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Michael W. Lark

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61H指数
195论文数
1.4W被引数
收录论文 45
发表时间
TRV0109101, a G Protein-Biased Agonist of the μ-Opioid Receptor, Does Not Promote Opioid-Induced Mechanical Allodynia following Chronic Administration
err2017-08-01
err32
errOAAI
errKoblish, Michael; Carr, Richard, III; Siuda, Edward R.; Rominger, David H.; Gowen-MacDonald, William; Cowan, Conrad L.; Crombie, Aimee L.; Violin, Jonathan D.; Lark, Michael W.
err分享
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Biased agonism of the μ-opioid receptor by TRV130 increases analgesia and reduces on-target adverse effects versus morphine: A randomized, double-blind, placebo-controlled, crossover study in healthy volunteers
errPAIN
IF5.5
err2014-09-01
err260
PREAI
errSoergel, David G.; Subach, Ruth Ann; Burnham, Nancy; Lark, Michael W.; James, Ian E.; Sadler, Brian M.; Skobieranda, Franck; Violin, Jonathan D.; Webster, Lynn R.
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TRV130, a novel biased opioid ligand, elicits increased analgesia with reduced adverse effects compared to morphine in healthy volunteers
err2014-04-01
err0
errOAAI
errSoergel, D.; Subach, R.; James, I.; Violin, I.; Skobieranda, F.; Sadler, B.; Burnham, N.; Theisen, T.; Lark, M.; Webster, L.
err分享
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GPCR biased ligands as novel heart failure therapeutics
err2013-10-01
err35
PREAI
errViolin, Jonathan D.; Soergel, David G.; Boerrigter, Guido; Burnett, John C., Jr.; Lark, Michael W.
err分享
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An orally available mu-opioid receptor biased ligand is analgesic with reduced constipation in rodents
err2013-04-01
err0
errOAAI
errViolin, J.; DeWire, S.; Koblish, M.; Chen, D.; Crombie, A.; Yamashita, D.; Soergel, D.; Lark, M.
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A G Protein-Biased Ligand at the μ-Opioid Receptor Is Potently Analgesic with Reduced Gastrointestinal and Respiratory Dysfunction Compared with Morphines
err2013-03-01
err577
PREAI
errDeWire, Scott M.; Yamashita, Dennis S.; Rominger, David H.; Liu, Guodong; Cowan, Conrad L.; Graczyk, Thomas M.; Chen, Xiao-Tao; Pitis, Philip M.; Gotchev, Dimitar; Yuan, Catherine; Koblish, Michael; Lark, Michael W.; Violin, Jonathan D.
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First Human Dosing Experience With TRV027, a Novel Therapy for Acute Heart Failure
err2012-08-01
err0
errOAAI
errSoergel, David G.; Subach, Ruth Ann; Violin, Jonathan D.; Yamashita, Dennis; Gowen, Maxine; Lark, Michael W.
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Selectively Engaging β-Arrestins at the Angiotensin II Type 1 Receptor Reduces Blood Pressure and Increases Cardiac Performance
err2010-12-01
err335
PREAI
errViolin, Jonathan D.; DeWire, Scott M.; Yamashita, Dennis; Rominger, David H.; Nguyen, Lisa; Schiller, Kevin; Whalen, Erin J.; Gowen, Maxine; Lark, Michael W.
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TRV120027, a β-Arrestin Biased Ligand at the Angiotensin II Type 1 Receptor, Produces Unique Pharmacology and Is a Novel Potential Therapy for Heart Failure
err2010-08-01
err3
PREAI
errViolin, Jonathan D.; Soergel, David G.; DeWire, Scott M.; Yamashita, Dennis; Rominger, David; Whalen, Erin J.; Gowen, Maxine; Lark, Michael W.
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Antagonism of the osteoclast vitronectin receptor with an orally active nonpeptide inhibitor prevents cancellous bone loss in the ovariectomized rat
err2009-12-02
err54
errOAAI
errLark, MW; Stroup, GB; Dodds, RA; Kapadia, R; Hoffman, SJ; Hwang, SM; James, IE; Lechowska, B; Liang, XG; Rieman, DJ; Salyers, KL; Ward, K; Smith, BR; Miller, WH; Huffman, WF; Gowen, M
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Human osteoclast cathepsin K is processed intracellularly prior to attachment and bone resorption
err2009-12-02
err88
PREAI
errDodds, RA; James, IE; Rieman, D; Ahern, R; Hwang, SM; Connor, JR; Thompson, SD; Veber, DF; Drake, FH; Holmes, S; Lark, MW; Gowen, M
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Potent and selective inhibition of human cathepsin K leads to inhibition of bone resorption in vivo in a nonhuman primate人组织蛋白酶K的有效和选择性抑制导致非人灵长类动物体内骨吸收的抑制
err2009-12-02
err161
PREAI
errStroup, GB; Lark, MW; Veber, DF; Bhattacharyya, A; Blake, S; Dare, LC; Erhard, KF; Hoffman, SJ; James, IE; Marquis, RW; Ru, Y; Vasko-Moser, JA; Smith, BR; Tomaszek, T; Gowen, M
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Interference with tissue factor prolongs intrahepatic islet allograft survival in a nonhuman primate marginal mass model
err2007-08-15
err75
errOAAI
errBerman, Dora M.; Cabrera, Over; Kenyon, Norman M.; Miller, Joshua; Tam, Susan H.; Khandekar, Vrinda S.; Picha, Kristen M.; Soderman, Avery R.; Jordan, Robert E.; Bugelski, Peter J.; Horninger, Denison; Lark, Michael; Davis, Janet E.; Alejandro, Rodolfo; Berggren, Per-Olof; Zimmerman, Mark; O'Neil, John J.; Ricordi, Camillo; Kenyon, Norma S.
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A highly potent inhibitor of cathepsin K (relacatib) reduces biomarkers of bone resorption both in vitro and in an acute model of elevated bone turnover in vivo in monkeys组织蛋白酶K的高效抑制剂 (relacatib) 在体外和猴子体内骨转换升高的急性模型中均降低了骨吸收的生物标志物
errBONE
IF3.6
err2007-01-01
err120
PREAI
errKumar, S.; Dare, L.; Vasko-Moser, J. A.; James, I. E.; Blake, S. M.; Rickard, D. J.; Hwang, S. -M.; Tomaszek, T.; Yamashita, D. S.; Marquis, R. W.; Oh, H.; Jeong, J. U.; Veber, D. F.; Gowen, M.; Lark, M. W.; Stroup, G.
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Structure activity relationships of 5-, 6-, and 7-methyl -substituted azepan-3-one cathepsin K inhibitors
err2006-02-15
err61
PREAI
errYamashita, DS; Marquis, RW; Xie, R; Nidamarthy, SD; Oh, HJ; Jeong, JU; Erhard, KF; Ward, KW; Roethke, TJ; Smith, BR; Cheng, HY; Geng, XL; Lin, F; Offen, PH; Wang, B; Nevins, N; Head, MS; Haltiwanger, RC; Sarjeant, AAN; Liable-Sands, LM; Zhao, BG; Smith, WW; Janson, CA; Gao, E; Tomaszek, T; McQueney, M; Jarnes, IE; Gress, CJ; Zembryki, DL; Lark, MW; Veber, DF
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