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G7731A mutation in mouse mitochondrial tRNA regulates late-onset disorders in transmitochondrial mice

Biochemical and biophysical research communications, 2015-03, Vol.459 (1), p.66-70

2015

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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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A somatic T15091C mutation in the Cytb gene of mouse mitochondrial DNA dominantly induces respiration defects

Biochemical and biophysical research communications, 2015-08, Vol.463 (4), p.1021-1027

2015

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Over-expression of Tfam improves the mitochondrial disease phenotypes in a mouse model system

Biochemical and biophysical research communications, 2010-10, Vol.401 (1), p.26-31

2010

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Transmitochondrial mito-miceΔ and mtDNA mutator mice, but not aged mice, share the same spectrum of musculoskeletal disorders

Biochemical and biophysical research communications, 2015-01, Vol.456 (4), p.933-937

2015

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Cytoplasmic transfer of heritable elements other than mtDNA from SAMP1 mice into mouse tumor cells suppresses their ability to form tumors in C57BL6 mice

Biochemical and biophysical research communications, 2017-11, Vol.493 (1), p.252-257

2017

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Interaction Theory of Mammalian Mitochondria

Biochemical and biophysical research communications, 2001-11, Vol.288 (4), p.743-746

2001

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Accumulation of pathogenic ΔmtDNA induced deafness but not diabetic phenotypes in mito-mice

Biochemical and biophysical research communications, 2004-10, Vol.323 (1), p.175-184

2004

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Nuclear DNA but not mtDNA controls tumor phenotypes in mouse cells

Biochemical and biophysical research communications, 2005-02, Vol.327 (4), p.1028-1035

2005

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Hypoxic induction of hypoxia-inducible factor-1α and oxygen-regulated gene expression in mitochondrial DNA-depleted HeLa cells

Biochemical and biophysical research communications, 2002-09, Vol.297 (2), p.346-352

2002

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Isolation and Characterization of Mitochondrial DNA-less Lines from Various Mammalian Cell Lines by Application of an Anticancer Drug, Ditercalinium

Biochemical and biophysical research communications, 1997-10, Vol.239 (1), p.257-260

1997

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Presence of interaction but not complementation between human mtDNAs carrying different mutations within a tRNA(Leu(UUR)) gene

Biochemical and biophysical research communications, 2004-02, Vol.314 (4), p.1107-1112

2004

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Application of ES cells for generation of respiration-deficient mice carrying mtDNA with a large-scale deletion

Biochemical and biophysical research communications, 2005-07, Vol.333 (2), p.590-595

2005

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Cytoplasmic Transfer of Platelet mtDNA from Elderly Patients with Parkinson's Disease to mtDNA-less HeLa Cells Restores Complete Mitochondrial Respiratory Function

Biochemical and biophysical research communications, 2001-01, Vol.280 (1), p.265-273

2001

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A Patient with Type 2 Diabetes Mellitus Associated with Mutations in Calcium Sensing Receptor Gene and Mitochondrial DNA

Biochemical and biophysical research communications, 2000-11, Vol.278 (3), p.808-813

2000

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Mice with Only Rat mtDNA Are Required as Models of Mitochondrial Diseases

Biochemical and biophysical research communications, 2001-04, Vol.282 (3), p.707-711

2001

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Effects of ethidium bromide treatment of mouse cells on expression and assembly of nuclear-coded subunits of complexes involved in the oxidative phosphorylation

Biochemical and biophysical research communications, 1990-02, Vol.167 (1), p.216-221

1990

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Long-Term Postmortem Survival of Mitochondrial Genomes in Mouse Synaptosomes and Their Rescue in a Mitochondrial DNA-less Mouse Cell Line

Biochemical and biophysical research communications, 1998-06, Vol.247 (2), p.432-435

1998

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A Mitochondrial DNA Mutation Cosegregates with the Pathophysiological U Wave

Biochemical and biophysical research communications, 1999-04, Vol.257 (1), p.228-233

1999

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

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

2015

Volltextzugriff (PDF)

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

Biochemical and biophysical research communications, 2015-01, Vol.467 (4), p.1097-1102

2015

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Strictly maternal inheritance of rat mitochondrial DNA

Biochemical and biophysical research communications, 1978-08, Vol.83 (3), p.1032-1038

1978

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G7731A mutation in mouse mitochondrial tRNALys regulates late-onset disorders in transmitochondrial mice

Biochemical and biophysical research communications, 2015-03, Vol.459 (1), p.66-70

2015

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Two different molecular types of rat mitochondrial DNAS

Biochemical and biophysical research communications, 1978-04, Vol.81 (3), p.871-877

1978

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Presence of interaction but not complementation between human mtDNAs carrying different mutations within a tRNALeu(UUR) gene

Biochemical and biophysical research communications, 2004-02, Vol.314 (4), p.1107-1112

2004

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G7731A mutation in mouse mitochondrial tRNA regulates late-onset disorders in transmitochondrial mice

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

A somatic T15091C mutation in the Cytb gene of mouse mitochondrial DNA dominantly induces respiration defects

Over-expression of Tfam improves the mitochondrial disease phenotypes in a mouse model system

Transmitochondrial mito-miceΔ and mtDNA mutator mice, but not aged mice, share the same spectrum of musculoskeletal disorders

Cytoplasmic transfer of heritable elements other than mtDNA from SAMP1 mice into mouse tumor cells suppresses their ability to form tumors in C57BL6 mice

Interaction Theory of Mammalian Mitochondria

Accumulation of pathogenic ΔmtDNA induced deafness but not diabetic phenotypes in mito-mice

Nuclear DNA but not mtDNA controls tumor phenotypes in mouse cells

Hypoxic induction of hypoxia-inducible factor-1α and oxygen-regulated gene expression in mitochondrial DNA-depleted HeLa cells

Isolation and Characterization of Mitochondrial DNA-less Lines from Various Mammalian Cell Lines by Application of an Anticancer Drug, Ditercalinium

Presence of interaction but not complementation between human mtDNAs carrying different mutations within a tRNA(Leu(UUR)) gene

Application of ES cells for generation of respiration-deficient mice carrying mtDNA with a large-scale deletion

Cytoplasmic Transfer of Platelet mtDNA from Elderly Patients with Parkinson's Disease to mtDNA-less HeLa Cells Restores Complete Mitochondrial Respiratory Function

A Patient with Type 2 Diabetes Mellitus Associated with Mutations in Calcium Sensing Receptor Gene and Mitochondrial DNA

Mice with Only Rat mtDNA Are Required as Models of Mitochondrial Diseases

Effects of ethidium bromide treatment of mouse cells on expression and assembly of nuclear-coded subunits of complexes involved in the oxidative phosphorylation

Long-Term Postmortem Survival of Mitochondrial Genomes in Mouse Synaptosomes and Their Rescue in a Mitochondrial DNA-less Mouse Cell Line

A Mitochondrial DNA Mutation Cosegregates with the Pathophysiological U Wave

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

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

Strictly maternal inheritance of rat mitochondrial DNA

G7731A mutation in mouse mitochondrial tRNALys regulates late-onset disorders in transmitochondrial mice

Two different molecular types of rat mitochondrial DNAS

Presence of interaction but not complementation between human mtDNAs carrying different mutations within a tRNALeu(UUR) gene

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