felix Cheysson, Valentin Bonnet, Minh Son Phan, Sébastien Herbert, Pierre Mahou, Emilie Menant, Sébastien Bedu, Jean-Yves Tinevez, Charles Baroud, Emmanuel Beaurepaire, Yohanns Bellaiche, Laure Bally-Cuif, Nicolas Dray, Apical size and deltaA expression predict adult neural stem cell decisions along lineage progression, Science Advances , 2023, 9 (35), pp.eadg7519. ⟨10.1126/sciadv.adg7519⟩.

Thaller AL, Jönsson F, Fiquet O, Marie S, Doisne JM, Girelli-Zubani G, Eri T, Fernandes P, Tatirovsky E, Langa-Vives F, Bruhns P, Strick-Marchand H, Di Santo JP, A human immune system (HIS) mouse model that dissociates roles for mouse and human FcR+ cells during antibody-mediated immune responses., Eur J Immunol 2023 Aug; (): e2350454.

Gozlan S, Batoumeni V, Fournier T, Nanteau C, Potey A, Clémençon M, Orieux G, Sahel JA, Goureau O, Roger JE, Reichman S, Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells., Commun Biol 2023 Jul; 6(1): 762.

Sutcu HH, Montagne B, Ricchetti M, DNA-PKcs regulates myogenesis in an Akt-dependent manner independent of induced DNA damage., Cell Death Differ 2023 Jul; (): .

Cumming T, Levayer R, Toward a predictive understanding of epithelial cell death., Semin Cell Dev Biol 2023 Jul; (): .

Brückner DB, Chen H, Barinov L, Zoller B, Gregor T, Stochastic motion and transcriptional dynamics of pairs of distal DNA loci on a compacted chromosome., Science 2023 Jun; 380(6652): 1357-1362.

Villars A, Letort G, Valon L, Levayer R, DeXtrusion: automatic recognition of epithelial cell extrusion through machine learning in vivo., Development 2023 Jul; 150(13): .

Le Chevalier F, Authié P, Chardenoux S, Bourgine M, Vesin B, Cussigh D, Sassier Y, Fert I, Noirat A, Nemirov K, Anna F, Bérard M, Guinet F, Hardy D, Charneau P, Lemonnier F, Langa-Vives F, Majlessi L, Mice Humanized for MHC and hACE2 with High Permissiveness to SARS-CoV-2 Omicron Replication., Microbes Infect 2023 Apr; (): 105142.

Núria Ros-Rocher, Thibaut Brunet, What is it like to be a choanoflagellate? Sensation, processing and behavior in the closest unicellular relatives of animals, Animal Cognition, 2023, ⟨10.1007/s10071-023-01776-z⟩.

Davidescu MR, Romanczuk P, Gregor T, Couzin ID, , Growth produces coordination trade-offs in Trichoplax adhaerens, an animal lacking a central nervous system., Proc Natl Acad Sci U S A 2023 Mar; 120(11): e2206163120.

Mathieu Mateo, Stéphanie Reynard, Natalia Pietrosemoli, Emeline Perthame, Alexandra Journeaux, Kodie Noy, Clara Germain, Xavier Carnec, Caroline Picard, Virginie Borges-Cardoso, Jimmy Hortion, Hélène Lopez-Maestre, Pierrick Regnard, Lyne Fellmann, Audrey Vallve, Stéphane Barron, Ophélie Jourjon, Orianne Lacroix, Aurélie Duthey, Manon Dirheimer, Maïlys Daniau, Catherine Legras-Lachuer, Caroline Carbonnelle, Hervé Raoul, Frédéric Tangy, Sylvain Baize, Rapid protection induced by a single-shot Lassa vaccine in male cynomolgus monkeys, Nature Communications, 2023, 14 (1), pp.1352. ⟨10.1038/s41467-023-37050-6⟩.

Slaoui L, Gilbert A, Rancillac A, Delaunay-Piednoir B, Chagnot A, Gerard Q, Letort G, Mailly P, Robil N, Gelot A, Lefebvre M, Favier M, Dias K, Jourdren L, Federici L, Auvity S, Cisternino S, Vivien D, Cohen-Salmon M, Boulay AC, In mice and humans, brain microvascular contractility matures postnatally., Brain Struct Funct 2023 Mar; 228(2): 475-492.

Rjiba K, Slimani W, Gaddas M, Hassine IH, Jelloul A, Khelifa HB, El Amri F, Zaouali M, Mcelreavey K, Saad A, Mougou-Zerelli S, Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis., J Clin Res Pediatr Endocrinol 2023 Feb; 15(1): 25-34.

Moigneu C, Abdellaoui S, Ramos-Brossier M, Pfaffenseller B, Wollenhaupt-Aguiar B, de Azevedo Cardoso T, Chiche A, Kuperwasser N, Azevedo da Silva R, Pedrotti Moreira F, Li H, Oury F, Kapczinski F, Lledo PM, Katsimpardi L, , Systemic GDF11 attenuates depression-like phenotype in aged mice via stimulation of neuronal autophagy., Nat Aging 2023 Feb; 3(2): 213-228.

Rjiba K, Mougou-Zerelli S, Hamida IH, Saad G, Khadija B, Jelloul A, Slimani W, Hasni Y, Dimassi S, Khelifa HB, Sallem A, Kammoun M, Abdallah HH, Gribaa M, Bignon-Topalovic J, Chelly S, Khairi H, Bibi M, Kacem M, Saad A, Bashamboo A, McElreavey K, Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development., Reprod Biol Endocrinol 2023 Jan; 21(1): 2.

Gonen N, Eozenou C, Mitter R, Elzaiat M, Stévant I, Aviram R, Bernardo AS, Chervova A, Wankanit S, Frachon E, Commère PH, Brailly-Tabard S, Valon L, Barrio Cano L, Levayer R, Mazen I, Gobaa S, Smith JC, McElreavey K, Lovell-Badge R, Bashamboo A, , In vitro cellular reprogramming to model gonad development and its disorders., Sci Adv 2023 Jan; 9(1): eabn9793.

Staneva R, Levayer R, Cell polarity and extrusion: How to polarize extrusion and extrude misspolarized cells?, Curr Top Dev Biol 2023 ; 154(): 131-167.

Dumont L, Lopez Maestre H, Chalmel F, Huber L, Rives-Feraille A, Moutard L, Bateux F, Rondanino C, Rives N, Throughout in vitro first spermatogenic wave: Next-generation sequencing gene expression patterns of fresh and cryopreserved prepubertal mice testicular tissue explants., Front Endocrinol (Lausanne) 2023 ; 14(): 1112834.

McElreavey K, Bashamboo A, Monogenic Forms of DSD: An Update., Horm Res Paediatr 2023 ; 96(2): 144-168.

Thibaut Brunet, David S Booth, Cell polarity in the protist-to-animal transition, Ulrich Tepass. Cell Polarity in Development and Disease, 154, Academic Press, pp.1-36, 2023, Current Topics in Developmental Biology, 9780128201657. ⟨10.1016/bs.ctdb.2023.03.001⟩.

Netta Haroush, Michal Levo, Eric Wieschaus, Thomas Gregor, Functional analysis of the Drosophila eve locus in response to non-canonical combinations of gap gene expression levels, Developmental Cell, In press, ⟨10.1016/j.devcel.2023.10.001⟩.

Rossine FW, Vercelli GT, Tarnita CE, Gregor T, , Structured foraging of soil predators unveils functional responses to bacterial defenses., Proc Natl Acad Sci U S A 2022 Dec; 119(52): e2210995119.

Laure Mancini, Boris Guirao, Sara Ortica, Miriam Labusch, Felix Cheysson, Valentin Bonnet, Minh Son Phan, Sébastien Herbert, Pierre Mahou, Emilie Menant, Sébastien Bedu, Jean-Yves Tinevez, Charles Baroud, Emmanuel Beaurepaire, Yohanns Bellaiche, Laure Bally-Cuif, Nicolas Dray, Apical size and deltaA expression predict adult neural stem cell decisions along lineage progression, 2023.

Couturier L, Luna J, Mazouni K, Mestdagh C, Phan MS, Corson F, Schweisguth F, , HaloTag-based reporters for sparse labeling and cell tracking., Fly (Austin) 2022 Dec; 16(1): 360-366.

Benjamin Zoller, Thomas Gregor, Gašper Tkačik, Eukaryotic gene regulation at equilibrium, or non?, Curr. Opin. Syst. Biol. 2022 Sep;31:100435..

Chervova A, Festuccia N, Altamirano-Pacheco L, Dubois A, Navarro P, , A gene subset requires CTCF bookmarking during the fast post-mitotic reactivation of mouse ES cells., EMBO Rep 2022 Nov; (): e56075.

Boquet-Pujadas A, Feaugas T, Petracchini A, Grassart A, Mary H, Manich M, Gobaa S, Olivo-Marin JC, Sauvonnet N, Labruyère E, , 4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion., Science advances.

Alla A, Ongoth FEM, Tahiri A, Karrou M, Rouf S, Benhaddou H, Kamaoui I, Mcelreavey K, Latrech H, Novel homozygous inactivating mutation in the luteinizing hormone receptor gene (LHCGR) associated with 46, XY DSD in a Moroccan family., J Pediatr Endocrinol Metab 2022 Sep; 35(9): 1215-1221.

Dubois A, Vincenti L, Chervova A, Greenberg MVC, Vandormael-Pournin S, Bourc'his D, Cohen-Tannoudji M, Navarro P, , H3K9 tri-methylation at Nanog times differentiation commitment and enables the acquisition of primitive endoderm fate., Development 2022 Sep; 149(17): .

Al Jord A, Letort G, Chanet S, Tsai FC, Antoniewski C, Eichmuller A, Da Silva C, Huynh JR, Gov NS, Voituriez R, Terret MÉ, Verlhac MH, Cytoplasmic forces functionally reorganize nuclear condensates in oocytes., Nat Commun 2022 Aug; 13(1): 5070.

Rujano MA, Briand D, Ðelić B, Marc J, Spéder P, , An interplay between cellular growth and atypical fusion defines morphogenesis of a modular glial niche in Drosophila., Nat Commun 2022 Aug; 13(1): 4999.

Russo E, Lemaître F, Corre B, Chikina AS, Langa-Vives F, Bousso P, , SPICE-Met: profiling and imaging energy metabolism at the single-cell level using a fluorescent reporter mouse., EMBO J 2022 Aug; (): e111528.

Voortman L, Anderson C, Urban E, Yuan L, Tran S, Neuhaus-Follini A, Derrick J, Gregor T, Johnston RJ, , Temporally dynamic antagonism between transcription and chromatin compaction controls stochastic photoreceptor specification in flies., Dev Cell 2022 08; 57(15): 1817-1832.e5.

Chatre L, Ducat A, Spradley FT, Palei AC, Chéreau C, Couderc B, Thomas KC, Wilson AR, Amaral LM, Gaillard I, Méhats C, Lagoutte I, Jacques S, Miralles F, Batteux F, Granger JP, Ricchetti M, Vaiman D, , Increased NOS coupling by the metabolite tetrahydrobiopterin (BH4) reduces preeclampsia/IUGR consequences., Redox Biol 2022 Jul; 55(): 102406.

Bernard LD, Dubois A, Heurtier V, Fischer V, Gonzalez I, Chervova A, Tachtsidi A, Gil N, Owens N, Bates LE, Vandormael-Pournin S, Silva JCR, Ulitsky I, Cohen-Tannoudji M, Navarro P, , OCT4 activates a Suv39h1-repressive antisense lncRNA to couple histone H3 Lysine 9 methylation to pluripotency., Nucleic Acids Res 2022 07; 50(13): 7367-7379.

von Joest M, Chen C, Douché T, Chantrel J, Chiche A, Gianetto QG, Matondo M, Li H, , Amphiregulin mediates non-cell-autonomous effect of senescence on reprogramming., Cell Rep 2022 Jul; 40(2): 111074.

Crochemore C, Cimmaruta C, Fernández-Molina C, Ricchetti M, , Reactive Species in Progeroid Syndromes and Aging-Related Processes., Antioxid Redox Signal 2022 07; 37(1-3): 208-228.

Phan MS, Matho K, Beaurepaire E, Livet J, Chessel A, , nAdder: A scale-space approach for the 3D analysis of neuronal traces., PLoS Comput Biol 2022 07; 18(7): e1010211.

Letort G, Eichmuller A, Da Silva C, Nikalayevich E, Crozet F, Salle J, Minc N, Labrune E, Wolf JP, Terret ME, Verlhac MH, An interpretable and versatile machine learning approach for oocyte phenotyping., J Cell Sci 2022 Jul; 135(13): .

Seyboldt R, Lavoie J, Henry A, Vanaret J, Petkova MD, Gregor T, François P, , Latent space of a small genetic network: Geometry of dynamics and information., Proc Natl Acad Sci U S A 2022 06; 119(26): e2113651119.

Ichim G, Gibert B, Adriouch S, Brenner C, Davoust N, Desagher S, Devos D, Dokudovskaya S, Dubrez L, Estaquier J, Gillet G, Guénal I, Juin PP, Kroemer G, Legembre P, Levayer R, Manon S, Mehlen P, Meurette O, Micheau O, Mignotte B, Nguyen-Khac F, Popgeorgiev N, Poyet JL, Priault M, Ricci JE, Riquet FB, Susin SA, Suzanne M, Vacher P, Walter L, Mollereau B, Keeping Cell Death Alive: An Introduction into the French Cell Death Research Network., Biomolecules 2022 Jun; 12(7): .

Villars A, Matamoro-Vidal A, Levillayer F, Levayer R, , Microtubule disassembly by caspases is an important rate-limiting step of cell extrusion., Nat Commun 2022 Jun; 13(1): 3632.

Allègre N, Chauveau S, Dennis C, Renaud Y, Meistermann D, Estrella LV, Pouchin P, Cohen-Tannoudji M, David L, Chazaud C, , NANOG initiates epiblast fate through the coordination of pluripotency genes expression., Nat Commun 2022 Jun; 13(1): 3550.

