I. Gicquel

发表

Transcriptome variations in human CaCo-2 cells: a model for enterocyte differentiation and its link to iron absorption.

P. Fergelot, S. Mottier, J. Mosser, 2004, Genomics.

The Clathrin adaptor AP-1 and Stratum act in parallel pathways to control Notch activation in Drosophila sensory organ precursors cells

I. Gicquel, R. Le Borgne, K. Bellec, 2020, Development.

Non-hyperfunctioning nodules from multinodular goiters: A minor role in pathogenesis for somatic activating mutations in the TSH-receptor and Gsα subunit genes

I. Gicquel, J. L. Le Gall, V. David, 2001, Journal of endocrinological investigation.

Localization of seven new genes around the HLA-A locus.

I. Gicquel, J. L. Le Gall, B. Chauvel, 1994, Advances in experimental medicine and biology.

Localization of seven new genes around the HLA-A locus.

I. Gicquel, J. L. Le Gall, B. Chauvel, 1993, Human molecular genetics.

New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases

I. Gicquel, N. Garcelon, L. Pasquier, 2011, Journal of Medical Genetics.

Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis

I. Gicquel, A. Laquérriere, L. Pasquier, 2013, Molecular Syndromology.

NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos

I. Gicquel, V. Dupé, S. Mercier, 2012, Disease Models & Mechanisms.

A new polymorphic probe close to HLA-A.

I. Gicquel, P. Pontarotti, V. David, 1991, Nucleic acids research.

A 1200-kilobase transcription map encompassing the D6S105 locus at 6p21.3.

F. Galibert, P. Fergelot, V. Lelaure, 1997, Genomics.

MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly

S. Mottier, I. Gicquel, L. Pasquier, 2007, Human mutation.

Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes

I. Gicquel, T. Frebourg, L. Pasquier, 2006, Human Genetics.

Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype

I. Gicquel, M. Huizing, L. Pasquier, 2005, Journal of Medical Genetics.

NOTCH, a new signaling pathway implicated in holoprosencephaly.

T. Bohan, I. Gicquel, V. Dupé, 2011, Human molecular genetics.

Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother.

I. Gicquel, L. Pasquier, S. Odent, 2007, European journal of medical genetics.

Novel genes upregulated when NOTCH signalling is disrupted during hypothalamic development

Michelle Ware, Frédérique Barloy-Hubler, I. Gicquel, 2013, Neural Development.

Identification of an endogenous RNA transcribed from the antisense strand of the HFE gene.

P. Fergelot, J. Mosser, I. Gicquel, 2001, Human molecular genetics.

The HFE gene undergoes alternate splicing processes.

P. Fergelot, J. Mosser, I. Gicquel, 2000, Blood cells, molecules & diseases.

Haemochromatosis and HLA–H

P. Fergelot, J. Mosser, I. Gicquel, 1996, Nature Genetics.

Array‐CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci

J. Mosser, I. Gicquel, A. Laquérriere, 2009, Human mutation.

Holoprosencephaly: An update on cytogenetic abnormalities

I. Gicquel, V. Dupé, C. Dubourg, 2010, American journal of medical genetics. Part C, Seminars in medical genetics.

DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family

I. Gicquel, R. Fauchet, M. Simon, 1986, Human Genetics.

The Clathrin adaptor AP-1 and Stratum act in parallel pathways to control Notch activation in Drosophila sensory organ precursors cells

I. Gicquel, R. Le Borgne, K. Bellec, 2020, Development.

The Clathrin adaptor AP-1 and the Rab-stabilizing chaperone Stratum act in two parallel pathways to control the activation of the Notch pathway in Drosophila

I. Gicquel, K. Bellec, R. L. Borgne, 2019, bioRxiv.

Stratum recruits Rab8 at Golgi exit sites to regulate the basolateral sorting of Notch and Sanpodo

I. Gicquel, R. Le Borgne, K. Bellec, 2018, Development.

A human homologue to the yeast omnipotent suppressor 45 maps 100 kb centromeric to HLA-A

P. Fergelot, I. Gicquel, B. Chauvel, 1995, Immunogenetics.

NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos

I. Gicquel, V. Dupé, L. Ratié, 2013, Development.

NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos

I. Gicquel, V. Dupé, L. Ratié, 2022 .

Holoprosencephaly: An update on cytogenetic abnormalities

I. Gicquel, V. Dupé, C. Dubourg, 2010, American journal of medical genetics. Part C, Seminars in medical genetics.