Works by Schon, Eric A.
Results: 59
Aberrant ER-mitochondria communication is a common pathomechanism in mitochondrial disease.
- Published in:
- Cell Death & Disease, 2024, v. 15, n. 6, p. 1, doi. 10.1038/s41419-024-06781-9
- By:
- Publication type:
- Article
A key role for MAM in mediating mitochondrial dysfunction in Alzheimer disease.
- Published in:
- Cell Death & Disease, 2018, v. 9, n. 3, p. 1, doi. 10.1038/s41419-017-0215-0
- By:
- Publication type:
- Article
A toolkit for the cell's powerhouse.
- Published in:
- Nature Biotechnology, 2008, v. 26, n. 3, p. 294, doi. 10.1038/nbt0308-294
- By:
- Publication type:
- Article
α-Synuclein Is Localized to Mitochondria-Associated ER Membranes.
- Published in:
- Journal of Neuroscience, 2014, v. 34, n. 1, p. 249, doi. 10.1523/JNEUROSCI.2507-13.2014
- By:
- Publication type:
- Article
Germ-Line Therapy to Cure Mitochondrial Disease: Protocol and Ethics of In Vitro Ovum Nuclear Transplantation.
- Published in:
- Cambridge Quarterly of Healthcare Ethics, 1995, v. 4, n. 3, p. 316, doi. 10.1017/S0963180100006071
- By:
- Publication type:
- Article
Clinical and Biochemical Studies on Cytochrome Oxidase Deficienciesa.
- Published in:
- Annals of the New York Academy of Sciences, 1988, v. 550, n. 1, p. 348, doi. 10.1111/j.1749-6632.1988.tb35349.x
- By:
- Publication type:
- Article
Identification of a mutation in the mitochondrial tRNA<sup>Cys</sup> gene associated with mitochondrial encephalopathy.
- Published in:
- Human Mutation, 1996, v. 7, n. 2, p. 158, doi. 10.1002/(SICI)1098-1004(1996)7:2<158::AID-HUMU12>3.0.CO;2-1
- By:
- Publication type:
- Article
Human mitochondrial DNA: roles of inherited and somatic mutations.
- Published in:
- Nature Reviews Genetics, 2012, v. 13, n. 12, p. 878, doi. 10.1038/nrg3275
- By:
- Publication type:
- Article
Is Alzheimer's Disease a Disorder of Mitochondria-Associated Membranes?
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 20, p. 281, doi. 10.3233/JAD-2010-100495
- By:
- Publication type:
- Article
Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 978, doi. 10.1093/hmg/ddr529
- By:
- Publication type:
- Article
Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 1, p. 170, doi. 10.1093/hmg/ddp477
- By:
- Publication type:
- Article
A functionally dominant mitochondrial DNA mutation.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 12, p. 1814, doi. 10.1093/hmg/ddn073
- By:
- Publication type:
- Article
Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene.
- Published in:
- Muscle & Nerve, 1995, v. 18, n. S14, p. S119, doi. 10.1002/mus.880181424
- By:
- Publication type:
- Article
Differential expression of nuclear genes for cytochrome c oxidase during myogenesis.
- Published in:
- Muscle & Nerve, 1990, v. 13, n. 4, p. 330, doi. 10.1002/mus.880130409
- By:
- Publication type:
- Article
Mitochondrial Respiratory Chain Diseases and Mutations in Nuclear DNA: A Promising Start?
- Published in:
- Brain Pathology, 2000, v. 10, n. 3, p. 442, doi. 10.1111/j.1750-3639.2000.tb00276.x
- By:
- Publication type:
- Article
Myoclonic Epilepsy with Ragged-red Fibers (MERRF): An Immunohistochemical Study of the Brain.
- Published in:
- Brain Pathology, 1995, v. 5, n. 2, p. 125, doi. 10.1111/j.1750-3639.1995.tb00586.x
- By:
- Publication type:
- Article
Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variability.
- Published in:
- EMBO Journal, 2016, v. 35, n. 18, p. 1979, doi. 10.15252/embj.201694892
- By:
- Publication type:
- Article
Upregulated function of mitochondria-associated ER membranes in Alzheimer disease.
- Published in:
- EMBO Journal, 2012, v. 31, n. 21, p. 4106, doi. 10.1038/emboj.2012.202
- By:
- Publication type:
- Article
Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects.
- Published in:
- Muscle & Nerve, 2002, v. 26, n. 5, p. 597, doi. 10.1002/mus.10194
- By:
- Publication type:
- Article
Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reaction.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Ketogenic treatment reduces deleted mitochondrial DNAs in cultured human cells.
- Published in:
- Annals of Neurology, 2004, v. 56, n. 5, p. 662
- By:
- Publication type:
- Article
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy.
- Published in:
- Annals of Neurology, 2002, v. 52, n. 5, p. 534, doi. 10.1002/ana.10354
- By:
- Publication type:
- Article
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency.
