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P C White

Showing results (171-180 of 183) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|October 16, 1999
Apparent cortisone reductase deficiency: a functional defect in 11beta-hydroxysteroid dehydrogenase type 1A Jamieson, A M Wallace, R Andrew, et al.
Biochemistry|May 20, 1986
Bovine steroid 21-hydroxylase: regulation of biosynthesisM E John, T Okamura, A Dee, et al.
Journal of Periodontal Research|March 26, 2018
Cigarette smoke modifies neutrophil chemotaxis, neutrophil extracellular trap formation and inflammatory response-related gene expressionP C White, J Hirschfeld, M R Milward, et al.
The Journal of Biological Chemistry|January 15, 1989
Structural and functional analysis of the promoter region of the gene encoding mouse steroid 11 beta-hydroxylaseA R Mouw, D A Rice, J C Meade, et al.
Clinical Endocrinology|September 5, 2001
Possible association but no linkage of the HSD11B2 gene encoding the kidney isozyme of 11beta-hydroxysteroid dehydrogenase to hypertension in Black peopleP C White, A K Agarwal, A Li, et al.
Immunogenetics|January 1, 1992
A novel gene constitutively expressed in human lymphoid cells is inducible with interferon-gamma in myeloid cellsJ A Trapani, K A Browne, M J Dawson, et al.
The Journal of Clinical Investigation|August 1, 1992
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyP W Speiser, J Dupont, D Zhu, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1990
First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)P W Speiser, N Laforgia, K Kato, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1992
Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)L P Karaviti, A B Mercado, M B Mercado, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1996
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyS Geley, K Kapelari, K Jöhrer, et al.
Pageof 19

Showing results (171-180 of 183) with videos related to

Sort By:
Pageof 19
The Journal of Clinical Endocrinology and Metabolism|October 16, 1999
Apparent cortisone reductase deficiency: a functional defect in 11beta-hydroxysteroid dehydrogenase type 1A Jamieson, A M Wallace, R Andrew, et al.
Biochemistry|May 20, 1986
Bovine steroid 21-hydroxylase: regulation of biosynthesisM E John, T Okamura, A Dee, et al.
Journal of Periodontal Research|March 26, 2018
Cigarette smoke modifies neutrophil chemotaxis, neutrophil extracellular trap formation and inflammatory response-related gene expressionP C White, J Hirschfeld, M R Milward, et al.
The Journal of Biological Chemistry|January 15, 1989
Structural and functional analysis of the promoter region of the gene encoding mouse steroid 11 beta-hydroxylaseA R Mouw, D A Rice, J C Meade, et al.
Clinical Endocrinology|September 5, 2001
Possible association but no linkage of the HSD11B2 gene encoding the kidney isozyme of 11beta-hydroxysteroid dehydrogenase to hypertension in Black peopleP C White, A K Agarwal, A Li, et al.
Immunogenetics|January 1, 1992
A novel gene constitutively expressed in human lymphoid cells is inducible with interferon-gamma in myeloid cellsJ A Trapani, K A Browne, M J Dawson, et al.
The Journal of Clinical Investigation|August 1, 1992
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyP W Speiser, J Dupont, D Zhu, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1990
First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)P W Speiser, N Laforgia, K Kato, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1992
Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)L P Karaviti, A B Mercado, M B Mercado, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1996
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyS Geley, K Kapelari, K Jöhrer, et al.
Pageof 19