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Rui Zhou

Mitochondrial dysfunction is associated with hypertrophic cardiomyopathy in Pompe disease‐specific induced pluripotent stem cell‐derived cardiomyocytes
2023 · Wenjun Huang, Rui Zhou, et al. · Cell Proliferation · 15
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Generation of two heterozygous GAA mutation-carrying human induced pluripotent stem cell lines (XACHi005-A, XACHi006-A) from parents of an infant with Pompe disease
2022 · Wenjun Huang, Yafei Zhou, et al. · Stem Cell Research · 8
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Induced pluripotent stem cell for modeling Pompe disease
2022 · Wenjun Huang, Yanmin Zhang, et al. · Frontiers in Cardiovascular Medicine · 6
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Irisin links Claudin-5 preservation and Mfn2-mediated mitochondrial dynamics to resist doxorubicin-induced cardiac endothelial damage
2024 · Jun He, Lin Hou, et al. · Biochemical and Biophysical Research Communications · 5
Regulation of heart regeneration by LSD1 through suppressing CEND1
2025 · Huahua Liu, Jinling Dong, et al. · Theranostics · 4
Generation of one human induced pluripotent stem cell line (XACHi004-A) with heterozygous mutation of RYR2 gene from an atrial fibrillation patient
2022 · Yafei Zhou, Congshan Jiang, et al. · Stem Cell Research · 3
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Generation and characterization of a novel Gaa compound heterozygous mouse model recapitulating human Pompe disease
2026 · Wenjun Huang, Jie Wang, et al. · Orphanet Journal of Rare Diseases · 1
Clinical features and genetic characteristics of ovotesticular disorders of sex development: 24 cases from a single center
2025 · Dian Li, Xiangliang Tang, et al. · World Journal of Urology · 1
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Wnt pathway activation unlocks disease-neutral proliferative potential in human iPSC-derived cardiomyocytes: A comparative study across healthy and inherited cardiac disease models
2025 · Yafei Zhou, Wenjun Huang, et al. · Tissue and Cell · 1
Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient
2023 · Benchang Li, Yafei Zhou, et al. · Stem Cell Research · 1
Deep Learning-Based Detection of Facial Dysmorphic Features for Rare Genetic Disorders in Pediatric Populations
2026 · Fengyu Che, Tianwei Lin, et al. · Preprints.org
Generation and characterization of a human iPSC line (XACHi022-A) derived from an asymptomatic carrier of the GAA c.2051C > A (p.P684Q) variant
2026 · Yafei Zhou, Rui Zhou, et al. · Stem Cell Research
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Methyl 4‐ O ‐Demethylbarbatate Destabilises HIF ‐1α and Enhances Temozolomide Sensitivity in Glioma Cells
2026 · Rui Zhou, Mücahit Varlı, et al. · Cell Proliferation
Works count: 13
Citation count: 45
H-index: 4
I10-index: 1
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