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Polyglutamine repeat disorders

Davies SW, Beardsall K, Turmaine M, DiFiglia M, Aronin N, Bates GP. Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions Lancet 1998 351 131-133. [Pg.270]

Salminen A, Tapiola T, Korhonen P, Suuronen T (1998) Neuronal optosis induced by histone deacetylase inhibitors. Brain Res Mol Brain Res 61(l-2) 203-206 Sanchez I, Xu CJ, Juo P, Kakizaka A, Blenis J, Yuan J (1999) Caspase-8 is required for cell death induced by expanded polyglutamine repeats. Neuron 22(3) 623-633 Sanchez I, Mahlke C, Yuan J (2003) Pivotal role of oligomerization in expanded polyglutamine neurode-generative disorders. Nature 421(6921) 373-379... [Pg.291]

Huntington s disease is an autosomal dominant inherited disorder caused by an abnormality (expansion of a CAG trinucleotide repeat that codes for a polyglutamine tract) of the huntingtin gene on chromosome 4. An autosomal... [Pg.614]

Huntington s disease (HD) is a devastating disorder caused by an excess number of GAG repeats in the gene for huntingtin on chromosome 4. The expanded polyglutamine... [Pg.340]

See other pages where Polyglutamine repeat disorders is mentioned: [Pg.779]    [Pg.779]    [Pg.268]    [Pg.413]    [Pg.353]    [Pg.357]    [Pg.607]    [Pg.662]    [Pg.772]    [Pg.198]    [Pg.266]    [Pg.39]    [Pg.40]    [Pg.1092]    [Pg.317]    [Pg.271]    [Pg.208]    [Pg.136]    [Pg.174]    [Pg.226]    [Pg.241]    [Pg.1092]    [Pg.204]    [Pg.319]    [Pg.390]    [Pg.390]    [Pg.408]    [Pg.491]    [Pg.259]    [Pg.387]   
See also in sourсe #XX -- [ Pg.779 ]



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