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Sequence and organization of the human mitochondrial genome

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Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

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Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

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Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by Complementation

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

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Abnormalities of the electron transport chain in idiopathic parkinson's disease

Parker, W. D., Boyson, S. J., & Parks, J. K. (1989) · Annals of Neurology · doi:10.1002/ana.410260606 · Cited by 1,061 · see citing works

Deletions of mitochondrial DNA in Kearns‐Sayre syndrome

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Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for Replication

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Paternal Inheritance of Mitochondrial DNA

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Origin and functional consequences of the complex I defect in Parkinson's disease

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INTRAMITOCHONDRIAL FIBERS WITH DNA CHARACTERISTICS

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Pluripotent embryonal carcinoma clones derived from the human teratocarcinoma cell line Tera-2. Differentiation in vivo and in vitro.

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Pure, postmitotic, polarized human neurons derived from NTera 2 cells provide a system for expressing exogenous proteins in terminally differentiated neurons

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Cytochrome oxidase deficiency in Alzheimer’s disease

Parker, W. D., Filley, C. M., & Parks, J. K. (1990) · Neurology · doi:10.1212/wnl.40.8.1302 · Cited by 598 · see citing works

Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication

Coskun, P. E., Beal, M. F., & Wallace, D. C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0403649101 · Cited by 556 · see citing works

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

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Untitled work

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Ethidium bromide induced mutation of yeast mitochondria: Complete transformation of cells into respiratory deficient non-chromosomal “petites”

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MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

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Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

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Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes

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High aggregate burden of somatic mtDNA point mutations in aging and Alzheimer's disease brain

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[27] Isolation of human cell lines lacking mitochondrial DNA

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INTRAMITOCHONDRIAL FIBERS WITH DNA CHARACTERISTICS

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Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants

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Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease

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KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

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Abnormal Mitochondrial Morphology in Sporadic Parkinson's and Alzheimer's Disease Cybrid Cell Lines

Trimmer, P. A., Swerdlow, R. H., Parks, J. K., Keeney, P. M., Bennett, J. P., Miller, S. W., Davis, R. E., & Parker, W. D. (2000) · Experimental Neurology · doi:10.1006/exnr.2000.7333 · Cited by 296 · see citing works

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.

Yoneda, M., Chomyn, A., Martinuzzi, A., Hurko, O., & Attardi, G. M. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.23.11164 · Cited by 291 · see citing works

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNALys and premature translation termination

Enriquez, J. A., Chomyn, A., & Attardi, G. (1995) · Nature Genetics · doi:10.1038/ng0595-47 · Cited by 285 · see citing works

Cybrids in Alzheimer's disease: a cellular model of the disease?

Swerdlow, R. H., Parks, J. K., Cassarino, D. S., Maguire, D. J., Maguire, R. S., Bennett, J. P., Davis, R. E., & Parker, W. D. (1997) · Neurology · doi:10.1212/wnl.49.4.918 · Cited by 272 · see citing works

Elevated reactive oxygen species and antioxidant enzyme activities in animal and cellular models of Parkinson's disease

Cassarino, D. S., Fall, C. P., Swerdlow, R. H., Smith, T. S., Halvorsen, E. M., Miller, S. W., Parks, J. K., Parker, W. D., & Bennett, J. P. (1997) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/s0925-4439(97)00070-7 · Cited by 265 · see citing works

Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis

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Mitochondria dysfunction of Alzheimer's disease cybrids enhances Aβ toxicity

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Functional Analysis of Lymphoblast and Cybrid Mitochondria Containing the 3460, 11778, or 14484 Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation

Brown, M. D., Trounce, I. A., Jun, A. S., Allen, J. C., & Wallace, D. C. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m006476200 · Cited by 260 · see citing works

Cybrids in Alzheimer's disease: A cellular model of the disease?

