Publications by authors named "Isabelle Gicquel"

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The Clathrin adaptor AP-1 and Stratum act in parallel pathways to control Notch activation in sensory organ precursors cells.
Karen Bellec, Mathieu Pinot, Isabelle Gicquel, Roland Le Borgne

Development· January 2021

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Stratum recruits Rab8 at Golgi exit sites to regulate the basolateral sorting of Notch and Sanpodo.
Karen Bellec, Isabelle Gicquel, Roland Le Borgne

Development· July 2018

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Novel genes upregulated when NOTCH signalling is disrupted during hypothalamic development.
Leslie Ratié, Michelle Ware, Frédérique Barloy-Hubler, Hélène Romé, Isabelle Gicquel

Neural Dev· December 2013

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NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos.
Sandra Mercier, Véronique David, Leslie Ratié, Isabelle Gicquel, Sylvie Odent

Dis Model Mech· March 2013

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New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Sandra Mercier, Christèle Dubourg, Nicolas Garcelon, Boris Campillo-Gimenez, Isabelle Gicquel

J Med Genet· November 2011

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NOTCH, a new signaling pathway implicated in holoprosencephaly.
Valérie Dupé, Lucie Rochard, Sandra Mercier, Yann Le Pétillon, Isabelle Gicquel

Hum Mol Genet· March 2011

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Holoprosencephaly: An update on cytogenetic abnormalities.
Claude Bendavid, Valérie Dupé, Lucie Rochard, Isabelle Gicquel, Christèle Dubourg

Am J Med Genet C Semin Med Genet· February 2010

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Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci.
Claude Bendavid, Lucie Rochard, Christèle Dubourg, Jonathan Seguin, Isabelle Gicquel

Hum Mutat· August 2009

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MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly.
Claude Bendavid, Christèle Dubourg, Laurent Pasquier, Isabelle Gicquel, Simon Le Gallou

Hum Mutat· December 2007

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Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother.
Claude Bendavid, Laurent Pasquier, Tanguy Watrin, Karine Morcel, Josette Lucas, Isabelle Gicquel

Eur J Med Genet· March 2007

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Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes.
Claude Bendavid, Christèle Dubourg, Isabelle Gicquel, Laurent Pasquier, Pascale Saugier-Veber

Hum Genet· March 2006

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Transcriptome variations in human CaCo-2 cells: a model for enterocyte differentiation and its link to iron absorption.
Hélène Bédrine-Ferran, Nolwenn Le Meur, Isabelle Gicquel, Martine Le Cunff, Nicolas Soriano

Genomics· May 2004

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