Author

Taixiang Liu

Observed names: Liu, Tongyingzi, T. X. Liu, Tongyingzi Liu

Institution: Jiangsu Province Blood Center

Observed institutions: Shandong University, Guizhou University, Zunyi Medical University, Shenzhen Center for Disease Control and Prevention, Jiangsu Province Blood Center, Children's Hospital of Zhejiang University, State Key Laboratory of Pharmaceutical Biotechnology, Zhejiang University, Nanjing University

ORCID: 0000-0002-8264-3258

Observed ORCID: 0000-0002-8264-3258

OpenAlex ID: A5103091376

Inhibition of herpes simplex virus infection by oligomeric stilbenoids through ROS generation

2012 · Xiaoqing Chen, Haishi Qiao, et al. · Antiviral Research · 67

Respiratory Syncytial Virus Infection Upregulates NLRC5 and Major Histocompatibility Complex Class I Expression through RIG-I Induction in Airway Epithelial Cells

2015 · Xuancheng Guo, Taixiang Liu, et al. · Journal of Virology · 49

Epidemiological characteristics and spatial−temporal analysis of COVID-19 in Shandong Province, China

2020 · C. Qi, Y. C. Zhu, et al. · Epidemiology and Infection · 20

NM_000148.4( FUT1 ):c.[ 229C >T; 302C >T]with 2 missense variations in the FUT1 gene associated with a para‐Bombay phenotype

2021 · Qing Chen, Chenchen Feng, et al. · Transfusion · 4

HPA1-29w Genotyping and the Foundation for the Platelet Apheresis Registry in Jiangsu Province of China by MassARRAY Spectrometry

2024 · Xin Dai, Chengcheng Liu, et al. · Transfusion Medicine and Hemotherapy · 3

Clinical and variant spectrum of patients harboring ATAD3A variants

2025 · Hongfang Mei, Xinyin Zhang, et al. · Translational Pediatrics · 2

Role of NADPH Oxidase 4 on Dry Eye Syndrome in Mice

2024 · Mian Guo, Taixiang Liu, et al. · Journal of Ocular Pharmacology and Therapeutics · 2

Rare Pk phenotype caused by a novel frameshift mutation in B3GALNT1

2022 · Ling Ma, Enbo Wang, et al. · Transfusion Medicine · 1

ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype

2021 · Chenchen Feng, Hui Li, et al. · Transfusion · 1

[Molecular screening for Vel- blood type and analysis of SMIM1 gene variants].

2020 · Taixiang Liu, Ting Xu, et al. · PubMed · 1

[A study on HNA-1~-5 genotypes and frequencies in the blood donor population of jiangsu province].

2026 · Xi Yu, Ling Ma, et al. · PubMed

UMPlex™: a targeted next-generation sequencing primer design workflow

2025 · Dachuan Lin, Xiaomin Zhang, et al. · Virology Journal

PacBio third‐generation sequencing detects a new variant, c.27delC, in exon 1 of the ABO gene resulting in a weak B phenotype

2024 · L. Shao, L. Ma, et al. · Transfusion Medicine

RHD*509G Allele Associated with an RhD Variant Phenotype: A Case Report

2024 · Ling Ma, Taixiang Liu, et al. · Blood and genomics discovery.

[Pedigree investigation and genetic analysis of a case with Vel heterozygous deletion mutation].

2017 · Taixiang Liu, Yanchun Liu, et al. · PubMed

Molecular screening of Vel‐blood donors using DNA pools in Nanjing, China

2017 · T. X. Liu, Y. C. Liu, et al. · Transfusion Medicine

Works count: 19

Citation count: 150

H-index: 4

I10-index: 3