Cholinergic neuronal defect without cell loss in Huntington's disease. (2006)
Smith, Ruben, Chung, Hinfan, Rundquist, Sara, Colgan, Lesley, Englund, Elisabet, ...
Abstract is not available
Cholinergic neuronal defect without cell loss in Huntington's disease (2006)
Smith, Ruben, Chung, Hinfan, Rundquist, Sara, Colgan, Lesley, Englund, Elisabet, ...
Huntington's disease (HD) is a neurodegenerative disorder caused by a CAG-repeat expansion in the huntingtin (IT15) gene. The striatum is one of the regions most affected by neurodegeneration,...
Cholinergic neuronal defect without cell loss in Huntington's disease (2006)
Smith, Ruben, Chung, Hinfan, Rundquist, Sara, Colgan, Lesley, Englund, Elisabet, ...
Huntington's Disease (HD) is a neurodegenerative disorder caused by a CAG-repeat expansion in the huntingtin (IT15) gene. The striatum is one of the regions most affected by neurodegeneration,...
Orexin loss in Huntington's disease (2005)
Petersén, Åsa, Gil, Joana, Björkqvist, Maria, Tanila, Heikki, Araújo, Inês M., ...
Huntington's disease (HD) is a devastating neurodegenerative disorder caused by an expanded CAG repeat in the gene encoding huntingtin, a protein of unknown function. Mutant huntingtin forms...
De Pril, Remko, Fischer, David F., Hobo, Barbara, Brunt, Ewout R., ...
Polyglutamine diseases are characterized by neuronal intranuclear inclusions of expanded polyglutamine proteins, indicating failing protein degradation. UBB+1, an aberrant form of ubiquitin, is a...
De Pril, Remko, Fischer, David F., Hobo, Barbara, Brunt, Ewout R., ...
Polyglutamine diseases are characterized by neuronal intranuclear inclusions (NIIs) of expanded polyglutamine proteins, indicating the failure of protein degradation. UBB+1, an aberrant form of...
De Pril, Remko, Fischer, David F., Hobo, Barbara, Brunt, Ewout R., ...
Polyglutamine diseases are characterized by neuronal intranuclear inclusions of expanded polyglutamine proteins, indicating failing protein degradation. UBB+1, an aberrant form of ubiquitin, is a...
Characterization and localization of the Huntington disease gene product (1993)
Hoogeveen, André T., Willemsen, Rob, Meyer, Nicolle, Roolj, Karien E.de, Roos, Raymund A.C., ...
The recent identification of the Huntington's disease (HD) gene, enabled us to synthesize oligopeptides corresponding with the carboxy-terminal end of the predicted HD-gene (IT15) product....
Delayed onset of the diurnal melatonin rise in patients with Huntington’s disease
Aziz, N. Ahmad, Pijl, Hanno, Frölich, Marijke, Van Der Bent, Chris, Roelfsema, Ferdinand, ...
Sleep disturbances are very prevalent in Huntington’s disease (HD) patients and can substantially impair their quality of life. Accumulating evidence suggests considerable dysfunction of the...