| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 6066485 | Journal of Allergy and Clinical Immunology | 2013 | 10 Pages | 
Abstract
												The present study delineates a number of novel proteins, TLR3-related pathways, and cellular phenotypes that may help elucidate the genetic basis of childhood HSE. Furthermore, our results reveal superoxide dismutase 2 as a potential therapeutic target for amelioration of the neurologic sequelae caused by HSE.
											Keywords
												ppifHerpes simplex virus 1 (HSV-1)HSV-1HSETLR3SOD2Herpes simplex virus encephalitisIFNstable isotope labeling of amino acids in cell cultureCNSSuperoxide dismutase 2central nervous systemSILACMass spectrometryFibroblastintercellular adhesion molecule-1Herpes simplex virus 1Proteomicspoly(I:C)Toll-like receptor 3
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											Authors
												Rebeca PhD, Claire PhD, Mark BSc, Matthew W.B. PhD, Lazaro BSc, Vanessa PhD, Laurent MD, PhD, Shen-Ying MD, PhD, Jean-Laurent MD, PhD, Jasminka PhD, 
											