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Annals of the New York Academy of Sciences|May 6, 2004
Molecular pathogenetic mechanism of maternally inherited deafnessMin-Xin GuanMitochondrion|November 5, 2010
Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicityMin-Xin GuanZhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 9, 2012
[Mitochondrial genetics and human essential hypertension]Hong Chen, Min-xin GuanJournal of Biomedical Science|September 22, 2023
Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutationsChao Chen, Min-Xin GuanMolecular and Cellular Biology|October 9, 2002
A human mitochondrial GTP binding protein related to tRNA modification may modulate phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutationXiaoming Li, Min-Xin GuanHuman Molecular Genetics|April 25, 2022
Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patientsChao Chen, Min-Xin GuanAntimicrobial Agents and Chemotherapy|August 19, 2009
Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutationYaping Qian, Min-Xin GuanBiochimica Et Biophysica Acta|January 30, 2004
Identification and characterization of mouse TRMU gene encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferaseQingfeng Yan, Min-Xin GuanBiochemical and Biophysical Research Communications|December 19, 2003
Identification and characterization of mouse GTPBP3 gene encoding a mitochondrial GTP-binding protein involved in tRNA modificationXiaoming Li, Min-Xin GuanMolecular and Cellular Biology|March 3, 2010
Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetesRonghua Li, Min-Xin GuanPageof 37