3 results match your criteria: "Veterans Affairs Medical Center (151B)[Affiliation]"
J Hepatol
June 2005
Department of Medicine, Veterans Affairs Medical Center (151B), 2002 Holcombe Blvd., Houston, TX 77030, USA.
Background/aims: The mechanism of interferon (IFN)-alpha-induced depression remains poorly understood. Recently, modulation of glucocorticoid receptor (GR) and serotonin receptor 1A (5-HTR1A) were implicated in mechanism(s) leading to depression. To gain insight into this mechanism, we assessed the effect of IFN-alpha on the modulation of GR and 5-HTR1A expression.
View Article and Find Full Text PDFCancer Lett
February 2003
Department of Medicine, Baylor College of Medicine and Veterans Affairs Medical Center (151B), 2002 Holcombe Boulevard, Houston, TX 77030, USA.
Endoplasmic reticulum (ER) was recently suggested as a third subcellular compartment in apoptotic execution. Survivin is a member of inhibitors of apoptosis and ursodeoxycholic acid (UDCA) prevents apoptosis from various apoptotic stimuli. To assess the activity of survivin and the effect of UDCA on the survivin in ER stress-mediated apoptosis, we treated hepatoma cell lines with thapsigargin (TG).
View Article and Find Full Text PDFInt J Hematol
April 1996
Department of Veterans Affairs Medical Center (151B), University of Nevada School of Medicine, Reno 89520, USA.
Although not 'ideal', xenograft models of human hematopoiesis have proved to be extremely useful experimental systems for the study of the in vivo engraftment/proliferation potential of human hematopoietic stem/progenitor cells (HSC). Among these, the human/sheep xenograft model is unique in several respects. This model takes advantage of fetal immunologic immaturity and developing 'homing' spaces in the fetal bone marrow to obtain donor HSC engraftment in normal recipients without marrow conditioning.
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