Resources

Biphasic development of the mammalian ventricular conduction system.

Sigolène Meilhac

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Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes.

Arnold Munnich, Sophie Saunier, Sophie Thomas, Tania Attié-Bitach

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FOG1 requires NuRD to promote hematopoiesis and maintain lineage fidelity within the megakaryocytic-erythroid compartment.

Annarita Miccio

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NuRD mediates activating and repressive functions of GATA-1 and FOG-1 during blood development.

Annarita Miccio

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Human embryonic stem cells and genomic instability.

Nathalie Lefort

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Sucrose-utilizing transglucosidases for biocatalysis.

Isabelle André

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Identification of CANT1 mutations in Desbuquois dysplasia.

Céline Huber, Arnold Munnich, Valérie Cormier-Daire

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Identification of CANT1 mutations in Desbuquois dysplasia.

Céline Huber, Arnold Munnich, Valérie Cormier-Daire

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Identification of CANT1 mutations in Desbuquois dysplasia.

Céline Huber, Arnold Munnich, Valérie Cormier-Daire

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CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation.

Sophie Thomas, Jeanne Amiel, Nathalie Boddaert, Arnold Munnich, Sophie Saunier, Tania Attié-Bitach

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Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease.

Jeanne Amiel

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Active cell movements coupled to positional induction are involved in lineage segregation in the mouse blastocyst.

Sigolène Meilhac

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Cerebral cortex development: From progenitors patterning to neocortical size during evolution.

Alessandra Pierani

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Landmarks and lineages in the developing heart.

Sigolène Meilhac

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FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function.

Frédéric Rieux-Laucat

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