Goellner JR - Search Results

1

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: goellner jr. J Clin Endocrinol Metab. 1997 Nov;82(11):3684-91. doi: 10.1210/jcem.82.11.4352. J Clin Endocrinol Metab. 1997. PMID: 9360526

2

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: goellner jr. J Clin Endocrinol Metab. 2002 Oct;87(10):4715-21. doi: 10.1210/jc.2002-020708. J Clin Endocrinol Metab. 2002. PMID: 12364463

3

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: goellner jr. 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

4

FHIT and TSG101 in thyroid tumours: aberrant transcripts reflect rare abnormal RNA processing events of uncertain pathogenetic or clinical significance.

McIver B, Grebe SKG, Wang L, Hay ID, Yokomizo, Liu W, Goellner JR, Grant CS, Smith DI, Eberhardt NL. McIver B, et al. Among authors: goellner jr. Clin Endocrinol (Oxf). 2000 Jun;52(6):749-757. doi: 10.1046/j.1365-2265.2000.01009.x. Clin Endocrinol (Oxf). 2000. PMID: 28796361

5

Frequent occurrence of cytogenetic abnormalities in sporadic nonmedullary thyroid carcinoma.

Jenkins RB, Hay ID, Herath JF, Schultz CG, Spurbeck JL, Grant CS, Goellner JR, Dewald GW. Jenkins RB, et al. Among authors: goellner jr. Cancer. 1990 Sep 15;66(6):1213-20. doi: 10.1002/1097-0142(19900915)66:6<1213::aid-cncr2820660622>3.0.co;2-9. Cancer. 1990. PMID: 2400971

6

Distant metastases in papillary thyroid carcinoma: 100 cases observed at one institution during 5 decades.

Dinneen SF, Valimaki MJ, Bergstralh EJ, Goellner JR, Gorman CA, Hay ID. Dinneen SF, et al. Among authors: goellner jr. J Clin Endocrinol Metab. 1995 Jul;80(7):2041-5. doi: 10.1210/jcem.80.7.7608252. J Clin Endocrinol Metab. 1995. PMID: 7608252

7

Extracervical fibrosclerosis causing obstruction of a ventriculo-peritoneal shunt in a patient with hydrocephalus and invasive fibrous thyroiditis (Riedel's struma).

Natt N, Heufelder AE, Hay ID, Grant CS, Goellner JR. Natt N, et al. Among authors: goellner jr. Clin Endocrinol (Oxf). 1997 Jul;47(1):107-11. doi: 10.1046/j.1365-2265.1997.1941028.x. Clin Endocrinol (Oxf). 1997. PMID: 9302380

8

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. Zhang JS, et al. Among authors: goellner jr. Oncogene. 1998 Aug 13;17(6):789-93. doi: 10.1038/sj.onc.1201996. Oncogene. 1998. PMID: 9715281

9

FHIT and TSG101 in thyroid tumours: aberrant transcripts reflect rare abnormal RNA processing events of uncertain pathogenetic or clinical significance.

McIver B, Grebe SK, Wang L, Hay ID, Yokomizo A, Liu W, Goellner JR, Grant CS, Smith DI, Eberhardt NL. McIver B, et al. Among authors: goellner jr. Clin Endocrinol (Oxf). 2000 Jun;52(6):749-57. Clin Endocrinol (Oxf). 2000. PMID: 10848880

10

Immunohistochemical analysis of sodium iodide symporter expression in metastatic differentiated thyroid cancer: correlation with radioiodine uptake.

Castro MR, Bergert ER, Goellner JR, Hay ID, Morris JC. Castro MR, et al. Among authors: goellner jr. J Clin Endocrinol Metab. 2001 Nov;86(11):5627-32. doi: 10.1210/jcem.86.11.8048. J Clin Endocrinol Metab. 2001. PMID: 11701745

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