Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Steele, Ronald A."'
Autor:
Mulatero, Paolo, Wuerzner, Gregoire, Groessl, Michael, Sconfienza, Elisa, Damianaki, Aikaterini, Forestiero, Vittorio, Vogt, Bruno, Brunner, Hans, Gerlock, Teresa, Steele, Ronald, Schumacher, Christoph
Publikováno v:
In eClinicalMedicine May 2024 71
Autor:
Pignatti, Emanuele, Kollar, Jakub, Hafele, Evelyn, Schuster, Daniela, Steele, Ronald E., Vogt, Bruno, Schumacher, Christoph, Groessl, Michael
Publikováno v:
In Journal of Steroid Biochemistry and Molecular Biology December 2023 235
Akademický článek
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Autor:
Kuo, Ramsay L, Paterson, Ryan F, Siqueira, Tibério M, Jr, Watkins, Stephanie L, Simmons, Garrick R, Steele, Ronald E, Lingeman, James E
Publikováno v:
In Urology 2003 62(1):59-63
Autor:
KUO, RAMSAY L., KIM, SAMUEL C., LINGEMAN, JAMES E., PATERSON, RYAN F., WATKINS, STEPHANIE L., SIMMONS, GARRICK R., STEELE, RONALD E.
Publikováno v:
In The Journal of Urology 2003 170(1):149-152
Publikováno v:
Journal of Hypertension
Context: We describe the clinical investigation of the first generation aldosterone synthase inhibitor, LCI699, in patients with essential, uncontrolled, resistant, or secondary hypertension. LCI699 competitively reduced blood pressure at lower doses
Autor:
Kenneth S. Leonards, Steele Ronald Edward, Jong M. Wasvary, E.C. Yurachek, Zouhair F. Stephan, Chii Whei Hu, Robin Sharif, Thomas H. Hintze
Publikováno v:
Atherosclerosis. 126:53-63
A potent lipid-lowering thyromimetic (CGS 26214) devoid of cardiac and thermogenic activity was identified based on its ability to preferentially access and bind the nuclear fraction of hepatocytes over that of myocytes in culture. The difference in
Publikováno v:
ChemInform. 22
A new class of potent, selective, nonsteroidal inhibitors of aromatase have been discovered. The most potent member of this series is fadrozole hydrochloride, CGS 16949 A, 4-(5,6,7,8-tetrahydroimidazo[1,5-alpha]pyridin-5-yl)benzonitrile monohydrochlo
Autor:
Colin Howes, Jong M. Wasvary, Zouhair F. Stephan, Steele Ronald Edward, E.C. Yurachek, Robin Sharif
Publikováno v:
Biochemical Pharmacology. 43:1969-1974
This study was designed to determine whether the conjugation product of L-T3 with cholic acid would result in a liver-targeted compound (CGH 509A) with hypocholesterolemic (HC) activity significantly dissociable from cardiovascular (CV) and thyroxine
Publikováno v:
Journal of Medicinal Chemistry. 34:725-736
A new class of potent, selective, nonsteroidal inhibitors of aromatase have been discovered. The most potent member of this series is fadrozole hydrochloride, CGS 16949 A, 4-(5,6,7,8-tetrahydroimidazo[1,5-alpha]pyridin-5-yl)benzonitrile monohydrochlo