FAQ

15q15.2

A chromosome band present on 15q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2015
01219952015

Related topics

Related topics

4 relations
15qCDAN1 wt AlleleChromosomesUSP8 wt Allele

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
15q15.2
Chromosomes
15q
CDAN1 wt Allele
USP8 wt Allele

Papers overview

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2015
2015
Implication of a Chromosome 15q15.2 Locus in Regulating UBR1 and Predisposing Smokers to MGMT Methylation in Lung.
O(6)-Methylguanine-DNA methyltransferase (MGMT) is a DNA repair enzyme that protects cells from carcinogenic effects of… (More)
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2015
2015
Prevention and Epidemiology Implication of a Chromosome 15q15.2 Locus in Regulating UBR1 and Predisposing Smokers to MGMT Methylation in Lung
O-Methylguanine-DNA methyltransferase (MGMT) is a DNA repair enzyme that protects cells from carcinogenic effects of alkylating… (More)
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2011
2011
Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.
Genome-wide association studies (GWAS) have identified 3 genomic regions, at 15q24-25.1, 5p15.33, and 6p21.33, which associate… (More)
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2011
2011
Prevention and Epidemiology Genome-Wide Significant Association Between a Sequence Variant at 15q15.2 and Lung Cancer Risk
Genome-wide association studies (GWAS) have identified 3 genomic regions, at 15q24–25.1, 5p15.33, and 6p21.33, which associate… (More)
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Highly Cited
2009
Highly Cited
2009
Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.
To explore the impact of common variation on the risk of developing lung cancer, we conducted a two-phase genome-wide association… (More)
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2008
2008
Craniosynostosis in a patient with a de novo 15q15-q22 deletion.
Interstitial deletions involving the chromosomal band 15q15 are very rare. A total of five cases were previously reported. Here… (More)
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2005
2005
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome.
Peeling skin syndrome is an autosomal recessive genodermatosis characterized by the shedding of the outer epidermis. In the acral… (More)
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2001
2001
Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. Structure of the gene encoding transglutaminase X and a novel gene family member…
We isolated and characterized the gene encoding human transglutaminase (TG)(X) (TGM5) and mapped it to the 15q15.2 region of… (More)
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2001
2001
The C/At is out of the bag: a gene for mental illness
Has the first ‘schizophrenia’ gene been identified? The knowledge that genes play a considerable role in the etiology of… (More)
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1995
1995
An STS map of the limb girdle muscular dystrophy type 2A region
A gene for the recessive limb girdle muscular dystrophy LGMD2A (MIM 253600) was mapped within a 7-cM interval along Chromosome… (More)
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