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T P Dryja

Showing results (41-50 of 141) with videos related to

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Nature Genetics|July 1, 1996
Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindnessT P Dryja, L B Hahn, T Reboul, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 24, 1999
Photoreceptor rosettes in autosomal dominant retinitis pigmentosa with reduced penetranceW Tulvatana, M Adamian, E L Berson, et al.
American Journal of Human Genetics|April 25, 2000
Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing lossC Rivolta, E A Sweklo, E L Berson, et al.
Experimental Eye Research|November 1, 1977
Presence of cysteinyldopa in the mature bovine eyeT P Dryja, D M Albert, E Rosengren, et al.
Nature Genetics|March 1, 1993
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescensK Kajiwara, M A Sandberg, E L Berson, et al.
Nature Genetics|February 1, 1997
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindnessS Yamamoto, K C Sippel, E L Berson, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segmentsT Li, W K Snyder, J E Olsson, et al.
Survey of Ophthalmology|November 1, 1995
Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutationT A Ciulla, F Tolentino, J F Morrow, et al.
Nucleic Acids Research|August 25, 1990
PCR detection of the Tth 111 I RFLP at the RB locusG L Vaughn, J Toguchida, T L McGee, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His)E L Berson, B Rosner, M A Sandberg, et al.
Pageof 15

Showing results (41-50 of 141) with videos related to

Sort By:
Pageof 15
Nature Genetics|July 1, 1996
Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindnessT P Dryja, L B Hahn, T Reboul, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 24, 1999
Photoreceptor rosettes in autosomal dominant retinitis pigmentosa with reduced penetranceW Tulvatana, M Adamian, E L Berson, et al.
American Journal of Human Genetics|April 25, 2000
Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing lossC Rivolta, E A Sweklo, E L Berson, et al.
Experimental Eye Research|November 1, 1977
Presence of cysteinyldopa in the mature bovine eyeT P Dryja, D M Albert, E Rosengren, et al.
Nature Genetics|March 1, 1993
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescensK Kajiwara, M A Sandberg, E L Berson, et al.
Nature Genetics|February 1, 1997
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindnessS Yamamoto, K C Sippel, E L Berson, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segmentsT Li, W K Snyder, J E Olsson, et al.
Survey of Ophthalmology|November 1, 1995
Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutationT A Ciulla, F Tolentino, J F Morrow, et al.
Nucleic Acids Research|August 25, 1990
PCR detection of the Tth 111 I RFLP at the RB locusG L Vaughn, J Toguchida, T L McGee, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His)E L Berson, B Rosner, M A Sandberg, et al.
Pageof 15