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Human Molecular Genetics|November 28, 2013
Functional interaction of Parkinson's disease-associated LRRK2 with members of the dynamin GTPase superfamilyKlodjan Stafa, Elpida Tsika, Roger Moser, et al.
Human Molecular Genetics|January 4, 2007
Parkinson's disease-associated mutations in LRRK2 link enhanced GTP-binding and kinase activities to neuronal toxicityAndrew B West, Darren J Moore, Catherine Choi, et al.
Human Molecular Genetics|April 18, 2014
Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegenerationElpida Tsika, Liliane Glauser, Roger Moser, et al.
Human Molecular Genetics|February 24, 2012
Neurodegenerative phenotypes in an A53T α-synuclein transgenic mouse model are independent of LRRK2João Paulo L Daher, Olga Pletnikova, Saskia Biskup, et al.
Human Molecular Genetics|June 10, 2005
Mitochondrial localization of the Parkinson's disease related protein DJ-1: implications for pathogenesisLi Zhang, Mika Shimoji, Bobby Thomas, et al.
Brain Research|May 22, 2007
Localization of Parkinson's disease-associated LRRK2 in normal and pathological human brainShinji Higashi, Saskia Biskup, Andrew B West, et al.
Human Molecular Genetics|November 1, 2016
Human R1441C LRRK2 regulates the synaptic vesicle proteome and phosphoproteome in a Drosophila model of Parkinson's diseaseMd Shariful Islam, Hendrik Nolte, Wright Jacob, et al.
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