White PC - Search Results

1

Apparent cortisone reductase deficiency: a functional defect in 11beta-hydroxysteroid dehydrogenase type 1.

Jamieson A, Wallace AM, Andrew R, Nunez BS, Walker BR, Fraser R, White PC, Connell JM. Jamieson A, et al. Among authors: white pc. J Clin Endocrinol Metab. 1999 Oct;84(10):3570-4. doi: 10.1210/jcem.84.10.6031. J Clin Endocrinol Metab. 1999. PMID: 10522997

2

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.

3

Glucocorticoid-suppressible hyperaldosteronism: effects of crossover site and parental origin of chimaeric gene on phenotypic expression.

Jamieson A, Slutsker L, Inglis GC, Fraser R, White PC, Connell JM. Jamieson A, et al. Among authors: white pc. Clin Sci (Lond). 1995 May;88(5):563-70. doi: 10.1042/cs0880563. Clin Sci (Lond). 1995. PMID: 7614815

4

Defects in the HSD11 gene encoding 11 beta-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency.

Nikkilä H, Tannin GM, New MI, Taylor NF, Kalaitzoglou G, Monder C, White PC. Nikkilä H, et al. Among authors: white pc. J Clin Endocrinol Metab. 1993 Sep;77(3):687-91. doi: 10.1210/jcem.77.3.8370690. J Clin Endocrinol Metab. 1993. PMID: 8370690

5

Variation in placental type 2 11beta-hydroxysteroid dehydrogenase activity is not related to birth weight or placental weight.

Rogerson FM, Kayes KM, White PC. Rogerson FM, et al. Among authors: white pc. Mol Cell Endocrinol. 1997 Apr 4;128(1-2):103-9. doi: 10.1016/s0303-7207(97)04027-6. Mol Cell Endocrinol. 1997. PMID: 9140081

6

Expression of human kidney 11beta-hydroxysteroid dehydrogenase (11-HSD2) in bacteria.

Nunez BS, Mune T, White PC. Nunez BS, et al. Among authors: white pc. Biochem Biophys Res Commun. 1999 Feb 24;255(3):652-6. doi: 10.1006/bbrc.1999.0259. Biochem Biophys Res Commun. 1999. PMID: 10049765

7

Functional analysis of four CYP21 mutations from spanish patients with congenital adrenal hyperplasia.

Nunez BS, Lobato MN, White PC, Meseguer A. Nunez BS, et al. Among authors: white pc. Biochem Biophys Res Commun. 1999 Sep 7;262(3):635-7. doi: 10.1006/bbrc.1999.1271. Biochem Biophys Res Commun. 1999. PMID: 10471376

8

Mutants of 11beta-hydroxysteroid dehydrogenase (11-HSD2) with partial activity: improved correlations between genotype and biochemical phenotype in apparent mineralocorticoid excess.

Nunez BS, Rogerson FM, Mune T, Igarashi Y, Nakagawa Y, Phillipov G, Moudgil A, Travis LB, Palermo M, Shackleton C, White PC. Nunez BS, et al. Among authors: white pc. Hypertension. 1999 Oct;34(4 Pt 1):638-42. doi: 10.1161/01.hyp.34.4.638. Hypertension. 1999. PMID: 10523339

9

Nikkila H, McMillan DR, Nunez BS, Pascoe L, Curnow KM, White PC. Nikkila H, et al. Among authors: white pc. Mol Endocrinol. 2000 Sep;14(9):1351-64. doi: 10.1210/mend.14.9.0511. Mol Endocrinol. 2000. PMID: 10976914

10

Genotype-phenotype correlations of mutations and polymorphisms in HSD11B2, the gene encoding the kidney isozyme of 11beta-hydroxysteroid dehydrogenase.

White PC, Agarwal AK, Nunez BS, Giacchetti G, Mantero F, Stewart PM. White PC, et al. Endocr Res. 2000 Nov;26(4):771-80. doi: 10.3109/07435800009048598. Endocr Res. 2000. PMID: 11196453 Review.

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