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Michael Cheetham
Michael Cheetham
Professor of Molecular Cell Biology, UCL Institute of Ophthalmology
Dirección de correo verificada de ucl.ac.uk
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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
13055*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
14932009
Structure, function and evolution of DnaJ: conservation and adaptation of chaperone function
ME Cheetham, AJ Caplan
Cell stress & chaperones 3 (1), 28, 1998
7721998
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
4732005
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
4452007
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
4112002
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
4092005
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
4082001
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
3702005
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
3132016
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
3082004
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
2892018
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
2622006
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
2522009
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
2232007
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
2192008
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
2062019
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
2002008
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
1892009
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
1702012
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20