BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

618 related articles for article (PubMed ID: 16001432)

  • 21. Rapid detection of methylation change at H19 in human imprinting disorders using methylation-sensitive high-resolution melting.
    Wojdacz TK; Dobrovic A; Algar EM
    Hum Mutat; 2008 Oct; 29(10):1255-60. PubMed ID: 18473334
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Characterization of differentially methylated regions in 3 bovine imprinted genes: a model for studying human germ-cell and embryo development.
    Hansmann T; Heinzmann J; Wrenzycki C; Zechner U; Niemann H; Haaf T
    Cytogenet Genome Res; 2011; 132(4):239-47. PubMed ID: 21160170
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Methylation status of imprinting centers for H19/IGF2 and SNURF/SNRPN in primate embryonic stem cells.
    Mitalipov S; Clepper L; Sritanaudomchai H; Fujimoto A; Wolf D
    Stem Cells; 2007 Mar; 25(3):581-8. PubMed ID: 17170068
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene.
    Bell AC; Felsenfeld G
    Nature; 2000 May; 405(6785):482-5. PubMed ID: 10839546
    [TBL] [Abstract][Full Text] [Related]  

  • 25. CTCF binding is not the epigenetic mark that establishes post-fertilization methylation imprinting in the transgenic H19 ICR.
    Matsuzaki H; Okamura E; Fukamizu A; Tanimoto K
    Hum Mol Genet; 2010 Apr; 19(7):1190-8. PubMed ID: 20047949
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma.
    el-Naggar AK; Lai S; Tucker SA; Clayman GL; Goepfert H; Hong WK; Huff V
    Oncogene; 1999 Nov; 18(50):7063-9. PubMed ID: 10597307
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hypomethylated and hypermethylated profiles of H19DMR are associated with the aberrant imprinting of IGF2 and H19 in human hepatocellular carcinoma.
    Wu J; Qin Y; Li B; He WZ; Sun ZL
    Genomics; 2008 May; 91(5):443-50. PubMed ID: 18358696
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus.
    Hark AT; Schoenherr CJ; Katz DJ; Ingram RS; Levorse JM; Tilghman SM
    Nature; 2000 May; 405(6785):486-9. PubMed ID: 10839547
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Expression, promoter usage and parental imprinting status of insulin-like growth factor II (IGF2) in human hepatoblastoma: uncoupling of IGF2 and H19 imprinting.
    Li X; Adam G; Cui H; Sandstedt B; Ohlsson R; Ekström TJ
    Oncogene; 1995 Jul; 11(2):221-9. PubMed ID: 7624139
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.
    Squire JA; Li M; Perlikowski S; Fei YL; Bayani J; Zhang ZM; Weksberg R
    Genomics; 2000 May; 65(3):234-42. PubMed ID: 10857747
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Activation of Wnt/beta-catenin signaling in distinct histologic subtypes of human germ cell tumors.
    Fritsch MK; Schneider DT; Schuster AE; Murdoch FE; Perlman EJ
    Pediatr Dev Pathol; 2006; 9(2):115-31. PubMed ID: 16822086
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Equivalent parental distribution of frequently lost alleles and biallelic expression of the H19 gene in human testicular germ cell tumors.
    Mishina M; Ogawa O; Kinoshita H; Oka H; Okumura K; Mitsumori K; Kakehi Y; Reeve AE; Yoshida O
    Jpn J Cancer Res; 1996 Aug; 87(8):816-23. PubMed ID: 8797887
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [The aberrant imprinting of insulin-like growth factor II and H19 in human hepatocellular carcinoma].
    Wu J; Qin Y; Li B; He WZ; Sun ZL
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2007 Jan; 38(1):49-52. PubMed ID: 17294726
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor.
    Ichikawa M; Arai Y; Haruta M; Furukawa S; Ariga T; Kajii T; Kaneko Y
    Genes Chromosomes Cancer; 2013 Mar; 52(3):274-86. PubMed ID: 23225212
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Establishment of functional imprinting of the H19 gene in human developing placentae.
    Jinno Y; Ikeda Y; Yun K; Maw M; Masuzaki H; Fukuda H; Inuzuka K; Fujishita A; Ohtani Y; Okimoto T
    Nat Genet; 1995 Jul; 10(3):318-24. PubMed ID: 7670470
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site.
    Ulaner GA; Vu TH; Li T; Hu JF; Yao XM; Yang Y; Gorlick R; Meyers P; Healey J; Ladanyi M; Hoffman AR
    Hum Mol Genet; 2003 Mar; 12(5):535-49. PubMed ID: 12588801
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Abnormal methylation patterns at the IGF2/H19 imprinting control region in phenotypically normal babies conceived by assisted reproductive technologies.
    Shi X; Ni Y; Zheng H; Chen S; Zhong M; Wu F; Xia R; Luo Y
    Eur J Obstet Gynecol Reprod Biol; 2011 Sep; 158(1):52-5. PubMed ID: 21555179
    [TBL] [Abstract][Full Text] [Related]  

  • 40. CTCF-dependent chromatin bias constitutes transient epigenetic memory of the mother at the H19-Igf2 imprinting control region in prospermatogonia.
    Lee DH; Singh P; Tsai SY; Oates N; Spalla A; Spalla C; Brown L; Rivas G; Larson G; Rauch TA; Pfeifer GP; Szabó PE
    PLoS Genet; 2010 Nov; 6(11):e1001224. PubMed ID: 21124827
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 31.