Matches in SemOpenAlex for { <https://semopenalex.org/work/W2338410065> ?p ?o ?g. }
- W2338410065 abstract "Polyglutamine expansion diseases are inherited neurodegenerative disorders including Huntington’s disease, several types of spino-cerebellar ataxia, dentatorubral-pallido-luysian atrophy and spinobulbar muscular atrophy. The diseases are caused by an expansion of the CAG trinucleotide in the corresponding genes coding for an expanded tract of glutamine in the mutated proteins. Generally, the diseases appear in mid-life, progress over time and lead to death ten to twenty years after the onset of the first symptoms. The mutation is mainly reflected by changes in the structural properties of the host protein and thereby leads to several cellular dysfunctions. Currently, research focus on identifying key actors of the neurodegenerative process in order to develop effective therapies directed against these diseases." @default.
- W2338410065 created "2016-06-24" @default.
- W2338410065 creator A5004447443 @default.
- W2338410065 creator A5086057942 @default.
- W2338410065 date "2010-01-01" @default.
- W2338410065 modified "2023-09-27" @default.
- W2338410065 title "Maladies par expansion de polyglutamine: Avancées récentes et perspectives thérapeutiques Polyglutamine expansion diseases: Recent advances and therapeutic perspectives Revue de la littérature" @default.
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