Dopamine

huntingtin ; Homo sapiens







12 Article(s)
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1 32004439 Genome-wide In Vivo CNS Screening Identifies Genes that Modify CNS Neuronal Survival and mHTT Toxicity. 2020 Apr 8 1
2 28532681 Resveratrol protects neuronal-like cells expressing mutant Huntingtin from dopamine toxicity by rescuing ATG4-mediated autophagosome formation. 2018 Jul 2
3 27840125 Dopamine exacerbates mutant Huntingtin toxicity via oxidative-mediated inhibition of autophagy in SH-SY5Y neuroblastoma cells: Beneficial effects of anti-oxidant therapeutics. 2016 Dec 2
4 24374792 A mitochondrial basis for Huntington's disease: therapeutic prospects. 2014 Apr 1
5 19682570 Mitochondria in Huntington's disease. 2010 Jan 1
6 18267960 Dopamine determines the vulnerability of striatal neurons to the N-terminal fragment of mutant huntingtin through the regulation of mitochondrial complex II. 2008 May 15 3
7 18403126 Dopamine D1 receptor-mediated aggregation of N-terminal fragments of mutant huntingtin and cell death in a neuroblastoma cell line. 2008 May 15 1
8 18829967 Dopaminergic and glutamatergic signaling crosstalk in Huntington's disease neurodegeneration: the role of p25/cyclin-dependent kinase 5. 2008 Oct 1 4
9 18844975 Mutant huntingtin activates Nrf2-responsive genes and impairs dopamine synthesis in a PC12 model of Huntington's disease. 2008 Oct 9 1
10 16854064 Synthesis and monoamine transporter binding properties of 2,3-cyclo analogues of 3beta-(4'-aminophenyl)-2beta-tropanemethanol. 2006 Jul 27 1
11 11406606 Expanded CAG repeats in exon 1 of the Huntington's disease gene stimulate dopamine-mediated striatal neuron autophagy and degeneration. 2001 Jun 1 1
12 10362304 Forskolin and dopamine D1 receptor activation increase huntingtin's association with endosomes in immortalized neuronal cells of striatal origin. 1999 2