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Stephen T. Smiley
Researcher at Trudeau Institute
Publications - 71
Citations - 10110
Stephen T. Smiley is an academic researcher from Trudeau Institute. The author has contributed to research in topics: T cell & Yersinia pestis. The author has an hindex of 37, co-authored 71 publications receiving 9727 citations. Previous affiliations of Stephen T. Smiley include Millennium Pharmaceuticals & Bristol-Myers Squibb.
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Journal ArticleDOI
Stat6 Is Required for Mediating Responses to IL-4 and for the Development of Th2 Cells
TL;DR: It is demonstrated that, despite the existence of multiple signaling pathways activated by IL-4, Stat6 is essential for mediating responses toIL-4 lymphocytes.
Journal ArticleDOI
Intracellular heterogeneity in mitochondrial membrane potentials revealed by a J-aggregate-forming lipophilic cation JC-1.
Stephen T. Smiley,Martin Reers,Cristina Mottola-Hartshorn,Mei Lin,A. P. Chen,Thomas W. Smith,Glenn Steele,Lan Bo Chen +7 more
TL;DR: It is found that membrane potentials across mitochondria in a living cell can be heterogeneous, and even within a long contiguous mitochondrion, regional heterogeneity in membranes potentials appears to be possible.
Journal ArticleDOI
Fibrinogen Stimulates Macrophage Chemokine Secretion Through Toll-Like Receptor 4
TL;DR: It is suggested that innate responses to fibrinogen and bacterial endotoxin may converge at the evolutionarily conserved Toll-like recognition molecules, thereby promoting immune surveillance at sites of inflammation.
Book ChapterDOI
Mitochondrial membrane potential monitored by JC-1 dye.
TL;DR: This chapter uses JC-1 to investigate the remaining questions about mitochondrial membrane potential in living cells, including the component of the electrochemical gradient that is responsible for the formation of J-aggregates, and the study of the variation of membrane potential within a given mitochondrion.
Journal ArticleDOI
Requirement of the Chemokine Receptor CXCR3 for Acute Allograft Rejection
Wayne W. Hancock,Bao Lu,Wei Gao,Vilmos Csizmadia,Kerrie L. Faia,Jennifer A. King,Stephen T. Smiley,Mai Ling,Norma P. Gerard,Craig Gerard +9 more
TL;DR: It is shown that acute cardiac allograft rejection is accompanied by progressive intragraft production of the chemokines interferon (IFN)-γ–inducible protein of 10 kD (IP-10), monokine induced by IFN-γ (Mig), andIFN-inducable T cell α chemoattractant (I-TAC), and by infiltration of activated T cells bearing the corresponding chemokine receptor, CXCR3.