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Markus R. Wenk

Researcher at National University of Singapore

Publications -  332
Citations -  25285

Markus R. Wenk is an academic researcher from National University of Singapore. The author has contributed to research in topics: Medicine & Lipid metabolism. The author has an hindex of 81, co-authored 292 publications receiving 21516 citations. Previous affiliations of Markus R. Wenk include Swiss Tropical and Public Health Institute & University of Geneva.

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Characterization of a dynamic metabolon producing the defense compound dhurrin in sorghum.

TL;DR: The isolation of the dynamic metabolon that catalyzes the formation of the cyanogenic glucoside dhurrin, a defense compound produced in sorghum plants is reported, which demonstrated the importance of membrane surface charge and the presence of the glucosyltransferase for metabolic channeling.
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Rhinovirus Uses a Phosphatidylinositol 4-Phosphate/Cholesterol Counter-Current for the Formation of Replication Compartments at the ER-Golgi Interface

TL;DR: It is shown that rhinovirus replication depends on host factors driving phosphatidylinositol 4-phosphate (PI4P)-cholesterol counter-currents at viral replication membranes, and data support a PI4P-ch cholesterol counter-flux model for rhinOVirus replication.
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Extensive diversity in circadian regulation of plasma lipids and evidence for different circadian metabolic phenotypes in humans

TL;DR: Healthy subjects showed substantial variation in the timing and strength of rhythms across different lipid species, suggesting that there are different circadian metabolic phenotypes in the general population and potential implications for lipid metabolism disorders linked to circadian clock disruption.
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Regulation of synaptojanin 1 by cyclin-dependent kinase 5 at synapses

TL;DR: It is shown that cyclin-dependent kinase 5 (Cdk5) phosphorylates synaptojanin 1 and regulates its function both in vitro and in intact synaptosomes, and suggests that Cdk5 and calcineurin may have an antagonistic role in the regulation of synaptobic recruitment and activity, and therefore in theregulation of phosphatidylinositol 4,5-bisphosphate turnover at synapses.