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Reduced levels of proteasome products in a mouse striatal cell model of huntington's disease
(2015-12-01)
Huntington's disease is the result of a long polyglutamine tract in the gene encoding huntingtin protein, which in turn causes a large number of cellular changes and ultimately results in neurodegeneration of striatal ...
Overexpression of heat shock protein 70 in R6/2 Huntington's disease mice has only modest effects on disease progression
(Elsevier Science BvAmsterdamHolanda, 2003)
Peptide based therapeutics and their use for the treatment of neurodegenerative and other diseases
(Elsevier Masson SAS, 2018)
Mr Imaging In Spinocerebellar Ataxias: A Systematic Review
(Amer Soc NeuroradiologyDenville, 2016)
Análise molecular da Ataxina 1Molecular analysis Ataxin 1
([s.n.], 2012)
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)
(Oxford Univ PressOxfordInglaterra, 2000)