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The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogensA Morishima, M M Grumbach, E R Simpson, et al.
Molecular Endocrinology (Baltimore, Md.)|July 1, 1987
Vasoactive intestinal peptide regulates cholesterol side-chain cleavage cytochrome P-450 (P-450scc) gene expression in granulosa cells from immature rat ovariesW H Trzeciak, M R Waterman, E R Simpson, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1982
Prostaglandin biosynthesis in the human fetal adrenal gland: regulation by glucocorticosteroidsM D Mitchell, B R Carr, J I Mason, et al.
American Journal of Obstetrics and Gynecology|April 15, 1981
Low-density lipoprotein as a potential vehicle for chemotherapeutic agents and radionucleotides in the management of gynecologic neoplasmsD Gal, M Ohashi, P C MacDonald, et al.
Biochimica Et Biophysica Acta|October 13, 1976
Electron paramagnetic resonance studies of cytochrome P-450 and adrenal ferredoxin in single whole rat adrenal glands. Effect of corticotropinD L Williams-Smith, E R Simpson, S M Barlow, et al.
Human Genetics|April 1, 1992
Canadian Mennonites and individuals residing in the Friesland region of The Netherlands share the same molecular basis of 17 alpha-hydroxylase deficiencyT Imai, T Yanase, M R Waterman, et al.
Princess Takamatsu Symposia|January 1, 1990
The aromatase enzyme: from cloning to cancerE R Simpson, T Price, J Aitken, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1992
Compound heterozygous mutations (Arg 239----stop, Pro 342----Thr) in the CYP17 (P45017 alpha) gene lead to ambiguous external genitalia in a male patient with partial combined 17 alpha-hydroxylase/17,20-lyase deficiencyR Ahlgren, T Yanase, E R Simpson, et al.
The Journal of Steroid Biochemistry and Molecular Biology|July 24, 2007
Estrogen and adiposity--utilizing models of aromatase deficiency to explore the relationshipM E E Jones, K J McInnes, W C Boon, et al.
Molecular Endocrinology (Baltimore, Md.)|June 1, 1988
Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiencyM Kagimoto, J S Winter, K Kagimoto, et al.
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