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678 related items for PubMed ID: 1281384

  • 1. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.
    Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW.
    Am J Hum Genet; 1992 Dec; 51(6):1229-39. PubMed ID: 1281384
    [Abstract] [Full Text] [Related]

  • 2. Methylation of HpaII site at the human DXS16 locus on Xp22 as an assay for abnormal patterns of X inactivation.
    Khalifa MM, Struthers JL, Maurice S, Harrison K, Duncan AM.
    Am J Med Genet; 2001 Jan 01; 98(1):64-9. PubMed ID: 11426457
    [Abstract] [Full Text] [Related]

  • 3. The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome.
    Hendriks RW, Hinds H, Chen ZY, Craig IW.
    Genomics; 1992 Nov 01; 14(3):598-603. PubMed ID: 1385307
    [Abstract] [Full Text] [Related]

  • 4. A PCR based X-chromosome inactivation assay for carrier detection in X-linked immunodeficiencies using differential methylation of the androgen receptor gene.
    Schmucker B, Meindl A, Achatz H, Mittermüller J, Krüger G, Hergersberg M, Spiegel R, Schinzel A, Belohradsky BH, Murken J.
    Immunodeficiency; 1995 Nov 01; 5(3):187-92. PubMed ID: 7749438
    [Abstract] [Full Text] [Related]

  • 5. Methylation patterns in human androgen receptor gene and clonality analysis.
    Jang SJ, Mao L.
    Cancer Res; 2000 Feb 15; 60(4):864-6. PubMed ID: 10706095
    [Abstract] [Full Text] [Related]

  • 6. An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene.
    Hendriks RW, Chen ZY, Hinds H, Schuurman RK, Craig IW.
    Hum Mol Genet; 1992 Jun 15; 1(3):187-94. PubMed ID: 1303176
    [Abstract] [Full Text] [Related]

  • 7. Clonal analysis of hematopoietic cells using a novel polymorphic site of the X chromosome.
    Okamoto T, Okada M, Wada H, Kanamaru A, Kakishita E, Hashimoto T, Furuyama J.
    Am J Hematol; 1998 Aug 15; 58(4):263-6. PubMed ID: 9692387
    [Abstract] [Full Text] [Related]

  • 8. The role of the CAG repeat polymorphism in the androgen receptor gene and of skewed X-chromosome inactivation, in the pathogenesis of hirsutism.
    Calvo RM, Asunción M, Sancho J, San Millán JL, Escobar-Morreale HF.
    J Clin Endocrinol Metab; 2000 Apr 15; 85(4):1735-40. PubMed ID: 10770223
    [Abstract] [Full Text] [Related]

  • 9. Clonal X-inactivation analysis of human tumours using the human androgen receptor gene (HUMARA) polymorphism: a non-radioactive and semiquantitative strategy applicable to fresh and archival tissue.
    Kopp P, Jaggi R, Tobler A, Borisch B, Oestreicher M, Sabacan L, Jameson JL, Fey MF.
    Mol Cell Probes; 1997 Jun 15; 11(3):217-28. PubMed ID: 9232621
    [Abstract] [Full Text] [Related]

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  • 11. Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27 beta): correlation with X-inactivation status.
    Boyd Y, Fraser NJ.
    Genomics; 1990 Jun 15; 7(2):182-7. PubMed ID: 1693357
    [Abstract] [Full Text] [Related]

  • 12. Androgen receptor gene methylation and exon one CAG repeat length in ovarian cancer: differences from breast cancer.
    Kassim S, Zoheiry NM, Hamed WM, Going JJ, Craft JA.
    IUBMB Life; 2004 Jul 15; 56(7):417-26. PubMed ID: 15545219
    [Abstract] [Full Text] [Related]

  • 13. Clonality analysis by methylation-specific PCR for the human androgen-receptor gene (HUMARA-MSP).
    Uchida T, Ohashi H, Aoki E, Nakahara Y, Hotta T, Murate T, Saito H, Kinoshita T.
    Leukemia; 2000 Jan 15; 14(1):207-12. PubMed ID: 10637497
    [Abstract] [Full Text] [Related]

  • 14. Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiency.
    Schmalstieg FC, Leonard WJ, Noguchi M, Berg M, Rudloff HE, Denney RM, Dave SK, Brooks EG, Goldman AS.
    J Clin Invest; 1995 Mar 15; 95(3):1169-73. PubMed ID: 7883965
    [Abstract] [Full Text] [Related]

  • 15. Skewed X inactivation in manifesting carriers of Duchenne muscular dystrophy.
    Yoshioka M, Yorifuji T, Mituyoshi I.
    Clin Genet; 1998 Feb 15; 53(2):102-7. PubMed ID: 9611069
    [Abstract] [Full Text] [Related]

  • 16. X chromosome inactivation patterns in 45,X/46,XX mosaics.
    Uehara S, Sato K, Hashiyada M, Obara Y, Matsuzaki S, Nata M, Okamura K.
    J Hum Genet; 2001 Feb 15; 46(3):126-31. PubMed ID: 11310579
    [Abstract] [Full Text] [Related]

  • 17. Nonrandom X chromosome inactivation detection.
    Jones JR.
    Curr Protoc Hum Genet; 2014 Jan 21; 80():9.7.1-9.7.7. PubMed ID: 24510685
    [Abstract] [Full Text] [Related]

  • 18. An assay for X inactivation based on differential methylation at the fragile X locus, FMR1.
    Carrel L, Willard HF.
    Am J Med Genet; 1996 Jul 12; 64(1):27-30. PubMed ID: 8826444
    [Abstract] [Full Text] [Related]

  • 19. Desmoid tumor is a clonal cellular proliferation: PCR amplification of HUMARA for analysis of patterns of X-chromosome inactivation.
    Lucas DR, Shroyer KR, McCarthy PJ, Markham NE, Fujita M, Enomoto TE.
    Am J Surg Pathol; 1997 Mar 12; 21(3):306-11. PubMed ID: 9060600
    [Abstract] [Full Text] [Related]

  • 20. Clonality of tuberous sclerosis harmatomas shown by non-random X-chromosome inactivation.
    Green AJ, Sepp T, Yates JR.
    Hum Genet; 1996 Feb 12; 97(2):240-3. PubMed ID: 8566961
    [Abstract] [Full Text] [Related]

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