Nollmann M, Bennabi I, Götz M, Gregor T, , The Impact of Space and Time on the Functional Output of the Genome., Cold Spring Harb Perspect Biol 2022 05; 14(4): .

Isaac Esteban, Patrick Schmidt, Audrey Desgrange, Morena Raiola, Susana Temiño, Sigolène M. Meilhac, Leif Kobbelt and Miguel Torres, Pseudodynamic analysis of heart tube formation in the mouse reveals strong regional variability and early left–right asymmetry, Nature Cardiovascular Research 2022 ; 1:504–517 .

Schreier HK, Wiehe RS, Ricchetti M, Wiesmüller L, , Polymerase ζ Is Involved in Mitochondrial DNA Maintenance Processes in Concert with APE1 Activity., Genes (Basel) 2022 05; 13(5): .

Levo M, Raimundo J, Bing XY, Sisco Z, Batut PJ, Ryabichko S, Gregor T, Levine MS, , Transcriptional coupling of distant regulatory genes in living embryos., Nature 2022 05; 605(7911): 754-760.

Vesin B, Lopez J, Noirat A, Authié P, Fert I, Le Chevalier F, Moncoq F, Nemirov K, Blanc C, Planchais C, Mouquet H, Guinet F, Hardy D, Vives FL, Gerke C, Anna F, Bourgine M, Majlessi L, Charneau P, , An intranasal lentiviral booster reinforces the waning mRNA vaccine-induced SARS-CoV-2 immunity that it targets to lung mucosa., Mol Ther 2022 Apr; (): .

Reyes-Rivera J, Wu Y, Guthrie BGH, Marletta MA, King N, Brunet T, , Nitric oxide signaling controls collective contractions in a colonial choanoflagellate., Curr Biol 2022 Apr; (): .

Chaigne A, Brunet T, , Incomplete abscission and cytoplasmic bridges in the evolution of eukaryotic multicellularity., Curr Biol 2022 Apr; 32(8): R385-R397.

Rituparna Sarkar, Daniel Darby, Sigolène Meilhac and Jean-Christophe Olivo-Marin, 3D cell morphology detection by association for embryo heart morphogenesis, Volume 2 , 2022 , e2.

Freyer L, Lallemand Y, Dardenne P, Sommer A, Biton A, Gomez Perdiguero E, , Erythro-myeloid progenitor origin of Hofbauer cells in the early mouse placenta., Development 2022 Apr; 149(8): .

Parada C, Banavar SP, Khalilian P, Rigaud S, Michaut A, Liu Y, Joshy DM, Campàs O, Gros J, , Mechanical feedback defines organizing centers to drive digit emergence., Dev Cell 2022 Apr; 57(7): 854-866.e6.

Ertekin Ö, Monavari M, Krüger R, Fuentes-Chandía M, Parma B, Letort G, Tripal P, Boccaccini AR, Bosserhoff AK, Ceppi P, Kappelmann-Fenzl M, Leal-Egaña A, 3D hydrogel-based microcapsules as an in vitro model to study tumorigenicity, cell migration and drug resistance., Acta Biomater 2022 Apr; 142(): 208-220.

Quarato P, Singh M, Bourdon L, Cecere G, , Inheritance and maintenance of small RNA-mediated epigenetic effects., Bioessays 2022 Mar; (): e2100284.

Singh AP, Wu P, Ryabichko S, Raimundo J, Swan M, Wieschaus E, Gregor T, Toettcher JE, , Optogenetic control of the Bicoid morphogen reveals fast and slow modes of gap gene regulation., Cell Rep 2022 03; 38(12): 110543.

Chikhaoui A, Kraoua I, Calmels N, Bouchoucha S, Obringer C, Zayoud K, Montagne B, M'rad R, Abdelhak S, Laugel V, Ricchetti M, Turki I, Yacoub-Youssef H, , Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations., Orphanet J Rare Dis 2022 03; 17(1): 121.

Grimaldi A, Comai G, Mella S, Tajbakhsh S, , Identification of bipotent progenitors that give rise to myogenic and connective tissues in mouse., Elife 2022 Feb; 11(): .

Dos Santos M, Backer S, Auradé F, Wong MM, Wurmser M, Pierre R, Langa F, Do Cruzeiro M, Schmitt A, Concordet JP, Sotiropoulos A, Jeffrey Dilworth F, Noordermeer D, Relaix F, Sakakibara I, Maire P, , A fast Myosin super enhancer dictates muscle fiber phenotype through competitive interactions with Myosin genes., Nat Commun 2022 02; 13(1): 1039.

Cornes E, Bourdon L, Singh M, Mueller F, Quarato P, Wernersson E, Bienko M, Li B, Cecere G, , piRNAs initiate transcriptional silencing of spermatogenic genes during C. elegans germline development., Dev Cell 2022 Jan; 57(2): 180-196.e7.

Palmquist-Gomes P, Meilhac SM, , Shaping the mouse heart tube from the second heart field epithelium., Curr Opin Genet Dev 2022 Jan; 73(): 101896.

Globa E, Zelinska N, Shcherbak Y, Bignon-Topalovic J, Bashamboo A, MсElreavey K, , Disorders of Sex Development in a Large Ukrainian Cohort: Clinical Diversity and Genetic Findings., Front Endocrinol (Lausanne) 2022 ; 13(): 810782.

McElreavey K, Sinclair A, Genetics of Differences of Sex Development., Sex Dev 2022 ; 16(2-3): 77-79.

Elzaiat M, McElreavey K, Bashamboo A, Genetics of 46,XY gonadal dysgenesis., Best Pract Res Clin Endocrinol Metab 2022 Jan; 36(1): 101633.

McElreavey K, Pailhoux E, Bashamboo A, DHX37 and 46,XY DSD: A New Ribosomopathy?, Sex Dev 2022 ; 16(2-3): 194-206.

Zidoune H, Ladjouze A, Chellat-Rezgoune D, Boukri A, Dib SA, Nouri N, Tebibel M, Sifi K, Abadi N, Satta D, Benelmadani Y, Bignon-Topalovic J, El-Zaiat-Munsch M, Bashamboo A, McElreavey K, Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort., Front Genet 2022 ; 13(): 900574.

Piergiuseppe Quarato, Germano Cecere, Global Run-On sequencing to measure nascent transcription in C. elegans, STAR Protocols.

Singh M, Chazal M, Quarato P, Bourdon L, Malabat C, Vallet T, Vignuzzi M, van der Werf S, Behillil S, Donati F, Sauvonnet N, Nigro G, Bourgine M, Jouvenet N, Cecere G, , A virus-derived microRNA targets immune response genes during SARS-CoV-2 infection., EMBO Rep 2021 Dec; (): e54341.

Ku MW, Authié P, Bourgine M, Anna F, Noirat A, Moncoq F, Vesin B, Nevo F, Lopez J, Souque P, Blanc C, Fert I, Chardenoux S, Lafosse L, Cussigh D, Hardy D, Nemirov K, Guinet F, Langa Vives F, Majlessi L, Charneau P, , Brain cross-protection against SARS-CoV-2 variants by a lentiviral vaccine in new transgenic mice., EMBO Mol Med 2021 12; 13(12): e14459.

Ibarra-Morales D, Rauer M, Quarato P, Rabbani L, Zenk F, Schulte-Sasse M, Cardamone F, Gomez-Auli A, Cecere G, Iovino N, Histone variant H2A.Z regulates zygotic genome activation., Nat Commun 2021 12; 12(1): 7002.

Grimaldi A, Tajbakhsh S, Diversity in cranial muscles: Origins and developmental programs., Curr Opin Cell Biol 2021 Dec; 73(): 110-116.

Zayoud K, Kraoua I, Chikhaoui A, Calmels N, Bouchoucha S, Obringer C, Crochemore C, Najjar D, Zarrouk S, Miladi N, Laugel V, Ricchetti M, Turki I, Yacoub-Youssef H, , Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B., Genes (Basel) 2021 11; 12(12): .

Foray AP, Candon S, Hildebrand S, Marquet C, Valette F, Pecquet C, Lemoine S, Langa-Vives F, Dumas M, Hu P, Santamaria P, You S, Lyon S, Scott L, Bu CH, Wang T, Xu D, Moresco EMY, Scazzocchio C, Bach JF, Beutler B, Chatenoud L, , De novo germline mutation in the dual specificity phosphatase 10 gene accelerates autoimmune diabetes., Proc Natl Acad Sci U S A 2021 11; 118(47): .

Bauer M, Petkova MD, Gregor T, Wieschaus EF, Bialek W, , Trading bits in the readout from a genetic network., Proc Natl Acad Sci U S A 2021 11; 118(46): .

Bessy T, Candelas A, Souquet B, Saadallah K, Schaeffer A, Vianay B, Cuvelier D, Gobaa S, Nakid-Cordero C, Lion J, Bories JC, Mooney N, Jaffredo T, Larghero J, Blanchoin L, Faivre L, Brunet S, Théry M, , Hematopoietic progenitors polarize in contact with bone marrow stromal cells in response to SDF1., J Cell Biol 2021 Nov; 220(11): .

Winkler B, Funke D, Benmimoun B, Spéder P, Rey S, Logan MA, Klämbt C, , Brain inflammation triggers macrophage invasion across the blood-brain barrier in Drosophila during pupal stages., Sci Adv 2021 Oct; 7(44): eabh0050.

Germano Cecere, Small RNAs in epigenetic inheritance: from mechanisms to trait transmission, FEBS Lett. 2021 Oct 20. doi: 10.1002/1873-3468.14210. Epub ahead of print. PMID: 34671979..

Benmimoun B, Spéder P, , Breaking down barriers: Tumors make a leaky brain., Dev Cell 2021 Oct; 56(19): 2683-2685.

Villars A, Levayer R, , Collective effects in epithelial cell death and cell extrusion., Curr Opin Genet Dev 2022 02; 72(): 8-14.

Dubois-Vedrenne I, Al Delbany D, De Henau O, Robert V, Vernimmen M, Langa F, Lefort A, Libert F, Wittamer V, Parmentier M, , The antitumoral effects of chemerin are independent from leukocyte recruitment and mediated by inhibition of neoangiogenesis., Oncotarget 2021 Sep; 12(19): 1903-1919.

Decourty L, Malabat C, Frachon E, Jacquier A, Saveanu C., Investigation of RNA metabolism through large-scale genetic interaction profiling in yeast., Nucleic Acids Res 2021 09; 49(15): 8535-8555.

Rjiba K, Soyah N, Kammoun M, Hadj Hmida I, Saad A, Mcelreavey K, Mougou-Zerelli S, Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case., Eur J Med Genet 2021 Sep; 64(9): 104285.

Derbel R, Sellami H, Rebai A, Gdoura R, Mcelreavey E, Ammar-Keskes L, , Can leukocytospermia predict prostate cancer via its effects on mitochondrial DNA?, Andrologia 2021 Sep; 53(8): e14129.

Houyel L, Meilhac SM, Heart Development and Congenital Structural Heart Defects., Annu Rev Genomics Hum Genet 2021 08; 22(): 257-284.

Festuccia N, Owens N, Chervova A, Dubois A, Navarro P, , The combined action of Esrrb and Nr5a2 is essential for murine naïve pluripotency., Development 2021 Aug; (): .

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Aizel K, Clark AG, Simon A, Geraldo S, Funfak A, Vargas P, Bibette J, Vignjevic DM, Bremond N, A tuneable microfluidic system for long duration chemotaxis experiments in a 3D collagen matrix, Lab Chip 2017 Nov;17(22):3851-3861.

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Couturier L, Mazouni K, Bernard F, Besson C, Reynaud E, Schweisguth F, Regulation of cortical stability by RhoGEF3 in mitotic sensory organ precursor cells in Drosophila, Biol Open 2017 Nov;.

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Festuccia N, Owens N, Navarro P, Esrrb, an estrogen-related receptor involved in early development, pluripotency, and reprogramming, FEBS Lett. 2018 03;592(6):852-877.

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Baghdadi MB, Tajbakhsh S, Regulation and phylogeny of skeletal muscle regeneration, Dev. Biol. 2018 01;433(2):200-209.

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Festuccia N, Gonzalez I, Navarro P, The Epigenetic Paradox of Pluripotent ES Cells, J. Mol. Biol. 2017 05;429(10):1476-1503.

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Tajbakhsh S, lncRNA-Encoded Polypeptide SPAR(s) with mTORC1 to Regulate Skeletal Muscle Regeneration, Cell Stem Cell 2017 Apr;20(4):428-430.

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Kinnaird JH, Singh M, Gillan V, Weir W, Calder ED, Hostettler I, Tatu U, Devaney E, Shiels BR, , Characterization of HSP90 isoforms in transformed bovine leukocytes infected with Theileria annulata., Cell Microbiol 2017 03; 19(3): .

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Tajbakhsh S, Losing stem cells in the aged skeletal muscle niche, Cell Res. 2013 Apr;23(4):455-7.

Brunet T, Bouclet A, Ahmadi P, Mitrossilis D, Driquez B, Brunet AC, Henry L, Serman F, Béalle G, Ménager C, Dumas-Bouchiat F, Givord D, Yanicostas C, Le-Roy D, Dempsey NM, Plessis A, Farge E, , Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria., Nat Commun 2013 ; 4(): 2821.

Rochani AK, Singh M, Tatu U, , Heat shock protein 90 inhibitors as broad spectrum anti-infectives., Curr Pharm Des 2013 ; 19(3): 377-86.

Avgousti DC, Cecere G, Grishok A, The conserved PHD1-PHD2 domain of ZFP-1/AF10 is a discrete functional module essential for viability in Caenorhabditis elegans, Mol. Cell. Biol. 2013 Mar;33(5):999-1015.

Lallemand Y, Moreau J, Cloment CS, Vives FL, Robert B, Generation and characterization of a tamoxifen inducible Msx1(CreERT2) knock-in allele, Genesis 2013 Feb;51(2):110-9.

Li H, Collado M, Villasante A, Matheu A, Lynch CJ, Cañamero M, Rizzoti K, Carneiro C, Martínez G, Vidal A, Lovell-Badge R, Serrano M, p27(Kip1) directly represses Sox2 during embryonic stem cell differentiation, Cell Stem Cell 2012 Dec;11(6):845-52.

