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Case report

First published 2017

Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene

Elena Martín-Hernández, María Teresa García-Silva, Pilar Quijada-Fraile [...]

Pediatric and Developmental Pathology

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Review article

First published 2011-7

Infantile-Onset Disorders of Mitochondrial Replication and Protein Synthesis

Célia Nogueira, Rosalba Carrozzo, Laura Vilarinho [...]

Journal of Child Neurology

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Research article

First published 2015-1

Novel Deoxyguanosine Kinase Gene Mutations in the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome

Taner Sezer, Figen Ozçay, Oya Balci [...]

Journal of Child Neurology

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Research article

First published 2013-11

Liver Pathology in Infantile Mitochondrial DNA Depletion Syndrome

Florette K. Hazard, Can H. Ficicioglu, Jaya Ganesh [...]

Pediatric and Developmental Pathology

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Research article

First published 2017-2

A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder

Caterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi [...]

Journal of Child Neurology

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Research article

First published 2008-10

Mitochondrial Oxidative Phosphorylation Protein Levels in Peripheral Blood Mononuclear Cells Correlate with Levels in Subcutaneous Adipose Tissue within Samples Differing by HIV and Lipoatrophy Status

Cecilia M. Shikuma, Mariana Gerschenson, Dominic Chow [...]

AIDS Research and Human Retroviruses

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Research article

First published 2005-03

Stable Transformation of CHO Cells and Human NARP Cybrids Confers Oligomycin Resistance (oli r ) Following Transfer of a Mitochondrial DNA–Encoded oli r ATPase6 Gene to the Nuclear Genome: A Model System for mtDNA Gene Therapy

S.J. Zullo, W.T. Parks, M. Chloupkova [...]

Rejuvenation Research

Search results

Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene

Infantile-Onset Disorders of Mitochondrial Replication and Protein Synthesis

Novel Deoxyguanosine Kinase Gene Mutations in the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome

Liver Pathology in Infantile Mitochondrial DNA Depletion Syndrome

A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder

Mitochondrial Oxidative Phosphorylation Protein Levels in Peripheral Blood Mononuclear Cells Correlate with Levels in Subcutaneous Adipose Tissue within Samples Differing by HIV and Lipoatrophy Status

Stable Transformation of CHO Cells and Human NARP Cybrids Confers Oligomycin Resistance (oli r ) Following Transfer of a Mitochondrial DNA–Encoded oli r ATPase6 Gene to the Nuclear Genome: A Model System for mtDNA Gene Therapy