Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation

Hereditary Early-Onset Parkinson's Disease Caused by Mutations in <i>PINK1</i>

Enza Maria Valente, Patrick M. Abou‐Sleiman, Viviana Caputo et al. · Science · 2004 · 3.5K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused by inactivation of <i>Drosophila</i> Pink1 is rescued by Parkin

Yufeng Yang, Stephan Gehrke, Yuzuru Imai et al. · Proceedings of the National Academy of Sciences · 2006 · 789 citations · Full text

Life Sciences, Genetics, Neuroscience +17

The Active Sites of the Eukaryotic 20 S Proteasome and Their Involvement in Subunit Precursor Processing

Wolfgang Heinemeyer, Michael B. Fischer, Thomas Krimmer et al. · Journal of Biological Chemistry · 1997 · 517 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

PINK1 mutations are associated with sporadic early‐onset parkinsonism

Enza Maria Valente, Sergio Salvi, Tàmara Ialongo et al. · Annals of Neurology · 2004 · 498 citations

Life Sciences, Genetics, Neurology +16

Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism

Laura Silvestri, Viviana Caputo, Emanuele Bellacchio et al. · Human Molecular Genetics · 2005 · 447 citations · Full text

Life Sciences, Genetics, Neuroscience +17