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- W2109249715 abstract "Huntington’s disease (HD) is a progressive neurological disorder caused by a CAG/polyglutamine repeat expansion. We have previously generated the R6/2 mouse model that expresses exon 1 of the human HD gene containing CAG repeats in excess of 150. These mice develop a progressive neurological phenotype with a rapid onset and progression. We show here that it is impossible to establish fibroblast lines from these mice at 12 weeks of age, whilst this can be achieved without difficulty at 6 and 9 weeks. Cultures derived from mice at 12 weeks contained a high frequency of dysmorphic cells, including cells with an aberrant nuclear morphology and a high frequency of micronuclei and large vacuoles. All of these features were also present in a line derived from a juvenile HD patient. Fibroblast lines derived from R6/2 mice and from HD patients were found to have a high frequency of multiple centrosomes which could account for all of the observed phenotypes including a reduced mitotic index, high frequency of aneuploidy and persistence of the midbody. We were unable to detect large insoluble polyglutamine aggregates in either the mouse or human lines. We have identified a novel progressive HD pathology that occurs in cells of non-central nervous system origin. An investigation of the pathological consequences of the HD mutation in these cells will provide insight into cellular basis of the disease." @default.
- W2109249715 created "2016-06-24" @default.
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- W2109249715 date "2001-10-01" @default.
- W2109249715 modified "2023-10-17" @default.
- W2109249715 title "Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington's disease (HD) transgenic mice and HD patients" @default.
- W2109249715 cites W1509279614 @default.
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- W2109249715 cites W1565788467 @default.
- W2109249715 cites W1599271861 @default.
- W2109249715 cites W1599366903 @default.
- W2109249715 cites W1940885739 @default.
- W2109249715 cites W1962249623 @default.
- W2109249715 cites W1974683080 @default.
- W2109249715 cites W1977383752 @default.
- W2109249715 cites W1978104052 @default.
- W2109249715 cites W1985474993 @default.
- W2109249715 cites W1988146888 @default.
- W2109249715 cites W1996381116 @default.
- W2109249715 cites W1996789718 @default.
- W2109249715 cites W1997312506 @default.
- W2109249715 cites W1998425738 @default.
- W2109249715 cites W1998974178 @default.
- W2109249715 cites W2004969253 @default.
- W2109249715 cites W2021549542 @default.
- W2109249715 cites W2029948374 @default.
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- W2109249715 cites W2073282970 @default.
- W2109249715 cites W2073342372 @default.
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- W2109249715 cites W2112072636 @default.
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- W2109249715 cites W2156079900 @default.
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- W2109249715 cites W2159269805 @default.
- W2109249715 cites W2160779871 @default.
- W2109249715 cites W2166131777 @default.
- W2109249715 cites W2167647748 @default.
- W2109249715 cites W2168802470 @default.
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- W2109249715 doi "https://doi.org/10.1093/hmg/10.21.2425" @default.
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- W2109249715 hasPublicationYear "2001" @default.
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