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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 ...
Disaggregases, Molecular Chaperones That Resolubilize Protein Aggregates
(ACAD BRASILEIRA DE CIENCIASRIO JANEIRO, 2015)
Dentatorubro-Pallidoluysian Atrophy (DRPLA) among 700 Families with Ataxia in Brazil
(Springer, 2017)
Dentatorubro-pallidoluysian atrophy (DRPLA) is a spinocerebellar ataxia (SCA) very rare in non-Asian populations. To date, DRPLA was undetected in the general Brazilian population. Adult-onset ataxic patients have been ...
Clock gene variation in Tachycineta swallows
(Wiley, 2012-01)
Many animals use photoperiod cues to synchronize reproduction with environmental conditions and thereby improve their reproductive success. The circadian clock, which creates endogenous behavioral and physiological rhythms ...
Overexpression of heat shock protein 70 in R6/2 Huntington's disease mice has only modest effects on disease progression
(Elsevier Science BvAmsterdamHolanda, 2003)
Análise molecular da Ataxina 1Molecular analysis Ataxin 1
([s.n.], 2012)
Mr Imaging In Spinocerebellar Ataxias: A Systematic Review
(Amer Soc NeuroradiologyDenville, 2016)