Lidong D. Zhao
Taiyuan, China
Last Updated: 09/26/2026
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Found 9 publications
Pathogenesis of Haemophilia in 20 Women and Girls.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: February 21, 2025
Phylogenetic analysis and pathogenesis study of a new deletion mutation causing inherited FⅩ deficiency
Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Published: December 02, 2024
Pedigree Analysis and Molecular Mechanism Study of Hereditary Glanzmann Thrombasthenia Caused by Compound Heterozygous Mutation of the ITGA2B Gene
Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Published: July 01, 2024
A Novel Splicing Mutation Leading to Wiskott-Aldrich Syndrome from a Family.
Journal: International journal of genomics
Published: October 12, 2023
Targeted genome engineering based on CRISPR/Cas9 system to enhance FVIII expression in vitro.
Journal: Gene
Published: August 30, 2023
Molecular pathogenesis of a novel Met394Thr variant causing hemophilia B.
Journal: Molecular genetics & genomic medicine
Published: October 12, 2022
Generation of an mESC model with a human hemophilia B nonsense mutation via CRISPR/Cas9 technology.
Journal: Stem cell research & therapy
Published: March 04, 2022
Generation of iPSC line from urine cells of hemophilia A with F8 (p. R814X) mutation.
Journal: Stem cell research
Published: December 17, 2021
Generation an induced pluripotent stem cell line SXMUi001-A derived from a hemophilia B patient carries variant F9 c.223C＞T(p.R75X).
Journal: Stem cell research
Published: November 17, 2021
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Last Updated: 09/26/2026