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Van Luu-The

Showing results (31-40 of 89) with videos related to

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Bioorganic & Medicinal Chemistry|November 18, 2006
C6-(N,N-butyl-methyl-heptanamide) derivatives of estrone and estradiol as inhibitors of type 1 17beta-hydroxysteroid dehydrogenase: Chemical synthesis and biological evaluationChristine Cadot, Yannick Laplante, Fatima Kamal, et al.
Biochemistry|July 16, 2008
The crystal structure of human Delta4-3-ketosteroid 5beta-reductase defines the functional role of the residues of the catalytic tetrad in the steroid double bond reduction mechanismFrédérick Faucher, Line Cantin, Van Luu-The, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|May 20, 2003
3Beta-sulfamate derivatives of C19 and C21 steroids bearing a t-butylbenzyl or a benzyl group: synthesis and evaluation as non-estrogenic and non-androgenic steroid sulfatase inhibitorsLiviu C Ciobanu, Roch P Boivin, Van Luu-The, et al.
Biochemistry|December 17, 2008
Crystal structures of human Delta4-3-ketosteroid 5beta-reductase (AKR1D1) reveal the presence of an alternative binding site responsible for substrate inhibitionFrédérick Faucher, Line Cantin, Van Luu-The, et al.
Breast Cancer Research and Treatment|June 9, 2012
Specific transcriptional response of four blockers of estrogen receptors on estradiol-modulated genes in the mouse mammary glandEzequiel Calvo, Van Luu-The, Pascal Belleau, et al.
The Journal of Steroid Biochemistry and Molecular Biology|May 12, 2009
Differential estrogenic 17beta-hydroxysteroid dehydrogenase activity and type 12 17beta-hydroxysteroid dehydrogenase expression levels in preadipocytes and differentiated adipocytesVéronique Bellemare, Philippe Laberge, Suzanne Noël, et al.
Cancer Research|October 16, 2003
Inhibition of estrone sulfate-induced uterine growth by potent nonestrogenic steroidal inhibitors of steroid sulfataseLiviu C Ciobanu, Van Luu-The, Céline Martel, et al.
Molecular and Cellular Endocrinology|December 20, 2005
3Beta-alkyl-androsterones as inhibitors of type 3 17beta-hydroxysteroid dehydrogenase: inhibitory potency in intact cells, selectivity towards isoforms 1, 2, 5 and 7, binding affinity for steroid receptors, and proliferative/antiproliferative activities on AR+ and ER+ cell linesBéatrice Tchédam Ngatcha, Yannick Laplante, Fernand Labrie, et al.
BMC Biochemistry|February 7, 2007
Expression and localization of estrogenic type 12 17beta-hydroxysteroid dehydrogenase in the cynomolgus monkeyHong Liu, Shufang Zheng, Véronique Bellemare, et al.
The Journal of Steroid Biochemistry and Molecular Biology|July 31, 2007
Steroid metabolism and profile of steroidogenic gene expression in Episkin: high similarity with human epidermisVan Luu-The, Corinne Ferraris, Daniel Duche, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
Bioorganic & Medicinal Chemistry|November 18, 2006
C6-(N,N-butyl-methyl-heptanamide) derivatives of estrone and estradiol as inhibitors of type 1 17beta-hydroxysteroid dehydrogenase: Chemical synthesis and biological evaluationChristine Cadot, Yannick Laplante, Fatima Kamal, et al.
Biochemistry|July 16, 2008
The crystal structure of human Delta4-3-ketosteroid 5beta-reductase defines the functional role of the residues of the catalytic tetrad in the steroid double bond reduction mechanismFrédérick Faucher, Line Cantin, Van Luu-The, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|May 20, 2003
3Beta-sulfamate derivatives of C19 and C21 steroids bearing a t-butylbenzyl or a benzyl group: synthesis and evaluation as non-estrogenic and non-androgenic steroid sulfatase inhibitorsLiviu C Ciobanu, Roch P Boivin, Van Luu-The, et al.
Biochemistry|December 17, 2008
Crystal structures of human Delta4-3-ketosteroid 5beta-reductase (AKR1D1) reveal the presence of an alternative binding site responsible for substrate inhibitionFrédérick Faucher, Line Cantin, Van Luu-The, et al.
Breast Cancer Research and Treatment|June 9, 2012
Specific transcriptional response of four blockers of estrogen receptors on estradiol-modulated genes in the mouse mammary glandEzequiel Calvo, Van Luu-The, Pascal Belleau, et al.
The Journal of Steroid Biochemistry and Molecular Biology|May 12, 2009
Differential estrogenic 17beta-hydroxysteroid dehydrogenase activity and type 12 17beta-hydroxysteroid dehydrogenase expression levels in preadipocytes and differentiated adipocytesVéronique Bellemare, Philippe Laberge, Suzanne Noël, et al.
Cancer Research|October 16, 2003
Inhibition of estrone sulfate-induced uterine growth by potent nonestrogenic steroidal inhibitors of steroid sulfataseLiviu C Ciobanu, Van Luu-The, Céline Martel, et al.
Molecular and Cellular Endocrinology|December 20, 2005
3Beta-alkyl-androsterones as inhibitors of type 3 17beta-hydroxysteroid dehydrogenase: inhibitory potency in intact cells, selectivity towards isoforms 1, 2, 5 and 7, binding affinity for steroid receptors, and proliferative/antiproliferative activities on AR+ and ER+ cell linesBéatrice Tchédam Ngatcha, Yannick Laplante, Fernand Labrie, et al.
BMC Biochemistry|February 7, 2007
Expression and localization of estrogenic type 12 17beta-hydroxysteroid dehydrogenase in the cynomolgus monkeyHong Liu, Shufang Zheng, Véronique Bellemare, et al.
The Journal of Steroid Biochemistry and Molecular Biology|July 31, 2007
Steroid metabolism and profile of steroidogenic gene expression in Episkin: high similarity with human epidermisVan Luu-The, Corinne Ferraris, Daniel Duche, et al.
Pageof 9