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Journal of Neural Transmission|January 1, 1979
Responses of plasma renin activity and dopamine-beta-hydroxylase to increased intravascular volumeF Lamprecht, W L Miller, T Kawasaki, et al.
Molecular Endocrinology (Baltimore, Md.)|March 1, 1994
Modeling and mutagenesis of the active site of human P450c17D Lin, L H Zhang, E Chiao, et al.
The Journal of Biological Chemistry|December 23, 1999
Transcriptional regulatory elements of the human gene for cytochrome P450c21 (steroid 21-hydroxylase) lie within intron 35 of the linked C4B geneS D Wijesuriya, G Zhang, A Dardis, et al.
The Journal of Steroid Biochemistry and Molecular Biology|January 6, 2012
Analysis of the duplicated human C4/P450c21/X gene clusterW L Miller, S E Gitelman, J Bristow, et al.
The Journal of Clinical Investigation|December 1, 1991
Normal genes for the cholesterol side chain cleavage enzyme, P450scc, in congenital lipoid adrenal hyperplasiaD Lin, S E Gitelman, P Saenger, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Transcription of the human genes for cytochrome P450scc and P450c17 is regulated differently in human adrenal NCI-H295 cells than in mouse adrenal Y1 cellsH Rodriguez, D W Hum, B Staels, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 1, 1993
Congenital lipoid adrenal hyperplasia--genes for P450scc, side chain cleavage enzyme, are normalP Saenger, D Lin, S E Gitelman, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locusY Morel, J Bristow, S E Gitelman, et al.
Endocrine Research|February 24, 2001
Probing structural and functional domains of human P450c17R J Auchus, K Worthy, D H Geller, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1994
Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiencyC E Fardella, D W Hum, J Homoki, et al.
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