Xu Zhang

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 10

Top Topics

Respiratory Syndrome Coronavirus

Transcription Factor

Genome Wide Identification

Top Venues

Journal of translational medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Jian-Ping Li, Ying Liu, Xu Zhang, Ying-Dong Wei, Xiao-Feng Li
Identification of the novel HLA-B*15:270 allele by Sanger dideoxy nucleotide sequencing. HLA (2023)
Xiao-Feng Li, Xu Zhang, Feng-Qiu Lin, Jian-Ping Li
Characterization of the novel HLA-B*15:269 allele by sequencing-based typing. HLA (2023)
Xu Zhang, Zhuren Zhou, Xuying Huang, Lichun Li, Xiao-Feng Li, Jian-Ping Li
A c.1046_1048delAGG deletion causes a novel O allele on an ABO*O.01.04 allele in a Chinese Han blood donor. Transfusion (2023)
Jian-Ping Li, Xu Zhang, Feng-Qiu Lin, Xiao-Feng Li
The novel HLA-A*02:404 allele, identified by Sanger dideoxy nucleotide sequencing in a Chinese individual. HLA (2023)
Xiao-Feng Li, Xu Zhang, Feng-Qiu Lin, Min-Jie Wei, Jian-Ping Li
The novel HLA-A*02:405 allele characterized by sequencing-based typing. HLA (2023)
Xu Zhang, Xiao-Feng Li, Zhuren Zhou, Xuying Huang, Lichun Li, Jian-Ping Li
A novel RHD allele, RHD*1166delA, with D-negative phenotype identified in a Chinese family. Transfusion (2021)
Xu Zhang, Xiao-Feng Li, Ying Liu, Jian-Ping Li
A novel allele arising from c.912C>A mutation in the α-1,3-N-acetylgalactosaminyltransferase gene in a Chinese individual. Transfusion 61 (2) (2020)
Feng-Qiu Lin, Kun-Lian Zhang, Xiao-Feng Li, Xu Zhang, Ying Liu, Jian-Ping Li
Two novel FUT1 alleles that cause para-Bombay phenotype in a Chinese individual. Transfusion 60 (12) (2020)
Xu Zhang, Guiji Li, Zhuren Zhou, Chaopeng Shao, Xuying Huang, Lichun Li, Xiaofeng Li, Ying Liu, Hua Fan, Jianping Li
Molecular and computational analysis of 45 samples with a serologic weak D phenotype detected among 132,479 blood donors in northeast China. Journal of translational medicine 17 (1) (2019)
Xu Zhang, Jianping Li
A novel cis-AB allele with c.797 T>C mutation identified in three unrelated Chinese individuals. Transfusion 58 (10) (2018)