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- W2890822878 abstract "Summary Background To investigate the difference in frequency of RAS mutations between nodular hyperplasia (NH), follicular thyroid adenomas (FTAs) and follicular thyroid carcinomas (FTCs) in a Korean population. Methods RAS mutations in 50 NH, 57 FTAs and 39 FTCs between January 2002 and May 2015 were analysed by pyrosequencing. Results Nine nodules of 50 NHs (18%), 18 nodules of 39 FTCs (46.2%) and 19 nodules of 57 FTAs (33.3%) harboured RAS mutations. Three FTCs and three FTAs showed two point mutations simultaneously. N‐RAS codon 61 (n = 6 of 9, 66.7%) and H‐RAS codon 61 (n = 3 of 9, 33.3%) were found in NHs. K‐RAS codons 12‐13, K‐RAS codon 61, N‐RAS codons 12‐13 and H‐RAS codons 12‐13 were not found in NHs. N‐RAS codon 61 (n = 7 of 21, 33.3%), K‐RAS codons 12‐13 (n = 6 of 21, 28.6%), H‐RAS codon 61 (n = 4 of 21, 19.0%), K‐RAS codon 61 (n = 3 of 21, 14.3%) and N‐RAS codons 12‐13 (n = 1 of 21, 4.7%) were found in FTCs, and N‐RAS codon 61 (n = 10 of 22, 45.5%), K‐RAS codons 12‐13 (n = 5 of 22, 22.7%), H‐RAS codon 61 (n = 5 of 22, 22.7%), K‐RAS codon 61 (n = 1 of 22, 4.5%) and N‐RAS codons 12‐13 (n = 1 of 22, 4.5%) were observed in FTAs. Conclusions The frequencies of RAS mutations among our Korean population were 18% in NHs, 46.2% in FTC and 33.3% in FTAs. N‐RAS codon 61 was the most frequent mutation in NHs, FTCs and FTAs, and the frequency was not significantly different among the three groups. K‐RAS codons 12‐13 were the second most commonly involved site in FTCs and FTAs, whereas no mutation was detected at this site in NHs." @default.
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- W2890822878 date "2018-09-03" @default.
- W2890822878 modified "2023-10-14" @default.
- W2890822878 title "Analysis of<i>RAS</i>mutation in thyroid nodular hyperplasia and follicular neoplasm in a Korean population" @default.
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- W2890822878 doi "https://doi.org/10.1002/edm2.40" @default.
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