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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 complex
C 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 rats
Y 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 syndrome
Daniel 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 cataracts
E 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 genes
F 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 development
L Le Gat, S Bonnel, K Gogat, et al.
Molecular Vision
|
January 6, 2009
Analysis of partner of inscuteable (mPins) expression in the developing mouse eye
B 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 retinopathy
L 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 rats
M 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 regeneration
Tomokatsu Udagawa, Patrick J Atkinson, Beatrice Milon, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 155) with videos related to
Sort By:
Page
of 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 complex
C 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 rats
Y 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 syndrome
Daniel 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 cataracts
E 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 genes
F 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 development
L Le Gat, S Bonnel, K Gogat, et al.
Molecular Vision
|
January 6, 2009
Analysis of partner of inscuteable (mPins) expression in the developing mouse eye
B 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 retinopathy
L 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 rats
M 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 regeneration
Tomokatsu Udagawa, Patrick J Atkinson, Beatrice Milon, et al.
Page
of 16