Cargando…
Exome sequencing identifies somatic mutations in novel driver genes in non-small cell lung cancer
Lung cancer is the leading cause of cancer death worldwide and accounts for more than one-third of all newly diagnosed cancer cases in China. Therefore, it is of great clinical significance to explore new driver gene mutations in non-small-cell lung cancer (NSCLC). Using an initial bioinformatic ana...
Autores principales: | Zhang, Manman, Zhang, Lele, Li, Yan, Sun, Feng, Fang, Ya, Zhang, Ruijia, Wu, Jin, Zhou, Guanbiao, Song, Huaidong, Xue, Liqiong, Han, Bing, Zheng, Cuixia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377869/ https://www.ncbi.nlm.nih.gov/pubmed/32629428 http://dx.doi.org/10.18632/aging.103500 |
Ejemplares similares
-
Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma
por: Krauthammer, Michael, et al.
Publicado: (2012) -
Whole exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas
por: Fishbein, Lauren, et al.
Publicado: (2015) -
Whole-Exome Sequencing Identifies Novel Somatic Mutations in Chinese Breast Cancer Patients
por: Zhang, Yanfeng, et al.
Publicado: (2015) -
Whole-exome sequencing identifies somatic mutations and intratumor heterogeneity in inflammatory breast cancer
por: Luo, Rui, et al.
Publicado: (2021) -
Exome sequencing identifies somatic gain-of-function PPM1D mutations in brainstem gliomas
por: Zhang, Liwei, et al.
Publicado: (2014)