Swerdlow, R. H., & Parker, D. W. (1998) · Neurology · doi:10.1212/wnl.51.1.326-a · Cited by 260 · see citing works

Calcium homeostasis and reactive oxygen species production in cells transformed by mitochondria from individuals with sporadic Alzheimer's disease

Sheehan, J. P., Swerdlow, R. H., Miller, S. W., Davis, R. E., Parks, J. K., Parker, W. D., & Tuttle, J. B. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-12-04612.1997 · Cited by 249 · see citing works

Clonal Human (hNT) Neuron Grafts for Stroke Therapy

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Evidence for a defect in NADH

Parker, W. D., Boyson, S. J., LUDER, A. S., & Parks, J. K. (1990) · Neurology · doi:10.1212/wnl.40.8.1231 · Cited by 230 · see citing works

Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids

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Tissue heterogeneity of the mammalian mitochondrial proteome

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Mitochondrial DNA modifies cognition in interaction with the nuclear genome and age in mice

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Mitochondrial DNA deficient petite mutants of yeast

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Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.

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Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.

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Ethidium Bromide-Induced Loss of Mitochondrial DNA from Primary Chicken Embryo Fibroblasts

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Human Xenomitochondrial Cybrids

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Cytoplasmic Inheritance of Chloramphenicol Resistance in Mouse Tissue Culture Cells

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Mitochondria in Sporadic Amyotrophic Lateral Sclerosis

Swerdlow, R. H., Parks, J. K., Cassarino, D. S., Trimmer, P. A., Miller, S. W., Maguire, D., Sheehan, J. P., Maguire, R. S., Pattee, G. L., Juel, V. C., et al. (1998) · Experimental Neurology · doi:10.1006/exnr.1998.6866 · Cited by 180 · see citing works

Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells

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Alzheimer's disease cybrids replicate beta-amyloid abnormalities through cell death pathways.

Khan, S. M., Cassarino, D. S., Abramova, N. N., Keeney, P. M., Borland, M. K., Pa, T., Krebs, C. T., Bennett, J. C., Parks, J. K., Swerdlow, R. H., et al. (2000) · PubMed · Cited by 176 · see citing works

Detection of mitochondrial DNA depletion in living human cells using PicoGreen staining

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Cytoplasmic transfer of chloramphenicol resistance in human tissue culture cells.

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Respiration and Growth Defects in Transmitochondrial Cell Lines Carrying the 11778 Mutation Associated with Leber's Hereditary Optic Neuropathy

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Severe Impairment of Complex I–Driven Adenosine Triphosphate Synthesis in Leber Hereditary Optic Neuropathy Cybrids

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Use of Transmitochondrial Cybrids To Assign a Complex I Defect to the Mitochondrial DNA-Encoded NADH Dehydrogenase Subunit 6 Gene Mutation at Nucleotide Pair 14459 That Causes Leber Hereditary Optic Neuropathy and Dystonia

Jun, A. S., Trounce, I. A., Brown, M. D., Shoffner, J. M., & Wallace, D. C. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.3.771 · Cited by 158 · see citing works

Altered Calcium Homeostasis in Cells Transformed by Mitochondria from Individuals with Parkinson's Disease

Sheehan, J. P., Swerdlow, R. H., Parker, W. D., Miller, S. W., Davis, R. E., & Tuttle, J. B. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.68031221.x · Cited by 151 · see citing works

Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family

Swerdlow, R. H., Parks, J. K., Davis, J. N., Cassarino, D. S., Trimmer, P. A., Currie, L. J., Dougherty, J., Bridges, W. S., Bennett, J. P., Wooten, G. F., et al. (1998) · Annals of Neurology · doi:10.1002/ana.410440605 · Cited by 148 · see citing works

Ethidium bromide-induced loss of mitochondrial DNA from primary chicken embryo fibroblasts.

Desjardins, P., Frost, E., & Morais, R. (1985) · Molecular and Cellular Biology · doi:10.1128/mcb.5.5.1163 · Cited by 139 · see citing works

High frequency of mitochondrial complex I mutations in Parkinson’s disease and aging

Smigrodzki, R. M., Parks, J. K., & Parker, W. D. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2004.02.020 · Cited by 138 · see citing works

Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers.

