Publications

Found 1969 results
2017
Paupe V & Prudent J (2017) New insights into the role of mitochondrial calcium homeostasis in cell migration. Biochem Biophys Res Commun
Sugiura A, Mattie S, Prudent J & McBride HM (2017) Newly born peroxisomes are a hybrid of mitochondrial and ER-derived pre-peroxisomes. Nature 542, 251-254
Geissler JM, Romanos M, Gerlach M, Berg D & Schulte C (2017) No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson's disease in nine ADHD candidate SNPs. Atten Defic Hyperact Disord 9, 121-127
James AM, Hoogewijs K, Logan A, Hall AR, Ding S, Fearnley IM & Murphy MP (2017) Non-enzymatic N-acetylation of Lysine Residues by AcetylCoA Often Occurs via a Proximal S-acetylated Thiol Intermediate Sensitive to Glyoxalase II. Cell Rep 18, 2105-2112
Legati A, Reyes A, Berti CCeccatelli, Stehling O, Marchet S, Lamperti C, Ferrari A, Robinson AJ, Mühlenhoff U, Lill R, Zeviani M, Goffrini P & Ghezzi D (2017) A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy. J Med Genet 54, 815-824
Del Dotto V, Mishra P, Vidoni S, Fogazza M, Maresca A, Caporali L, J McCaffery M, Cappelletti M, Baruffini E, Lenaers G, Chan D, Rugolo M, Carelli V & Zanna C (2017) OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions. Cell Rep 19, 2557-2571
Sommerville EW, Jones RL, Hardy SA, Blakely EL, Pyle A, Schaefer AM, Chinnery PF, Turnbull DM, Gorman GS & Taylor RW (2017) Opening One's Eyes to Mosaicism in Progressive External Ophthalmoplegia. Neurol Genet 3, e202
Robinson WE, Bassegoda A, Reisner E & Hirst J (2017) Oxidation-State-Dependent Binding Properties of the Active Site in a Mo-Containing Formate Dehydrogenase. J Am Chem Soc 139, 9927-9936
Bénit P, Pelhaître A, Saunier E, Bortoli S, Coulibaly A, Rak M, Schiff M, Kroemer G, Zeviani M & Rustin P (2017) Paradoxical Inhibition of Glycolysis by Pioglitazone Opposes the Mitochondriopathy Caused by AIF Deficiency. EBioMedicine 17, 75-87
Hewitt VL & Whitworth AJ (2017) Parkinson's Disease: Mitochondrial Fission and Fusion, Elsevier
Parikh S, Goldstein A, Karaa A, Koenig MKay, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Raboisson MJosee, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Cunningham ZZolkipli, Rahman S & Chinnery PF (2017) Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society. Genet Med
Majander A, Robson AG, João C, Holder GE, Chinnery PF, Moore AT, Votruba M, Stockman A & Yu-Wai-Man P (2017) The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy. Mitochondrion
He J, Carroll J, Ding S, Fearnley IM & Walker JE (2017) Permeability transition in human mitochondria persists in the absence of peripheral stalk subunits of ATP synthase. Proc Natl Acad Sci U S A 114, 9086-9091
He J, Ford HC, Carroll J, Ding S, Fearnley IM & Walker JE (2017) Persistence of the mitochondrial permeability transition in the absence of subunit c of human ATP synthase. Proc Natl Acad Sci U S A 114, 3409-3414
Sallevelt SCEH, Dreesen JCFM, Drüsedau M, Hellebrekers DMEI, Paulussen ADC, Coonen E, van Golde RJT, Geraedts JPM, Gianaroli L, Magli MC, Zeviani M, Smeets HJM & de Die-Smulders CEM (2017) PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy. Hum Reprod 32, 698-703
Whitworth AJ & Pallanck LJ (2017) PINK1/Parkin mitophagy and neurodegeneration-what do we really know in vivo?. Curr Opin Genet Dev 44, 47-53
Tsuchiya Y, Peak-Chew SYeu, Newell C, Miller-Aidoo S, Mangal S, Zhyvoloup A, Bakovic J, Malanchuk O, Pereira GC, Kotiadis V, Szabadkai G, Duchen MR, Campbell M, Cuenca SRodriguez, Vidal-Puig A, James AM, Murphy MP, Filonenko V, Skehel M & Gout I (2017) Protein CoAlation: a redox-regulated protein modification by coenzyme A in mammalian cells. Biochem J 474, 2489-2508
Zaganelli S, Rebelo-Guiomar P, Maundrell K, Rozanska A, Pierredon S, Powell CA, Jourdain AA, Hulo N, Lightowlers RN, Chrzanowska-Lightowlers ZM, Minczuk MA & Martinou J-C (2017) The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules. J Biol Chem 292, 4519-4532
Zanolini A, Potic A, Carrara F, Lamantea E, Diodato D, Blasevich F, Marchet S, Mora M, Pallotti F, Morandi L, Zeviani M & Lamperti C (2017) Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene. Mol Genet Metab Rep 10, 24-27
Nasca A, Scotton C, Zaharieva I, Neri M, Selvatici R, Magnusson OThor, Gal A, Weaver D, Rossi R, Armaroli A, Pane M, Phadke R, Sarkozy A, Muntoni F, Hughes I, Cecconi A, Hajnóczky G, Donati A, Mercuri E, Zeviani M, Ferlini A & Ghezzi D (2017) Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia. Hum Mutat
Pearce SF, Rebelo-Guiomar P, D'Souza AR, Powell CA, Van Haute L & Minczuk MA (2017) Regulation of Mammalian Mitochondrial Gene Expression: Recent Advances. Trends Biochem Sci
J Y Jones A, Blaza JN, Varghese F & Hirst J (2017) Respiratory Complex I in Bos taurus and Paracoccus denitrificans Pumps Four Protons across the Membrane for Every NADH Oxidized. J Biol Chem 292, 4987-4995
Parikh S, Goldstein A, Karaa A, Koenig MKay, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Raboisson MJosee, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Cunningham ZZolkipli, Rahman S & Chinnery PF (2017) Response to Newman et al. Genet Med 19
Wei W, Keogh MJ, Ironside JW & Chinnery PF (2017) Response to Simon et al. Acta Neuropathol Commun 5, 34
Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, Federico A, Minetti C, Moggio M, Mongini T, Santorelli FM, Servidei S, Tonin P, Ardissone A, Bello L, Bruno C, E Ienco C, Diodato D, Filosto M, Lamperti C, Moroni I, Musumeci O, Pegoraro E, Primiano G, Ronchi D, Rubegni A, Salvatore S, Sciacco M, Valentino ML, Vercelli L, Toscano A, Zeviani M, Siciliano G & Mancuso M (2017) Revisiting mitochondrial ocular myopathies: a study from the Italian Network. J Neurol 264, 1777-1784

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