Paola Martinelli

Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases

Tyler Mark Pierson, David R. Adams, Florian Bonn et al. · PLoS Genetics · 2011 · 226 citations · Full text

Neurodegenerative Diseases, Peripheral Neuropathy, Mendelian Disorder +14

Loss of Prohibitin Membrane Scaffolds Impairs Mitochondrial Architecture and Leads to Tau Hyperphosphorylation and Neurodegeneration

Carsten Merkwirth, Paola Martinelli, Anne Korwitz et al. · PLoS Genetics · 2012 · 166 citations · Full text

Mitophagy, Molecular Biology, Social Sciences +16

CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins

Jie Gao, Désirée Schatton, Paola Martinelli et al. · The Journal of Cell Biology · 2014 · 143 citations · Full text

AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival

Eva R. Almajan, Ricarda Richter, Lars Paeger et al. · Journal of Clinical Investigation · 2012 · 109 citations · Full text

Mitophagy, Cell Death, Molecular Biology +16

Loss of the m-AAA protease subunit AFG3L2 causes mitochondrial transport defects and tau hyperphosphorylation

Arun Kumar Kondadi, Shaomeng Wang, Sara Montagner et al. · The EMBO Journal · 2014 · 76 citations · Full text

Mitochondrial Biogenesis, Mitochondrial Function, Biochemistry +9