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P C White

Showing results (111-120 of 183) with videos related to

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The New England Journal of Medicine|January 17, 1991
Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylaseP W Speiser, L Agdere, H Ueshiba, et al.
The Journal of General Physiology|January 1, 1976
Nonelectrolyte diffusion across lipid bilayer systemsM Poznansky, S Tong, P C White, et al.
Molecular and Cellular Endocrinology|July 31, 1998
Prominent sex steroid metabolism in human lymphocytesZ Zhou, C H Shackleton, S Pahwa, et al.
The Journal of Biological Chemistry|June 8, 1999
Processing, activity, and inhibition of recombinant cyprosin, an aspartic proteinase from cardoon (Cynara cardunculus)P C White, M C Cordeiro, D Arnold, et al.
Journal of Molecular Endocrinology|April 5, 2002
Differential regulation of aldosterone synthase and 11beta-hydroxylase transcription by steroidogenic factor-1M H Bassett, Y Zhang, C Clyne, et al.
Human Mutation|January 1, 1994
Mutations in steroid 21-hydroxylase (CYP21)P C White, M T Tusie-Luna, M I New, et al.
Molecular Endocrinology (Baltimore, Md.)|August 1, 1992
R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversionsA Helmberg, M T Tusie-Luna, M Tabarelli, et al.
The Journal of Clinical Endocrinology and Metabolism|March 10, 2001
Type 1 aldosterone synthase deficiency presenting in a middle-aged manK M Kayes-Wandover, R E Schindler, H C Taylor, et al.
Nature Genetics|August 1, 1995
Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenaseT Mune, F M Rogerson, H Nikkilä, et al.
The Journal of Clinical Investigation|July 1, 1988
Nonsense mutation causing steroid 21-hydroxylase deficiencyH Globerman, M Amor, K L Parker, et al.
Pageof 19

Showing results (111-120 of 183) with videos related to

Sort By:
Pageof 19
The New England Journal of Medicine|January 17, 1991
Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylaseP W Speiser, L Agdere, H Ueshiba, et al.
The Journal of General Physiology|January 1, 1976
Nonelectrolyte diffusion across lipid bilayer systemsM Poznansky, S Tong, P C White, et al.
Molecular and Cellular Endocrinology|July 31, 1998
Prominent sex steroid metabolism in human lymphocytesZ Zhou, C H Shackleton, S Pahwa, et al.
The Journal of Biological Chemistry|June 8, 1999
Processing, activity, and inhibition of recombinant cyprosin, an aspartic proteinase from cardoon (Cynara cardunculus)P C White, M C Cordeiro, D Arnold, et al.
Journal of Molecular Endocrinology|April 5, 2002
Differential regulation of aldosterone synthase and 11beta-hydroxylase transcription by steroidogenic factor-1M H Bassett, Y Zhang, C Clyne, et al.
Human Mutation|January 1, 1994
Mutations in steroid 21-hydroxylase (CYP21)P C White, M T Tusie-Luna, M I New, et al.
Molecular Endocrinology (Baltimore, Md.)|August 1, 1992
R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversionsA Helmberg, M T Tusie-Luna, M Tabarelli, et al.
The Journal of Clinical Endocrinology and Metabolism|March 10, 2001
Type 1 aldosterone synthase deficiency presenting in a middle-aged manK M Kayes-Wandover, R E Schindler, H C Taylor, et al.
Nature Genetics|August 1, 1995
Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenaseT Mune, F M Rogerson, H Nikkilä, et al.
The Journal of Clinical Investigation|July 1, 1988
Nonsense mutation causing steroid 21-hydroxylase deficiencyH Globerman, M Amor, K L Parker, et al.
Pageof 19