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Blood|November 23, 2020
A natural DNMT1 mutation elevates the fetal hemoglobin level via epigenetic derepression of the γ-globin gene in β-thalassemiaYi Gong, Xinhua Zhang, Qianqian Zhang, et al.
Blood Advances|April 8, 2025
A common TBP-binding site mutation elevates γ-globin levels by competitive globin switching change in β-thalassemiaMengyang Song, Xiaolei Wei, Hualei Luo, et al.
Blood Cells, Molecules & Diseases|February 25, 2018
Role of tissue-specific promoter DNA methylation in regulating the human EKLF geneYihong Li, Dun Liu, Zhiming Li, et al.
Experimental Hematology|March 31, 2018
miR-326 regulates HbF synthesis by targeting EKLF in human erythroid cellsYihong Li, Dun Liu, Xinhua Zhang, et al.
British Journal of Haematology|May 17, 2021
GATA zinc finger domain-containing protein 2A (GATAD2A) deficiency reactivates fetal haemoglobin in patients with β-thalassaemia through impaired formation of methyl-binding domain protein 2 (MBD2)-containing nucleosome remodelling and deacetylation (NuRD) complexYunhao Liang, Xinhua Zhang, Yongqiong Liu, et al.
Transfusion Medicine Reviews|November 16, 2024
Exploring Novel Strategies to Alleviate Symptoms of β-Globinopathies: Examining the Potential Role of Embryonic ε-globin InductionJun Liu, Kevin Park, Ziyang Shen, et al.
Hematology (Amsterdam, Netherlands)|May 5, 2025
A Chinese pediatric patient with thalassemia traits and compound heterozygous mutations in the PIEZO1 gene suspected of having dehydrated hereditary stomatocytosisWeijie Chen, Xinyu Li, Huaqing Yang, et al.
Hemoglobin|December 11, 2025
Identification of a Patient with Transfusion-Dependent β-Thalassemia Caused by Compound Heterozygous Mutations of HBB: C.84_85insC and Common Linked Intronic Variants in HBBLang Qin, Xinyu Li, Yin Wang, et al.
Nature Communications|November 20, 2025
Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East AsiaQianqian Zhang, Jialong Li, Haoyang Huang, et al.
Journal of Medical Biochemistry|November 24, 2025
Impact of transferrin levels on iron accumulation in transfusion-dependent beta-thalassemia: A genotype-specific analysisYidan Liang, Xinhua Zhang, Binbin Huang, et al.
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