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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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Review
2008
Review
2008
3p deletion syndrome is a rare disorder involving developmental delay, dysmorphic physical features, and growth retardation… Expand
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
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
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
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