Universität zu Köln

2022

Ralevski, Alexandra, Apelt, Federico, Olas, Justyna J., Mueller-Roeber, Bernd, Rugarli, Elena I., Kragler, Friedrich and Horvath, Tamas L. (2022). Plant mitochondrial FMT and its mammalian homolog CLUH controls development and behavior in Arabidopsis and locomotion in mice. Cell. Mol. Life Sci., 79 (6). BASEL: SPRINGER BASEL AG. ISSN 1420-9071

Wani, Gulzar A., Sprenger, Hans-Georg, Ndoci, Kristiano, Chandragiri, Srikanth, Acton, Richard James ORCID: 0000-0002-2574-9611, Schatton, Desiree, Kochan, Sandra M. V., Sakthivelu, Vignesh, Jevtic, Milica, Seeger, Jens M., Mueller, Stefan, Giavalisco, Patrick, Rugarli, Elena I., Motori, Elisa ORCID: 0000-0001-5997-6866, Langer, Thomas and Bergami, Matteo (2022). Metabolic control of adult neural stem cell self-renewal by the mitochondrial protease YME1L. Cell Reports, 38 (7). CAMBRIDGE: CELL PRESS. ISSN 2211-1247

2019

Iershov, Anton, Nemazanyy, Ivan, Alkhoury, Chantal, Girard, Muriel, Barth, Esther, Cagnard, Nicolas, Montagner, Alexandra ORCID: 0000-0002-4800-5105, Chretien, Dominique, Rugarli, Elena I. ORCID: 0000-0002-5782-1067, Guillou, Herve ORCID: 0000-0002-5363-9081, Pende, Mario ORCID: 0000-0002-7864-8937 and Panasyuk, Ganna (2019). The class 3 PI3K coordinates autophagy and mitochondrial lipid catabolism by controlling nuclear receptor PPAR alpha. Nat. Commun., 10. LONDON: NATURE PUBLISHING GROUP. ISSN 2041-1723

Sprenger, Hans-Georg, Wani, Gulzar, Hesseling, Annika, Koenig, Tim, Patron, Maria, MacVicar, Thomas, Ahola, Sofia, Wai, Timothy, Barth, Esther, Rugarli, Elena I. ORCID: 0000-0002-5782-1067, Bergami, Matteo ORCID: 0000-0001-5525-5025 and Langer, Thomas (2019). Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy. EMBO Mol. Med., 11 (1). HOBOKEN: WILEY. ISSN 1757-4684

2018

Schatton, Desiree and Rugarli, Elena I. ORCID: 0000-0002-5782-1067 (2018). Post-transcriptional regulation of mitochondrial function. Curr. Opin. Physiol., 3. S. 6 - 16. AMSTERDAM: ELSEVIER SCIENCE BV. ISSN 2468-8673

Schatton, Desiree and Rugarli, Elena I. ORCID: 0000-0002-5782-1067 (2018). A concert of RNA-binding proteins coordinates mitochondrial function. Crit. Rev. Biochem. Mol. Biol., 53 (6). S. 652 - 667. ABINGDON: TAYLOR & FRANCIS LTD. ISSN 1549-7798

2017

Schatton, Desiree, Pla-Martin, David, Marx, Marie-Charlotte, Hansen, Henriette, Mourier, Arnaud, Nemazanyy, Ivan, Pessia, Alberto ORCID: 0000-0001-8607-9191, Zentis, Peter, Corona, Teresa, Kondylis, Vangelis ORCID: 0000-0002-6970-8731, Barth, Esther, Schauss, Astrid C., Velagapudi, Vidya ORCID: 0000-0002-8261-7164 and Rugarli, Elena I. ORCID: 0000-0002-5782-1067 (2017). CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAs. J. Cell Biol., 216 (3). S. 675 - 694. NEW YORK: ROCKEFELLER UNIV PRESS. ISSN 1540-8140

2016

Koenig, Tim, Troeder, Simon E., Bakka, Kavya, Korwitz, Anne, Richter-Dennerlein, Ricarda, Lampe, Philipp A., Patron, Maria, Muhlmeister, Mareike, Guerrero-Castillo, Sergio ORCID: 0000-0002-6630-0562, Brandt, Ulrich ORCID: 0000-0003-1869-6811, Decker, Thorsten, Lauria, Ines ORCID: 0000-0001-5813-3103, Paggio, Angela, Rizzuto, Rosario ORCID: 0000-0001-7044-5097, Rugarli, Elena I. ORCID: 0000-0002-5782-1067, De Stefani, Diego ORCID: 0000-0003-3796-8907 and Langer, Thomas ORCID: 0000-0003-1250-1462 (2016). The m-AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria. Mol. Cell, 64 (1). S. 148 - 163. CAMBRIDGE: CELL PRESS. ISSN 1097-4164

Korwitz, Anne, Merkwirth, Carsten ORCID: 0000-0001-8895-3495, Richter-Dennerlein, Ricarda, Troeder, Simon E., Sprenger, Hans-Georg, Quiros, Pedro M., Lopez-Otin, Carlos ORCID: 0000-0001-6964-1904, Rugarli, Elena I. ORCID: 0000-0002-5782-1067 and Langer, Thomas ORCID: 0000-0003-1250-1462 (2016). Loss of OMA1 delays neurodegeneration by preventing stress-induced OPA1 processing in mitochondria. J. Cell Biol., 212 (2). S. 157 - 167. NEW YORK: ROCKEFELLER UNIV PRESS. ISSN 1540-8140

