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Journal Abstract Search

124 related items for PubMed ID: 9192806

  • 1. Frequent mutation of the E2F-4 cell cycle gene in primary human gastrointestinal tumors.
    Souza RF, Yin J, Smolinski KN, Zou TT, Wang S, Shi YQ, Rhyu MG, Cottrell J, Abraham JM, Biden K, Simms L, Leggett B, Bova GS, Frank T, Powell SM, Sugimura H, Young J, Harpaz N, Shimizu K, Matsubara N, Meltzer SJ.
    Cancer Res; 1997 Jun 15; 57(12):2350-3. PubMed ID: 9192806
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  • 2. E2F-4 mutation in hereditary non-polyposis colorectal cancer.
    Moriyama H, Sasamoto H, Kambara T, Matsubara N, Ikeda M, Baba S, Meltzer SJ, Lynch HT, Shimizu K, Tanaka N.
    J Exp Clin Cancer Res; 2002 Jun 15; 21(2):185-9. PubMed ID: 12148576
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  • 3. Mutations of E2F-4 trinucleotide repeats in colorectal cancer with microsatellite instability.
    Yoshitaka T, Matsubara N, Ikeda M, Tanino M, Hanafusa H, Tanaka N, Shimizu K.
    Biochem Biophys Res Commun; 1996 Oct 14; 227(2):553-7. PubMed ID: 8878551
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  • 4. Various AGC repeat numbers in the coding region of the human transcription factor gene E2F-4.
    Zhong X, Hemmi H, Koike J, Tsujita K, Shimatake H.
    Hum Mutat; 2000 Mar 14; 15(3):296-7. PubMed ID: 10679953
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  • 5. Frequent alterations of the beta-catenin and TCF-4 genes, but not of the APC gene, in colon cancers with high-frequency microsatellite instability.
    Fukushima H, Yamamoto H, Itoh F, Horiuchi S, Min Y, Iku S, Imai K.
    J Exp Clin Cancer Res; 2001 Dec 14; 20(4):553-9. PubMed ID: 11876551
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  • 8. Multiple epithelial and nonepithelial tumors in hereditary nonpolyposis colorectal cancer: characterization of germline and somatic mutations of the MSH2 gene and heterogeneity of replication error phenotypes.
    Huang RL, Chao CF, Ding DC, Yu CP, Chang CC, Lai HC, Yu MH, Liu HS, Chu TY.
    Cancer Genet Cytogenet; 2004 Sep 14; 153(2):108-14. PubMed ID: 15350299
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  • 10. Frequent frameshift mutations of the TCF-4 gene in colorectal cancers with microsatellite instability.
    Duval A, Gayet J, Zhou XP, Iacopetta B, Thomas G, Hamelin R.
    Cancer Res; 1999 Sep 01; 59(17):4213-5. PubMed ID: 10485457
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  • 15. Exon 3 beta-catenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome.
    Johnson V, Volikos E, Halford SE, Eftekhar Sadat ET, Popat S, Talbot I, Truninger K, Martin J, Jass J, Houlston R, Atkin W, Tomlinson IP, Silver AR.
    Gut; 2005 Feb 01; 54(2):264-7. PubMed ID: 15647192
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  • 16. Accumulated frameshift mutations at coding nucleotide repeats during the progression of gastric carcinoma with microsatellite instability.
    Kim JJ, Baek MJ, Kim L, Kim NG, Lee YC, Song SY, Noh SH, Kim H.
    Lab Invest; 1999 Sep 01; 79(9):1113-20. PubMed ID: 10496529
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  • 18. p300 gene alterations in colorectal and gastric carcinomas.
    Muraoka M, Konishi M, Kikuchi-Yanoshita R, Tanaka K, Shitara N, Chong JM, Iwama T, Miyaki M.
    Oncogene; 1996 Apr 04; 12(7):1565-9. PubMed ID: 8622873
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  • 19. Mutations in beta-catenin and APC genes are uncommon in esophageal and esophagogastric junction adenocarcinomas.
    Choi YW, Heath EI, Heitmiller R, Forastiere AA, Wu TT.
    Mod Pathol; 2000 Oct 04; 13(10):1055-9. PubMed ID: 11048797
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  • 20. Genetic alteration of the beta-catenin gene (CTNNB1) in human lung cancer and malignant mesothelioma and identification of a new 3p21.3 homozygous deletion.
    Shigemitsu K, Sekido Y, Usami N, Mori S, Sato M, Horio Y, Hasegawa Y, Bader SA, Gazdar AF, Minna JD, Hida T, Yoshioka H, Imaizumi M, Ueda Y, Takahashi M, Shimokata K.
    Oncogene; 2001 Jul 12; 20(31):4249-57. PubMed ID: 11464291
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