Mechanisms of tissue damage in Huntington's disease involve excitotoxicity, mitochondrial damage, and neuroinflammation, including microglia activation. In the present study, we investigate the role of pyroptosis process in the striatal neurons of the R6/2 mouse model of Huntington's disease. Transgenic mice were sacrificed at 4 and 13 weeks of age. After sacrifice, histological and immunohistochemical studies were performed. We found that NLRP3 and Caspase-1 were intensely expressed in 13-week-old R6/2 mice. Moreover, NLRP3 expression levels were higher in striatal spiny projection neurons and in parvalbumin interneurons, which are prone to degenerate in HD
Neurodegenerative diseases (NDs), such as Alzheimer’s disease, Parkinson’s disease, Huntington’s dis...
Huntington's disease, with its dominant loss of striatal neurons, is triggered by an expanded glutam...
Huntington's disease is an autosomal dominant hereditary neurodegenerative disorder characterized by...
Huntington’s disease (HD) is a neurodegenerative disease characterized by several symptoms encompass...
This thesis investigates the possible role of apoptosis, or programmed cell death, in Huntington's d...
Huntington Disease (HD) is a neurodegenerative disorder caused by expansion of a poly-glutamine trac...
Huntington's disease (HD) is a hereditary neurodegenerative disorder presenting with chorea, dementi...
Huntington's disease (HD) is a fatally progressive neurodegenerative disease that is characterized a...
Huntington's disease (HD) is a fatal hereditary neurodegenerative disease causing degeneration of st...
SummaryCleavage of huntingtin (htt) has been characterized in vitro, and accumulation of caspase cle...
Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor, ...
Transgenic Huntington's disease (HD) mice, expressing exon 1 of the HD gene with an expanded CAG rep...
Many pathways have been proposed as contributing to Huntington's disease (HD) pathogenesis, but gene...
Several mouse models for Huntington’s disease (HD) have been produced to date. Based on differences...
Hereditary Huntington's disease (HD) is associated with progressive motor, cognitive and psychiatric...
Neurodegenerative diseases (NDs), such as Alzheimer’s disease, Parkinson’s disease, Huntington’s dis...
Huntington's disease, with its dominant loss of striatal neurons, is triggered by an expanded glutam...
Huntington's disease is an autosomal dominant hereditary neurodegenerative disorder characterized by...
Huntington’s disease (HD) is a neurodegenerative disease characterized by several symptoms encompass...
This thesis investigates the possible role of apoptosis, or programmed cell death, in Huntington's d...
Huntington Disease (HD) is a neurodegenerative disorder caused by expansion of a poly-glutamine trac...
Huntington's disease (HD) is a hereditary neurodegenerative disorder presenting with chorea, dementi...
Huntington's disease (HD) is a fatally progressive neurodegenerative disease that is characterized a...
Huntington's disease (HD) is a fatal hereditary neurodegenerative disease causing degeneration of st...
SummaryCleavage of huntingtin (htt) has been characterized in vitro, and accumulation of caspase cle...
Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor, ...
Transgenic Huntington's disease (HD) mice, expressing exon 1 of the HD gene with an expanded CAG rep...
Many pathways have been proposed as contributing to Huntington's disease (HD) pathogenesis, but gene...
Several mouse models for Huntington’s disease (HD) have been produced to date. Based on differences...
Hereditary Huntington's disease (HD) is associated with progressive motor, cognitive and psychiatric...
Neurodegenerative diseases (NDs), such as Alzheimer’s disease, Parkinson’s disease, Huntington’s dis...
Huntington's disease, with its dominant loss of striatal neurons, is triggered by an expanded glutam...
Huntington's disease is an autosomal dominant hereditary neurodegenerative disorder characterized by...