NeuralCipher Open access
MAP1B rescues LRRK2 mutant-mediated cytotoxicity.
DOI: 10.1186/1756-6606-7-29PMID: 24754922
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14.046 articles found
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A revised picture of the Cu(II)-α-synuclein complex: the role of N-terminal acetylation.
DOI: 10.1021/bi5003025PMID: 24739028
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Genetic variants and animal models in SNCA and Parkinson disease.
DOI: 10.1016/j.arr.2014.04.002PMID: 24768741
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Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations.
DOI: 10.1002/mds.25883PMID: 24752924
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PAR2-mediated epigenetic upregulation of α-synuclein contributes to the pathogenesis of Parkinson׳s disease.
DOI: 10.1016/j.brainres.2014.04.014PMID: 24747612
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Residue histidine 50 plays a key role in protecting α-synuclein from aggregation at physiological pH.
DOI: 10.1074/jbc.m113.544049PMID: 24742669
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Co-existence of two different α-synuclein oligomers with different core structures determined by hydrogen/deuterium exchange mass spectrometry.
DOI: 10.1002/anie.201400491PMID: 24740651
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Hsp27 suppresses the Cu(2+)-induced amyloidogenicity, redox activity, and cytotoxicity of α-synuclein by metal ion stripping.
DOI: 10.1016/j.freeradbiomed.2014.04.012PMID: 24746619
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The beneficial effect of a prolyl oligopeptidase inhibitor, KYP-2047, on alpha-synuclein clearance and autophagy in A30P transgenic mouse.
DOI: 10.1016/j.nbd.2014.04.003PMID: 24746855
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Unaltered striatal dopamine release levels in young Parkin knockout, Pink1 knockout, DJ-1 knockout and LRRK2 R1441G transgenic mice.
DOI: 10.1371/journal.pone.0094826PMID: 24733019
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Multiple system atrophy: a prototypical synucleinopathy for disease-modifying therapeutic strategies.
DOI: 10.1016/j.nbd.2014.03.021PMID: 24727096
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Differential LRRK2 expression in the cortex, striatum, and substantia nigra in transgenic and nontransgenic rodents.
DOI: 10.1002/cne.23583PMID: 24633735
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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