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Frequent loss of heterozygosity on chromosomes 3p and 17p without VHL or p53 mutations suggests involvement of unidentified tumor suppressor genes in follicular thyroid carcinoma.
Grebe SK, McIver B, Hay ID, Wu PS, Maciel LM, Drabkin HA, Goellner JR, Grant CS, Jenkins RB, Eberhardt NL. Grebe SK, et al. Among authors: eberhardt nl. J Clin Endocrinol Metab. 1997 Nov;82(11):3684-91. doi: 10.1210/jcem.82.11.4352. J Clin Endocrinol Metab. 1997. PMID: 9360526
High resolution loss of heterozygosity mapping of 17p13 in thyroid cancer: Hurthle cell carcinomas exhibit a small 411-kilobase common region of allelic imbalance, probably containing a novel tumor suppressor gene.
Farrand K, Delahunt B, Wang XL, McIver B, Hay ID, Goellner JR, Eberhardt NL, Grebe SK. Farrand K, et al. Among authors: eberhardt nl. J Clin Endocrinol Metab. 2002 Oct;87(10):4715-21. doi: 10.1210/jc.2002-020708. J Clin Endocrinol Metab. 2002. PMID: 12364463
PPARgamma staining as a surrogate for PAX8/PPARgamma fusion oncogene expression in follicular neoplasms: clinicopathological correlation and histopathological diagnostic value.
Sahin M, Allard BL, Yates M, Powell JG, Wang XL, Hay ID, Zhao Y, Goellner JR, Sebo TJ, Grebe SK, Eberhardt NL, McIver B. Sahin M, et al. Among authors: eberhardt nl. J Clin Endocrinol Metab. 2005 Jan;90(1):463-8. doi: 10.1210/jc.2004-1203. Epub 2004 Oct 13. J Clin Endocrinol Metab. 2005. PMID: 15483076
116 results