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Michael E. Cheetham

Researcher at UCL Institute of Ophthalmology

Publications -  207
Citations -  19348

Michael E. Cheetham is an academic researcher from UCL Institute of Ophthalmology. The author has contributed to research in topics: Retinitis pigmentosa & Retinal degeneration. The author has an hindex of 58, co-authored 192 publications receiving 16311 citations. Previous affiliations of Michael E. Cheetham include University of London & Moorfields Eye Hospital.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky, +2983 more
- 08 Feb 2021 - 
TL;DR: In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
Journal ArticleDOI

Guidelines for the nomenclature of the human heat shock proteins

Harm H. Kampinga, +10 more
- 01 Jan 2009 - 
TL;DR: New guidelines for the nomenclature of the human HSP families, HSPH (HSP110), HSPC (H SP90), HSPA (HSPA70), DNAJ, and HSPB (small HSP) as well as for the human chaperonin families HSPD/E (Hsp60/HSP10) and CCT (TRiC).
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Structure, function and evolution of DnaJ: conservation and adaptation of chaperone function

Michael E. Cheetham, +1 more
- 01 Mar 1998 - 
Journal ArticleDOI

Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2.

Louise A. Metherell, +12 more
- 01 Jan 2005 - 
TL;DR: It is shown that MRAP interacts withMC2R and may have a role in the trafficking of MC2R from the endoplasmic reticulum to the cell surface and may be involved in the Trafficking of melanocortin 2 receptor accessory protein (MRAP).