Results 81 to 90 of about 53,372 (96)

The chemokine receptor antagonist, TAK‐779, decreased experimental autoimmune encephalomyelitis by reducing inflammatory cell migration into the central nervous system, without affecting T cell function

open access: yesBritish Journal of Pharmacology, 2009
Jia Ni   +9 more
semanticscholar   +1 more source

Editorial

open access: yesTherapeutic Advances in Respiratory Disease, 2007
Mario Cazzola
doaj   +1 more source
Some of the next articles are maybe not open access.

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“It Is Better If I Kill Her”: Perceptions and Opinions of Violence Against Women and Femicide in Ocotal, Nicaragua, After Law 779

, 2015
The objective of this research is to examine women's perceptions and opinions of violence against women (VAW) and femicide in Ocotal, Nicaragua, since the introduction of Law 779, a national law implemented in 2012 meant to eradicate VAW.
M. LuffySamantha   +2 more
semanticscholar   +1 more source

Diverse modifications of the 4-methylphenyl moiety of TAK-779 by late-stage Suzuki-Miyaura cross-coupling.

Organic and biomolecular chemistry, 2014
Chemokine receptor 5 (CCR5) antagonists provide a new therapeutic approach in the treatment of HIV-1 (AIDS). TAK-779 displays high affinity and selectivity for the CCR5 receptor and serves as a lead compound for the development of further antagonists. In
Anna Junker   +7 more
semanticscholar   +1 more source

Synthesis of thiophene-based TAK-779 analogues by C-H arylation.

Journal of Organic Chemistry, 2013
A rapid synthesis of thiophene-based TAK-779 analogues 1 is reported using a late-stage diversification strategy. At the end of the synthesis, the key building block 2, which was prepared in six steps from thiophene, was arylated regioselectively at the ...
Anna Junker   +3 more
semanticscholar   +1 more source

Radiation therapy and concurrent plus adjuvant temsirolimus (CCI-779) versus chemoirradiation with temozolomide in newly diagnosed glioblastoma without methylation of the MGMT gene promoter.

, 2014
Background: Preclinical data indicate activity of mammalian target of rapamycin inhibitors and synergistic activity together with radiotherapy in glioblastoma.
W. Wick   +15 more
semanticscholar   +1 more source

Phase II trial of single-agent temsirolimus (CCI-779) for relapsed mantle cell lymphoma.

Journal of Clinical Oncology, 2005
PURPOSE Mantle cell lymphoma (MCL) is characterized by a t(11;14) resulting in overexpression of cyclin D1 messenger RNA. This study tested whether temsirolimus (previously known as CCI-779), an inhibitor of the mammalian target of rapamycin kinase that ...
T. Witzig   +12 more
semanticscholar   +1 more source

Phase I/II trial of CCI 779 and bevacizumab in advanced renal cell carcinoma (RCC): Safety and activity in RTKI refractory RCC patients.

Journal of Clinical Oncology, 2009
5039 Background: Combined mTOR and VEGF blockade is a potentially promising and rational strategy for the treatment of advanced RCC. We previously reported the phase I safety and efficacy results of CCI 779 (C) +bevacizumab (B) n RTKI naïve stage IV RCC ...
J. Merchan   +7 more
semanticscholar   +1 more source

A Phase 1 clinical study of temsirolimus (CCI-779) in Japanese patients with advanced solid tumors.

Japanese Journal of Clinical Oncology, 2010
OBJECTIVE Temsirolimus (CCI-779) is a novel inhibitor of the mammalian target of rapamycin. This Phase 1 study was aimed at investigating the maximum-tolerated dose, toxicity, pharmacokinetics and antitumor activity in Japanese patients with advanced ...
Y. Fujisaka   +4 more
semanticscholar   +1 more source

Rapamycin Ester Analog CCI-779/Temsirolimus Alleviates Tau Pathology and Improves Motor Deficit in Mutant Tau Transgenic Mice

Journal of Alzheimer's Disease, 2015
C. Frédérick   +6 more
semanticscholar   +1 more source

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