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Coordinate reciprocal trends in glycolytic and mitochondrial transcript accumulations during the in vitro differentiation of human myoblasts.
- Published in:
- Journal of Cellular Physiology, 1990, v. 142, n. 3, p. 566, doi. 10.1002/jcp.1041420316
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- Publication type:
- Article
Altered methionine metabolism occurs in all members of a set of diverse human tumor cell lines.
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- 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.
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- Journal of Cellular Physiology, 1983, v. 117, n. 1, p. 9, doi. 10.1002/jcp.1041170103
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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
MISSOURI RIVER FLOOD OF 1993: ROLE OF WOODY CORRIDOR WIDTH IN LEVEE PROTECTION.
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- 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
A mitochondrial bioenergetic etiology of disease.
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- 2013
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- Publication type:
- journal article
A mitochondrial bioenergetic etiology of disease.
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- Journal of Clinical Investigation, 2013, v. 123, n. 4, p. 1405, doi. 10.1172/JCI61398
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- Publication type:
- Article
Perspectives: Anecdotal, Historical and Critical Commentaries on Genetics.
- Published in:
- Genetics, 2008, v. 179, n. 2, p. 727
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- Publication type:
- Article
Classification of European mtDNAs from an analysis of three European populations.
- Published in:
- Genetics, 1996, v. 144, n. 4, p. 1835, doi. 10.1093/genetics/144.4.1835
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- Publication type:
- Article
Mitochondrial DNA Complex I and III Mutations Associated With Leber's Hereditary Optic Neuropathy.
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- Genetics, 1992, v. 130, n. 1, p. 163, doi. 10.1093/genetics/130.1.163
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- Publication type:
- Article
Native American Mitochondrial DNA Analysis Indicates That the Amerind and the Nadene Populations Were Founded by Two Independent Migrations.
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- Genetics, 1992, v. 130, n. 1, p. 153, doi. 10.1093/genetics/130.1.153
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- Publication type:
- Article
Southeast Asian Mitochondrial DNA Analysis Reveals Genetic Continuity of Ancient Mongoloid Migrations.
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- Genetics, 1992, v. 130, n. 1, p. 139, doi. 10.1093/genetics/130.1.139
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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.
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- 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
An enhanced MITOMAP with a global mtDNA mutational phylogeny.
- Published in:
- Nucleic Acids Research, 2007, v. 35, p. d823, doi. 10.1093/nar/gkl927
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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
Survivin promotes oxidative phosphorylation, subcellular mitochondrial repositioning, and tumor cell invasion.
- Published in:
- Science Signaling, 2015, v. 8, n. 389, p. 1, doi. 10.1126/scisignal.aab1624
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- Publication type:
- Article
Hypoxemia Is Associated With Mitochondrial DNA Damage and Gene Induction.
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- 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
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
DNA microarrays as a method to monitor changes in mitochondria-related gene expression during development and mitochondrial dysfunction.
- Published in:
- 1999
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- Publication type:
- Abstract
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
Cristae remodeling causes acidification detected by integrated graphene sensor during mitochondrial outer membrane permeabilization.
- Published in:
- Scientific Reports, 2016, p. 35907, doi. 10.1038/srep35907
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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
Peripheral Blood Mitochondrial DNA as a Biomarker of Cerebral Mitochondrial Dysfunction following Traumatic Brain Injury in a Porcine Model.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0130927
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- Publication type:
- Article
Human Retinal Transmitochondrial Cybrids with J or H mtDNA Haplogroups Respond Differently to Ultraviolet Radiation: Implications for Retinal Diseases.
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- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099003
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- Publication type:
- Article
Mitochondrial DNA Variants Mediate Energy Production and Expression Levels for CFH, C3 and EFEMP1 Genes: Implications for Age-Related Macular Degeneration.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054339
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- Publication type:
- Article
Succinate Dehydrogenase Is a Direct Target of Sirtuin 3 Deacetylase Activity.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023295
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- Publication type:
- Article
VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease.
- Published in:
- PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013183
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- Publication type:
- Article
Mitochondrial Variants in Schizophrenia, Bipolar Disorder, and Major Depressive Disorder.
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- PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004913
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- Publication type:
- Article
Heterozygous Mutation of Opa1 in Drosophila Shortens Lifespan Mediated through Increased Reactive Oxygen Species Production.
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- PLoS ONE, 2009, v. 4, n. 2, p. 1, doi. 10.1371/journal.pone.0004492
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- Publication type:
- Article
Premature Lambs Exhibit Normal Mitochondrial Respiration after Long-Term Extrauterine Support.
- Published in:
- 2019
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- Publication type:
- journal article
Conformational mutations in human mitochondrial DNA.
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- Nature, 1987, v. 329, n. 6136, p. 270, doi. 10.1038/329270a0
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- Publication type:
- Article
Elevated male European and female African contributions to the genomes of African American individuals.
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- 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.
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- 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
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
TGF-β1 induction of the adenine nucleotide translocator 1 in astrocytes occurs through Smads and Sp1 transcription factors.
- Published in:
- BMC Neuroscience, 2004, v. 5, p. 1, doi. 10.1186/1471-2202-5-1
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- Publication type:
- 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
GENOME SIZE AND LIFE CYCLE OF THE MYCOPLASMA*.
- Published in:
- Annals of the New York Academy of Sciences, 1973, v. 225, n. 1, p. 62, doi. 10.1111/j.1749-6632.1973.tb45637.x
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- Publication type:
- Article
Fast capillary electrophoresis-laser induced fluorescence analysis of ligase chain reaction products: Human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy.
- Published in:
- Electrophoresis, 1996, v. 17, n. 12, p. 1875, doi. 10.1002/elps.1150171212
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- Publication type:
- Article
Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41398-019-0643-y
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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
MITOMAP: a human mitochondrial genome database—2004 update.
- Published in:
- Nucleic Acids Research, 2005, v. 33, n. suppl 1, p. d611
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- Publication type:
- Article
Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells.
- Published in:
- Nucleic Acids Research, 2000, v. 28, n. 10, p. 2164, doi. 10.1093/nar/28.10.2164
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- Publication type:
- Article
MITOMAP: a human mitochondrial genome database—1998 update.
- Published in:
- Nucleic Acids Research, 1998, v. 26, n. 1, p. 112, doi. 10.1093/nar/26.1.112
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- Publication type:
- Article