Linear mitochondrial DNA is rapidly degraded by components of the replication machinery
Peeva, Viktoriya, Blei, Daniel, Trombly, Genevieve, Corsi, Sarah, Szukszto, Maciej J., Rebelo-Guiomar, Pedro, Gammage, Payam A., Kudin, Alexei P., Becker, Christian, Altmüller, Janine, Minczuk, Michal, Zsurka, Gábor, Kunz, Wolfram S.
Published in Nature communications (30.04.2018)
Published in Nature communications (30.04.2018)
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Selenium Ameliorated Oxidized Fish Oil-Induced Lipotoxicity via the Inhibition of Mitochondrial Oxidative Stress, Remodeling of Usp4-Mediated Deubiquitination, and Stabilization of Pparα
Zhang, Dian-Guang, Kunz, Wolfram S, Lei, Xi-Jun, Zito, Ester, Zhao, Tao, Xu, Yi-Chuang, Wei, Xiao-Lei, Lv, Wu-Hong, Luo, Zhi
Published in Antioxidants & redox signaling (01.03.2024)
Published in Antioxidants & redox signaling (01.03.2024)
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Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease
Kornblum, Cornelia, Nicholls, Thomas J, Haack, Tobias B, Schöler, Susanne, Peeva, Viktoriya, Danhauser, Katharina, Hallmann, Kerstin, Zsurka, Gábor, Rorbach, Joanna, Iuso, Arcangela, Wieland, Thomas, Sciacco, Monica, Ronchi, Dario, Comi, Giacomo P, Moggio, Maurizio, Quinzii, Catarina M, DiMauro, Salvatore, Calvo, Sarah E, Mootha, Vamsi K, Klopstock, Thomas, Strom, Tim M, Meitinger, Thomas, Minczuk, Michal, Kunz, Wolfram S, Prokisch, Holger
Published in Nature genetics (01.02.2013)
Published in Nature genetics (01.02.2013)
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Mosaic Deficiency in Mitochondrial Oxidative Metabolism Promotes Cardiac Arrhythmia during Aging
Baris, Olivier R., Ederer, Stefan, Neuhaus, Johannes F.G., von Kleist-Retzow, Jürgen-Christoph, Wunderlich, Claudia M., Pal, Martin, Wunderlich, F. Thomas, Peeva, Viktoriya, Zsurka, Gabor, Kunz, Wolfram S., Hickethier, Tilman, Bunck, Alexander C., Stöckigt, Florian, Schrickel, Jan W., Wiesner, Rudolf J.
Published in Cell metabolism (05.05.2015)
Published in Cell metabolism (05.05.2015)
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Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue
Winter, Lilli, Wittig, Ilka, Peeva, Viktoriya, Eggers, Britta, Heidler, Juliana, Chevessier, Frederic, Kley, Rudolf A., Barkovits, Katalin, Strecker, Valentina, Berwanger, Carolin, Herrmann, Harald, Marcus, Katrin, Kornblum, Cornelia, Kunz, Wolfram S., Schröder, Rolf, Clemen, Christoph S.
Published in Acta neuropathologica (01.09.2016)
Published in Acta neuropathologica (01.09.2016)
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A mitochondria-specific mutational signature of aging: increased rate of A > G substitutions on the heavy strand
Mikhailova, Alina G, Mikhailova, Alina A, Ushakova, Kristina, Tretiakov, Evgeny O, Iliushchenko, Dmitrii, Shamansky, Victor, Lobanova, Valeria, Kozenkov, Ivan, Efimenko, Bogdan, Yurchenko, Andrey A, Kozenkova, Elena, Zdobnov, Evgeny M, Makeev, Vsevolod, Yurov, Valerian, Tanaka, Masashi, Gostimskaya, Irina, Fleischmann, Zoe, Annis, Sofia, Franco, Melissa, Wasko, Kevin, Denisov, Stepan, Kunz, Wolfram S, Knorre, Dmitry, Mazunin, Ilya, Nikolaev, Sergey, Fellay, Jacques, Reymond, Alexandre, Khrapko, Konstantin, Gunbin, Konstantin, Popadin, Konstantin
Published in Nucleic acids research (14.10.2022)
Published in Nucleic acids research (14.10.2022)
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Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration
Gispert, Suzana, Ricciardi, Filomena, Kurz, Alexander, Azizov, Mekhman, Hoepken, Hans-Hermann, Becker, Dorothea, Voos, Wolfgang, Leuner, Kristina, Müller, Walter E, Kudin, Alexei P, Kunz, Wolfram S, Zimmermann, Annabelle, Roeper, Jochen, Wenzel, Dirk, Jendrach, Marina, García-Arencíbia, Moisés, Fernández-Ruiz, Javier, Huber, Leslie, Rohrer, Hermann, Barrera, Miguel, Reichert, Andreas S, Rüb, Udo, Chen, Amy, Nussbaum, Robert L, Auburger, Georg
Published in PloS one (03.06.2009)
Published in PloS one (03.06.2009)
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Primary Skin Fibroblasts as a Model of Parkinson's Disease
Auburger, Georg, Klinkenberg, Michael, Drost, Jessica, Marcus, Katrin, Morales-Gordo, Blas, Kunz, Wolfram S., Brandt, Ulrich, Broccoli, Vania, Reichmann, Heinz, Gispert, Suzana, Jendrach, Marina
Published in Molecular neurobiology (01.08.2012)
Published in Molecular neurobiology (01.08.2012)
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Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy
Hallmann, Kerstin, Kudin, Alexei P, Zsurka, Gábor, Kornblum, Cornelia, Reimann, Jens, Stüve, Burkhard, Waltz, Stephan, Hattingen, Elke, Thiele, Holger, Nürnberg, Peter, Rüb, Cornelia, Voos, Wolfgang, Kopatz, Jens, Neumann, Harald, Kunz, Wolfram S
Published in Brain (London, England : 1878) (01.02.2016)
Published in Brain (London, England : 1878) (01.02.2016)
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Metabolic Epilepsies-Commemorative Issue in Honor of Professor Uwe Heinemann
Kovács, Richard, Kunz, Wolfram S
Published in International journal of molecular sciences (22.11.2017)
Published in International journal of molecular sciences (22.11.2017)
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Sonography of the median nerve in CMT1A, CMT2A, CMTX, and HNPP
Schreiber, Stefanie, Oldag, Andreas, Kornblum, Cornelia, Kollewe, Katja, Kropf, Siegfried, Schoenfeld, Ariel, Feistner, Helmut, Jakubiczka, Sibylle, Kunz, Wolfram S., Scherlach, Cordula, Tempelmann, Claus, Mawrin, Christian, Dengler, Reinhard, Schreiber, Frank, Goertler, Michael, Vielhaber, Stefan
Published in Muscle & nerve (01.03.2013)
Published in Muscle & nerve (01.03.2013)
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Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion
Vielhaber, Stefan, Debska-Vielhaber, Grazyna, Peeva, Viktoriya, Schoeler, Susanne, Kudin, Alexei P., Minin, Irina, Schreiber, Stefanie, Dengler, Reinhard, Kollewe, Katja, Zuschratter, Werner, Kornblum, Cornelia, Zsurka, Gábor, Kunz, Wolfram S.
Published in Acta neuropathologica (01.02.2013)
Published in Acta neuropathologica (01.02.2013)
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