Hughes IA, Morel Y, McElreavey K, Rogol A, Biological assessment of abnormal genitalia, J Pediatr Urol 2012 Dec;8(6):592-6.

Mourikis P, Gopalakrishnan S, Sambasivan R, Tajbakhsh S, Cell-autonomous Notch activity maintains the temporal specification potential of skeletal muscle stem cells, Development 2012 Dec;139(24):4536-48.

Guardiola O, Lafuste P, Brunelli S, Iaconis S, Touvier T, Mourikis P, De Bock K, Lonardo E, Andolfi G, Bouché A, Liguori GL, Shen MM, Tajbakhsh S, Cossu G, Carmeliet P, Minchiotti G, Cripto regulates skeletal muscle regeneration and modulates satellite cell determination by antagonizing myostatin, Proc. Natl. Acad. Sci. U.S.A. 2012 Nov;109(47):E3231-40.

Dornier E, Coumailleau F, Ottavi JF, Moretti J, Boucheix C, Mauduit P, Schweisguth F, Rubinstein E, TspanC8 tetraspanins regulate ADAM10/Kuzbanian trafficking and promote Notch activation in flies and mammals, J. Cell Biol. 2012 Oct;199(3):481-96.

Liu S, Bonner JM, Chanet S, Commisso C, Skwarek LC, Schweisguth F, Boulianne GL, Functional analysis of the NHR2 domain indicates that oligomerization of Neuralized regulates ubiquitination and endocytosis of Delta during Notch signaling, Mol. Cell. Biol. 2012 Dec;32(24):4933-45.

Bashamboo A, McElreavey K, Gene mutations associated with anomalies of human gonad formation, Sex Dev 2013;7(1-3):126-46.

Anderson C, Williams VC, Moyon B, Daubas P, Tajbakhsh S, Buckingham ME, Shiroishi T, Hughes SM, Borycki AG, Sonic hedgehog acts cell-autonomously on muscle precursor cells to generate limb muscle diversity, Genes Dev. 2012 Sep;26(18):2103-17.

Harvey RP, Tajbakhsh S, Biased DNA segregation and cardiac stem cell therapies, Circ. Res. 2012 Sep;111(7):827-30.

Mounier J, Boncompain G, Senerovic L, Lagache T, Chrétien F, Perez F, Kolbe M, Olivo-Marin JC, Sansonetti PJ, Sauvonnet N, Shigella effector IpaB-induced cholesterol relocation disrupts the Golgi complex and recycling network to inhibit host cell secretion, Cell Host Microbe 2012 Sep;12(3):381-9.

Domínguez JN, Meilhac SM, Bland YS, Buckingham ME, Brown NA, Asymmetric fate of the posterior part of the second heart field results in unexpected left/right contributions to both poles of the heart, Circ. Res. 2012 Oct;111(10):1323-35.

Le Grand F, Grifone R, Mourikis P, Houbron C, Gigaud C, Pujol J, Maillet M, Pagès G, Rudnicki M, Tajbakhsh S, Maire P, Six1 regulates stem cell repair potential and self-renewal during skeletal muscle regeneration, J. Cell Biol. 2012 Sep;198(5):815-32.

Lescroart F, Mohun T, Meilhac SM, Bennett M, Buckingham M, Lineage tree for the venous pole of the heart: clonal analysis clarifies controversial genealogy based on genetic tracing, Circ. Res. 2012 Oct;111(10):1313-22.

Dulauroy S, Di Carlo SE, Langa F, Eberl G, Peduto L, Lineage tracing and genetic ablation of ADAM12(+) perivascular cells identify a major source of profibrotic cells during acute tissue injury, Nat. Med. 2012 Aug;18(8):1262-70.

Gomez Perdiguero E, Schulz C, Geissmann F, Development and homeostasis of “resident” myeloid cells: the case of the microglia, Glia 2013 Jan;61(1):112-20.

Cecere G, Zheng GX, Mansisidor AR, Klymko KE, Grishok A, Promoters recognized by forkhead proteins exist for individual 21U-RNAs, Mol. Cell 2012 Sep;47(5):734-45.

Nouët Y, Dahan J, Labalette C, Levillayer F, Julien B, Jouvion G, Cairo S, Vives FL, Ribeiro A, Huerre M, Colnot S, Perret C, Nhieu JT, Tordjmann T, Buendia MA, Wei Y, The four and a half LIM-only protein 2 regulates liver homeostasis and contributes to carcinogenesis, J. Hepatol. 2012 Nov;57(5):1029-36.

Galeotti C, Lahlou Z, Goullon D, Sarda-Thibault H, Cahen-Varsaux J, Bignon-Topalovic J, Bashamboo A, McElreavey K, Brauner R, Longitudinal evaluation of the hypothalamic-pituitary-testicular function in 8 boys with adrenal hypoplasia congenita (AHC) due to NR0B1 mutations, PLoS ONE 2012;7(6):e39828.

Fenina M, Simon-Chazottes D, Vandormael-Pournin S, Soueid J, Langa F, Cohen-Tannoudji M, Bernard BA, Panthier JJ, I-SceI-mediated double-strand break does not increase the frequency of homologous recombination at the Dct locus in mouse embryonic stem cells, PLoS ONE 2012;7(6):e39895.

Ghorbel M, Gargouri SB, Zribi N, Abdallah FB, Cherif M, Keskes R, Chakroun N, Sellami A, McElreavey K, Fakhfakh F, Ammar-Keskes L, Partial microdeletions in the Y-chromosome AZFc region are not a significant risk factor for spermatogenic impairment in Tunisian infertile men, Genet Test Mol Biomarkers 2012 Jul;16(7):775-9.

Latil M, Rocheteau P, Châtre L, Sanulli S, Mémet S, Ricchetti M, Tajbakhsh S, Chrétien F, , Skeletal muscle stem cells adopt a dormant cell state post mortem and retain regenerative capacity., Nat Commun 2012 Jun; 3(): 903.

Coolen M, Thieffry D, Drivenes Ø, Becker TS, Bally-Cuif L, miR-9 controls the timing of neurogenesis through the direct inhibition of antagonistic factors, Dev. Cell 2012 May;22(5):1052-64.

Strähle U, Bally-Cuif L, Kelsh R, Beis D, Mione M, Panula P, Figueras A, Gothilf Y, Brösamle C, Geisler R, Knedlitschek G, EuFishBioMed (COST Action BM0804): a European network to promote the use of small fishes in biomedical research, Zebrafish 2012 Jun;9(2):90-3.

Chanet S, Schweisguth F, Regulation of epithelial polarity by the E3 ubiquitin ligase Neuralized and the Bearded inhibitors in Drosophila, Nat. Cell Biol. 2012 May;14(5):467-76.

Eloualid A, Rhaissi H, Reguig A, Bounaceur S, El Houate B, Abidi O, Charif M, Louanjli N, Chadli E, Barakat A, Bashamboo A, McElreavey K, Rouba H, Association of spermatogenic failure with the b2/b3 partial AZFc deletion, PLoS ONE 2012;7(4):e34902.

Petzoldt AG, Coutelis JB, Géminard C, Spéder P, Suzanne M, Cerezo D, Noselli S, DE-Cadherin regulates unconventional Myosin ID and Myosin IC in Drosophila left-right asymmetry establishment, Development 2012 May;139(10):1874-84.

Boucherma R, Kridane-Miledi H, Vives FL, Vauchy C, Borg C, Kleinclauss F, Fiette L, Tiberghien P, Lemonnier FA, Rohrlich PS, Huetz F, Loss of central and peripheral CD8+ T-cell tolerance to HFE in mouse models of human familial hemochromatosis, Eur. J. Immunol. 2012 Apr;42(4):851-62.

Radhakrishna U, Nath SK, McElreavey K, Ratnamala U, Sun C, Maiti AK, Gagnebin M, Béna F, Newkirk HL, Sharp AJ, Everman DB, Murray JC, Schwartz CE, Antonarakis SE, Butler MG, Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele, J. Med. Genet. 2012 Apr;49(4):270-6.

Eloualid A, Abidi O, Charif M, El Houate B, Benrahma H, Louanjli N, Chadli E, Ajjemami M, Barakat A, Bashamboo A, McElreavey K, Rhaissi H, Rouba H, Association of the MTHFR A1298C variant with unexplained severe male infertility, PLoS ONE 2012;7(3):e34111.

Schulz C, Gomez Perdiguero E, Chorro L, Szabo-Rogers H, Cagnard N, Kierdorf K, Prinz M, Wu B, Jacobsen SE, Pollard JW, Frampton J, Liu KJ, Geissmann F, A lineage of myeloid cells independent of Myb and hematopoietic stem cells, Science 2012 Apr;336(6077):86-90.

Coïc YM, Baleux F, Poyraz Ö, Thibeaux R, Labruyere E, Chretien F, Sobhani I, Lazure T, Wyplosz B, Schneider G, Mulard L, Sansonetti PJ, Marteyn BS, Design of a specific colonic mucus marker using a human commensal bacterium cell surface domain, J. Biol. Chem. 2012 May;287(19):15916-22.

Gayraud-Morel B, Chrétien F, Jory A, Sambasivan R, Negroni E, Flamant P, Soubigou G, Coppée JY, Di Santo J, Cumano A, Mouly V, Tajbakhsh S, Myf5 haploinsufficiency reveals distinct cell fate potentials for adult skeletal muscle stem cells, J. Cell. Sci. 2012 Apr;125(Pt 7):1738-49.

Mourikis P, Sambasivan R, Castel D, Rocheteau P, Bizzarro V, Tajbakhsh S, A critical requirement for notch signaling in maintenance of the quiescent skeletal muscle stem cell state, Stem Cells 2012 Feb;30(2):243-52.

Amir-Zilberstein L, Blechman J, Sztainberg Y, Norton WH, Reuveny A, Borodovsky N, Tahor M, Bonkowsky JL, Bally-Cuif L, Chen A, Levkowitz G, Homeodomain protein otp and activity-dependent splicing modulate neuronal adaptation to stress, Neuron 2012 Jan;73(2):279-91.

Couturier L, Vodovar N, Schweisguth F, Endocytosis by Numb breaks Notch symmetry at cytokinesis, Nat. Cell Biol. 2012 Feb;14(2):131-9.

Rocheteau P, Gayraud-Morel B, Siegl-Cachedenier I, Blasco MA, Tajbakhsh S, A subpopulation of adult skeletal muscle stem cells retains all template DNA strands after cell division, Cell 2012 Jan;148(1-2):112-25.

Masson JB, Voisinne G, Wong-Ng J, Celani A, Vergassola M, Noninvasive inference of the molecular chemotactic response using bacterial trajectories, Proc. Natl. Acad. Sci. U.S.A. 2012 Jan;109(5):1802-7.

Ravel C, Bashamboo A, Bignon-Topalovic J, Siffroi JP, McElreavey K, Darai E, Polymorphisms in DLGH1 and LAMC1 in Mayer-Rokitansky-Kuster-Hauser syndrome, Reprod. Biomed. Online 2012 Apr;24(4):462-5.

Chayot R, Montagne B, Ricchetti M, , DNA polymerase μ is a global player in the repair of non-homologous end-joining substrates., DNA Repair (Amst) 2012 Jan; 11(1): 22-34.

Seeherunvong T, Ukarapong S, McElreavey K, Berkovitz GD, Perera EM, Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD, J. Pediatr. Endocrinol. Metab. 2012;25(1-2):121-3.

Lescroart F, Meilhac SM, Cell lineages, growth and repair of the mouse heart, Results Probl Cell Differ 2012;55:263-89.

Freyer L, Aggarwal V, Morrow BE, Dual embryonic origin of the mammalian otic vesicle forming the inner ear, Development 2011 Dec;138(24):5403-14.

Baumgart EV, Barbosa JS, Bally-Cuif L, Götz M, Ninkovic J, Stab wound injury of the zebrafish telencephalon: a model for comparative analysis of reactive gliosis, Glia 2012 Mar;60(3):343-57.

Galaup A, Gomez E, Souktani R, Durand M, Cazes A, Monnot C, Teillon J, Le Jan S, Bouleti C, Briois G, Philippe J, Pons S, Martin V, Assaly R, Bonnin P, Ratajczak P, Janin A, Thurston G, Valenzuela DM, Murphy AJ, Yancopoulos GD, Tissier R, Berdeaux A, Ghaleh B, Germain S, Protection against myocardial infarction and no-reflow through preservation of vascular integrity by angiopoietin-like 4, Circulation 2012 Jan;125(1):140-9.

Menendez S, Camus S, Herreria A, Paramonov I, Morera LB, Collado M, Pekarik V, Maceda I, Edel M, Consiglio A, Sanchez A, Li H, Serrano M, Belmonte JC, Increased dosage of tumor suppressors limits the tumorigenicity of iPS cells without affecting their pluripotency, Aging Cell 2012 Feb;11(1):41-50.

Pontier SM, Schweisguth F, Glycosphingolipids in signaling and development: from liposomes to model organisms, Dev. Dyn. 2012 Jan;241(1):92-106.

Allali S, Muller JB, Brauner R, Lourenço D, Boudjenah R, Karageorgou V, Trivin C, Lottmann H, Lortat-Jacob S, Nihoul-Fékété C, De Dreuzy O, McElreavey K, Bashamboo A, Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadias, PLoS ONE 2011;6(10):e24117.

Grey C, Barthès P, Chauveau-Le Friec G, Langa F, Baudat F, de Massy B, Mouse PRDM9 DNA-binding specificity determines sites of histone H3 lysine 4 trimethylation for initiation of meiotic recombination, PLoS Biol. 2011 Oct;9(10):e1001176.

Mansisidor AR, Cecere G, Hoersch S, Jensen MB, Kawli T, Kennedy LM, Chavez V, Tan MW, Lieb JD, Grishok A, A conserved PHD finger protein and endogenous RNAi modulate insulin signaling in Caenorhabditis elegans, PLoS Genet. 2011 Sep;7(9):e1002299.

