Mutually exclusive mutations in NOTCH1 and PIK3CA associated with clinical prognosis and chemotherapy responses of esophageal squamous cell carcinoma in China

BACKGROUND: Recurrent genetic abnormalities that correlate with clinical features could be used to determine patients' prognosis, select treatments and predict responses to therapy. Esophageal squamous cell carcinoma (ESCC) contains genomic alterations of undefined clinical significance. We aim...

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Detalles Bibliográficos
Autores principales: Song, Bin, Cui, Heyang, Li, Yaoping, Cheng, Caixia, Yang, Bin, Wang, Fang, Kong, Pengzhou, Li, Hongyi, Zhang, Ling, Jia, Zhiwu, Bi, Yanghui, Wang, Jiaqian, Zhou, Yong, Liu, Jing, Wang, Juan, Zhao, Zhenxiang, Zhang, Yanyan, Hu, Xiaoling, Shi, Ruyi, Yang, Jie, Liu, Haiyan, Yan, Ting, Li, Yike, Xu, Enwei, Qian, Yu, Xi, Yanfeng, Guo, Shiping, Chen, Yunqing, Wang, Jinfen, Li, Guodong, Liang, Jianfang, Jia, Junmei, Chen, Xing, Guo, Jiansheng, Wang, Tong, Zhang, Yanbo, Li, Qingshan, Wang, Chuangui, Cheng, Xiaolong, Zhan, Qimin, Cui, Yongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Clinical Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823130/
https://www.ncbi.nlm.nih.gov/pubmed/26528858
http://dx.doi.org/10.18632/oncotarget.6120

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