BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

306 related articles for article (PubMed ID: 24990148)

  • 1. Tissue-specific insulator function at H19/Igf2 revealed by deletions at the imprinting control region.
    Ideraabdullah FY; Thorvaldsen JL; Myers JA; Bartolomei MS
    Hum Mol Genet; 2014 Dec; 23(23):6246-59. PubMed ID: 24990148
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model.
    Freschi A; Del Prete R; Pignata L; Cecere F; Manfrevola F; Mattia M; Cobellis G; Sparago A; Bartolomei MS; Riccio A; Cerrato F
    Hum Mol Genet; 2021 Jul; 30(16):1509-1520. PubMed ID: 34132339
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.
    Cerrato F; Sparago A; Verde G; De Crescenzo A; Citro V; Cubellis MV; Rinaldi MM; Boccuto L; Neri G; Magnani C; D'Angelo P; Collini P; Perotti D; Sebastio G; Maher ER; Riccio A
    Hum Mol Genet; 2008 May; 17(10):1427-35. PubMed ID: 18245780
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality.
    Lee DH; Singh P; Tsark WM; Szabó PE
    PLoS One; 2010 Sep; 5(9):e12630. PubMed ID: 20838620
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel cis-regulatory function in ICR-mediated imprinted repression of H19.
    Ideraabdullah FY; Abramowitz LK; Thorvaldsen JL; Krapp C; Wen SC; Engel N; Bartolomei MS
    Dev Biol; 2011 Jul; 355(2):349-57. PubMed ID: 21600199
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.
    Beygo J; Citro V; Sparago A; De Crescenzo A; Cerrato F; Heitmann M; Rademacher K; Guala A; Enklaar T; Anichini C; Cirillo Silengo M; Graf N; Prawitt D; Cubellis MV; Horsthemke B; Buiting K; Riccio A
    Hum Mol Genet; 2013 Feb; 22(3):544-57. PubMed ID: 23118352
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2.
    Kurukuti S; Tiwari VK; Tavoosidana G; Pugacheva E; Murrell A; Zhao Z; Lobanenkov V; Reik W; Ohlsson R
    Proc Natl Acad Sci U S A; 2006 Jul; 103(28):10684-9. PubMed ID: 16815976
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.
    Higashimoto K; Jozaki K; Kosho T; Matsubara K; Fuke T; Yamada D; Yatsuki H; Maeda T; Ohtsuka Y; Nishioka K; Joh K; Koseki H; Ogata T; Soejima H
    Clin Genet; 2014 Dec; 86(6):539-44. PubMed ID: 24299031
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.
    Sparago A; Russo S; Cerrato F; Ferraiuolo S; Castorina P; Selicorni A; Schwienbacher C; Negrini M; Ferrero GB; Silengo MC; Anichini C; Larizza L; Riccio A
    Hum Mol Genet; 2007 Feb; 16(3):254-64. PubMed ID: 17158821
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sox-Oct motifs contribute to maintenance of the unmethylated H19 ICR in YAC transgenic mice.
    Sakaguchi R; Okamura E; Matsuzaki H; Fukamizu A; Tanimoto K
    Hum Mol Genet; 2013 Nov; 22(22):4627-37. PubMed ID: 23821645
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epigenetic regulation of Igf2/H19 imprinting at CTCF insulator binding sites.
    Yang Y; Hu JF; Ulaner GA; Li T; Yao X; Vu TH; Hoffman AR
    J Cell Biochem; 2003 Dec; 90(5):1038-55. PubMed ID: 14624463
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel large deletion of the ICR1 region including H19 and putative enhancer elements.
    Fryssira H; Amenta S; Kanber D; Sofocleous C; Lykopoulou E; Kanaka-Gantenbein C; Cerrato F; Lüdecke HJ; Bens S; Riccio A; Buiting K
    BMC Med Genet; 2015 May; 16():30. PubMed ID: 25943194
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.
    Sparago A; Cerrato F; Vernucci M; Ferrero GB; Silengo MC; Riccio A
    Nat Genet; 2004 Sep; 36(9):958-60. PubMed ID: 15314640
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Oct4/Sox2 binding sites contribute to maintaining hypomethylation of the maternal igf2/h19 imprinting control region.
    Zimmerman DL; Boddy CS; Schoenherr CS
    PLoS One; 2013; 8(12):e81962. PubMed ID: 24324735
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes.
    Hur SK; Freschi A; Ideraabdullah F; Thorvaldsen JL; Luense LJ; Weller AH; Berger SL; Cerrato F; Riccio A; Bartolomei MS
    Proc Natl Acad Sci U S A; 2016 Sep; 113(39):10938-43. PubMed ID: 27621468
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CTCF is the master organizer of domain-wide allele-specific chromatin at the H19/Igf2 imprinted region.
    Han L; Lee DH; Szabó PE
    Mol Cell Biol; 2008 Feb; 28(3):1124-35. PubMed ID: 18039862
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Mutation of a single CTCF target site within the H19 imprinting control region leads to loss of Igf2 imprinting and complex patterns of de novo methylation upon maternal inheritance.
    Pant V; Kurukuti S; Pugacheva E; Shamsuddin S; Mariano P; Renkawitz R; Klenova E; Lobanenkov V; Ohlsson R
    Mol Cell Biol; 2004 Apr; 24(8):3497-504. PubMed ID: 15060168
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders.
    Demars J; Shmela ME; Rossignol S; Okabe J; Netchine I; Azzi S; Cabrol S; Le Caignec C; David A; Le Bouc Y; El-Osta A; Gicquel C
    Hum Mol Genet; 2010 Mar; 19(5):803-14. PubMed ID: 20007505
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.