BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

405 related articles for article (PubMed ID: 12466290)

  • 1. Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.
    Yatsuki H; Joh K; Higashimoto K; Soejima H; Arai Y; Wang Y; Hatada I; Obata Y; Morisaki H; Zhang Z; Nakagawachi T; Satoh Y; Mukai T
    Genome Res; 2002 Dec; 12(12):1860-70. PubMed ID: 12466290
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.
    Higashimoto K; Urano T; Sugiura K; Yatsuki H; Joh K; Zhao W; Iwakawa M; Ohashi H; Oshimura M; Niikawa N; Mukai T; Soejima H
    Am J Hum Genet; 2003 Oct; 73(4):948-56. PubMed ID: 12949703
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome.
    Horike S; Mitsuya K; Meguro M; Kotobuki N; Kashiwagi A; Notsu T; Schulz TC; Shirayoshi Y; Oshimura M
    Hum Mol Genet; 2000 Sep; 9(14):2075-83. PubMed ID: 10958646
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.
    Yatsuki H; Joh K; Higashimoto K; Soejima H; Arai Y; Wang Y; Hatada I; Obata Y; Morisaki H; Zhang Z; Nakagawachi T; Satoh Y; Mukai T
    Genome Res; 2004 Sep; 14(9):1820. PubMed ID: 15378833
    [No Abstract]   [Full Text] [Related]  

  • 7. Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.
    Caspary T; Cleary MA; Baker CC; Guan XJ; Tilghman SM
    Mol Cell Biol; 1998 Jun; 18(6):3466-74. PubMed ID: 9584186
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human.
    Yatsuki H; Watanabe H; Hattori M; Joh K; Soejima H; Komoda H; Xin Z; Zhu X; Higashimoto K; Nishimura M; Kuratomi S; Sasaki H; Sakaki Y; Mukai T
    DNA Res; 2000 Jun; 7(3):195-206. PubMed ID: 10907850
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The testis-specific factor CTCFL cooperates with the protein methyltransferase PRMT7 in H19 imprinting control region methylation.
    Jelinic P; Stehle JC; Shaw P
    PLoS Biol; 2006 Oct; 4(11):e355. PubMed ID: 17048991
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.
    Paulsen M; Davies KR; Bowden LM; Villar AJ; Franck O; Fuermann M; Dean WL; Moore TF; Rodrigues N; Davies KE; Hu RJ; Feinberg AP; Maher ER; Reik W; Walter J
    Hum Mol Genet; 1998 Jul; 7(7):1149-59. PubMed ID: 9618174
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
    Vu TH; Li T; Nguyen D; Nguyen BT; Yao XM; Hu JF; Hoffman AR
    Genomics; 2000 Mar; 64(2):132-43. PubMed ID: 10729220
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors.
    Chung WY; Yuan L; Feng L; Hensle T; Tycko B
    Hum Mol Genet; 1996 Aug; 5(8):1101-8. PubMed ID: 8842727
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome.
    John RM; Ainscough JF; Barton SC; Surani MA
    Hum Mol Genet; 2001 Jul; 10(15):1601-9. PubMed ID: 11468278
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lsh controls silencing of the imprinted Cdkn1c gene.
    Fan T; Hagan JP; Kozlov SV; Stewart CL; Muegge K
    Development; 2005 Feb; 132(4):635-44. PubMed ID: 15647320
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.
    Engemann S; Strödicke M; Paulsen M; Franck O; Reinhardt R; Lane N; Reik W; Walter J
    Hum Mol Genet; 2000 Nov; 9(18):2691-706. PubMed ID: 11063728
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization and imprinting status of OBPH1/Obph1 gene: implications for an extended imprinting domain in human and mouse.
    Higashimoto K; Soejima H; Yatsuki H; Joh K; Uchiyama M; Obata Y; Ono R; Wang Y; Xin Z; Zhu X; Masuko S; Ishino F; Hatada I; Jinno Y; Iwasaka T; Katsuki T; Mukai T
    Genomics; 2002 Dec; 80(6):575-84. PubMed ID: 12504849
    [TBL] [Abstract][Full Text] [Related]  

  • 17. IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch.
    Li T; Vu TH; Ulaner GA; Littman E; Ling JQ; Chen HL; Hu JF; Behr B; Giudice L; Hoffman AR
    Mol Hum Reprod; 2005 Sep; 11(9):631-40. PubMed ID: 16219628
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: relation to expression and imprinting.
    Weber M; Milligan L; Delalbre A; Antoine E; Brunel C; Cathala G; Forné T
    Mech Dev; 2001 Mar; 101(1-2):133-41. PubMed ID: 11231066
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19.
    Takada S; Paulsen M; Tevendale M; Tsai CE; Kelsey G; Cattanach BM; Ferguson-Smith AC
    Hum Mol Genet; 2002 Jan; 11(1):77-86. PubMed ID: 11773001
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Methylation at mouse Cdkn1c is acquired during postimplantation development and functions to maintain imprinted expression.
    Bhogal B; Arnaudo A; Dymkowski A; Best A; Davis TL
    Genomics; 2004 Dec; 84(6):961-70. PubMed ID: 15533713
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.