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Journal Abstract Search

123 related items for PubMed ID: 15239143

  • 41. Frequent loss of heterozygosity at 11p loci in testicular cancer.
    Smith RC, Rukstalis DB.
    J Urol; 1995 May; 153(5):1684-7. PubMed ID: 7715010
    [Abstract] [Full Text] [Related]

  • 42. Loss of methylation at chromosome 11p15.5 is common in human adult tumors.
    Scelfo RA, Schwienbacher C, Veronese A, Gramantieri L, Bolondi L, Querzoli P, Nenci I, Calin GA, Angioni A, Barbanti-Brodano G, Negrini M.
    Oncogene; 2002 Apr 11; 21(16):2564-72. PubMed ID: 11971191
    [Abstract] [Full Text] [Related]

  • 43. SSA/RO52gene and expressed sequence tags in an 85 kb region of chromosome segment 11p15.5.
    Kim YC, Cao Y, Pitterle DM, O'Briant KC, Bepler G.
    Int J Cancer; 2000 Jul 01; 87(1):61-7. PubMed ID: 10861453
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  • 45. 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 20; 11(2):221-9. PubMed ID: 7624139
    [Abstract] [Full Text] [Related]

  • 46. [Evidence of genetic alterations in chromosome 11 in embryonal and alveolar rhabdomyosarcoma].
    Brinkschmidt C, Poremba C, Schäfer KL, Simon R, Jürgens H, Böcker W, Dockhorn-Dworniczak B.
    Verh Dtsch Ges Pathol; 1998 Jul 20; 82():210-4. PubMed ID: 10095436
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  • 48. Childhood hepatoblastomas frequently carry a mutated degradation targeting box of the beta-catenin gene.
    Koch A, Denkhaus D, Albrecht S, Leuschner I, von Schweinitz D, Pietsch T.
    Cancer Res; 1999 Jan 15; 59(2):269-73. PubMed ID: 9927029
    [Abstract] [Full Text] [Related]

  • 49. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
    Kubota T, Saitoh S, Matsumoto T, Narahara K, Fukushima Y, Jinno Y, Niikawa N.
    Am J Med Genet; 1994 Feb 15; 49(4):378-83. PubMed ID: 7909196
    [Abstract] [Full Text] [Related]

  • 50. Genomic imprinting and Wilms' tumor.
    Moulton T, Chung WY, Yuan L, Hensle T, Waber P, Nisen P, Tycko B.
    Med Pediatr Oncol; 1996 Nov 15; 27(5):476-83. PubMed ID: 8827077
    [Abstract] [Full Text] [Related]

  • 51. Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays.
    Suzuki M, Kato M, Yuyan C, Takita J, Sanada M, Nannya Y, Yamamoto G, Takahashi A, Ikeda H, Kuwano H, Ogawa S, Hayashi Y.
    Cancer Sci; 2008 Mar 15; 99(3):564-70. PubMed ID: 18271875
    [Abstract] [Full Text] [Related]

  • 52. Expression profiling and differential screening between hepatoblastomas and the corresponding normal livers: identification of high expression of the PLK1 oncogene as a poor-prognostic indicator of hepatoblastomas.
    Yamada S, Ohira M, Horie H, Ando K, Takayasu H, Suzuki Y, Sugano S, Hirata T, Goto T, Matsunaga T, Hiyama E, Hayashi Y, Ando H, Suita S, Kaneko M, Sasaki F, Hashizume K, Ohnuma N, Nakagawara A.
    Oncogene; 2004 Aug 05; 23(35):5901-11. PubMed ID: 15221005
    [Abstract] [Full Text] [Related]

  • 53. Elevated expression of Wnt antagonists is a common event in hepatoblastomas.
    Koch A, Waha A, Hartmann W, Hrychyk A, Schüller U, Waha A, Wharton KA, Fuchs SY, von Schweinitz D, Pietsch T.
    Clin Cancer Res; 2005 Jun 15; 11(12):4295-304. PubMed ID: 15958610
    [Abstract] [Full Text] [Related]

  • 54. Loss of heterozygosity at 11p13 and 11p15 in Wilms tumor: a study of 22 cases from India.
    Sigamani E, Wari MN, Iyer VK, Agarwala S, Sharma A, Bakhshi S, Dinda A.
    Pediatr Surg Int; 2013 Mar 15; 29(3):223-7. PubMed ID: 23292539
    [Abstract] [Full Text] [Related]

  • 55. Investigation in liver tissues and cell lines of the transcription of 13 genes mapping to the 16q24 region that are frequently deleted in hepatocellular carcinoma.
    Riou P, Saffroy R, Comoy J, Gross-Goupil M, Thiéry JP, Emile JF, Azoulay D, Piatier-Tonneau D, Lemoine A, Debuire B.
    Clin Cancer Res; 2002 Oct 15; 8(10):3178-86. PubMed ID: 12374686
    [Abstract] [Full Text] [Related]

  • 56. Genome-wide analysis of allelic imbalances reveals 4q deletions as a poor prognostic factor and MDM4 amplification at 1q32.1 in hepatoblastoma.
    Arai Y, Honda S, Haruta M, Kasai F, Fujiwara Y, Ohshima J, Sasaki F, Nakagawara A, Horie H, Yamaoka H, Hiyama E, Kaneko Y.
    Genes Chromosomes Cancer; 2010 Jul 15; 49(7):596-609. PubMed ID: 20461752
    [Abstract] [Full Text] [Related]

  • 57. Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?
    Aretz S, Koch A, Uhlhaas S, Friedl W, Propping P, von Schweinitz D, Pietsch T.
    Pediatr Blood Cancer; 2006 Nov 15; 47(6):811-8. PubMed ID: 16317745
    [Abstract] [Full Text] [Related]

  • 58. Activation of beta-catenin in epithelial and mesenchymal hepatoblastomas.
    Wei Y, Fabre M, Branchereau S, Gauthier F, Perilongo G, Buendia MA.
    Oncogene; 2000 Jan 27; 19(4):498-504. PubMed ID: 10698519
    [Abstract] [Full Text] [Related]

  • 59. Inactivation of the tumor suppressor WTX in a subset of pediatric tumors.
    Akhavanfard S, Vargas SO, Han M, Nitta M, Chang CB, Le LP, Fazlollahi L, Nguyen Q, Ma Y, Cosper A, Dias-Santagata D, Han JY, Bergethon K, Borger DR, Ellisen LW, Pomeroy SL, Haber DA, Iafrate AJ, Rivera MN.
    Genes Chromosomes Cancer; 2014 Jan 27; 53(1):67-77. PubMed ID: 24249259
    [Abstract] [Full Text] [Related]

  • 60. Prognostic significance of aminopeptidase-N (CD13) in hepatoblastoma.
    Saida S, Watanabe K, Kato I, Fujino H, Umeda K, Okamoto S, Uemoto S, Hishiki T, Yoshida H, Tanaka S, Adachi S, Niwa A, Nakahata T, Heike T.
    Pediatr Int; 2015 Aug 27; 57(4):558-66. PubMed ID: 25682862
    [Abstract] [Full Text] [Related]

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