RepAHR: an improved approach for de novo repeat identification by assembly of the high-frequency reads

por Liao, Xingyu, Gao, Xin, Zhang, Xiankai, Wu, Fang-Xiang, Wang, Jianxin
Publicado 2020

Prognostic role of Toll-like receptors in cancer: a meta-analysis

por Wang, Qingwen, Zhang, Xiankai, Xiao, Tingting, Pan, Chenhua, Liu, Xing, Zhao, Yulan
Publicado 2018

Identification and Characterization of a Germline Mutation in CARD11 From a Chinese Case of B Cell Expansion With NF-κB and T Cell Anergy

por Zhao, Peiwei, Meng, Qingjie, Huang, Yufeng, Zhang, Lei, Luo, Sukun, Zhang, Xiankai, Tan, Li, Zhou, Aifen, Xiong, Hao, He, Xuelian
Publicado 2021

Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

por Zhang, Lei, Hu, Yanqiu, Lu, Jingjing, Zhao, Peiwei, Zhang, Xiankai, Tan, Li, Li, Jun, Xiao, Cuiping, Zeng, Linkong, He, Xuelian
Publicado 2022

A novel CARD11 germline mutation in a Chinese patient of B cell expansion with NF-κB and T cell anergy (BENTA) and literature review

por Zhao, Peiwei, Hu, Yanqiu, Sun, Dongming, Meng, Qingjie, Zhang, Lei, Zhang, Xiankai, Tan, Li, Zhang, Yong, Ding, Yan, He, Xuelian
Publicado 2022

Corrigendum: Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

por Zhang, Lei, Hu, Yanqiu, Lu, Jingjing, Zhao, Peiwei, Zhang, Xiankai, Tan, Li, Li, Jun, Xiao, Cuiping, Zeng, Linkong, He, Xuelian
Publicado 2022

Pathohistological investigation of osteochondral tissue obtained during total knee arthroplasty after osteochondral autologous transfer: a case report

por Tanima-Nagai, Momoko, Harada, Hideto, Aoyama, Tomoki, Yamaguchi, Shoki, Ito, Akira, Tajino, Junichi, Iijima, Hirotaka, Zhang, Xiankai, Kuroki, Hiroshi, Kobayashi, Masahiko
Publicado 2017