NeuralCipher Source record
The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease.
DOI: 10.1017/s0317167100005783PMID: 17352347
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
14.777 articles found
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Mutant alpha-synuclein exacerbates age-related decrease of neurogenesis.
DOI: 10.1016/j.neurobiolaging.2006.12.016PMID: 17275140
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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GM1 specifically interacts with alpha-synuclein and inhibits fibrillation.
DOI: 10.1021/bi061749aPMID: 17253773
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Wild-type and mutant alpha-synuclein induce a multi-component gene expression profile consistent with shared pathophysiology in different transgenic mouse models of PD.
DOI: 10.1016/j.expneurol.2006.12.005PMID: 17254569
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Frequency of the LRRK2 G2019S mutation in Italian patients affected by Parkinson's disease.
DOI: 10.1007/s10038-006-0105-2PMID: 17235449
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's disease.
DOI: 10.1007/s10048-006-0075-8PMID: 17225181
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia.
DOI: 10.1016/j.parkreldis.2006.12.001PMID: 17222580
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease.
DOI: 10.1212/01.wnl.0000254483.19854.efPMID: 17215492
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies.
DOI: 10.1136/jnnp.2006.107904PMID: 17210620
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
Prostaglandin E2 receptor subtype 2 (EP2) regulates microglial activation and associated neurotoxicity induced by aggregated alpha-synuclein.
DOI: 10.1186/1742-2094-4-2PMID: 17204153
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Analysis of alpha-synuclein, dopamine and parkin pathways in neuropathologically confirmed parkinsonian nigra.
DOI: 10.1007/s00401-006-0181-6PMID: 17203291
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Dopaminergic neuron loss and up-regulation of chaperone protein mRNA induced by targeted over-expression of alpha-synuclein in mouse substantia nigra.
DOI: 10.1111/j.1471-4159.2006.04310.xPMID: 17241127
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.