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Van Luu-The

Showing results (11-20 of 89) with videos related to

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Hormone Molecular Biology and Clinical Investigation|May 12, 2015
Sequential transformation of 4-androstenedione into dihydrotestosterone in prostate carcinoma (DU-145) cells indicates that 4-androstenedione and not testosterone is the substrate of 5α-reductaseMelanie Samson, Fernand Labrie, Van Luu-The
Journal of Medicinal Chemistry|January 25, 2002
Synthesis and optimization of a new family of type 3 17 beta-hydroxysteroid dehydrogenase inhibitors by parallel liquid-phase chemistryRené Maltais, Van Luu-The, Donald Poirier
The Journal of Steroid Biochemistry and Molecular Biology|May 3, 2005
Inhibition of human-type 1 3beta-hydroxysteroid deshydrogenase/Delta(5)-Delta(4)-isomerase expression using siRNAMélanie Samson, Fernand Labrie, Van Luu-The
European Journal of Biochemistry|March 13, 2003
Assessment of porcine and human 16-ene-synthase, a third activity of P450c17, in the formation of an androstenol precursor. Role of recombinant cytochrome b5 and P450 reductasePenny Soucy, Lucille Lacoste, Van Luu-The
Hormone Molecular Biology and Clinical Investigation|May 12, 2015
Target deletion of the bifunctional type 12 17β-hydroxysteroid dehydrogenase in mice results in reduction of androgen and estrogen levels in heterozygotes and embryonic lethality in homozygotesVéronique Bellemare, Daniel Phaneuf, Van Luu-The
The Journal of Steroid Biochemistry and Molecular Biology|September 30, 2005
Isolation and characterization of a cDNA encoding mouse 3alpha-hydroxysteroid dehydrogenase: an androgen-inactivating enzyme selectively expressed in female tissuesVéronique Bellemare, Fernand Labrie, Van Luu-The
The Journal of Steroid Biochemistry and Molecular Biology|April 30, 2005
Quantitative appreciation of steroidogenic gene expression in mouse tissues: new roles for type 2 5alpha-reductase, 20alpha-hydroxysteroid dehydrogenase and estrogen sulfotransferaseVan Luu-The, Georges Pelletier, Fernand Labrie
Molecular Endocrinology (Baltimore, Md.)|September 17, 2005
Characterization of type 12 17beta-hydroxysteroid dehydrogenase, an isoform of type 3 17beta-hydroxysteroid dehydrogenase responsible for estradiol formation in womenVan Luu-The, Philippe Tremblay, Fernand Labrie
Best Practice & Research. Clinical Endocrinology & Metabolism|May 13, 2008
Androgen biosynthetic pathways in the human prostateVan Luu-The, Alain Bélanger, Fernand Labrie
Journal of Enzyme Inhibition and Medicinal Chemistry|November 22, 2002
Androsterone derivatives substituted at position 16: chemical synthesis, inhibition of type 3 17beta-hydroxysteroid dehydrogenase, binding affinity for steroid receptors and proliferative/antiproliferative activity on Shionogi (AR+) cellsBéatrice Tchédam-Ngatcha, Van Luu-The, Donald Poirier
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
Hormone Molecular Biology and Clinical Investigation|May 12, 2015
Sequential transformation of 4-androstenedione into dihydrotestosterone in prostate carcinoma (DU-145) cells indicates that 4-androstenedione and not testosterone is the substrate of 5α-reductaseMelanie Samson, Fernand Labrie, Van Luu-The
Journal of Medicinal Chemistry|January 25, 2002
Synthesis and optimization of a new family of type 3 17 beta-hydroxysteroid dehydrogenase inhibitors by parallel liquid-phase chemistryRené Maltais, Van Luu-The, Donald Poirier
The Journal of Steroid Biochemistry and Molecular Biology|May 3, 2005
Inhibition of human-type 1 3beta-hydroxysteroid deshydrogenase/Delta(5)-Delta(4)-isomerase expression using siRNAMélanie Samson, Fernand Labrie, Van Luu-The
European Journal of Biochemistry|March 13, 2003
Assessment of porcine and human 16-ene-synthase, a third activity of P450c17, in the formation of an androstenol precursor. Role of recombinant cytochrome b5 and P450 reductasePenny Soucy, Lucille Lacoste, Van Luu-The
Hormone Molecular Biology and Clinical Investigation|May 12, 2015
Target deletion of the bifunctional type 12 17β-hydroxysteroid dehydrogenase in mice results in reduction of androgen and estrogen levels in heterozygotes and embryonic lethality in homozygotesVéronique Bellemare, Daniel Phaneuf, Van Luu-The
The Journal of Steroid Biochemistry and Molecular Biology|September 30, 2005
Isolation and characterization of a cDNA encoding mouse 3alpha-hydroxysteroid dehydrogenase: an androgen-inactivating enzyme selectively expressed in female tissuesVéronique Bellemare, Fernand Labrie, Van Luu-The
The Journal of Steroid Biochemistry and Molecular Biology|April 30, 2005
Quantitative appreciation of steroidogenic gene expression in mouse tissues: new roles for type 2 5alpha-reductase, 20alpha-hydroxysteroid dehydrogenase and estrogen sulfotransferaseVan Luu-The, Georges Pelletier, Fernand Labrie
Molecular Endocrinology (Baltimore, Md.)|September 17, 2005
Characterization of type 12 17beta-hydroxysteroid dehydrogenase, an isoform of type 3 17beta-hydroxysteroid dehydrogenase responsible for estradiol formation in womenVan Luu-The, Philippe Tremblay, Fernand Labrie
Best Practice & Research. Clinical Endocrinology & Metabolism|May 13, 2008
Androgen biosynthetic pathways in the human prostateVan Luu-The, Alain Bélanger, Fernand Labrie
Journal of Enzyme Inhibition and Medicinal Chemistry|November 22, 2002
Androsterone derivatives substituted at position 16: chemical synthesis, inhibition of type 3 17beta-hydroxysteroid dehydrogenase, binding affinity for steroid receptors and proliferative/antiproliferative activity on Shionogi (AR+) cellsBéatrice Tchédam-Ngatcha, Van Luu-The, Donald Poirier
Pageof 9