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P A Sieving

Showing results (51-60 of 91) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1984
Multiple evanescent white dot syndrome. I. Clinical findingsL M Jampol, P A Sieving, D Pugh, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 31, 1995
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutationP A Sieving, J E Richards, F Naarendorp, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Bietti crystalline retinopathy and juvenile retinoschisis in a family with a novel RS1 mutationD V Weinberg, P A Sieving, E L Bingham, et al.
Human Heredity|November 1, 1996
X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YACH Pawar, E L Bingham, K Hiriyanna, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 15, 2000
Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 geneR Ayyagari, I B Griesinger, E Bingham, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2000
Retinal toxicity of commercial intravitreal tissue plasminogen activator solution in cat eyesC J Hrach, M W Johnson, A S Hassan, et al.
Human Molecular Genetics|January 12, 2010
Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisisY V Sergeev, R C Caruso, M R Meltzer, et al.
Gene Therapy|May 22, 2009
Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouseT K Park, Z Wu, S Kjellstrom, et al.
Molecular Vision|July 31, 1999
Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment geneR Ayyagari, L E Kakuk, C L Coats, et al.
Human Heredity|July 1, 1995
Refined genetic mapping of juvenile X-linked retinoschisisH Pawar, E L Bingham, K L Lunetta, et al.
Pageof 10

Showing results (51-60 of 91) with videos related to

Sort By:
Pageof 10
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1984
Multiple evanescent white dot syndrome. I. Clinical findingsL M Jampol, P A Sieving, D Pugh, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 31, 1995
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutationP A Sieving, J E Richards, F Naarendorp, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Bietti crystalline retinopathy and juvenile retinoschisis in a family with a novel RS1 mutationD V Weinberg, P A Sieving, E L Bingham, et al.
Human Heredity|November 1, 1996
X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YACH Pawar, E L Bingham, K Hiriyanna, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 15, 2000
Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 geneR Ayyagari, I B Griesinger, E Bingham, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2000
Retinal toxicity of commercial intravitreal tissue plasminogen activator solution in cat eyesC J Hrach, M W Johnson, A S Hassan, et al.
Human Molecular Genetics|January 12, 2010
Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisisY V Sergeev, R C Caruso, M R Meltzer, et al.
Gene Therapy|May 22, 2009
Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouseT K Park, Z Wu, S Kjellstrom, et al.
Molecular Vision|July 31, 1999
Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment geneR Ayyagari, L E Kakuk, C L Coats, et al.
Human Heredity|July 1, 1995
Refined genetic mapping of juvenile X-linked retinoschisisH Pawar, E L Bingham, K L Lunetta, et al.
Pageof 10