155 related articles for article (PubMed ID: 17121536)
21. Molecular analysis of 12 Chinese patients with 11β-hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants.
Sun B; Lu L; Xie S; Zhang W; Zhang X; Tong A; Chen S; Wu X; Mao J; Wang X; Qiu L; Nie M
FASEB J; 2023 Apr; 37(4):e22869. PubMed ID: 36929050
[TBL] [Abstract][Full Text] [Related]
22. 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; 52(6):523-8. PubMed ID: 7779756
[TBL] [Abstract][Full Text] [Related]
23. Is altered adrenal steroid biosynthesis a key intermediate phenotype in hypertension?
Connell JM; Fraser R; MacKenzie S; Davies E
Hypertension; 2003 May; 41(5):993-9. PubMed ID: 12654713
[TBL] [Abstract][Full Text] [Related]
24. Analyzing the functional and structural consequences of two point mutations (P94L and A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia resulting from 11-hydroxylase deficiency.
Krone N; Grischuk Y; Müller M; Volk RE; Grötzinger J; Holterhus PM; Sippell WG; Riepe FG
J Clin Endocrinol Metab; 2006 Jul; 91(7):2682-8. PubMed ID: 16670167
[TBL] [Abstract][Full Text] [Related]
25. 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; 63(6):284-93. PubMed ID: 16024935
[TBL] [Abstract][Full Text] [Related]
26. Mutations in CYP11B1 gene converting 11beta-hydroxylase into an aldosterone-producing enzyme are not present in aldosterone-producing adenomas.
Pilon C; Mulatero P; Barzon L; Veglio F; Garrone C; Boscaro M; Sonino N; Fallo F
J Clin Endocrinol Metab; 1999 Nov; 84(11):4228-31. PubMed ID: 10566677
[TBL] [Abstract][Full Text] [Related]
27. Biotransformation of the mineralocorticoid receptor antagonists spironolactone and canrenone by human CYP11B1 and CYP11B2: Characterization of the products and their influence on mineralocorticoid receptor transactivation.
Schiffer L; Müller AR; Hobler A; Brixius-Anderko S; Zapp J; Hannemann F; Bernhardt R
J Steroid Biochem Mol Biol; 2016 Oct; 163():68-76. PubMed ID: 27125452
[TBL] [Abstract][Full Text] [Related]
28. A de novo unequal cross-over mutation between CYP11B1 and CYP11B2 genes causes familial hyperaldosteronism type I.
Carvajal CA; Stehr CB; González PA; Riquelme EM; Montero T; Santos MJ; Kalergis AM; Fardella CE
J Endocrinol Invest; 2011 Feb; 34(2):140-4. PubMed ID: 20634641
[TBL] [Abstract][Full Text] [Related]
29. Novel missense mutations, GCC [Ala306]- > GTC [Val] and ACG [Thr318]- > CCG [Pro], in the CYP11B1 gene cause steroid 11beta-hydroxylase deficiency in the Chinese.
Lee HH; Won GS; Chao HT; Lee YJ; Chung BC
Clin Endocrinol (Oxf); 2005 Apr; 62(4):418-22. PubMed ID: 15807871
[TBL] [Abstract][Full Text] [Related]
30. Effects of 18-hydroxylated steroids on corticosteroid production by human aldosterone synthase and 11beta-hydroxylase.
Fisher A; Friel EC; Bernhardt R; Gomez-Sanchez C; Connell JM; Fraser R; Davies E
J Clin Endocrinol Metab; 2001 Sep; 86(9):4326-9. PubMed ID: 11549669
[TBL] [Abstract][Full Text] [Related]
31. Histopathological and genetic characterization of aldosterone-producing adenomas with concurrent subclinical cortisol hypersecretion: a case series.
Fallo F; Castellano I; Gomez-Sanchez CE; Rhayem Y; Pilon C; Vicennati V; Santini D; Maffeis V; Fassina A; Mulatero P; Beuschlein F; Reincke M
Endocrine; 2017 Dec; 58(3):503-512. PubMed ID: 28405879
[TBL] [Abstract][Full Text] [Related]
32. 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; 25():S42-6. PubMed ID: 9809191
[TBL] [Abstract][Full Text] [Related]
33. Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency.
Peter M
Semin Reprod Med; 2002 Aug; 20(3):249-54. PubMed ID: 12428205
[TBL] [Abstract][Full Text] [Related]
34. Amino acid residue 147 of human aldosterone synthase and 11beta-hydroxylase plays a key role in 11beta-hydroxylation.
Fisher A; Fraser R; Mc Connell J; Davies E
J Clin Endocrinol Metab; 2000 Mar; 85(3):1261-6. PubMed ID: 10720073
[TBL] [Abstract][Full Text] [Related]
35. Congenital adrenal hyperplasia caused by compound heterozygosity of two novel CYP11B1 gene variants.
Fylaktou I; Smyrnaki P; Sertedaki A; Dracopoulou M; Kanaka-Gantenbein C
Hormones (Athens); 2022 Mar; 21(1):155-161. PubMed ID: 34697763
[TBL] [Abstract][Full Text] [Related]
36. 11 beta-Hydroxylase activity in glucocorticoid suppressible hyperaldosteronism: lessons for essential hypertension?
Connell JM; Jamieson AJ; Davies E; Ingram M; Soro A; Fraser R
Endocr Res; 1996 Nov; 22(4):691-700. PubMed ID: 8969929
[TBL] [Abstract][Full Text] [Related]
37. Unequal crossing over between CYP11B2 and CYP11B1 causes 11 β -hydroxylase deficiency in a consanguineous family.
Xiong Y; Zeng Z; Liang T; Yang P; Lu Q; Yang J; Zhang J; Fang W; Luo P; Hu Y; Zhang M; Zhou D
J Steroid Biochem Mol Biol; 2023 Oct; 233():106375. PubMed ID: 37572761
[TBL] [Abstract][Full Text] [Related]
38. Efficient conversion of 11-deoxycortisol to cortisol (hydrocortisone) by recombinant fission yeast Schizosaccharomyces pombe.
Drăgan CA; Zearo S; Hannemann F; Bernhardt R; Bureik M
FEMS Yeast Res; 2005 Apr; 5(6-7):621-5. PubMed ID: 15780661
[TBL] [Abstract][Full Text] [Related]
39. The combination of a novel 2 bp deletion mutation and p.D63H in CYP11B1 cause congenital adrenal hyperplasia due to steroid 11β-hydroxylase deficiency.
Long Y; Han S; Zhang X; Zhang X; Chen T; Gao Y; Tian H
Endocr J; 2016; 63(3):301-10. PubMed ID: 26806323
[TBL] [Abstract][Full Text] [Related]
40. Genetic study of patients with dexamethasone-suppressible aldosteronism without the chimeric CYP11B1/CYP11B2 gene.
Fardella CE; Pinto M; Mosso L; Gómez-Sánchez C; Jalil J; Montero J
J Clin Endocrinol Metab; 2001 Oct; 86(10):4805-7. PubMed ID: 11600544
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]