Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure.
about
Global metabolic consequences of the chromogranin A-null model of hypertension: transcriptomic detection, pathway identification, and experimental verification.Long human CHGA flanking chromosome 14 sequence required for optimal BAC transgenic "rescue" of disease phenotypes in the mouse Chga knockout.Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach.Genome-wide case/control studies in hypertension: only the 'tip of the iceberg'.Chromogranin a and the autonomic system: decomposition of heart rate variability and rescue by its catestatin fragment.Single nucleotide polymorphism in gene encoding transcription factor Prep1 is associated with HIV-1-associated dementia.Naturally occurring genetic variants in human chromogranin A (CHGA) associated with hypertension as well as hypertensive renal disease.Role of reactive oxygen species in hyperadrenergic hypertension: biochemical, physiological, and pharmacological evidence from targeted ablation of the chromogranin a (Chga) geneProteomic analysis yields an unexpected trans-acting point in control of the human sympathochromaffin phenotype.The extended granin family: structure, function, and biomedical implicationsGenetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins.Adrenergic genetic mechanisms in hypertension and hypertensive kidney disease.MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension.Chromogranin A regulates renal function by triggering Weibel-Palade body exocytosis.Analysis and validation of traits associated with a single nucleotide polymorphism Gly364Ser in catestatin using humanized chromogranin A mouse models.A haplotype variant of the human chromogranin A gene (CHGA) promoter increases CHGA expression and the risk for cardiometabolic disorders.Common genetic variants in the chromogranin a promoter are associated with renal injury in IgA nephropathy patients with malignant hypertension.
P2860
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P2860
Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Common genetic variants in the ...... c activity and blood pressure.
@en
type
label
Common genetic variants in the ...... c activity and blood pressure.
@en
prefLabel
Common genetic variants in the ...... c activity and blood pressure.
@en
P2093
P2860
P50
P356
P1433
P1476
Common genetic variants in the ...... ic activity and blood pressure
@en
P2093
B A Hamilton
D T O'Connor
M G Ziegler
N J Schork
P-A B Shih
S K Mahata
P2860
P2888
P304
P356
10.1038/KI.2008.113
P407
P577
2008-04-23T00:00:00Z