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Complete mitochondrial DNA sequence analysis in a family with early-onset dystonia and optic atrophy.
- Published in:
- Movement Disorders, 2004, v. 19, n. 2, p. 235, doi. 10.1002/mds.10646
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- Publication type:
- Article
Elevated male European and female African contributions to the genomes of African American individuals.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 713, doi. 10.1007/s00439-006-0261-7
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- Publication type:
- Article
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
- Published in:
- Human Genetics, 2002, v. 110, n. 2, p. 130, doi. 10.1007/s00439-001-0660-8
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- Publication type:
- Article
Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families.
- Published in:
- Human Genetics, 2001, v. 109, n. 1, p. 33, doi. 10.1007/s004390100538
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- Publication type:
- Article
An Inherited Heteroplasmic Mutation in Mitochondrial Gene COI in a Patient with Prostate Cancer Alters Reactive Oxygen, Reactive Nitrogen and Proliferation.
- Published in:
- BioMed Research International, 2013, v. 2013, p. 1, doi. 10.1155/2013/239257
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- Publication type:
- Article
Systemic Mitochondrial Dysfunction and the Etiology of Alzheimer's Disease and Down Syndrome Dementia.
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- Journal of Alzheimer's Disease, 2010, v. 20, p. S293, doi. 10.3233/JAD-2010-100351
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- Publication type:
- Article
Systemic mitochondrial dysfunction and the etiology of Alzheimer's disease and down syndrome dementia.
- Published in:
- 2010
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- Publication type:
- journal article
Unlocking the Complexity of Mitochondrial DNA: A Key to Understanding Neurodegenerative Disease Caused by Injury.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 12, p. 3460, doi. 10.3390/cells10123460
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- Publication type:
- Article
BKCa (Slo) Channel Regulates Mitochondrial Function and Lifespan in Drosophila melanogaster.
- Published in:
- Cells (2073-4409), 2019, v. 8, n. 9, p. 945, doi. 10.3390/cells8090945
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- Publication type:
- Article
SARS-COV-2 viroporins activate the NLRP3-inflammasome by the mitochondrial permeability transition pore.
- Published in:
- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.1064293
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- Publication type:
- Article
APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40797-7
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- Publication type:
- Article
Detection of Low Levels of the Mitochondrial tRNA<sup>Leu(UUR)</sup> 3243A>G Mutation in Blood Derived from Patients with Diabetes.
- Published in:
- Molecular Diagnosis & Therapy, 2006, v. 10, n. 6, p. 381, doi. 10.1007/BF03256215
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- Publication type:
- Article
Vascular assessment of the periarticular ligaments of the rabbit knee.
- Published in:
- Journal of Orthopaedic Research, 1991, v. 9, n. 6, p. 787, doi. 10.1002/jor.1100090603
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- Publication type:
- Article
Essential role of mitochondrial energy metabolism in Foxp3<sup>+</sup> T-regulatory cell function and allograft survival.
- Published in:
- FASEB Journal, 2015, v. 29, n. 6, p. 2315, doi. 10.1096/fj.14-268409
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- Publication type:
- Article
Heteroplasmic mutations of the mitochondrial genome cause paradoxical effects on mitochondrial functions.
- Published in:
- FASEB Journal, 2012, v. 26, n. 12, p. 4914, doi. 10.1096/fj.12-206532
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- Publication type:
- Article
A Mitochondrial Etiology of Neurodegenerative Diseases: Evidence from Parkinson's Disease.
- Published in:
- Annals of the New York Academy of Sciences, 2008, v. 1147, p. 1, doi. 10.1196/annals.1427.001
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- Publication type:
- Article
Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders.
- Published in:
- Genetic Epidemiology, 1996, v. 13, n. 6, p. 605, doi. 10.1002/(SICI)1098-2272(1996)13:6<605::AID-GEPI6>3.0.CO;2-Z
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- Publication type:
- Article
The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore.
- Published in:
- Nature, 2004, v. 427, n. 6973, p. 461, doi. 10.1038/nature02229
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- Publication type:
- Article
Association of Mitochondrial Biogenesis With Variable Penetrance of Schizophrenia.
- Published in:
- 2021
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- Publication type:
- journal article
Mitochondrial Etiology of Psychiatric Disorders-Reply.
- Published in:
- 2018
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- Publication type:
- letter
Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders.
- Published in:
- 2017
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- Publication type:
- journal article
A Mitochondrial Etiology of Neuropsychiatric Disorders.
- Published in:
- 2017
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- Publication type:
- journal article
Inherited mitochondrial DNA variants can affect complement, inflammation and apoptosis pathways: insights into mitochondrial–nuclear interactions.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 13, p. 3537, doi. 10.1093/hmg/ddu065
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- Publication type:
- Article
Corrigendum: Landscape of the mitochondrial Hsp90 metabolome in tumours.
- Published in:
- Nature Communications, 2015, v. 6, n. 6, p. 7605, doi. 10.1038/ncomms8605
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- Publication type:
- Article
Trans-mitochondrial coordination of cristae at regulated membrane junctions.
- Published in:
- Nature Communications, 2015, v. 6, n. 2, p. 6259, doi. 10.1038/ncomms7259
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- Publication type:
- Article
Landscape of the mitochondrial Hsp90 metabolome in tumours.
- Published in:
- Nature Communications, 2013, v. 4, n. 7, p. 2139, doi. 10.1038/ncomms3139
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- Publication type:
- Article
Host mitochondria influence gut microbiome diversity: A role for ROS.
