BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 38772516)

  • 1. Imprinted lncRNA KCNQ1OT1 regulates CDKN1C expression through promoter binding and chromatin folding in pigs.
    Zhou Y; Yu H; Zhang D; Wang Z; Li Q; An X; Zhang S; Li Z
    Gene; 2024 Sep; 923():148590. PubMed ID: 38772516
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Estrogen-mediated epigenetic repression of the imprinted gene cyclin-dependent kinase inhibitor 1C in breast cancer cells.
    Rodriguez BA; Weng YI; Liu TM; Zuo T; Hsu PY; Lin CH; Cheng AL; Cui H; Yan PS; Huang TH
    Carcinogenesis; 2011 Jun; 32(6):812-21. PubMed ID: 21304052
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The long non-coding RNA Kcnq1ot1 controls maternal p57 expression in muscle cells by promoting H3K27me3 accumulation to an intragenic MyoD-binding region.
    Andresini O; Rossi MN; Matteini F; Petrai S; Santini T; Maione R
    Epigenetics Chromatin; 2019 Jan; 12(1):8. PubMed ID: 30651140
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.
    Higashimoto K; Soejima H; Saito T; Okumura K; Mukai T
    Cytogenet Genome Res; 2006; 113(1-4):306-12. PubMed ID: 16575194
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine.
    Robbins KM; Chen Z; Wells KD; Rivera RM
    J Biomed Sci; 2012 Nov; 19(1):95. PubMed ID: 23153226
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A cross-talk between DNA methylation and H3 lysine 9 dimethylation at the KvDMR1 region controls the induction of Cdkn1c in muscle cells.
    Andresini O; Ciotti A; Rossi MN; Battistelli C; Carbone M; Maione R
    Epigenetics; 2016 Nov; 11(11):791-803. PubMed ID: 27611768
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Evolution of the CDKN1C-KCNQ1 imprinted domain.
    Ager EI; Pask AJ; Gehring HM; Shaw G; Renfree MB
    BMC Evol Biol; 2008 May; 8():163. PubMed ID: 18510768
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Imprinted gene alterations in the kidneys of growth restricted offspring may be mediated by a long non-coding RNA.
    Doan TNA; Cowley JM; Phillips AL; Briffa JF; Leemaqz SY; Burton RA; Romano T; Wlodek ME; Bianco-Miotto T
    Epigenetics; 2024 Dec; 19(1):2294516. PubMed ID: 38126131
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Aberrant CpG methylation of the imprinting control region KvDMR1 detected in assisted reproductive technology-produced calves and pathogenesis of large offspring syndrome.
    Hori N; Nagai M; Hirayama M; Hirai T; Matsuda K; Hayashi M; Tanaka T; Ozawa T; Horike S
    Anim Reprod Sci; 2010 Dec; 122(3-4):303-12. PubMed ID: 21035970
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.
    Arima T; Kamikihara T; Hayashida T; Kato K; Inoue T; Shirayoshi Y; Oshimura M; Soejima H; Mukai T; Wake N
    Nucleic Acids Res; 2005; 33(8):2650-60. PubMed ID: 15888726
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients.
    Rovina D; La Vecchia M; Cortesi A; Fontana L; Pesant M; Maitz S; Tabano S; Bodega B; Miozzo M; Sirchia SM
    Sci Rep; 2020 May; 10(1):8275. PubMed ID: 32427849
    [TBL] [Abstract][Full Text] [Related]  

  • 14.
    Hara-Isono K; Yamazawa K; Tanaka S; Nishi E; Fukami M; Kagami M
    J Med Genet; 2022 Dec; 59(12):1241-1246. PubMed ID: 35906012
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome.
    Diaz-Meyer N; Day CD; Khatod K; Maher ER; Cooper W; Reik W; Junien C; Graham G; Algar E; Der Kaloustian VM; Higgins MJ
    J Med Genet; 2003 Nov; 40(11):797-801. PubMed ID: 14627666
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases.
    Chiesa N; De Crescenzo A; Mishra K; Perone L; Carella M; Palumbo O; Mussa A; Sparago A; Cerrato F; Russo S; Lapi E; Cubellis MV; Kanduri C; Cirillo Silengo M; Riccio A; Ferrero GB
    Hum Mol Genet; 2012 Jan; 21(1):10-25. PubMed ID: 21920939
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domain.
    Schultz BM; Gallicio GA; Cesaroni M; Lupey LN; Engel N
    Nucleic Acids Res; 2015 Jan; 43(2):745-59. PubMed ID: 25539921
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Long noncoding RNA-mediated intrachromosomal interactions promote imprinting at the Kcnq1 locus.
    Zhang H; Zeitz MJ; Wang H; Niu B; Ge S; Li W; Cui J; Wang G; Qian G; Higgins MJ; Fan X; Hoffman AR; Hu JF
    J Cell Biol; 2014 Jan; 204(1):61-75. PubMed ID: 24395636
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer.
    Soejima H; Nakagawachi T; Zhao W; Higashimoto K; Urano T; Matsukura S; Kitajima Y; Takeuchi M; Nakayama M; Oshimura M; Miyazaki K; Joh K; Mukai T
    Oncogene; 2004 May; 23(25):4380-8. PubMed ID: 15007390
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndrome.
    Diaz-Meyer N; Yang Y; Sait SN; Maher ER; Higgins MJ
    J Med Genet; 2005 Aug; 42(8):648-55. PubMed ID: 16061564
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.