Your browser doesn't support javascript.
loading
Next-generation sequencing reveals heterogeneous genetic alterations in key signaling pathways of mismatch repair deficient colorectal carcinomas.
Wang, Jing; Li, Ruiyu; He, Yangzhige; Yi, Yuting; Wu, Huanwen; Liang, Zhiyong.
Afiliação
  • Wang J; Department of Pathology, Molecular Pathology Research Center, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Li R; Department of Pathology, Molecular Pathology Research Center, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • He Y; Department of Medical Research Center, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Yi Y; Geneplus-Beijing Institute, Beijing, China.
  • Wu H; Department of Pathology, Molecular Pathology Research Center, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. wuhuanwen10700@pumch.cn.
  • Liang Z; Department of Pathology, Molecular Pathology Research Center, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. liangzhiyong1220@yahoo.com.
Mod Pathol ; 33(12): 2591-2601, 2020 12.
Article em En | MEDLINE | ID: mdl-32620917
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise Mutacional de DNA / Neoplasias Colorretais / Transdução de Sinais / Biomarcadores Tumorais / Heterogeneidade Genética / Reparo de Erro de Pareamento de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise Mutacional de DNA / Neoplasias Colorretais / Transdução de Sinais / Biomarcadores Tumorais / Heterogeneidade Genética / Reparo de Erro de Pareamento de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article