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Cell lineages, growth and repair of the mouse heart.

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Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.

Sandrine Marlin, Jean-Laurent CASANOVA , Arnold Munnich, Valérie Cormier-Daire

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Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans.

Jeanne Amiel

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Tracing cells for tracking cell lineage and clonal behavior.

Sigolène Meilhac

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Dbx1-expressing cells are necessary for the survival of the mammalian anterior neural and craniofacial structures.

Alessandra Pierani, Frédéric Causeret

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KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes.

Sophie Thomas, Patrick Nitschké, Arnold Munnich, Valérie Cormier-Daire, Stanislas Lyonnet, Tania Attié-Bitach

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Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation.

Frédéric Rieux-Laucat

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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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