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29 related items for PubMed ID: 10089275

  • 1. Analysis of Four Common Salt-Wasting Mutations in CYP21 (Steroid 21-Hydroxylase) by Cleavase Fragment Length Polymorphism Analysis and Characterization of a Frequent Polymorphism in Intron 6.
    Wei WL, Killeen AA.
    Mol Diagn; 1998 Sep; 3(3):171-177. PubMed ID: 10089275
    [Abstract] [Full Text] [Related]

  • 2. Characterization of frequent polymorphisms in intron 2 of CYP21: application to analysis of segregation of CYP21 alleles.
    Killeen AA, Jiddou RR, Sane KS.
    Clin Chem; 1998 Dec; 44(12):2410-5. PubMed ID: 9836705
    [Abstract] [Full Text] [Related]

  • 3. Comparative Evaluation of Cleavase Fragment Length Polymorphism With PCR-SSCP and PCR-RFLP to Detect Antimicrobial Agent Resistance in Mycobacterium tuberculosis.
    Sreevatsan S, Bookout JB, Ringpis FM, Mogazeh SL, Kreiswirth BN, Pottathil RR, Barathur RR.
    Mol Diagn; 1998 Jun; 3(2):81-91. PubMed ID: 10029659
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Single-nucleotide polymorphisms in intron 2 of CYP21P: evidence for a higher rate of mutation at CpG dinucleotides in the functional steroid 21-hydroxylase gene and application to segregation analysis in congenital adrenal hyperplasia.
    Jiddou RR, Wei WL, Sane KS, Killeen AA.
    Clin Chem; 1999 May; 45(5):625-9. PubMed ID: 10222348
    [Abstract] [Full Text] [Related]

  • 6. Detection of p53 gene mutations: analysis by single-strand conformation polymorphism and Cleavase fragment length polymorphism.
    O'Connell CD, Atha DH, Oldenburg MC, Tian J, Siebert M, Handrow R, Grooms K, Heisler L, de Arruda M.
    Electrophoresis; 1999 Jun; 20(6):1211-23. PubMed ID: 10380761
    [Abstract] [Full Text] [Related]

  • 7. Genetic diagnosis of 21-hydroxylase deficiency: DGGE-based mutation scanning of CYP21.
    Ohlsson G, Müller J, Schwartz M.
    Hum Mutat; 1999 Jun; 13(5):385-9. PubMed ID: 10338093
    [Abstract] [Full Text] [Related]

  • 8. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 9. Frequency of CYP21 gene mutations in Czech patients with steroid 21-hydroxylase deficiency and statistical comparison with other populations.
    Kotaska K, Průsa R.
    Med Princ Pract; 2003 Aug; 12(4):243-7. PubMed ID: 12966197
    [Abstract] [Full Text] [Related]

  • 10. Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 gene.
    Bobba A, Iolascon A, Giannattasio S, Albrizio M, Sinisi A, Prisco F, Schettini F, Marra E.
    J Med Genet; 1997 Mar; 34(3):223-8. PubMed ID: 9132494
    [Abstract] [Full Text] [Related]

  • 11. The Importance of Heteroduplexes in Interpreting the Results of PCR-RED Diagnostic Assays: Application to the Analysis of Mutations in the Steroid 21-Hydroxylase Gene in a Case of Congenital Adrenal Hyperplasia.
    Bradley JF, Baker D, Schwartz ID, Rothberg PG.
    Mol Diagn; 1998 Jun; 3(2):119-123. PubMed ID: 10029663
    [Abstract] [Full Text] [Related]

  • 12. Detection of germline BRCA1 mutations by Multiple-Dye Cleavase Fragment Length Polymorphism (MD-CFLP) method.
    Casadei S, Cortesi L, Pensotti V, Radice P, Pierotti M, Amadori D, Calistri D.
    Br J Cancer; 2001 Sep 14; 85(6):845-9. PubMed ID: 11556835
    [Abstract] [Full Text] [Related]

  • 13. Characterization of a novel DNA polymorphism in the human CYP21 gene and application for DNA diagnosis of congenital adrenal hyperplasia.
    Lee YH, Park ES, Kang SH, Kim H, Lee JY, Lee JS.
    Clin Endocrinol (Oxf); 2000 Oct 14; 53(4):419-22. PubMed ID: 11012565
    [Abstract] [Full Text] [Related]

  • 14. New Cleavase Fragment Length Polymorphism method improves the mutation detection assay.
    Oldenburg MC, Siebert M.
    Biotechniques; 2000 Feb 14; 28(2):351-7. PubMed ID: 10683747
    [Abstract] [Full Text] [Related]

  • 15. Vertical transmission of Chlamydia trachomatis in Chongqing China.
    Yu J, Wu S, Li F, Hu L.
    Curr Microbiol; 2009 Apr 14; 58(4):315-20. PubMed ID: 19123031
    [Abstract] [Full Text] [Related]

  • 16. An overview of molecular diagnosis of steroid 21-hydroxylase deficiency.
    Keegan CE, Killeen AA.
    J Mol Diagn; 2001 May 14; 3(2):49-54. PubMed ID: 11393164
    [No Abstract] [Full Text] [Related]

  • 17. Analysis of CYP21 coding polymorphisms in three ethnic populations: further evidence of nonamplifying CYP21 alleles among whites.
    Ozturk IC, Wei WL, Palaniappan L, Rubenfire M, Killeen AA.
    Mol Diagn; 2000 Mar 14; 5(1):47-52. PubMed ID: 10837089
    [Abstract] [Full Text] [Related]

  • 18. Analysis of Four Common Salt-Wasting Mutations in CYP21 (Steroid 21-Hydroxylase) by Cleavase Fragment Length Polymorphism Analysis and Characterization of a Frequent Polymorphism in Intron 6.
    Wei WL, Killeen AA.
    Mol Diagn; 1998 Sep 14; 3(3):171-177. PubMed ID: 10089275
    [Abstract] [Full Text] [Related]

  • 19. Characterization of frequent polymorphisms in intron 2 of CYP21: application to analysis of segregation of CYP21 alleles.
    Killeen AA, Jiddou RR, Sane KS.
    Clin Chem; 1998 Dec 14; 44(12):2410-5. PubMed ID: 9836705
    [Abstract] [Full Text] [Related]

  • 20. Comparative Evaluation of Cleavase Fragment Length Polymorphism With PCR-SSCP and PCR-RFLP to Detect Antimicrobial Agent Resistance in Mycobacterium tuberculosis.
    Sreevatsan S, Bookout JB, Ringpis FM, Mogazeh SL, Kreiswirth BN, Pottathil RR, Barathur RR.
    Mol Diagn; 1998 Jun 14; 3(2):81-91. PubMed ID: 10029659
    [Abstract] [Full Text] [Related]

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