Publications by authors named "Maurice Menasche"

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Truncation of PITX2 differentially affects its activity on physiological targets.
Marie-Hélène Quentien, Véronique Vieira, Maurice Menasche, Jean-Louis Dufier, Jean-Paul Herman

J Mol Endocrinol· February 2011

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Sirt1 involvement in rd10 mouse retinal degeneration.
Carolina Jaliffa, Ilhame Ameqrane, Anouk Dansault, Julia Leemput, Véronique Vieira, Maurice Menasche

Invest Ophthalmol Vis Sci· August 2009

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Morphologic and electroretinographic phenotype of SR-BI knockout mice after a long-term atherogenic diet.
Alexandra C Provost, Leonie Vede, Karine Bigot, Nicole Keller, Anne Tailleux, Maurice Menasche

Invest Ophthalmol Vis Sci· August 2009

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Expression of 8-oxoguanine DNA glycosylase (Ogg1) in mouse retina.
Karine Bigot, Julia Leemput, Monique Vacher, Anna Campalans, J Pablo Radicella, Maurice Menasche

Mol Vis· June 2009

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ATM localization and gene expression in the adult mouse eye.
Julia Leemput, Christel Masson, Karine Bigot, Abdelmounaim Errachid, Anouk Dansault, Maurice Menasche

Mol Vis· March 2009

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Novel mouse model of monocular amaurosis fugax.
Dominique Claude Lelong, Ivan Bieche, Elodie Perez, Karine Bigot, Julia Leemput, Maurice Menasche

Stroke· December 2007

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Novel human pathological mutations. Gene symbol: FZD4. Disease: exudative vitreoretinopathy.
Véronique Vieira, de la Houssaye Guillaume, Dansault Anouk, Perez Elodie, Menasche Maurice

Hum Genet· November 2007

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Novel human pathological mutations. Gene symbol: FZD4. Disease: familial exudative vitreoretinopathy.
Véronique Vieira, Guillaume de la Houssaye, Anouk Dansault, Elodie Perez, Olivier Roche, Maurice Menasche

Hum Genet· June 2007

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Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
Anouk Dansault, Gabriel David, Claire Schwartz, Carolina Jaliffa, Véronique Vieira, Maurice Menasche

Mol Vis· April 2007

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Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Veronique Vieira, Gabriel David, Olivier Roche, Guillaume de la Houssaye, Sandrine Boutboul, Maurice Menasche

Mol Vis· December 2006

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Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report.
Guillaume de la Houssaye, Ivan Bieche, Olivier Roche, Véronique Vieira, Ingrid Laurendeau, Maurice Menasche

BMC Med Genet· November 2006

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A subset of patients with epithelial basement membrane corneal dystrophy have mutations in TGFBI/BIGH3.
Sandrine Boutboul, Graeme C M Black, John E Moore, Janet Sinton, Maurice Menasche

Hum Mutat· June 2006

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Eight previously unidentified mutations found in the OA1 ocular albinism gene.
Hélène Mayeur, Olivier Roche, Christelle Vêtu, Carolina Jaliffa, Dominique Marchant, Maurice Menasche

BMC Med Genet· April 2006

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The beta3 integrin gene is expressed at high levels in the major haematopoietic and lymphoid organs, vascular system, and skeleton during mouse embryo development.
Laurence Le Gat, Karïn Gogat, Loïc Van Den Berghe, Mara Brizard, Alexandra Kobetz

Cell Commun Adhes· August 2004

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Prosaposin gene expression in normal and dystrophic RCS rat retina.
Loïc Van Den Berghe, Karine Sainton, Karïn Gogat, Dominique Marchant, Eric Dufour, Maurice Menasche

Invest Ophthalmol Vis Sci· May 2004

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VEGF and KDR gene expression during human embryonic and fetal eye development.
Karïn Gogat, Laurence Le Gat, Loïc Van Den Berghe, Dominique Marchant, Alexandra Kobetz, Maurice Menasche

Invest Ophthalmol Vis Sci· January 2004

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Identification of novel genes and altered signaling pathways in the retinal pigment epithelium during the Royal College of Surgeons rat retinal degeneration.
Eric M Dufour, Emeline Nandrot, Dominique Marchant, Loïc Van Den Berghe, Stéphanie Gadin, Maurice Menasche

Neurobiol Dis· November 2003

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Mutational analysis of the OA1 gene in ocular albinism.
Olivier Camand, Sandrine Boutboul, Laurence Arbogast, Olivier Roche, Claude Sternberg, Maurice Menasche

Ophthalmic Genet· September 2003

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