These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 1594605)

  • 1. Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency.
    Pascoe L; Curnow KM; Slutsker L; Rösler A; White PC
    Proc Natl Acad Sci U S A; 1992 Jun; 89(11):4996-5000. PubMed ID: 1594605
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in human 11 beta-hydroxylase genes: 11 beta-hydroxylase deficiency in Jews of Morocco and corticosterone methyl-oxidase II deficiency in Jews of Iran.
    Rösler A; White PC
    J Steroid Biochem Mol Biol; 1993 Apr; 45(1-3):99-106. PubMed ID: 8481357
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gene conversion in the CYP11B2 gene encoding P450c11AS is associated with, but does not cause, the syndrome of corticosterone methyloxidase II deficiency.
    Fardella CE; Hum DW; Rodriguez H; Zhang G; Barry FL; Ilicki A; Bloch CA; Miller WL
    J Clin Endocrinol Metab; 1996 Jan; 81(1):321-6. PubMed ID: 8550772
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Amino acid substitution R384P in aldosterone synthase causes corticosterone methyloxidase type I deficiency.
    Geley S; Jöhrer K; Peter M; Denner K; Bernhardt R; Sippell WG; Kofler R
    J Clin Endocrinol Metab; 1995 Feb; 80(2):424-9. PubMed ID: 7852500
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylase.
    Globerman H; Rösler A; Theodor R; New MI; White PC
    N Engl J Med; 1988 Nov; 319(18):1193-7. PubMed ID: 3262827
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenitally defective aldosterone biosynthesis in humans: the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients.
    Mitsuuchi Y; Kawamoto T; Naiki Y; Miyahara K; Toda K; Kuribayashi I; Orii T; Yasuda K; Miura K; Nakao K
    Biochem Biophys Res Commun; 1992 Jan; 182(2):974-9. PubMed ID: 1346492
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation T318M in the CYP11B2 gene encoding P450c11AS (aldosterone synthase) causes corticosterone methyl oxidase II deficiency.
    Zhang G; Rodriguez H; Fardella CE; Harris DA; Miller WL
    Am J Hum Genet; 1995 Nov; 57(5):1037-43. PubMed ID: 7485152
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Isolated aldosterone synthase deficiency caused by simultaneous E198D and V386A mutations in the CYP11B2 gene.
    Portrat-Doyen S; Tourniaire J; Richard O; Mulatero P; Aupetit-Faisant B; Curnow KM; Pascoe L; Morel Y
    J Clin Endocrinol Metab; 1998 Nov; 83(11):4156-61. PubMed ID: 9814506
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene.
    Wasniewska M; De Luca F; Valenzise M; Lombardo F; De Luca F
    Eur J Endocrinol; 2001 Jan; 144(1):59-62. PubMed ID: 11174838
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inborn errors of aldosterone biosynthesis in humans.
    Shizuta Y; Kawamoto T; Mitsuuchi Y; Miyahara K; Rösler A; Ulick S; Imura H
    Steroids; 1995 Jan; 60(1):15-21. PubMed ID: 7792802
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CMO I deficiency caused by a point mutation in exon 8 of the human CYP11B2 gene encoding steroid 18-hydroxylase (P450C18).
    Nomoto S; Massa G; Mitani F; Ishimura Y; Miyahara K; Toda K; Nagano I; Yamashiro T; Ogoshi S; Fukata J; Onishi S; Hashimoto K; Doi Y; Imura H; Shizuta Y
    Biochem Biophys Res Commun; 1997 May; 234(2):382-5. PubMed ID: 9177280
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients.
    Mitsuuchi Y; Kawamoto T; Miyahara K; Ulick S; Morton DH; Naiki Y; Kuribayashi I; Toda K; Hara T; Orii T
    Biochem Biophys Res Commun; 1993 Feb; 190(3):864-9. PubMed ID: 8439335
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Congenital hypoaldosteronism: the Visser-Cost syndrome revisited.
    Peter M; Sippell WG
    Pediatr Res; 1996 Mar; 39(3):554-60. PubMed ID: 8929880
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multisteroid analysis in children with terminal aldosterone biosynthesis defects.
    Peter M; Partsch CJ; Sippell WG
    J Clin Endocrinol Metab; 1995 May; 80(5):1622-7. PubMed ID: 7745009
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dietary potassium supplementation and sodium restriction stimulate aldosterone synthase but not 11 beta-hydroxylase P-450 messenger ribonucleic acid accumulation in rat adrenals and require angiotensin II production.
    Tremblay A; Parker KL; Lehoux JG
    Endocrinology; 1992 Jun; 130(6):3152-8. PubMed ID: 1597135
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Homozygous deletion of arginine-173 in the CYP11B2 gene in a girl with congenital hypoaldosteronism. Corticosterone methyloxidase deficiency type II.
    Peter M; Nikischin W; Heinz-Erian P; Fussenegger W; Kapelari K; Sippell WG
    Horm Res; 1998; 50(4):222-5. PubMed ID: 9838244
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The impact of the clinical CYP11B2 mutation V386A strongly depends on the enzyme's genetic background.
    Neunzig J; Khatri Y; Bernhardt R
    Endocr J; 2017 Apr; 64(4):457-461. PubMed ID: 28190867
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.