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Showing results (131-140 of 155) with videos related to

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Prenatal Diagnosis|December 11, 1999
First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complexC Rouillac, B Aral, F Fouque, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Intravitreous transplantation of encapsulated fibroblasts secreting the human fibroblast growth factor 2 delays photoreceptor cell degeneration in Royal College of Surgeons ratsY Uteza, J S Rouillot, A Kobetz, et al.
American Journal of Human Genetics|April 22, 2008
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndromeDaniel F Schorderet, Olivia Nichini, Gaëlle Boisset, et al.
Journal of Medical Genetics|April 5, 2003
Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataractsE Nandrot, C Slingsby, A Basak, et al.
Human Molecular Genetics|December 23, 1999
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genesF Fougerousse, P Bullen, M Herasse, et al.
Cell Communication & Adhesion|April 9, 2002
Prominent beta-5 gene expression in the cardiovascular system and in the cartilaginous primordiae of the skeleton during mouse developmentL Le Gat, S Bonnel, K Gogat, et al.
Molecular Vision|January 6, 2009
Analysis of partner of inscuteable (mPins) expression in the developing mouse eyeB Raji, A Dansault, V Vieira, et al.
Gene Therapy|November 5, 2003
In vivo adenovirus-mediated delivery of a uPA/uPAR antagonist reduces retinal neovascularization in a mouse model of retinopathyL Le Gat, K Gogat, C Bouquet, et al.
Human Gene Therapy|September 15, 2000
Ocular cell transfection with the human basic fibroblast growth factor gene delays photoreceptor cell degeneration in RCS ratsM Neuner-Jehle, L V Berghe, S Bonnel, et al.
Plos Biology|November 10, 2021
Lineage-tracing and translatomic analysis of damage-inducible mitotic cochlear progenitors identifies candidate genes regulating regenerationTomokatsu Udagawa, Patrick J Atkinson, Beatrice Milon, et al.
Pageof 16

Showing results (131-140 of 155) with videos related to

Sort By:
Pageof 16
Prenatal Diagnosis|December 11, 1999
First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complexC Rouillac, B Aral, F Fouque, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Intravitreous transplantation of encapsulated fibroblasts secreting the human fibroblast growth factor 2 delays photoreceptor cell degeneration in Royal College of Surgeons ratsY Uteza, J S Rouillot, A Kobetz, et al.
American Journal of Human Genetics|April 22, 2008
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndromeDaniel F Schorderet, Olivia Nichini, Gaëlle Boisset, et al.
Journal of Medical Genetics|April 5, 2003
Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataractsE Nandrot, C Slingsby, A Basak, et al.
Human Molecular Genetics|December 23, 1999
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genesF Fougerousse, P Bullen, M Herasse, et al.
Cell Communication & Adhesion|April 9, 2002
Prominent beta-5 gene expression in the cardiovascular system and in the cartilaginous primordiae of the skeleton during mouse developmentL Le Gat, S Bonnel, K Gogat, et al.
Molecular Vision|January 6, 2009
Analysis of partner of inscuteable (mPins) expression in the developing mouse eyeB Raji, A Dansault, V Vieira, et al.
Gene Therapy|November 5, 2003
In vivo adenovirus-mediated delivery of a uPA/uPAR antagonist reduces retinal neovascularization in a mouse model of retinopathyL Le Gat, K Gogat, C Bouquet, et al.
Human Gene Therapy|September 15, 2000
Ocular cell transfection with the human basic fibroblast growth factor gene delays photoreceptor cell degeneration in RCS ratsM Neuner-Jehle, L V Berghe, S Bonnel, et al.
Plos Biology|November 10, 2021
Lineage-tracing and translatomic analysis of damage-inducible mitotic cochlear progenitors identifies candidate genes regulating regenerationTomokatsu Udagawa, Patrick J Atkinson, Beatrice Milon, et al.
Pageof 16