Copy number variation in the human genome and its implications for cardiovascular disease.
about
Cellular hyperproliferation and cancer as evolutionary variablesGenetics of type 2 diabetes: pathophysiologic and clinical relevanceGenomic structural variations for cardiovascular and metabolic comorbidityComputing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio testGenetics and cardiovascular disease: Design and development of a DNA biobank.Early identification of cardiovascular risk using genomics and proteomics.Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.Genetic Polymorphisms and Peritoneal Membrane Function.Variation in inflammation-related genes and risk of incident nonfatal myocardial infarction or ischemic stroke.The pressure of finding human hypertension genes: new tools, old dilemmas.Genome-wide association studies for atherosclerotic vascular disease and its risk factors.A common copy number variation on chromosome 6 association with the gene expression level of endothelin 1 in transformed B lymphocytes from three racial groups.The relationship between apolipoprotein E epsilon2/epsilon3/epsilon4 polymorphisms and hypertension: a meta-analysis of six studies comprising 1812 cases and 1762 controls.Predictive genetic testing for coronary artery disease.Translating genomic analyses into improved management of coronary artery disease.Implications of gene copy-number variation in health and diseases.Optimal Sparse Segment Identification with Application in Copy Number Variation Analysis.The utility of copy number variation (CNV) in studies of hypertension-related left ventricular hypertrophy (LVH): rationale, potential and challengesWhole genome survey of copy number variation in the spontaneously hypertensive rat: relationship to quantitative trait loci, gene expression, and blood pressure.Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia.A genome-wide characterization of copy number variations in native populations of Peninsular Malaysia.Identification of Copy Number Variations in Isolated Tetralogy of Fallot.Analyses of copy number variation reveal putative susceptibility loci in MTX-induced mouse neural tube defects.Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease
P2860
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P2860
Copy number variation in the human genome and its implications for cardiovascular disease.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Copy number variation in the h ...... ns for cardiovascular disease.
@en
type
label
Copy number variation in the h ...... ns for cardiovascular disease.
@en
prefLabel
Copy number variation in the h ...... ns for cardiovascular disease.
@en
P1433
P1476
Copy number variation in the h ...... ns for cardiovascular disease.
@en
P304
P356
10.1161/CIRCULATIONAHA.106.677591
P407
P577
2007-06-01T00:00:00Z