Perdigoto CN, Schweisguth F, Bardin AJ, Distinct levels of Notch activity for commitment and terminal differentiation of stem cells in the adult fly intestine, Development 2011 Nov;138(21):4585-95.

Norton WH, Stumpenhorst K, Faus-Kessler T, Folchert A, Rohner N, Harris MP, Callebert J, Bally-Cuif L, Modulation of Fgfr1a signaling in zebrafish reveals a genetic basis for the aggression-boldness syndrome, J. Neurosci. 2011 Sep;31(39):13796-807.

Spéder P, Liu J, Brand AH, Nutrient control of neural stem cells, Curr. Opin. Cell Biol. 2011 Dec;23(6):724-9.

Buckingham ME, Meilhac SM, Tracing cells for tracking cell lineage and clonal behavior, Dev. Cell 2011 Sep;21(3):394-409.

Sambasivan R, Yao R, Kissenpfennig A, Van Wittenberghe L, Paldi A, Gayraud-Morel B, Guenou H, Malissen B, Tajbakhsh S, Galy A, Pax7-expressing satellite cells are indispensable for adult skeletal muscle regeneration, Development 2011 Sep;138(17):3647-56.

Tajbakhsh S, Cavalli G, Richet E, Integrated gene regulatory circuits: celebrating the 50(th) anniversary of the operon model, Mol. Cell 2011 Aug;43(4):505-14.

Brauner R, Neve M, Allali S, Trivin C, Lottmann H, Bashamboo A, McElreavey K, Clinical, biological and genetic analysis of anorchia in 26 boys, PLoS ONE 2011;6(8):e23292.

Perdiguero EG, Galaup A, Durand M, Teillon J, Philippe J, Valenzuela DM, Murphy AJ, Yancopoulos GD, Thurston G, Germain S, Alteration of developmental and pathological retinal angiogenesis in angptl4-deficient mice, J. Biol. Chem. 2011 Oct;286(42):36841-51.

Chapouton P, Webb KJ, Stigloher C, Alunni A, Adolf B, Hesl B, Topp S, Kremmer E, Bally-Cuif L, Expression of hairy/enhancer of split genes in neural progenitors and neurogenesis domains of the adult zebrafish brain, J. Comp. Neurol. 2011 Jun;519(9):1748-69.

Sambasivan R, Kuratani S, Tajbakhsh S, An eye on the head: the development and evolution of craniofacial muscles, Development 2011 Jun;138(12):2401-15.

Webb KJ, Coolen M, Gloeckner CJ, Stigloher C, Bahn B, Topp S, Ueffing M, Bally-Cuif L, The Enhancer of split transcription factor Her8a is a novel dimerisation partner for Her3 that controls anterior hindbrain neurogenesis in zebrafish, BMC Dev. Biol. 2011;11:27.

Dumitrache LC, Hu L, Son MY, Li H, Wesevich A, Scully R, Stark J, Hasty P, Trex2 enables spontaneous sister chromatid exchanges without facilitating DNA double-strand break repair, Genetics 2011 Aug;188(4):787-97.

Villasante A, Piazzolla D, Li H, Gomez-Lopez G, Djabali M, Serrano M, Epigenetic regulation of Nanog expression by Ezh2 in pluripotent stem cells, Cell Cycle 2011 May;10(9):1488-98.

Nowlan NC, Dumas G, Tajbakhsh S, Prendergast PJ, Murphy P, Biophysical stimuli induced by passive movements compensate for lack of skeletal muscle during embryonic skeletogenesis, Biomech Model Mechanobiol 2012 Jan;11(1-2):207-19.

Zou Z, Hu H, Song M, Shen Y, Guo X, McElreavey K, Bittles AH, Wang W, Semen quality analysis of military personnel from six geographical areas of the People’s Republic of China, Fertil. Steril. 2011 May;95(6):2018-23, 2023.e1-3.

Chatre L, Ricchetti M, , Nuclear mitochondrial DNA activates replication in Saccharomyces cerevisiae., PLoS One 2011 Mar; 6(3): e17235.

Rothenaigner I, Krecsmarik M, Hayes JA, Bahn B, Lepier A, Fortin G, Götz M, Jagasia R, Bally-Cuif L, Clonal analysis by distinct viral vectors identifies bona fide neural stem cells in the adult zebrafish telencephalon and characterizes their division properties and fate, Development 2011 Apr;138(8):1459-69.

Adam L, Kozar M, Letort G, Mirat O, Srivastava A, Stewart T, Wilson ML, Peccoud J, Strengths and limitations of the federal guidance on synthetic DNA., Nat Biotechnol 2011 Mar; 29(3): 208-10.

Montjean D, Benkhalifa M, Dessolle L, Cohen-Bacrie P, Belloc S, Siffroi JP, Ravel C, Bashamboo A, McElreavey K, Polymorphisms in MTHFR and MTRR genes associated with blood plasma homocysteine concentration and sperm counts, Fertil. Steril. 2011 Feb;95(2):635-40.

Radosevic M, Robert-Moreno A, Coolen M, Bally-Cuif L, Alsina B, Her9 represses neurogenic fate downstream of Tbx1 and retinoic acid signaling in the inner ear, Development 2011 Feb;138(3):397-408.

Guo X, Freyer L, Morrow B, Zheng D, Characterization of the past and current duplication activities in the human 22q11.2 region, BMC Genomics 2011 Jan;12:71.

del Álamo D, Rouault H, Schweisguth F, Mechanism and significance of cis-inhibition in Notch signalling, Curr. Biol. 2011 Jan;21(1):R40-7.

Lourenço D, Brauner R, Rybczynska M, Nihoul-Fékété C, McElreavey K, Bashamboo A, Loss-of-function mutation in GATA4 causes anomalies of human testicular development, Proc. Natl. Acad. Sci. U.S.A. 2011 Jan;108(4):1597-602.

Dumic M, New MI, Lin-Su K, McElreavey K, Leibel NI, Ciglar S, Nimkarn S, Vinci G, Wilson J, Lasan R, Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual development, Adv. Exp. Med. Biol. 2011;707:169-70.

McElreavey K, Bashamboo A, Genetic disorders of sex differentiation, Adv. Exp. Med. Biol. 2011;707:91-9.

Todorovic V, Finnegan E, Freyer L, Zilberberg L, Ota M, Rifkin DB, Long form of latent TGF-β binding protein 1 (Ltbp1L) regulates cardiac valve development, Dev. Dyn. 2011 Jan;240(1):176-87.

Funfak A, Cao J, Knauer A, Martin K, Köhler JM, Synergistic effects of metal nanoparticles and a phenolic uncoupler using microdroplet-based two-dimensional approach, J Environ Monit 2011 Feb;13(2):410-5.

Ghozzi S, Wong Ng J, Chatenay D, Robert J, Inference of plasmid-copy-number mean and noise from single-cell gene expression data, Phys Rev E Stat Nonlin Soft Matter Phys 2010 Nov;82(5 Pt 1):051916.

Chayot R, Danckaert A, Montagne B, Ricchetti M, , Lack of DNA polymerase μ affects the kinetics of DNA double-strand break repair and impacts on cellular senescence., DNA Repair (Amst) 2010 Nov; 9(11): 1187-99.

Gros J, Hu JK, Vinegoni C, Feruglio PF, Weissleder R, Tabin CJ, WNT5A/JNK and FGF/MAPK pathways regulate the cellular events shaping the vertebrate limb bud, Curr. Biol. 2010 Nov;20(22):1993-2002.

Lynch CJ, Shah ZH, Allison SJ, Ahmed SU, Ford J, Warnock LJ, Li H, Serrano M, Milner J, SIRT1 undergoes alternative splicing in a novel auto-regulatory loop with p53, PLoS ONE 2010;5(10):e13502.

Bashamboo A, Ferraz-de-Souza B, Lourenço D, Lin L, Sebire NJ, Montjean D, Bignon-Topalovic J, Mandelbaum J, Siffroi JP, Christin-Maitre S, Radhakrishna U, Rouba H, Ravel C, Seeler J, Achermann JC, McElreavey K, Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1, Am. J. Hum. Genet. 2010 Oct;87(4):505-12.

Lescroart F, Kelly RG, Le Garrec JF, Nicolas JF, Meilhac SM, Buckingham M, Clonal analysis reveals common lineage relationships between head muscles and second heart field derivatives in the mouse embryo, Development 2010 Oct;137(19):3269-79.

Sawa S, Cherrier M, Lochner M, Satoh-Takayama N, Fehling HJ, Langa F, Di Santo JP, Eberl G, Lineage relationship analysis of RORgammat+ innate lymphoid cells, Science 2010 Oct;330(6004):665-9.

Suzanne M, Petzoldt AG, Spéder P, Coutelis JB, Steller H, Noselli S, Coupling of apoptosis and L/R patterning controls stepwise organ looping, Curr. Biol. 2010 Oct;20(19):1773-8.

Theis S, Patel K, Valasek P, Otto A, Pu Q, Harel I, Tzahor E, Tajbakhsh S, Christ B, Huang R, The occipital lateral plate mesoderm is a novel source for vertebrate neck musculature, Development 2010 Sep;137(17):2961-71.

Norton W, Bally-Cuif L, Adult zebrafish as a model organism for behavioural genetics, BMC Neurosci 2010;11:90.

Tajbakhsh S, [Unravelling the mysteries of biased DNA segregation during mitosis], Med Sci (Paris) 2010 Aug-Sep;26(8-9):696-8.

Rouault H, Mazouni K, Couturier L, Hakim V, Schweisguth F, Genome-wide identification of cis-regulatory motifs and modules underlying gene coregulation using statistics and phylogeny, Proc. Natl. Acad. Sci. U.S.A. 2010 Aug;107(33):14615-20.

Weiss L, Piketty C, Assoumou L, Didier C, Caccavelli L, Donkova-Petrini V, Levy Y, Girard PM, Burgard M, Viard JP, Rouzioux C, Costagliola D, , Relationship between regulatory T cells and immune activation in human immunodeficiency virus-infected patients interrupting antiretroviral therapy, PLoS ONE 2010;5(7):e11659.

Bashamboo A, Ledig S, Wieacker P, Achermann JC, Achermann J, McElreavey K, New technologies for the identification of novel genetic markers of disorders of sex development (DSD), Sex Dev 2010 Sep;4(4-5):213-24.

Rousset R, Bono-Lauriol S, Gettings M, Suzanne M, Spéder P, Noselli S, The Drosophila serine protease homologue Scarface regulates JNK signalling in a negative-feedback loop during epithelial morphogenesis, Development 2010 Jul;137(13):2177-86.

Brauner R, Bashamboo A, Rouget S, Goulet M, Philibert P, Sarda-Thibault H, Trivin C, Misrahi M, Sultan C, McElreavey K, Clinical, biological and genetic analysis of prepubertal isolated ovarian cyst in 11 girls, PLoS ONE 2010;5(6):e11282.

Chapouton P, Skupien P, Hesl B, Coolen M, Moore JC, Madelaine R, Kremmer E, Faus-Kessler T, Blader P, Lawson ND, Bally-Cuif L, Notch activity levels control the balance between quiescence and recruitment of adult neural stem cells, J. Neurosci. 2010 Jun;30(23):7961-74.

Henrique D, Bally-Cuif L, A cross-disciplinary approach to understanding neural stem cells in development and disease, Development 2010 Jun;137(12):1933-8.

Sinha DK, Neveu P, Gagey N, Aujard I, Le Saux T, Rampon C, Gauron C, Kawakami K, Leucht C, Bally-Cuif L, Volovitch M, Bensimon D, Jullien L, Vriz S, Photoactivation of the CreER T2 recombinase for conditional site-specific recombination with high spatiotemporal resolution, Zebrafish 2010 Jun;7(2):199-204.

Freyer L, Morrow BE, Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle, Dev. Dyn. 2010 Jun;239(6):1708-22.

Aggarwal VS, Carpenter C, Freyer L, Liao J, Petti M, Morrow BE, Mesodermal Tbx1 is required for patterning the proximal mandible in mice, Dev. Biol. 2010 Aug;344(2):669-81.

Miquerol L, Moreno-Rascon N, Beyer S, Dupays L, Meilhac SM, Buckingham ME, Franco D, Kelly RG, Biphasic development of the mammalian ventricular conduction system, Circ. Res. 2010 Jul;107(1):153-61.

März M, Chapouton P, Diotel N, Vaillant C, Hesl B, Takamiya M, Lam CS, Kah O, Bally-Cuif L, Strähle U, Heterogeneity in progenitor cell subtypes in the ventricular zone of the zebrafish adult telencephalon, Glia 2010 May;58(7):870-88.

Benhra N, Vignaux F, Dussert A, Schweisguth F, Le Borgne R, Neuralized promotes basal to apical transcytosis of delta in epithelial cells, Mol. Biol. Cell 2010 Jun;21(12):2078-86.

Shimeld SM, Boyle MJ, Brunet T, Luke GN, Seaver EC, , Clustered Fox genes in lophotrochozoans and the evolution of the bilaterian Fox gene cluster., Dev Biol 2010 Apr; 340(2): 234-48.

Bashamboo A, McElreavey K, NR5A1/SF-1 and development and function of the ovary, Ann. Endocrinol. (Paris) 2010 May;71(3):177-82.

Bardin AJ, Perdigoto CN, Southall TD, Brand AH, Schweisguth F, Transcriptional control of stem cell maintenance in the Drosophila intestine, Development 2010 Mar;137(5):705-14.

Hamel S, Fantini J, Schweisguth F, Notch ligand activity is modulated by glycosphingolipid membrane composition in Drosophila melanogaster, J. Cell Biol. 2010 Feb;188(4):581-94.

Chayot R, Montagne B, Mazel D, Ricchetti M, , An end-joining repair mechanism in Escherichia coli., Proc Natl Acad Sci U S A 2010 Feb; 107(5): 2141-6.

Wong Ng J, Chatenay D, Robert J, Poirier MG, Plasmid copy number noise in monoclonal populations of bacteria, Phys Rev E Stat Nonlin Soft Matter Phys 2010 Jan;81(1 Pt 1):011909.

