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Journal Abstract Search

123 related items for PubMed ID: 15239143

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Pediatric adrenocortical tumors: molecular events leading to insulin-like growth factor II gene overexpression.
    Wilkin F, Gagné N, Paquette J, Oligny LL, Deal C.
    J Clin Endocrinol Metab; 2000 May; 85(5):2048-56. PubMed ID: 10843195
    [Abstract] [Full Text] [Related]

  • 23. Genetic alterations in hepatoblastoma and hepatocellular carcinoma: common and distinctive aspects.
    Buendia MA.
    Med Pediatr Oncol; 2002 Nov; 39(5):530-5. PubMed ID: 12228912
    [Abstract] [Full Text] [Related]

  • 24. The 11p15.5 ribonucleotide reductase M1 subunit locus is not imprinted in Wilms' tumour and hepatoblastoma.
    Byrne JA, Smith PJ.
    Hum Genet; 1993 Apr; 91(3):275-7. PubMed ID: 8386696
    [Abstract] [Full Text] [Related]

  • 25. Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.
    Lee MP, Reeves C, Schmitt A, Su K, Connors TD, Hu RJ, Brandenburg S, Lee MJ, Miller G, Feinberg AP.
    Cancer Res; 1998 Sep 15; 58(18):4155-9. PubMed ID: 9751628
    [Abstract] [Full Text] [Related]

  • 26. Loss of heterozygosity at chromosome 11p15 in Wilms tumors: identification of two independent regions.
    Karnik P, Chen P, Paris M, Yeger H, Williams BR.
    Oncogene; 1998 Jul 16; 17(2):237-40. PubMed ID: 9674708
    [Abstract] [Full Text] [Related]

  • 27. Amplification and overexpression of the IGF2 regulator PLAG1 in hepatoblastoma.
    Zatkova A, Rouillard JM, Hartmann W, Lamb BJ, Kuick R, Eckart M, von Schweinitz D, Koch A, Fonatsch C, Pietsch T, Hanash SM, Wimmer K.
    Genes Chromosomes Cancer; 2004 Feb 16; 39(2):126-37. PubMed ID: 14695992
    [Abstract] [Full Text] [Related]

  • 28. Blocking the hedgehog pathway inhibits hepatoblastoma growth.
    Eichenmüller M, Gruner I, Hagl B, Häberle B, Müller-Höcker J, von Schweinitz D, Kappler R.
    Hepatology; 2009 Feb 16; 49(2):482-90. PubMed ID: 19177589
    [Abstract] [Full Text] [Related]

  • 29. Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples.
    Schwienbacher C, Sabbioni S, Campi M, Veronese A, Bernardi G, Menegatti A, Hatada I, Mukai T, Ohashi H, Barbanti-Brodano G, Croce CM, Negrini M.
    Proc Natl Acad Sci U S A; 1998 Mar 31; 95(7):3873-8. PubMed ID: 9520460
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Molecular cloning and characterization of a novel human BTB domain-containing gene, BTBD10, which is down-regulated in glioma.
    Chen J, Xu J, Ying K, Cao G, Hu G, Wang L, Luo C, Lou M, Mao Y, Xie Y, Lu Y.
    Gene; 2004 Sep 29; 340(1):61-9. PubMed ID: 15556295
    [Abstract] [Full Text] [Related]

  • 32. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
    Gaston V, Le Bouc Y, Soupre V, Burglen L, Donadieu J, Oro H, Audry G, Vazquez MP, Gicquel C.
    Eur J Hum Genet; 2001 Jun 29; 9(6):409-18. PubMed ID: 11436121
    [Abstract] [Full Text] [Related]

  • 33. Analysis of loss of heterozygosity on chromosomes 10q, 11, and 16 in medulloblastomas.
    Yin XL, Pang JC, Liu YH, Chong EY, Cheng Y, Poon WS, Ng HK.
    J Neurosurg; 2001 May 29; 94(5):799-805. PubMed ID: 11354413
    [Abstract] [Full Text] [Related]

  • 34. High-density marker analysis of 11p15.5 in non-small cell lung carcinomas reveals allelic deletion of one shared and one distinct region when compared to breast carcinomas.
    Tran YK, Newsham IF.
    Cancer Res; 1996 Jul 01; 56(13):2916-21. PubMed ID: 8674040
    [Abstract] [Full Text] [Related]

  • 35. [Genomic imbalance and chromosome disorders in hepatoblastoma].
    Gao H, Zhang ZB, Ou YL, Zhang KR, Wang WL.
    Zhonghua Zhong Liu Za Zhi; 2006 Dec 01; 28(12):915-9. PubMed ID: 17533743
    [Abstract] [Full Text] [Related]

  • 36. MicroRNA-492 is processed from the keratin 19 gene and up-regulated in metastatic hepatoblastoma.
    von Frowein J, Pagel P, Kappler R, von Schweinitz D, Roscher A, Schmid I.
    Hepatology; 2011 Mar 01; 53(3):833-42. PubMed ID: 21319197
    [Abstract] [Full Text] [Related]

  • 37. Selective maternal-allele loss in human lung cancers of the maternally expressed p57KIP2 gene at 11p15.5.
    Kondo M, Matsuoka S, Uchida K, Osada H, Nagatake M, Takagi K, Harper JW, Takahashi T, Elledge SJ, Takahashi T.
    Oncogene; 1996 Mar 21; 12(6):1365-8. PubMed ID: 8649840
    [Abstract] [Full Text] [Related]

  • 38. Genetic mosaicism at the insulin locus in liver associated with childhood hepatoblastoma.
    Simms LA, Reeve AE, Smith PJ.
    Genes Chromosomes Cancer; 1995 May 21; 13(1):72-3. PubMed ID: 7541647
    [Abstract] [Full Text] [Related]

  • 39. Loss of imprinting in hepatoblastoma.
    Rainier S, Dobry CJ, Feinberg AP.
    Cancer Res; 1995 May 01; 55(9):1836-8. PubMed ID: 7728748
    [Abstract] [Full Text] [Related]

  • 40. Mutational spectrum of beta-catenin, AXIN1, and AXIN2 in hepatocellular carcinomas and hepatoblastomas.
    Taniguchi K, Roberts LR, Aderca IN, Dong X, Qian C, Murphy LM, Nagorney DM, Burgart LJ, Roche PC, Smith DI, Ross JA, Liu W.
    Oncogene; 2002 Jul 18; 21(31):4863-71. PubMed ID: 12101426
    [Abstract] [Full Text] [Related]

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