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T P Dryja

Showing results (91-100 of 141) with videos related to

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American Journal of Human Genetics|May 1, 1991
Allele-specific hypermethylation of the retinoblastoma tumor-suppressor geneT Sakai, J Toguchida, N Ohtani, et al.
Experimental Eye Research|July 1, 1990
Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNAP R Cotran, P J Ringens, J W Crabb, et al.
Journal of Medical Genetics|June 7, 2005
Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophyJ Lin, K M Nishiguchi, M Nakamura, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1991
Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosaT P Dryja, L B Hahn, G S Cowley, et al.
Medical and Pediatric Oncology|September 25, 2001
RB1 genetic testing as a clinical service: a follow-up studyJ G Cohen, T P Dryja, K B Davis, et al.
Nature Genetics|February 14, 1998
Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosaS A Hagstrom, M A North, P L Nishina, et al.
Investigative Ophthalmology & Visual Science|October 1, 1995
Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutationP J Rosenfeld, L B Hahn, M A Sandberg, et al.
Oncogene|June 1, 1994
A silencer element in the retinoblastoma tumor-suppressor geneN Ohtani-Fujita, T Fujita, R Takahashi, et al.
Nature|June 15, 1989
Parental origin of mutations of the retinoblastoma geneT P Dryja, S Mukai, R Petersen, et al.
Nature|December 12, 1991
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosaK Kajiwara, L B Hahn, S Mukai, et al.
Pageof 15

Showing results (91-100 of 141) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|May 1, 1991
Allele-specific hypermethylation of the retinoblastoma tumor-suppressor geneT Sakai, J Toguchida, N Ohtani, et al.
Experimental Eye Research|July 1, 1990
Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNAP R Cotran, P J Ringens, J W Crabb, et al.
Journal of Medical Genetics|June 7, 2005
Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophyJ Lin, K M Nishiguchi, M Nakamura, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1991
Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosaT P Dryja, L B Hahn, G S Cowley, et al.
Medical and Pediatric Oncology|September 25, 2001
RB1 genetic testing as a clinical service: a follow-up studyJ G Cohen, T P Dryja, K B Davis, et al.
Nature Genetics|February 14, 1998
Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosaS A Hagstrom, M A North, P L Nishina, et al.
Investigative Ophthalmology & Visual Science|October 1, 1995
Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutationP J Rosenfeld, L B Hahn, M A Sandberg, et al.
Oncogene|June 1, 1994
A silencer element in the retinoblastoma tumor-suppressor geneN Ohtani-Fujita, T Fujita, R Takahashi, et al.
Nature|June 15, 1989
Parental origin of mutations of the retinoblastoma geneT P Dryja, S Mukai, R Petersen, et al.
Nature|December 12, 1991
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosaK Kajiwara, L B Hahn, S Mukai, et al.
Pageof 15