Minxin Guan

Yiwu, 322000, China

Last Updated: 09/26/2026

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Found 48 publications

The "Triple-hit" pathogenic mechanism of Leber hereditary optic neuropathy

The "Triple-hit" pathogenic mechanism of Leber hereditary optic neuropathy

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences
Published: June 08, 2026

Pathogenic mechanisms of Leber hereditary optic neuropathy caused by m.3472T>C mutation

Pathogenic mechanisms of Leber hereditary optic neuropathy caused by m.3472T>C mutation

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences
Published: November 18, 2025

Mechanism of BNIP3-mediated mitophagy in m.3635G>A related Leber hereditary optic neuropathy

Mechanism of BNIP3-mediated mitophagy in m.3635G>A related Leber hereditary optic neuropathy

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 11, 2025

Impact of POU3F4 mutation on cochlear development and auditory function.

Impact of POU3F4 mutation on cochlear development and auditory function.

Journal: Cell communication and signaling : CCS
Published: December 17, 2024

A Novel Mutation Located in the N-Terminal Domain of MYO15A Caused Sensorineural Hearing Loss.

A Novel Mutation Located in the N-Terminal Domain of MYO15A Caused Sensorineural Hearing Loss.

Journal: Molecular genetics & genomic medicine
Published: July 30, 2024

Clinical and genetic analysis of essential hypertension with mitochondrial tRNAMet 4435A>G and YARS2 mutation.

Clinical and genetic analysis of essential hypertension with mitochondrial tRNAMet 4435A>G and YARS2 mutation.

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences
Published: April 02, 2024

A homozygous mutation of TWNK identified in premature ovarian insufficiency warns of late-onset perrault syndrome.

A homozygous mutation of TWNK identified in premature ovarian insufficiency warns of late-onset perrault syndrome.

Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: December 29, 2023

Clinical and genetic analysis of essential hypertension with CYB gene m.15024G>A mutation.

Clinical and genetic analysis of essential hypertension with CYB gene m.15024G>A mutation.

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences
Published: August 29, 2023

Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations.

Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations.

Journal: Journal of biomedical science
Published: April 05, 2023

Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation.

Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation.

Journal: Journal of biomedical science
Published: March 09, 2023

Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene.

Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene.

Journal: Stem cell research
Published: January 25, 2022

Lipidomic Alterations and PPARα Activation Induced by Resveratrol Lead to Reduction in Lesion Size in Endometriosis Models.

Lipidomic Alterations and PPARα Activation Induced by Resveratrol Lead to Reduction in Lesion Size in Endometriosis Models.

Journal: Oxidative medicine and cellular longevity
Published: April 01, 2021
Showing 1-12 of 48

Last Updated: 09/26/2026