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The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells

Protein & cell, 2017-06, Vol.8 (6), p.439-445

2017

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

Journal of biomedical science, 2023-09, Vol.30 (1), p.1-82, Article 82

2023

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Investigating the Broad Matrix-Gate Network in the Mitochondrial ADP/ATP Carrier through Molecular Dynamics Simulations

Molecules (Basel, Switzerland), 2022-02, Vol.27 (3), p.1071

2022

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CXCR4-mediated signaling regulates autophagy and influences acute myeloid leukemia cell survival and drug resistance

Cancer letters, 2018-07, Vol.425, p.1-12

2018

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A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis

Nucleic acids research, 2019-02, Vol.47 (4), p.2056-2074

2019

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Species identification through mitochondrial rRNA genetic analysis

Scientific reports, 2014-02, Vol.4 (1), p.4089-4089, Article 4089

2014

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Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated Mutation

Antimicrobial Agents and Chemotherapy, 2009-11, Vol.53 (11), p.4612-4618

2009

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Deletion of Gtpbp3 in zebrafish revealed the hypertrophic cardiomyopathy manifested by aberrant mitochondrial tRNA metabolism

Nucleic acids research, 2019-06, Vol.47 (10), p.5341-5355

2019

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A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis

Scientific reports, 2017-07, Vol.7 (1), p.5704-13, Article 5704

2017

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

Journal of biomedical science, 2023-08, Vol.30 (1), p.63-63, Article 63

2023

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Exportin 4 depletion leads to nuclear accumulation of a subset of circular RNAs

Nature communications, 2022-10, Vol.13 (1), p.5769-5769, Article 5769

2022

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GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss

PloS one, 2015-06, Vol.10 (6), p.e0128691-e0128691

2015

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Molecular Pathogenetic Mechanism of Maternally Inherited Deafness

Annals of the New York Academy of Sciences, 2004-04, Vol.1011 (1), p.259-271

GUAN, MIN-XIN

2004

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A peep into mitochondrial disorder： multifaceted from mitochondrial DNA mutations to nuclear gene modulation

Protein & Cell, 2015-12, Vol.6 (12), p.862-870

2015

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Association of MTHFR C677T polymorphism and type 2 diabetes mellitus (T2DM) susceptibility

Molecular genetics & genomic medicine, 2019-12, Vol.7 (12), p.e1020-n/a

2019

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Transcriptome-Based Analysis Reveals Therapeutic Effects of Resveratrol on Endometriosis in aRat Model

Drug design, development and therapy, 2021-01, Vol.15, p.4141-4155

2021

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Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity

Journal of otology (Beijing), 2017-03, Vol.12 (1), p.1-8

2017

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Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation

Human molecular genetics, 2016-08, Vol.25 (16), p.3613-3625

2016

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Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patients

Human molecular genetics, 2022-09, Vol.31 (18), p.3068-3082

2022

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Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets

Stem cell research & therapy, 2016-01, Vol.7 (2), p.2-2, Article 2

2016

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Emerging functions of mitochondria-encoded noncoding RNAs

Trends in genetics, 2023-02, Vol.39 (2), p.125-139

2023

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The defective expression of gtpbp3 related to tRNA modification alters the mitochondrial function and development of zebrafish

The international journal of biochemistry & cell biology, 2016-08, Vol.77 (Pt A), p.1-9

2016

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Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

American journal of human genetics, 2006-08, Vol.79 (2), p.291-302

2006

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Deficient tRNA posttranscription modification dysregulated the mitochondrial quality controls and apoptosis

iScience, 2024-02, Vol.27 (2), p.108883-108883, Article 108883

2024

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Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity

Mitochondrion, 2011-03, Vol.11 (2), p.237-245

Guan, Min-Xin

2011

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The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells

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

Investigating the Broad Matrix-Gate Network in the Mitochondrial ADP/ATP Carrier through Molecular Dynamics Simulations

CXCR4-mediated signaling regulates autophagy and influences acute myeloid leukemia cell survival and drug resistance

A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis

Species identification through mitochondrial rRNA genetic analysis

Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated Mutation

Deletion of Gtpbp3 in zebrafish revealed the hypertrophic cardiomyopathy manifested by aberrant mitochondrial tRNA metabolism

A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis

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

Exportin 4 depletion leads to nuclear accumulation of a subset of circular RNAs

GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss

Molecular Pathogenetic Mechanism of Maternally Inherited Deafness

A peep into mitochondrial disorder： multifaceted from mitochondrial DNA mutations to nuclear gene modulation

Association of MTHFR C677T polymorphism and type 2 diabetes mellitus (T2DM) susceptibility

Transcriptome-Based Analysis Reveals Therapeutic Effects of Resveratrol on Endometriosis in aRat Model

Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity

Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation

Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patients

Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets

Emerging functions of mitochondria-encoded noncoding RNAs

The defective expression of gtpbp3 related to tRNA modification alters the mitochondrial function and development of zebrafish

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

Deficient tRNA posttranscription modification dysregulated the mitochondrial quality controls and apoptosis

Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity

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