- Published in:
- Science Signaling, 2019, v. 12, n. 588, p. N.PAG, doi. 10.1126/scisignal.aaw3159
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- Publication type:
- Article
Microchambers with Solid-State Phosphorescent Sensor for Measuring Single Mitochondrial Respiration.
- Published in:
- Sensors (14248220), 2016, v. 16, n. 7, p. 1065, doi. 10.3390/s16071065
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- Publication type:
- Article
Homozygous boricua TBCK mutation causes neurodegeneration and aberrant autophagy.
- Published in:
- 2018
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- Publication type:
- journal article
MitoScape: A big-data, machine-learning platform for obtaining mitochondrial DNA from next-generation sequencing data.
- Published in:
- PLoS Computational Biology, 2021, v. 17, n. 11, p. 1, doi. 10.1371/journal.pcbi.1009594
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- Publication type:
- Article
Altered methionine metabolism occurs in all members of a set of diverse human tumor cell lines.
- Published in:
- Journal of Cellular Physiology, 1984, v. 119, n. 1, p. 29, doi. 10.1002/jcp.1041190106
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- Publication type:
- Article
Reduced free-methionine in methionine-dependent SV40-transformed human fibroblasts synthesizing apparently normal amounts of methionine.
- Published in:
- Journal of Cellular Physiology, 1983, v. 117, n. 1, p. 9, doi. 10.1002/jcp.1041170103
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- Publication type:
- Article
Novel mitochondrial DNA deletion found in a renal cell carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 1996, v. 15, n. 2, p. 95, doi. 10.1002/(SICI)1098-2264(199602)15:2<95::AID-GCC3>3.0.CO;2-Z
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- Publication type:
- Article
Multi-organ characterization of mitochondrial genomic rearrangements in ad libitum and caloric restricted mice show striking somatic mitochondrial DNA rearrangements with age.
- Published in:
- Nucleic Acids Research, 1997, v. 25, n. 5, p. 974, doi. 10.1093/nar/25.5.974
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- Publication type:
- Article
MITOMAP: an update on the status of the human mitochondrial genome database.
- Published in:
- Nucleic Acids Research, 1997, v. 25, n. 1, p. 196, doi. 10.1093/nar/25.1.196
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- Publication type:
- Article
MITOMAP: A Human Mitochondrial Genome Database.
- Published in:
- Nucleic Acids Research, 1996, v. 24, n. 1, p. 177, doi. 10.1093/nar/24.1.177
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- Publication type:
- Article
Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 2, p. 200, doi. 10.1038/ejhg.2010.169
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- Publication type:
- Article
MISSOURI RIVER FLOOD OF 1993: ROLE OF WOODY CORRIDOR WIDTH IN LEVEE PROTECTION.
- Published in:
- Journal of the American Water Resources Association, 2003, v. 39, n. 4, p. 923, doi. 10.1111/j.1752-1688.2003.tb04416.x
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- Publication type:
- Article
Reply.
- Published in:
- Annals of Neurology, 1986, v. 20, n. 4, p. 546, doi. 10.1002/ana.410200425
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- Publication type:
- Article
Maternally inherited mitochondrial myopathy and myoclonic epilepsy.
- Published in:
- Annals of Neurology, 1985, v. 17, n. 3, p. 228, doi. 10.1002/ana.410170303
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- Publication type:
- Article
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss.
- Published in:
- Nature Genetics, 2011, v. 43, n. 6, p. 595, doi. 10.1038/ng.830
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- Publication type:
- Article
Giuseppe Attardi 1923–2008.
- Published in:
- 2008
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- Publication type:
- Obituary
Life extension through neurofibromin mitochondrial regulation and antioxidant therapy for neurofibromatosis-1 in Drosophila melanogaster.
- Published in:
- Nature Genetics, 2007, v. 39, n. 4, p. 476, doi. 10.1038/ng2004
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- Publication type:
- Article
Immunocytochemical Characterization of the Mitochondrially Encoded ND1 Subunit of Complex I (NADH: Ubiquinone Oxidoreductase) in Rat Brain.
- Published in:
- Journal of Neurochemistry, 2000, v. 75, n. 1, p. 383, doi. 10.1046/j.1471-4159.2000.0750383.x
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- Publication type:
- Article
TSPO, a Mitochondrial Outer Membrane Protein, Controls Ethanol-Related Behaviors in Drosophila.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 8, p. 1, doi. 10.1371/journal.pgen.1005366
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- Publication type:
- Article
Ancient mtDNA Genetic Variants Modulate mtDNA Transcription and Replication.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 5, p. 1, doi. 10.1371/journal.pgen.1000474
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- Publication type:
- Article
The Molecular Mechanisms of OPA1-Mediated Optic Atrophy in Drosophila Model and Prospects for Antioxidant Treatment.
- Published in:
- PLoS Genetics, 2008, v. 4, n. 1, p. e6, doi. 10.1371/journal.pgen.0040006
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- Publication type:
- Article
Mitochondrial respiration is sensitive to cytoarchitectural breakdown.
- Published in:
- Integrative Biology, 2016, v. 8, n. 11, p. 1170, doi. 10.1039/c6ib00192k
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- Publication type:
- Article
Hypoxemia Is Associated With Mitochondrial DNA Damage and Gene Induction.
- Published in:
- JAMA: Journal of the American Medical Association, 1991, v. 266, n. 13, p. 1812, doi. 10.1001/jama.1991.03470130092035
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- Publication type:
- Article
Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups.
- Published in:
- Annals of Human Genetics, 2005, v. 69, n. 1, p. 67, doi. 10.1046/j.1529-8817.2003.00127.x
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- Publication type:
- Article