Timeline

Yvan Lallemand

Permanent Researcher

15 Apr 2022

publication

Erythro-myeloid progenitor origin of Hofbauer cells in the early mouse placenta.

31 May 2021

news

The embryonic megakaryopoiesis is a two-tier process

25 May 2021

publication

Megakaryocyte production is sustained by direct differentiation from erythromyeloid progenitors in the yolk sac until midgestation.

14 Jan 2020

project

ERC-2016-StG _ResidentMacroPhage – Development, Maintenance and Functions of Resident Macrophages

17 Jul 2017

publication

Identification Of Erythromyeloid Progenitors And Their Progeny In The Mouse Embryo By Flow Cytometry

11 May 2015

team

Macrophages and Endothelial Cells

29 Jan 2013

publication

BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb development

20 Dec 2012

publication

Generation and characterization of a tamoxifen inducible Msx1(CreERT2) knock-in allele

01 Jul 2011

publication

Msx genes define a population of mural cell precursors required for head blood vessel maturation

04 Apr 2011

publication

Msx1 and Msx2 in limb mesenchyme modulate digit number and identity

05 May 2009

publication

Msx genes are important apoptosis effectors downstream of the Shh/Gli3 pathway in the limb

18 Apr 2007

publication

Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan

01 Sep 2006

publication

Anteroposterior patterning in the limb and digit specification: contribution of mouse genetics

01 Jun 2005

publication

Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development

01 Jun 2004

publication

Msx1-deficient mice fail to form prosomere 1 derivatives, subcommissural organ, and posterior commissure and develop hydrocephalus

01 Dec 2003

publication

A new mouse limb mutation identifies a Twist allele that requires interacting loci on chromosome 4 for its phenotypic expression

01 Sep 2003

publication

Msx1 is required for dorsal diencephalon patterning

01 Mar 1998

publication

Maternally expressed PGK-Cre transgene as a tool for early and uniform activation of the Cre site-specific recombinase

18 Mar 1997

publication

Function and regulation of heat shock factor 2 during mouse embryogenesis

01 Oct 1996

publication

Epilepsy and brain abnormalities in mice lacking the Otx1 gene

01 Oct 1995

publication

Forebrain and midbrain regions are deleted in Otx2-/- mutants due to a defective anterior neuroectoderm specification during gastrulation

01 Mar 1995

publication

Abnormal avoidance learning in mice lacking functional high-affinity nicotine receptor in the brain

17 Apr 1992

publication

Homeosis in the mouse induced by a null mutation in the Hox-3.1 gene

01 Dec 1990

publication

An in situ assessment of the routes and extents of colonisation of the mouse embryo by embryonic stem cells and their descendants

01 Jun 1990

publication

A little guide for advanced search:

Timeline

Erythro-myeloid progenitor origin of Hofbauer cells in the early mouse placenta.

The embryonic megakaryopoiesis is a two-tier process

Megakaryocyte production is sustained by direct differentiation from erythromyeloid progenitors in the yolk sac until midgestation.

ERC-2016-StG _ResidentMacroPhage – Development, Maintenance and Functions of Resident Macrophages

Identification Of Erythromyeloid Progenitors And Their Progeny In The Mouse Embryo By Flow Cytometry

Macrophages and Endothelial Cells

BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb development

Generation and characterization of a tamoxifen inducible Msx1(CreERT2) knock-in allele

Msx genes define a population of mural cell precursors required for head blood vessel maturation

Msx1 and Msx2 in limb mesenchyme modulate digit number and identity

Msx genes are important apoptosis effectors downstream of the Shh/Gli3 pathway in the limb

Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan

Anteroposterior patterning in the limb and digit specification: contribution of mouse genetics

Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development

Msx1-deficient mice fail to form prosomere 1 derivatives, subcommissural organ, and posterior commissure and develop hydrocephalus

A new mouse limb mutation identifies a Twist allele that requires interacting loci on chromosome 4 for its phenotypic expression

Msx1 is required for dorsal diencephalon patterning

Maternally expressed PGK-Cre transgene as a tool for early and uniform activation of the Cre site-specific recombinase

Function and regulation of heat shock factor 2 during mouse embryogenesis

Epilepsy and brain abnormalities in mice lacking the Otx1 gene

Forebrain and midbrain regions are deleted in Otx2-/- mutants due to a defective anterior neuroectoderm specification during gastrulation

Abnormal avoidance learning in mice lacking functional high-affinity nicotine receptor in the brain

Homeosis in the mouse induced by a null mutation in the Hox-3.1 gene

An in situ assessment of the routes and extents of colonisation of the mouse embryo by embryonic stem cells and their descendants

Targeted replacement of the homeobox gene Hox-3.1 by the Escherichia coli lacZ in mouse chimeric embryos