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Leucine-Rich Repeat Kinase 2 (LRRK2)

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Attention for Chapter 9: Models of LRRK2-Associated Parkinson’s Disease
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Chapter title
Models of LRRK2-Associated Parkinson’s Disease
Chapter number 9
Book title
Leucine-Rich Repeat Kinase 2 (LRRK2)
Published in
Advances in neurobiology, March 2017
DOI 10.1007/978-3-319-49969-7_9
Pubmed ID
Book ISBNs
978-3-31-949967-3, 978-3-31-949969-7
Authors

Xiong, Yulan, Dawson, Ted M., Dawson, Valina L., Yulan Xiong, Ted M. Dawson, Valina L. Dawson

Editors

Hardy J. Rideout

Abstract

Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common genetic causes of Parkinson's disease (PD) and also one of the strongest genetic risk factors in sporadic PD. The LRRK2 protein contains a GTPase and a kinase domain and several protein-protein interaction domains. Both in vitro and in vivo assays in different model systems have provided tremendous insights into the molecular mechanisms underlying LRRK2-induced dopaminergic neurodegeneration. Among all the model systems, animal models are crucial tools to study the pathogenesis of human disease. How do the animal models recapitulate LRRK2-induced dopaminergic neuronal loss in human PD? To answer this question, this review focuses on the discussion of the animal models of LRRK2-associated PD including genetic- and viral-based models.

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Mendeley readers

The data shown below were compiled from readership statistics for 84 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 84 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 14 17%
Student > Ph. D. Student 12 14%
Researcher 6 7%
Student > Bachelor 5 6%
Student > Doctoral Student 4 5%
Other 9 11%
Unknown 34 40%
Readers by discipline Count As %
Neuroscience 18 21%
Biochemistry, Genetics and Molecular Biology 11 13%
Medicine and Dentistry 6 7%
Agricultural and Biological Sciences 3 4%
Pharmacology, Toxicology and Pharmaceutical Science 3 4%
Other 4 5%
Unknown 39 46%