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15q15

A chromosome band present on 15q
National Institutes of Health

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7 relations
15qBUB1B wt AlleleChromosomesPDIA3 wt Allele

Papers overview

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Highly Cited
2012
Highly Cited
2012
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls
Recent genome-wide association studies (GWASs) have identified common genetic variants at 5p15.33, 6p21–6p22 and 15q25.1… 
2004
2004
A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population
Developmental dyslexia (dyslexia) is a heritable condition typically diagnosed in the first school years, characterised by an… 
Highly Cited
2001
Highly Cited
2001
Evolution of Transglutaminase Genes: Identification of a Transglutaminase Gene Cluster on Human Chromosome 15q15
We isolated and characterized the gene encoding human transglutaminase (TG)X(TGM5) and mapped it to the 15q15.2 region of… 
Highly Cited
1999
Highly Cited
1999
Purification of a Novel Flavoprotein Involved in the Thyroid NADPH Oxidase
Hydrogen peroxide is the final electron acceptor for the biosynthesis of thyroid hormone catalyzed by thyroperoxidase at the… 
Highly Cited
1999
Highly Cited
1999
Tumor suppression in human skin carcinoma cells by chromosome 15 transfer or thrombospondin-1 overexpression through halted tumor vascularization.
The development of skin carcinomas presently is believed to be correlated with mutations in the p53 tumor suppressor and ras gene… 
Highly Cited
1998
Highly Cited
1998
Stimulation of p53-mediated Transcriptional Activation by the p53-binding Proteins, 53BP1 and 53BP2*
p53 is a tumor suppressor protein that controls cell proliferation by regulating the expression of growth control genes. In a… 
Highly Cited
1998
Highly Cited
1998
Molecular cloning, functional expression and chromosomal localization of a cDNA encoding a human Na+/nucleoside cotransporter (hCNT2) selective for purine nucleosides and uridine.
Two Na(+)-dependent nucleoside transporters implicated in adenosine and uridine transport in mammalian cells are distinguished… 
Review
1997
Review
1997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey
Autosomal recessive limb girdle muscular dystrophy (LGMD2) is a clinically and genetically heterogenous group of diseases… 
1995
1995
A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.
Previous genetic and physical studies of LGMD2A, an autosomal recessive form of limb-girdle muscular dystrophy, have led to the… 
Highly Cited
1988
Highly Cited
1988
Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase.
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