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An integrated transcriptomics and proteomics analysis reveals functional endocytic dysregulation caused by mutations in LRRK2

Abstract:
Background Mutations in LRRK2 are the most common cause of autosomal dominant Parkinson's disease, and the relevance of LRRK2 to the sporadic form of the disease is becoming ever more apparent. It is therefore essential that studies are conducted to improve our understanding of the cellular role of this protein. Here we use multiple models and techniques to identify the pathways through which LRRK2 mutations may lead to the development of Parkinson's disease.

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.nbd.2019.04.005

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Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Role:
Author
ORCID:
0000-0001-8350-6928
Publisher:
Elsevier Publisher's website
Journal:
Neurobiology of Disease Journal website
Volume:
127
Pages:
512-526
Publication date:
2019-04-05
Acceptance date:
2019-04-03
DOI:
ISSN:
0969-9961
Language:
English
Keywords:
Pubs id:
pubs:987997
UUID:
uuid:61334663-ec44-4d89-bbcc-ae51f2a2f004
Local pid:
pubs:987997
Deposit date:
2019-04-15

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