NeuralCipher Open access
Molecular basis for N-terminal alpha-synuclein acetylation by human NatB.
DOI: 10.7554/elife.57491PMID: 32885784
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15.286 articles found
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Letter to the editor, "Movement disorders rounds: A case of missing pathology in a patient with LRRK2 Parkinson's disease".
DOI: 10.1016/j.parkreldis.2020.08.036PMID: 32921567
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
A Phase 1 Randomized Trial of Specific Active α-Synuclein Immunotherapies PD01A and PD03A in Multiple System Atrophy.
DOI: 10.1002/mds.28218PMID: 32882100
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
Signs of Chronic Hypoxia Suggest a Novel Pathophysiological Event in α-Synucleinopathies.
DOI: 10.1002/mds.28229PMID: 32881058
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Age at Onset of LRRK2 p.Gly2019Ser Is Related to Environmental and Lifestyle Factors.
DOI: 10.1002/mds.28238PMID: 32875616
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Degradation of LRRK2 in the Treatment of Parkinson's Disease.
DOI: 10.1021/acsmedchemlett.0c00453PMID: 33214810
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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A genetic analysis of a Spanish population with early onset Parkinson's disease.
DOI: 10.1371/journal.pone.0238098PMID: 32870915
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Anti-amyloidogenic effect of artemin on α-synuclein.
DOI: 10.1515/hsz-2019-0446PMID: 32673279
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Aspirin and ibuprofen could lower risk of LRRK2 Parkinson disease.
DOI: 10.1038/s41582-020-0394-7PMID: 32719503
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Lack of evidence for genetic association of saposins A, B, C and D with Parkinson's disease.
DOI: 10.1093/brain/awaa214PMID: 32793944
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Reply: Saposin D variants are not a common cause of familial Parkinson's disease among Italians; and Lack of evidence for genetic association of saposins A, B, C and D with Parkinson's disease.
DOI: 10.1093/brain/awaa215PMID: 32793945
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How Parkinson's disease-related mutations disrupt the dimerization of WD40 domain in LRRK2: a comparative molecular dynamics simulation study.
DOI: 10.1039/d0cp03171bPMID: 32914822
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