|
||||||||||
![]()
|
Narayan R. Bhat, Ph.D.
Phone: (843) The current research interests of our laboratory (supported by NIH and other grants) focus on the cellular and molecular mechanisms underlying:
In addition, we are interested in neuroglial stem cells with respect to their lineage determination, malignant transformation (gliomagenesis) due to dysregulated growth factor signaling as well as their potential utility in CNS gene trans
Bhat NR, Feinstein DL, Shen Q, Bhat AN. p38 MAPK-mediated transcriptional activation of inducible nitric oxide synthase in glial cells: roles of nuclear factors, NFkb, CREB, C/EBP and ATF-2. J Biol Chem 2002; 277:29584-29592. Bhat NR, Fan F. Adenovirus infection induces microglial activation: Involvement of mitogen-activated protein kinase pathways. Brain Res 2002; 948:93-101. Bhat NR, Zhang P, Lee JC and Hogan EL. Extracellular signal-regulated kinase and p38 subgroups of mitogen-activated protein kinases regulate inducible nitric oxide synthase and tumor necrosis factor-a gene expression in endotoxin-stimulated primary glial cultures. J Neurosci 1998; 18:1633-1641. Andrews T, Zhang P and Bhat NR. TNFa potentiates IFNg-induced cell death in ligodendrocyte progenitors. J Neurosci Res 1998; 54:574-583. Bhat NR, Zhang P. Activation of MAP kinases in oligodendrocytes. J Neurochem 1996; 66:1986-1994. Zhang P, Miller BS, Rosenzweig SA, Bhat NR. Activation of c-Jun N-terminal kinase/stress-activated protein kinase in primary glial cultures. J Neurosci Res 1996;46:114-121.
|
|||||||||
© Copyright 2008 The Neuroscience
Institute, Medical University of South Carolina, Charleston SC. For site
queries and comments please contact the webmaster |
||||||||||