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Your search keyword '"Martin, Ruth L"' showing total 156 results

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1. Selective MCL-1 inhibitor ABBV-467 is efficacious in tumor models but is associated with cardiac troponin increases in patients

4. Discovery of A-910, a Highly Potent and Orally Bioavailable Dual MerTK/Axl-Selective Tyrosine Kinase Inhibitor

6. Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours

10. Author Correction: Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours

17. Preclinical Characterization of A-582941: A Novel α7 Neuronal Nicotinic Receptor Agonist with Broad Spectrum Cognition-Enhancing Properties

20. Alterations in ATP-sensitive potassium channel sensitivity to ATP in failing human hearts

21. Cardiac sodium channels expressed in a peripheral neurotumor-derived cell line, RT4-B8

23. A 3,4-diaminopyridine-insensitive, Ca(super 2+)-independent transient outward K(super +) current in cardiac ventricular myocytes

24. Abstract LB-A23: Discovery of a potent catalytic p300/CBP inhibitor that targets lineage-specific tumors

25. Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours

28. Abstract C202: Discovery and initial characterization of the clinical compound ABT-348, a potent inhibitor of the VEGF, PDGF, and Aurora kinase families.

32. Cannabinoid (CB) Receptors are not Involved in A-955840 Induced Negative Inotropic Effects in Isolated Cardiac Myocytes

33. Do hERG Enhancers and Blockers Compete?

36. An evaluation of 3,4-methylenedioxy phenyl replacements in the aminopiperidine chromone class of MCHr1 antagonists

37. Preclinical Characterization of A-582941: A Novel α7 Neuronal Nicotinic Receptor Agonist with Broad Spectrum Cognition-Enhancing Properties

39. Syntheses of Potent, Selective, and Orally Bioavailable Indazole-Pyridine Series of Protein Kinase B/Akt Inhibitors with Reduced Hypotension

41. 1,4-Dihydroindeno[1,2-c]pyrazoles with Acetylenic Side Chains as Novel and Potent Multitargeted Receptor Tyrosine Kinase Inhibitors with Low Affinity for the hERG Ion Channel

42. Discovery of N-(4-(3-Amino-1H-indazol-4-yl)phenyl)-N‘-(2-fluoro-5-methylphenyl)urea (ABT-869), a 3-Aminoindazole-Based Orally Active Multitargeted Receptor Tyrosine Kinase Inhibitor

44. ABT-089: Pharmacological Properties of a Neuronal Nicotinic Acetylcholine Receptor Agonist for the Potential Treatment of Cognitive Disorders

48. ABT-089: Pharmacological Properties of a Neuronal Nicotinic Acetylcholine Receptor Agonist for the Potential Treatment of Cognitive Disorders.

49. A 3,4-diaminopyridine-insensitive, Ca2+-independent transient outward K+ current in cardiac...

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