Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Marc Abitbol"'
Autor:
Guillaume Bassez, Olivier J.A Camand, Valère Cacheux, Alexandra Kobetz, Florence Dastot-Le Moal, Dominique Marchant, Martin Catala, Marc Abitbol, Michel Goossens
Publikováno v:
Neurobiology of Disease, Vol 15, Iss 2, Pp 240-250 (2004)
ZFHX1B encodes Smad-interacting protein 1, a transcriptional corepressor involved in the transforming growth factors β (TGFβ) signaling pathway. ZFHX1B mutations cause a complex developmental phenotype characterized by severe mental retardation (MR
Externí odkaz:
https://doaj.org/article/539d4b8aa3af4c7ca3c6c2d3bc2a4c40
Autor:
Eric M Dufour, Emeline Nandrot, Dominique Marchant, Loïc Van Den Berghe, Stéphanie Gadin, Moussa Issilame, Jean-Louis Dufier, Cécile Marsac, Deborah Carper, Maurice Menasche, Marc Abitbol
Publikováno v:
Neurobiology of Disease, Vol 14, Iss 2, Pp 166-180 (2003)
Shed photoreceptor outer segments (POS) are phagocytosed by RPE cells in a circadian manner. The homozygous deletion of the c-mer gene abolishes the ingestion phase of this phagocytosis in the Royal College of Surgeons (RCS) rat strain, which in turn
Externí odkaz:
https://doaj.org/article/22bfd756c8a343619d23562edd127bc1
Autor:
D. Bremond-Gignac, M. Robert, A. Daruich, V. Borderie, F. Chiambaretta, S. Valleix, Dominique Bremond-Gignac, Vincent Borderie, Jean-Louis Bourges, Patrick Calvas, Frédéric Chiambaretta, Henri Copin, Vincent Daien, Antoine Labbé, Béatrice Le Bail, Bruno Mortemousque, Matthieu Robert, Jean-Michel Rozet, Arnaud Sauer, Sophie Valleix, Daniel Aberdam, Marc Abitbol, Nathalie Aidan, Isabelle Audo, Nadia Bahi-Buisson, Emmanuelle Barbieri, Fernand Basille, Aurélie Bouet, Lénaïc Bruere, Joseph Bursztyn, Béatrice Cochener-Lamard, Alejandra Daruich-Matet, Danièle Denis, Philippe Denis, Nathalie De Vergnes, Adil El Maftouhi, Audrey Forbeaux Glize, Eric Gabison, Jean Philippe Grundeler, Louis Hoffart, Sophie Igla, Gaëlle Jouanjan, Elsa Laumonier Demory, Camille Leroy, Guylène Le Meur, Zoia Mincheva, Elisabeth Plat, Charlotte Rigal-Sastourne, Serge Romana, Antoine Rousseau, Rémi Salomon, Julie Steffann, Valérie Touitou, Alain Verloes
Publikováno v:
Journal Français d'Ophtalmologie. 45:647-652
Publikováno v:
Acta Ophthalmologica. 100
Purpose Retinal vascular abnormalities (RVA) have been recently described in patients with neurofibromatosis type 1 (NF1) as vascular tortuosity, best visible on infrared imaging. This study assessed clinical RVA's characteristics in a large series o
Autor:
Gabrielle Goldman, Marc Putterman, Fabien Guimiot, Thierry Jo Molina, Alexandre Moulin, Claudine Versaux-Botteri, Loïc Van Den Berghe, Francine Behar-Cohen, Alejandra Daruich, Eric Krejci, Matthieu P. Robert, Benoit Terris, Dominique Marchant, Christophe Klein, Maud Valensi, Laurent Jonet, Frederic Mascarelli, Dominique Bremond-Gignac, Marc Abitbol
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology
Graefe's Archive for Clinical and Experimental Ophthalmology, Springer Verlag, 2019, 257 (11), pp.2401-2427. ⟨10.1007/s00417-019-04462-4⟩
Graefe's Archive for Clinical and Experimental Ophthalmology, Springer Verlag, 2019, 257 (11), pp.2401-2427. ⟨10.1007/s00417-019-04462-4⟩
This study was conducted in order to study Sostdc1 expression in rat and human developing and adult eyes.Using the yeast signal sequence trap screening method, we identified the Sostdc1 cDNA encoding a protein secreted by the adult rat retinal pigmen
Autor:
Marc Abitbol
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 257:453-454
Autor:
Hoai Viet Tran, E. Moret, F. Marcelli, Daniel F. Schorderet, Francis L. Munier, Veronika Vaclavik, Marc Abitbol
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 233:475-477
Reference EPFL-ARTICLE-219311doi:10.1055/s-0042-102585View record in Web of Science Record created on 2016-07-19, modified on 2017-05-12
Autor:
Caroline Seghir, Pierre-Antoine Aymard, Charlotte Denier, Matthieu P. Robert, Marc Abitbol, Nathalie Boddaert, Dominique Bremond-Gignac, Gilles C. Martin
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 21(6)
Introduction Whereas apraclonidine has eclipsed cocaine test in the exploration of unilateral miosis in adults, its use in infants is avoided because of the risk of central nervous system depression. This chart review evaluates the usefulness of coca
Publikováno v:
Annales d'Endocrinologie. 73:510-514
Background PAX6 is a transcription factor involved in the regulation of eye and islet cell development in humans and has also been shown to be an early marker of the pituitary gland in mice. While some subjects with PAX6 mutations were found to have
Autor:
Marc Abitbol, Virginie Dinet, Roberto Cappai, Yvan Arsenijevic, Na An, Francine Behar-Cohen, Mohamed El Sanharawi, Giuseppe D. Ciccotosto, Laurent Jonet, Frédéric Mascarelli, Céline Borras, Michèle Savoldelli, Kimberley Delaunay, Corinne Kostic, Caroline Pirou, Isabelle Ranchon-Cole
Publikováno v:
Molecular Brain
Molecular Brain, 2015, 9 (1), pp.64. ⟨10.1186/s13041-016-0245-z⟩
Molecular Brain, BioMed Central, 2016, <10.1186/s13041-016-0245-z>
Molecular Brain, 2015, 9 (1), pp.64. 〈10.1186/s13041-016-0245-z〉
Molecular brain, vol. 9, no. 1, pp. 64
Molecular Brain, 2015, 9 (1), pp.64. ⟨10.1186/s13041-016-0245-z⟩
Molecular Brain, BioMed Central, 2016, <10.1186/s13041-016-0245-z>
Molecular Brain, 2015, 9 (1), pp.64. 〈10.1186/s13041-016-0245-z〉
Molecular brain, vol. 9, no. 1, pp. 64
Background Amyloid precursor protein knockout mice (APP-KO) have impaired differentiation of amacrine and horizontal cells. APP is part of a gene family and its paralogue amyloid precursor-like protein 2 (APLP2) has both shared as well as distinct ex