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cystadenocarcinoma/tyrosine

Veza se sprema u međuspremnik
ČlanciKliničkim ispitivanjimaPatenti
3 rezultati
Gain-of-function mutations in the gene encoding the receptor tyrosine kinase RET have been identified as the aetiological factor for multiple endocrine neoplasia type 2A (MEN2A). MEN2A is a dominantly-inherited cancer predisposition syndrome characterized by medullary thyroid carcinoma, a tumour of
Exosomes have emerged as important mediators of diverse biological functions including tumor suppression, tumor progression, invasion, immune escape and cell-to-cell communication, through the release of molecules such as mRNAs, miRNAs, and proteins. Here, we identified differentially expressed

Clinicopathologic and molecular characterization of mammary analogue secretory carcinoma of salivary gland origin.

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Prijavite se / prijavite se
BACKGROUND Mammary analogue secretory carcinoma (MASC) is a newly recognized salivary gland tumor that harbors a characteristic balanced chromosomal translocation t (12; 15) (p13; q25) resulting in an ETV6-NTRK3 fusion gene. METHODS Retrospective study of 111 salivary gland carcinomas revealed 37
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