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The Journal of Steroid Biochemistry and Molecular Biology|August 26, 2010
Selective inhibition of human 3β-hydroxysteroid dehydrogenase type 1 as a potential treatment for breast cancerJames L Thomas, Kevin M Bucholtz, Balint Kacsoh
Organic Letters|February 12, 2005
Self-selection in olefin cross-metathesis: the effect of remote functionalityBrian R McNaughton, Kevin M Bucholtz, Ana Camaaño-Moure, et al.
Organic & Biomolecular Chemistry|October 19, 2006
Synthesis and evaluation of the first cis-cyclobutane-containing receptor for lipid AKevin M Bucholtz, Peter C Gareiss, Stephen G Tajc, et al.
Molecular and Cellular Endocrinology|October 29, 2008
Structural basis for the selective inhibition of human 3beta-hydroxysteroid dehydrogenase 1 in human breast tumor MCF-7 cellsJames L Thomas, Kevin M Bucholtz, Jingping Sun, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 28, 2010
The functions of key residues in the inhibitor, substrate and cofactor sites of human 3beta-hydroxysteroid dehydrogenase type 1 are validated by mutagenesisJames L Thomas, Vance L Mack, Jingping Sun, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 6, 2008
Structure/function of the inhibition of human 3beta-hydroxysteroid dehydrogenase type 1 and type 2 by trilostaneJames L Thomas, Vance L Mack, Jason A Glow, et al.
The Journal of Steroid Biochemistry and Molecular Biology|October 17, 2017
Structure-function relationships for the selective inhibition of human 3β-hydroxysteroid dehydrogenase type 1 by a novel androgen analogJenny H Pham, Catherine M Will, Vance L Mack, et al.
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