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David N. Hauser

Researcher at National Institutes of Health

Publications -  24
Citations -  2591

David N. Hauser is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Parkin & LRRK2. The author has an hindex of 14, co-authored 23 publications receiving 2057 citations. Previous affiliations of David N. Hauser include Brown University & University of Pittsburgh.

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p62/SQSTM1 is required for Parkin-induced mitochondrial clustering but not mitophagy; VDAC1 is dispensable for both

TL;DR: It is demonstrated that mitochondria are aggregated by p62, following its recruitment by Parkin in a VDAC1-independent manner, and it is suggested that proteins other than p62 are likely required for mitophagy downstream of Parkin substrates other than VD AC1.
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Dopamine: Functions, Signaling, and Association with Neurological Diseases

TL;DR: The aspects of dopamine as a catecholaminergic neurotransmitter and dopamine signaling pathways elicited through dopamine receptor activation in normal brain function are summarized and the potential involvement of these signaling pathways in evoking the onset and progression of some diseases in the nervous system are described.
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Mitochondrial dysfunction and oxidative stress in Parkinson's disease and monogenic parkinsonism

TL;DR: Evidence from both sporadic and genetic forms of Parkinson's disease that implicate both mitochondria and oxidative stress as central players in disease pathogenesis are reviewed.
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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

Alexandra Beilina, +168 more
TL;DR: It is shown, using the specific example of Parkinson disease, that identification of protein–protein interactions can help determine the most likely candidate for several GWAS loci, and proposed that three different genes for PD have a common biological function.
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mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortex

TL;DR: A high-resolution transcriptome data set of mouse cerebral cortex at embryonic and adult stages using RNA sequencing (RNA-Seq) is reported, finding many differences in gene expression, splicing and RNA editing between embryonic andadult cerebral cortex.