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19q13.31

A chromosome band present on 19q
National Institutes of Health

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3 relations
19qChromosomesPOU2F2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Identification of breast cancer associated variants that modulate transcription factor binding
Genome-wide association studies (GWAS) have discovered thousands loci associated with disease risk and quantitative traits, yet… Expand
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Highly Cited
2012
Highly Cited
2012
Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients
BackgroundSpecific genetic contributions for preeclampsia (PE) are currently unknown. This genome-wide association study (GWAS… Expand
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2010
2010
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family.
BACKGROUND The bladder exstrophy-epispadias complex (BEEC) is a spectrum of anomalies involving the abdominal wall, pelvis… Expand
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2010
2010
Arsenic-related DNA copy-number alterations in lung squamous cell carcinomas
Background:Lung squamous cell carcinomas (SqCCs) occur at higher rates following arsenic exposure. Somatic DNA copy-number… Expand
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2009
2009
Chromosomal imbalances and partial uniparental disomies in primary central nervous system lymphoma
To determine the pattern of genetic alterations in primary central nervous system lymphomas (PCNSL), 19 PCNSL were studied by… Expand
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Highly Cited
2006
Highly Cited
2006
Integration specificity of phage phiC31 integrase in the human genome.
The site-specific integrase from bacteriophage phiC31 functions in mammalian cells and is being applied for genetic engineering… Expand
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2006
2006
The gene overexpressed in polycythemia rubra vera, PRV-1, and the gene encoding a neutrophil alloantigen, NB1, are alleles of a single gene, CD177, in chromosome band 19q13.31.
BACKGROUND PRV-1 mRNA is overexpressed by neutrophils from polycythemia vera patients and is homologous to NB1 a gene… Expand
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Highly Cited
2006
Highly Cited
2006
Molecular analysis of chromosomal rearrangements in mammalian cells after phiC31-mediated integration.
Reports on insertional mutagenesis due to integration of gene therapy vectors into the host genome have raised concerns about the… Expand
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2005
2005
Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions
Lipid levels in plasma strongly influence the risk for coronary heart disease. To localise and subsequently identify genes… Expand
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2005
2005
Genome-wide analyses demonstrate novel loci that predispose to drusen formation.
PURPOSE To test whether genes for drusen formation are independent of age-related macular degeneration (AMD) pathogenesis… Expand
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