Publications

Found 1941 results
2018
Murphy MP (2018) Newly made mitochondrial DNA drives inflammation. Nature 560, 176-177
Joon S, Ragunathan P, Sundararaman L, Nartey W, Kundu S, Manimekalai MSS, Bogdanović N, Dick T & Grüber G (2018) The NMR solution structure of Mycobacterium tuberculosis F-ATP synthase subunit ε provides new insight into energy coupling inside the rotary engine. FEBS J 285, 1111-1128
Bartsakoulia M, Pyle A, Troncoso-Chandía D, Vial-Brizzi J, Paz-Fiblas MV, Duff J, Griffin H, Boczonadi V, Lochmüller H, Kleinle S, Chinnery PF, Grünert S, Kirschner J, Eisner V & Horvath R (2018) A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies. Hum Mol Genet 27, 1186-1195
Leslie M (2018) 'Old' genome editors might treat mitochondrial diseases. Science 361, 1302
Keogh MJ, Wei W, Aryaman J, Wilson I, Talbot K, Turner MR, McKenzie C-A, Troakes C, Attems J, Smith C, Sarraj SAl, Morris CM, Ansorge O, Pickering-Brown S, Jones N, Ironside JW & Chinnery PF (2018) Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains. J Neurol Neurosurg Psychiatry
Hirst J (2018) Open questions: respiratory chain supercomplexes-why are they there and what do they do?. BMC Biol 16, 111
Mootha VK & Chinnery PF (2018) Oxygen in mitochondrial disease: can there be too much of a good thing?. J Inherit Metab Dis 41, 761-763
Majd H, King MS, Smith AC & Kunji ERS (2018) Pathogenic mutations of the human mitochondrial citrate carrier SLC25A1 lead to impaired citrate export required for lipid, dolichol, ubiquinone and sterol synthesis. Biochim Biophys Acta 1859, 1-7
Friederich MW, Timal S, Powell CA, Dallabona C, Kurolap A, Palacios-Zambrano S, Bratkovic D, Derks TGJ, Bick D, Bouman K, Chatfield KC, Damouny-Naoum N, Dishop MK, Falik-Zaccai TC, Fares F, Fedida A, Ferrero I, Gallagher RC, Garesse R, Gilberti M, González C, Gowan K, Habib C, Halligan RK, Kalfon L, Knight K, Lefeber D, Mamblona L, Mandel H, Mory A, Ottoson J, Paperna T, Pruijn GJM, Rebelo-Guiomar PF, Saada A, Sainz B, Salvemini H, Schoots MH, Smeitink JA, Szukszto MJ, Horst HJTer, van den Brandt F, van Spronsen FJ, Veltman JA, Wartchow E, Wintjes LT, Zohar Y, Fernández-Moreno MA, Baris HN, Donnini C, Minczuk MA, Rodenburg RJ & Van Hove JLK (2018) Pathogenic variants in glutamyl-tRNA amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder. Nat Commun 9, 4065
Chipot C, Dehez F, Schnell JR, Zitzmann N, Pebay-Peyroula E, Catoire LJ, Miroux B, Kunji ERS, Veglia G, Cross TA & Schanda P (2018) Perturbations of Native Membrane Protein Structure in Alkyl Phosphocholine Detergents: A Critical Assessment of NMR and Biophysical Studies. Chem Rev 118, 3559-3607
Dogan SAnil, Cerutti R, Benincá C, Brea-Calvo G, Jacobs HTrevor, Zeviani M, Szibor M & Viscomi C (2018) Perturbed Redox Signaling Exacerbates a Mitochondrial Myopathy. Cell Metab
Stovell MG, Mada MO, T Carpenter A, Yan J-L, Guilfoyle MR, Jalloh I, Welsh KE, Helmy A, Howe DJ, Grice P, Mason A, Giorgi-Coll S, Gallagher CN, Murphy MP, Menon DK, Hutchinson PJ & Carpenter KLh (2018) Phosphorus spectroscopy in acute TBI demonstrates metabolic changes that relate to outcome in the presence of normal structural MRI. J Cereb Blood Flow Metab, 271678X18799176
