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Investigative Ophthalmology & Visual Science|April 1, 1994
In vivo transfer of a reporter gene to the retina mediated by an adenoviral vectorT Li, M Adamian, D J Roof, et al.Human Mutation|July 21, 2009
A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetranceThomas Rio Frio, Terri L McGee, Nicholas M Wade, et al.Proceedings of the National Academy of Sciences of the United States of America|September 30, 1998
Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell culturesT Li, M A Sandberg, B S Pawlyk, et al.Investigative Ophthalmology & Visual Science|October 27, 2004
A novel mutation (I143NT) in guanylate cyclase-activating protein 1 (GCAP1) associated with autosomal dominant cone degenerationKoji M Nishiguchi, Izabela Sokal, Lili Yang, et al.Investigative Ophthalmology & Visual Science|August 1, 1990
Analysis of genes coding for S-antigen, interstitial retinol binding protein, and the alpha-subunit of cone transducin in patients with retinitis pigmentosaP J Ringens, M Fang, T Shinohara, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1993
A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosaE L Berson, B Rosner, M A Sandberg, et al.Proceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophyV Ramesh, A I McClatchey, N Ramesh, et al.American Journal of Human Genetics|November 1, 1990
Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophyA I McClatchey, D L Kaufman, E L Berson, et al.Ophthalmic Genetics|September 27, 2007
Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogramSureka Thiagalingam, Terri L McGee, Richard G Weleber, et al.Journal of Lipid Research|July 1, 1995
Red blood cell membrane phosphatidylethanolamine fatty acid content in various forms of retinitis pigmentosaE J Schaefer, S J Robins, G M Patton, et al.Pageof 22