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Sambasivan R, Tajbakhsh S, Skeletal muscle stem cell birth and properties, Semin. Cell Dev. Biol. 2007 Dec;18(6):870-82.

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Ravel C, Chantot-Bastaraud S, McElreavey K, Siffroi JP, [Molecular anomalies of the Y chromosome: Consequences on male fertility], Gynecol Obstet Fertil 2006 Oct;34(10):885-93.

Ravel C, El Houate B, Chantot S, Lourenço D, Dumaine A, Rouba H, Bandyopadahyay A, Radhakrishna U, Das B, Sengupta S, Mandelbaum J, Siffroi JP, McElreavey K, Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26, Mol. Hum. Reprod. 2006 Oct;12(10):643-6.

Stigloher C, Ninkovic J, Laplante M, Geling A, Tannhäuser B, Topp S, Kikuta H, Becker TS, Houart C, Bally-Cuif L, Segregation of telencephalic and eye-field identities inside the zebrafish forebrain territory is controlled by Rx3, Development 2006 Aug;133(15):2925-35.

Ninkovic J, Bally-Cuif L, The zebrafish as a model system for assessing the reinforcing properties of drugs of abuse, Methods 2006 Jul;39(3):262-74.

Shinin V, Gayraud-Morel B, Gomès D, Tajbakhsh S, Asymmetric division and cosegregation of template DNA strands in adult muscle satellite cells, Nat. Cell Biol. 2006 Jul;8(7):677-87.

Delmaghani S, del Castillo FJ, Michel V, Leibovici M, Aghaie A, Ron U, Van Laer L, Ben-Tal N, Van Camp G, Weil D, Langa F, Lathrop M, Avan P, Petit C, Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy, Nat. Genet. 2006 Jul;38(7):770-8.

Alves BC, Mayer MG, Taber AP, Egito AA, Fagundes V, McElreavey K, Moreira-Filho CA, Molecular characterization of a bovine Y-specific DNA sequence conserved in taurine and zebu breeds, DNA Seq. 2006 Jun;17(3):199-202.

Stefano G, Renna L, Hanton SL, Chatre L, Haas TA, Brandizzi F, ARL1 plays a role in the binding of the GRIP domain of a peripheral matrix protein to the Golgi apparatus in plant cells, Plant Mol. Biol. 2006 Jun;61(3):431-49.

Adolf B, Chapouton P, Lam CS, Topp S, Tannhäuser B, Strähle U, Götz M, Bally-Cuif L, Conserved and acquired features of adult neurogenesis in the zebrafish telencephalon, Dev. Biol. 2006 Jul;295(1):278-93.

Franco D, Meilhac SM, Christoffels VM, Kispert A, Buckingham M, Kelly RG, Left and right ventricular contributions to the formation of the interventricular septum in the mouse heart, Dev. Biol. 2006 Jun;294(2):366-75.

Foucher I, Mione M, Simeone A, Acampora D, Bally-Cuif L, Houart C, Differentiation of cerebellar cell identities in absence of Fgf signalling in zebrafish Otx morphants, Development 2006 May;133(10):1891-900.

Cheng HH, Ying M, Tian YH, Guo Y, McElreavey K, Zhou RJ, Transcriptional diversity of DMRT1 (dsx- and mab3-related transcription factor 1) in human testis, Cell Res. 2006 Apr;16(4):389-93.

Spéder P, Adám G, Noselli S, Type ID unconventional myosin controls left-right asymmetry in Drosophila, Nature 2006 Apr;440(7085):803-7.

Hozumi S, Maeda R, Taniguchi K, Kanai M, Shirakabe S, Sasamura T, Spéder P, Noselli S, Aigaki T, Murakami R, Matsuno K, An unconventional myosin in Drosophila reverses the default handedness in visceral organs, Nature 2006 Apr;440(7085):798-802.

Stefano G, Renna L, Chatre L, Hanton SL, Moreau P, Hawes C, Brandizzi F, In tobacco leaf epidermal cells, the integrity of protein export from the endoplasmic reticulum and of ER export sites depends on active COPI machinery, Plant J. 2006 Apr;46(1):95-110.

Ninkovic J, Folchert A, Makhankov YV, Neuhauss SC, Sillaber I, Straehle U, Bally-Cuif L, Genetic identification of AChE as a positive modulator of addiction to the psychostimulant D-amphetamine in zebrafish, J. Neurobiol. 2006 Apr;66(5):463-75.

Bajanca F, Luz M, Raymond K, Martins GG, Sonnenberg A, Tajbakhsh S, Buckingham M, Thorsteinsdóttir S, Integrin alpha6beta1-laminin interactions regulate early myotome formation in the mouse embryo, Development 2006 May;133(9):1635-44.

Palmer CN, Irvine AD, Terron-Kwiatkowski A, Zhao Y, Liao H, Lee SP, Goudie DR, Sandilands A, Campbell LE, Smith FJ, O'Regan GM, Watson RM, Cecil JE, Bale SJ, Compton JG, DiGiovanna JJ, Fleckman P, Lewis-Jones S, Arseculeratne G, Sergeant A, Munro CS, El Houate B, McElreavey K, Halkjaer LB, Bisgaard H, Mukhopadhyay S, McLean WH, Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis, Nat. Genet. 2006 Apr;38(4):441-6.

Bardin AJ, Schweisguth F, Bearded family members inhibit Neuralized-mediated endocytosis and signaling activity of Delta in Drosophila, Dev. Cell 2006 Feb;10(2):245-55.

McElreavey K, Ravel C, Chantot-Bastaraud S, Siffroi JP, Y chromosome variants and male reproductive function, Int. J. Androl. 2006 Feb;29(1):298-303; discussion 304-6.

Esner M, Meilhac SM, Relaix F, Nicolas JF, Cossu G, Buckingham ME, Smooth muscle of the dorsal aorta shares a common clonal origin with skeletal muscle of the myotome, Development 2006 Feb;133(4):737-49.

Patin E, Barreiro LB, Sabeti PC, Austerlitz F, Luca F, Sajantila A, Behar DM, Semino O, Sakuntabhai A, Guiso N, Gicquel B, McElreavey K, Harding RM, Heyer E, Quintana-Murci L, Deciphering the ancient and complex evolutionary history of human arylamine N-acetyltransferase genes, Am. J. Hum. Genet. 2006 Mar;78(3):423-36.

Barreiro LB, Neyrolles O, Babb CL, Tailleux L, Quach H, McElreavey K, Helden PD, Hoal EG, Gicquel B, Quintana-Murci L, Promoter variation in the DC-SIGN-encoding gene CD209 is associated with tuberculosis, PLoS Med. 2006 Feb;3(2):e20.

Ravel C, Chantot-Bastaraud S, El Houate B, Mandelbaum J, Siffroi JP, McElreavey K, GR/GR deletions within the azoospermia factor c region on the Y chromosome might not be associated with spermatogenic failure, Fertil. Steril. 2006 Jan;85(1):229-31.

Bally-Cuif L, Teleosts: simple organisms? Complex behavior, Zebrafish 2006;3(2):127-30.

Relaix F, Montarras D, Zaffran S, Gayraud-Morel B, Rocancourt D, Tajbakhsh S, Mansouri A, Cumano A, Buckingham M, Pax3 and Pax7 have distinct and overlapping functions in adult muscle progenitor cells, J. Cell Biol. 2006 Jan;172(1):91-102.

Radtke F, Schweisguth F, Pear W, The Notch ‘gospel’, EMBO Rep. 2005 Dec;6(12):1120-5.

Hamade A, Deries M, Begemann G, Bally-Cuif L, Genêt C, Sabatier F, Bonnieu A, Cousin X, Retinoic acid activates myogenesis in vivo through Fgf8 signalling, Dev. Biol. 2006 Jan;289(1):127-40.

David NB, Martin CA, Segalen M, Rosenfeld F, Schweisguth F, Bellaïche Y, Drosophila Ric-8 regulates Galphai cortical localization to promote Galphai-dependent planar orientation of the mitotic spindle during asymmetric cell division, Nat. Cell Biol. 2005 Nov;7(11):1083-90.

Manceau M, Marcelle C, Gros J, [A common somitic origin for embryonic muscle progenitors], Med Sci (Paris) 2005 Nov;21(11):915-7.

Buckingham M, Meilhac S, Zaffran S, Building the mammalian heart from two sources of myocardial cells, Nat. Rev. Genet. 2005 Nov;6(11):826-35.

Chatre L, Brandizzi F, Hocquellet A, Hawes C, Moreau P, Sec22 and Memb11 are v-SNAREs of the anterograde endoplasmic reticulum-Golgi pathway in tobacco leaf epidermal cells, Plant Physiol. 2005 Nov;139(3):1244-54.

Hanton SL, Renna L, Bortolotti LE, Chatre L, Stefano G, Brandizzi F, Diacidic motifs influence the export of transmembrane proteins from the endoplasmic reticulum in plant cells, Plant Cell 2005 Nov;17(11):3081-93.

Yaneva M, Li H, Marple T, Hasty P, Non-homologous end joining, but not homologous recombination, enables survival for cells exposed to a histone deacetylase inhibitor, Nucleic Acids Res. 2005;33(16):5320-30.

Dufour A, Shinin V, Tajbakhsh S, Guillén-Aghion N, Olivo-Marin JC, Zimmer C, Segmenting and tracking fluorescent cells in dynamic 3-D microscopy with coupled active surfaces, IEEE Trans Image Process 2005 Sep;14(9):1396-410.

Linker C, Lesbros C, Gros J, Burrus LW, Rawls A, Marcelle C, beta-Catenin-dependent Wnt signalling controls the epithelial organisation of somites through the activation of paraxis, Development 2005 Sep;132(17):3895-905.

Beis D, Bartman T, Jin SW, Scott IC, D'Amico LA, Ober EA, Verkade H, Frantsve J, Field HA, Wehman A, Baier H, Tallafuss A, Bally-Cuif L, Chen JN, Stainier DY, Jungblut B, Genetic and cellular analyses of zebrafish atrioventricular cushion and valve development, Development 2005 Sep;132(18):4193-204.

Ergun-Longmire B, Vinci G, Alonso L, Matthew S, Tansil S, Lin-Su K, McElreavey K, New MI, Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature, J. Pediatr. Endocrinol. Metab. 2005 Aug;18(8):739-48.

Holzschuh J, Wada N, Wada C, Schaffer A, Javidan Y, Tallafuss A, Bally-Cuif L, Schilling TF, Requirements for endoderm and BMP signaling in sensory neurogenesis in zebrafish, Development 2005 Aug;132(16):3731-42.

Kassar-Duchossoy L, Giacone E, Gayraud-Morel B, Jory A, Gomès D, Tajbakhsh S, Pax3/Pax7 mark a novel population of primitive myogenic cells during development, Genes Dev. 2005 Jun;19(12):1426-31.

Tajbakhsh S, Skeletal muscle stem and progenitor cells: reconciling genetics and lineage, Exp. Cell Res. 2005 Jun;306(2):364-72.

Meau-Petit V, Marcou V, Trivin C, Lortat-Jacob S, McElreavey K, Brauner R, Idiopathic male pseudohermaphroditism: variations in presentation and management, J. Pediatr. Endocrinol. Metab. 2005 Jun;18(6):569-75.

Patsalis PC, Skordis N, Sismani C, Kousoulidou L, Koumbaris G, Eftychi C, Stavrides G, Ioulianos A, Kitsiou-Tzeli S, Galla-Voumvouraki A, Kosmaidou Z, Hadjiathanasiou CG, McElreavey K, Identification of high frequency of Y chromosome deletions in patients with sex chromosome mosaicism and correlation with the clinical phenotype and Y-chromosome instability, Am. J. Med. Genet. A 2005 Jun;135(2):145-9.

Langevin J, Le Borgne R, Rosenfeld F, Gho M, Schweisguth F, Bellaïche Y, Lethal giant larvae controls the localization of notch-signaling regulators numb, neuralized, and Sanpodo in Drosophila sensory-organ precursor cells, Curr. Biol. 2005 May;15(10):955-62.

Schweisguth F, Temporal regulation of planar cell polarity: insights from the Drosophila eye, Cell 2005 May;121(4):497-9.

Gros J, Manceau M, Thomé V, Marcelle C, A common somitic origin for embryonic muscle progenitors and satellite cells, Nature 2005 Jun;435(7044):954-8.

Le Borgne R, Bardin A, Schweisguth F, The roles of receptor and ligand endocytosis in regulating Notch signaling, Development 2005 Apr;132(8):1751-62.

Le Borgne R, Remaud S, Hamel S, Schweisguth F, Two distinct E3 ubiquitin ligases have complementary functions in the regulation of delta and serrate signaling in Drosophila, PLoS Biol. 2005 Apr;3(4):e96.

McElreavey K, Quintana-Murci L, A population genetics perspective of the Indus Valley through uniparentally-inherited markers, Ann. Hum. Biol. 2005 Mar-Apr;32(2):154-62.

Vinci G, Raicu F, Popa L, Popa O, Cocos R, McElreavey K, A deletion of a novel heat shock gene on the Y chromosome associated with azoospermia, Mol. Hum. Reprod. 2005 Apr;11(4):295-8.

Loeb-Hennard C, Kremmer E, Bally-Cuif L, Prominent transcription of zebrafish N-myc (nmyc1) in tectal and retinal growth zones during embryonic and early larval development, Gene Expr. Patterns 2005 Feb;5(3):341-7.

Aknin-Seifer IE, Touraine RL, Lejeune H, Jimenez C, Chouteau J, Siffroi JP, McElreavey K, Bienvenu T, Patrat C, Levy R, Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study, Hum. Reprod. 2005 Mar;20(3):736-40.

Quintana-Murci L, Gal I, Bakhan T, Quach H, Sayar SH, Shiri-Sverdlov R, Baruch RG, McElreavey K, Dagan E, Narod S, Friedman E, The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi Jews, Fam. Cancer 2005;4(2):85-8.

