Publications and ressources

BBS10 mutations are common in 'Meckel'-type cystic kidneys.

Sophie Thomas, Tania Attié-Bitach

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Regulation of Frizzled-dependent planar polarity signaling by a V-ATPase subunit.

Matias Simons

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Patterning the cerebral cortex: traveling with morphogens.

Alessandra Pierani

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A novel role for Dbx1-derived Cajal-Retzius cells in early regionalization of the cerebral cortical neuroepithelium.

Alessandra Pierani, Frédéric Causeret

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Clonal analysis reveals common lineage relationships between head muscles and second heart field derivatives in the mouse embryo.

Sigolène Meilhac

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Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathy.

Nadine CERF-BENSUSSAN

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A novel transient glutamatergic population migrating from the pallial-subpallial boundary contributes to neocortical development.

Alessandra Pierani

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Role of the GATA-1/FOG-1/NuRD pathway in the expression of human beta-like globin genes.

Annarita Miccio

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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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