A team has shown the most common genetic cause of Parkinson’s disease – a mutant LRRK2 kinase enzyme – contributes to the formation of inclusions in neurons, resembling one of the hallmark pathologies seen in Parkinson’s disease. These inclusions are made up of aggregated alpha synuclein protein, which – the research also shows – can be prevented from forming by using 2 LRRK2 kinase inhibitor drugs now being developed for clinical use.
The interaction between mutant LRRK2 kinase and alph...
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