AR wt Allele

Known as: SMAX1, NR3C4, DHTR 
Human AR wild-type allele is located within Xq11.2-q12 and is approximately 180 kb in length. This allele, which encodes androgen receptor protein… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1975-2018
0102019752018

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Highly Cited
2012
Highly Cited
2012
Spinal and bulbar muscular atrophy (SBMA) is an inherited neurodegenerative disorder caused by the expansion of the polyglutamine… (More)
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Highly Cited
2009
Highly Cited
2009
Expansion of a polyglutamine tract in the androgen receptor (AR) causes spinal and bulbar muscular atrophy (SBMA). We previously… (More)
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Highly Cited
2006
Highly Cited
2006
Expansion of the polyglutamine (polyQ) stretch in the androgen receptor (AR) protein leads to spinal and bulbar muscular atrophy… (More)
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Highly Cited
2005
Highly Cited
2005
Spinal and bulbar muscular atrophy (SBMA) is an adult-onset motor neuron disease caused by the expansion of a trinucleotide CAG… (More)
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Highly Cited
2005
Highly Cited
2005
Spinal and bulbar muscular atrophy (SBMA) is an inherited adult onset motor neuron disease caused by the expansion of a… (More)
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Highly Cited
2004
Highly Cited
2004
X-linked spinal and bulbar muscular atrophy (SBMA) is an inherited neuromuscular disorder characterized by lower motor neuron… (More)
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Highly Cited
2003
Highly Cited
2003
Spinal and bulbar muscular atrophy (SBMA) is an inherited motor neuron disease caused by the expansion of the polyglutamine… (More)
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Highly Cited
2000
Highly Cited
2000
Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused… (More)
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Highly Cited
2000
Highly Cited
2000
Spinal and bulbar muscular atrophy (SBMA) is one of a group of human inherited neurodegenerative diseases caused by polyglutamine… (More)
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Highly Cited
1998
Highly Cited
1998
Spinal and bulbar muscular atrophy (SBMA) is an X-linked motor neuronopathy caused by the expansion of an unstable CAG repeat in… (More)
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