Nuzzo AM, Camm EJ, Sferruzzi-Perri AN, Ashmore TJ, Yung H-W, Cindrova-Davies T, Spiroski A-M, Sutherland MR, Logan A, Austin-Williams S, Burton GJ, Rolfo A, Todros T, Murphy MP & Giussani DA (2018) Placental Adaptation to Early-Onset Hypoxic Pregnancy and Mitochondria-Targeted Antioxidant Therapy in a Rodent Model. Am J Pathol 188, 2704-2716
Chong KLeong, Chalmers BA, Cullen JK, Kaur A, Kolanowski JL, Morrow BJ, Fairfull-Smith KE, Lavin MJ, Barnett NL, New EJ, Murphy MP & Bottle SE (2018) Pro-fluorescent mitochondria-targeted real-time responsive redox probes synthesised from carboxy isoindoline nitroxides: Sensitive probes of mitochondrial redox status in cells. Free Radic Biol Med
James AM, Smith AC, Smith CL, Robinson AJ & Murphy MP (2018) Proximal Cysteines that Enhance Lysine N-Acetylation of Cytosolic Proteins in Mice Are Less Conserved in Longer-Living Species. Cell Rep 24, 1445-1455
King MS, Crichton PG, Ruprecht JJ & Kunji ERS (2018) Publisher Correction: Concerns with yeast mitochondrial ADP/ATP carrier's integrity in DPC. Nat Struct Mol Biol 25, 988
Farmery JHR, Smith ML & Lynch AG (2018) Publisher Correction: Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data. Sci Rep 8, 13376
Civiletto G, Dogan SAnil, Cerutti R, Fagiolari G, Moggio M, Lamperti C, Benincá C, Viscomi C & Zeviani M (2018) Rapamycin rescues mitochondrial myopathy via coordinated activation of autophagy and lysosomal biogenesis. EMBO Mol Med 10
Sielaff H, Duncan TM & Börsch M (2018) The regulatory subunit ε in Escherichia coli FF-ATP synthase. Biochim Biophys Acta Bioenerg 1859, 775-788
Foote K, Reinhold J, Yu EPK, Figg NL, Finigan A, Murphy MP & Bennett MR (2018) Restoring mitochondrial DNA copy number preserves mitochondrial function and delays vascular aging in mice. Aging Cell, e12773
Garone C, Taylor RW, Nascimento A, Poulton J, Fratter C, Domínguez-González C, Evans JC, Loos M, Isohanni P, Suomalainen A, Ram D, M Hughes I, McFarland R, Barca E, Gomez CLopez, Jayawant S, Thomas ND, Manzur AY, Kleinsteuber K, Martin MA, Kerr T, Gorman GS, Sommerville EW, Chinnery PF, Hofer M, Karch C, Ralph J, Cámara Y, Madruga-Garrido M, Domínguez-Carral J, Ortez C, Emperador S, Montoya J, Chakrapani A, Kriger JF, Schoenaker R, Levin B, Thompson JLP, Long Y, Rahman S, Donati MAlice, DiMauro S & Hirano M (2018) Retrospective natural history of thymidine kinase 2 deficiency. J Med Genet
Majd H, King MS, Palmer SM, Smith AC, Elbourne LDh, Paulsen IT, Sharples D, Henderson PJf & Kunji ERs (2018) Screening of candidate substrates and coupling ions of transporters by thermostability shift assays. Elife 7
Floros VI, Pyle A, Dietmann S, Wei W, Tang WWC, Irie N, Payne B, Capalbo A, Noli L, Coxhead J, Hudson G, Crosier M, Strahl H, Khalaf Y, Saitou M, Ilic D, M Surani A & Chinnery PF (2018) Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos. Nat Cell Biol 20, 144-151
Nicolas G, Acuna-Hidalgo R, Keogh MJ, Quenez O, Steehouwer M, Lelieveld S, Rousseau S, Richard A-C, Oud MS, Marguet F, Laquerrière A, Morris CM, Attems J, Smith C, Ansorge O, Sarraj SAl, Frebourg T, Campion D, Hannequin D, Wallon D, Gilissen C, Chinnery PF, Veltman JA & Hoischen A (2018) Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease. Alzheimers Dement
Rocha MC & Springett R (2018) Spectral components of detergent-solubilized bovine cytochrome oxidase. Biochim Biophys Acta Bioenerg 1859, 555-566

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