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Let's make it clear: systematic exploration of mitochondrial DNA– and RNA–protein complexes by complexome profiling.
- Published in:
- Nucleic Acids Research, 2023, v. 51, n. 19, p. 10619, doi. 10.1093/nar/gkad697
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- Article
Top3α is the replicative topoisomerase in mitochondrial DNA replication.
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- Nucleic Acids Research, 2022, v. 50, n. 15, p. 8733, doi. 10.1093/nar/gkac660
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- Article
Mitochondrial RNA processing defect caused by a SUPV3L1 mutation in two siblings with a novel neurodegenerative syndrome.
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- Journal of Inherited Metabolic Disease, 2022, v. 45, n. 2, p. 292, doi. 10.1002/jimd.12476
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- Article
Mitochondrial RNA granules are critically dependent on mtDNA replication factors Twinkle and mtSSB.
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- Nucleic Acids Research, 2019, v. 47, n. 7, p. 3680, doi. 10.1093/nar/gkz047
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- Article
Transcript availability dictates the balance between strand-asynchronous and strand-coupled mitochondrial DNA replication.
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- Nucleic Acids Research, 2018, v. 46, n. 20, p. 10771, doi. 10.1093/nar/gky852
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- Article
A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome.
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- Human Molecular Genetics, 2017, v. 26, n. 13, p. 2541, doi. 10.1093/hmg/ddx152
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- Article
Corrigendum: Human Mitochondrial DNA-Protein Complexes Attach to a Cholesterol-Rich Membrane Structure.
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- Scientific Reports, 2015, p. 17119, doi. 10.1038/srep17119
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- Article
The hexameric structure of the human mitochondrial replicative helicase Twinkle.
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- Nucleic Acids Research, 2015, v. 43, n. 8, p. 4284, doi. 10.1093/nar/gkv189
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- Article
The multikinase inhibitor Sorafenib enhances glycolysis and synergizes with glycolysis blockade for cancer cell killing.
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- Scientific Reports, 2015, p. 9149, doi. 10.1038/srep09149
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- Article
Whole Cell Formaldehyde Cross-Linking Simplifies Purification of Mitochondrial Nucleoids and Associated Proteins Involved in Mitochondrial Gene Expression.
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- PLoS ONE, 2015, v. 10, n. 2, p. 1, doi. 10.1371/journal.pone.0116726
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- Article
Replication factors transiently associate with mtDNA at the mitochondrial inner membrane to facilitate replication.
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- Nucleic Acids Research, 2014, v. 42, n. 2, p. 952, doi. 10.1093/nar/gkt988
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- Article
Analysis of 953 Human Proteins from a Mitochondrial HEK293 Fraction by Complexome Profiling.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068340
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- Article
Mytoe: automatic analysis of mitochondrial dynamics.
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- Bioinformatics, 2012, v. 28, n. 7, p. 1050, doi. 10.1093/bioinformatics/bts073
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- Article
Sequence-specific stalling of DNA polymerase γ and the effects of mutations causing progressive ophthalmoplegia†.
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- Human Molecular Genetics, 2011, v. 20, n. 6, p. 1212, doi. 10.1093/hmg/ddq565
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- Article
Functional organization of mammalian mitochondrial DNA in nucleoids: History, recent developments, and future challenges.
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- IUBMB Life, 2010, v. 62, n. 1, p. 19, doi. 10.1002/iub.282
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- Article
A New Splice Variant of the Mouse SIRT3 Gene Encodes the Mitochondrial Precursor Protein.
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- PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004986
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- Article
Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling.
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- Human Molecular Genetics, 2009, v. 18, n. 2, p. 328, doi. 10.1093/hmg/ddn359
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- Article
Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.
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- Human Molecular Genetics, 2008, v. 17, n. 23, p. 3822, doi. 10.1093/hmg/ddn280
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- Article
What causes mitochondrial DNA deletions in human cells?
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- Nature Genetics, 2008, v. 40, n. 3, p. 275, doi. 10.1038/ng.f.94
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- Article
Twinkle helicase (PEO1) gene mutation causes mitochondrial DNA depletion.
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- Annals of Neurology, 2007, v. 62, n. 6, p. 579, doi. 10.1002/ana.21207
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- Article
The mitochondrial transcription termination factor mTERF modulates replication pausing in human mitochondrial DNA.
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- Nucleic Acids Research, 2007, v. 35, n. 19, p. 6458, doi. 10.1093/nar/gkm676
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- Article
Expression of catalytic mutants of the mtDNA helicase Twinkle and polymerase POLG causes distinct replication stalling phenotypes.
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- Nucleic Acids Research, 2007, v. 35, n. 10, p. 3238, doi. 10.1093/nar/gkm215
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- Article
The AAA<sup>+</sup> protein ATAD3 has displacement loop binding properties and is involved in mitochondrial nucleoid organization.
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- Journal of Cell Biology, 2007, v. 176, n. 2, p. 141, doi. 10.1083/jcb.200609158
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- Article
Alterations to the expression level of mitochondrial transcription factor A, TFAM, modify the mode of mitochondrial DNA replication in cultured human cells.
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- Nucleic Acids Research, 2006, v. 34, n. 20, p. 5815
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- Article
Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky.
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- Human Molecular Genetics, 2005, v. 14, n. 20, p. 2981, doi. 10.1093/hmg/ddi328
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- Article
Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number.
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- Human Molecular Genetics, 2004, v. 13, n. 24, p. 3219, doi. 10.1093/hmg/ddh342
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- Article
Twinkle and POLG defects enhance age‐dependent accumulation of mutations in the control region of mtDNA.
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- Nucleic Acids Research, 2004, v. 32, n. 10, p. 3053, doi. 10.1093/nar/gkh634
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- Article
Premature ageing in mice expressing defective mitochondrial DNA polymerase.
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- Nature, 2004, v. 429, n. 6990, p. 417, doi. 10.1038/nature02517
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- Article
Ditercalinium chloride, a pro-anticancer drug, intimately associates with mammalian mitochondrial DNA and inhibits its replication.
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- Current Genetics, 2003, v. 43, n. 5, p. 364, doi. 10.1007/s00294-003-0393-4
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- Article
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.
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- Nature Genetics, 2001, v. 28, n. 3, p. 223, doi. 10.1038/90058
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- Article
Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states.
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- Human Molecular Genetics, 2000, v. 9, n. 19, p. 2821, doi. 10.1093/hmg/9.19.2821
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- Article
The dangers of extended PCR in the clinic.
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- Nature Medicine, 1999, v. 5, n. 9, p. 965, doi. 10.1038/12379
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Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individuals.
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- European Journal of Human Genetics, 1999, v. 7, n. 2, p. 140, doi. 10.1038/sj.ejhg.5200244
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- Article
The pre-mRNA of nuclear respiratory factor 1, a regulator of mitochondrial biogenesis, is alternatively spliced in human tissues and cell lines.
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- Human Molecular Genetics, 1995, v. 4, n. 9, p. 1591
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The relationship between mitochondrial genotype and mitochondrial phenotype in lymphoblasts with a heteroplasmic mtDNA deletion.
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- Human Molecular Genetics, 1994, v. 3, n. 11, p. 1989
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