Nuclear Receptors and Their Selective Pharmacologic Modulators-Reference-Cited by-同舟云学术

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Nuclear Receptors and Their Selective Pharmacologic Modulators

Published:2013-03-01 Issue:2 Volume:65 Page:710-778
ISSN:0031-6997
Container-title:Pharmacological Reviews
language:en
Short-container-title:Pharmacol Rev

Author:

Burris Thomas P.,Solt Laura A.,Wang Yongjun,Crumbley Christine,Banerjee Subhashis,Griffett Kristine,Lundasen Thomas,Hughes Travis,Kojetin Douglas J.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference850 articles.

1. Discovery of (2R)-2-(3-{3-[(4-Methoxyphenyl)carbonyl]-2-methyl-6-(trifluoromethoxy)-1H-indol-1-yl}phenoxy)butanoic Acid (MK-0533): A Novel Selective Peroxisome Proliferator-Activated Receptor γ Modulator for the Treatment of Type 2 Diabetes Mellitus with a Reduced Potential to Increase Plasma and Extracellular Fluid Volume

2. Benzoyl 2-methyl indoles as selective PPARγ modulators

3. Transcriptional Activation by Peroxisome Proliferator-activated Receptor γ Is Inhibited by Phosphorylation at a Consensus Mitogen-activated Protein Kinase Site

4. A phase I trial to assess the pharmacology of the new oestrogen receptor antagonist fulvestrant on the endometrium in healthy postmenopausal volunteers

5. 1,25-Dihydroxyvitamin D3 analogs as potential therapies in transplantation;Adorini;Curr Opin Investig Drugs,2002

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