G
Gregory M. Anstead
Researcher at University of Texas Health Science Center at San Antonio
Publications - 83
Citations - 6333
Gregory M. Anstead is an academic researcher from University of Texas Health Science Center at San Antonio. The author has contributed to research in topics: Indene & Estrogen receptor binding. The author has an hindex of 24, co-authored 80 publications receiving 6107 citations. Previous affiliations of Gregory M. Anstead include University of Kentucky & United States Department of Veterans Affairs.
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Reversible dilated cardiomyopathy related to amphotericin B therapy
TL;DR: A patient who developed dilated cardiomyopathy and clinical congestive heart failure after 2 months of therapy with amphotericin B (AmB) for disseminated coccidioidomycosis resolved after posaconazole was substituted for AmB.
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Cognitive efficiency is associated with endogenous cytokine levels in patients with chronic hepatitis C.
Robin C. Hilsabeck,Gregory M. Anstead,Amy Webb,Anastasio Hoyumpa,Paul Ingmundson,Steve Holliday,Qiong Zhang,Angela M. Casas,Marci Jovel,Stephen L. Stern +9 more
TL;DR: In patients with detectable IFN-alpha, higher levels of IL-6 and TNF-alpha were related to poorer cognitive functioning and suggest CHC patients with immune responses characterized by elevated IFn-alpha may be at risk for cognitive difficulties.
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The malnutrition-related increase in early visceralization of Leishmania donovani is associated with a reduced number of lymph node phagocytes and altered conduit system flow.
Marwa K. Ibrahim,Jeffrey L. Barnes,Jeffrey L. Barnes,Gregory M. Anstead,Gregory M. Anstead,Fabio Jimenez,Bruno L. Travi,Alex G. Peniche,E. Yaneth Osorio,Seema S. Ahuja,Seema S. Ahuja,Peter C. Melby +11 more
TL;DR: Results indicate that the impaired capacity of the lymph node to act as a barrier to dissemination of L. donovani infection is associated with a reduced number of lymph node phagocytes, which most likely leads to reduced capture of parasites as they transit through the sinuses and conduit system.
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Molecular structures, conformational analysis, and preferential modes of binding of 3-aroyl-2-arylbenzo[b]thiophene estrogen receptor ligands: LY117018 and aryl azide photoaffinity labeling analogs.
TL;DR: In this paper, structural and computational modeling studies were performed on the antiestrogen LY117018 and two photoaffinity labeling analogs, in which an azide replaces the basic ether side chain (methyl ether tetrafluoro azide 7 and its protio analog 8).
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