Smith, Ruben, Bacos, Karl, Fedele, Valentina, Soulet, Denis, Walz, Helena A., Obermüller, Stefanie, ...
Huntington's disease is a severe progressive neurodegenerative disorder caused by a CAG expansion in the IT15 gene, which encodes huntingtin. The disease primarily affects the neostriatum and...
Communication breakdown - synaptic dysfunction in Huntington's disease. (2007)
Huntington's disease (HD) is a neurodegenerative disease caused by a CAG-triplet expansion in the gene encoding the protein huntingtin. The disease typically starts in mid-life and progresses for...
Loss of SNAP-25 and rabphilin 3a in sensory-motor cortex in Huntington's disease. (2007)
Smith, Ruben, Klein, Pontus, Koc-Schmitz, Yeliz, Waldvogel, Henry J, Faull, Richard L M, Brundin, Patrik, ...
Abstract is not available
Increased metabolism in the R6/2 mouse model of Huntington's disease. (2007)
Bacos, Karl, Wood, Nigel I, Lindqvist, Andreas, Wierup, Nils, Woodman, Ben, ...
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, ...
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,...
Smith, Ruben, Petersén, Asa, Bates, Gillian P, Brundin, Patrik, Li, Jia-Yi
Abstract is not available
Orexin loss in Huntington's disease. (2004)
Petersén, Asa, Gil, Joana, Maat-Schieman, Marion Lc, Björkqvist, Maria, Tanila, Heikki, Araújo, Ines M, ...
Abstract is not available
Orexin loss in Huntington's disease (2004)
Petersén, Åsa, Gil, Joana, Maat-Schieman, Marion LC, Björkqvist, Maria, Tanila, Heikki, Araújo, Ines M, ...
Huntington's disease is a devastating neurodegenerative disorder caused by an expanded CAG repeat in the gene encoding huntingtin, a protein of unknown function. Mutant huntingtin forms intracellular...
Orexin loss in Huntington's disease (2004)
Petersén, Åsa, Gil, Joana, Maat-Schieman, Marion LC, Björkqvist, Maria, Tanila, Heikki, Araújo, Ines M, ...
Huntington's disease is a devastating neurodegenerative disorder caused by an expanded CAG repeat in the gene encoding huntingtin, a protein of unknown function. Mutant huntingtin forms intracellular...
Smith, Ruben, Lotharius, Julie, Brundin, Patrik
Abstract is not available