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Michael E Cheetham

Showing results (21-30 of 161) with videos related to

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Human Molecular Genetics|October 5, 2010
Molecular chaperone-mediated rescue of mitophagy by a Parkin RING1 domain mutantJohanna M Rose, Sergey S Novoselov, Philip A Robinson, et al.
Trends in Endocrinology and Metabolism: TEM|November 8, 2005
Inherited ACTH insensitivity illuminates the mechanisms of ACTH actionAdrian J L Clark, Louise A Metherell, Michael E Cheetham, et al.
Trends in Molecular Medicine|April 13, 2005
Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapyHugo F Mendes, Jacqueline van der Spuy, J Paul Chapple, et al.
Journal of Cell Science|June 26, 2002
The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formationRichard S Saliba, Peter M G Munro, Philip J Luthert, et al.
Protein Science : a Publication of the Protein Society|July 1, 2005
Not all J domains are created equal: implications for the specificity of Hsp40-Hsp70 interactionsFritha Hennessy, William S Nicoll, Richard Zimmermann, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|December 6, 2017
DNAJ Proteins in neurodegeneration: essential and protective factorsChristina Zarouchlioti, David A Parfitt, Wenwen Li, et al.
Plos One|January 10, 2018
Correlative light and immuno-electron microscopy of retinal tissue cryostat sectionsThomas Burgoyne, Amelia Lane, William E Laughlin, et al.
Journal of Neurochemistry|August 5, 2008
Late stage treatment with arimoclomol delays disease progression and prevents protein aggregation in the SOD1 mouse model of ALSBernadett Kalmar, Sergey Novoselov, Anna Gray, et al.
Human Molecular Genetics|October 17, 2017
The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosaDimitra Athanasiou, Monica Aguila, James Bellingham, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 11, 2021
Induced Pluripotent Stem Cells for Inherited Optic Neuropathies-Disease Modeling and Therapeutic DevelopmentJoshua Paul Harvey, Paul Edward Sladen, Patrick Yu-Wai-Man, et al.
Pageof 17

Showing results (21-30 of 161) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|October 5, 2010
Molecular chaperone-mediated rescue of mitophagy by a Parkin RING1 domain mutantJohanna M Rose, Sergey S Novoselov, Philip A Robinson, et al.
Trends in Endocrinology and Metabolism: TEM|November 8, 2005
Inherited ACTH insensitivity illuminates the mechanisms of ACTH actionAdrian J L Clark, Louise A Metherell, Michael E Cheetham, et al.
Trends in Molecular Medicine|April 13, 2005
Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapyHugo F Mendes, Jacqueline van der Spuy, J Paul Chapple, et al.
Journal of Cell Science|June 26, 2002
The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formationRichard S Saliba, Peter M G Munro, Philip J Luthert, et al.
Protein Science : a Publication of the Protein Society|July 1, 2005
Not all J domains are created equal: implications for the specificity of Hsp40-Hsp70 interactionsFritha Hennessy, William S Nicoll, Richard Zimmermann, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|December 6, 2017
DNAJ Proteins in neurodegeneration: essential and protective factorsChristina Zarouchlioti, David A Parfitt, Wenwen Li, et al.
Plos One|January 10, 2018
Correlative light and immuno-electron microscopy of retinal tissue cryostat sectionsThomas Burgoyne, Amelia Lane, William E Laughlin, et al.
Journal of Neurochemistry|August 5, 2008
Late stage treatment with arimoclomol delays disease progression and prevents protein aggregation in the SOD1 mouse model of ALSBernadett Kalmar, Sergey Novoselov, Anna Gray, et al.
Human Molecular Genetics|October 17, 2017
The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosaDimitra Athanasiou, Monica Aguila, James Bellingham, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 11, 2021
Induced Pluripotent Stem Cells for Inherited Optic Neuropathies-Disease Modeling and Therapeutic DevelopmentJoshua Paul Harvey, Paul Edward Sladen, Patrick Yu-Wai-Man, et al.
Pageof 17