Jiangxi G. Xiao
No. 8 Xishiku St
Beijing, 100034, China
Beijing, 100034, China
Last Updated: 09/26/2026
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Found 53 publications
Acute megakaryoblastic leukemia with CBFA2T3::GLIS2 fusion gene: 3 cases report and literature review
Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Published: April 16, 2026
Spatial lipidomics reveals altered lipid profiles in TMEM63A mutant rats with hypomyelination.
Journal: Scientific reports
Published: February 20, 2025
Mitoxantrone hydrochloride liposome combined with cytarabine for treating pediatric acute myeloid leukemia with RUNX1∷MTG16 fusion gene: a case report and literature review
Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Published: January 07, 2025
Quantitative MRI Findings and Their Relationship to Muscle Histopathology and Ambulatory Clinical Function in Duchenne Muscular Dystrophy.
Journal: Journal of cachexia, sarcopenia and muscle
Published: August 12, 2024
Use of the ETV6/RUNX1 probe to verify the performance of the fluorescence in situ hybridization probe before clinical detection
Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Published: March 25, 2024
Unraveling rare form of adult-onset NIID by characteristic brain MRI features: A single-center retrospective review.
Journal: Frontiers in neurology
Published: October 31, 2022
The recurrent mutation in RNF220 also causes hypomyelination in China and is a CpG hot spot.
Journal: Brain : a journal of neurology
Published: July 23, 2022
Clinical and genetic analysis of three children with 22q13 deletion syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 10, 2022
Functional Study of TMEM163 Gene Variants Associated with Hypomyelination Leukodystrophy.
Journal: Cells
Published: December 20, 2021
Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients.
Journal: Frontiers in genetics
Published: November 30, 2021
Last Updated: 09/26/2026