Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies
Hess, John F., Parisi, Melissa A., Bennett, Jeffrey L., Clayton, David A.·1991·Nature
DOI 10.1038/351236a0
Cited by (234)
Items 201–234 of 234
- Quantifying phenotype and genotype distributions in single muscle fibres from patients carrying the pathogenic mtDNA variant m.3243A>GSyeda T Ahmed, Robert William Taylor, Douglass M. Turnbull, Conor Lawless, Sarah J. Pickett · 2022 · medRxiv
- Mitochondrial Disturbances in Parkinson’s DiseaseHeinz Reichmann, Bernd Janetzky, Peter Franz Riederer · 1994 · Birkhäuser Boston eBooks
- Astrocytes in Acute Energy Deprivation SyndromesMartin A. Philbert, E Spencer Williams, David E. Ray, Amanda D. Phelka · 2004 · CRC Press eBooks
- Extranuclear DNAAnil Day, Joanna Poulton · 1996 · Foundations of modern biochemistry
- Defining the nuclear genetic architecture of a common maternally inherited mitochondrial disorderRóisín M. Boggan, Yi Shiau Ng, Imogen G. Franklin, Charlotte L. Alston, Emma L. Blakely, Boriana Büchner, Enrico Bugiardini, Kevin Colclough, Catherine L Feeney, Michael G. Hanna et al. · 2022 · medRxiv
- MELAS Syndrome: Mediated by Impaired Taurinomethyluridine SynthesisStephen W. Schaffer, Chian Ju Jong · 2011 · Springer eBooks
- Mitochondrial DNA and Heart DiseaseChihiro Shikata, Masami Nemoto, Takanori Ebisawa, Akihiro Nishiyama, Nobuakira Takeda · 2011 · Springer eBooks
- Molecular biology of neurological diseasesW. J. K. Cumming · 1992 · Postgraduate Medical Journal
- Biochemie und Molekularbiologie 1991Horst Domdey · 1992 · Nachrichten aus Chemie Technik und Laboratorium
- Langzeitergebnisse von Patienten mit einem Cochlea-ImplantatMichael Riebandt, Patricia Sandrieser, Peter Matulat, Antoinette Lamprecht-Dinnesen, Eberhard Seifert · 1999 · Oto-Rhino-Laryngologia Nova
- Diabetic conditions induce intolerance to accumulation of pathogenic mitochondrial DNAsEmi Ogasawara, Shun Katada, Takayuki Mito, Jun‐Ichi Hayashi, Kazuto Nakada · 2019 · bioRxiv (Cold Spring Harbor Laboratory)
- ReferencesCecilia Saccone, Graziano Pesole · 2003 · Wiley eBooks
- The Role of Mitochondrial DNA in TumorigenesisKa Yu Yeung, Adam Dickinson, Justin C. St. John · 2012 · Humana Press eBooks
- Mitochondriale DNA des MenschenBernd Wissinger · 2008 · Springer eBooks
- Models of mitochondrial diseaseDanae Liolitsa, Michael G. Hanna · 2002 · International review of neurobiology
- Mechanism and Regulation of Mitochondrial Transcription in Animal CellsPaola Loguercio Polosa, Marina Roberti, Palmiro Cantatore · 2011 · Springer eBooks
- Molecular mechanisms for transcription in mammalian mitochondriaMartina Gaspari · 2006 · Figshare
- [Mitochondrial genome analysis in the probands of six Chinese families with MELAS].Li Liu, Yuquan Shao, BaoRong Zhang, Pingping Jiang, Ailian Du, Guan Minxin · 2014 · PubMed
- The pathophysiology of respiratory chain dysfunctionJosé Pablo Silva · 2005 · Figshare
- RESEARCH ARTICLE Increased Prevalence 12308 A > G mutation in Mitochondrial tRNA Leu (CUN) Gene Associated with earlier Age of Onset in Friedreich AtaxiaMohammad Heidari, Mehri Khatami, Massoud Houshmand, Eisa Mahmoudi, Shahriar Nafissi · 2011
- Mitochondrial DNA sequence variation in patients with sensorineural hearing impairment and in the Finnish populationMervi S. Lehtonen · 2002
- Genetic Selection in Human MitochondriaSanna K. Lehtinen · 2001 · Tampere University Institutional Repository (Tampere University)
- Estudio de la función de FASTKD3 en la mitocondriaRebeca Torres Merino · 2015
- Neurodegeneration in Mitochondrial DisordersJonathan Phillips, Hannah Hayhurst, Nichola Zoe Lax · 2016 · Springer eBooks
- Mitochondrial DNA in CardiomyopathiesNobuakira Takeda · 2005 · Oxidative stress and disease
- Diseases esulting fro Point MutationsDouglas C. Wallace, Marie T. Lott, John M. Shoffner, M.D. Brown · 1992
- Mechanisms of onset and accumulation of mtDNA mutationsIan James Holt, Antonella Spinazzola · 2020 · Elsevier eBooks
- Comparative genomics of mitochondrial DNA in Branchiostoma speciesYuzo Takada, Toshio Imai · 2009 · 生物試料分析 = Journal of analytical bio-science
- Heart Mitochondrial Biogenesis2005 · Developments in cardiovascular medicine
- Mitochondriale DNA des MenschenBernd Wissinger · 2003 · Springer eBooks
- 人线粒体tRNALeu(UUR)及其突变体的基因克隆、表达和纯化*2000 · Science in China Series C-Life Sciences (in Chinese)
- Expression métabolique des polymorphismes mitochondriaux : mutations pathogènes et haplogroupesNicolas Gutierrez C. · 2011
- Etude de la dysfonction cellulaire et moléculaire du syndrome mitochondrial MELAS.Guillaume Geffroy · 2017
- Identification of Nuclear Genetic Loci Linked to Clinical Features of the m.3243A>G Mitochondrial DNA VariantRóisín M. Boggan, Theodora-Dafni Michalettou, Yi Shiau Ng, Imogen G. Franklin, Lucas T. Cortés, Charlotte L. Alston, Emma L. Blakely, Boriana Büchner, Enrico Bugiardini, Kevin Colclough et al. · 2026 · Neurology Genetics