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Harm H. Kampinga

Researcher at University Medical Center Groningen

Publications -  274
Citations -  26693

Harm H. Kampinga is an academic researcher from University Medical Center Groningen. The author has contributed to research in topics: Heat shock protein & Protein aggregation. The author has an hindex of 72, co-authored 266 publications receiving 23597 citations. Previous affiliations of Harm H. Kampinga include University of Groningen & University of Pennsylvania.

Papers
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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

`The HSP70 chaperone machinery: J proteins as drivers of functional specificity

Harm H. Kampinga, +1 more
- 01 Aug 2010 - 
TL;DR: Heat shock 70 kDa proteins are ubiquitous molecular chaperones that function in a myriad of biological processes, modulating polypeptide folding, degradation and translocation across membranes, and protein–protein interactions.
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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Rescue of salivary gland function after stem cell transplantation in irradiated glands.

Isabelle M.A. Lombaert, +9 more
- 30 Apr 2008 - 
TL;DR: In vivo, intra-glandular transplantation of a small number of c-Kit+ cells resulted in long-term restoration of salivary gland morphology and function and is the first proof for the potential use of stem cell transplantation to functionally rescue salivARY gland deficiency.