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J Fielding

Showing results (381-390 of 493) with videos related to

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Molecular Vision|December 2, 2005
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 geneQingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
Ophthalmic Genetics|March 10, 2011
An atypical form of Bietti crystalline dystrophySettimio Rossi, Francesco Testa, Anren Li, et al.
Molecular Vision|March 30, 2007
Mutations in NYX of individuals with high myopia, but without night blindnessQingjiong Zhang, Xueshan Xiao, Shiqiang Li, et al.
Structure (London, England : 1993)|November 15, 2016
Structural Basis for Selective Interaction between the ESCRT Regulator HD-PTP and UBAP1Deepankar Gahloth, Colin Levy, Graham Heaven, et al.
Experimental Eye Research|June 4, 2025
DAPL1 inhibits epithelial-mesenchymal transition of retinal pigment epithelial cells by regulating the TGF-β/MITF pathwayYaqi You, Youjia Liu, Lijing Huang, et al.
Genes|August 26, 2022
A Mouse Model with Ablated Asparaginase and Isoaspartyl Peptidase 1 (<i>Asrgl1</i>) Develops Early Onset Retinal Degeneration (RD) Recapitulating the Human PhenotypePooja Biswas, Anne Marie Berry, Qais Zawaydeh, et al.
Molecular Vision|June 10, 2011
Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosaShahbaz Ali, S Amer Riazuddin, Amber Shahzadi, et al.
Human Genome Variation|September 8, 2022
A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataractsBushra Irum, Firoz Kabir, Nadav Shoshany, et al.
Ophthalmology|December 3, 2014
Phenotypic variability associated with the D226N allele of IMPDH1Shahbaz Ali, Shahid Y Khan, Muhammad Asif Naeem, et al.
Molecular Vision|July 24, 2013
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophyFiroz Kabir, Shagufta Naz, S Amer Riazuddin, et al.
Pageof 50

Showing results (381-390 of 493) with videos related to

Sort By:
Pageof 50
Molecular Vision|December 2, 2005
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 geneQingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
Ophthalmic Genetics|March 10, 2011
An atypical form of Bietti crystalline dystrophySettimio Rossi, Francesco Testa, Anren Li, et al.
Molecular Vision|March 30, 2007
Mutations in NYX of individuals with high myopia, but without night blindnessQingjiong Zhang, Xueshan Xiao, Shiqiang Li, et al.
Structure (London, England : 1993)|November 15, 2016
Structural Basis for Selective Interaction between the ESCRT Regulator HD-PTP and UBAP1Deepankar Gahloth, Colin Levy, Graham Heaven, et al.
Experimental Eye Research|June 4, 2025
DAPL1 inhibits epithelial-mesenchymal transition of retinal pigment epithelial cells by regulating the TGF-β/MITF pathwayYaqi You, Youjia Liu, Lijing Huang, et al.
Genes|August 26, 2022
A Mouse Model with Ablated Asparaginase and Isoaspartyl Peptidase 1 (<i>Asrgl1</i>) Develops Early Onset Retinal Degeneration (RD) Recapitulating the Human PhenotypePooja Biswas, Anne Marie Berry, Qais Zawaydeh, et al.
Molecular Vision|June 10, 2011
Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosaShahbaz Ali, S Amer Riazuddin, Amber Shahzadi, et al.
Human Genome Variation|September 8, 2022
A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataractsBushra Irum, Firoz Kabir, Nadav Shoshany, et al.
Ophthalmology|December 3, 2014
Phenotypic variability associated with the D226N allele of IMPDH1Shahbaz Ali, Shahid Y Khan, Muhammad Asif Naeem, et al.
Molecular Vision|July 24, 2013
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophyFiroz Kabir, Shagufta Naz, S Amer Riazuddin, et al.
Pageof 50