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Edwin M Stone

Showing results (151-160 of 384) with videos related to

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Investigative Ophthalmology & Visual Science|June 27, 2007
Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damageRuth E Swiderski, Darryl Y Nishimura, Robert F Mullins, et al.
Neurology. Genetics|November 22, 2019
A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an <i>ELOVL4</i> mutationChangrui Xiao, Elaine M Binkley, Jessica Rexach, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 2011
Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypesQihong Zhang, Darryl Nishimura, Seongjin Seo, et al.
Human Molecular Genetics|July 22, 2010
Deducing the pathogenic contribution of recessive ABCA4 alleles in an outbred populationEmily I Schindler, Erik L Nylen, Audrey C Ko, et al.
American Journal of Ophthalmology|July 24, 2021
Long-Term Outcomes and Risk Factors for Severe Vision Loss in Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy (ADNIV)Timothy M Boyce, S Scott Whitmore, Katayoun Varzavand, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 13, 2011
Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitisAudrey C Ko, Jason P Brinton, Vinit B Mahajan, et al.
Molecular Vision|February 16, 2011
Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohortMarkus H Kuehn, Kai Wang, Ben Roos, et al.
Molecular Vision|May 23, 2009
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataractEsther Meyer, Fatimah Rahman, Jessica Owens, et al.
Investigative Ophthalmology & Visual Science|June 10, 2008
Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Human Gene Therapy|April 9, 2002
Gene transfer to the nonhuman primate retina with recombinant feline immunodeficiency virus vectorsAndrew J Lotery, Todd A Derksen, Stephen R Russell, et al.
Pageof 39

Showing results (151-160 of 384) with videos related to

Sort By:
Pageof 39
Investigative Ophthalmology & Visual Science|June 27, 2007
Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damageRuth E Swiderski, Darryl Y Nishimura, Robert F Mullins, et al.
Neurology. Genetics|November 22, 2019
A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an <i>ELOVL4</i> mutationChangrui Xiao, Elaine M Binkley, Jessica Rexach, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 2011
Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypesQihong Zhang, Darryl Nishimura, Seongjin Seo, et al.
Human Molecular Genetics|July 22, 2010
Deducing the pathogenic contribution of recessive ABCA4 alleles in an outbred populationEmily I Schindler, Erik L Nylen, Audrey C Ko, et al.
American Journal of Ophthalmology|July 24, 2021
Long-Term Outcomes and Risk Factors for Severe Vision Loss in Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy (ADNIV)Timothy M Boyce, S Scott Whitmore, Katayoun Varzavand, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 13, 2011
Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitisAudrey C Ko, Jason P Brinton, Vinit B Mahajan, et al.
Molecular Vision|February 16, 2011
Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohortMarkus H Kuehn, Kai Wang, Ben Roos, et al.
Molecular Vision|May 23, 2009
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataractEsther Meyer, Fatimah Rahman, Jessica Owens, et al.
Investigative Ophthalmology & Visual Science|June 10, 2008
Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Human Gene Therapy|April 9, 2002
Gene transfer to the nonhuman primate retina with recombinant feline immunodeficiency virus vectorsAndrew J Lotery, Todd A Derksen, Stephen R Russell, et al.
Pageof 39