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pro vyhledávání: '"J T, Nguyen"'
Akademický článek
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Autor:
F. Lin, B. Lu, J. T. Nguyen, H. E. Kinecki, T. N. Watkins, Robert B. Raffa, V. Phan, G. Burdge, J. Gambrah, M. A. Sesay, A. Ruan
Publikováno v:
Journal of Clinical Pharmacy and Therapeutics. 42:8-17
SummaryWhat is known and objective Chronic pain presents a difficult clinical challenge because of the limited efficacy, the limiting adverse-effect profile or the abuse potential of current analgesic options. Cebranopadol is a novel new agent in cli
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 165(5)
Galectin-1, an endogenous lectin expressed in lymphoid organs and immune-privileged sites, induces death of human and murine thymocytes and T cells. Galectin-1 binds to several glycoproteins on the T cell surface, including CD7. However, the T cell s
Autor:
J T, Nguyen
Publikováno v:
Advances in experimental medicine and biology. 465
Autor:
J T, Nguyen
Publikováno v:
Advances in experimental medicine and biology. 465
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 162(2)
Galectin-1 is an endogenous lectin expressed by thymic and lymph node stromal cells at sites of Ag presentation and T cell death during normal development. It is known to have immunomodulatory activity in vivo and can induce apoptosis in thymocytes a
Publikováno v:
Cancer research. 58(24)
Antiangiogenic tumor therapies have recently attracted intense interest for their broad-spectrum action, low toxicity, and, in the case of direct endothelial targeting, an absence of drug resistance. To promote tumor regression and to maintain dorman
Autor:
Richard Essner, S. Kuhns, J. T. Nguyen, D. van Epps, D. Buckman, L. Zhang, Mark B. Faries, J. Thomas, Eddy C. Hsueh, C. R. Ill, Leland J. Foshag
Publikováno v:
Journal of Clinical Oncology. 23:2574-2574
2574 Background: Although few nonsurgical treatment options offer significant benefit for patients with high-risk melanoma, extensive matched-pair control studies of phase II trials indicate that C...
Akademický článek
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Publikováno v:
Scopus-Elsevier
To understand the molecular interactions leading to the assembly of beta/44 protein into the hallmark fibrils of Alzheimer's disease (AD), we have examined the ability of synthetic peptides that correspond to the beta/A4 extracellular sequence to for
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