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Journal Abstract Search

241 related items for PubMed ID: 8595411

  • 1. Intragenic mutations of CDKN2B and CDKN2A in primary human esophageal cancers.
    Suzuki H, Zhou X, Yin J, Lei J, Jiang HY, Suzuki Y, Chan T, Hannon GJ, Mergner WJ, Abraham JM.
    Hum Mol Genet; 1995 Oct; 4(10):1883-7. PubMed ID: 8595411
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  • 2. Genomic DNA and messenger RNA expression alterations of the CDKN2B and CDKN2 genes in esophageal squamous carcinoma cell lines.
    Zhou X, Suzuki H, Shimada Y, Imamura M, Yin J, Jiang HY, Tarmin L, Abraham JM, Meltzer SJ.
    Genes Chromosomes Cancer; 1995 Aug; 13(4):285-90. PubMed ID: 7547637
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  • 3. Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas.
    Boström J, Meyer-Puttlitz B, Wolter M, Blaschke B, Weber RG, Lichter P, Ichimura K, Collins VP, Reifenberger G.
    Am J Pathol; 2001 Aug; 159(2):661-9. PubMed ID: 11485924
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  • 4. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients.
    Bassi CL, Martelli L, Cipolotti R, Scrideli CA, Defávery R, Tone LG.
    Braz J Med Biol Res; 2004 Nov; 37(11):1683-7. PubMed ID: 15517085
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  • 5. Fine-mapping loss of gene architecture at the CDKN2B (p15INK4b), CDKN2A (p14ARF, p16INK4a), and MTAP genes in head and neck squamous cell carcinoma.
    Worsham MJ, Chen KM, Tiwari N, Pals G, Schouten JP, Sethi S, Benninger MS.
    Arch Otolaryngol Head Neck Surg; 2006 Apr; 132(4):409-15. PubMed ID: 16618910
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  • 9. Infrequent mutations and no methylation of CDKN2A (P16/MTS1) and CDKN2B (p15/MTS2) in hepatocellular carcinoma in Taiwan.
    Lin YW, Chen CH, Huang GT, Lee PH, Wang JT, Chen DS, Lu FJ, Sheu JC.
    Eur J Cancer; 1998 Oct; 34(11):1789-95. PubMed ID: 9893670
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  • 11. Aberrant methylation of p16INK4a and deletion of p15INK4b are frequent events in human esophageal cancer in Linxian, China.
    Xing EP, Nie Y, Wang LD, Yang GY, Yang CS.
    Carcinogenesis; 1999 Jan; 20(1):77-84. PubMed ID: 9934853
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  • 12. High frequency of CDKN2A alterations in esophageal squamous cell carcinoma from a high-risk Chinese population.
    Hu N, Wang C, Su H, Li WJ, Emmert-Buck MR, Li G, Roth MJ, Tang ZZ, Lu N, Giffen C, Albert PS, Taylor PR, Goldstein AM.
    Genes Chromosomes Cancer; 2004 Mar; 39(3):205-16. PubMed ID: 14732922
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  • 13. Loss of chromosome arm 9p DNA and analysis of the p16 and p15 cyclin-dependent kinase inhibitor genes in human parathyroid adenomas.
    Tahara H, Smith AP, Gaz RD, Arnold A.
    J Clin Endocrinol Metab; 1996 Oct; 81(10):3663-7. PubMed ID: 8855819
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  • 15. Homozygous deletions at chromosome 9p21 and mutation analysis of p16 and p15 in microdissected primary non-small cell lung cancers.
    Packenham JP, Taylor JA, White CM, Anna CH, Barrett JC, Devereux TR.
    Clin Cancer Res; 1995 Jul; 1(7):687-90. PubMed ID: 9816033
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  • 18. Homozygous deletions but no sequence mutations in coding regions of p15 or p16 in human primary bladder tumors.
    Packenham JP, Taylor JA, Anna CH, White CM, Devereux TR.
    Mol Carcinog; 1995 Nov; 14(3):147-51. PubMed ID: 7576106
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