BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 7749438)

  • 1. 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; 5(3):187-92. PubMed ID: 7749438
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus.
    Hendriks RW; Chen ZY; Hinds H; Schuurman RK; Craig IW
    Immunodeficiency; 1993; 4(1-4):209-11. PubMed ID: 8167702
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.
    Hinds H; Craig IW; Chen ZY; Kraakman ME; Schuurman RK; Hendriks RW
    Immunodeficiency; 1993; 4(1-4):213-5. PubMed ID: 8167703
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 95(3):1169-73. PubMed ID: 7883965
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inheritance of skewed X chromosome inactivation in a large family with an X-linked recessive deafness syndrome.
    Orstavik KH; Orstavik RE; Eiklid K; Tranebjaerg L
    Am J Med Genet; 1996 Jul; 64(1):31-4. PubMed ID: 8826445
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation.
    Fearon ER; Winkelstein JA; Civin CI; Pardoll DM; Vogelstein B
    N Engl J Med; 1987 Feb; 316(8):427-31. PubMed ID: 2880293
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Patterns of X chromosome inactivation in haematopoietic cells of female carriers of X linked severe combined immunodeficiency.
    Hendriks RW; Kraakman ME; Schuurman RK
    Immunodeficiency; 1993; 4(1-4):263-5. PubMed ID: 8167715
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Carrier detection and prenatal diagnosis of X-linked agammaglobulinemia.
    Journet O; Durandy A; Doussau M; Le Deist F; Couvreur J; Griscelli C; Fischer A; de Saint-Basile G
    Am J Med Genet; 1992 Jul; 43(5):885-7. PubMed ID: 1642281
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 64(1):27-30. PubMed ID: 8826444
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of meningiomas by methylation- and transcription-based clonality assays.
    Zhu J; Frosch MP; Busque L; Beggs AH; Dashner K; Gilliland DG; Black PM
    Cancer Res; 1995 Sep; 55(17):3865-72. PubMed ID: 7641206
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact.
    Hendriks RW; Kraakman ME; Craig IW; Espanol T; Schuurman RK
    Eur J Immunol; 1990 Dec; 20(12):2603-8. PubMed ID: 1980111
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X chromosome linked immunodeficiency.
    Schwaber J; Rosen FS
    Immunodefic Rev; 1990; 2(3):233-51. PubMed ID: 1981831
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 56(7):417-26. PubMed ID: 15545219
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular genetics of X-linked primary immunodeficiencies: advances in diagnosis and prevention].
    Carbonara A; Brusco A; Carbonara C
    Ann Ital Med Int; 1996; 11(3):180-6. PubMed ID: 8998263
    [TBL] [Abstract][Full Text] [Related]  

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

  • 16. Quantification of X-chromosome inactivation patterns in haematological samples using the DNA PCR-based HUMARA assay.
    Gale RE; Mein CA; Linch DC
    Leukemia; 1996 Feb; 10(2):362-7. PubMed ID: 8637249
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X chromosome methylation-based chimerism assay for sex-mismatched hematopoietic stem cell transplantation.
    Yamane A; Karasawa M; Maehara T; Tsukamoto N; Nojima Y
    Bone Marrow Transplant; 2001 Nov; 28(10):969-73. PubMed ID: 11753553
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.
    Lose F; Duffy DL; Kay GF; Kedda MA; Spurdle AB; ;
    J Natl Cancer Inst; 2008 Nov; 100(21):1519-29. PubMed ID: 18957670
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locus.
    Hendriks RW; De Weers M; Mensink RG; Kraakman ME; Mollee-Versteegde IF; Veerman AJ; Sandkuyl LA; Schuurman RK
    Clin Exp Immunol; 1991 May; 84(2):219-22. PubMed ID: 1709069
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carrier identification in X-linked immunodeficiency diseases.
    Li SL; Ting SS; Lindeman R; Ffrench R; Ziegler JB
    J Paediatr Child Health; 1998 Jun; 34(3):273-9. PubMed ID: 9633977
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.