Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Xiankai Zhang"'
Autor:
Peiwei Zhao, Juan Huang, Huicong Fu, Jiali Xu, Tianhong Li, Xiankai Zhang, Qingjie Meng, Lei Zhang, Li Tan, Wen Zhang, Hebin Chen, Xiaoxia Lu, Yan Ding, Xuelian He
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-8 (2024)
Abstract Background Germline heterozygous gain-of-function (GOF) mutations in the PIK3CD gene lead to a rare primary immunodeficiency disease known as activated phosphoinositide 3-kinase (PI3K) δ syndrome type 1(APDS1). Affected patients present a s
Externí odkaz:
https://doaj.org/article/2cbeb84ea3e94977b23db5c4f24a9164
Autor:
Lei Zhang, Yanqiu Hu, Jingjing Lu, Peiwei Zhao, Xiankai Zhang, Li Tan, Jun Li, Cuiping Xiao, Linkong Zeng, Xuelian He
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/859d5ddd4cf84b5ab4d60d3a123ba291
Autor:
Peiwei Zhao, Yanqiu Hu, Dongming Sun, Qingjie Meng, Lei Zhang, Xiankai Zhang, Li Tan, Yong Zhang, Yan Ding, Xuelian He
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Germline gain-of-function (GOF) mutations in the CARD11 gene lead to a rare primary immunodeficiency disease known as B cell expansion with NF-κB and T cell anergy (BENTA). Affected patients present with a polyclonal expansion of B cells, lymphadeno
Externí odkaz:
https://doaj.org/article/8f266e0a99594ea8baac04f9cf55bc8f
Autor:
Lei Zhang, Yanqiu Hu, Jingjing Lu, Peiwei Zhao, Xiankai Zhang, Li Tan, Jun Li, Cuiping Xiao, Linkong Zeng, Xuelian He
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Uniparental disomy (UPD) is a rare genetic event caused by errors during gametogenesis and fertilization leading to two copies of a chromosome or chromosomal region inherited from one parent. MixUPD is one type of UPD that contains isodisomic and het
Externí odkaz:
https://doaj.org/article/0b826dc9a6a740369c7406c54be25cd3
Publikováno v:
BMC Bioinformatics, Vol 21, Iss 1, Pp 1-24 (2020)
Abstract Background Repetitive sequences account for a large proportion of eukaryotes genomes. Identification of repetitive sequences plays a significant role in many applications, such as structural variation detection and genome assembly. Many exis
Externí odkaz:
https://doaj.org/article/63e368c2f83e4ecfac65fa8f27828ce2
Autor:
Peiwei Zhao, Qingjie Meng, Yufeng Huang, Lei Zhang, Sukun Luo, Xiankai Zhang, Li Tan, Aifen Zhou, Hao Xiong, Xuelian He
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder caused by gain-of-function (GOF) mutations in the CARD11 gene. Affected patients present with persistent B cell lymphocytosis in early childhood paired
Externí odkaz:
https://doaj.org/article/efbc2bbdd54040c3ac21b25946ae20c4
Autor:
Momoko Tanima-Nagai, Hideto Harada, Tomoki Aoyama, Shoki Yamaguchi, Akira Ito, Junichi Tajino, Hirotaka Iijima, Xiankai Zhang, Hiroshi Kuroki, Masahiko Kobayashi
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
Abstract Background Osteochondral autologous transfer is one of the repair techniques for cartilage defects of knee with promising knee function recovery. There are no reports including histopathological images concerning human osteochondral tissue a
Externí odkaz:
https://doaj.org/article/ffd26b50b303401293e782db4edb69cb
Autor:
Peiwei Zhao, Qingjie Meng, Chunhui Wan, Tao Lei, Lei Zhang, Xiankai Zhang, Li Tan, Hongmin Zhu, Xuelian He
Publikováno v:
neurogenetics. 24:129-136
Autor:
Juan Du, Yanqiu Hu, Miaomiao Hou, Jingyi Zhou, Feiyan Xiang, Hao Zheng, Xiankai Zhang, Xuelian He, Han Xiao
Publikováno v:
Fish & Shellfish Immunology. 137:108803
Autor:
Lei Zhang, Yufeng Huang, Xuelian He, Sukun Luo, Xiankai Zhang, Aifen Zhou, Hao Xiong, Peiwei Zhao, Qingjie Meng, Li Tan
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology, Vol 12 (2021)
B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder caused by gain-of-function (GOF) mutations in the CARD11 gene. Affected patients present with persistent B cell lymphocytosis in early childhood paired