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Vacuolar protein sorting 35 (Vps35) rescues locomotor deficits and shortened lifespan in Drosophila expressing a Parkinson’s disease mutant of Leucine-rich repeat kinase 2 (LRRK2)

Overview of attention for article published in Molecular Neurodegeneration, June 2014
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Title
Vacuolar protein sorting 35 (Vps35) rescues locomotor deficits and shortened lifespan in Drosophila expressing a Parkinson’s disease mutant of Leucine-rich repeat kinase 2 (LRRK2)
Published in
Molecular Neurodegeneration, June 2014
DOI 10.1186/1750-1326-9-23
Pubmed ID
Authors

Radek Linhart, Sarah Anne Wong, Jieyun Cao, Melody Tran, Anne Huynh, Casey Ardrey, Jong Min Park, Christine Hsu, Saher Taha, Rentia Peterson, Shannon Shea, Jason Kurian, Katerina Venderova

Abstract

Parkinson's disease (PD) is the most common movement neurodegenerative movement disorder. An incomplete understanding of the molecular pathways involved in its pathogenesis impedes the development of effective disease-modifying treatments. To address this gap, we have previously generated a Drosophila model of PD that overexpresses PD pathogenic mutant form of the second most common causative gene of PD, Leucine-Rich Repeat Kinase 2 (LRRK2).

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 99 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 1%
India 1 1%
Unknown 97 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 26 26%
Researcher 20 20%
Student > Bachelor 11 11%
Student > Master 9 9%
Student > Doctoral Student 6 6%
Other 11 11%
Unknown 16 16%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 24 24%
Agricultural and Biological Sciences 23 23%
Neuroscience 16 16%
Medicine and Dentistry 9 9%
Pharmacology, Toxicology and Pharmaceutical Science 3 3%
Other 3 3%
Unknown 21 21%