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Shin-Huei Fu
Researcher at National Defense Medical Center
Publications - 51
Citations - 678
Shin-Huei Fu is an academic researcher from National Defense Medical Center. The author has contributed to research in topics: Transplantation & Islet. The author has an hindex of 11, co-authored 50 publications receiving 564 citations. Previous affiliations of Shin-Huei Fu include Johns Hopkins University & Memorial Hospital of South Bend.
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Journal ArticleDOI
Phenylbutyrate-induced G1 arrest and apoptosis in myeloid leukemia cells: structure-function analysis.
Joseph A. DiGiuseppe,Li Jun Weng,K H Yu,Shin-Huei Fu,Michael B. Kastan,Samid D,Steven D. Gore +6 more
TL;DR: It appears that the fatty acid moiety of PB, rather than its aromatic ring, is critical for its activity in myeloid leukemic cells, which provides a potential mechanistic basis for the increased potency of PB over PA previously demonstrated in primary leukedmic samples, and support the further clinical development of PB in the treatment of hematologic malignancies.
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New insights into Blimp-1 in T lymphocytes: a divergent regulator of cell destiny and effector function.
TL;DR: The emerging roles of Blimp-1 in the complex regulation of gene networks that regulate the destiny and effector function of T cells and provide a Blimp-1-dominated transcriptional framework for T lymphocyte homeostasis are discussed.
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Microencapsulation of islets in PEG-amine modified alginate-poly(l-lysine)-alginate microcapsules for constructing bioartificial pancreas
TL;DR: Intraperitoneal transplantation of the microencapsulated islets into streptozotocin-induced diabetic mice could maintain normal blood glucose levels in test animals for up to 200 d without immunosuppression.
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Loofa Sponge as a Scaffold for the Culture of Human Hepatocyte Cell Line
TL;DR: Experimental results and observations by SEM suggested that loofa sponge is a suitable scaffold for high‐density culture of human hepatocyte cell line and the immobilized cells could express high levels of liver‐specific functions.
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Glucosamine Modulates T Cell Differentiation through Down-regulating N-Linked Glycosylation of CD25
Ming-Wei Chien,Ming-Hong Lin,Shing-Hwa Huang,Shin-Huei Fu,Chao-Yuan Hsu,B. Linju Yen,Jiann-Torng Chen,Deh-Ming Chang,Huey-Kang Sytwu +8 more
TL;DR: It is demonstrated that glucosamine impedes Th1, Th2, and iTreg cells but promotes Th17 differentiation through down-regulating N-linked glycosylation of CD25 and subsequently inhibiting its downstream Stat5 signaling in a dose-dependent manner.