McElreavey K, Wang W, Bittles AH, First Asian workshop on genomics and community genetics, Shenzhen, PR China, 10-22 April 2004, Community Genet 2005;8(2):130-2.

Ninkovic J, Tallafuss A, Leucht C, Topczewski J, Tannhäuser B, Solnica-Krezel L, Bally-Cuif L, Inhibition of neurogenesis at the zebrafish midbrain-hindbrain boundary by the combined and dose-dependent activity of a new hairy/E(spl) gene pair, Development 2005 Jan;132(1):75-88.

Vinci G, Anjot MN, Trivin C, Lottmann H, Brauner R, McElreavey K, An analysis of the genetic factors involved in testicular descent in a cohort of 14 male patients with anorchia, J. Clin. Endocrinol. Metab. 2004 Dec;89(12):6282-5.

Machev N, Saut N, Longepied G, Terriou P, Navarro A, Levy N, Guichaoua M, Metzler-Guillemain C, Collignon P, Frances AM, Belougne J, Clemente E, Chiaroni J, Chevillard C, Durand C, Ducourneau A, Pech N, McElreavey K, Mattei MG, Mitchell MJ, Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility, J. Med. Genet. 2004 Nov;41(11):814-25.

Prunotto C, Crepaldi T, Forni PE, Ieraci A, Kelly RG, Tajbakhsh S, Buckingham M, Ponzetto C, Analysis of Mlc-lacZ Met mutants highlights the essential function of Met for migratory precursors of hypaxial muscles and reveals a role for Met in the development of hyoid arch-derived facial muscles, Dev. Dyn. 2004 Nov;231(3):582-91.

Adolf B, Bellipanni G, Huber V, Bally-Cuif L, atoh1.2 and beta3.1 are two new bHLH-encoding genes expressed in selective precursor cells of the zebrafish anterior hindbrain, Gene Expr. Patterns 2004 Nov;5(1):35-41.

Marple T, Li H, Hasty P, A genotoxic screen: rapid analysis of cellular dose-response to a wide range of agents that either damage DNA or alter genome maintenance pathways, Mutat. Res. 2004 Oct;554(1-2):253-66.

Kassar-Duchossoy L, Gayraud-Morel B, Gomès D, Rocancourt D, Buckingham M, Shinin V, Tajbakhsh S, Mrf4 determines skeletal muscle identity in Myf5:Myod double-mutant mice, Nature 2004 Sep;431(7007):466-71.

Ricchetti M, Tekaia F, Dujon B, , Continued colonization of the human genome by mitochondrial DNA., PLoS Biol 2004 Sep; 2(9): E273.

Orgogozo V, Schweisguth F, Evolution of the larval peripheral nervous system in Drosophila species has involved a change in sensory cell lineage, Dev. Genes Evol. 2004 Sep;214(9):442-52.

Haffner C, Frauli M, Topp S, Irmler M, Hofmann K, Regula JT, Bally-Cuif L, Haass C, Nicalin and its binding partner Nomo are novel Nodal signaling antagonists, EMBO J. 2004 Aug;23(15):3041-50.

Zaffran S, Kelly RG, Meilhac SM, Buckingham ME, Brown NA, Right ventricular myocardium derives from the anterior heart field, Circ. Res. 2004 Aug;95(3):261-8.

Schweisguth F, Formation and remodeling of epithelial polarity, Dev. Cell 2004 Jun;6(6):749-55.

Gros J, Scaal M, Marcelle C, A two-step mechanism for myotome formation in chick, Dev. Cell 2004 Jun;6(6):875-82.

Chang TH, Primig M, Hadchouel J, Tajbakhsh S, Rocancourt D, Fernandez A, Kappler R, Scherthan H, Buckingham M, An enhancer directs differential expression of the linked Mrf4 and Myf5 myogenic regulatory genes in the mouse, Dev. Biol. 2004 May;269(2):595-608.

Orgogozo V, Schweisguth F, Bellaïche Y, Slit-Robo signalling prevents sensory cells from crossing the midline in Drosophila, Mech. Dev. 2004 May;121(5):427-36.

Meilhac SM, Esner M, Kelly RG, Nicolas JF, Buckingham ME, The clonal origin of myocardial cells in different regions of the embryonic mouse heart, Dev. Cell 2004 May;6(5):685-98.

Quintana-Murci L, Chaix R, Wells RS, Behar DM, Sayar H, Scozzari R, Rengo C, Al-Zahery N, Semino O, Santachiara-Benerecetti AS, Coppa A, Ayub Q, Mohyuddin A, Tyler-Smith C, Qasim Mehdi S, Torroni A, McElreavey K, Where west meets east: the complex mtDNA landscape of the southwest and Central Asian corridor, Am. J. Hum. Genet. 2004 May;74(5):827-45.

Schweisguth F, [Genetic basis of planar polarity], Med Sci (Paris) 2004 Apr;20(4):424-30.

Geling A, Plessy C, Rastegar S, Strähle U, Bally-Cuif L, Her5 acts as a prepattern factor that blocks neurogenin1 and coe2 expression upstream of Notch to inhibit neurogenesis at the midbrain-hindbrain boundary, Development 2004 May;131(9):1993-2006.

Scaal M, Gros J, Lesbros C, Marcelle C, In ovo electroporation of avian somites, Dev. Dyn. 2004 Mar;229(3):643-50.

Quintana-Murci L, Bigham A, Rouba H, Barakat A, McElreavey K, Hammer M, Y-chromosomal STR haplotypes in Berber and Arabic-speaking populations from Morocco, Forensic Sci. Int. 2004 Feb;140(1):113-5.

Bardin AJ, Le Borgne R, Schweisguth F, Asymmetric localization and function of cell-fate determinants: a fly’s view, Curr. Opin. Neurobiol. 2004 Feb;14(1):6-14.

Schweisguth F, Regulation of notch signaling activity, Curr. Biol. 2004 Feb;14(3):R129-38.

Bellaïche Y, Beaudoin-Massiani O, Stuttem I, Schweisguth F, The planar cell polarity protein Strabismus promotes Pins anterior localization during asymmetric division of sensory organ precursor cells in Drosophila, Development 2004 Jan;131(2):469-78.

Meilhac SM, Esner M, Kerszberg M, Moss JE, Buckingham ME, Oriented clonal cell growth in the developing mouse myocardium underlies cardiac morphogenesis, J. Cell Biol. 2004 Jan;164(1):97-109.

Boyer J, Badis G, Fairhead C, Talla E, Hantraye F, Fabre E, Fischer G, Hennequin C, Koszul R, Lafontaine I, Ozier-Kalogeropoulos O, Ricchetti M, Richard GF, Thierry A, Dujon B, , Large-scale exploration of growth inhibition caused by overexpression of genomic fragments in Saccharomyces cerevisiae., Genome Biol 2004 ; 5(9): R72.

Chapouton P, Bally-Cuif L, Neurogenesis, Methods Cell Biol. 2004;76:163-206.

Maskell PD, Speder P, Newberry NR, Bermudez I, Inhibition of human alpha 7 nicotinic acetylcholine receptors by open channel blockers of N-methyl-D-aspartate receptors, Br. J. Pharmacol. 2003 Dec;140(7):1313-9.

Tallafuss A, Bally-Cuif L, Tracing of her5 progeny in zebrafish transgenics reveals the dynamics of midbrain-hindbrain neurogenesis and maintenance, Development 2003 Sep;130(18):4307-23.

Henrique D, Schweisguth F, Cell polarity: the ups and downs of the Par6/aPKC complex, Curr. Opin. Genet. Dev. 2003 Aug;13(4):341-50.

Tajbakhsh S, Stem cells to tissue: molecular, cellular and anatomical heterogeneity in skeletal muscle, Curr. Opin. Genet. Dev. 2003 Aug;13(4):413-22.

Hadchouel J, Carvajal JJ, Daubas P, Bajard L, Chang T, Rocancourt D, Cox D, Summerbell D, Tajbakhsh S, Rigby PW, Buckingham M, Analysis of a key regulatory region upstream of the Myf5 gene reveals multiple phases of myogenesis, orchestrated at each site by a combination of elements dispersed throughout the locus, Development 2003 Aug;130(15):3415-26.

Meilhac SM, Kelly RG, Rocancourt D, Eloy-Trinquet S, Nicolas JF, Buckingham ME, A retrospective clonal analysis of the myocardium reveals two phases of clonal growth in the developing mouse heart, Development 2003 Aug;130(16):3877-89.

Tallafuss A, Adolf B, Bally-Cuif L, Selective control of neuronal cluster size at the forebrain/midbrain boundary by signaling from the prechordal plate, Dev. Dyn. 2003 Aug;227(4):524-35.

Le Borgne R, Schweisguth F, Unequal segregation of Neuralized biases Notch activation during asymmetric cell division, Dev. Cell 2003 Jul;5(1):139-48.

McElreavey K, Quintana-Murci L, Male reproductive function and the human Y chromosome: is selection acting on the Y?, Reprod. Biomed. Online 2003 Jul-Aug;7(1):17-23.

De La Rochebrochard E, McElreavey K, Thonneau P, Paternal age over 40 years: the “amber light” in the reproductive life of men?, J. Androl. 2003 Jul-Aug;24(4):459-65.

Kablar B, Krastel K, Tajbakhsh S, Rudnicki MA, Myf5 and MyoD activation define independent myogenic compartments during embryonic development, Dev. Biol. 2003 Jun;258(2):307-18.

Jawaheer D, Juo SH, Le Caignec C, David A, Petit C, Gregersen P, Dowbak S, Damle A, McElreavey K, Ostrer H, Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis, Clin. Genet. 2003 Jun;63(6):530-5.

Ricchetti M, Dujon B, Fairhead C, , Distance from the chromosome end determines the efficiency of double strand break repair in subtelomeres of haploid yeast., J Mol Biol 2003 May; 328(4): 847-62.

Le Borgne R, Schweisguth F, Notch signaling: endocytosis makes delta signal better, Curr. Biol. 2003 Apr;13(7):R273-5.

Krausz C, Forti G, McElreavey K, The Y chromosome and male fertility and infertility, Int. J. Androl. 2003 Apr;26(2):70-5.

Geling A, Itoh M, Tallafuss A, Chapouton P, Tannhäuser B, Kuwada JY, Chitnis AB, Bally-Cuif L, bHLH transcription factor Her5 links patterning to regional inhibition of neurogenesis at the midbrain-hindbrain boundary, Development 2003 Apr;130(8):1591-604.

Quintana-Murci L, Weale ME, Thomas MG, Erdei E, Bradman N, Shanks JH, Krausz C, McElreavey K, Y chromosome haplotypes and testicular cancer in the English population, J. Med. Genet. 2003 Mar;40(3):e20.

Morel V, Le Borgne R, Schweisguth F, Snail is required for Delta endocytosis and Notch-dependent activation of single-minded expression, Dev. Genes Evol. 2003 Mar;213(2):65-72.

Bally-Cuif L, Hammerschmidt M, Induction and patterning of neuronal development, and its connection to cell cycle control, Curr. Opin. Neurobiol. 2003 Feb;13(1):16-25.

Schweisguth F, [Cell polarity and asymmetric division in the peripheral nervous system of Drosophila], J. Soc. Biol. 2003;197(1):17-22.

McElreavey K, Quintana-Murci L, Y chromosome haplogroups: a correlation with testicular dysgenesis syndrome?, APMIS 2003 Jan;111(1):106-13; discussion 114.

Le Caignec C, Baron S, McElreavey K, Joubert M, Rival JM, Mechinaud F, David A, 46,XY gonadal dysgenesis: evidence for autosomal dominant transmission in a large kindred, Am. J. Med. Genet. A 2003 Jan;116A(1):37-43.

Meilhac S, Kelly R, Rocancourt D, Buckingham M, [The mouse as a model of heart morphogenesis in mammals: origin and lineage of myocytes], J. Soc. Biol. 2003;197(2):179-86.

Buckingham M, Bajard L, Chang T, Daubas P, Hadchouel J, Meilhac S, Montarras D, Rocancourt D, Relaix F, The formation of skeletal muscle: from somite to limb, J. Anat. 2003 Jan;202(1):59-68.

Frydelund-Larsen L, Krausz C, Leffers H, Andersson AM, Carlsen E, Bangsboell S, McElreavey K, Skakkebaek NE, Rajpert-De Meyts E, Inhibin B: a marker for the functional state of the seminiferous epithelium in patients with azoospermia factor C microdeletions, J. Clin. Endocrinol. Metab. 2002 Dec;87(12):5618-24.

Bellipanni G, Rink E, Bally-Cuif L, Cloning of two tryptophan hydroxylase genes expressed in the diencephalon of the developing zebrafish brain, Mech. Dev. 2002 Dec;119 Suppl 1:S215-20.

Bellipanni G, Rink E, Bally-Cuif L, Cloning of two tryptophan hydroxylase genes expressed in the diencephalon of the developing zebrafish brain, Gene Expr. Patterns 2002 Dec;2(3-4):251-6.

Zammit PS, Heslop L, Hudon V, Rosenblatt JD, Tajbakhsh S, Buckingham ME, Beauchamp JR, Partridge TA, Kinetics of myoblast proliferation show that resident satellite cells are competent to fully regenerate skeletal muscle fibers, Exp. Cell Res. 2002 Nov;281(1):39-49.

Patsalis PC, Sismani C, Quintana-Murci L, Taleb-Bekkouche F, Krausz C, McElreavey K, Effects of transmission of Y chromosome AZFc deletions, Lancet 2002 Oct;360(9341):1222-4.

Orgogozo V, Schweisguth F, Bellaïche Y, Binary cell death decision regulated by unequal partitioning of Numb at mitosis, Development 2002 Oct;129(20):4677-84.

Manni F, Leonardi P, Barakat A, Rouba H, Heyer E, Klintschar M, McElreavey K, Quintana-Murci L, Y-chromosome analysis in Egypt suggests a genetic regional continuity in Northeastern Africa, Hum. Biol. 2002 Oct;74(5):645-58.

