Author Response: K320E-Twinkle(skm) Mice Are Genetically Heterogeneous for Secondary mtDNA Deletions Impairing Comparison With Controls

par Kimoloi, Sammy, Pla-Martín, David, Oexner, Rafael R., Baris, Olivier R., Wiesner, Rudolf J.
Publié dans Invest Ophthalmol Vis Sci (2021)

Overexpression of the Mitochondrial T3 Receptor p43 Induces a Shift in Skeletal Muscle Fiber Types

par Casas, François, Pessemesse, Laurence, Grandemange, Stéphanie, Seyer, Pascal, Gueguen, Naïg, Baris, Olivier, Lepourry, Laurence, Cabello, Gérard, Wrutniak-Cabello, Chantal
Publié 2008

Extraocular Muscle Reveals Selective Vulnerability of Type IIB Fibers to Respiratory Chain Defects Induced by Mitochondrial DNA Alterations

par Oexner, Rafael R., Pla-Martín, David, Paß, Thomas, Wiesen, Martin H. J., Zentis, Peter, Schauss, Astrid, Baris, Olivier R., Kimoloi, Sammy, Wiesner, Rudolf J.
Publié dans Invest Ophthalmol Vis Sci (2020)

Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor

par Imhof, Thomas, Rosenblatt, Katharina, Pryymachuk, Galyna, Weiland, Daniela, Noetzel, Nicolas, Deschner, James, Baris, Olivier R., Kimoloi, Sammy, Koch, Manuel, Wiesner, Rudolf J., Korkmaz, Yüksel
Publié dans Sci Rep (2020)

Overexpression of the Mitochondrial T3 Receptor Induces Skeletal Muscle Atrophy during Aging

par Casas, François, Pessemesse, Laurence, Grandemange, Stéphanie, Seyer, Pascal, Baris, Olivier, Gueguen, Naïg, Ramonatxo, Christelle, Perrin, Florence, Fouret, Gilles, Lepourry, Laurence, Cabello, Gérard, Wrutniak-Cabello, Chantal
Publié 2009

Mitochondrial Dysfunction Combined with High Calcium Load Leads to Impaired Antioxidant Defense Underlying the Selective Loss of Nigral Dopaminergic Neurons

par Ricke, Konrad M., Paß, Thomas, Kimoloi, Sammy, Fährmann, Kai, Jüngst, Christian, Schauss, Astrid, Baris, Olivier R., Aradjanski, Marijana, Trifunovic, Aleksandra, Eriksson Faelker, Therese M., Bergami, Matteo, Wiesner, Rudolf J.
Publié dans J Neurosci (2020)

Efficient Isolation of Pure and Functional Mitochondria from Mouse Tissues Using Automated Tissue Disruption and Enrichment with Anti-TOM22 Magnetic Beads

par Franko, Andras, Baris, Olivier R., Bergschneider, Eva, von Toerne, Christine, Hauck, Stefanie M., Aichler, Michaela, Walch, Axel K., Wurst, Wolfgang, Wiesner, Rudolf J., Johnston, Ian C. D., de Angelis, Martin Hrabĕ
Publié 2013

Respiratory chain inactivation links cartilage-mediated growth retardation to mitochondrial diseases

par Holzer, Tatjana, Probst, Kristina, Etich, Julia, Auler, Markus, Georgieva, Veronika S., Bluhm, Björn, Frie, Christian, Heilig, Juliane, Niehoff, Anja, Nüchel, Julian, Plomann, Markus, Seeger, Jens M., Kashkar, Hamid, Baris, Olivier R., Wiesner, Rudolf J., Brachvogel, Bent
Publié dans J Cell Biol (2019)

Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing

par Basu, Swaraj, Xie, Xie, Uhler, Jay P., Hedberg-Oldfors, Carola, Milenkovic, Dusanka, Baris, Olivier R., Kimoloi, Sammy, Matic, Stanka, Stewart, James B., Larsson, Nils-Göran, Wiesner, Rudolf J., Oldfors, Anders, Gustafsson, Claes M., Falkenberg, Maria, Larsson, Erik
Publié dans PLoS Genet (2020)

Inhibition of insulin/IGF-1 receptor signaling protects from mitochondria-mediated kidney failure

par Ising, Christina, Koehler, Sybille, Brähler, Sebastian, Merkwirth, Carsten, Höhne, Martin, Baris, Olivier R, Hagmann, Henning, Kann, Martin, Fabretti, Francesca, Dafinger, Claudia, Bloch, Wilhelm, Schermer, Bernhard, Linkermann, Andreas, Brüning, Jens C, Kurschat, Christine E, Müller, Roman-Ulrich, Wiesner, Rudolf J, Langer, Thomas, Benzing, Thomas, Brinkkoetter, Paul Thomas
Publié dans EMBO Mol Med (2015)

FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders

par Lehtonen, Jenni M., Forsström, Saara, Bottani, Emanuela, Viscomi, Carlo, Baris, Olivier R., Isoniemi, Helena, Höckerstedt, Krister, Österlund, Pia, Hurme, Mikko, Jylhävä, Juulia, Leppä, Sirpa, Markkula, Ritva, Heliö, Tiina, Mombelli, Giuliana, Uusimaa, Johanna, Laaksonen, Reijo, Laaksovirta, Hannu, Auranen, Mari, Zeviani, Massimo, Smeitink, Jan, Wiesner, Rudolf J., Nakada, Kazuto, Isohanni, Pirjo, Suomalainen, Anu
Publié dans Neurology (2016)