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Similar articles for PubMed (Select 10559665)

1.

Disorders of the aldosterone synthase and steroid 11beta-hydroxylase deficiencies.

Peter M, Dubuis JM, Sippell WG.

Horm Res. 1999;51(5):211-22. Review.

PMID:
10559665
2.

Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency.

Peter M.

Semin Reprod Med. 2002 Aug;20(3):249-54. Review.

PMID:
12428205
3.

Molecular biology of 11β-hydroxylase and 11β-hydroxysteroid dehydrogenase enzymes.

White PC, Pascoe L, Curnow KM, Tannin G, Rösler A.

J Steroid Biochem Mol Biol. 1992 Dec;43(8):827-35. doi: 10.1016/0960-0760(92)90309-7. Review.

PMID:
22217826
4.

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. Epub 2005 Jul 15.

PMID:
16024935
5.

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. Review.

PMID:
15134824
6.

Disorders of steroid 11 beta-hydroxylase isozymes.

White PC, Curnow KM, Pascoe L.

Endocr Rev. 1994 Aug;15(4):421-38. Review.

PMID:
7988480
7.

Steroid 11 beta-hydroxylase deficiency and related disorders.

White PC.

Endocrinol Metab Clin North Am. 2001 Mar;30(1):61-79, vi. Review.

PMID:
11344939
8.

Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family.

Ben Charfeddine I, Riepe FG, Kahloul N, Kulle AE, Adala L, Mamaï O, Amara A, Mili A, Amri F, Saad A, Holterhus PM, Gribaa M.

Gen Comp Endocrinol. 2012 Feb 1;175(3):514-8. doi: 10.1016/j.ygcen.2011.12.017. Epub 2011 Dec 22.

PMID:
22210247
9.

In vitro release of aldosterone and cortisol in human adrenal adenomas correlates to mRNA expression of steroidogenic enzymes for genes CYP11B2 and CYP17.

Enberg U, Farnebo LO, Wedell A, Gröndal S, Thorén M, Grimelius L, Kjellman M, Bäckdahl M, Hamberger B.

World J Surg. 2001 Jul;25(7):957-66.

PMID:
11572038
10.
11.

Hormonal hypertension in children: 11beta-hydroxylase deficiency and apparent mineralocorticoid excess.

Cerame BI, New MI.

J Pediatr Endocrinol Metab. 2000 Nov-Dec;13(9):1537-47. Review.

PMID:
11154148
13.

Genetic analysis of the cytochrome P-450c17alpha (CYP17) and aldosterone synthase (CYP11B2) in Japanese patients with 17alpha-hydroxylase deficiency.

Takeda Y, Yoneda T, Demura M, Furukawa K, Koshida H, Miyamori I, Mabuchi H.

Clin Endocrinol (Oxf). 2001 Jun;54(6):751-8.

PMID:
11422109
14.

Quantitative assessment of CYP11B1 and CYP11B2 expression in aldosterone-producing adenomas.

Fallo F, Pezzi V, Barzon L, Mulatero P, Veglio F, Sonino N, Mathis JM.

Eur J Endocrinol. 2002 Dec;147(6):795-802.

15.

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.

16.

Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia.

Nimkarn S, New MI.

Trends Endocrinol Metab. 2008 Apr;19(3):96-9. doi: 10.1016/j.tem.2008.01.002. Epub 2008 Feb 21. Review.

PMID:
18294861
17.

Unequal crossing-over between aldosterone synthase and 11beta-hydroxylase genes causes congenital adrenal hyperplasia.

Hampf M, Dao NT, Hoan NT, Bernhardt R.

J Clin Endocrinol Metab. 2001 Sep;86(9):4445-52.

PMID:
11549691
18.

Congenital hypoaldosteronism: the Visser-Cost syndrome revisited.

Peter M, Sippell WG.

Pediatr Res. 1996 Mar;39(3):554-60.

PMID:
8929880
19.

Differential regulation of aldosterone synthase and 11beta-hydroxylase transcription by steroidogenic factor-1.

Bassett MH, Zhang Y, Clyne C, White PC, Rainey WE.

J Mol Endocrinol. 2002 Apr;28(2):125-35.

20.

Progress in molecular-genetic studies on congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.

Zhao LQ, Han S, Tian HM.

World J Pediatr. 2008 May;4(2):85-90. doi: 10.1007/s12519-008-0016-8. Review.

PMID:
18661760
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