alfa-sinüklein agregasyonu: mitokondriyal defektler ile Parkinson hastalığı arasındaki bağlantı?
alpha-synuclein aggregation: a link between mitochondrial defects and Parkinson's disease?
DOI: 10.1089/152308603322110904PMID: 12880487
“Parkinson alpha synuclein” Aramayı temizle
alpha-synuclein aggregation: a link between mitochondrial defects and Parkinson's disease?
DOI: 10.1089/152308603322110904PMID: 12880487
Residual substantia nigra neuromelanin in Parkinson's disease is cross-linked to alpha-synuclein.
DOI: 10.1016/s0197-0186(02)00161-4PMID: 12590943
Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece.
DOI: 10.1046/j.1468-1331.2003.00576.xPMID: 12752402
Differential cytotoxicity of dopamine and H2O2 in a human neuroblastoma divided cell line transfected with alpha-synuclein and its familial Parkinson's disease-linked mutants.
DOI: 10.1016/s0304-3940(03)00212-xPMID: 12727333
Beta-synuclein inhibits formation of alpha-synuclein protofibrils: a possible therapeutic strategy against Parkinson's disease.
DOI: 10.1021/bi020604aPMID: 12667059
Parkinson's disease-associated alpha-synuclein is a calmodulin substrate.
DOI: 10.1074/jbc.m209020200PMID: 12610000
Nigrostriatal alpha-synucleinopathy induced by viral vector-mediated overexpression of human alpha-synuclein: a new primate model of Parkinson's disease.
DOI: 10.1073/pnas.0536383100PMID: 12601150
Tissue transglutaminase-induced aggregation of alpha-synuclein: Implications for Lewy body formation in Parkinson's disease and dementia with Lewy bodies.
DOI: 10.1073/pnas.0438021100PMID: 12576551
The formation of highly soluble oligomers of alpha-synuclein is regulated by fatty acids and enhanced in Parkinson's disease.
DOI: 10.1016/s0896-6273(03)00024-2PMID: 12597857
Parkinson's disease: alpha-synuclein and parkin in protein aggregation and the reversal of unfolded protein stress.
DOI: 10.1385/1-59259-394-1:57PMID: 12840539
Alpha-synuclein and Parkinson's disease.
DOI: 10.1201/9780203508596-22PMID: 12442675
Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.
DOI: 10.1093/brain/awg010PMID: 12477695
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