- A Korean Family of Familial Medullary Thyroid Cancer with Cys618Ser RET Germline Mutation
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Jung J, Uchino S, Lee Y, Park H
- KMID: 1779251
- J Korean Med Sci.
- 2010 Feb;25(2):226-229.
- doi: 10.3346/jkms.2010.25.2.226
Familial medullary thyroid carcinoma (FMTC) is caused by autosomal dominant gain-of-function mutations in the RET proto-oncogene. An identifiable RET mutation can be detected in about 85% of FMTC families. The... -
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- Detection of Plasma BRAF(V600E) Mutation Is Associated with Lung Metastasis in Papillary Thyroid Carcinomas
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Kim BH, Kim IJ, Lee BJ, Lee JC, Kim IS, Kim SJ, Kim WJ, Jeon YK, Kim SS, Kim YK
- KMID: 2450335
- Yonsei Med J.
- 2015 May;56(3):634-640.
- doi: 10.3349/ymj.2015.56.3.634
PURPOSE: The BRAF(V600E) mutation represents a novel indicator of the progression and aggressiveness of papillary thyroid carcinoma (PTC). The purpose of this study was to determine the clinical significance of... -
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- NAD(P)H: Quinone Oxidoreductase 1 and NRH:Quinone Oxidoreductase 2 Polymorphisms in Papillary Thyroid Microcarcinoma: Correlation with Phenotype
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Lee J, Kim KS, Lee MH, Kim YS, Lee MH, Lee SE, Kim YK, Ryu MJ, Kim SJ, Choi MJ, Jo YS
- KMID: 1793163
- Yonsei Med J.
- 2013 Sep;54(5):1158-1167.
- doi: 10.3349/ymj.2013.54.5.1158
PURPOSE: NAD(P)H:Quinone Oxidoreductase 1 (NQO1) C609T missense variant (NQO1*2) and 29 basepair (bp)-insertion/deletion (I29/D) polymorphism of the NRH:Quinone Oxidoreductase 2 (NQO2) gene promoter have been proposed as predictive and prognostic... -
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