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470 related items for PubMed ID: 11832364
1. Mutations in aldosterone synthase gene of Milan hypertensive rats: phenotypic consequences. Lloyd-MacGilp SA, Torielli L, Bechtel S, Tripodi G, Gomez-Sanchez CE, Zagato L, Bernhardt R, Kenyon CJ. Am J Physiol Endocrinol Metab; 2002 Mar; 282(3):E608-17. PubMed ID: 11832364 [Abstract] [Full Text] [Related]
2. The impact of polymorphisms in the gene encoding aldosterone synthase (CYP11B2) on steroid synthesis and blood pressure regulation. Connell JM, Fraser R, MacKenzie SM, Friel EC, Ingram MC, Holloway CD, Davies E. Mol Cell Endocrinol; 2004 Mar 31; 217(1-2):243-7. PubMed ID: 15134824 [Abstract] [Full Text] [Related]
3. Steroid 11-beta-hydroxylase deficiency caused by compound heterozygosity for a novel mutation, p.G314R, in one CYP11B1 allele, and a chimeric CYP11B2/CYP11B1 in the other allele. Kuribayashi I, Nomoto S, Massa G, Oostdijk W, Wit JM, Wolffenbuttel BH, Shizuta Y, Honke K. Horm Res; 2005 Mar 31; 63(6):284-93. PubMed ID: 16024935 [Abstract] [Full Text] [Related]
4. Mutation analysis of CYP11B1 and CYP11B2 in patients with increased 18-hydroxycortisol production. Nicod J, Dick B, Frey FJ, Ferrari P. Mol Cell Endocrinol; 2004 Feb 12; 214(1-2):167-74. PubMed ID: 15062555 [Abstract] [Full Text] [Related]
5. Aldosterone synthase gene variation and adrenocortical response to sodium status, angiotensin II and ACTH in normal male subjects. Kennon B, Ingram MC, Friel EC, Anderson NH, MacKenzie SM, Davies E, Shakerdi L, Wallace AM, Fraser R, Connell JM. Clin Endocrinol (Oxf); 2004 Aug 12; 61(2):174-81. PubMed ID: 15272911 [Abstract] [Full Text] [Related]
6. Coexistence of different phenotypes in a family with glucocorticoid-remediable aldosteronism. Fallo F, Pilon C, Williams TA, Sonino N, Morra Di Cella S, Veglio F, De Iasio R, Montanari P, Mulatero P. J Hum Hypertens; 2004 Jan 12; 18(1):47-51. PubMed ID: 14688810 [Abstract] [Full Text] [Related]
7. Association of DNA polymorphisms within the CYP11B2/CYP11B1 locus and postoperative hypertension risk in the patients with aldosterone-producing adenomas. Wang B, Zhang G, Ouyang J, Deng X, Shi T, Ma X, Li H, Ju Z, Wang C, Wu Z, Liu S, Zhang X. Urology; 2010 Oct 12; 76(4):1018.e1-7. PubMed ID: 20708777 [Abstract] [Full Text] [Related]
8. Neonatal salt-wasting and 11 beta-hydroxylase deficiency in a child carrying a homozygous deletion hybrid CYP11B2 (aldosterone synthase)-CYP11B1 (11 beta-hydroxylase). Ezquieta B, Luzuriaga C. Clin Genet; 2004 Sep 12; 66(3):229-35. PubMed ID: 15324322 [Abstract] [Full Text] [Related]
9. Stable expression of rat cytochrome P450 11 beta-hydroxylase (CYP11B1) and aldosterone synthase (CYP11B2) in MA-10 cells. Zhou M, Xue D, Foecking MF, Gomez-Sanchez CE. J Steroid Biochem Mol Biol; 1995 Jun 12; 52(6):523-8. PubMed ID: 7779756 [Abstract] [Full Text] [Related]
10. Structure-function relationships of aldosterone synthase and 11 beta-hydroxylase enzymes: implications for human hypertension. Fisher A, Davies E, Fraser R, Connell JM. Clin Exp Pharmacol Physiol Suppl; 1998 Nov 12; 25():S42-6. PubMed ID: 9809191 [Abstract] [Full Text] [Related]
11. Polymorphisms in CYP11B2 and CYP11B1 genes associated with primary hyperaldosteronism. Zhang GX, Wang BJ, Ouyang JZ, Deng XY, Ma X, Li HZ, Wu Z, Liu SL, Xu H, Zhang X. Hypertens Res; 2010 May 12; 33(5):478-84. PubMed ID: 20339375 [Abstract] [Full Text] [Related]
12. Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasia. Portrat S, Mulatero P, Curnow KM, Chaussain JL, Morel Y, Pascoe L. J Clin Endocrinol Metab; 2001 Jul 12; 86(7):3197-201. PubMed ID: 11443188 [Abstract] [Full Text] [Related]
13. Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study. Freel EM, Ingram M, Friel EC, Fraser R, Brown M, Samani NJ, Caulfield M, Munroe P, Farrall M, Webster J, Clayton D, Dominiczak AF, Davies E, Connell JM. Clin Endocrinol (Oxf); 2007 Dec 12; 67(6):832-8. PubMed ID: 17651452 [Abstract] [Full Text] [Related]
14. Microsatellite polymorphism analysis allows the individual assignment of the rat 11 beta-hydroxylase gene (Cyp11b1) and the rat aldosterone synthase gene (Cyp11b2) to chromosome 7 using rat x mouse somatic cell hybrids and identifies differences between and within various rat strains. Inglis GC, Kenyon CJ, Szpirer C, Klinga-Levan K, Sutcliffe RG, Connell JM. J Mol Endocrinol; 1995 Jun 12; 14(3):303-11. PubMed ID: 7669222 [Abstract] [Full Text] [Related]
15. Interacting influence of potassium and polychlorinated biphenyl on cortisol and aldosterone biosynthesis. Li LA, Lin TC. Toxicol Appl Pharmacol; 2007 May 01; 220(3):252-61. PubMed ID: 17350062 [Abstract] [Full Text] [Related]
16. Coexpression of CYP11B2 or CYP11B1 with adrenodoxin and adrenodoxin reductase for assessing the potency and selectivity of aldosterone synthase inhibitors. LaSala D, Shibanaka Y, Jeng AY. Anal Biochem; 2009 Nov 01; 394(1):56-61. PubMed ID: 19622340 [Abstract] [Full Text] [Related]
17. High-resolution mapping of the blood pressure QTL on chromosome 7 using Dahl rat congenic strains. Cicila GT, Garrett MR, Lee SJ, Liu J, Dene H, Rapp JP. Genomics; 2001 Feb 15; 72(1):51-60. PubMed ID: 11247666 [Abstract] [Full Text] [Related]
18. Disorders of the aldosterone synthase and steroid 11beta-hydroxylase deficiencies. Peter M, Dubuis JM, Sippell WG. Horm Res; 1999 Feb 15; 51(5):211-22. PubMed ID: 10559665 [Abstract] [Full Text] [Related]
19. Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency. Peter M. Semin Reprod Med; 2002 Aug 15; 20(3):249-54. PubMed ID: 12428205 [Abstract] [Full Text] [Related]
20. Regulation of human CYP11B1 and CYP11B2 promoters by transposable elements and conserved cis elements. Cheng LC, Pai TW, Li LA. Steroids; 2012 Jan 15; 77(1-2):100-9. PubMed ID: 22079243 [Abstract] [Full Text] [Related] Page: [Next] [New Search]