DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)
|
0.720 |
GeneticVariation
|
disease |
BEFREE |
Four mutations in the TyrH gene have recently been described in cases of autosomal recessive DOPA-responsive dystonia (Swaans et al., Ann Hum Genet 2000;64:25-31).
|
15468323 |
2005 |
DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)
|
0.720 |
AlteredExpression
|
disease |
BEFREE |
Autosomal recessive mutations in the TH gene cause impaired TH activity and are associated with phenotypes ranging from autosomal recessive dopa-responsive dystonia (DRD) to progressive infantile encephalopathy.
|
23939262 |
2011 |
Parkinsonian Disorders
|
0.700 |
AlteredExpression
|
group |
BEFREE |
For example, α-synuclein represses TH not only by inhibiting phosphorylation at Ser40 of TH, but also by stimulating protein phosphatase 2A activity, which decreases dopamine synthesis and leads to parkinsonism.
|
22483316 |
2012 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections.
|
15747353 |
2005 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
Missense mutation in both alleles of the TH gene is known to cause dopamine-related phenotypes, including dystonia and infantile Parkinsonism.
|
20809526 |
2010 |
Parkinsonian Disorders
|
0.700 |
Biomarker
|
group |
BEFREE |
To overcome this problem, we developed a non-invasive intranasal delivery system, chitosan coated niosomes with entrapped pentamidine (inPentasomes), in the attempt to provide a novel pharmacological approach to ameliorate parkinsonism induced by subchronic MPTP administration in C57BL-6 J mice. inPentasomes, prepared by evaporation method was administered daily by intranasal route in subchronic MPTP-intoxicated rodents and resulted in a dose-dependent manner (0.001-0.004 mg/kg) capable for a significant Tyrosine Hydroxylase (TH) positive neuronal density rescue in both striatum and substantia nigra of parkinsonian mice.
|
30529726 |
2019 |
Parkinsonian Disorders
|
0.700 |
Biomarker
|
group |
BEFREE |
Intravenous nonviral gene therapy causes normalization of striatal tyrosine hydroxylase and reversal of motor impairment in experimental parkinsonism.
|
12573054 |
2003 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonism.
|
11246459 |
2000 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
GTP cyclohydrolase I gene, tetrahydrobiopterin, and tyrosine hydroxylase gene: their relations to dystonia and parkinsonism.
|
9182249 |
1996 |
Parkinsonian Disorders
|
0.700 |
AlteredExpression
|
group |
BEFREE |
Since TH protein has been shown to be involved in the dopamine-producing pathway in previous studies, our results indicate the possibility that manganese-mediated reduction of TH expression and phosphorylation via decreased expression of c-RET protein in neural cells is involved in parkinsonism induced by manganese.
|
28730349 |
2017 |
Parkinsonian Disorders
|
0.700 |
AlteredExpression
|
group |
BEFREE |
Our results indicate that the differential regulation of mRNAs encoding TH and DAT is similar in the parkinsonian disorders (PD and AD/Park) even though the degree of cell death is very different.
|
9399211 |
1997 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
Consistent with the essential role of TH in dopamine homeostasis, missense mutations in both alleles of TH have been associated with severe Parkinsonism-related phenotypes including infantile Parkinsonism.
|
22583432 |
2012 |
Parkinsonian Disorders
|
0.700 |
Biomarker
|
group |
BEFREE |
Preliminary investigations have examined possible allelic associations, e.g., with alleles of MAO-A and debrisoquine hydroxylase and linkage to the tyrosine hydroxylase gene on chromosome 11p15.5 has been excluded in one study of juvenile familial parkinsonism.
|
1341965 |
1992 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
Functional polymorphisms of the TH gene may be involved in the pathogenesis of neuropsychiatric diseases such as schizophrenia, affective disorders, and Parkinsonism.
|
9613851 |
1998 |
Parkinsonian Disorders
|
0.700 |
Biomarker
|
group |
BEFREE |
In an in vivo MPTP-induced animal model of Parkinson's disease, oral administration of compound 5b showed neuroprotection of nigrostriatal dopaminergic neurons as revealed by tyrosine hydroxylase staining and prevention of MPTP-induced parkinsonism as revealed by motor behavioral assay of vertical grid test.
|
28332824 |
2017 |
Parkinsonian Disorders
|
0.700 |
Biomarker
|
group |
BEFREE |
The provocation test was developed by a systemic administration of α-methyl-p-tyrosine (αMpT), a reversible inhibitor of tyrosine hydroxylase to MPTP-treated mice at the presymptomatic stage of parkinsonism.
|
27194433 |
2017 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene.
|
8817341 |
1996 |
Parkinsonian Disorders
|
0.700 |
AlteredExpression
|
group |
BEFREE |
In the combined forms, dystonia is accompanied by parkinsonism (GCH1/DYT5a; TH/DYT5b; ATP1A3/DYT12; TAF1/DYT3) or myoclonus (SGCE/DYT11).
|
24262166 |
2014 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
Patients with the dystonia plus syndrome DYT5 display levodopa-responsive dystonia sometimes associated with tremor or parkinsonism (DYT5a, mutations in GCH1); a more severe phenotype with psychomotor involvement can be seen in recessive forms (DYT5b with TH mutations, SPR-deficiency syndrome).
|
22166420 |
2012 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
The phenotype of AR-DRD with the Leu205Pro mutation in the TH gene, which produces a severe decrease in TH activity to 1.5% of that of the wild type, was severe, not dystonia/Segawa's syndrome, but early-onset parkinsonism.
|
10661862 |
1999 |
Parkinsonian Disorders
|
0.700 |
GeneticVariation
|
group |
BEFREE |
The mutation p.Arg233His was predicted to link to the second type of TH deficiency (dopa-responsive infantile parkinsonism with delayed motor development).
|
28087438 |
2017 |
Parkinsonian Disorders
|
0.700 |
Biomarker
|
group |
BEFREE |
Here, we investigated sex differences in motor deficits and tyrosine hydroxylase (TH) immunoreactivity induced by a progressive model of parkinsonism.
|
30690108 |
2019 |
Parkinsonian Disorders
|
0.700 |
AlteredExpression
|
group |
BEFREE |
BAs taken by rats with rotenone-induced parkinsonism showed enhanced general motor performance, reduced inflammatory markers, and increased striatal dopamine level and nigral tyrosine hydroxylase immunostaining.
|
28249117 |
2017 |
Parkinson Disease
|
0.600 |
Biomarker
|
disease |
BEFREE |
Following the establishment of a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson's disease (PD) model, AQP4-deficient (AQP4<sup>-/-</sup> ) mice displayed significantly stronger microglial inflammatory responses and remarkably greater losses of tyrosine hydroxylase (TH<sup>+</sup> )-positive neurons than did wild-type AQP4 (AQP4<sup>+/+</sup> ) controls.
|
30680924 |
2019 |
Parkinson Disease
|
0.600 |
Biomarker
|
disease |
BEFREE |
Because activation of the innate cellular immune response, mediated by microglia, has been linked to the neurodegeneration in PD, in the present study, we evaluated the effects of lipopolysaccharide (LPS) and 6-hydroxydopamine (6-OHDA) on microglia's morphology, reflective of their activity, as well as tyrosine hydroxylase (TH)-positive neurons in SNpc and motor behavior.
|
31478124 |
2020 |