These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

317 related articles for article (PubMed ID: 17245608)

  • 1. A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA.
    Green K; Lewis A; Dawson C; Dean W; Reinhart B; Chaillet JR; Reik W
    Mamm Genome; 2007 Jan; 18(1):32-42. PubMed ID: 17245608
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epigenetic dynamics of the Kcnq1 imprinted domain in the early embryo.
    Lewis A; Green K; Dawson C; Redrup L; Huynh KD; Lee JT; Hemberger M; Reik W
    Development; 2006 Nov; 133(21):4203-10. PubMed ID: 17021040
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1.
    Mohammad F; Mondal T; Guseva N; Pandey GK; Kanduri C
    Development; 2010 Aug; 137(15):2493-9. PubMed ID: 20573698
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Domain-specific response of imprinted genes to reduced DNMT1.
    Weaver JR; Sarkisian G; Krapp C; Mager J; Mann MR; Bartolomei MS
    Mol Cell Biol; 2010 Aug; 30(16):3916-28. PubMed ID: 20547750
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo.
    Hudson QJ; Seidl CI; Kulinski TM; Huang R; Warczok KE; Bittner R; Bartolomei MS; Barlow DP
    Dev Biol; 2011 May; 353(2):420-31. PubMed ID: 21354127
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The long noncoding RNA Kcnq1ot1 organises a lineage-specific nuclear domain for epigenetic gene silencing.
    Redrup L; Branco MR; Perdeaux ER; Krueger C; Lewis A; Santos F; Nagano T; Cobb BS; Fraser P; Reik W
    Development; 2009 Feb; 136(4):525-30. PubMed ID: 19144718
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial Loss of Genomic Imprinting Reveals Important Roles for Kcnq1 and Peg10 Imprinted Domains in Placental Development.
    Koppes E; Himes KP; Chaillet JR
    PLoS One; 2015; 10(8):e0135202. PubMed ID: 26241757
    [TBL] [Abstract][Full Text] [Related]  

  • 8. DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation.
    Das R; Lee YK; Strogantsev R; Jin S; Lim YC; Ng PY; Lin XM; Chng K; Yeo GSh; Ferguson-Smith AC; Ding C
    BMC Genomics; 2013 Oct; 14():685. PubMed ID: 24094292
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Long noncoding RNA-mediated maintenance of DNA methylation and transcriptional gene silencing.
    Mohammad F; Pandey GK; Mondal T; Enroth S; Redrup L; Gyllensten U; Kanduri C
    Development; 2012 Aug; 139(15):2792-803. PubMed ID: 22721776
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing.
    Monk D; Wagschal A; Arnaud P; Müller PS; Parker-Katiraee L; Bourc'his D; Scherer SW; Feil R; Stanier P; Moore GE
    Genome Res; 2008 Aug; 18(8):1270-81. PubMed ID: 18480470
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Kcnq1ot1 long non-coding RNA affects chromatin conformation and expression of Kcnq1, but does not regulate its imprinting in the developing heart.
    Korostowski L; Sedlak N; Engel N
    PLoS Genet; 2012 Sep; 8(9):e1002956. PubMed ID: 23028363
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes.
    Mancini-Dinardo D; Steele SJ; Levorse JM; Ingram RS; Tilghman SM
    Genes Dev; 2006 May; 20(10):1268-82. PubMed ID: 16702402
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An extended domain of Kcnq1ot1 silencing revealed by an imprinted fluorescent reporter.
    Jones MJ; Bogutz AB; Lefebvre L
    Mol Cell Biol; 2011 Jul; 31(14):2827-37. PubMed ID: 21576366
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females.
    McGraw S; Oakes CC; Martel J; Cirio MC; de Zeeuw P; Mak W; Plass C; Bartolomei MS; Chaillet JR; Trasler JM
    PLoS Genet; 2013 Nov; 9(11):e1003873. PubMed ID: 24278026
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Antisense noncoding RNA promoter regulates the timing of de novo methylation of an imprinting control region.
    Guseva N; Mondal T; Kanduri C
    Dev Biol; 2012 Jan; 361(2):403-11. PubMed ID: 22119056
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality.
    Biniszkiewicz D; Gribnau J; Ramsahoye B; Gaudet F; Eggan K; Humpherys D; Mastrangelo MA; Jun Z; Walter J; Jaenisch R
    Mol Cell Biol; 2002 Apr; 22(7):2124-35. PubMed ID: 11884600
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Maintenance of paternal methylation and repression of the imprinted H19 gene requires MBD3.
    Reese KJ; Lin S; Verona RI; Schultz RM; Bartolomei MS
    PLoS Genet; 2007 Aug; 3(8):e137. PubMed ID: 17708683
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Telomeric NAP1L4 and OSBPL5 of the KCNQ1 cluster, and the DECORIN gene are not imprinted in human trophoblast stem cells.
    Frost JM; Udayashankar R; Moore HD; Moore GE
    PLoS One; 2010 Jul; 5(7):e11595. PubMed ID: 20644730
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Depletion of Kcnq1ot1 non-coding RNA does not affect imprinting maintenance in stem cells.
    Golding MC; Magri LS; Zhang L; Lalone SA; Higgins MJ; Mann MR
    Development; 2011 Sep; 138(17):3667-78. PubMed ID: 21775415
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.
    Oh-McGinnis R; Bogutz AB; Lee KY; Higgins MJ; Lefebvre L
    BMC Dev Biol; 2010 May; 10():50. PubMed ID: 20459838
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.