BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 2882404)

  • 21. Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.
    O'Neill GJ; Dupont B; Pollack MS; Levine LS; New MI
    Clin Immunol Immunopathol; 1982 May; 23(2):312-22. PubMed ID: 6980755
    [No Abstract]   [Full Text] [Related]  

  • 22. Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.
    Speiser PW; New MI; White PC
    N Engl J Med; 1988 Jul; 319(1):19-23. PubMed ID: 3260007
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Steroid 21-hydroxylase deficiency and the major histocompatibility complex.
    White PC; Werkmeister J; New MI; Dupont B
    Hum Immunol; 1986 Apr; 15(4):404-15. PubMed ID: 3009365
    [TBL] [Abstract][Full Text] [Related]  

  • 24. DNA and RNA analysis of cytochrome P-450 21-hydroxylase: transcriptional activity in congenital adrenal hyperplasia.
    al-Othman AN; Docherty K; Makgoba MW; Sheppard MC; London DR
    J Mol Endocrinol; 1988 Nov; 1(3):157-64. PubMed ID: 2475127
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.
    White PC; Grossberger D; Onufer BJ; Chaplin DD; New MI; Dupont B; Strominger JL
    Proc Natl Acad Sci U S A; 1985 Feb; 82(4):1089-93. PubMed ID: 2983330
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Localization of the pathologic gene for 21-hydroxylase enzyme deficiency within the HLA system].
    Brkljacić-Surkalović L; Dumić M; Mardesić D; Plavsić V; Kastelan A
    Lijec Vjesn; 1988; 110(9-10):306-11. PubMed ID: 3264873
    [No Abstract]   [Full Text] [Related]  

  • 27. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.
    White PC; New MI; Dupont B
    Proc Natl Acad Sci U S A; 1984 Dec; 81(23):7505-9. PubMed ID: 6334310
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital adrenal hyperplasia: molecular mechanisms resulting in 21-hydroxylase deficiency.
    Donohoue PA; Van Dop C; Jospe N; Migeon CJ
    Acta Endocrinol Suppl (Copenh); 1986; 279():315-20. PubMed ID: 3022524
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.
    Rumsby G; Fielder AH; Hague WM; Honour JW
    J Med Genet; 1988 Sep; 25(9):596-9. PubMed ID: 3263505
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Heterogeneity of steroid 21-hydroxylase genes in classical congenital adrenal hyperplasia.
    Dawkins RL; Martin E; Kay PH; Garlepp MJ; Wilton AN; Stuckey MS
    J Immunogenet; 1987; 14(2-3):89-98. PubMed ID: 2891769
    [TBL] [Abstract][Full Text] [Related]  

  • 31. HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.
    Pollack MS; Levine LS; O'Neill GJ; Pang S; Lorenzen F; Kohn B; Rondanini GF; Chiumello G; New MI; Dupont B
    Am J Hum Genet; 1981 Jul; 33(4):540-50. PubMed ID: 6789674
    [TBL] [Abstract][Full Text] [Related]  

  • 32. RFLPs of 21-hydroxylase and C4 genes: application to pedigree analysis on 21-hydroxylase deficiency.
    Matsumoto T; Kondoh T; Baba T; Yoshimoto M; Niikawa N; Tsuji Y
    Acta Paediatr Jpn; 1988; 30 Suppl():111-6. PubMed ID: 2906201
    [No Abstract]   [Full Text] [Related]  

  • 33. [Steroid 21-hydroxylase deficiency--congenital adrenal hyperplasia].
    Urabe K; Harada F; Sasazuki T
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):903-8. PubMed ID: 3270907
    [No Abstract]   [Full Text] [Related]  

  • 34. [HLA haplotypes in congenital adrenal hyperplasia (21-hydroxylase deficiency].
    González-Díaz JP; González T; González-Espinosa C; Gantes M; Santisteban M; Bustad S
    An Esp Pediatr; 1984 Oct; 21(6):583-6. PubMed ID: 6335362
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The biochemical basis for genotyping 21-hydroxylase deficiency.
    New MI; Dupont B; Pollack MS; Levine LS
    Hum Genet; 1981; 58(1):123-7. PubMed ID: 6269988
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Different gene defects in the salt-wasting (SW), simple virilizing (SV), and nonclassical (NC) types of congenital adrenal hyperplasia (CAH).
    Knorr D; Albert ED; Bidlingmaier F; Höller W; Scholz S
    Ann N Y Acad Sci; 1985; 458():71-5. PubMed ID: 3879133
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S; Pollack MS; Loo M; Green O; Nussbaum R; Clayton G; Dupont B; New MI
    J Clin Endocrinol Metab; 1985 Jul; 61(1):89-97. PubMed ID: 3873469
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Molecular genetics of 21-hydroxylase deficiency in congenital adrenal hyperplasia].
    Lobaccaro JM; Ghanem N; Lefranc G; Sultan C
    C R Seances Soc Biol Fil; 1990; 184(1):75-86. PubMed ID: 1964845
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The immunological detection of a 21-OH deficiency mutation HLA supratype.
    Pollack MS; Keenan B; Christiansen FT; Cobain TJ; Dawkins RL; Clayton G
    Am J Hum Genet; 1986 May; 38(5):688-98. PubMed ID: 3013005
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A rare TaqI polymorphism in a human complement C4 gene is caused by an additional restriction site in the first intron.
    Koppens PF; Hoogenboezem T; Degenhart HJ
    Immunol Lett; 1992; 34(2):93-7. PubMed ID: 1362564
    [TBL] [Abstract][Full Text] [Related]  

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