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肝细胞肝癌组织中PTEN和p53蛋白的表达 被引量:4

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出处 《临床与实验病理学杂志》 CAS CSCD 2002年第1期113-114,共2页 Chinese Journal of Clinical and Experimental Pathology
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  • 1[1]Steck PA, Pershouse MA, Jasser SA et al. Identification of candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancer. Nat Genet, 1997;15:356~62
  • 2[2]Li J, Yen C, Liaw D et al. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast and prostate cancer. Science, 1997;275:1943~7
  • 3[3]Myers MP, Stolarov P, Eng C. PTEN, the tumor suppressor form human 10q23, is a dual specificity phosphatase. Proc Natl Acad Sci USA, 1997;94:9052~7
  • 4[4]Maehama T, Dixon JE. The tumor suppressor, PTEN/MMAC1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-triphosphate. J Biol Chem, 1998;273:13375~8
  • 5[5]Piao Z, Park C, Park JH et al. Allelotype analysis of hepatocellular carcinomas. Int J Cancer, 1998;75:29~33
  • 6[6]Furnari FB, Lin H, Huang HS et al. Growth suppression of glioma cells by PTEN requires a functional phosphatase canalytic domain. Proc Natl Acad Sci USA, 1997;94:12479~84
  • 7[7]Myers MP, Pass I, Barry IH et al. The lipid phosphatase activity of PTEN is critical for its tumor suppressor function. Proc Natl Acad Sci USA, 1998;95:13513~8
  • 8[8]Li J, Simpson L, Takaheshi M et al. The PTEN/MMAC1 tumor suppressor induces cell death that is rescued by the AKT/protein kinase B oncogene. Cancer Res, 1998;58:5667~72

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