RET原癌基因 - Suppr

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The RET Protooncogene.

作者信息

Traugott Amber L, Moley Jeffrey F

出版信息

Cancer Treat Res. 2010;153:303-19. doi: 10.1007/978-1-4419-0857-5_17.

DOI:10.1007/978-1-4419-0857-5_17

PMID:19957232

Abstract

摘要

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The RET Protooncogene.RET原癌基因

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Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma.由于独特的C609S RET突变导致的多发性内分泌腺瘤病2A型表现为嗜铬细胞瘤和甲状腺髓样癌的低外显率。

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Experience of prophylactic thyroidectomy in multiple endocrine neoplasia type 2A kindreds with RET codon 804 mutations.2A 型多发性内分泌腺瘤病家系中 RET 密码子 804 突变患者预防性甲状腺切除术的经验。

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RET proto-oncogene mutations are restricted to codons 634 and 918 in mainland Chinese families with MEN2A and MEN2B.在患有MEN2A和MEN2B的中国大陆家系中，RET原癌基因突变仅限于密码子634和918。

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