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Journal Abstract Search
404 related items for PubMed ID: 9354427
1. Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors. Dahia PL, Marsh DJ, Zheng Z, Zedenius J, Komminoth P, Frisk T, Wallin G, Parsons R, Longy M, Larsson C, Eng C. Cancer Res; 1997 Nov 01; 57(21):4710-3. PubMed ID: 9354427 [Abstract] [Full Text] [Related]
2. Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas. Marsh DJ, Zheng Z, Zedenius J, Kremer H, Padberg GW, Larsson C, Longy M, Eng C. Cancer Res; 1997 Feb 01; 57(3):500-3. PubMed ID: 9012481 [Abstract] [Full Text] [Related]
3. Mitochondrial D-Loop instability in thyroid tumours is not a marker of malignancy. Máximo V, Lima J, Soares P, Botelho T, Gomes L, Sobrinho-Simões M. Mitochondrion; 2005 Oct 01; 5(5):333-40. PubMed ID: 16183030 [Abstract] [Full Text] [Related]
4. Somatic mutations of the PTEN tumor suppressor gene in sporadic follicular thyroid tumors. Halachmi N, Halachmi S, Evron E, Cairns P, Okami K, Saji M, Westra WH, Zeiger MA, Jen J, Sidransky D. Genes Chromosomes Cancer; 1998 Nov 01; 23(3):239-43. PubMed ID: 9790504 [Abstract] [Full Text] [Related]
5. Genetic mutations in thyroid carcinoma. Taccaliti A, Boscaro M. Minerva Endocrinol; 2009 Mar 01; 34(1):11-28. PubMed ID: 19209125 [Abstract] [Full Text] [Related]
11. PTEN/MMAC1 mutations in endometrial cancers. Risinger JI, Hayes AK, Berchuck A, Barrett JC. Cancer Res; 1997 Nov 01; 57(21):4736-8. PubMed ID: 9354433 [Abstract] [Full Text] [Related]
14. Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome. Marsh DJ, Roth S, Lunetta KL, Hemminki A, Dahia PL, Sistonen P, Zheng Z, Caron S, van Orsouw NJ, Bodmer WF, Cottrell SE, Dunlop MG, Eccles D, Hodgson SV, Järvinen H, Kellokumpu I, Markie D, Neale K, Phillips R, Rozen P, Syngal S, Vijg J, Tomlinson IP, Aaltonen LA, Eng C. Cancer Res; 1997 Nov 15; 57(22):5017-21. PubMed ID: 9371495 [Abstract] [Full Text] [Related]
15. Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas. Gimm O, Chi H, Dahia PL, Perren A, Hinze R, Komminoth P, Dralle H, Reynolds PR, Eng C. J Clin Endocrinol Metab; 2001 Apr 15; 86(4):1801-5. PubMed ID: 11297621 [Abstract] [Full Text] [Related]
16. Silencing of the PTEN tumor-suppressor gene in anaplastic thyroid cancer. Frisk T, Foukakis T, Dwight T, Lundberg J, Höög A, Wallin G, Eng C, Zedenius J, Larsson C. Genes Chromosomes Cancer; 2002 Sep 15; 35(1):74-80. PubMed ID: 12203792 [Abstract] [Full Text] [Related]
17. Differential loss of heterozygosity at 7q31.2 in follicular and papillary thyroid tumors. Zhang JS, Nelson M, McIver B, Hay ID, Goellner JR, Grant CS, Eberhardt NL, Smith DI. Oncogene; 1998 Aug 13; 17(6):789-93. PubMed ID: 9715281 [Abstract] [Full Text] [Related]
18. The natural protein kinase C alpha mutant is present in human thyroid neoplasms. Prévostel C, Alvaro V, de Boisvilliers F, Martin A, Jaffiol C, Joubert D. Oncogene; 1995 Aug 17; 11(4):669-74. PubMed ID: 7651730 [Abstract] [Full Text] [Related]