Search Results - Christopher A. Powell
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The mammalian mitochondrial epitranscriptome by Pedro Rebelo‐Guiomar, Christopher A. Powell, Lindsey Van Haute, Michal Minczuk
Published 2018Revisão -
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PrimPol, an Archaic Primase/Polymerase Operating in Human Cells by Sara García-Gómez, Aurelio Reyes, María I. Martínez-Jiménez, E. Sandra Chocrón, Silvana Mourón, Gloria Terrados, Christopher A. Powell, Eduardo Salido, Juan Méndez, Ian Holt, Luis Blanco
Published 2013Artigo -
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METTL15 introduces N4-methylcytidine into human mitochondrial 12S rRNA and is required for mitoribosome biogenesis by Lindsey Van Haute, Alan G. Hendrick, Aaron R. D’Souza, Christopher A. Powell, Pedro Rebelo‐Guiomar, Michael E. Harbour, Shujing Ding, Ian M. Fearnley, Byron Andrews, Michal Minczuk
Published 2019Artigo -
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Clinically translatable mitochondrial gene therapy in muscle using tandem mtZFN architecture by P. Nash, Keira Turner, Christopher A. Powell, Lindsey Van Haute, Pedro Silva-Pinheiro, Felix Bubeck, Ellen Wiedtke, Eloïse Marques, Dylan G. Ryan, Dirk Grimm, Payam A. Gammage, Michal Minczuk
Published 2025Artigo -
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The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules by Sofia Zaganelli, Pedro Rebelo‐Guiomar, Kinsey Maundrell, Agata Rozanska, Sandra Pierredon, Christopher A. Powell, Alexis A. Jourdain, Nicolas Hulo, Robert N. Lightowlers, Zofia M. Chrzanowska‐Lightowlers, Michal Minczuk, Jean‐Claude Martinou
Published 2017Artigo -
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Balancing of mitochondrial translation through METTL8-mediated m3C modification of mitochondrial tRNAs by Eva Schöller, James Marks, Virginie Marchand, Astrid Bruckmann, Christopher A. Powell, Markus Reichold, Christian D. Mutti, Katja Dettmer, Regina Feederle, Stefan Hüttelmaier, Mark Helm, Peter J. Oefner, Michal Minczuk, Yuri Motorin, Markus Hafner, Gunter Meister
Published 2021Artigo -
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Two Siblings with Homozygous Pathogenic Splice-Site Variant in Mitochondrial Asparaginyl-tRNA Synthetase (<i>NARS2</i>) by Arnaud Vanlander, Björn Menten, Joél Smet, Linda De Meırleır, Tom Sante, Boél De Paepe, Sara Seneca, Sarah F. Pearce, Christopher A. Powell, Sarah Vergult, Alex Michotte, Elien De Latter, Lies Vantomme, Michal Minczuk, Rudy Van Coster
Published 2014Artigo -
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TRNT1 deficiency: clinical, biochemical and molecular genetic features by Yehani Wedatilake, Rojeen Niazi, Elisa Fassone, Christopher A. Powell, Sarah F. Pearce, Vincent Plagnol, José W. Saldanha, Robert Kleta, W.K. Chong, Emma Footitt, Philippa B. Mills, Jan‐Willem Taanman, Michal Minczuk, Peter T. Clayton, Shamima Rahman
Published 2016Artigo -
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Disruption of the TCA cycle reveals an ATF4-dependent integration of redox and amino acid metabolism by Dylan G. Ryan, Ming Yang, Hiran A. Prag, Giovanny Rodriguez Blanco, Efterpi Nikitopoulou, Marc Segarra‐Mondejar, Christopher A. Powell, Tim Young, Nils Burger, Jan Lj. Miljković, Michal Minczuk, Michael P. Murphy, Alex von Kriegsheim, Christian Frezza
Published 2021Artigo -
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NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs by Lindsey Van Haute, Song-Yi Lee, Beverly J. McCann, Christopher A. Powell, Dhiru Bansal, Lina Vasiliauskaitė, Caterina Garone, Sanghee Shin, Jong‐Seo Kim, Michaela Frye, Joseph G. Gleeson, Eric A. Miska, Hyun‐Woo Rhee, Michal Minczuk
Published 2019Artigo -
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New insights into the phenotype of FARS2 deficiency by Elise Vantroys, Austin Larson, Marisa W. Friederich, Kaz M. Knight, Michael A. Swanson, Christopher A. Powell, Joél Smet, Sarah Vergult, Boél De Paepe, Sara Seneca, Herbert Roeyers, Björn Menten, Michal Minczuk, Arnaud Vanlander, Johan Van Hove, Rudy Van Coster
Published 2017Artigo -
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Mutations in the mitochondrial cysteinyl-tRNA synthase gene,<i>CARS2,</i>lead to a severe epileptic encephalopathy and complex movement disorder by Curtis R. Coughlin, Gunter Scharer, Marisa W. Friederich, Hung‐Chun Yu, Elizabeth A. Geiger, Geralyn Creadon‐Swindell, Abigail E. Collins, Arnaud Vanlander, Rudy Van Coster, Christopher A. Powell, Michael A. Swanson, Michal Minczuk, Johan L.K. Van Hove, Tamim H. Shaikh
Published 2015Artigo -
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<i>VARS2</i>and<i>TARS2</i>Mutations in Patients with Mitochondrial Encephalomyopathies by Daria Diodato, Laura Melchionda, Tobias B. Haack, Cristina Dallabona, Enrico Baruffini, Claudia Donnini, Tiziana Granata, Francesca Ragona, Paolo Balestri, Maria Margollicci, Eleonora Lamantea, Alessia Nasca, Christopher A. Powell, Michal Minczuk, Tim M. Strom, Thomas Meitinger, Holger Prokisch, Costanza Lamperti, Massimo Zeviani, Daniele Ghezzi
Published 2014Artigo
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