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Adriano Gonnelli

University of Padua

5

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278

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MFN2 mutations in Charcot–Marie–Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics

2019 Human Molecular Genetics
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Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation

2018 Molecular Neurodegeneration
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GTP binding regulates cellular localization of Parkinson's disease-associated LRRK2

2017 Human Molecular Genetics
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Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation

2017 Alzheimers & Dementia
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LRRK2 phosphorylates pre-synaptic N-ethylmaleimide sensitive fusion (NSF) protein enhancing its ATPase activity and SNARE complex disassembling rate.

2016 Molecular Neurodegeneration
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Citations (133)