Wang, Shuaiyu, Jacquemyn, Julie, Murru, Sara, Martinelli, Paola, Barth, Esther, Langer, Thomas, Niessen, Carien M. and Rugarli, Elena I. ORCID: 0000-0002-5782-1067 (2016). The Mitochondrial m-AAA Protease Prevents Demyelination and Hair Greying. PLoS Genet., 12 (12). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1553-7404

2014

Andree, Maria, Seeger, Jens M., Schuell, Stephan, Coutelle, Oliver, Wagner-Stippich, Diana, Wiegmann, Katja, Wunderlich, Claudia M., Brinkmann, Kerstin, Broxtermann, Pia, Witt, Axel, Fritsch, Melanie, Martinelli, Paola, Bielig, Harald, Lamkemeyer, Tobias, Rugarli, Elena I. ORCID: 0000-0002-5782-1067, Kaufmann, Thomas ORCID: 0000-0001-9906-874X, Sterner-Kock, Anja, Wunderlich, F. Thomas, Villunger, Andreas, Martins, L. Miguel, Kroenke, Martin, Kufer, Thomas A., Utermoehlen, Olaf and Kashkar, Hamid (2014). BID-dependent release of mitochondrial SMAC dampens XIAP-mediated immunity against Shigella. Embo J., 33 (19). S. 2171 - 2188. HOBOKEN: WILEY. ISSN 1460-2075

Dogan, Sukru Anil ORCID: 0000-0002-1800-2923, Pujol, Claire, Maiti, Priyanka ORCID: 0000-0003-4207-0341, Kukat, Alexandra, Wang, Shuaiyu, Hermans, Steffen, Senft, Katharina, Wibom, Rolf, Rugarli, Elena I. ORCID: 0000-0002-5782-1067 and Trifunovic, Aleksandra (2014). Tissue-Specific Loss of DARS2 Activates Stress Responses Independently of Respiratory Chain Deficiency in the Heart. Cell Metab., 19 (3). S. 458 - 470. CAMBRIDGE: CELL PRESS. ISSN 1932-7420

Gao, Jie ORCID: 0000-0002-5229-9249, Schatton, Desiree, Martinelli, Paola, Hansen, Henriette, Pla-Martin, David, Barth, Esther, Becker, Christian, Altmueller, Janine, Frommolt, Peter ORCID: 0000-0002-1966-8014, Sardiello, Marco and Rugarli, Elena I. ORCID: 0000-0002-5782-1067 (2014). CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins. J. Cell Biol., 207 (2). S. 213 - 224. NEW YORK: ROCKEFELLER UNIV PRESS. ISSN 1540-8140

Kondadi, Arun Kumar ORCID: 0000-0002-5888-7834, Wang, Shuaiyu, Montagner, Sara, Kladt, Nikolay, Korwitz, Anne, Martinelli, Paola, Herholz, David, Baker, Michael J., Schauss, Astrid C., Langer, Thomas ORCID: 0000-0003-1250-1462 and Rugarli, Elena I. ORCID: 0000-0002-5782-1067 (2014). Loss of the m-AAA protease subunit AFG3L2 causes mitochondrial transport defects and tau hyperphosphorylation. Embo J., 33 (9). S. 1011 - 1027. HOBOKEN: WILEY. ISSN 1460-2075

Richter-Dennerlein, Ricarda, Korwitz, Anne, Haag, Mathias, Tatsuta, Takashi, Dargazanli, Sascha, Baker, Michael, Decker, Thorsten, Lamkemeyer, Tobias, Rugarli, Elena I. ORCID: 0000-0002-5782-1067 and Langer, Thomas ORCID: 0000-0003-1250-1462 (2014). DNAJC19, a Mitochondrial Cochaperone Associated with Cardiomyopathy, Forms a Complex with Prohibitins to Regulate Cardiolipin Remodeling. Cell Metab., 20 (1). S. 158 - 172. CAMBRIDGE: CELL PRESS. ISSN 1932-7420

2012

Almajan, Eva R., Richter, Ricarda, Paeger, Lars ORCID: 0000-0001-8716-3483, Martinelli, Paola, Barth, Esther, Decker, Thorsten, Larsson, Nils-Goeran, Kloppenburg, Peter, Langer, Thomas ORCID: 0000-0003-1250-1462 and Rugarli, Elena I. (2012). AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival. J. Clin. Invest., 122 (11). S. 4048 - 4059. ANN ARBOR: AMER SOC CLINICAL INVESTIGATION INC. ISSN 1558-8238

Merkwirth, Carsten ORCID: 0000-0001-8895-3495, Martinelli, Paola, Korwitz, Anne, Morbin, Michela ORCID: 0000-0001-8034-3123, Broenneke, Hella S., Jordan, Sabine D., Rugarli, Elena I. and Langer, Thomas ORCID: 0000-0003-1250-1462 (2012). Loss of Prohibitin Membrane Scaffolds Impairs Mitochondrial Architecture and Leads to Tau Hyperphosphorylation and Neurodegeneration. PLoS Genet., 8 (11). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1553-7404

2011

Pierson, Tyler Mark, Adams, David, Bonn, Florian, Martinelli, Paola, Cherukuri, Praveen F., Teer, Jamie K., Hansen, Nancy F., Cruz, Pedro, Mullikin, James C., Blakesley, Robert W., Golas, Gretchen, Kwan, Justin, Sandler, Anthony ORCID: 0000-0001-9440-2964, Fajardo, Karin Fuentes, Markello, Thomas, Tifft, Cynthia, Blackstone, Craig, Rugarli, Elena I., Langer, Thomas ORCID: 0000-0003-1250-1462, Gahl, William A. and Toro, Camilo (2011). Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases. PLoS Genet., 7 (10). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1553-7390