Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Neurodegenerative protein

Interactions of Glycolytic Enzymes with Neurodegenerative Proteins 239... [Pg.239]

Mucolipin, also known as mucolipin 1 or mucolipidin (encoded by the MCOLN1 gene), is a TRP channel-related membrane protein, most probably residing in intracellular membranes. Is defective in mucolipidosis type IV disease, a developmental neurodegenerative disorder characterized by lysosomal storage disorder and abnormal endocytosis of lipids. The fimction of mucolipin is unknown. [Pg.793]

The transmissible spongiform encephalopathies, or prion diseases, are fatal neurodegenerative diseases characterized by spongiform changes, astrocytic gliomas, and neuronal loss resulting from the deposition of insoluble protein aggregates in neural cells. They include Creutzfeldt-Jakob disease in humans, scrapie in... [Pg.37]

Zhao M, Su J, Head E, Cotman CW (2003) Accumulation of caspase cleaved amyloid precursor protein represents an early neurodegenerative event in aging and in Alzheimer s disease. Neurobiol Dis 14 391-403... [Pg.300]

Protein Misfolding and Neurodegenerative Disease Therapeutic Opportunities... [Pg.7]

Kakizuka A. Protein precipitation a common etiology in neurodegener-ative disorders Trends Genet 1998 14 396 -02. [Pg.270]

The conformational plasticity supported by mobile regions within native proteins, partially denatured protein states such as molten globules, and natively unfolded proteins underlies many of the conformational (protein misfolding) diseases (Carrell and Lomas, 1997 Dobson et al., 2001). Many of these diseases involve amyloid fibril formation, as in amyloidosis from mutant human lysozymes, neurodegenerative diseases such as Parkinson s and Alzheimer s due to the hbrillogenic propensities of a -synuclein and tau, and the prion encephalopathies such as scrapie, BSE, and new variant Creutzfeldt-Jacob disease (CJD) where amyloid fibril formation is triggered by exposure to the amyloid form of the prion protein. In addition, aggregation of serine protease inhibitors such as a j-antitrypsin is responsible for diseases such as emphysema and cirrhosis. [Pg.105]


See other pages where Neurodegenerative protein is mentioned: [Pg.238]    [Pg.250]    [Pg.206]    [Pg.238]    [Pg.250]    [Pg.206]    [Pg.189]    [Pg.66]    [Pg.162]    [Pg.824]    [Pg.826]    [Pg.826]    [Pg.1166]    [Pg.1245]    [Pg.1257]    [Pg.432]    [Pg.443]    [Pg.444]    [Pg.444]    [Pg.14]    [Pg.236]    [Pg.236]    [Pg.289]    [Pg.289]    [Pg.295]    [Pg.369]    [Pg.137]    [Pg.284]    [Pg.288]    [Pg.48]    [Pg.4]    [Pg.250]    [Pg.251]    [Pg.256]    [Pg.268]    [Pg.1148]    [Pg.75]    [Pg.25]    [Pg.293]    [Pg.347]    [Pg.352]    [Pg.353]    [Pg.354]   
See also in sourсe #XX -- [ Pg.239 , Pg.250 ]




SEARCH



Glycolytic Enzymes with Neurodegenerative Proteins

© 2024 chempedia.info