Xinyu Li
Huizhou, 516000, China
Last Updated: 09/26/2026
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Found 8 publications
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 HBB.
Journal: Hemoglobin
Published: December 11, 2025
Genetic dissection of clinical heterogeneity in hemoglobin H patients by targeted long-read sequencing.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: December 11, 2025
Clinical patterns of thalidomide in the treatment of transfusion-dependent β-thalassaemia in children: a prospective single-arm study in China.
Journal: Annals of medicine
Published: October 11, 2025
A Chinese pediatric patient with thalassemia traits and compound heterozygous mutations in the PIEZO1 gene suspected of having dehydrated hereditary stomatocytosis.
Journal: Hematology (Amsterdam, Netherlands)
Published: May 05, 2025
Creating New Cis-Regulatory Elements of HBD to Reactivate Delta-Globin.
Journal: Human gene therapy
Published: March 21, 2025
A novel conditioning regimen with pre-transplantation immunosuppression reduces the complication rates in hematopoietic stem cell transplantation in transfusion-dependent β-thalassemia.
Journal: Stem cell research & therapy
Published: September 27, 2024
Stem Leydig cells support macrophage immunological homeostasis through mitochondrial transfer in mice.
Journal: Nature communications
Published: June 03, 2023
Quantitative evaluation of the clinical severity of hemoglobin H disease in a cohort of 591 patients using a scoring system based on regression analysis.
Journal: Haematologica
Published: March 24, 2023
Showing 1-8 of 8
Last Updated: 09/26/2026