BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 2592361)

  • 21. Study of cholesterol side-chain cleavage (20,22 desmolase) deficiency causing congenital lipoid adrenal hyperplasia using bovine-sequence P450scc oligodeoxyribonucleotide probes.
    Matteson KJ; Chung BC; Urdea MS; Miller WL
    Endocrinology; 1986 Apr; 118(4):1296-305. PubMed ID: 2419119
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin.
    White PC; Dupont J; New MI; Leiberman E; Hochberg Z; Rösler A
    J Clin Invest; 1991 May; 87(5):1664-7. PubMed ID: 2022736
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Characterization of the CYP2C5 gene in 21L III/J rabbits. Allelic variation affects the expression of P450IIC5.
    Pendurthi UR; Lamb JG; Nguyen N; Johnson EF; Tukey RH
    J Biol Chem; 1990 Aug; 265(24):14662-8. PubMed ID: 2387874
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Cloning and expression of a rat cytochrome P-450 11 beta-hydroxylase/aldosterone synthase (CYP11B2) cDNA variant.
    Zhou M; Gomez-Sanchez CE
    Biochem Biophys Res Commun; 1993 Jul; 194(1):112-7. PubMed ID: 8333830
    [TBL] [Abstract][Full Text] [Related]  

  • 27. CYP11B1 mutations causing non-classic adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
    Joehrer K; Geley S; Strasser-Wozak EM; Azziz R; Wollmann HA; Schmitt K; Kofler R; White PC
    Hum Mol Genet; 1997 Oct; 6(11):1829-34. PubMed ID: 9302260
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Regulation of cholesterol 7 alpha-hydroxylase in the liver. Cloning, sequencing, and regulation of cholesterol 7 alpha-hydroxylase mRNA.
    Li YC; Wang DP; Chiang JY
    J Biol Chem; 1990 Jul; 265(20):12012-9. PubMed ID: 1694852
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A gene structure of testosterone 6 beta-hydroxylase (P450IIIA).
    Miyata M; Nagata K; Yamazoe Y; Kato R
    Biochem Biophys Res Commun; 1991 May; 177(1):68-73. PubMed ID: 2043144
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Role of steroid 11 beta-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans.
    Kawamoto T; Mitsuuchi Y; Toda K; Yokoyama Y; Miyahara K; Miura S; Ohnishi T; Ichikawa Y; Nakao K; Imura H
    Proc Natl Acad Sci U S A; 1992 Feb; 89(4):1458-62. PubMed ID: 1741400
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Isolation and characterization of the human UGT2B15 gene, localized within a cluster of UGT2B genes and pseudogenes on chromosome 4.
    Turgeon D; Carrier JS; Lévesque E; Beatty BG; Bélanger A; Hum DW
    J Mol Biol; 2000 Jan; 295(3):489-504. PubMed ID: 10623541
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. The hybrid rat cytochrome P450 containing the first 5 exons of the CYP11B1 and last 4 exons from the CYP11B2 enzyme retains 11 beta-hydroxylase activity, but the alternative hybrid is inactive.
    Zhou MY; Gomez-Sanchez CE; Xue D; Foecking MF
    Biochem Biophys Res Commun; 1994 Feb; 199(1):130-5. PubMed ID: 8123004
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cloning and expression of the rat adrenal cytochrome P-450 11B3 (CYP11B3) enzyme cDNA: preferential 18-hydroxylation over 11 beta-hydroxylation of DOC.
    Zhou MY; Gomez-Sanchez EP; Foecking MF; Gomez-Sanchez CE
    Mol Cell Endocrinol; 1995 Oct; 114(1-2):137-45. PubMed ID: 8674838
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia.
    Rodrigues NR; Dunham I; Yu CY; Carroll MC; Porter RR; Campbell RD
    EMBO J; 1987 Jun; 6(6):1653-61. PubMed ID: 3038528
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Classic steroid 11 beta-hydroxylase deficiency caused by a C-->G transversion in exon 7 of CYP11B1.
    Yang LX; Toda K; Miyahara K; Nomoto S; Kinoshita E; Baba T; Yoshimoto M; Araki K; Kurashige T; Hashimoto K
    Biochem Biophys Res Commun; 1995 Nov; 216(2):723-8. PubMed ID: 7488170
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Missense mutation in CYP11B1 (CGA[Arg-384]-->GGA[Gly]) causes steroid 11 beta-hydroxylase deficiency.
    Nakagawa Y; Yamada M; Ogawa H; Igarashi Y
    Eur J Endocrinol; 1995 Mar; 132(3):286-9. PubMed ID: 7889175
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Structure of an ovine CYP11B1 gene.
    Anwar A; Coghlan JP; Jeyaseelan K
    DNA Seq; 1998; 8(6):357-74. PubMed ID: 10728821
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular genetics of congenital adrenal hyperplasia.
    White PC; New MI
    Baillieres Clin Endocrinol Metab; 1988 Nov; 2(4):941-65. PubMed ID: 3077248
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.