NeuralCipher Source record
ERKed by LRRK2: a cell biological perspective on hereditary and sporadic Parkinson's disease.
DOI: 10.1016/j.bbadis.2013.11.005PMID: 24225420
A bibliographic record traceable to Europe PMC.
9.897 articles found
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Jmjd3 is essential for the epigenetic modulation of microglia phenotypes in the immune pathogenesis of Parkinson's disease.
DOI: 10.1038/cdd.2013.159PMID: 24212761
A bibliographic record traceable to Europe PMC.
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Progression of intestinal permeability changes and alpha-synuclein expression in a mouse model of Parkinson's disease.
DOI: 10.1002/mds.25736PMID: 24898698
A bibliographic record traceable to Europe PMC.
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What's wrong with epigenetics in Huntington's disease?
DOI: 10.1016/j.neuropharm.2013.10.025PMID: 24184315
A bibliographic record traceable to Europe PMC.
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Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population.
DOI: 10.1016/j.neurobiolaging.2013.10.094PMID: 24239437
A bibliographic record traceable to Europe PMC.
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FOXO3 determines the accumulation of α-synuclein and controls the fate of dopaminergic neurons in the substantia nigra.
DOI: 10.1093/hmg/ddt530PMID: 24158851
A bibliographic record traceable to Europe PMC.
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Metabolic abnormalities and hypoleptinemia in α-synuclein A53T mutant mice.
DOI: 10.1016/j.neurobiolaging.2013.10.088PMID: 24239384
A bibliographic record traceable to Europe PMC.
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α-Synuclein in the olfactory system in Parkinson's disease: role of neural connections on spreading pathology.
DOI: 10.1007/s00429-013-0651-2PMID: 24135772
A bibliographic record traceable to Europe PMC.
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Association of common genetic variants of HOMER1 gene with levodopa adverse effects in Parkinson's disease patients.
DOI: 10.1038/tpj.2013.37PMID: 24126708
A bibliographic record traceable to Europe PMC.
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Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease.
DOI: 10.1016/j.neurobiolaging.2013.09.019PMID: 24126159
A bibliographic record traceable to Europe PMC.
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Yet another polymorph of α-synuclein: solid-state sequential assignments.
DOI: 10.1007/s12104-013-9526-yPMID: 24114178
A bibliographic record traceable to Europe PMC.
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Clinical profiles of Parkinson's disease associated with common leucine-rich repeat kinase 2 and glucocerebrosidase genetic variants in Chinese individuals.
DOI: 10.1016/j.neurobiolaging.2013.08.012PMID: 24095219
A bibliographic record traceable to Europe PMC.
Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.