BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

211 related articles for article (PubMed ID: 2325662)

  • 1. Direct analysis of CYP21B genes in 21-hydroxylase deficiency using polymerase chain reaction amplification.
    Owerbach D; Crawford YM; Draznin MB
    Mol Endocrinol; 1990 Jan; 4(1):125-31. PubMed ID: 2325662
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency.
    Mornet E; Crété P; Kuttenn F; Raux-Demay MC; Boué J; White PC; Boué A
    Am J Hum Genet; 1991 Jan; 48(1):79-88. PubMed ID: 1985465
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B.
    Donohoue PA; Jospe N; Migeon CJ; Van Dop C
    Genomics; 1989 Oct; 5(3):397-406. PubMed ID: 2613228
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.
    Amor M; Parker KL; Globerman H; New MI; White PC
    Proc Natl Acad Sci U S A; 1988 Mar; 85(5):1600-4. PubMed ID: 3257825
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of mutations causing steroid 21-hydroxylase deficiency.
    White PC
    Endocr Res; 1989; 15(1-2):239-56. PubMed ID: 2788080
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exon 7 Ncol restriction site within CYP21B (steroid 21-hydroxylase) is a normal polymorphism.
    Donohoue PA; Sandrini Neto R; Collins MM; Migeon CJ
    Mol Endocrinol; 1990 Sep; 4(9):1354-62. PubMed ID: 1978247
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nonsense mutation causing steroid 21-hydroxylase deficiency.
    Globerman H; Amor M; Parker KL; New MI; White PC
    J Clin Invest; 1988 Jul; 82(1):139-44. PubMed ID: 3267225
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular analysis of patient and carrier genes with congenital steroid 21-hydroxylase deficiency by using polymerase chain reaction and single strand conformation polymorphism.
    Tajima T; Fujieda K; Nakayama K; Fujii-Kuriyama Y
    J Clin Invest; 1993 Nov; 92(5):2182-90. PubMed ID: 8227333
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of molecular defects causing congenital adrenal hyperplasia by cloning and differential hybridization of polymerase chain reaction-amplified 21-hydroxylase (CYP21) genes.
    Helmberg A; Tabarelli M; Fuchs MA; Keller E; Dobler G; Schnegg I; Knorr D; Albert E; Kofler R
    DNA Cell Biol; 1992 Jun; 11(5):359-68. PubMed ID: 1605859
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pseudogene/functional gene ratio in late-onset 21-hydroxylase-deficient adrenal hyperplasia.
    Azziz R; Wells G; Acton RT; Zacur HA
    Am J Obstet Gynecol; 1990 Mar; 162(3):633-8. PubMed ID: 2316563
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mutations in 21-hydroxylase gene caused by gene conversion-like events].
    Urabe K
    Fukuoka Igaku Zasshi; 1990 Feb; 81(2):77-87. PubMed ID: 2328938
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CYP21B gene conversion and complete CYP21A gene deletion in congenital adrenal hyperplasia.
    Lobaccaro JM; Ghanem N; Lefranc G; Sultan C
    Ann Genet; 1990; 33(2):70-5. PubMed ID: 1978631
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Molecular analysis of the most frequent mutations associated with congenital adrenal hyperplasia secondary to 21-hydroxylase enzyme deficiency].
    Dardis A; Marino R; Bergadá I; Escobar ME; Gryngarten M; Rivarola MA; Belgorosky A
    Medicina (B Aires); 2001; 61(1):28-34. PubMed ID: 11265620
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia.
    Ghanem N; Lobaccaro JM; Buresi C; Abbal M; Halaby G; Sultan C; Lefranc G
    Hum Genet; 1990 Dec; 86(2):117-25. PubMed ID: 1979956
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.
    White PC; Vitek A; Dupont B; New MI
    Proc Natl Acad Sci U S A; 1988 Jun; 85(12):4436-40. PubMed ID: 3260033
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Salt-wasting congenital adrenal hyperplasia: detection and characterization of mutations in the steroid 21-hydroxylase gene, CYP21, using the polymerase chain reaction.
    Owerbach D; Ballard AL; Draznin MB
    J Clin Endocrinol Metab; 1992 Mar; 74(3):553-8. PubMed ID: 1740489
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A molecular method of diagnosis of congenital adrenal hyperplasia].
    Israel S; Brautbar C
    Harefuah; 2000 Dec; 139(11-12):429-33, 494. PubMed ID: 11341187
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of the recombination site within the steroid 21-hydroxylase gene (CYP21) of the HLA-B47,DR7 haplotype.
    Chu X; Braun-Heimer L; Rittner C; Schneider PM
    Exp Clin Immunogenet; 1992; 9(2):80-5. PubMed ID: 1489553
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Concordance of 21-hydroxylase gene ratio, human leukocyte antigen haplotyping and adrenal testing results in a family with late-onset adrenal hyperplasia.
    Wells G; Acton RT; Azziz R
    J Reprod Med; 1993 Aug; 38(8):615-20. PubMed ID: 8410868
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.