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Jocelyn Laporte

Researcher at University of Strasbourg

Publications -  229
Citations -  22550

Jocelyn Laporte is an academic researcher from University of Strasbourg. The author has contributed to research in topics: Centronuclear myopathy & Myotubularin. The author has an hindex of 61, co-authored 212 publications receiving 19003 citations. Previous affiliations of Jocelyn Laporte include Collège de France & French Institute of Health and Medical Research.

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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

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy 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

A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast

Jocelyn Laporte, +8 more
- 01 Jun 1996 - 
TL;DR: The presence of frameshift or missense mutations in seven patients proved that one of these genes is indeed implicated in MTM1, a new family of putative tyrosine phosphatases in man.
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Mutations in dynamin 2 cause dominant centronuclear myopathy.

Marc Bitoun, +13 more
- 16 Oct 2005 - 
TL;DR: In 11 families affected by centronuclear myopathy, recurrent and de novo missense mutations in the gene dynamin 2 (DNM2), which encodes a protein involved in endocytosis and membrane trafficking, actin assembly and centrosome cohesion, were identified.