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Michael E Cheetham

Showing results (71-80 of 161) with videos related to

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American Journal of Human Genetics|January 28, 2021
Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse modelClarissa Patrizi, Manel Llado, Daniela Benati, et al.
Journal of Neurochemistry|July 5, 2005
Treatment with extracellular HSP70/HSC70 protein can reduce polyglutamine toxicity and aggregationTatiana V Novoselova, Boris A Margulis, Sergey S Novoselov, et al.
International Journal of Molecular Sciences|July 12, 2025
CRISPRa-Mediated Increase of OPA1 Expression in Dominant Optic AtrophyGiada Becchi, Michael Whitehead, Joshua P Harvey, et al.
Ophthalmic Genetics|October 18, 2017
A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataractVanita Berry, Nikolas Pontikos, Monica Albarca-Aguilera, et al.
Human Molecular Genetics|June 2, 2022
Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cellsPaul E Sladen, Katarina Jovanovic, Rosellina Guarascio, et al.
Gene|July 19, 2005
Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2Suzanne L Inglis-Broadgate, Louise Ocaka, Ruby Banerjee, et al.
Cell Stress & Chaperones|July 30, 2008
Guidelines for the nomenclature of the human heat shock proteinsHarm H Kampinga, Jurre Hageman, Michel J Vos, et al.
Human Molecular Genetics|September 12, 2012
NUB1 modulation of GSK3β reduces tau aggregationEmma Richet, Amy M Pooler, Teresa Rodriguez, et al.
The Biochemical Journal|March 22, 2003
Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sortingJ Paul Chapple, Celene Grayson, Alison J Hardcastle, et al.
Molecular Vision|March 16, 2012
Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosaCécilia Maubaret, Maria Kosmaoglou, Sancy Low, et al.
Pageof 17

Showing results (71-80 of 161) with videos related to

Sort By:
Pageof 17
American Journal of Human Genetics|January 28, 2021
Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse modelClarissa Patrizi, Manel Llado, Daniela Benati, et al.
Journal of Neurochemistry|July 5, 2005
Treatment with extracellular HSP70/HSC70 protein can reduce polyglutamine toxicity and aggregationTatiana V Novoselova, Boris A Margulis, Sergey S Novoselov, et al.
International Journal of Molecular Sciences|July 12, 2025
CRISPRa-Mediated Increase of OPA1 Expression in Dominant Optic AtrophyGiada Becchi, Michael Whitehead, Joshua P Harvey, et al.
Ophthalmic Genetics|October 18, 2017
A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataractVanita Berry, Nikolas Pontikos, Monica Albarca-Aguilera, et al.
Human Molecular Genetics|June 2, 2022
Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cellsPaul E Sladen, Katarina Jovanovic, Rosellina Guarascio, et al.
Gene|July 19, 2005
Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2Suzanne L Inglis-Broadgate, Louise Ocaka, Ruby Banerjee, et al.
Cell Stress & Chaperones|July 30, 2008
Guidelines for the nomenclature of the human heat shock proteinsHarm H Kampinga, Jurre Hageman, Michel J Vos, et al.
Human Molecular Genetics|September 12, 2012
NUB1 modulation of GSK3β reduces tau aggregationEmma Richet, Amy M Pooler, Teresa Rodriguez, et al.
The Biochemical Journal|March 22, 2003
Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sortingJ Paul Chapple, Celene Grayson, Alison J Hardcastle, et al.
Molecular Vision|March 16, 2012
Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosaCécilia Maubaret, Maria Kosmaoglou, Sancy Low, et al.
Pageof 17