Min‐Xin Guan

Zhejiang International Studies University — China

Biochemistry, Genetics and Molecular Biology · Life Sciences

57h-index10.7kcitations325works3.22yr avg
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Research Topics

Mitochondrial Function and Pathology(224), RNA modifications and cancer(89), RNA and protein synthesis mechanisms(84), ATP Synthase and ATPases Research(73), Metabolism and Genetic Disorders(62)

Publications325 total

Pathogenic Mechanism of the <i>KCNQ4</i> Gene Variant in Hearing Loss and Functional Validation in a Zebrafish Model
The FASEB Journal·2025
Pathogenic mechanisms of Leber hereditary optic neuropathy caused by m.3472T&gt;C mutation
Journal of Zhejiang University (Medical Sciences)·2025Open Access
Sunspot dynamics and magnetic evolution in the active region 12192
Physics of Fluids·2025· 1 cited
Clinical characteristics and predictors for the presence of pediatric intussusception secondary to pathological lead points
2025Open Access
Stress granule sequestration of OXPHOS gene transcripts exacerbates glycolytic restriction
2025Open Access
Leber's hereditary optic neuropathy–associated ND1 3733G&gt;C mutation ameliorates the mitochondrial quality control and cellular homeostasis
Journal of Biological Chemistry·2025· 3 citedOpen Access
Surgical Invasiveness, Hidden Blood Loss, and Outcomes of 2 Endoscopic Lumbar Fusion Techniques for Degenerative Disease: A Comparative Study
World Neurosurgery·2025Open Access
Mitochondrial tRNA processing defects reprogram mitochondrial and cellular homeostasis
Journal of Biological Chemistry·2025· 3 citedOpen Access
Impact of POU3F4 mutation on cochlear development and auditory function
Cell Communication and Signaling·2025· 1 citedOpen Access
Machine Learning-Based Measurement and Prediction of Ground Settlement Induced by Shield Tunneling Undercrossing Existing Tunnels in Composite Strata
Sensors·2025· 5 citedOpen Access
Vitamin A treatment restores vision failures arising from Leber’s hereditary optic neuropathy–linked mtDNA mutation
JCI Insight·2025· 4 citedOpen Access
[Mechanism of BNIP3-mediated mitophagy in m.3635G>A related Leber hereditary optic neuropathy].
PubMed·2025
Deafness-associated mitochondrial 12S rRNA mutation reshapes mitochondrial and cellular homeostasis
Journal of Biological Chemistry·2024· 5 citedOpen Access
A simplified method for evaluating shallow slope stability of slopes based on an indirectly coupled runoff and groundwater seepage model
Hydrogeology Journal·2024· 4 cited
A Novel Mutation Located in the N‐Terminal Domain of <scp>MYO15A</scp> Caused Sensorineural Hearing Loss
Molecular Genetics & Genomic Medicine·2024· 2 citedOpen Access
Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophy
JCI Insight·2024· 5 citedOpen Access
Signal Generator Based Prescribed-Time Anti-Disturbance Containment Control for Multi-agent Systems with An Application to Multiple Manipulator System
2024· 1 cited
SpliceTransformer predicts tissue-specific splicing linked to human diseases
Nature Communications·2024· 27 citedOpen Access
Up-regulation of HIF-1α in refractory sudden sensorineural hearing loss
Acta Otorhinolaryngologica Italica·2024· 1 citedOpen Access
Mitochondrial tRNA<sup>Glu</sup> 14693A &gt; G Mutation, an “Enhancer” to the Phenotypic Expression of Leber's Hereditary Optic Neuropathy
Advanced Science·2024· 1 citedOpen Access
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Frequent Co-authors

Ronghua Li(15), Yaping Qian(11), Li Yang(8), Taosheng Huang(6), Meng Wang(6), Jun Qin Mo(5), Pingping Jiang(5), Xiangtian Zhou(5), Wie‐Yen Young(5), Qingfeng Yan(4), Dongyi Han(4), Ye Chen(4), Xinjian Wang(4), Jing Zheng(4), Yuqi Liu(4), Jia Qu(4), Fuxin Zhao(4), Yanchun Ji(4), Jianxin Lü(3), Ling Xue(3)