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ROS-Generating Mitochondrial DNA Mutations Can Regulate Tumor Cell Metastasis

Science (American Association for the Advancement of Science), 2008-05, Vol.320 (5876), p.661-664

2008

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Propofol induces a metabolic switch to glycolysis and cell death in a mitochondrial electron transport chain-dependent manner

PloS one, 2018-02, Vol.13 (2), p.e0192796

2018

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Epigenetic regulation of the nuclear-coded GCAT and SHMT2 genes confers human age-associated mitochondrial respiration defects

Scientific reports, 2015-05, Vol.5 (1), p.10434-10434, Article 10434

2015

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A novel function of mtDNA: its involvement in metastasis

Annals of the New York Academy of Sciences, 2010-07, Vol.1201 (1), p.40-43

2010

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Mitochondrial DNA mutations regulate metastasis of human breast cancer cells

PloS one, 2011-08, Vol.6 (8), p.e23401-e23401

2011

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New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice

PLoS genetics, 2009-12, Vol.5 (12), p.e1000756-e1000756

2009

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Mitochondria-Related Male Infertility

Proceedings of the National Academy of Sciences - PNAS, 2006-10, Vol.103 (41), p.15148-15153

2006

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Specific mitochondrial DNA mutation in mice regulates diabetes and lymphoma development

Proceedings of the National Academy of Sciences - PNAS, 2012-06, Vol.109 (26), p.10528-10533

2012

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Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria

Nature genetics, 2001-07, Vol.28 (3), p.272-275

2001

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A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy

Journal of human genetics, 2017-05, Vol.62 (5), p.539-547

2017

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Mouse somatic mutation orthologous to MELAS A3302G mutation in the mitochondrial tRNA(Leu(UUR)) gene confers respiration defects

Biochemical and biophysical research communications, 2015-11, Vol.467 (4), p.1097-1102

2015

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Gene Therapy for Progeny of Mito-Mice Carrying Pathogenic mtDNA by Nuclear Transplantation

Proceedings of the National Academy of Sciences - PNAS, 2005-11, Vol.102 (46), p.16765-16770

2005

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Mitochondrial DNA mutations in mutator mice confer respiration defects and B-cell lymphoma development

PloS one, 2013-02, Vol.8 (2), p.e55789-e55789

2013

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Association of predicted pathogenic mutations in mitochondrial ND genes with distant metastasis in NSCLC and colon cancer

Scientific reports, 2017-11, Vol.7 (1), p.15535-11, Article 15535

2017

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Regulation of metastasis; mitochondrial DNA mutations have appeared on stage

Journal of bioenergetics and biomembranes, 2012-12, Vol.44 (6), p.639-644

2012

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A specific nuclear DNA background is required for high frequency lymphoma development in transmitochondrial mice with G13997A mtDNA

PloS one, 2015-03, Vol.10 (3), p.e0118561-e0118561

2015

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A 5-bp insertion in Mip causes recessive congenital cataract in KFRS4/Kyo rats

PloS one, 2012-11, Vol.7 (11), p.e50737

2012

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Mito-mice∆ and mitochondrial DNA mutator mice as models of human osteoporosis caused not by aging but by hyperparathyroidism

Experimental Animals, 2018, Vol.67(4), pp.509-516

2018

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Specific mtDNA mutations in mouse carcinoma cells suppress their tumor formation via activation of the host innate immune system

PloS one, 2013-09, Vol.8 (9), p.e75981

2013

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Mice deficient in the Shmt2 gene have mitochondrial respiration defects and are embryonic lethal

Scientific reports, 2018-01, Vol.8 (1), p.425-425, Article 425

2018

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Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNALeu(UUR) with a pathogenic A2748G mutation

Nucleic acids research, 2022-09, Vol.50 (16), p.9382-9396

2022

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Transmitochondrial Mice as Models for Mitochondrial DNA-Based Diseases

Experimental Animals, 2011, Vol.60(5), pp.421-431

2011

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Polymorphic mutations in mouse mitochondrial DNA regulate a tumor phenotype

Mitochondrion, 2013-11, Vol.13 (6), p.881-887

2013

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Mammalian Copper Chaperone Cox17p Has an Essential Role in Activation of Cytochrome c Oxidase and Embryonic Development

Molecular and Cellular Biology, 2002-11, Vol.22 (21), p.7614-7621

2002

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Mitochondrial functional complementation in mitochondrial DNA-based diseases

The international journal of biochemistry & cell biology, 2009-10, Vol.41 (10), p.1907-1913

2009

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ROS-Generating Mitochondrial DNA Mutations Can Regulate Tumor Cell Metastasis

Propofol induces a metabolic switch to glycolysis and cell death in a mitochondrial electron transport chain-dependent manner

Epigenetic regulation of the nuclear-coded GCAT and SHMT2 genes confers human age-associated mitochondrial respiration defects

A novel function of mtDNA: its involvement in metastasis

Mitochondrial DNA mutations regulate metastasis of human breast cancer cells

New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice

Mitochondria-Related Male Infertility

Specific mitochondrial DNA mutation in mice regulates diabetes and lymphoma development

Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria

A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy

Mouse somatic mutation orthologous to MELAS A3302G mutation in the mitochondrial tRNA(Leu(UUR)) gene confers respiration defects

Gene Therapy for Progeny of Mito-Mice Carrying Pathogenic mtDNA by Nuclear Transplantation

Mitochondrial DNA mutations in mutator mice confer respiration defects and B-cell lymphoma development

Association of predicted pathogenic mutations in mitochondrial ND genes with distant metastasis in NSCLC and colon cancer

Regulation of metastasis; mitochondrial DNA mutations have appeared on stage

A specific nuclear DNA background is required for high frequency lymphoma development in transmitochondrial mice with G13997A mtDNA

A 5-bp insertion in Mip causes recessive congenital cataract in KFRS4/Kyo rats

Mito-mice∆ and mitochondrial DNA mutator mice as models of human osteoporosis caused not by aging but by hyperparathyroidism

Specific mtDNA mutations in mouse carcinoma cells suppress their tumor formation via activation of the host innate immune system

Mice deficient in the Shmt2 gene have mitochondrial respiration defects and are embryonic lethal

Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNALeu(UUR) with a pathogenic A2748G mutation

Transmitochondrial Mice as Models for Mitochondrial DNA-Based Diseases

Polymorphic mutations in mouse mitochondrial DNA regulate a tumor phenotype

Mammalian Copper Chaperone Cox17p Has an Essential Role in Activation of Cytochrome c Oxidase and Embryonic Development

Mitochondrial functional complementation in mitochondrial DNA-based diseases

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