MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention

door Tischner, Christin, Hofer, Annette, Wulff, Veronika, Stepek, Joanna, Dumitru, Iulia, Becker, Lore, Haack, Tobias, Kremer, Laura, Datta, Alexandre N., Sperl, Wolfgang, Floss, Thomas, Wurst, Wolfgang, Chrzanowska-Lightowlers, Zofia, De Angelis, Martin Hrabe, Klopstock, Thomas, Prokisch, Holger, Wenz, Tina
Gepubliceerd in Hum Mol Genet (2015)

MTO1-Deficient Mouse Model Mirrors the Human Phenotype Showing Complex I Defect and Cardiomyopathy

door Becker, Lore, Kling, Eva, Schiller, Evelyn, Zeh, Ramona, Schrewe, Anja, Hölter, Sabine M., Mossbrugger, Ilona, Calzada-Wack, Julia, Strecker, Valentina, Wittig, Ilka, Dumitru, Iulia, Wenz, Tina, Bender, Andreas, Aichler, Michaela, Janik, Dirk, Neff, Frauke, Walch, Axel, Quintanilla-Fend, Leticia, Floss, Thomas, Bekeredjian, Raffi, Gailus-Durner, Valérie, Fuchs, Helmut, Wurst, Wolfgang, Meitinger, Thomas, Prokisch, Holger, de Angelis, Martin Hrabě, Klopstock, Thomas
Gepubliceerd in PLoS One (2014)