BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 21252296)

  • 1. Epigenetic profile of the euchromatic region of human Y chromosome.
    Singh NP; Madabhushi SR; Srivastava S; Senthilkumar R; Neeraja C; Khosla S; Mishra RK
    Nucleic Acids Res; 2011 May; 39(9):3594-606. PubMed ID: 21252296
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DXZ4 chromatin adopts an opposing conformation to that of the surrounding chromosome and acquires a novel inactive X-specific role involving CTCF and antisense transcripts.
    Chadwick BP
    Genome Res; 2008 Aug; 18(8):1259-69. PubMed ID: 18456864
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distinct epigenetic domains separated by a CTCF bound insulator between the tandem genes, BLU and RASSF1A.
    Chang JW; Hsu HS; Ni HJ; Chuang CT; Hsiung CH; Huang TH; Wang YC
    PLoS One; 2010 Sep; 5(9):e12847. PubMed ID: 20877461
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Aberrant epigenetic modifications in the CTCF binding domain of the IGF2/H19 gene in prostate cancer compared with benign prostate hyperplasia.
    Paradowska A; Fenic I; Konrad L; Sturm K; Wagenlehner F; Weidner W; Steger K
    Int J Oncol; 2009 Jul; 35(1):87-96. PubMed ID: 19513555
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The 5' regulatory sequences of active miR-146a promoters are hypomethylated and associated with euchromatic histone modification marks in B lymphoid cells.
    Szenthe K; Koroknai A; Banati F; Bathori Z; Lozsa R; Burgyan J; Wolf H; Salamon D; Nagy K; Niller HH; Minarovits J
    Biochem Biophys Res Commun; 2013 Apr; 433(4):489-95. PubMed ID: 23528241
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of DXZ4 conservation in primates implies important functional roles for CTCF binding, array expression and tandem repeat organization on the X chromosome.
    McLaughlin CR; Chadwick BP
    Genome Biol; 2011; 12(4):R37. PubMed ID: 21489251
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Euchromatin islands in large heterochromatin domains are enriched for CTCF binding and differentially DNA-methylated regions.
    Wen B; Wu H; Loh YH; Briem E; Daley GQ; Feinberg AP
    BMC Genomics; 2012 Oct; 13():566. PubMed ID: 23102236
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NF-Y dependent epigenetic modifications discriminate between proliferating and postmitotic tissue.
    Gurtner A; Fuschi P; Magi F; Colussi C; Gaetano C; Dobbelstein M; Sacchi A; Piaggio G
    PLoS One; 2008 Apr; 3(4):e2047. PubMed ID: 18431504
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
    Nativio R; Sparago A; Ito Y; Weksberg R; Riccio A; Murrell A
    Hum Mol Genet; 2011 Apr; 20(7):1363-74. PubMed ID: 21282187
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The mouse DXZ4 homolog retains Ctcf binding and proximity to Pls3 despite substantial organizational differences compared to the primate macrosatellite.
    Horakova AH; Calabrese JM; McLaughlin CR; Tremblay DC; Magnuson T; Chadwick BP
    Genome Biol; 2012 Aug; 13(8):R70. PubMed ID: 22906166
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gonadoblastoma Y locus genes expressed in germ cells of individuals with dysgenetic gonads and a Y chromosome in their karyotypes include DDX3Y and TSPY.
    Vogt PH; Besikoglu B; Bettendorf M; Frank-Herrmann P; Zimmer J; Bender U; Knauer-Fischer S; Choukair D; Sinn P; Lau YC; Heidemann PH; Strowitzki T
    Hum Reprod; 2019 Apr; 34(4):770-779. PubMed ID: 30753444
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CTCF prevents the epigenetic drift of EBV latency promoter Qp.
    Tempera I; Wiedmer A; Dheekollu J; Lieberman PM
    PLoS Pathog; 2010 Aug; 6(8):e1001048. PubMed ID: 20730088
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A region of euchromatin coincides with an extensive tandem repeat on the mouse (Mus musculus) inactive X chromosome.
    Darrow EM; Seberg AP; Das S; Figueroa DM; Sun Z; Moseley SC; Chadwick BP
    Chromosome Res; 2014 Sep; 22(3):335-50. PubMed ID: 24821208
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The macrosatellite DXZ4 mediates CTCF-dependent long-range intrachromosomal interactions on the human inactive X chromosome.
    Horakova AH; Moseley SC; McLaughlin CR; Tremblay DC; Chadwick BP
    Hum Mol Genet; 2012 Oct; 21(20):4367-77. PubMed ID: 22791747
    [TBL] [Abstract][Full Text] [Related]  

  • 15. JHDM3A module as an effector molecule in guide-directed modification of target chromatin.
    Jeong YS; Park JS; Ko Y; Kang YK
    J Biol Chem; 2011 Feb; 286(6):4461-70. PubMed ID: 21148561
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epigenetic profiling at mouse imprinted gene clusters reveals novel epigenetic and genetic features at differentially methylated regions.
    Dindot SV; Person R; Strivens M; Garcia R; Beaudet AL
    Genome Res; 2009 Aug; 19(8):1374-83. PubMed ID: 19542493
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cell cycle-dependent accumulation of histone H3.3 and euchromatic histone modifications in pericentromeric heterochromatin in response to a decrease in DNA methylation levels.
    Sugimura K; Fukushima Y; Ishida M; Ito S; Nakamura M; Mori Y; Okumura K
    Exp Cell Res; 2010 Oct; 316(17):2731-46. PubMed ID: 20599948
    [TBL] [Abstract][Full Text] [Related]  

  • 18. YY1 associates with the macrosatellite DXZ4 on the inactive X chromosome and binds with CTCF to a hypomethylated form in some male carcinomas.
    Moseley SC; Rizkallah R; Tremblay DC; Anderson BR; Hurt MM; Chadwick BP
    Nucleic Acids Res; 2012 Feb; 40(4):1596-608. PubMed ID: 22064860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular landscape of modified histones in Drosophila heterochromatic genes and euchromatin-heterochromatin transition zones.
    Yasuhara JC; Wakimoto BT
    PLoS Genet; 2008 Jan; 4(1):e16. PubMed ID: 18208336
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).
    Zeng W; de Greef JC; Chen YY; Chien R; Kong X; Gregson HC; Winokur ST; Pyle A; Robertson KD; Schmiesing JA; Kimonis VE; Balog J; Frants RR; Ball AR; Lock LF; Donovan PJ; van der Maarel SM; Yokomori K
    PLoS Genet; 2009 Jul; 5(7):e1000559. PubMed ID: 19593370
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.