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Michael E Cheetham

Showing results (51-60 of 161) with videos related to

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Eye (London, England)|June 24, 2018
Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataractVanita Berry, Alexander C W Ionides, Nikolas Pontikos, et al.
Brain : a Journal of Neurology|March 8, 2012
Suppression of protein aggregation by chaperone modification of high molecular weight complexesJohn Labbadia, Sergey S Novoselov, John S Bett, et al.
Cell Stress & Chaperones|November 17, 2004
Downstream caspases are novel targets for the antiapoptotic activity of the molecular chaperone hsp70Elena Yu Komarova, Elena A Afanasyeva, Marina M Bulatova, et al.
Investigative Ophthalmology & Visual Science|December 7, 2007
Novel retinal and cone photoreceptor transcripts revealed by human macular expression profilingDaniel M Hornan, Stuart N Peirson, Alison J Hardcastle, et al.
Endocrinology|September 27, 2008
Distinct melanocortin 2 receptor accessory protein domains are required for melanocortin 2 receptor interaction and promotion of receptor traffickingTom R Webb, Li Chan, Sadani N Cooray, et al.
Cellular and Molecular Life Sciences : CMLS|August 22, 2021
A look into retinal organoids: methods, analytical techniques, and applicationsTess A V Afanasyeva, Julio C Corral-Serrano, Alejandro Garanto, et al.
The Journal of Biological Chemistry|September 24, 2011
Molecular mechanisms of disease for mutations at Gly-90 in rhodopsinDarwin Toledo, Eva Ramon, Mònica Aguilà, et al.
Human Molecular Genetics|April 4, 2002
The Leber congenital amaurosis gene product AIPL1 is localized exclusively in rod photoreceptors of the adult human retinaJacqueline van der Spuy, J Paul Chapple, Brian J Clark, et al.
Investigative Ophthalmology & Visual Science|February 2, 2011
Knockdown of the zebrafish ortholog of the retinitis pigmentosa 2 (RP2) gene results in retinal degenerationXinhua Shu, Zhiqiang Zeng, Philippe Gautier, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 24, 2020
Symmetric arrangement of mitochondria:plasma membrane contacts between adjacent photoreceptor cells regulated by Opa1Ingrid P Meschede, Nicholas C Ovenden, Miguel C Seabra, et al.
Pageof 17

Showing results (51-60 of 161) with videos related to

Sort By:
Pageof 17
Eye (London, England)|June 24, 2018
Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataractVanita Berry, Alexander C W Ionides, Nikolas Pontikos, et al.
Brain : a Journal of Neurology|March 8, 2012
Suppression of protein aggregation by chaperone modification of high molecular weight complexesJohn Labbadia, Sergey S Novoselov, John S Bett, et al.
Cell Stress & Chaperones|November 17, 2004
Downstream caspases are novel targets for the antiapoptotic activity of the molecular chaperone hsp70Elena Yu Komarova, Elena A Afanasyeva, Marina M Bulatova, et al.
Investigative Ophthalmology & Visual Science|December 7, 2007
Novel retinal and cone photoreceptor transcripts revealed by human macular expression profilingDaniel M Hornan, Stuart N Peirson, Alison J Hardcastle, et al.
Endocrinology|September 27, 2008
Distinct melanocortin 2 receptor accessory protein domains are required for melanocortin 2 receptor interaction and promotion of receptor traffickingTom R Webb, Li Chan, Sadani N Cooray, et al.
Cellular and Molecular Life Sciences : CMLS|August 22, 2021
A look into retinal organoids: methods, analytical techniques, and applicationsTess A V Afanasyeva, Julio C Corral-Serrano, Alejandro Garanto, et al.
The Journal of Biological Chemistry|September 24, 2011
Molecular mechanisms of disease for mutations at Gly-90 in rhodopsinDarwin Toledo, Eva Ramon, Mònica Aguilà, et al.
Human Molecular Genetics|April 4, 2002
The Leber congenital amaurosis gene product AIPL1 is localized exclusively in rod photoreceptors of the adult human retinaJacqueline van der Spuy, J Paul Chapple, Brian J Clark, et al.
Investigative Ophthalmology & Visual Science|February 2, 2011
Knockdown of the zebrafish ortholog of the retinitis pigmentosa 2 (RP2) gene results in retinal degenerationXinhua Shu, Zhiqiang Zeng, Philippe Gautier, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 24, 2020
Symmetric arrangement of mitochondria:plasma membrane contacts between adjacent photoreceptor cells regulated by Opa1Ingrid P Meschede, Nicholas C Ovenden, Miguel C Seabra, et al.
Pageof 17