Genomic comparison of esophageal squamous cell carcinoma and its precursor lesions by multi-region whole-exome sequencing
The pathogenesis of oesophageal squamous cell carcinoma is a multi-step process but the genetic determinants behind this progression are unknown. Here the authors use multi-region exome sequencing to comprehensively investigate the genetic evolution of precursor dysplastic lesions and untransformed...
Guardado en:
Autores principales: | Xi-Xi Chen, Qian Zhong, Yang Liu, Shu-Mei Yan, Zhang-Hua Chen, Shan-Zhao Jin, Tian-Liang Xia, Ruo-Yan Li, Ai-Jun Zhou, Zhe Su, Yu-Hua Huang, Qi-Tao Huang, Li-Yun Huang, Xing Zhang, Yan-Na Zhao, Jin-Ping Yun, Qiu-Liang Wu, Dong-Xin Lin, Fan Bai, Mu-Sheng Zeng |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/3432ab8a3ea44a19a8be00b2d3f5e2fc |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Comparative genomic analysis of esophageal squamous cell carcinoma between Asian and Caucasian patient populations
por: Jiaying Deng, et al.
Publicado: (2017) -
Exome sequencing identifies novel somatic variants in African American esophageal squamous cell carcinoma
por: Hayriye Verda Erkizan, et al.
Publicado: (2021) -
Whole-exome sequencing reveals the origin and evolution of hepato-cholangiocarcinoma
por: Anqiang Wang, et al.
Publicado: (2018) -
High expression of GOLPH3 in esophageal squamous cell carcinoma correlates with poor prognosis.
por: Jian-Hua Wang, et al.
Publicado: (2012) -
Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability
por: Chunyan Jin, et al.
Publicado: (2021)