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Michael E Cheetham

Showing results (61-70 of 161) with videos related to

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The International Journal of Biochemistry & Cell Biology|May 4, 2010
The binding of the molecular chaperone Hsc70 to the prion protein PrP is modulated by pH and copperSimon Wilkins, Ashraf A Choglay, J Paul Chapple, et al.
Investigative Ophthalmology & Visual Science|November 26, 2003
The expression of the Leber congenital amaurosis protein AIPL1 coincides with rod and cone photoreceptor developmentJacqueline van der Spuy, Jeong H Kim, Young S Yu, et al.
The Journal of Biological Chemistry|November 1, 2014
Differential light-induced responses in sectorial inherited retinal degenerationEva Ramon, Arnau Cordomí, Mònica Aguilà, et al.
Molecular Biology of the Cell|August 3, 2012
BiP prevents rod opsin aggregationDimitra Athanasiou, Maria Kosmaoglou, Naheed Kanuga, et al.
Human Molecular Genetics|March 25, 2010
The Nance-Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphologySimon P Brooks, Margherita Coccia, Hao R Tang, et al.
Investigative Ophthalmology & Visual Science|April 28, 2004
Modulation of Sub-RPE deposits in vitro: a potential model for age-related macular degenerationSepideh Amin, N H Victor Chong, Tracey A Bailey, et al.
Progress in Retinal and Eye Research|February 18, 2024
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicityMarzena Kurzawa-Akanbi, Nikolaos Tzoumas, Julio C Corral-Serrano, et al.
Molecular Vision|July 30, 2005
Predominant rod photoreceptor degeneration in Leber congenital amaurosisJacqueline van der Spuy, Peter M G Munro, Philip J Luthert, et al.
Plos One|September 12, 2013
Molecular chaperone mediated late-stage neuroprotection in the SOD1(G93A) mouse model of amyotrophic lateral sclerosisSergey S Novoselov, Wendy J Mustill, Anna L Gray, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
Pageof 17

Showing results (61-70 of 161) with videos related to

Sort By:
Pageof 17
The International Journal of Biochemistry & Cell Biology|May 4, 2010
The binding of the molecular chaperone Hsc70 to the prion protein PrP is modulated by pH and copperSimon Wilkins, Ashraf A Choglay, J Paul Chapple, et al.
Investigative Ophthalmology & Visual Science|November 26, 2003
The expression of the Leber congenital amaurosis protein AIPL1 coincides with rod and cone photoreceptor developmentJacqueline van der Spuy, Jeong H Kim, Young S Yu, et al.
The Journal of Biological Chemistry|November 1, 2014
Differential light-induced responses in sectorial inherited retinal degenerationEva Ramon, Arnau Cordomí, Mònica Aguilà, et al.
Molecular Biology of the Cell|August 3, 2012
BiP prevents rod opsin aggregationDimitra Athanasiou, Maria Kosmaoglou, Naheed Kanuga, et al.
Human Molecular Genetics|March 25, 2010
The Nance-Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphologySimon P Brooks, Margherita Coccia, Hao R Tang, et al.
Investigative Ophthalmology & Visual Science|April 28, 2004
Modulation of Sub-RPE deposits in vitro: a potential model for age-related macular degenerationSepideh Amin, N H Victor Chong, Tracey A Bailey, et al.
Progress in Retinal and Eye Research|February 18, 2024
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicityMarzena Kurzawa-Akanbi, Nikolaos Tzoumas, Julio C Corral-Serrano, et al.
Molecular Vision|July 30, 2005
Predominant rod photoreceptor degeneration in Leber congenital amaurosisJacqueline van der Spuy, Peter M G Munro, Philip J Luthert, et al.
Plos One|September 12, 2013
Molecular chaperone mediated late-stage neuroprotection in the SOD1(G93A) mouse model of amyotrophic lateral sclerosisSergey S Novoselov, Wendy J Mustill, Anna L Gray, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
Pageof 17