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Neurochemical Aspects of Neurodegenerative Diseases

Oligomerization of unfolded proteins, formation of ditfiused deposits [Pg.250]

misfolded Ap peptide 1-42 accumulates in the neuronal endoplasmic reticulum extracellularly as plaques. In contrast, in PD and dementia with Lewy bodies (DLB) abnormal accumulation of a-synuclein occurs in neuronal cell bodies, axons, and synapses. Furthermore, in DLB, Ap 1-42 has been reported to promote a-synuclein accumulation and neurodegeneration (Hashimoto et ah, 2003). [Pg.250]

Neurodegenerative disease Protein Type of aggregate Location References [Pg.251]

PD a-Synuclein Fibrillar non-amyloid Intracellular Beyer (2007), Burke (2004) [Pg.251]

HD Huntingtin Fibrillar non-amyloid Intracellular Bonilla (2000), Gil and Rego (2008) [Pg.251]


See other pages where Neurochemical Aspects of Neurodegenerative Diseases is mentioned: [Pg.249]    [Pg.250]    [Pg.254]    [Pg.256]    [Pg.258]    [Pg.260]    [Pg.262]    [Pg.264]    [Pg.266]    [Pg.268]    [Pg.270]    [Pg.272]    [Pg.274]    [Pg.276]    [Pg.278]    [Pg.280]    [Pg.282]    [Pg.284]    [Pg.286]    [Pg.288]    [Pg.290]    [Pg.292]    [Pg.294]    [Pg.296]    [Pg.298]    [Pg.300]    [Pg.302]    [Pg.304]    [Pg.306]    [Pg.308]    [Pg.310]    [Pg.312]    [Pg.314]    [Pg.316]    [Pg.320]    [Pg.322]    [Pg.324]   


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Neurodegenerative diseases

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