Mandon-Pépin B, Derbois C, Matsuda F, Cotinot C, Wolgemuth DJ, Smith K, McElreavey K, Nicolas A, Fellous M, [Human infertility: meiotic genes as potential candidates], Gynecol Obstet Fertil 2002 Oct;30(10):817-21.

Gorlov IP, Kamat A, Bogatcheva NV, Jones E, Lamb DJ, Truong A, Bishop CE, McElreavey K, Agoulnik AI, Mutations of the GREAT gene cause cryptorchidism, Hum. Mol. Genet. 2002 Sep;11(19):2309-18.

Morel F, Duguépéroux I, McElreavey K, Le Bris MJ, Herry A, Parent P, Le Martelot MT, Fellous M, De Braekeleer M, Transmission of an unbalanced (Y;1) translocation in Brittany, France, J. Med. Genet. 2002 Sep;39(9):e52.

Vialard F, Ottolenghi C, Gonzales M, Choiset A, Girard S, Siffroi JP, McElreavey K, Vibert-Guigue C, Sebaoun M, Joyé N, Portnoï MF, Jaubert F, Fellous M, Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses, J. Med. Genet. 2002 Jul;39(7):514-8.

Geling A, Steiner H, Willem M, Bally-Cuif L, Haass C, A gamma-secretase inhibitor blocks Notch signaling in vivo and causes a severe neurogenic phenotype in zebrafish, EMBO Rep. 2002 Jul;3(7):688-94.

Lele Z, Folchert A, Concha M, Rauch GJ, Geisler R, Rosa F, Wilson SW, Hammerschmidt M, Bally-Cuif L, parachute/n-cadherin is required for morphogenesis and maintained integrity of the zebrafish neural tube, Development 2002 Jul;129(14):3281-94.

McElreavey K, Krausz C, Patrat C, Fellous M, [Male infertility and microdeletions of the Y chromosome], Gynecol Obstet Fertil 2002 May;30(5):405-12.

Ortenberg J, Oddoux C, Craver R, McElreavey K, Salas-Cortes L, Guillen-Navarro E, Ostrer H, Sarafoglou K, Clarke V, Yee H, SRY gene expression in the ovotestes of XX true hermaphrodites, J. Urol. 2002 Apr;167(4):1828-31.

Tallafuss A, Bally-Cuif L, Formation of the head-trunk boundary in the animal body plan: an evolutionary perspective, Gene 2002 Apr;287(1-2):23-32.

Ottolenghi C, Fellous M, Barbieri M, McElreavey K, Novel paralogy relations among human chromosomes support a link between the phylogeny of doublesex-related genes and the evolution of sex determination, Genomics 2002 Mar;79(3):333-43.

Le Borgne R, Bellaïche Y, Schweisguth F, Drosophila E-cadherin regulates the orientation of asymmetric cell division in the sensory organ lineage, Curr. Biol. 2002 Jan;12(2):95-104.

McElreavey K, Quintana-Murci L, Understanding inherited disease through human migrations: a south-west Asian perspective, Community Genet 2002;5(3):153-6.

Pieri Pde C, Pereira DH, Glina S, Hallak J, McElreavey K, Moreira-Filho CA, A cost-effective screening test for detecting AZF microdeletions on the human Y chromosome, Genet. Test. 2002;6(3):185-94.

McElreavey K, Mitchell MJ, The sexually transmitted genome, Trends Genet. 2002 Jan;18(1):13-4.

Tajbakhsh S, The genetics of murine skeletal muscle biogenesis, Results Probl Cell Differ 2002;38:61-79.

Krausz C, Quintana-Murci L, Rajpert-De Meyts E, Jørgensen N, Jobling MA, Rosser ZH, Skakkebaek NE, McElreavey K, Identification of a Y chromosome haplogroup associated with reduced sperm counts, Hum. Mol. Genet. 2001 Sep;10(18):1873-7.

Bellaïche Y, Radovic A, Woods DF, Hough CD, Parmentier ML, O'Kane CJ, Bryant PJ, Schweisguth F, The Partner of Inscuteable/Discs-large complex is required to establish planar polarity during asymmetric cell division in Drosophila, Cell 2001 Aug;106(3):355-66.

Bellaïche Y, Schweisguth F, Lineage diversity in the Drosophila nervous system, Curr. Opin. Genet. Dev. 2001 Aug;11(4):418-23.

Bienvenu T, Patrat C, McElreavey K, de Almeida M, Jouannet P, Reduction in the DAZ gene copy number in two infertile men with impaired spermatogenesis, Ann. Genet. 2001 Jul-Sep;44(3):125-8.

McElreavey K, Cortes LS, X-Y translocations and sex differentiation, Semin. Reprod. Med. 2001 Jun;19(2):133-9.

Krausz C, Rajpert-De Meyts E, Frydelund-Larsen L, Quintana-Murci L, McElreavey K, Skakkebaek NE, Double-blind Y chromosome microdeletion analysis in men with known sperm parameters and reproductive hormone profiles: microdeletions are specific for spermatogenic failure, J. Clin. Endocrinol. Metab. 2001 Jun;86(6):2638-42.

Ottolenghi C, Moreira-Filho C, Mendonça BB, Barbieri M, Fellous M, Berkovitz GD, McElreavey K, Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis, J. Clin. Endocrinol. Metab. 2001 Jun;86(6):2465-9.

Krausz C, McElreavey K, Y chromosome microdeletions in ‘fertile’ males, Hum. Reprod. 2001 Jun;16(6):1306-7.

Quintana-Murci L, Krausz C, McElreavey K, The human Y chromosome: function, evolution and disease, Forensic Sci. Int. 2001 May;118(2-3):169-81.

Morel V, Lecourtois M, Massiani O, Maier D, Preiss A, Schweisguth F, Transcriptional repression by suppressor of hairless involves the binding of a hairless-dCtBP complex in Drosophila, Curr. Biol. 2001 May;11(10):789-92.

Nunes M, Blanc I, Maes J, Fellous M, Robert B, McElreavey K, NSPc1, a novel mammalian Polycomb gene, is expressed in neural crest-derived structures of the peripheral nervous system, Mech. Dev. 2001 Apr;102(1-2):219-22.

Orgogozo V, Schweisguth F, Bellaïche Y, Lineage, cell polarity and inscuteable function in the peripheral nervous system of the Drosophila embryo, Development 2001 Mar;128(5):631-43.

Ben-Yaacov S, Le Borgne R, Abramson I, Schweisguth F, Schejter ED, Wasp, the Drosophila Wiskott-Aldrich syndrome gene homologue, is required for cell fate decisions mediated by Notch signaling, J. Cell Biol. 2001 Jan;152(1):1-13.

Quintana-Murci L, Krausz C, Heyer E, Gromoll J, Seifer I, Barton DE, Barrett T, Skakkebaek NE, Rajpert-De Meyts E, Mitchell M, Lee AC, Jobling MA, McElreavey K, The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertility, Hum. Genet. 2001 Jan;108(1):55-8.

Bellaïche Y, Gho M, Kaltschmidt JA, Brand AH, Schweisguth F, Frizzled regulates localization of cell-fate determinants and mitotic spindle rotation during asymmetric cell division, Nat. Cell Biol. 2001 Jan;3(1):50-7.

Quintana-Murci L, Krausz C, Zerjal T, Sayar SH, Hammer MF, Mehdi SQ, Ayub Q, Qamar R, Mohyuddin A, Radhakrishna U, Jobling MA, Tyler-Smith C, McElreavey K, Y-chromosome lineages trace diffusion of people and languages in southwestern Asia, Am. J. Hum. Genet. 2001 Feb;68(2):537-42.

Siffroi JP, Le Bourhis C, Krausz C, Barbaux S, Quintana-Murci L, Kanafani S, Rouba H, Bujan L, Bourrouillou G, Seifer I, Boucher D, Fellous M, McElreavey K, Dadoune JP, Sex chromosome mosaicism in males carrying Y chromosome long arm deletions, Hum. Reprod. 2000 Dec;15(12):2559-62.

Rosser ZH, Zerjal T, Hurles ME, Adojaan M, Alavantic D, Amorim A, Amos W, Armenteros M, Arroyo E, Barbujani G, Beckman G, Beckman L, Bertranpetit J, Bosch E, Bradley DG, Brede G, Cooper G, Côrte-Real HB, de Knijff P, Decorte R, Dubrova YE, Evgrafov O, Gilissen A, Glisic S, Gölge M, Hill EW, Jeziorowska A, Kalaydjieva L, Kayser M, Kivisild T, Kravchenko SA, Krumina A, Kucinskas V, Lavinha J, Livshits LA, Malaspina P, Maria S, McElreavey K, Meitinger TA, Mikelsaar AV, Mitchell RJ, Nafa K, Nicholson J, Nørby S, Pandya A, Parik J, Patsalis PC, Pereira L, Peterlin B, Pielberg G, Prata MJ, Previderé C, Roewer L, Rootsi S, Rubinsztein DC, Saillard J, Santos FR, Stefanescu G, Sykes BC, Tolun A, Villems R, Tyler-Smith C, Jobling MA, Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language, Am. J. Hum. Genet. 2000 Dec;67(6):1526-43.

Ottolenghi C, McElreavey K, Deletions of 9p and the quest for a conserved mechanism of sex determination, Mol. Genet. Metab. 2000 Sep-Oct;71(1-2):397-404.

Le Bourhis C, Siffroi JP, McElreavey K, Dadoune JP, Y chromosome microdeletions and germinal mosaicism in infertile males, Mol. Hum. Reprod. 2000 Aug;6(8):688-93.

Krausz C, Quintana-Murci L, McElreavey K, Prognostic value of Y deletion analysis: what is the clinical prognostic value of Y chromosome microdeletion analysis?, Hum. Reprod. 2000 Jul;15(7):1431-4.

Schweisguth F, Cell polarity: fixing cell polarity with Pins, Curr. Biol. 2000 Apr;10(7):R265-7.

Krausz C, Quintana-Murci L, Fellous M, Siffroi JP, McElreavey K, Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism, Mol. Hum. Reprod. 2000 Apr;6(4):298-302.

Ottolenghi C, Veitia R, Barbieri M, Fellous M, McElreavey K, The human doublesex-related gene, DMRT2, is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript, Genomics 2000 Mar;64(2):179-86.

Ottolenghi C, Veitia R, Quintana-Murci L, Torchard D, Scapoli L, Souleyreau-Therville N, Beckmann J, Fellous M, McElreavey K, The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain, Genomics 2000 Mar;64(2):170-8.

Hanley NA, Hagan DM, Clement-Jones M, Ball SG, Strachan T, Salas-Cortés L, McElreavey K, Lindsay S, Robson S, Bullen P, Ostrer H, Wilson DI, SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development, Mech. Dev. 2000 Mar;91(1-2):403-7.

Lehembre F, Badenhorst P, Müller S, Travers A, Schweisguth F, Dejean A, Covalent modification of the transcriptional repressor tramtrack by the ubiquitin-related protein Smt3 in Drosophila flies, Mol. Cell. Biol. 2000 Feb;20(3):1072-82.

Morel V, Schweisguth F, Repression by suppressor of hairless and activation by Notch are required to define a single row of single-minded expressing cells in the Drosophila embryo, Genes Dev. 2000 Feb;14(3):377-88.

McElreavey K, Krausz C, Bishop CE, The human Y chromosome and male infertility, Results Probl Cell Differ 2000;28:211-32.

McElreavey K, Fellous M, Sex determination and the Y chromosome, Am. J. Med. Genet. 1999 Dec;89(4):176-85.

Quintana-Murci L, Semino O, Bandelt HJ, Passarino G, McElreavey K, Santachiara-Benerecetti AS, Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africa, Nat. Genet. 1999 Dec;23(4):437-41.

Damiani D, Guedes DR, Fellous M, Barbaux S, McElreavey K, Kalil J, Goldberg AC, Moreira-Filho CA, Barbosa A, Della Manna T, Dichtchekenian V, Setian N, Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments, J. Pediatr. Endocrinol. Metab. 1999 Nov-Dec;12(6):827-31.

Hurles ME, Veitia R, Arroyo E, Armenteros M, Bertranpetit J, Pérez-Lezaun A, Bosch E, Shlumukova M, Cambon-Thomsen A, McElreavey K, López De Munain A, Röhl A, Wilson IJ, Singh L, Pandya A, Santos FR, Tyler-Smith C, Jobling MA, Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism, Am. J. Hum. Genet. 1999 Nov;65(5):1437-48.

Ricchetti M, Fairhead C, Dujon B, Mitochondrial DNA repairs double-strand breaks in yeast chromosomes, Nature 1999 Nov;402(6757):96-100.

Krausz C, Quintana-Murci L, Barbaux S, Siffroi JP, Rouba H, Delafontaine D, Souleyreau-Therville N, Arvis G, Antoine JM, Erdei E, Taar JP, Tar A, Jeandidier E, Plessis G, Bourgeron T, Dadoune JP, Fellous M, McElreavey K, A high frequency of Y chromosome deletions in males with nonidiopathic infertility, J. Clin. Endocrinol. Metab. 1999 Oct;84(10):3606-12.

Demmer L, Primack W, Loik V, Brown R, Therville N, McElreavey K, Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46,XX female, J. Am. Soc. Nephrol. 1999 Oct;10(10):2215-8.

Schweisguth F, Dominant-negative mutation in the beta2 and beta6 proteasome subunit genes affect alternative cell fate decisions in the Drosophila sense organ lineage, Proc. Natl. Acad. Sci. U.S.A. 1999 Sep;96(20):11382-6.

Gho M, Bellaïche Y, Schweisguth F, Revisiting the Drosophila microchaete lineage: a novel intrinsically asymmetric cell division generates a glial cell, Development 1999 Aug;126(16):3573-84.

Krausz C, Bussani-Mastellone C, Granchi S, McElreavey K, Scarselli G, Forti G, Screening for microdeletions of Y chromosome genes in patients undergoing intracytoplasmic sperm injection, Hum. Reprod. 1999 Jul;14(7):1717-21.

Schweisguth F, Presenilins in their infancy, Chem. Biol. 1999 Jul;6(7):R187-90.

