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Genome-wide association studies (GWAS) have discovered thousands loci associated with disease risk and quantitative traits, yet… Expand BackgroundSpecific genetic contributions for preeclampsia (PE) are currently unknown. This genome-wide association study (GWAS… Expand Abstract The genetic origin of the three common variants of the human apolipoprotein E (apoE) protein, known as E2, E3 and E4… Expand Background:Lung squamous cell carcinomas (SqCCs) occur at higher rates following arsenic exposure. Somatic DNA copy-number… Expand BACKGROUND
The bladder exstrophy-epispadias complex (BEEC) is a spectrum of anomalies involving the abdominal wall, pelvis… Expand To determine the pattern of genetic alterations in primary central nervous system lymphomas (PCNSL), 19 PCNSL were studied by… Expand The site-specific integrase from bacteriophage phiC31 functions in mammalian cells and is being applied for genetic engineering… Expand BACKGROUND: PRV‐1 mRNA is overexpressed by neutrophils from polycythemia vera patients and is homologous to NB1 a gene… Expand Reports on insertional mutagenesis due to integration of gene therapy vectors into the host genome have raised concerns about the… Expand Lipid levels in plasma strongly influence the risk for coronary heart disease. To localise and subsequently identify genes… Expand