Dentatorubral-Pallidoluysian Atrophy

Known as: Disease, Naito-Oyanagi, NOD, Syndrome, Haw River 
A rare, autosomal dominant inherited progressive neurodegenerative disorder. It is caused by a mutation in the ATN1 gene, resulting in a combined… (More)

Topic mentions per year

Topic mentions per year

1981-2017
010020019812017

Papers overview

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Highly Cited
2009
Highly Cited
2009
FoxP3 is a key transcription factor for the development and function of natural CD4(+) regulatory T cells (Treg cells). Here we… (More)
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2008
2008
BACKGROUND Dentatorubral pallidoluysian atrophy (DRPLA) is a rare, autosomal dominant, clinically heterogeneous neurodegenerative… (More)
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Highly Cited
2008
Highly Cited
2008
A fundamental question in cancer biology is whether cells with tumorigenic potential are common or rare within human cancers… (More)
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Highly Cited
2008
Highly Cited
2008
Type 1 diabetes (T1D) is a debilitating autoimmune disease that results from T-cell-mediated destruction of insulin-producing… (More)
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Highly Cited
2001
Highly Cited
2001
Acrp30 is a circulating protein synthesized in adipose tissue. A single injection in mice of purified recombinant Acrp30 leads to… (More)
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1995
1995
An unstable expansion of CAG repeat in the coding region of the DRPLA gene on chromosome 12p is the mutation specific for… (More)
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1995
1995
Dentatorubral–pallidoluysian atrophy (DRPLA) is associated with the expansion of an unstable GAG repeat. Using antibodies against… (More)
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Highly Cited
1994
Highly Cited
1994
Hereditary dentatorubral–pallidoluysian atrophy (DRPLA) is an autosomal dominant neurologic disorder characterized by variable… (More)
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Highly Cited
1994
Highly Cited
1994
Dentatorubral and pallidoluysian atrophy (DRPLA) is an autosomal dominant neurodegenerative disorder characterized by combined… (More)
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1994
1994
Anticipation refers to the progressively earlier onset and increase in disease severity in successive generations. We studied… (More)
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