Absence OF D1CER1, CTCF, RPL22, DNMT3A, TRRAP, IDH1 and 1DH2 hotspot mutations in patients with various subtypes of ovarian carcinomas

Cancer is caused by multiple genetic alterations within cells. Recently, large-scale sequencing has identified frequent ribonuclease type III (DICER1), CCCTC-binding factor (CTCF), ribosomal protein L22 (RPL22), DNA (cytosine-5-)-methyltransferase 3α (DNMT3A), transformation/transcription domain-ass...

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Veröffentlicht in:	Biomedical reports 2015-01, p.33
Hauptverfasser:	Zou, Yang, Huang, Mei-Zhen, Liu, Fa-Ying, Yang, Bi-Cheng, Wang, Li-Qun, Wang, Feng, Yu, Xiao-Hong, Wan, Lei, Wan, Xi-Di, Xu, Xiao-Yun, Li, Wei, Huang, Ou-Ping, He, Ming
Format:	Artikel
Sprache:	eng
Schlagworte:	Analysis Care and treatment Gene mutations Genetic aspects Health aspects Ovarian cancer Risk factors
Online-Zugang:	Volltext
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