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Cell lineages, growth and repair of the mouse heart.
Source :
Results Probl Cell Differ2012 Jan 1Pmid / DOI:
22918812 -
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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Nat Genet2011 Dec 11Pmid / DOI:
22158539 -
Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans.
Jeanne Amiel
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Nat. Genet.2011 Nov 21Pmid / DOI:
21892160 -
Tracing cells for tracking cell lineage and clonal behavior.
Sigolène Meilhac
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Dev. Cell2011 Sep 13Pmid / DOI:
21920310 -
Alessandra Pierani, Frédéric Causeret
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PLoS ONE2011 Aug 23Pmid / DOI:
21552538 -
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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Nat Genet2011 Jun 1Pmid / DOI:
21552264 -
Frédéric Rieux-Laucat
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J. Clin. Invest.2011 Feb 3Pmid / DOI:
21183795 -
BBS10 mutations are common in 'Meckel'-type cystic kidneys.
Sophie Thomas, Tania Attié-Bitach
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J Med Genet2010 Dec 1Pmid / DOI:
20805367 -
Regulation of Frizzled-dependent planar polarity signaling by a V-ATPase subunit.
Matias Simons
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Curr. Biol.2010 Nov 26Pmid / DOI:
20579879 -
Patterning the cerebral cortex: traveling with morphogens.
Alessandra Pierani
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Curr. Opin. Genet. Dev.2010 Nov 16Pmid / DOI:
20542680 -
Alessandra Pierani, Frédéric Causeret
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PLoS Biol.2010 Oct 26Pmid / DOI:
20668538 -
Sigolène Meilhac
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Development2010 Oct 1Pmid / DOI:
20823066 -
Nadine CERF-BENSUSSAN
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Gastroenterology2010 Sep 20Pmid / DOI:
20537998 -
Alessandra Pierani
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J. Neurosci.2010 Aug 24Pmid / DOI:
20685999 -
Role of the GATA-1/FOG-1/NuRD pathway in the expression of human beta-like globin genes.
Annarita Miccio
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Mol. Cell. Biol.2010 Jul 14Pmid / DOI:
20439494