Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons-Reference-Cited by-同舟云学术

Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons

Published:2018-03 Issue: Volume:111 Page:26-35
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Schapansky Jason,Khasnavis Saurabh,DeAndrade Mark P.,Nardozzi Jonathan D.,Falkson Samuel R.,Boyd Justin D.,Sanderson John B.,Bartels Tim,Melrose Heather L.,LaVoie Matthew J.^ORCID

Funder

Michael J. Fox Foundation

NIH

Publisher

Elsevier BV

Subject

Neurology

Reference77 articles.

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4. Loss of leucine-rich repeat kinase 2 (LRRK2) in rats leads to progressive abnormal phenotypes in peripheral organs;Baptista;PLoS One,2013

5. alpha-Synuclein occurs physiologically as a helically folded tetramer that resists aggregation;Bartels;Nature,2011

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