Neuronal degeneration and mitochondrial dysfunction von Schon, Eric A, Manfredi, Giovanni

Volltext

Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition von Gilkerson, Robert W., De Vries, Rosa L.A., Lebot, Paul, Wikstrom, Jakob D., Torgyekes, Edina, Shirihai, Orian S., Przedborski, Serge, Schon, Eric A.

Volltext

Mitochondrial genetics and disease von Schon, E A

Volltext

Mitochondrial DNA and respiratory chain function in spinal cords of ALS patients von Wiedemann, Falk R., Manfredi, Giovanni, Mawrin, Christian, Beal, M. Flint, Schon, Eric A.

Volltext

Two direct repeats cause most human mtDNA deletions von Samuels, David C., Schon, Eric A., Chinnery, Patrick F.

Volltext

Mitochondria von Chinnery, P F, Schon, E A

Volltext

Ketogenic treatment reduces deleted mitochondrial DNAs in cultured human cells von Santra, Sumana, Gilkerson, Robert W., Davidson, Mercy, Schon, Eric A.

Volltext

Rescue of a deficiency in ATP synthesis by transfer of MTATP6 , a mitochondrial DNA-encoded gene, to the nucleus von Schon, Eric A, Manfredi, Giovanni, Fu, Jin, Ojaimi, Joseline, Sadlock, James E, Kwong, Jennifer Q, Guy, John

Volltext

Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy von Guy, John, Qi, Xiaoping, Pallotti, Francesco, Schon, Eric A., Manfredi, Giovanni, Carelli, Valerio, Martinuzzi, Andrea, Hauswirth, William W., Lewin, Alfred S.

Volltext

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2 , a COX assembly gene von Schon, Eric A, Papadopoulou, Lefkothea C, Sue, Carolyn M, Davidson, Mercy M, Tanji, Kurenai, Nishino, Ichizo, Sadlock, James E, Krishna, Sindu, Walker, Winsome, Selby, Jeanette, Glerum, D. Moira, Coster, Rudy Van, Lyon, Gilles, Scalais, Emmanuel, Lebel, Roger, Kaplan, Paige, Shanske, Sara, De Vivo, Darryl C, Bonilla, Eduardo, Hirano, Michio, DiMauro, Salvatore

Volltext

Crystal structure of human SCO1: implications for redox signaling by a mitochondrial cytochrome c oxidase "assembly" protein von Williams, John C, Sue, Carolyn, Banting, Graham S, Yang, Hua, Glerum, D Moira, Hendrickson, Wayne A, Schon, Eric A

Volltext

Hypocitrullinemia in patients with MELAS: an insight into the “MELAS paradox” von Naini, Ali, Kaufmann, Petra, Shanske, Sara, Engelstad, Kristin, De Vivo, Darryl C., Schon, Eric A.

Volltext

Mitochondrial DNA mutations and pathogenesis von Schon, E A, Bonilla, E, DiMauro, S

Volltext

Mitochondrial DNA mutations in cancer von Zanssen, Stefanie, Schon, Eric A

Volltext

Risk of developing a mitochondrial DNA deletion disorder von Chinnery, Patrick F, DiMauro, Salvatore, Shanske, Sara, Schon, Eric A, Zeviani, Massimo, Mariotti, Caterina, Carrara, Fanco, Lombes, Anne, Laforet, Pascal, Ogier, Heléne, Jaksch, Michaela, Lochmüller, Hanns, Horvath, Rita, Deschauer, Marcus, Thorburn, David R, Bindoff, Laurence A, Poulton, Joanna, Taylor, Robert W, Matthews, John NS, Turnbull, Douglass M

Volltext

Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations von Pallotti, Francesco, Baracca, Alessandra, Hernandez-Rosa, Evelyn, Walker, Winsome F, Solaini, Giancarlo, Lenaz, Giorgio, Melzi D'Eril, Gian Vico, Dimauro, Salvatore, Schon, Eric A, Davidson, Mercy M

Volltext

Mitochondrial DNA genotypes in nuclear transfer-derived cloned sheep von Schon, Eric A, Evans, Matthew J, Gurer, Cagan, Loike, John D, Wilmut, Ian, Schnieke, Angelika E

Volltext

Pathogenesis of primary defects in mitochondrial ATP synthesis von Schon, Eric A, Santra, Sumana, Pallotti, Francesco, Girvin, Mark E

Volltext

A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency von Rizzuto, Rosario, Brini, Marisa, Pinton, Paolo, King, Michael P, Davidson, Mercy, Schon, Eric A

Volltext

Mitochondria in neuromuscular disorders von DiMauro, Salvatore, Bonilla, Eduardo, Davidson, Mercy, Hirano, Michio, Schon, Eric A.

Volltext