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Journal Abstract Search

176 related items for PubMed ID: 1322376

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  • 3. Prognostic impact of multiple allelic losses on metastatic recurrence in hepatocellular carcinoma after curative resection.
    Nishida N, Fukuda Y, Komeda T, Ito T, Nishimura T, Minata M, Kuno M, Katsuma H, Ikai I, Yamaoka Y, Nakao K.
    Oncology; 2002; 62(2):141-8. PubMed ID: 11914600
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  • 4. Accumulation of genetic changes during development and progression of hepatocellular carcinoma: loss of heterozygosity of chromosome arm 1p occurs at an early stage of hepatocarcinogenesis.
    Kuroki T, Fujiwara Y, Tsuchiya E, Nakamori S, Imaoka S, Kanematsu T, Nakamura Y.
    Genes Chromosomes Cancer; 1995 Jul; 13(3):163-7. PubMed ID: 7669735
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  • 5. Comprehensive allelotype study of hepatocellular carcinoma: potential differences in pathways to hepatocellular carcinoma between hepatitis B virus-positive and -negative tumors.
    Okabe H, Ikai I, Matsuo K, Satoh S, Momoi H, Kamikawa T, Katsura N, Nishitai R, Takeyama O, Fukumoto M, Yamaoka Y.
    Hepatology; 2000 May; 31(5):1073-9. PubMed ID: 10796882
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  • 6. Evidence for the presence of two tumour-suppressor genes for hepatocellular carcinoma on chromosome 13q.
    Kuroki T, Fujiwara Y, Nakamori S, Imaoka S, Kanematsu T, Nakamura Y.
    Br J Cancer; 1995 Aug; 72(2):383-5. PubMed ID: 7640222
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  • 8. Loss of somatic heterozygosity in hepatocellular carcinoma.
    Walker GJ, Hayward NK, Falvey S, Cooksley WG.
    Cancer Res; 1991 Aug 15; 51(16):4367-70. PubMed ID: 1678314
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  • 9. Allelotype study of primary hepatocellular carcinoma.
    Fujimori M, Tokino T, Hino O, Kitagawa T, Imamura T, Okamoto E, Mitsunobu M, Ishikawa T, Nakagama H, Harada H.
    Cancer Res; 1991 Jan 01; 51(1):89-93. PubMed ID: 1670995
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  • 10. Accumulation of genetic alterations and progression of primary breast cancer.
    Sato T, Akiyama F, Sakamoto G, Kasumi F, Nakamura Y.
    Cancer Res; 1991 Nov 01; 51(21):5794-9. PubMed ID: 1682035
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  • 12. Clonality analysis of multiple hepatocellular carcinomas by loss of heterozygosity pattern determined by chromosomes 16q and 13q.
    Lin YW, Lee HS, Chen CH, Huang GT, Lee PH, Sheu JC.
    J Gastroenterol Hepatol; 2005 Apr 01; 20(4):536-46. PubMed ID: 15836701
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  • 14. Frequent loss of heterozygosity on chromosomes 16 and 4 in human hepatocellular carcinoma.
    Zhang WD, Hirohashi S, Tsuda H, Shimosato Y, Yokota J, Terada M, Sugimura T.
    Jpn J Cancer Res; 1990 Feb 01; 81(2):108-11. PubMed ID: 1970554
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  • 15. Molecular cytogenetic evaluation of virus-associated and non-viral hepatocellular carcinoma: analysis of 26 carcinomas and 12 concurrent dysplasias.
    Zondervan PE, Wink J, Alers JC, IJzermans JN, Schalm SW, de Man RA, van Dekken H.
    J Pathol; 2000 Oct 01; 192(2):207-15. PubMed ID: 11004697
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  • 16. Deletions of chromosome 13q, mutations in Retinoblastoma 1, and retinoblastoma protein state in human hepatocellular carcinoma.
    Zhang X, Xu HJ, Murakami Y, Sachse R, Yashima K, Hirohashi S, Hu SX, Benedict WF, Sekiya T.
    Cancer Res; 1994 Aug 01; 54(15):4177-82. PubMed ID: 8033150
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  • 17. Correlation of loss of alleles on the short arms of chromosomes 11 and 17 with metastasis of primary breast cancer to lymph nodes.
    Takita K, Sato T, Miyagi M, Watatani M, Akiyama F, Sakamoto G, Kasumi F, Abe R, Nakamura Y.
    Cancer Res; 1992 Jul 15; 52(14):3914-7. PubMed ID: 1617666
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