Nuclear Inclusion

Known as: Nuclear Inclusion Body, Inclusion Bodies, Intranuclear, Inclusion Body, Intranuclear 
Circumscribed masses of foreign or metabolically inactive materials, within the CELL NUCLEUS. Some are VIRAL INCLUSION BODIES.
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
Protein degradation by basal constitutive autophagy is important to avoid accumulation of polyubiquitinated protein aggregates… (More)
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Highly Cited
2002
Highly Cited
2002
Proteolytic processing of mutant huntingtin (mhtt) is regarded as a key event in the pathogenesis of Huntington's disease (HD… (More)
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Highly Cited
2000
Highly Cited
2000
Instability of CAG DNA trinucleotide repeats is the mutational mechanism for several neurodegenerative diseases resulting in the… (More)
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Highly Cited
1999
Highly Cited
1999
Huntington's disease (HD) is an inherited, neurodegenerative disorder caused by the expansion of a glutamine repeat in the N… (More)
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Highly Cited
1999
Highly Cited
1999
Mutant ataxin-1, the expanded polyglutamine protein causing spinocerebellar ataxia type 1 (SCA1), aggregates in ubiquitin… (More)
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Highly Cited
1998
Highly Cited
1998
The mechanisms by which mutant huntingtin induces neurodegeneration were investigated using a cellular model that recapitulates… (More)
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Highly Cited
1998
Highly Cited
1998
Spinocerebellar ataxia type 3 (SCA3/MJD) is one of at least eight human neurodegenerative diseases caused by glutamine-repeat… (More)
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Highly Cited
1998
Highly Cited
1998
Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disorder caused by expansion of a polyglutamine… (More)
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Highly Cited
1997
Highly Cited
1997
Huntington's disease (HD) is one of an increasing number of human neurodegenerative disorders caused by a CAG/polyglutamine… (More)
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Highly Cited
1997
Highly Cited
1997
The mechanism of neurodegeneration in CAG/polyglutamine repeat expansion diseases is unknown but is thought to occur at the… (More)
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