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P C White

Showing results (121-130 of 183) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiencyM Amor, K L Parker, H Globerman, et al.
The Veterinary Record|August 24, 2000
Fox predation as a cause of lamb mortality on hill farmsP C White, H L Groves, J R Savery, et al.
Steroids|January 1, 1997
Molecular analysis of 11 beta-hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excessP C White, T Mune, F M Rogerson, et al.
Molecular Endocrinology (Baltimore, Md.)|September 1, 1995
Alternatively spliced human type 1 angiotensin II receptor mRNAs are translated at different efficiencies and encode two receptor isoformsK M Curnow, L Pascoe, E Davies, et al.
The Journal of the Arkansas Medical Society|September 1, 1979
Amebic meningoencephalitis in ArkansasT Yamauchi, J F Jimenez, T W McKee, et al.
The Journal of Biological Chemistry|September 5, 1991
The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localizationG M Tannin, A K Agarwal, C Monder, et al.
The Journal of Clinical Investigation|May 1, 1991
A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan originP C White, J Dupont, M I New, et al.
Pediatric Research|January 1, 1997
11 beta-Hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excessP C White, T Mune, F M Rogerson, et al.
Clinical Science (London, England : 1979)|May 1, 1995
Glucocorticoid-suppressible hyperaldosteronism: effects of crossover site and parental origin of chimaeric gene on phenotypic expressionA Jamieson, L Slutsker, G C Inglis, et al.
Molecular Biology & Medicine|October 1, 1986
Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene regionB O Boehm, C Rosak, T L Boehm, et al.
Pageof 19

Showing results (121-130 of 183) with videos related to

Sort By:
Pageof 19
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiencyM Amor, K L Parker, H Globerman, et al.
The Veterinary Record|August 24, 2000
Fox predation as a cause of lamb mortality on hill farmsP C White, H L Groves, J R Savery, et al.
Steroids|January 1, 1997
Molecular analysis of 11 beta-hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excessP C White, T Mune, F M Rogerson, et al.
Molecular Endocrinology (Baltimore, Md.)|September 1, 1995
Alternatively spliced human type 1 angiotensin II receptor mRNAs are translated at different efficiencies and encode two receptor isoformsK M Curnow, L Pascoe, E Davies, et al.
The Journal of the Arkansas Medical Society|September 1, 1979
Amebic meningoencephalitis in ArkansasT Yamauchi, J F Jimenez, T W McKee, et al.
The Journal of Biological Chemistry|September 5, 1991
The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localizationG M Tannin, A K Agarwal, C Monder, et al.
The Journal of Clinical Investigation|May 1, 1991
A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan originP C White, J Dupont, M I New, et al.
Pediatric Research|January 1, 1997
11 beta-Hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excessP C White, T Mune, F M Rogerson, et al.
Clinical Science (London, England : 1979)|May 1, 1995
Glucocorticoid-suppressible hyperaldosteronism: effects of crossover site and parental origin of chimaeric gene on phenotypic expressionA Jamieson, L Slutsker, G C Inglis, et al.
Molecular Biology & Medicine|October 1, 1986
Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene regionB O Boehm, C Rosak, T L Boehm, et al.
Pageof 19