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Rearrangements of Human Mitochondrial DNA (mtDNA): New Insights into the Regulation of mtDNA Copy Number and Gene Expression

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Creation and Characterization of Mitochondrial DNA‐Depleted Cell Lines with “Neuronal‐Like” Properties

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Mitochondria in Alzheimer's disease

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MtDNA Mutations Associated with Leber′s Hereditary Optic Neuropathy: Studies on Cytoplasmic Hybrid (Cybrid) Cells

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Parkinson's disease transgenic mitochondrial cybrids generate Lewy inclusion bodies

Trimmer, P. A., Borland, M., Keeney, P. M., Bennett, J. P., & Parker, W. D. (2004) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02168.x · Cited by 121 · see citing works

Interaction Among Mitochondria, Mitogen‐Activated Protein Kinases, and Nuclear Factor‐κB in Cellular Models of Parkinson's Disease

Cassarino, D. S., Halvorsen, E. M., Swerdlow, R. H., Abramova, N. N., Parker, W. D., Sturgill, T. W., & Bennett, J. P. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0741384.x · Cited by 121 · see citing works

Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion.

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Nuclear but not mitochondrial genome involvement in human age-related mitochondrial dysfunction. Functional integrity of mitochondrial DNA from aged subjects.

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Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson’s disease

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In Vitro Analysis of Mutations Causing Myoclonus Epilepsy with Ragged-Red Fibers in the Mitochondrial tRNALys Gene: Two Genotypes Produce Similar Phenotypes

Masucci, J. P., Davidson, M. M., Koga, Y., Schon, E. A., & King, M. P. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.5.2872 · Cited by 111 · see citing works

On auxotrophy for pyrimidines of respiration‐deficient chick embryo cells

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Mitochondrial ND5 mutations in idiopathic Parkinson’s disease

Parker, W. D., & Parks, J. K. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.11.093 · Cited by 108 · see citing works

Cyclosporin A Increases Resting Mitochondrial Membrane Potential in SY5Y Cells and Reverses the Depressed Mitochondrial Membrane Potential of Alzheimer's Disease Cybrids

Cassarino, D. S., Swerdlow, R. H., Parks, J. K., Parker, W. D., & Bennett, J. P. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.8866 · Cited by 98 · see citing works

Mitochondrial Dysfunction in Idiopathic Parkinson Disease

Parker, W. D., & Swerdlow, R. H. (1998) · The American Journal of Human Genetics · doi:10.1086/301812 · Cited by 97 · see citing works

Transmission of mitochondrial DNA disorders: possibilities for the future

Brown, D., Herbert, M., Lamb, V. K., Chinnery, P. F., Taylor, R. W., Lightowlers, R., Craven, L., Cree, L. M., Gardner, J., & Turnbull, D. (2006) · The Lancet · doi:10.1016/s0140-6736(06)68972-1 · Cited by 97 · see citing works

Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations

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Mitochondrial Dysfunction in Cybrid Lines Expressing Mitochondrial Genes from Patients with Progressive Supranuclear Palsy

Swerdlow, R. H., Golbe, L. I., Parks, J. K., Cassarino, D. S., Binder, D. R., Grawey, A. E., Litvan, I., Bennett, J. P., Wooten, G. F., & Parker, W. D. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0751681.x · Cited by 95 · see citing works

Mitochondrial DNA as a Cancer Biomarker

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Aging-dependent Functional Alterations of Mitochondrial DNA (mtDNA) from Human Fibroblasts Transferred into mtDNA-less Cells

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Use of Cytoplasmic Hybrid Cell Lines for Elucidating the Role of Mitochondrial Dysfunction in Alzheimer's Disease and Parkinson's Disease

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Reversible tenfod reduction in mitochondrial DNA content of human cells treated with ethidium bromide

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Mitochondrial abnormalities in cybrid cell models of sporadic Alzheimer's disease worsen with passage in culture

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Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from elderly patients with Alzheimer’s disease

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Differentiated Alzheimer's Disease Transmitochondrial Cybrid Cell Lines Exhibit Reduced Organelle Movement

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