Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Olivier, Camand"'
Publikováno v:
The Journal of Neuroscience. 26:8082-8091
An early step in the formation of the optic pathway is the directed extension of retinal ganglion cell (RGC) axons into the optic fiber layer (OFL) of the retina in which they project toward the optic disc. Using analysis of knock-out mice andin vitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5df0968fba1f35b869e2e51b711b601b
https://doi.org/10.1523/jneurosci.1342-06.2006
https://doi.org/10.1523/jneurosci.1342-06.2006
Autor:
Olivier Camand, Michel Goossens, Guillaume Bassez, Florence Dastot-Le Moal, Alexandra Kobetz, Valère Cacheux, Marc Abitbol, Dominique Marchant, Martin Catala
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 beta (TGFbeta) signaling pathway. ZFHX1B mutations cause a complex developmental phenotype characterized by severe mental retardation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c4c8006838b0ed33be71ffcdfdc4a98
http://www.sciencedirect.com/science/article/pii/S0969996103002080
http://www.sciencedirect.com/science/article/pii/S0969996103002080
Autor:
Marie-Laure Sobrier, Olivier Camand, Juliane Léger, Paul Czernichow, Florence Dastot-Le Moal, Irene Netchine, Serge Amselem, Philippe Duquesnoy, Jacques Pantel, Marc Abitbol, Kalotina Machinis
Publikováno v:
The American Journal of Human Genetics. 69(5):961-968
Studies of genetically engineered flies and mice have revealed the role that orthologs of the human LIM homeobox LHX4 have in the control of motor-neuron–identity assignment and in pituitary development. Remarkably, these mouse strains, which bear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf3eeb514715ed309be9bf5097137aab
Autor:
Veronique, Vieira, Gabriel, David, Olivier, Roche, Guillaume, de la Houssaye, Sandrine, Boutboul, Laurence, Arbogast, Alexandra, Kobetz, Christophe, Orssaud, Olivier, Camand, Daniel F, Schorderet, Francis, Munier, Annick, Rossi, Anne Lise, Delezoide, Cecile, Marsac, Daniel, Ricquier, Jean-Louis, Dufier, Maurice, Menasche, Marc, Abitbol
Publikováno v:
Molecular vision. 12
Axenfeld Rieger syndrome (ARS) is an autosomal dominant inherited disorder affecting development of the ocular anterior chamber, abdomen, teeth and facial structures. The PITX2 gene is a major gene encoding a major transcription factor associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed28e5ec4a1dd490a36b5264e2a5537b
https://pubmed.ncbi.nlm.nih.gov/17167399
https://pubmed.ncbi.nlm.nih.gov/17167399
Autor:
Olivier Camand, Sandrine Boutboul, Laurence Gat, Laurence Arbogast, Olivier Roche, Claude Sternberg, Joanne Sutherland, Alex Levin, Elise Héon, Maurice Menasche, Jean-Louis Dufier, Marc Abitbol
Publikováno v:
Ophthalmic genetics. 24(3)
Ocular albinism type 1 (OA1) is an X-linked disorder, mainly characterized by a severe reduction in visual acuity, foveal hypoplasia, nystagmus, hypopigmentation of the retina, the presence of macromelanosomes in the skin and eyes, and the misrouting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dffcf25025c512904cb180b2f9eca6a7
https://pubmed.ncbi.nlm.nih.gov/12868035
https://pubmed.ncbi.nlm.nih.gov/12868035
Publikováno v:
Comptes rendus biologies. 325(2)
Leptin acts on the hypothalamus to reduce food intake and on a number of non-neuronal tissues via specific receptors (Lepr). The use of in situ hybridisation to map the Lepr gene in pre-natal mice revealed transcripts in the yolk sac in various struc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be91b1845ec86fc99af36217c5bf2707
https://pubmed.ncbi.nlm.nih.gov/11980179
https://pubmed.ncbi.nlm.nih.gov/11980179
Autor:
Dominique Marchant, Olivier Camand, Marie O. Pequignot, Elise Heon, Jean-Louis Dufier, Sandrine Boutboul, Cécile Marsac, Alex V. Levin, Hélène Dollfus, Sylvie Odent, Joanne Sutherland, Maurice Menasche, Marc Abitbol
Publikováno v:
Human Mutation. 17:352-352
Type I oculocutaneous albinism (OCA) is an autosomal recessive disorder caused by the reduction or the absence of tyrosinase (TYR) activity in melanocytes of the skin, hair and eyes. Here we report an analysis of 45 patients with OCA. We found five n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::163aac59d61c4f07fe0a312f992ed135
https://doi.org/10.1002/humu.38
https://doi.org/10.1002/humu.38
Publikováno v:
Developmental Biology. (2):476-484
RGC axons extend in the optic tracts in a manner that correlates with the expression in the hypothalamus and epithalamus of a soluble factor inhibitory to RGC axon outgrowth. Additionally, although the RGC axons extend adjacent to the telencephalon,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a996da7ba91d195009d86ead9bd0626b