Krausz C, Siffroi J, Souleyreau-Therville N, Bourgeron T, McElreavey K, Fellous M, [Genetic control of spermatogenesis: Y chromosome and male infertility], Ann. Biol. Clin. (Paris) 1999 May;57(3):309-17.

McElreavey K, Krausz C, Sex Chromosome Genetics ’99. Male infertility and the Y chromosome, Am. J. Hum. Genet. 1999 Apr;64(4):928-33.

Salas-Cortés L, Jaubert F, Barbaux S, Nessmann C, Bono MR, Fellous M, McElreavey K, Rosemblatt M, The human SRY protein is present in fetal and adult Sertoli cells and germ cells, Int. J. Dev. Biol. 1999 Mar;43(2):135-40.

Krausz C, McElreavey K, Y chromosome and male infertility, Front. Biosci. 1999 Jan;4:E1-8.

Veitia RA, Nunes M, Quintana-Murci L, Rappaport R, Thibaud E, Jaubert F, Fellous M, McElreavey K, Gonçalves J, Silva M, Rodrigues JC, Caspurro M, Boieiro F, Marques R, Lavinha J, Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome, Am. J. Hum. Genet. 1998 Sep;63(3):901-5.

Agulnik AI, Zharkikh A, Boettger-Tong H, Bourgeron T, McElreavey K, Bishop CE, Evolution of the DAZ gene family suggests that Y-linked DAZ plays little, or a limited, role in spermatogenesis but underlines a recent African origin for human populations, Hum. Mol. Genet. 1998 Sep;7(9):1371-7.

Lecourtois M, Schweisguth F, Indirect evidence for Delta-dependent intracellular processing of notch in Drosophila embryos, Curr. Biol. 1998 Jun;8(13):771-4.

Gho M, Schweisguth F, Frizzled signalling controls orientation of asymmetric sense organ precursor cell divisions in Drosophila, Nature 1998 May;393(6681):178-81.

Schweisguth F, Lecourtois M, The activity of Drosophila Hairless is required in pupae but not in embryos to inhibit Notch signal transduction, Dev. Genes Evol. 1998 Mar;208(1):19-27.

Ion R, Telvi L, Chaussain JL, Barbet JP, Nunes M, Safar A, Réthoré MO, Fellous M, McElreavey K, Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene, Hum. Genet. 1998 Feb;102(2):151-6.

Tajbakhsh S, Spörle R, Somite development: constructing the vertebrate body, Cell 1998 Jan;92(1):9-16.

Veitia R, Laurent A, Quintana-Murci L, Ottolenghi C, Fellous M, Vidaud M, McElreavey K, The INSL4 gene maps close to WI-5527 at 9p24.1–>p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome, Cytogenet. Cell Genet. 1998;81(3-4):275-7.

Barbaux S, Niaudet P, Gubler MC, Grünfeld JP, Jaubert F, Kuttenn F, Fékété CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K, Donor splice-site mutations in WT1 are responsible for Frasier syndrome, Nat. Genet. 1997 Dec;17(4):467-70.

McElreavey K, Fellous M, Sex-determining genes, Trends Endocrinol. Metab. 1997 Nov;8(9):342-6.

Veitia RA, Fellous M, McElreavey K, Conservation of Y chromosome-specific sequences immediately 5′ to the testis determining gene in primates, Gene 1997 Oct;199(1-2):63-70.

Tajbakhsh S, Cossu G, Establishing myogenic identity during somitogenesis, Curr. Opin. Genet. Dev. 1997 Oct;7(5):634-41.

Ricchetti M, Buc H, Telomerase activity of reverse transcriptase, Science 1997 Aug;277(5328):887.

Bourgeron T, Barbaux S, McElreavey K, Fellous M, [Y chromosome and spermatogenesis], Contracept Fertil Sex 1997 Jul-Aug;25(7-8):620-5.

Phillips CA, Repperger DW, Chelette TL, , The acceleration-velocity relationship: identification of normal and spastic upper extremity movement., Comput Biol Med 1997 Jul; 27(4): 309-28.

Veitia R, Ion A, Barbaux S, Jobling MA, Souleyreau N, Ennis K, Ostrer H, Tosi M, Meo T, Chibani J, Fellous M, McElreavey K, Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype, Hum. Genet. 1997 May;99(5):648-52.

Veitia R, Nunes M, Brauner R, Doco-Fenzy M, Joanny-Flinois O, Jaubert F, Lortat-Jacob S, Fellous M, McElreavey K, Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1, Genomics 1997 Apr;41(2):271-4.

Seboun E, Barbaux S, Bourgeron T, Nishi S, Agulnik A, Egashira M, Nikkawa N, Bishop C, Fellous M, McElreavey K, Kasahara M, Algonik A, Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene, Genomics 1997 Apr;41(2):227-35.

Tajbakhsh S, Rocancourt D, Cossu G, Buckingham M, Redefining the genetic hierarchies controlling skeletal myogenesis: Pax-3 and Myf-5 act upstream of MyoD, Cell 1997 Apr;89(1):127-38.

Damiani D, Fellous M, McElreavey K, Barbaux S, Barreto ES, Dichtchekenian V, Setian N, True hermaphroditism: clinical aspects and molecular studies in 16 cases, Eur. J. Endocrinol. 1997 Feb;136(2):201-4.

Tar A, Ion A, Sólyom J, Györvári B, Stephenson C, Barbaux S, Nunes M, Fellous M, McElreavey K, Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13, Am. J. Med. Genet. 1997 Jan;68(2):231-5.

Veitia R, Nunes M, McElreavey K, Fellous M, [Sex determination and differentiation in man: from pathology to genes], Arch Pediatr 1997;4(2 Suppl 2):118s-120s.

Lecourtois M, Schweisguth F, Role of suppressor of hairless in the delta-activated Notch signaling pathway, Perspect Dev Neurobiol 1997;4(4):305-11.

Ricchetti M, Buc H, A reiterative mode of DNA synthesis adopted by HIV-1 reverse transcriptase after a misincorporation, Biochemistry 1996 Nov;35(47):14970-83.

Tajbakhsh S, Rocancourt D, Buckingham M, Muscle progenitor cells failing to respond to positional cues adopt non-myogenic fates in myf-5 null mice, Nature 1996 Nov;384(6606):266-70.

Telvi L, Ion A, Carel JC, Desguerre I, Piraud M, Boutin AM, Feingold J, Ponsot G, Fellous M, McElreavey K, A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalities, J. Med. Genet. 1996 Sep;33(9):767-71.

McElreavey K, Vilain E, Barbaux S, Fuqua JS, Fechner PY, Souleyreau N, Doco-Fenzy M, Gabriel R, Quereux C, Fellous M, Berkovitz GD, Loss of sequences 3′ to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination, Proc. Natl. Acad. Sci. U.S.A. 1996 Aug;93(16):8590-4.

Tajbakhsh S, Bober E, Babinet C, Pournin S, Arnold H, Buckingham M, Gene targeting the myf-5 locus with nlacZ reveals expression of this myogenic factor in mature skeletal muscle fibres as well as early embryonic muscle, Dev. Dyn. 1996 Jul;206(3):291-300.

Ion A, Telvi L, Chaussain JL, Galacteros F, Valayer J, Fellous M, McElreavey K, A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome, Am. J. Hum. Genet. 1996 Jun;58(6):1185-91.

Gho M, Lecourtois M, Géraud G, Posakony JW, Schweisguth F, Subcellular localization of Suppressor of Hairless in Drosophila sense organ cells during Notch signalling, Development 1996 Jun;122(6):1673-82.

Cossu G, Tajbakhsh S, Buckingham M, How is myogenesis initiated in the embryo?, Trends Genet. 1996 Jun;12(6):218-23.

Tar A, Rácz K, Dobos M, Barbaux S, McElreavey K, Fellous M, [46,XX karyotype males, based on a specific case], Orv Hetil 1996 May;137(20):1085-7.

Kucheria K, Mohapatra I, Ammini AC, Bhargava VL, McElreavey K, Clinical and DNA studies on 46, XY females with gonadal dysgenesis. A report of six cases, J Reprod Med 1996 Apr;41(4):263-6.

Schweisguth F, Gho M, Lecourtois M, Control of cell fate choices by lateral signaling in the adult peripheral nervous system of Drosophila melanogaster, Dev. Genet. 1996;18(1):28-39.

McElreavey K, Barbaux S, Ion A, Fellous M, The genetic basis of murine and human sex determination: a review, Heredity (Edinb) 1995 Dec;75 ( Pt 6):599-611.

Lecourtois M, Schweisguth F, The neurogenic suppressor of hairless DNA-binding protein mediates the transcriptional activation of the enhancer of split complex genes triggered by Notch signaling, Genes Dev. 1995 Nov;9(21):2598-608.

Tar A, Sólyom J, Györvári B, Ion A, Telvi L, Barbaux S, Souleyreau N, Vilain E, Fellous M, McElreavey K, Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion, Hum. Genet. 1995 Oct;96(4):464-8.

Barbaux S, Vilain E, Raoul O, Gilgenkrantz S, Jeandidier E, Chadenas D, Souleyreau N, Fellous M, McElreavey K, Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata, Hum. Mol. Genet. 1995 Sep;4(9):1565-8.

Negroni M, Ricchetti M, Nouvel P, Buc H, Homologous recombination promoted by reverse transcriptase during copying of two distinct RNA templates, Proc. Natl. Acad. Sci. U.S.A. 1995 Jul;92(15):6971-5.

Schweisguth F, Suppressor of Hairless is required for signal reception during lateral inhibition in the Drosophila pupal notum, Development 1995 Jun;121(6):1875-84.

Tajbakhsh S, Houzelstein D, In situ hybridization and beta-galactosidase: a powerful combination for analysing transgenic mice, Trends Genet. 1995 Feb;11(2):42.

Ibnsouda S, Schweisguth F, Jullien D, Kücherer C, Lepesant JA, Vincent A, Evolutionarily conserved positive and negative cis-acting elements control the blastoderm-specific expression of the Drosophila serendipity alpha cellularisation gene, Mech. Dev. 1995 Jan;49(1-2):71-82.

Schweisguth F, Nero P, Posakony JW, The sequence similarity of the Drosophila suppressor of hairless protein to the integrase domain has no functional significance in vivo, Dev. Biol. 1994 Dec;166(2):812-4.

Brou C, Logeat F, Lecourtois M, Vandekerckhove J, Kourilsky P, Schweisguth F, Israël A, Inhibition of the DNA-binding activity of Drosophila suppressor of hairless and of its human homolog, KBF2/RBP-J kappa, by direct protein-protein interaction with Drosophila hairless, Genes Dev. 1994 Oct;8(20):2491-503.

Mendonça BB, Barbosa AS, Arnhold IJ, McElreavey K, Fellous M, Moreira-Filho CA, Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene, Am. J. Med. Genet. 1994 Aug;52(1):39-43.

Boucekkine C, Toublanc JE, Abbas N, Chaabouni S, Ouahid S, Semrouni M, Jaubert F, Toublanc M, McElreavey K, Vilain E, Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences, Clin. Endocrinol. (Oxf) 1994 Jun;40(6):733-42.

Schweisguth F, Posakony JW, Antagonistic activities of Suppressor of Hairless and Hairless control alternative cell fates in the Drosophila adult epidermis, Development 1994 Jun;120(6):1433-41.

Vilain E, Le Fiblec B, Morichon-Delvallez N, Brauner R, Dommergues M, Dumez Y, Jaubert F, Boucekkine C, McElreavey K, Vekemans M, SRY-negative XX fetus with complete male phenotype, Lancet 1994 Jan;343(8891):240-1.

Boucekkine C, Vilain E, McElreavey K, Jaubert F, Brauner R, Thibaud E, Battin J, Toublanc JE, Kucheria K, Chaabouni S, [Study of sex determination gene (SRY) in 46,XY gonadal dysgenesis], Ann. Endocrinol. (Paris) 1994;54(5):315-21.

McElreavey K, Vilain E, Cotinot C, Payen E, Fellous M, Control of sex determination in animals, Eur. J. Biochem. 1993 Dec;218(3):769-83.

Ibnsouda S, Schweisguth F, de Billy G, Vincent A, Relationship between expression of serendipity alpha and cellularisation of the Drosophila embryo as revealed by interspecific transformation, Development 1993 Oct;119(2):471-83.

Khodyreva SN, Podust VN, Sergeev DS, Ivanova EM, Frolova EI, Koshkin AA, Godovikova TS, Zarytova VF, Ricchetti M, Lavrik OI, Comparison of interactions of 5′-derivatives of deoxyoctathymidylate with human DNA polymerize alpha and HIV reverse transcriptase, Mol. Biol. Rep. 1993 Jun;18(1):43-7.

McElreavey K, Vilain E, Abbas N, Herskowitz I, Fellous M, A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development, Proc. Natl. Acad. Sci. U.S.A. 1993 Apr;90(8):3368-72.

Ricchetti M, Buc H, E. coli DNA polymerase I as a reverse transcriptase, EMBO J. 1993 Feb;12(2):387-96.

Vilain E, Jaubert F, Fellous M, McElreavey K, Pathology of 46,XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor, Differentiation 1993 Jan;52(2):151-9.

Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R, Nihoul-Fekete C, Rappaport R, Fellous M, Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome, C. R. Acad. Sci. III, Sci. Vie 1993;316(4):375-83.

Toublanc JE, Boucekkine C, Abbas N, Barama D, Vilain E, McElreavey K, Toublanc M, Fellous M, Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation, Eur. J. Pediatr. 1993;152 Suppl 2:S70-5.

McElreavey K, Rappaport R, Vilain E, Abbas N, Richaud F, Lortat-Jacob S, Berger R, Le Coniat M, Boucekkine C, Kucheria K, A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY, Hum. Genet. 1992 Sep-Oct;90(1-2):121-5.

McElreavey KD, Vilain E, Boucekkine C, Vidaud M, Jaubert F, Richaud F, Fellous M, XY sex reversal associated with a nonsense mutation in SRY, Genomics 1992 Jul;13(3):838-40.

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