Publications by authors named "Valerie Dupé"

28Publications

Recent advances in understanding inheritance of holoprosencephaly.

Am J Med Genet C Semin Med Genet 2018 06 22;178(2):258-269. Epub 2018 May 22.

Univ Rennes, CNRS, IGDR (Institut de génétique et développement de Rennes) - UMR 6290, F - 35000, Rennes, France.

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June 2018

[From cyclops to reality: a fresh look at the genetics of holoprosencephaly].

Med Sci (Paris) 2017 Nov 4;33(11):924-926. Epub 2017 Dec 4.

UMR 6290 CNRS, institut de génétique et développement de Rennes, université de Rennes1, France - Service de génétique moléculaire et génomique, CHU Pontchaillou, 2, rue Henri Le Guilloux, 35033 Rennes, France.

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November 2017

Regulation of downstream neuronal genes by proneural transcription factors during initial neurogenesis in the vertebrate brain.

Neural Dev 2016 12 7;11(1):22. Epub 2016 Dec 7.

Institut de Génétique et Développement de Rennes, Faculté de Médecine, CNRS UMR6290, Université de Rennes 1, IFR140 GFAS, 2 Avenue du Pr. Léon Bernard, 35043, Rennes Cedex, France.

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December 2016

Evolutionary Conservation of the Early Axon Scaffold in the Vertebrate Brain.

Dev Dyn 2015 Oct 13;244(10):1202-14. Epub 2015 Aug 13.

Institute of Biomedical and Biomolecular Sciences, University of Portsmouth, Portsmouth, United Kingdom.

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October 2015

Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings.

PLoS One 2015 6;10(2):e0117418. Epub 2015 Feb 6.

Institut de Génétique et Développement de Rennes, Equipe Génétique des Pathologies Liées au Développement, Faculté de Médecine, Université de Rennes 1, 35043 Rennes, France; Laboratoire de Génétique Moléculaire et Génomique, CHU Pontchaillou, 35033 Rennes, France.

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February 2016

Dynamic expression of Notch-dependent neurogenic markers in the chick embryonic nervous system.

Front Neuroanat 2014 18;8:158. Epub 2014 Dec 18.

CNRS UMR6290, Faculté de Médecine, Institut de Génétique et Développement de Rennes, Université de Rennes 1 Rennes, France.

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January 2015

Notch signaling and proneural genes work together to control the neural building blocks for the initial scaffold in the hypothalamus.

Front Neuroanat 2014 2;8:140. Epub 2014 Dec 2.

Institut de Génétique et Développement de Rennes, Faculté de Médecine, CNRS UMR6290, Université de Rennes 1 Rennes, France.

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December 2014

Novel genes upregulated when NOTCH signalling is disrupted during hypothalamic development.

Neural Dev 2013 Dec 23;8:25. Epub 2013 Dec 23.

Institut de Génétique et Développement de Rennes, CNRS UMR6290, Université de Rennes 1, IFR140 GFAS, Faculté de Médecine, Rennes, France.

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December 2013

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

Dis Model Mech 2013 Mar 20;6(2):537-43. Epub 2012 Dec 20.

Institut de Génétique et Développement, CNRS UMR6290, Université de Rennes 1, IFR140 GFAS, Faculté de Médecine, 35043 Rennes, France.

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March 2013

NOTCH, a new signaling pathway implicated in holoprosencephaly.

Hum Mol Genet 2011 Mar 31;20(6):1122-31. Epub 2010 Dec 31.

Institut de Génétique et Développement, CNRS UMR6061, Université de Rennes 1, IFR140 GFAS, Faculté de Médecine, Rennes, France.

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March 2011

Conditional ablation of integrin alpha-6 in mouse epidermis leads to skin fragility and inflammation.

Eur J Cell Biol 2011 Feb-Mar;90(2-3):270-7. Epub 2010 Oct 20.

Institut de génétique et de biologie moléculaire et cellulaire, Department of Cell Biology and Development, CNRS UdS UMR7104, Inserm U964, Illkirch, France.

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July 2011

Holoprosencephaly: An update on cytogenetic abnormalities.

Am J Med Genet C Semin Med Genet 2010 Feb;154C(1):86-92

Institut National de la Santé et de la Recherche Médicale, Rennes, France.

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February 2010

Retinoic acid receptors exhibit cell-autonomous functions in cranial neural crest cells.

Dev Dyn 2009 Oct;238(10):2701-11

Faculté de Médecine, Institut de Génétique et Développement, Université de Rennes 1, Rennes Cedex, France.

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October 2009

Impairing retinoic acid signalling in the neural crest cells is sufficient to alter entire eye morphogenesis.

Dev Biol 2008 Aug 11;320(1):140-8. Epub 2008 May 11.

UPR9022 du CNRS, IBMC, 15 rues Descartes, 67084 Strasbourg, France.

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August 2008

Identification of a new type of PBX1 partner that contains zinc finger motifs and inhibits the binding of HOXA9-PBX1 to DNA.

Mech Dev 2007 May 8;124(5):364-76. Epub 2007 Feb 8.

UMR CNRS 6061, Génétique et Développement, IFR 140, Faculté de Médecine, Université de Rennes 1, Campus Villejean, 2 avenue du Professeur Léon Bernard, CS34317, F-35043 Rennes Cedex, France.

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May 2007

Retinoic acid-dependent eye morphogenesis is orchestrated by neural crest cells.

Development 2005 Nov 5;132(21):4789-800. Epub 2005 Oct 5.

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC Collège de France, BP10142, 67404 Illkirch Cedex, CU de Strasbourg, France.

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November 2005

Contribution of cellular retinol-binding protein type 1 to retinol metabolism during mouse development.

Dev Dyn 2005 May;233(1):167-76

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Institut Clinique de la Souris (ICS), CNRS/INSERM/ULP, Collège de France, BP10142, 67404 Illkirch Cedex, CU de Strasbourg, France.

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May 2005

A newborn lethal defect due to inactivation of retinaldehyde dehydrogenase type 3 is prevented by maternal retinoic acid treatment.

Proc Natl Acad Sci U S A 2003 Nov 17;100(24):14036-41. Epub 2003 Nov 17.

Institut de Génétique et de Biologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, Université Louis Pasteur, Collège de France, BP10142, 67404 Illkirch Cedex, Communauté Urbaine de Strasbourg, France.

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November 2003