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收藏The identification of intestinal scavenger receptor class B, type I (SR-BI) by expression cloning and its role in cholesterol absorption通过表达克隆鉴定肠清道夫受体B,I型 (sr-bi) 及其在胆固醇吸收中的作用
Altmann, SW; Davis, HR; Yao, XR; Laverty, M; Compton, DS; Zhu, LJ; Crona, JH; Caplen, MA; Hoos, LM; Tetzloff, G; Priestley, T; Burnett, DA; Strader, CD; Graziano, MP
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收藏Facilitation of acetylcholine release and improvement in cognition by a selective M2 muscarinic antagonist, SCH 72788
Lachowicz, JE; Duffy, RA; Ruperto, V; Kozlowski, J; Zhou, GW; Clader, J; Billard, W; Binch, H; Crosby, G; Cohen-Williams, M; Strader, CD; Coffin, V
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收藏L-750355, a human β3-adrenoceptor agonist;: in vitro pharmacology and profile of activity in vivo in the rhesus monkey
Forrest, MJ; Hom, G; Bach, T; Candelore, MR; Cascieri, MA; Strader, C; Tota, L; Fisher, MH; Szumiloski, J; Ok, HO; Weber, AE; Wyvratt, M; Vicario, P; Marko, O; Deng, LP; Cioffe, C; Hegarty-Friscino, B; MacIntyre, E
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收藏A selective human β3 adrenergic receptor agonist increases metabolic rate in rhesus monkeys
Fisher, MH; Amend, AM; Bach, TJ; Barker, JM; Brady, EJ; Candelore, MR; Carroll, D; Cascieri, MA; Chiu, SHL; Deng, LP; Forrest, MJ; Hegarty-Friscino, B; Guan, XM; Hom, GJ; Hutchins, JE; Kelly, LJ; Mathvink, RJ; Metzger, JM; Miller, RR; Ok, HO; Parmee, ER; Saperstein, R; Strader, CD; Stearns, RA; Thompson, GM; Tota, L; Vicario, PP; Weber, AE; Woods, JW; Wyvratt, MJ; Zafian, PT; MacIntyre, DE
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收藏Cloning and expression of a novel neuropeptide Y receptor
Weinberg, DH; Sirinathsinghji, DJS; Tan, CP; Shiao, LL; Morin, N; Rigby, MR; Heavens, RH; Rapoport, DR; Bayne, ML; Cascieri, MA; Strader, CD; Linemeyer, DL; MacNeil, DJ
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收藏Synthesis of potent cyclic hexapeptide NK-1 antagonists. Use of a minilibrary in transforming a peptidal somatostatin receptor ligand into an NK-1 receptor ligand via a polyvalent peptidomimetic
Hirschmann, R; Yao, WQ; Cascieri, MA; Strader, CD; Maechler, L; CichyKnight, MA; Hynes, J; vanRijn, RD; Sprengeler, PA; Smith, AB
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收藏2(S)-((3,5-bis(trifluoromethyl)benzyl)oxy)-3(S)-phenyl-4-((3-oxo-1,2,4-triazol-5-yl)methyl)morpholine .1. A potent, orally active, morpholine-based human neurokinin-1 receptor antagonist
Hale, JJ; Mills, SG; MacCoss, M; Shah, SK; Qi, HB; Mathre, DJ; Cascieri, MA; Sadowski, S; Strader, CD; MacIntyre, DE; Metzger, JM
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收藏Down-regulation of the expression of the obese gene by an antidiabetic thiazolidinedione in Zucker diabetic fatty rats and db/db mice
Zhang, B; Graziano, MP; Doebber, TW; Leibowitz, MD; WhiteCarrington, S; Szalkowski, DM; Hey, PJ; Wu, M; Cullinan, CA; Bailey, P; Lollmann, B; Frederich, R; Flier, JS; Strader, CD; Smith, RG
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