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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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Targeting Lipid Esterases in Mycobacteria Grown Under Different Physiological Conditions Using Activity-based Profiling with Tetrahydrolipstatin (THL)

TL;DR: A THL analog and activity-based protein profiling is used to identify target proteins after enrichment from whole cell lysates of Mycobacterium bovis Bacillus Calmette-Guérin cultured under replicating and non-replicating conditions to define the target spectrum of THL in a biological species with particularly diverse lipid metabolic pathways.
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Recommendations for good practice in MS-based lipidomics

TL;DR: The Lipidomics Standards Initiative (LSI) as discussed by the authors is a community-based endeavor for the coordination of development of these best practice guidelines in lipidomics, and is embedded within the International lipidomics Society (ILS).
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Longitudinal changes in tear fluid lipidome brought about by eyelid-warming treatment in a cohort of meibomian gland dysfunction

TL;DR: Excess ocular surface phospholipase activity detrimental to tear film stability could be alleviated by eyelid warming alone without application of steroids and tear OAHFAs are identified as suitable markers to monitor treatment response in MGD.
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Changes in Plasma Lipids during Exposure to Total Sleep Deprivation.

TL;DR: The decrease in choline plasmalogen levels during sleep deprivation is consistent with prior work demonstrating that these lipids are susceptible to degradation by oxidative stress, and the increase in phosphatidylcholines and triacylglycerides suggests that sleep loss might modulate lipid metabolism, which has potential implications for metabolic health in individuals who do not achieve adequate sleep.
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A fluorescent sphingolipid binding domain peptide probe interacts with sphingolipids and cholesterol-dependent raft domains.

TL;DR: Using fluorescence correlation spectroscopy to assay the mobility of SBD in live cells, it is shown that SBD's behavior at the plasma membrane is similar to that of the previously described raft marker cholera toxin B, displaying both a fast and a slow component.