Bertrand Vernay

Otx2 regulates subtype specification and neurogenesis in the midbrain.

An essential function of the mitogen-activated protein kinase Erk2 in mouse trophoblast development.

Microcephalin coordinates mitosis in the syncytial Drosophila embryo.

Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling.

Bio-electrospraying primary cardiac cells: in vitro tissue creation and functional study.

Protein deiminases: new players in the developmentally regulated loss of neural regenerative ability.

Increased Wingless (Wnt) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans.

Human γδ T Lymphocytes Are Licensed for Professional Antigen Presentation by Interaction with Opsonized Target Cells.

Disease-associated missense mutations in the EVH1 domain disrupt intrinsic WASp function causing dysregulated actin dynamics and impaired dendritic cell migration.

Vascularisation is not necessary for gut colonisation by enteric neural crest cells.

Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome.

The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes.

The neural milieu of the developing choroid plexus: neural stem cells, neurons and innervation.

The CXCL12/CXCR4 Axis Plays a Critical Role in Coronary Artery Development.

Rho-kinase-dependent actin turnover and actomyosin disassembly are necessary for mouse spinal neural tube closure.