Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinA
Author:
Publisher
Wiley
Subject
Clinical Biochemistry
Reference58 articles.
1. Brainstem pathology in DYT1 primary torsion dystonia
2. TorsinA protein and neuropathology in early onset generalized dystonia with GAG deletion
3. Overexpression of human wildtype torsinA and human ΔGAG torsinA in a transgenic mouse model causes phenotypic abnormalities
4. Torsin A haplotype predisposes to idiopathic dystonia
5. Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier
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2. Transcriptome profiles in brains of mice heterozygous for a DYT1 dystonia-associated mutation in the endogenous Tor1a gene;2019-10-31
3. Emerging common molecular pathways for primary dystonia;Movement Disorders;2013-06-15
4. Molecular pathways in dystonia;Neurobiology of Disease;2011-05
5. Increased c-fos expression in the central nucleus of the amygdala and enhancement of cued fear memory in Dyt1 ΔGAG knock-in mice;Neuroscience Research;2009-11
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