T1799A BRAF Mutation is Common in PUVA Lentigines

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The T1799A BRAF mutation is present in iris melanoma.

PURPOSE An activating mutation in exon 15 of the BRAF gene has been found in a high proportion of cutaneous pigmented lesions, but only in one case of uveal melanoma. Iris melanoma is the least common uveal melanoma and displays a less aggressive clinical course compared with posterior uveal melanoma. To date, no study has been conducted to investigate the T1799A mutation in iris melanoma. The ...

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T1799A BRAF mutations in conjunctival melanocytic lesions.

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Factors influencing the detection of the BRAF T1799A mutation in papillary thyroid carcinoma.

The BRAF T1799A mutation is a heterozygous point mutation and its reported prevalence in papillary thyroid carcinoma (PTC) has varied from 29 to 83%, with an overall mean of 44%. In Korea, the reported mutation rate reached 83% in PTC and 52% in micropapillary carcinoma. We hypothesized that the differences in prevalence may be influenced by the methods of mutation analysis, the sizes of tumor ...

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Surgical perspective of T1799A BRAF mutation diagnostic value in papillary thyroid carcinoma.

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ژورنال

عنوان ژورنال: Journal of Investigative Dermatology

سال: 2006

ISSN: 0022-202X

DOI: 10.1038/sj.jid.5700250