Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.
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The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular diseasePharmacogenetics of erectile dysfunction: navigating into uncharted watersA comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseAn overview of the genetic structure within the Italian population from genome-wide dataGenetic Variation in the Human SORBS1 Gene is Associated With Blood Pressure Regulation and Age at Onset of Hypertension: A SAPPHIRe Cohort StudyGenetics of hypertension: discoveries from the bench to human populations.Rare mutations in renal sodium and potassium transporter genes exhibit impaired transport function.Imputing observed blood pressure for antihypertensive treatment: impact on population and genetic analyses.Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1.Pharmacogenetic association of NOS3 variants with cardiovascular disease in patients with hypertension: the GenHAT study.Soluble guanylate cyclase: a new therapeutic target for pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension.Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection.Progress and future aspects in genetics of human hypertensionLeft ventricular diastolic function associated with common genetic variation in ATP12A in a general population.Associations of Endothelial System Genes With Blood Pressure Changes and Hypertension Incidence: The GenSalt StudyFrontiers in renal and epithelial physiology - grand challenges.Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC).TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives.Angiogenesis related genes NOS3, CD14, MMP3 and IL4R are associated to VEGF gene expression and circulating levels in healthy adults.Genome-wide association studies and contribution to cardiovascular physiologyGenes and Cardiovascular Disease: Where do we go from here?Copy number variations and cognitive phenotypes in unselected populationsA genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaPathophysiology of hypertension in the absence of nitric oxide/cyclic GMP signaling.Genes for blood pressure: an opportunity to understand hypertensionLoci influencing blood pressure identified using a cardiovascular gene-centric array.Genetics, ancestry, and hypertension: implications for targeted antihypertensive therapiesAssociation Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian CohortCommon variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.Gene-environment interactions of selected pharmacogenes in arterial hypertension.cGMP: transition from bench to bedside: a report of the 6th International Conference on cGMP Generators, Effectors and Therapeutic Implications.Role of sGC-dependent NO signalling and myocardial infarction risk.A Review of the Genetics of Hypertension with a Focus on Gene-Environment Interactions.Novel Paradigms of Salt and Hypertension.Genetics of ion homeostasis in Ménière's Disease.New quality measure for SNP array based CNV detection.Association between variation in the genes DDAH1 and DDAH2 and hypertension among Uygur, Kazakh and Han ethnic groups in China.The burden of multiple sclerosis variants in continental Italians and Sardinians.Positional cloning of quantitative trait nucleotides for blood pressure and cardiac QT-interval by targeted CRISPR/Cas9 editing of a novel long non-coding RNA.
P2860
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P2860
Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Genomewide association study u ...... on of endothelial NO synthase.
@ast
Genomewide association study u ...... on of endothelial NO synthase.
@en
type
label
Genomewide association study u ...... on of endothelial NO synthase.
@ast
Genomewide association study u ...... on of endothelial NO synthase.
@en
prefLabel
Genomewide association study u ...... on of endothelial NO synthase.
@ast
Genomewide association study u ...... on of endothelial NO synthase.
@en
P2093
P2860
P50
P921
P1433
P1476
Genomewide association study u ...... on of endothelial NO synthase.
@en
P2093
Amnon Shabo
Chiara Troffa
Clive Hoggart
Costanza Conti
Daniele Cusi
Federica Rizzi
Francesca Frau
Galina Simonova
Giuseppe Argiolas
Hisatomi Arima
P2860
P304
P356
10.1161/HYPERTENSIONAHA.111.181990
P407
P50
P577
2011-12-19T00:00:00Z