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V. Wee Yong

Researcher at University of Calgary

Publications -  276
Citations -  21024

V. Wee Yong is an academic researcher from University of Calgary. The author has contributed to research in topics: Multiple sclerosis & Microglia. The author has an hindex of 73, co-authored 233 publications receiving 17556 citations. Previous affiliations of V. Wee Yong include Allen Institute for Brain Science & Foothills Medical Centre.

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Using magnetic resonance imaging in animal models to guide drug development in multiple sclerosis

TL;DR: Key papers showing how MR imaging has been combined with a range of animal models to evaluate potential therapeutics for multiple sclerosis are reviewed and advice is given on how to maximize the potential for incorporating MRI into preclinical studies evaluating possible therapeuticals for MS.
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Exercise rapidly alters proteomes in mice following spinal cord demyelination.

TL;DR: The authors showed that acute bouts of exercise in mice profoundly alters the proteome in demyelinating lesions following lysolecithin induced demyeling of the ventral spinal cord, mice were given immediate access to a running wheel for 4 days Lesioned spinal cords and peripheral blood serum were then subjected to tandem mass tag labeling to identify alteration in protein levels.
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Minocycline for axonal regeneration after nerve injury: a double-edged sword.

TL;DR: A focused background on nerve injury and regeneration is presented, the therapeutic use of minocycline in other neurological disorders is considered, and a few relevant comments are made regarding the potential role of mincycline as a therapeutic strategy for nerve repair in the future are presented.
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PD-1 independent of PD-L1 ligation promotes glioblastoma growth through the NFκB pathway.

TL;DR: This paper found that about 8% of cells within the human glioblastoma microenvironment coexpreses with brain tumor-initiating cells (BTICs) through not fully understood mechanisms.
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The regulation of reactive changes around multiple sclerosis lesions by phosphorylated signal transducer and activator of transcription.

TL;DR: The findings show that pSTAT3 does not correlate with inflammatory activity in MS lesions, but that it may play an important role in regulating reactive changes proximal to MS lesions.