- Published in:
- 2018
- By:
- Publication type:
- journal article
A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency.
- Published in:
- Nature Medicine, 1999, v. 5, n. 8, p. 951, doi. 10.1038/11396
- By:
- Publication type:
- Article
Kearns-Sayre syndrome: unusual pattern of expression of subunits of the respiratory chain in the cerebellar system.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Neurotrophin-4 is up-regulated in ragged-red fibers associated with pathogenic mitochondrial DNA mutations.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Association of myopathy with large-scale mitochondrial dna duplications and deletions: Which is pathogenic?
- Published in:
- Annals of Neurology, 1997, v. 42, n. 2, p. 180, doi. 10.1002/ana.410420208
- By:
- Publication type:
- Article
Mitochondrial DNA and RNA processing in MELAS.
- Published in:
- Annals of Neurology, 1996, v. 40, n. 2, p. 172, doi. 10.1002/ana.410400208
- By:
- Publication type:
- Article
On the Pathogenesis of Alzheimer's Disease: The MAM Hypothesis.
- Published in:
- FASEB Journal, 2017, v. 31, n. 3, p. 864, doi. 10.1096/fj.201601309
- By:
- Publication type:
- Article
ATP-binding cassette transporters and sterol O-acyltransferases interact at membrane microdomains to modulate sterol uptake and esterification.
- Published in:
- FASEB Journal, 2015, v. 29, n. 11, p. 4682, doi. 10.1096/fj.14-264796
- By:
- Publication type:
- Article
Mitochondrial DNA Mutations in Cancer.
- Published in:
- PLoS Medicine, 2005, v. 2, n. 11, p. 1082, doi. 10.1371/journal.pmed.0020401
- By:
- Publication type:
- Article
Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging?
- Published in:
- Aging Cell, 2006, v. 5, n. 3, p. 279, doi. 10.1111/j.1474-9726.2006.00209.x
- By:
- Publication type:
- Article
Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation.
- Published in:
- Journal of Cell Biology, 2008, v. 181, n. 7, p. 1117, doi. 10.1083/jcb.200712101
- By:
- Publication type:
- Article
Extremely high levels of mutant mtDNAs co-localize with cytocohrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 3, p. 449
- By:
- Publication type:
- Article
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 1, p. 13
- By:
- Publication type:
- Article
Mitochondrial diseases: Genetics.
- Published in:
- Biofactors, 1998, v. 7, n. 3, p. 191, doi. 10.1002/biof.5520070304
- By:
- Publication type:
- Article
Increased localization of APP-C99 in mitochondria-associated ER membranes causes mitochondrial dysfunction in Alzheimer disease.
- Published in:
- EMBO Journal, 2017, v. 36, n. 22, p. 3356, doi. 10.15252/embj.201796797
- By:
- Publication type:
- Article
Mitochondrial DNA genotypes in nuclear transfer-derived cloned sheep.
- Published in:
- Nature Genetics, 1999, v. 23, n. 1, p. 90, doi. 10.1038/12696
- By:
- Publication type:
- Article
Nuclear power and mitochondrial disease.
- Published in:
- Nature Genetics, 1998, v. 19, n. 3, p. 214, doi. 10.1038/883
- By:
- Publication type:
- Article
Mitochondria, OxPhos, and neurodegeneration: cells are not just running out of gas.
- Published in:
- 2019
- By:
- Publication type:
- journal article
ApoE4 upregulates the activity of mitochondria-associated ER membranes.
- Published in:
- EMBO Reports, 2016, v. 17, n. 1, p. 27, doi. 10.15252/embr.201540614
- By:
- Publication type:
- Article
Novel subcellular localization for - synuclein: possible functional consequences.
- Published in:
- Frontiers in Neuroanatomy, 2015, v. 9, p. 1, doi. 10.3389/fnana.2015.00017
- By:
- Publication type:
- Article
Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with SCO2 mutations.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with sco2 mutations.
- Published in:
- Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 21, doi. 10.1186/1750-1172-7-21
- By:
- Publication type:
- Article
Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus.
- Published in:
- Nature Genetics, 2002, v. 30, n. 4, p. 394, doi. 10.1038/ng851
- By:
- Publication type:
- Article
MFN2 mutations in Charcot–Marie–Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 11, p. 1782, doi. 10.1093/hmg/ddz008
- By:
- Publication type:
- Article
Low-dose rapamycin extends lifespan in a mouse model of mtDNA depletion syndrome.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 23, p. 4588, doi. 10.1093/hmg/ddx341
- By:
- Publication type:
- Article
Cardiac deficiency of single cytochrome oxidase assembly factor scox induces p53-dependent apoptosis in a Drosophila cardiomyopathy model.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 13, p. 3608, doi. 10.1093/hmg/ddv106
- By:
- Publication type:
- Article
Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Power, sex, suicide.
- Published in:
- 2006
- By:
- Publication type:
- Book Review