NeuralCipher Source record
Parkinson's disease: from monogenic forms to genetic susceptibility factors.
DOI: 10.1093/hmg/ddp012PMID: 19297401
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
14.936 articles found
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Nitrated {alpha}-synuclein-induced alterations in microglial immunity are regulated by CD4+ T cell subsets.
DOI: 10.4049/jimmunol.0803982PMID: 19299711
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Interplay between cytosolic dopamine, calcium, and alpha-synuclein causes selective death of substantia nigra neurons.
DOI: 10.1016/j.neuron.2009.01.033PMID: 19409267
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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[Analysis of the alpha-synuclein gene dosage variation associated with autosomal dominant form of ParkinsonTs disease].
DOI: 10.1134/s1022795409040176PMID: 19507712
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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[Parkinson disease: genetics and neuronal death].
PMID: 19593875
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study.
DOI: 10.1016/s1474-4422(09)70081-xPMID: 19345147
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
The G2019S LRRK2 Mutation is Rare in Korean Patients with Parkinson's Disease and Multiple System Atrophy.
DOI: 10.3988/jcn.2009.5.1.29PMID: 19513331
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Prevalence and clinical features of LRRK2 mutations in patients with Parkinson's disease in southern Spain.
DOI: 10.1111/j.1468-1331.2009.02620.xPMID: 19473361
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Alpha-synuclein induces migration of BV-2 microglial cells by up-regulation of CD44 and MT1-MMP.
DOI: 10.1111/j.1471-4159.2009.06075.xPMID: 19457162
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Different saccadic abnormalities in PINK1 mutation carriers and in patients with non-genetic Parkinson's disease.
DOI: 10.1007/s00415-009-5092-8PMID: 19330279
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Differences between subacute and chronic MPTP mice models: investigation of dopaminergic neuronal degeneration and alpha-synuclein inclusions.
DOI: 10.1111/j.1471-4159.2009.06072.xPMID: 19457163
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Source record
Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese.
DOI: 10.1016/j.neurobiolaging.2008.11.008PMID: 19329225
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.