White PC - Search Results

1

Disorders of aldosterone biosynthesis and action.

White PC. White PC. N Engl J Med. 1994 Jul 28;331(4):250-8. doi: 10.1056/NEJM199407283310408. N Engl J Med. 1994. PMID: 8015573 Review. No abstract available.

2

Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency.

Pascoe L, Curnow KM, Slutsker L, Rösler A, White PC. Pascoe L, et al. Among authors: white pc. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):4996-5000. doi: 10.1073/pnas.89.11.4996. Proc Natl Acad Sci U S A. 1992. PMID: 1594605 Free PMC article.

3

Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase.

Speiser PW, Agdere L, Ueshiba H, White PC, New MI. Speiser PW, et al. Among authors: white pc. N Engl J Med. 1991 Jan 17;324(3):145-9. doi: 10.1056/NEJM199101173240302. N Engl J Med. 1991. PMID: 1984191 Free article.

4

Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.

Speiser PW, New MI, White PC. Speiser PW, et al. Among authors: white pc. N Engl J Med. 1988 Jul 7;319(1):19-23. doi: 10.1056/NEJM198807073190104. N Engl J Med. 1988. PMID: 3260007

5

An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylase.

Globerman H, Rösler A, Theodor R, New MI, White PC. Globerman H, et al. Among authors: white pc. N Engl J Med. 1988 Nov 3;319(18):1193-7. doi: 10.1056/NEJM198811033191804. N Engl J Med. 1988. PMID: 3262827

6

Disorders of steroid 11 beta-hydroxylase isozymes.

White PC, Curnow KM, Pascoe L. White PC, et al. Endocr Rev. 1994 Aug;15(4):421-38. doi: 10.1210/edrv-15-4-421. Endocr Rev. 1994. PMID: 7988480 Review.

7

Steroid 11 beta-hydroxylase deficiency and related disorders.

White PC, Speiser PW. White PC, et al. Endocrinol Metab Clin North Am. 1994 Jun;23(2):325-39. Endocrinol Metab Clin North Am. 1994. PMID: 8070425 Review.

8

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2.

Pascoe L, Curnow KM, Slutsker L, Connell JM, Speiser PW, New MI, White PC. Pascoe L, et al. Among authors: white pc. Proc Natl Acad Sci U S A. 1992 Sep 1;89(17):8327-31. doi: 10.1073/pnas.89.17.8327. Proc Natl Acad Sci U S A. 1992. PMID: 1518866 Free PMC article.

9

Genetic basis of endocrine disease 2: congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

White PC, New MI. White PC, et al. J Clin Endocrinol Metab. 1992 Jan;74(1):6-11. doi: 10.1210/jcem.74.1.1727830. J Clin Endocrinol Metab. 1992. PMID: 1727830 Review. No abstract available.

10

The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex.

Curnow KM, Tusie-Luna MT, Pascoe L, Natarajan R, Gu JL, Nadler JL, White PC. Curnow KM, et al. Among authors: white pc. Mol Endocrinol. 1991 Oct;5(10):1513-22. doi: 10.1210/mend-5-10-1513. Mol Endocrinol. 1991. PMID: 1775135

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