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The common I172N mutation causes conformational change of cytochrome P450c21 revealed by systematic mutation, kinetic, and structural studies.

Periodical

Hsu, L C; Hsu, N C; Guzova, J A; Guzov, V M; Chang, S F; Chung, B C

Journal of Biological Chemistry; February 1996, Vol. 271 Issue: 6 p3306-10, 5p

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P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.

Periodical

Matteson, K J; Phillips, J A; Miller, W L; Chung, B C; Orlando, P J; Frisch, H; Ferrandez, A; Burr, I M

Proceedings of the National Academy of Sciences of the United States of America; August 1987, Vol. 84 Issue: 16 p5858-5862, 5p

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Human adrenodoxin: cloning of three cDNAs and cycloheximide enhancement in JEG-3 cells.

Periodical

Picado-Leonard, J; Voutilainen, R; Kao, L C; Chung, B C; Strauss, J F; Miller, W L

Journal of Biological Chemistry; March 1988, Vol. 263 Issue: 7 p3240-3244, 5p

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Structure of a bovine gene for P-450c21 (steroid 21-hydroxylase) defines a novel cytochrome P-450 gene family.

Periodical

Chung, B C; Matteson, K J; Miller, W L

Proceedings of the National Academy of Sciences of the United States of America; June 1986, Vol. 83 Issue: 12 p4243-4247, 5p

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Regulated expression of cytochrome P-450scc (cholesterol-side-chain cleavage enzyme) in cultured cell lines detected by antibody against bacterially expressed human protein

Periodical

Hu, M C; Guo, I C; Lin, J H; Chung, B C

Biochemical Journal; March 1991, Vol. 274 Issue: 3 p813-817, 5p

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Cytochrome P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues.

Periodical

Chung, B C; Picado-Leonard, J; Haniu, M; Bienkowski, M; Hall, P F; Shively, J E; Miller, W L

Proceedings of the National Academy of Sciences of the United States of America; January 1987, Vol. 84 Issue: 2 p407-411, 5p

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Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placenta.

Periodical

Chung, B C; Matteson, K J; Voutilainen, R; Mohandas, T K; Miller, W L

Proceedings of the National Academy of Sciences of the United States of America; December 1986, Vol. 83 Issue: 23 p8962-8966, 5p

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A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.

Periodical

Chiou, S H; Hu, M C; Chung, B C

Journal of Biological Chemistry; February 1990, Vol. 265 Issue: 6 p3549-3552, 4p

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Increased hair polyamine levels in patients with Alzheimer's disease.

Academic Journal

Choi, Man Ho; Kim, Kyoung-Rae; Kim, In Seong; Lho, Dong Seok; Chung, Bong Chul; Choi, M H; Kim, K R; Kim, I S; Lho, D S; Chung, B C

Annals of Neurology; 2001, Vol. 50 Issue 1, p128-128, 1p

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