BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 10441576)

  • 1. Polymorphic X-chromosome inactivation of the human TIMP1 gene.
    Anderson CL; Brown CJ
    Am J Hum Genet; 1999 Sep; 65(3):699-708. PubMed ID: 10441576
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Variability of X chromosome inactivation: effect on levels of TIMP1 RNA and role of DNA methylation.
    Anderson CL; Brown CJ
    Hum Genet; 2002 Mar; 110(3):271-8. PubMed ID: 11935340
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Epigenetic predisposition to expression of TIMP1 from the human inactive X chromosome.
    Anderson CL; Brown CJ
    BMC Genet; 2005 Sep; 6():48. PubMed ID: 16194278
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expression of genes from the human active and inactive X chromosomes.
    Brown CJ; Carrel L; Willard HF
    Am J Hum Genet; 1997 Jun; 60(6):1333-43. PubMed ID: 9199554
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Determination of X-chromosome inactivation status using X-linked expressed polymorphisms identified by database searching.
    Kutsche R; Brown CJ
    Genomics; 2000 Apr; 65(1):9-15. PubMed ID: 10777660
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X chromosome inactivation of the human TIMP gene.
    Brown CJ; Flenniken AM; Williams BR; Willard HF
    Nucleic Acids Res; 1990 Jul; 18(14):4191-5. PubMed ID: 2377460
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse.
    Carrel L; Clemson CM; Dunn JM; Miller AP; Hunt PA; Lawrence JB; Willard HF
    Hum Mol Genet; 1996 Mar; 5(3):391-401. PubMed ID: 8852665
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41.
    Rosati M; Franzé A; Matarazzo MR; Grimaldi G
    Cytogenet Cell Genet; 1999; 85(3-4):291-6. PubMed ID: 10449920
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiple in vivo footprints are specific to the active allele of the X-linked human hypoxanthine phosphoribosyltransferase gene 5' region: implications for X chromosome inactivation.
    Hornstra IK; Yang TP
    Mol Cell Biol; 1992 Dec; 12(12):5345-54. PubMed ID: 1448069
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Induction of XIST expression from the human active X chromosome in mouse/human somatic cell hybrids by DNA demethylation.
    Tinker AV; Brown CJ
    Nucleic Acids Res; 1998 Jun; 26(12):2935-40. PubMed ID: 9611238
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs).
    Vasques LR; Pereira LV
    DNA Res; 2001 Aug; 8(4):173-7. PubMed ID: 11572483
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-inactivation profile reveals extensive variability in X-linked gene expression in females.
    Carrel L; Willard HF
    Nature; 2005 Mar; 434(7031):400-4. PubMed ID: 15772666
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The human X-inactivation centre is not required for maintenance of X-chromosome inactivation.
    Brown CJ; Willard HF
    Nature; 1994 Mar; 368(6467):154-6. PubMed ID: 8139659
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status.
    Coleman MP; Ambrose HJ; Carrel L; Németh AH; Willard HF; Davies KE
    Genomics; 1996 Jan; 31(1):135-8. PubMed ID: 8808293
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reactivation of an inactive human X chromosome introduced into mouse embryonal carcinoma cells by microcell fusion with persistent expression of XIST.
    Yoshida I; Nishita Y; Mohandas TK; Takagi N
    Exp Cell Res; 1997 Feb; 230(2):208-19. PubMed ID: 9024780
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The severe phenotype of females with tiny ring X chromosomes is associated with inability of these chromosomes to undergo X inactivation.
    Migeon BR; Luo S; Jani M; Jeppesen P
    Am J Hum Genet; 1994 Sep; 55(3):497-504. PubMed ID: 8079992
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation.
    Chang PL; Mueller OT; Lafrenie RM; Varey PA; Rosa NE; Davidson RG; Henry WM; Shows TB
    Am J Hum Genet; 1990 Apr; 46(4):729-37. PubMed ID: 1690506
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant.
    Hansen RS; Stöger R; Wijmenga C; Stanek AM; Canfield TK; Luo P; Matarazzo MR; D'Esposito M; Feil R; Gimelli G; Weemaes CM; Laird CD; Gartler SM
    Hum Mol Genet; 2000 Nov; 9(18):2575-87. PubMed ID: 11063717
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A first-generation X-inactivation profile of the human X chromosome.
    Carrel L; Cottle AA; Goglin KC; Willard HF
    Proc Natl Acad Sci U S A; 1999 Dec; 96(25):14440-4. PubMed ID: 10588724
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E.
    Esposito T; Gianfrancesco F; Ciccodicola A; D'Esposito M; Nagaraja R; Mazzarella R; D'Urso M; Forabosco A
    Genomics; 1997 Jul; 43(2):183-90. PubMed ID: 9244435
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.