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2024
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2023Intrinsic factors and CD1d1 but not CD1d2 expression levels control invariant natural killer T cell subset differentiation, Nature Communications, 2023, 14 (1), pp.7922. ⟨10.1038/s41467-023-43424-7⟩.
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2023CCQTL: facilitating QTL mapping in the Collaborative Cross, 20th Annual Meeting of the Complex Trait Community | Rat Genome & Models, University of Tennessee Health Science Center [Memphis, Tennessee], Oct 2023, Memphis, TN, United States.
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2021A mouse-adapted SARS-CoV-2 strain replicating in standard laboratory mice, 2021.
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2021Variants with the N501Y mutation extend SARS-CoV-2 host range to mice, with contact transmission, 2021.
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2020Characterization of the developmental landscape of murine RORγt+ iNKT cells, International Immunology, 2019, 32 (2), pp.105-116. ⟨10.1093/intimm/dxz064⟩.
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2019A Loss-of-Function Mutation in the Integrin Alpha L ( Itgal ) Gene Contributes to Susceptibility to Salmonella enterica Serovar Typhimurium Infection in Collaborative Cross Strain CC042, Infection and Immunity, 2019, 88 (1), pp.e00656-19. ⟨10.1128/IAI.00656-19⟩.
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2018Deficient LRRC8A-dependent volume-regulated anion channel activity is associated with male infertility in mice, JCI Insight, 2018, 3 (16), pp.e99767. ⟨10.1172/jci.insight.99767⟩.
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2018Identification of new loci involved in the host susceptibility to Salmonella Typhimurium in collaborative cross mice, BMC Genomics, 2018, 19 (1), pp.303. ⟨10.1186/s12864-018-4667-0⟩.
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2017Enhanced Macrophage M1 Polarization and Resistance to Apoptosis Enable Resistance to Plague, Journal of Infectious Diseases, 2017, 216 (6), pp.761-770. ⟨10.1093/infdis/jix348⟩.
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2015Mucosal-associated invariant T cell–rich congenic mouse strain allows functional evaluation, Journal of Clinical Investigation, 2015, 125 (11), pp.4171 - 4185. ⟨10.1172/JCI82424⟩.
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2015Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene, Journal of Investigative Dermatology, 2015, 135 (12), pp.3133-3143. ⟨10.1038/jid.2015.314⟩.
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2014An Animal Model of Type A Cystinuria Due to Spontaneous Mutation in 129S2/SvPasCrl Mice, PLoS ONE, 2014, 9 (7), pp.e102700. ⟨10.1371/journal.pone.0102700⟩.
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2012Resistance to plague of Mus spretus SEG/Pas mice requires the combined action of at least four genetic factors, Genes and Immunity, 2013, 14 (1), pp.35-41. ⟨10.1038/gene.2012.50⟩.
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2011Early Systemic Bacterial Dissemination and a Rapid Innate Immune Response Characterize Genetic Resistance to Plague of SEG Mice, Journal of Infectious Diseases, 2012, 205 (1), pp.134-143. ⟨10.1093/infdis/jir696⟩.
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2010Mus spretus SEG/Pas mice resist virulent Yersinia pestis, under multigenic control, Genes and Immunity, 2011, 12 (1), pp.23-30. ⟨10.1038/gene.2010.45⟩.
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2010Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes, American Journal of Pathology, 2010, 177 (4), pp.1958-1968. ⟨10.2353/ajpath.2010.100118⟩.
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2008Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channels, Neurogenetics 2008 Oct;9(4):237-48.
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2006Cmv4, a new locus linked to the NK cell gene complex, controls innate resistance to cytomegalovirus in wild-derived mice, J. Immunol. 2006 May;176(9):5478-85.
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2004Tetracycline-regulated transactivators driven by the involucrin promoter to achieve epidermal conditional gene expression, J. Invest. Dermatol. 2004 Aug;123(2):313-8.
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2003Ectopic expression of kruppel like factor 4 (Klf4) accelerates formation of the epidermal permeability barrier, Development 2003 Jun;130(12):2767-77.
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2002A missense mutation in Tbce causes progressive motor neuronopathy in mice, Nat. Genet. 2002 Nov;32(3):443-7.
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2001Genetic and physical delineation of the region overlapping the progressive motor neuropathy (pmn) locus on mouse chromosome 13, Genomics 2001 Jul;75(1-3):9-16.
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2000A new family of genes and pseudogenes potentially expressing testis- and brain-specific leucine zipper proteins in man and mouse, Gene 2000 May;249(1-2):105-13.
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1999Three new allelic mouse mutations that cause skeletal overgrowth involve the natriuretic peptide receptor C gene (Npr3), Proc. Natl. Acad. Sci. U.S.A. 1999 Aug;96(18):10278-83.
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1996Mouse orphan nuclear receptor Rev-erb beta sequences are localized on chromosomes 19 and 14, Mamm. Genome 1996 Mar;7(3):243.