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P A Sieving

Showing results (71-80 of 91) with videos related to

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Investigative Ophthalmology & Visual Science|September 1, 2000
P23H rhodopsin transgenic rat: correlation of retinal function with histopathologyS Machida, M Kondo, J A Jamison, et al.
Ophthalmic Genetics|July 23, 1999
A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutationR Mendoza-Londono, K T Hiriyanna, E L Bingham, et al.
American Journal of Human Genetics|October 27, 1997
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.
Eye (London, England)|November 7, 2009
Long-term follow-up of a family with dominant X-linked retinitis pigmentosaD M Wu, H Khanna, P Atmaca-Sonmez, et al.
American Journal of Human Genetics|March 3, 1999
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosaA J Mears, L Gieser, D Yan, et al.
Human Heredity|July 1, 1996
Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American familyY C Hou, J E Richards, E L Bingham, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 24, 2001
Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell lossP A Sieving, M L Fowler, R A Bush, et al.
Human Molecular Genetics|June 17, 1999
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgeneN McNally, P Kenna, M M Humphries, et al.
Human Molecular Genetics|June 1, 1994
Dinucleotide repeat polymorphism at the DXS977 locusD Yan, D Wong, K Zheng, et al.
Genomics|March 2, 1999
Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22S M Walpole, K T Hiriyana, A Nicolaou, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
Investigative Ophthalmology & Visual Science|September 1, 2000
P23H rhodopsin transgenic rat: correlation of retinal function with histopathologyS Machida, M Kondo, J A Jamison, et al.
Ophthalmic Genetics|July 23, 1999
A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutationR Mendoza-Londono, K T Hiriyanna, E L Bingham, et al.
American Journal of Human Genetics|October 27, 1997
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.
Eye (London, England)|November 7, 2009
Long-term follow-up of a family with dominant X-linked retinitis pigmentosaD M Wu, H Khanna, P Atmaca-Sonmez, et al.
American Journal of Human Genetics|March 3, 1999
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosaA J Mears, L Gieser, D Yan, et al.
Human Heredity|July 1, 1996
Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American familyY C Hou, J E Richards, E L Bingham, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 24, 2001
Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell lossP A Sieving, M L Fowler, R A Bush, et al.
Human Molecular Genetics|June 17, 1999
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgeneN McNally, P Kenna, M M Humphries, et al.
Human Molecular Genetics|June 1, 1994
Dinucleotide repeat polymorphism at the DXS977 locusD Yan, D Wong, K Zheng, et al.
Genomics|March 2, 1999
Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22S M Walpole, K T Hiriyana, A Nicolaou, et al.
Pageof 10