MAGE‐C3 promotes cancer metastasis by inducing epithelial‐mesenchymal transition and immunosuppression in esophageal squamous cell carcinoma

por Wu, Qingnan, Zhang, Weimin, Wang, Yan, Min, Qingjie, Zhang, Hongyue, Dong, Dezuo, Zhan, Qimin
Publicado 2021

The m6A-induced lncRNA CASC8 promotes proliferation and chemoresistance via upregulation of hnRNPL in esophageal squamous cell carcinoma

por Wu, Qingnan, Zhang, Hongyue, Yang, Di, Min, Qingjie, Wang, Yan, Zhang, Weimin, Zhan, Qimin
Publicado 2022

Nuclear genome-derived circular RNA circPUM1 localizes in mitochondria and regulates oxidative phosphorylation in esophageal squamous cell carcinoma

por Gong, Wei, Xu, Jiancheng, Wang, Yan, Min, Qingjie, Chen, Xu, Zhang, Weimin, Chen, Jie, Zhan, Qimin
Publicado 2022

Exome-assistant: a rapid and easy detection of disease-related genes and genetic variations from exome sequencing

por Liu, Qi, Shen, Enjian, Min, Qingjie, Li, Xueying, Wang, Xin, Li, Xianfeng, Sun, Zhong Sheng, Wu, Jinyu
Publicado 2012

Genomic and epigenomic evolution of acquired resistance to combination therapy in esophageal squamous cell carcinoma

por Min, Qingjie, Wang, Yan, Wu, Qingnan, Li, Xianfeng, Teng, Huajing, Fan, Jiawen, Cao, Yiren, Fan, Pingsheng, Zhan, Qimin
Publicado 2021

Comparative transcriptome characterization of esophageal squamous cell carcinoma and adenocarcinoma

por Li, Xianfeng, Wang, Yan, Min, Qingjie, Zhang, Weimin, Teng, Huajing, Li, Chao, Zhang, Kun, Shi, Leisheng, Wang, Bin, Zhan, Qimin
Publicado 2023

Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

por Huang, Xiu-Feng, Xiang, Ping, Chen, Jie, Xing, Dong-Jun, Huang, Na, Min, Qingjie, Gu, Feng, Tong, Yi, Pang, Chi-Pui, Qu, Jia, Jin, Zi-Bing
Publicado 2013

The metabolic genomic atlas reveals potential drivers and clinically relevant insights into the etiology of esophageal squamous cell carcinoma

por Liu, Xuesong, Hong, Ruoxi, Du, Peina, Yang, Di, He, Meibo, Wu, Qingnan, Li, Lin, Wang, Yan, Chen, Jie, Min, Qingjie, Li, Jinting, Zhang, Weimin, Zhan, Qimin
Publicado 2022

Molecular Diagnosis of Putative Stargardt Disease by Capture Next Generation Sequencing

por Zhang, Xiao, Ge, Xianglian, Shi, Wei, Huang, Ping, Min, Qingjie, Li, Minghan, Yu, Xinping, Wu, Yaming, Zhao, Guangyu, Tong, Yi, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Publicado 2014

A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family

por Zhang, Liping, Shi, Wei, Song, Liming, Zhang, Xiao, Cheng, Lulu, Wang, Yanfang, Ge, Xianglian, Li, Wei, Zhang, Wei, Min, Qingjie, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Publicado 2014

Spatial transcriptomics delineates molecular features and cellular plasticity in lung adenocarcinoma progression

por Wang, Yan, Liu, Bing, Min, Qingjie, Yang, Xin, Yan, Shi, Ma, Yuanyuan, Li, Shaolei, Fan, Jiawen, Wang, Yaqi, Dong, Bin, Teng, Huajing, Lin, Dongmei, Zhan, Qimin, Wu, Nan
Publicado 2023

CDK7-YAP-LDHD axis promotes D-lactate elimination and ferroptosis defense to support cancer stem cell-like properties

por Lv, Mengzhu, Gong, Ying, Liu, Xuesong, Wang, Yan, Wu, Qingnan, Chen, Jie, Min, Qingjie, Zhao, Dongyu, Li, Xianfeng, Chen, Dongshao, Yang, Di, Yeerken, Danna, Liu, Rui, Li, Jinting, Zhang, Weimin, Zhan, Qimin
Publicado 2023