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3p26.2

A chromosome band present on 3p
National Institutes of Health

Papers overview

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2014
2014
A significant proportion (up to 62%) of oral squamous cell carcinomas (OSCCs) may arise from oral potential malignant lesions… Expand
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Review
2013
Review
2013
Disc-related disorders are highly genetic conditions with heritability estimates of up to 75 % and yet, few genomic locations… Expand
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2009
2009
Autism is a neurodevelopmental disorder characterized by three core symptom domains: ritualistic-repetitive behaviors, impaired… Expand
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2006
2006
Objective: To identify of the gene responsible for the onset of spinocerebellar ataxia type 16 (SCA16). Methods: We reanalyzed… Expand
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2004
2004
3p deletion syndrome is a rare contiguous-gene disorder involving the loss of the telomeric portion of the short arm of… Expand
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Review
2003
Review
2003
The oxytocin receptor belongs to the G-protein-coupled seven transmembrane receptor superfamily. Its main physiological role is… Expand
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Review
2001
Review
2001
8-Hydroxyguanine (oh8G) is a major base lesion produced by reactive oxygen species. oh8G in DNA causes G:C to T:A transversions… Expand
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Highly Cited
2000
Highly Cited
2000
Oxidative damage is implicated in several chronic diseases including cancer. 8-Hydroxyguanine (8-oxoG) is one of the major… Expand
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Highly Cited
1997
Highly Cited
1997
We report the cloning of a human homolog of the yeast OGG1 gene, which encodes a DNA glycosylase that excises an oxidatively… Expand
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Highly Cited
1994
Highly Cited
1994
We isolated and characterized the human oxytocin receptor gene. Southern blots indicated that the human genome has a single copy… Expand
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