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M Penning

Showing results (141-150 of 2,151) with videos related to

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The Biochemical Journal|September 15, 1985
Potent inhibition of mammalian progesterone synthesis by 2 alpha-cyanoprogesteroneR B Sharp, M B Senior, T M Penning
Chemico-Biological Interactions|February 27, 2003
Role of human type 3 3alpha-hydroxysteroid dehydrogenase (AKR1C2) in androgen metabolism of prostate cancer cellsTea Lanisnik Rizner, Hsueh K Lin, Trevor M Penning
Biochemistry|January 24, 1995
Bromoacetamido analogs of indomethacin and mefenamic acid as affinity-labeling agents and mechanistic probes for prostaglandin H2 synthaseM S Tang, L J Askonas, T M Penning
Chemical Research in Toxicology|September 16, 2008
Oxidation of PAH trans-dihydrodiols by human aldo-keto reductase AKR1B10Amy M Quinn, Ronald G Harvey, Trevor M Penning
Chemico-Biological Interactions|November 26, 2008
Aldo-keto reductases in which the conserved catalytic histidine is substitutedLuigi Di Costanzo, Trevor M Penning, David W Christianson
Biochemistry|May 16, 1989
Non-K-region o-quinones as enzyme-generated inactivators of dihydrodiol dehydrogenaseT M Penning, R B Sharp, T E Smithgall
Cancer Research|December 15, 1989
Characterization of dihydrodiol dehydrogenase in rat H-4IIe hepatoma cellsA L Buller, R B Sharp, T M Penning
Endocrinology|May 13, 2022
Conversion of Classical and 11-Oxygenated Androgens by Insulin-Induced AKR1C3 in a Model of Human PCOS AdipocytesRyan D Paulukinas, Clementina A Mesaros, Trevor M Penning
The Journal of Biological Chemistry|December 5, 1985
Purification and properties of 3 alpha-hydroxysteroid dehydrogenase from rat brain cytosol. Inhibition by nonsteroidal anti-inflammatory drugs and progestinsT M Penning, R B Sharp, N R Krieger
Chemico-Biological Interactions|February 27, 2003
Steroid-binding site residues dictate optimal substrate positioning in rat 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD or AKR1C9)Vladi V Heredia, Ryan G Kruger, Trevor M Penning
Pageof 216

Showing results (141-150 of 2,151) with videos related to

Sort By:
Pageof 216
The Biochemical Journal|September 15, 1985
Potent inhibition of mammalian progesterone synthesis by 2 alpha-cyanoprogesteroneR B Sharp, M B Senior, T M Penning
Chemico-Biological Interactions|February 27, 2003
Role of human type 3 3alpha-hydroxysteroid dehydrogenase (AKR1C2) in androgen metabolism of prostate cancer cellsTea Lanisnik Rizner, Hsueh K Lin, Trevor M Penning
Biochemistry|January 24, 1995
Bromoacetamido analogs of indomethacin and mefenamic acid as affinity-labeling agents and mechanistic probes for prostaglandin H2 synthaseM S Tang, L J Askonas, T M Penning
Chemical Research in Toxicology|September 16, 2008
Oxidation of PAH trans-dihydrodiols by human aldo-keto reductase AKR1B10Amy M Quinn, Ronald G Harvey, Trevor M Penning
Chemico-Biological Interactions|November 26, 2008
Aldo-keto reductases in which the conserved catalytic histidine is substitutedLuigi Di Costanzo, Trevor M Penning, David W Christianson
Biochemistry|May 16, 1989
Non-K-region o-quinones as enzyme-generated inactivators of dihydrodiol dehydrogenaseT M Penning, R B Sharp, T E Smithgall
Cancer Research|December 15, 1989
Characterization of dihydrodiol dehydrogenase in rat H-4IIe hepatoma cellsA L Buller, R B Sharp, T M Penning
Endocrinology|May 13, 2022
Conversion of Classical and 11-Oxygenated Androgens by Insulin-Induced AKR1C3 in a Model of Human PCOS AdipocytesRyan D Paulukinas, Clementina A Mesaros, Trevor M Penning
The Journal of Biological Chemistry|December 5, 1985
Purification and properties of 3 alpha-hydroxysteroid dehydrogenase from rat brain cytosol. Inhibition by nonsteroidal anti-inflammatory drugs and progestinsT M Penning, R B Sharp, N R Krieger
Chemico-Biological Interactions|February 27, 2003
Steroid-binding site residues dictate optimal substrate positioning in rat 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD or AKR1C9)Vladi V Heredia, Ryan G Kruger, Trevor M Penning
Pageof 216