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W L Miller

Showing results (221-230 of 256) with videos related to

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Molecular and Cellular Biochemistry|January 1, 1983
Regulation of beta-chain mRNA of ovine follicle-stimulating hormone by 17 beta-estradiolW L Miller, D C Alexander, J C Wu, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Genetic variation in P450c11AS in Chilean patients with low renin hypertensionC E Fardella, H Rodriguez, J Montero, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1989
Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA typesY Morel, M David, M G Forest, et al.
Biochemistry|October 3, 1995
Structure of the human steroidogenic acute regulatory protein (StAR) gene: StAR stimulates mitochondrial cholesterol 27-hydroxylase activityT Sugawara, D Lin, J A Holt, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissuesS B Solish, J Picado-Leonard, Y Morel, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1987
Cytochrome P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissuesB C Chung, J Picado-Leonard, M Haniu, et al.
European Journal of Biochemistry|November 1, 1975
Interactions between prostaglandin analogues and a receptor in bovine Corpora lutea. Correlation of dissociation constants with luteolytic potencies in hamstersW S Powell, S Hammarström, B Samuelsson, et al.
Human Molecular Genetics|December 1, 1995
T-->A transversion 11 bp from a splice acceptor site in the human gene for steroidogenic acute regulatory protein causes congenital lipoid adrenal hyperplasiaM K Tee, D Lin, T Sugawara, et al.
Journal of Pharmaceutical Sciences|July 1, 1979
Prostaglandin prodrugs. I: Stabilization of dinoprostone (prostaglandin E2) in solid state through formation of crystalline C1-phenyl estersW Morozowich, T O Oesterling, W L Miller, et al.
American Journal of Human Genetics|December 5, 1998
Genetics of vitamin D 1alpha-hydroxylase deficiency in 17 familiesJ T Wang, C J Lin, S M Burridge, et al.
Pageof 26

Showing results (221-230 of 256) with videos related to

Sort By:
Pageof 26
Molecular and Cellular Biochemistry|January 1, 1983
Regulation of beta-chain mRNA of ovine follicle-stimulating hormone by 17 beta-estradiolW L Miller, D C Alexander, J C Wu, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Genetic variation in P450c11AS in Chilean patients with low renin hypertensionC E Fardella, H Rodriguez, J Montero, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1989
Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA typesY Morel, M David, M G Forest, et al.
Biochemistry|October 3, 1995
Structure of the human steroidogenic acute regulatory protein (StAR) gene: StAR stimulates mitochondrial cholesterol 27-hydroxylase activityT Sugawara, D Lin, J A Holt, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissuesS B Solish, J Picado-Leonard, Y Morel, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1987
Cytochrome P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissuesB C Chung, J Picado-Leonard, M Haniu, et al.
European Journal of Biochemistry|November 1, 1975
Interactions between prostaglandin analogues and a receptor in bovine Corpora lutea. Correlation of dissociation constants with luteolytic potencies in hamstersW S Powell, S Hammarström, B Samuelsson, et al.
Human Molecular Genetics|December 1, 1995
T-->A transversion 11 bp from a splice acceptor site in the human gene for steroidogenic acute regulatory protein causes congenital lipoid adrenal hyperplasiaM K Tee, D Lin, T Sugawara, et al.
Journal of Pharmaceutical Sciences|July 1, 1979
Prostaglandin prodrugs. I: Stabilization of dinoprostone (prostaglandin E2) in solid state through formation of crystalline C1-phenyl estersW Morozowich, T O Oesterling, W L Miller, et al.
American Journal of Human Genetics|December 5, 1998
Genetics of vitamin D 1alpha-hydroxylase deficiency in 17 familiesJ T Wang, C J Lin, S M Burridge, et al.
Pageof 26