Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins.
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Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular riskNaturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion.Early inflammatory and metabolic changes in association with AGTR1 polymorphisms in prehypertensive subjects.Dopamine D1 receptor (DRD1) genetic polymorphism: pleiotropic effects on heritable renal traitsTwo functional serotonin polymorphisms moderate the effect of food reinforcement on BMI.Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressureProgression of chronic kidney disease: Adrenergic genetic influence on glomerular filtration rate decline in hypertensive nephrosclerosis.Effects of chromogranin A deficiency and excess in vivo: biphasic blood pressure and catecholamine responsesHuman tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension.Catecholamine storage vesicles: role of core protein genetic polymorphisms in hypertension.Genetic covariance between gamma-glutamyl transpeptidase and fatty liver risk factors: role of beta2-adrenergic receptor genetic variation in twins.Genome-wide linkage and regional association study of blood pressure response to the cold pressor test in Han Chinese: the genetic epidemiology network of salt sensitivity study.Human tyrosine hydroxylase natural genetic variation: delineation of functional transcriptional control motifs disrupted in the proximal promoter.Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traitsHeritable influence of DBH on adrenergic and renal function: twin and disease studiesCatecholamine pathway gene variation is associated with norepinephrine and epinephrine concentrations at rest and after exercise.Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system.Autonomic and hemodynamic origins of pre-hypertension: central role of heredity.Statistical genetics concepts and approaches in schizophrenia and related neuropsychiatric research.Chromogranin A polymorphisms are associated with hypertensive renal disease.Heredity and cardiometabolic risk: naturally occurring polymorphisms in the human neuropeptide Y(2) receptor promoter disrupt multiple transcriptional response motifsGenetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins.Analysis of ABCG2 and other urate transporters in uric acid homeostasis in chronic kidney disease: potential role of remote sensing and signaling.Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure.The cholinesterases: analysis by pharmacogenomics in man.Heritability and genome-wide linkage in US and australian twins identify novel genomic regions controlling chromogranin a: implications for secretion and blood pressure.Genetic variation at the delta-sarcoglycan (SGCD) locus elevates heritable sympathetic nerve activity in human twin pairsAdrenergic polymorphism and the human stress response.Tobacco addiction and pharmacogenetics of nicotine metabolism.Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs.Neuropeptide Y(1) Receptor NPY1R discovery of naturally occurring human genetic variants governing gene expression in cella as well as pleiotropic effects on autonomic activity and blood pressure in vivo.Human heart rate: heritability of resting and stress values in twin pairs, and influence of genetic variation in the adrenergic pathway at a microribonucleic acid (microrna) motif in the 3'-UTR of cytochrome b561 [corrected]Gene variants predisposing to SIDS: current knowledge.Statistical analysis strategies for association studies involving rare variants.Review: Neuropathological features of unexplained sudden unexpected death in infancy: current evidence and controversies.Genetic Variations of Tyrosine Hydroxylase in the Pathogenesis of Hypertension.The genetics of anxiety-related negative valence system traits.The USC Adult Twin Cohorts: International Twin Study and California Twin Program.Pleiotropic effects of novel trans-acting loci influencing human sympathochromaffin secretion.Contributions of the sympathetic nervous system, glutathione, body mass and gender to blood pressure increase with normal aging: influence of heredity.
P2860
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P2860
Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
Functional allelic heterogenei ...... d response to stress in twins.
@en
Functional allelic heterogenei ...... d response to stress in twins.
@nl
type
label
Functional allelic heterogenei ...... d response to stress in twins.
@en
Functional allelic heterogenei ...... d response to stress in twins.
@nl
prefLabel
Functional allelic heterogenei ...... d response to stress in twins.
@en
Functional allelic heterogenei ...... d response to stress in twins.
@nl
P2093
P2860
P1476
Functional allelic heterogenei ...... d response to stress in twins.
@en
P2093
Brian P Kennedy
Brinda K Rana
Daniel T O'Connor
Elizabeth O Lillie
Fangwen Rao
Lian Zhang
Michael G Ziegler
Myles Cockburn
Nicholas J Schork
P2860
P304
P356
10.1152/PHYSIOLGENOMICS.00151.2004
P577
2004-09-14T00:00:00Z