BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

328 related articles for article (PubMed ID: 9814482)

  • 1. Recombinant CYP11B genes encode enzymes that can catalyze conversion of 11-deoxycortisol to cortisol, 18-hydroxycortisol, and 18-oxocortisol.
    Mulatero P; Curnow KM; Aupetit-Faisant B; Foekling M; Gomez-Sanchez C; Veglio F; Jeunemaitre X; Corvol P; Pascoe L
    J Clin Endocrinol Metab; 1998 Nov; 83(11):3996-4001. PubMed ID: 9814482
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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
    Proc Natl Acad Sci U S A; 1992 Sep; 89(17):8327-31. PubMed ID: 1518866
    [TBL] [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; 214(1-2):167-74. PubMed ID: 15062555
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 86(7):3197-201. PubMed ID: 11443188
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Functional effects of genetic variants in the 11beta-hydroxylase (CYP11B1) gene.
    Barr M; MacKenzie SM; Wilkinson DM; Holloway CD; Friel EC; Miller S; MacDonald T; Fraser R; Connell JM; Davies E
    Clin Endocrinol (Oxf); 2006 Dec; 65(6):816-25. PubMed ID: 17121536
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new presentation of the chimeric CYP11B1/CYP11B2 gene with low prevalence of primary aldosteronism and atypical gene segregation pattern.
    Carvajal CA; Campino C; Martinez-Aguayo A; Tichauer JE; Bancalari R; Valdivia C; Trejo P; Aglony M; Baudrand R; Lagos CF; Mellado C; Garcia H; Fardella CE
    Hypertension; 2012 Jan; 59(1):85-91. PubMed ID: 22083159
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Disorders of steroid 11 beta-hydroxylase isozymes.
    White PC; Curnow KM; Pascoe L
    Endocr Rev; 1994 Aug; 15(4):421-38. PubMed ID: 7988480
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 18(1):47-51. PubMed ID: 14688810
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Disorders of the aldosterone synthase and steroid 11beta-hydroxylase deficiencies.
    Peter M; Dubuis JM; Sippell WG
    Horm Res; 1999; 51(5):211-22. PubMed ID: 10559665
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Primary hyperaldosteronism in essential hypertensives: prevalence, biochemical profile, and molecular biology.
    Fardella CE; Mosso L; Gómez-Sánchez C; Cortés P; Soto J; Gómez L; Pinto M; Huete A; Oestreicher E; Foradori A; Montero J
    J Clin Endocrinol Metab; 2000 May; 85(5):1863-7. PubMed ID: 10843166
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Diagnosis of glucocorticoid-remediable aldosteronism in hypertensive children.
    Kamrath C; Maser-Gluth C; Haag C; Schulze E
    Horm Res Paediatr; 2011; 76(2):93-8. PubMed ID: 21625068
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Effect of variation in CYP11B1 and CYP11B2 on corticosteroid phenotype and hypothalamic-pituitary-adrenal axis activity in hypertensive and normotensive subjects.
    Freel EM; Ingram M; Wallace AM; White A; Fraser R; Davies E; Connell JM
    Clin Endocrinol (Oxf); 2008 May; 68(5):700-6. PubMed ID: 17980006
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 67(6):832-8. PubMed ID: 17651452
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic analyses of the chimeric CYP11B1/CYP11B2 gene in a Korean family with glucocorticoid-remediable aldosteronism.
    Lee IS; Kim SY; Jang HW; Kim MK; Lee JH; Lee YH; Jo YS
    J Korean Med Sci; 2010 Sep; 25(9):1379-83. PubMed ID: 20808686
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 217(1-2):243-7. PubMed ID: 15134824
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.
    Keavney B; Mayosi B; Gaukrodger N; Imrie H; Baker M; Fraser R; Ingram M; Watkins H; Farrall M; Davies E; Connell J
    J Clin Endocrinol Metab; 2005 Feb; 90(2):1072-7. PubMed ID: 15522937
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.