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P A Sieving

Showing results (61-70 of 91) with videos related to

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American Journal of Human Genetics|October 1, 1990
Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probesP A Sieving, E L Bingham, M S Roth, et al.
Genomics|November 5, 1997
Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degenerationQ Farjo, A Jackson, S Pieke-Dahl, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 2, 2000
Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 geneL C Eksandh, V Ponjavic, R Ayyagari, et al.
Human Genetics|September 12, 2000
Spectrum of color gene deletions and phenotype in patients with blue cone monochromacyR Ayyagari, L E Kakuk, E L Bingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2001
Inhibition of the visual cycle in vivo by 13-cis retinoic acid protects from light damage and provides a mechanism for night blindness in isotretinoin therapyP A Sieving, P Chaudhry, M Kondo, et al.
Nature Genetics|November 6, 2001
Nrl is required for rod photoreceptor developmentA J Mears, M Kondo, P K Swain, et al.
Molecular Vision|December 5, 1995
A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1R Fujita, M Blumberg, D Anderson, et al.
Human Molecular Genetics|February 5, 1999
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor functionA Swaroop, Q L Wang, W Wu, et al.
Investigative Ophthalmology & Visual Science|March 29, 2001
Lens epithelium-derived growth factor promotes photoreceptor survival in light-damaged and RCS ratsS Machida, P Chaudhry, T Shinohara, et al.
Nature Genetics|May 31, 2001
Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophyD A Thompson, Y Li, C L McHenry, et al.
Pageof 10

Showing results (61-70 of 91) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|October 1, 1990
Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probesP A Sieving, E L Bingham, M S Roth, et al.
Genomics|November 5, 1997
Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degenerationQ Farjo, A Jackson, S Pieke-Dahl, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 2, 2000
Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 geneL C Eksandh, V Ponjavic, R Ayyagari, et al.
Human Genetics|September 12, 2000
Spectrum of color gene deletions and phenotype in patients with blue cone monochromacyR Ayyagari, L E Kakuk, E L Bingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2001
Inhibition of the visual cycle in vivo by 13-cis retinoic acid protects from light damage and provides a mechanism for night blindness in isotretinoin therapyP A Sieving, P Chaudhry, M Kondo, et al.
Nature Genetics|November 6, 2001
Nrl is required for rod photoreceptor developmentA J Mears, M Kondo, P K Swain, et al.
Molecular Vision|December 5, 1995
A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1R Fujita, M Blumberg, D Anderson, et al.
Human Molecular Genetics|February 5, 1999
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor functionA Swaroop, Q L Wang, W Wu, et al.
Investigative Ophthalmology & Visual Science|March 29, 2001
Lens epithelium-derived growth factor promotes photoreceptor survival in light-damaged and RCS ratsS Machida, P Chaudhry, T Shinohara, et al.
Nature Genetics|May 31, 2001
Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophyD A Thompson, Y Li, C L McHenry, et al.
Pageof 10