Michael Cheetham
Michael Cheetham
Professor of Molecular Cell Biology, UCL Institute of Ophthalmology
Verified email at
Cited by
Cited by
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
Guidelines for the nomenclature of the human heat shock proteins
HH Kampinga, J Hageman, MJ Vos, H Kubota, RM Tanguay, EA Bruford, ...
Cell Stress and Chaperones 14 (1), 105-111, 2009
Structure, function and evolution of DnaJ: conservation and adaptation of chaperone function
ME Cheetham, AJ Caplan
Cell stress & chaperones 3 (1), 28, 1998
Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
LA Metherell, JP Chapple, S Cooray, A David, C Becker, F Rüschendorf, ...
Nature genetics 37 (2), 166-170, 2005
Targeting amyloid-β in glaucoma treatment
L Guo, TE Salt, V Luong, N Wood, W Cheung, A Maass, G Ferrari, ...
Proceedings of the National Academy of Sciences 104 (33), 13444-13449, 2007
Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy
HF Mendes, J Van Der Spuy, JP Chapple, ME Cheetham
Trends in molecular medicine 11 (4), 177-185, 2005
The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formation
RS Saliba, PMG Munro, PJ Luthert, ME Cheetham
Journal of cell science 115 (14), 2907-2918, 2002
In vitro studies show that Hsp70 can be released by glia and that exogenous Hsp70 can enhance neuronal stress tolerance
I Guzhova, K Kislyakova, O Moskaliova, I Fridlanskaya, M Tytell, ...
Brain research 914 (1-2), 66-73, 2001
Not all J domains are created equal: implications for the specificity of Hsp40–Hsp70 interactions
F Hennessy, WS Nicoll, R Zimmermann, ME Cheetham, GL Blatch
Protein Science 14 (7), 1697-1709, 2005
Identification and correction of mechanisms underlying inherited blindness in human iPSC-derived optic cups
DA Parfitt, A Lane, CM Ramsden, AJF Carr, PM Munro, K Jovanovic, ...
Cell stem cell 18 (6), 769-781, 2016
Oxidative stress affects the junctional integrity of retinal pigment epithelial cells
TA Bailey, N Kanuga, IA Romero, J Greenwood, PJ Luthert, ...
Investigative ophthalmology & visual science 45 (2), 675-684, 2004
The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy
D Athanasiou, M Aguila, J Bellingham, W Li, C McCulley, PJ Reeves, ...
Progress in retinal and eye research 62, 1-23, 2018
Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase
M Borrell-Pagès, JM Canals, FP Cordelières, JA Parker, JR Pineda, ...
The Journal of clinical investigation 116 (5), 1410-1424, 2006
MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family
LF Chan, TR Webb, TT Chung, E Meimaridou, SN Cooray, L Guasti, ...
Proceedings of the National Academy of Sciences 106 (15), 6146-6151, 2009
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis
AI Den Hollander, RK Koenekoop, MD Mohamed, HH Arts, K Boldt, ...
Nature genetics 39 (7), 889-895, 2007
Late stage treatment with arimoclomol delays disease progression and prevents protein aggregation in the SOD1G93A mouse model of ALS
B Kalmar, S Novoselov, A Gray, ME Cheetham, B Margulis, L Greensmith
Journal of neurochemistry 107 (2), 339-350, 2008
Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect
AV Cideciyan, SG Jacobson, AV Drack, AC Ho, J Charng, AV Garafalo, ...
Nature medicine 25 (2), 225-228, 2019
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa
MM Abd El-Aziz, I Barragan, CA O'Driscoll, L Goodstadt, E Prigmore, ...
Nature genetics 40 (11), 1285-1287, 2008
The ataxia protein sacsin is a functional co-chaperone that protects against polyglutamine-expanded ataxin-1
DA Parfitt, GJ Michael, EGM Vermeulen, NV Prodromou, TR Webb, ...
Human molecular genetics 18 (9), 1556-1565, 2009
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)
TR Webb, DA Parfitt, JC Gardner, A Martinez, D Bevilacqua, AE Davidson, ...
Human molecular genetics 21 (16), 3647-3654, 2012
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