نتایج جستجو برای: 077 and 013

تعداد نتایج: 16828186  

Journal: :Pasado y Memoria 2021

Reseña:Pedro Oliver Olmo (coord.), La tortura en la España contemporánea, Madrid, Los Libros de Catarata, 2020, ISBN 978-84-1352-077-3, 288 pp.

Journal: :The Journal of pharmacology and experimental therapeutics 2015
Mei-Hong Li Rolf Swenson Miriam Harel Sampa Jana Erik Stolarzewicz Timothy Hla Linda H Shapiro Fernando Ferrer

The bioactive lipid sphingosine-1-phosphate (S1P) and its receptors (S1P1-5) play critical roles in many pathologic processes, including cancer. The S1P axis has become a bona fide therapeutic target in cancer. JTE-013 [N-​(2,​6-​dichloro-​4-​pyridinyl)-​2-​[1,​3-​dimethyl-​4-​(1-​methylethyl)-​1H-​pyrazolo[3,​4-​b]pyridin-​6-​yl]-​hydrazinecarboxamide], a known S1P2 antagonist, suffers from in...

Journal: :Pediatric Critical Care Medicine 2018

Journal: :Pediatric Critical Care Medicine 2018

Journal: :Journal of neurophysiology 2012
Chao Li Xian Xuan Chi Wenrui Xie J A Strong J-M Zhang G D Nicol

Previously we demonstrated that sphingosine 1-phosphate receptor 1 (S1PR(1)) played a prominent, but not exclusive, role in enhancing the excitability of small-diameter sensory neurons, suggesting that other S1PRs can modulate neuronal excitability. To examine the potential role of S1PR(2) in regulating neuronal excitability we used the established selective antagonist of S1PR(2), JTE-013. Here...

2010

Out[27]= 5 732 633 648 444 029 959 171 112 534 135 601 537 904 527 274 424 900 382 532 001 737 941 474 619 400 523 520 462 230 330 041Ö 125 536 677 017 734 855 696 154 228 338 013 057 234 856 311 747 239 817 067 594 543 153 099 451 342 467 908 368 438 222 191Ö 627 068 172 197 302 715 770 028 566 855 392 342 976 305 724 205 594 772 269 515 365 592 152 841 739 667 322 895 223 024 545Ö 931 314 017...

Journal: :Molecular pharmacology 2007
Trudy A Kohout Qiu Xie Shelby Reijmers Kenneth J Finn Zhiqiang Guo Yun-Fei Zhu R Scott Struthers

Drugs that exhibit insurmountable antagonism are proposed to provide improved clinical efficacy through extended receptor blockade. Long-term suppression of the gonadotropin-releasing hormone receptor (GnRHR) is an important therapeutic approach for a number of sex hormone-dependent diseases. In this study, we describe the mechanism and structural components required for insurmountable activity...

Journal: :J. Comput. Physics 2015
Yann Moguen Simon Delmas Vincent Perrier Pascal Bruel Erik Dick

aUniversité de Pau et des Pays de l’Adour LMAP UMR 5142 and Inria CAGIRE Team – Avenue de l’Université – 64 013 Pau, France bInria CAGIRE Team, Université de Pau et des Pays de l’Adour LMAP UMR 5142 – Avenue de l’Université – 64 013 Pau, France cCNRS, Université de Pau et des Pays de l’Adour LMAP UMR 5142 and Inria CAGIRE Team – Avenue de l’Université – 64 013 Pau, France dGhent University – De...

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