TH, tyrosine hydroxylase, 7054

N. diseases: 321; N. variants: 71
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 Biomarker group BEFREE The purpose of this study was to investigate immunoreactivity for dopamine β-hydroxylase (DBH) and tyrosine hydroxylase (TH) in carotid body (CB) glomus cells in spontaneously hypertensive rats (SHR/Izm) at 4 (prehypertensive stage), 8 (early stage of developmental hypertension), 12 (later stage of developmental hypertension), and 16weeks of age (established hypertensive stage). 28473232 2017
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 Biomarker group CTD_human Chronic infusion of epigallocatechin-3-O-gallate into the hypothalamic paraventricular nucleus attenuates hypertension and sympathoexcitation by restoring neurotransmitters and cytokines. 27659729 2016
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 GeneticVariation group BEFREE However, the contribution of the tyrosine hydroxylase C-824T single nucleotide polymorphism to hypertension could not be confirmed in our cohort. 23489065 2013
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 GeneticVariation group BEFREE The C-824T SNP in the proximal TH promoter influences BP and prevalence of hypertension in the general population. 20706199 2010
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 GeneticVariation group BEFREE Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension. 20571875 2010
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 Biomarker group BEFREE We designed a case-controlled study consisting of 503 HT (hypertensive) individuals and 490 NT (normotensive) individuals matched by region, age and gender to systematically investigate the association between the TH gene and hypertension. 18208403 2008
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 GeneticVariation group LHGDN Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo. 17698732 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 Biomarker group RGD The results show that TH and AGT mRNA expression changes during the different phases of experimental hypertension, suggesting that the noradrenaline (NOR) and angiotensin II (Ang II) might participate in the modulation/maintenance of coarctation hypertension. 16650497 2006
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 GeneticVariation group BEFREE We conclude that common allelic variation within the tyrosine hydroxylase locus exerts a powerful, heritable effect on autonomic control of the circulation and that such variation may have implications in later development of cardiovascular disease traits such as hypertension. 15367723 2004
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.580 Biomarker group BEFREE The position of tyrosine hydroxylase (TH) as the rate-limiting enzyme in catecholamine biosynthesis renders it a candidate gene for the etiology of hypertension. 9774362 1998