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Nils J. Færgeman

Researcher at University of Southern Denmark

Publications -  136
Citations -  12592

Nils J. Færgeman is an academic researcher from University of Southern Denmark. The author has contributed to research in topics: Acyl-CoA-binding protein & Caenorhabditis elegans. The author has an hindex of 44, co-authored 127 publications receiving 11229 citations. Previous affiliations of Nils J. Færgeman include Odense University & Novo Nordisk.

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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.
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Quantitative Phosphoproteomics Applied to the Yeast Pheromone Signaling Pathway

TL;DR: Of more than 700 identified phosphopeptides, 139 were differentially regulated at least 2-fold in response to mating pheromone and among these regulated proteins were components belonging to the mitogen-activated protein kinase signaling pathway and to downstream processes including transcriptional regulation, the establishment of polarized growth, and the regulation of the cell cycle.
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Role of long-chain fatty acyl-CoA esters in the regulation of metabolism and in cell signalling.

TL;DR: The observations that the ryanodine-senstitive Ca2+-release channel is regulated by long-chain acyl-CoA esters in the presence of a molar excess of acyl -CoA binding protein and that acetyl- coA carboxylase, the AMP kinase kinase and the Escherichia coli transcription factor FadR are affected by low nanomolar concentrations of Acyl- CoA indicate that long- chain acyl
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Sphingolipids: membrane microdomains in brain development, function and neurological diseases

TL;DR: The importance of microdomains with emphasis on sphingolipids in brain development and function is discussed as well as how disruption of the sphingoipid metabolism (and hence micro domains) contributes to the pathogenesis of several neurological diseases.