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15q25

A chromosome band present on 15q
National Institutes of Health

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4 relations
15qChromosomesMFGE8 wt AlleleNTRK3 wt Allele

Papers overview

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2017
2017
Genetic Risk Can Be Decreased: Quitting Smoking Decreases and Delays Lung Cancer for Smokers With High and Low CHRNA5 Risk Genotypes — A Meta-Analysis
Highly Cited
2013
Highly Cited
2013
The α3β4* nicotinic acetylcholine receptor subtype mediates nicotine reward and physical nicotine withdrawal signs independently of the α5 subunit in the mouse
2012
2012
Association of the 15q25 and 5p15 Lung Cancer Susceptibility Regions with Gene Expression in Lung Tumor Tissue
Background: Genome-wide association studies have identified two independent lung cancer susceptibility loci at chromosome 15q25… 
2011
2011
A Case–Control Study of a Sex-Specific Association between a 15q25 Variant and Lung Cancer Risk
Background: Genetic variants located at 15q25, including those in the cholinergic receptor nicotinic cluster (CHRNA5) have been… 
2001
2001
Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26
Hearing impairment is the most common inherited human sensory defect. Nonsyndromic Hearing Impairment (NSHI) is the most… 
2000
2000
Expression of brx proto-oncogene in normal ovary and in epithelial ovarian neoplasms.
2000
2000
Tetrasomy 15q25-->qter: cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome.
Tetrasomy for the distal long arm of chromosome 15 is a rare finding. It has been previously described in seven patients, all of… 
1998
1998
Expression analysis and chromosomal mapping of a novel human gene, APRIL, encoding an acidic protein rich in leucines.
1997
1997
A PAC containing the human mitochondrial DNA polymerase gamma gene (POLG) maps to chromosome 15q25.
The human mitochondrial DNA (mtDNA) is a closed circular, 16,569-bp double-stranded DNA, encoding 13 genes whose protein products… 
1996
1996
Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.
We describe a premature boy with metopic craniosynostosis, facial anomalies, atrial-septal defect, hydronephrosis and flexion… 
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