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Kari Branham

Showing results (31-40 of 54) with videos related to

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The New England Journal of Medicine|September 10, 2010
E2-2 protein and Fuchs's corneal dystrophyKeith H Baratz, Nirubol Tosakulwong, Euijung Ryu, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Toll-like receptor polymorphisms and age-related macular degenerationAlbert O Edwards, Dequan Chen, Brooke L Fridley, et al.
Physiological Genomics|October 30, 2016
Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencingKari Branham, Hiroko Matsui, Pooja Biswas, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2007
Molecular testing for hereditary retinal disease as part of clinical careKaty Downs, David N Zacks, Rafael Caruso, et al.
Human Mutation|August 7, 2018
Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsiaNicole Weisschuh, Katarina Stingl, Isabelle Audo, et al.
Physiological Genomics|January 29, 2017
Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype associationPooja Biswas, Jacque L Duncan, Bruno Maranhao, et al.
American Journal of Human Genetics|December 23, 2006
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degenerationJames S Friedman, Bo Chang, Chitra Kannabiran, et al.
Human Mutation|March 10, 2022
Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A studyRobert B Hufnagel, Wendi Liang, Jacque L Duncan, et al.
Investigative Ophthalmology & Visual Science|October 18, 2011
Complement factor D in age-related macular degenerationChloe M Stanton, John R W Yates, Anneke I den Hollander, et al.
Human Molecular Genetics|April 5, 2020
Family-based exome sequencing identifies rare coding variants in age-related macular degenerationRinki Ratnapriya, İlhan E Acar, Maartje J Geerlings, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
The New England Journal of Medicine|September 10, 2010
E2-2 protein and Fuchs's corneal dystrophyKeith H Baratz, Nirubol Tosakulwong, Euijung Ryu, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Toll-like receptor polymorphisms and age-related macular degenerationAlbert O Edwards, Dequan Chen, Brooke L Fridley, et al.
Physiological Genomics|October 30, 2016
Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencingKari Branham, Hiroko Matsui, Pooja Biswas, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2007
Molecular testing for hereditary retinal disease as part of clinical careKaty Downs, David N Zacks, Rafael Caruso, et al.
Human Mutation|August 7, 2018
Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsiaNicole Weisschuh, Katarina Stingl, Isabelle Audo, et al.
Physiological Genomics|January 29, 2017
Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype associationPooja Biswas, Jacque L Duncan, Bruno Maranhao, et al.
American Journal of Human Genetics|December 23, 2006
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degenerationJames S Friedman, Bo Chang, Chitra Kannabiran, et al.
Human Mutation|March 10, 2022
Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A studyRobert B Hufnagel, Wendi Liang, Jacque L Duncan, et al.
Investigative Ophthalmology & Visual Science|October 18, 2011
Complement factor D in age-related macular degenerationChloe M Stanton, John R W Yates, Anneke I den Hollander, et al.
Human Molecular Genetics|April 5, 2020
Family-based exome sequencing identifies rare coding variants in age-related macular degenerationRinki Ratnapriya, İlhan E Acar, Maartje J Geerlings, et al.
Pageof 6