MASON, J. IAN

Human 3β-Hydroxysteroid Dehydrogenase/ δ5→4Isomerase from Placenta: Expression in Nonsteroidogenic Cells of a Protein that Catalyzes the Dehydrogenation/Isomerization of C21 and C19 Steroids*

LORENCE, M. C., MURRY, B. A., TRANT, J. M., & MASON, J. I. (1990) · Endocrinology

Steroid Chemistry and BiochemistryAdrenal Hormones and Disorders

Cited by 212

Structural Analysis of the Gene Encoding Human 3β-Hydroxysteroid Dehydrogenase/δ5→4-lsomerase

Lorence, M. C., Corbin, C. J., Kamimura, N., Mahendroo, M. S., & Mason, J. I. (1990) · Molecular Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 80

Inherited congenital adrenal hyperplasia in the rabbit is caused by a deletion in the gene encoding cytochrome P450 cholesterol side-chain cleavage enzyme

Yang, X., Iwamoto, K., Wang, M., Artwohl, J., Mason, J. I., & Pang, S. (1993) · Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 73

Steroidogenesis in the Human Fetal Adrenal: A Role for Cholesterol Synthesized de Novo*

MASON, J. I., & RAINEY, W. E. (1987) · The Journal of Clinical Endocrinology & Metabolism

Cholesterol and Lipid MetabolismSteroid Chemistry and Biochemistry

Cited by 47

Battle of the kinases: Integration of adrenal responses to cAMP, DG and Ca2+at the level of steroidogenic cytochromes P450 and 3ßHSD expression in H295R cells.

Bird, I. M., Mason, J. I., & Rainey, W. E. (1998) · Endocrine Research

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 27

Carriers for type II 3β‐hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test

Pang, S., Carbunaru, G., Haider, A., Copeland, K. C., Chang, Y. T., Lutfallah, C., & Mason, J. I. (2003) · Clinical Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 24