Publikationen
Externes Mitglied: Larsson Gruppe
Zeitschriftenartikel (10)
2009
Zeitschriftenartikel
29 (50), S. 15923 - 32 (2009)
Nurr1 is required for maintenance of maturing and adult midbrain dopamine neurons. J Neurosci
Zeitschriftenartikel
11 (1), S. 1 (2009)
Point mutations are causing progeroid phenotypes in the mtDNA mutator mouse. Cell Metab
Zeitschriftenartikel
9 (2), S. 173 - 81 (2009)
MitoPark mice mirror the slow progression of key symptoms and L-DOPA response in Parkinson's disease. Genes Brain Behav
Zeitschriftenartikel
139 (2), S. 231 - 3 (2009)
Structure casts light on mtDNA replication. Cell
Zeitschriftenartikel
10 (2), S. 131 - 8 (2009)
Random point mutations with major effects on protein-coding genes are the driving force behind premature aging in mtDNA mutator mice. Cell Metab
Zeitschriftenartikel
5 (5), S. e1000499 (2009)
Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene. PLoS Genet
Zeitschriftenartikel
1787 (5), S. 296 - 302 (2009)
MTERF2 is a nucleoid component in mammalian mitochondria. Biochim Biophys Acta
Zeitschriftenartikel
9 (4), S. 386 - 97 (2009)
Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome. Cell Metab
Zeitschriftenartikel
265 (2), S. 170 - 3 (2009)
Introduction: Euromit VII--summarizing 50 years of research on mitochondrial disease. J Intern Med
Zeitschriftenartikel
1787 (5), S. 484 - 490 (2009)
MONA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome. SI