NeuralCipher Source record
Epigenetic Control of Rho-Associated Protein Kinase 2 in Neurodegeneration.
DOI: 10.3233/jad-190832PMID: 31658060
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15.097 articles found
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[Animal models of synucleinopathies: prion-like propagation of alpha-synuclein in wild-type animals].
DOI: 10.1254/fpj.154.301PMID: 31787680
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Alpha-synuclein oligomerization increases its effect on promoting NMDA receptor internalization.
PMID: 31933723
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Associations Between APOE Variants, Tau and α-Synuclein.
DOI: 10.1007/978-981-32-9358-8_15PMID: 32096038
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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A Comparative Study of the Diagnostic Potential of Plasma and Erythrocytic α-Synuclein in Parkinson's Disease.
DOI: 10.1159/000506480PMID: 32485710
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
Chemical genetic identification of GAK substrates reveals its role in regulating Na<sup>+</sup>/K<sup>+</sup>-ATPase.
DOI: 10.26508/lsa.201800118PMID: 30623173
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LRRK2-mediated Rab10 phosphorylation in immune cells from Parkinson's disease patients.
DOI: 10.1002/mds.27601PMID: 30597610
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Treadmill exercise intervention improves gait and postural control in alpha-synuclein mouse models without inducing cerebral autophagy.
DOI: 10.1016/j.bbr.2018.11.035PMID: 30599154
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Wild-type and mutant (G2019S) leucine-rich repeat kinase 2 (LRRK2) associate with subunits of the translocase of outer mitochondrial membrane (TOM) complex.
DOI: 10.1016/j.yexcr.2018.12.022PMID: 30597143
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The Parkinson's disease-associated mutation N1437H impairs conformational dynamics in the G domain of LRRK2.
DOI: 10.1096/fj.201802031rPMID: 30592623
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Radicicol rescues yeast cell death triggered by expression of human α-synuclein and its A53T mutant, but not by human βA4 peptide and proapoptotic protein bax.
DOI: 10.1016/j.bioorg.2018.12.033PMID: 30612081
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Glucocerebrosidase mutations and synucleinopathies: Toward a model of precision medicine.
DOI: 10.1002/mds.27583PMID: 30589955
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.