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: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE As a result, 6-hydroxydopamine could lead to PD-like lesions, including tremor, stiffness, attenuated spontaneous activity, and bradykinesia in mice, and the expression of tyrosine hydroxylase in the striatum was decreased. 31359520 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE After observation of behavioral alteration using the rotarod test, mice were sacrificed for the measurement of the PD- and mitochondrial quality control-related protein levels in the substantia nigra. tDCS improved the behavioral alterations and changes in tyrosine hydroxylase levels in MPTP-treated mice. 31229553 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE These results show a selective sparing of tyrosine hydroxylase isoform 2 in Parkinson's disease. 31276794 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE The severity of PD was evaluated through locomotor activity perceived in the open field test, histological examination and immunohistochemical detection of amyloid-β in brain tissues, in addition to the biochemical assessment of tyrosine hydroxylase activity in brain tissues. 31198107 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE Decreased tyrosine hydroxylase (TH) activity, due to degeneration of dopaminergic neurons contributes to the low dopamine content and the motor deficits that characterized Parkinson's disease (PD). 31463866 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE This manuscript provides an overview of the role of human TH in the pathophysiology of PD, covering the following aspects: (1) structures of the gene and protein of human TH in relation to PD; (2) similarity and dissimilarity between the phenotypes of aging-related sPD and those of young-onset fPD or DOPA-responsive dystonia due to DA deficiency in the striatum with decreased TH activity caused by mutations in either the TH gene or GTP cyclohydrolase I (GCH1) gene; and (3) genetic variants of the TH gene (polymorphisms, rare variants, and mutations) in PD, as discovered recently by advanced genome analysis. 29995172 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE We concluded that, FR and Ex improved the motor performance in rotenone-induced PD rodent model which might be due to increased Hsp70 expression and TH density in corpus striatum and combination of both did not offer more protection than FR alone. 30113007 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease CTD_human The PPARGC1A locus and CNS-specific PGC-1α isoforms are associated with Parkinson's Disease. 30236862 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE Our data show that scavenging intracellular or mitochondrial ROS inhibits the microglial activation and lipid peroxidation, while protecting the tyrosine hydroxylase (TH) in the striata of PD model mice. 29862623 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE In the present study, we first investigated the neuroprotective effect of tDCS in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced PD mouse model and then evaluated the effect of tDCS on the autophagy pathway. tDCS improved behavioral alterations, increased tyrosine hydroxylase protein levels and suppressed α-synuclein protein levels in MPTP-treated mice. 30310174 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE The prophylactic treatment of DML effectually improved the behavioral deficits, curbed the microglial-mediated neuroinflammation, and protected dopaminergic (DA) neuronal loss by restoring tyrosine hydroxylase (TH) levels in brain tissue of the MPTP-induced PD mouse model. 29849878 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE Notably, the oral administration of 4b remarkably improved dyskinesia, reduced the expression of glial fibrillary acidic protein (GFAP)-a marker of neuroinflammation, and increased tyrosine hydroxylase-positive cells in 1-methyl-4-phenyl-1,2,3,6-tetrahydro-pyridine-induced Parkinson's disease (PD) mouse models. 29626798 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE CaMKII inhibition ameliorated levodopa-induced dyskinesia by downregulating tyrosine hydroxylase activity in an experimental model of Parkinson's disease. 29452071 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE In this study, we have utilized two transgenic Cre-driver rat lines, a choline acetyl transferase ChAT-Cre transgenic rat and a novel double-transgenic tyrosine hydroxylase TH-Cre/ChAT-Cre rat to further elucidate the role of striatal ChIs in normal motor function and in Parkinson's disease. 29037828 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE Here, we demonstrate a novel type of lipid dysregulation involved in PD progression as evidenced by upregulated expression of Plin4 (a coating protein and regulator of LDs), and increased intracellular LD deposition that correlated with the loss of TH-ir (Tyrosine hydroxylase-immunoreactive) neurons in the MPTP/p-induced PD model mouse mesencephalon. 29967574 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE NBP significantly improved dyskinesia, reduced microglial activation, decreased nuclear α‑synuclein deposition and increased the survival of TH‑positive cells in the substantia nigra of LPS‑induced PD model mice. 29286148 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE Intervention with OCN could improve the behavioral dysfunction in PD rat models and reduce the tyrosine hydroxylase (TH) loss in the nigrostriatal system. 30319352 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE A significant decrease in dopamine (DA) and its metabolites 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) along with a marked decrease in the number of tyrosine hydroxylase (TH)-positive cells in the substantia nigra pars compacta (SNpc) and striatum (STr) confirms the validity of this model for studying PD. 28875428 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Our results indicate that to analyze the relationship between dopa-responsive dystonia-related genes and PD, it is important to screen GCH1 and test rs6356 of TH in a larger sample. 29724574 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE This suggests that increased ser31 TH phosphorylation may be an inherent compensatory mechanism to attenuate DA loss against TH loss, similar to that in an established PD model. 29782882 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE The latency reduction in PD mice was partially restored after MANF treatment (P<0.05); MANF significantly reduced the loss of tyrosine hydroxylase (TH)-positive dopaminergic neurons in the substantia nigra pars compacta (SNpc) (P<0.01); MANF significantly increased the striatal DA level in PD mice (P<0.05) and markedly increased the SOD activity (P<0.01) and GSH production (P<0.01). 29887945 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE Our results clearly demonstrate that the HFE genotype impacts the expression of tyrosine hydroxylase in the substantia nigra, the gut microbiome and the response to paraquat providing additional support that the HFE genotype is a disease modifier for Parkinson's disease. 29315562 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE In the MPTP-induced mouse model of Parkinson's disease (PD), 12c significantly protected the tyrosine hydroxylase (TH)-immunopositive DAergic neurons and attenuated the PD-associated behavioral deficits. 29198609 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE Lastly, neurons with α-synuclein inclusions displayed reductions in tyrosine hydroxylase expression that were comparable in subjects with both minimal motor features and PD. 29420861 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE Treating a cell culture model of PD with CAMP-hMT1A restored tyrosine hydroxylase expression and mitochondrial activity and reduced ROS production. 30120245 2018