V
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.
Papers
More filters
Journal ArticleDOI
Interferon beta in the treatment of multiple sclerosis Mechanisms of action
TL;DR: In this review, several biological activities of IFN-β are highlighted, including its inhibitory effects on proliferation of leukocytes and antigen presentation, and these activities are likely to act in concert to account for the mechanism of IFn-β in MS.
Journal ArticleDOI
Analyses of all matrix metalloproteinase members in leukocytes emphasize monocytes as major inflammatory mediators in multiple sclerosis
Amit Bar-Or,Robert K. Nuttall,Martin Duddy,Andrea Alter,Ho Jin Kim,Igal Ifergan,Caroline J. Pennington,Pierre Bourgoin,Dylan R. Edwards,V. Wee Yong +9 more
TL;DR: Monocytes are prominent contributors of the neuroinflammation in multiple sclerosis through a mechanism that involves their high MMP expression and that they identify specific MMP members as targets for novel therapeutics in the disease.
Journal ArticleDOI
Results of a phase II placebo-controlled randomized trial of minocycline in acute spinal cord injury
TL;DR: The minocycline regimen established in this study proved feasible, safe and was associated with a tendency towards improvement across several outcome measures, which are encouraging and warrant further investigation in a multi-centre phase III trial.
Journal ArticleDOI
A1 Adenosine Receptor Upregulation and Activation Attenuates Neuroinflammation and Demyelination in a Model of Multiple Sclerosis
Shigeki Tsutsui,Jurgen Schnermann,Farshid Noorbakhsh,Scot D. Henry,V. Wee Yong,Brent W. Winston,Kenneth G. Warren,Christopher Power +7 more
TL;DR: Modulation of neuroinflammation by the A1AR represents a novel mechanism that provides new therapeutic opportunities for MS and other demyelinating diseases.
Journal ArticleDOI
Matrix Metalloproteinase-9/Gelatinase B Is Required for Process Outgrowth by Oligodendrocytes
Luke Y. S. Oh,Peter H. Larsen,Craig A. Krekoski,Dylan R. Edwards,Frances Donovan,Zena Werb,V. Wee Yong +6 more
TL;DR: Genetic evidence that MMP-9 facilitates process outgrowth by OLs in vivo and in culture is provided, indicating a requirement for M MP-9 in process out growth.