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ab34540 has been referenced in 25 publications.

  • Bonsi P  et al. RGS9-2 rescues dopamine D2 receptor levels and signaling in DYT1 dystonia mouse models. EMBO Mol Med 11:N/A (2019). PubMed: 30552094
  • Beauvais G  et al. Efficient RNA interference-based knockdown of mutant torsinA reveals reversibility of PERK-eIF2a pathway dysregulation in DYT1 transgenic rats in vivo. Brain Res 1706:24-31 (2019). PubMed: 30366018
  • Pappas SS  et al. A cell autonomous torsinA requirement for cholinergic neuron survival and motor control. Elife 7:N/A (2018). PubMed: 30117805
  • Saunders CA  et al. TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movement. J Cell Biol 216:657-674 (2017). PubMed: 28242745
  • Bhagat SL  et al. Mouse model of rare TOR1A variant found in sporadic focal dystonia impairs domains affected in DYT1 dystonia patients and animal models. Neurobiol Dis 93:137-45 (2016). PubMed: 27168150
  • Beauvais G  et al. Disruption of Protein Processing in the Endoplasmic Reticulum of DYT1 Knock-in Mice Implicates Novel Pathways in Dystonia Pathogenesis. J Neurosci 36:10245-10256 (2016). WB ; Mouse . PubMed: 27707963
  • Zhang L  et al. Dopamine receptor and Ga(olf) expression in DYT1 dystonia mouse models during postnatal development. PLoS One 10:e0123104 (2015). WB . PubMed: 25860259
  • Yokoi F  et al. Behavioral and electrophysiological characterization of Dyt1 heterozygous knockout mice. PLoS One 10:e0120916 (2015). WB ; Mouse . PubMed: 25799505
  • Pappas SS  et al. Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons. Elife 4:e08352 (2015). PubMed: 26052670
  • Weisheit CE & Dauer WT A novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutation. Hum Mol Genet 24:6459-72 (2015). PubMed: 26370418
  • Ruiz M  et al. Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia. Hum Mol Genet 24:7159-70 (2015). PubMed: 26376866
  • Liang CC  et al. TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration. J Clin Invest 124:3080-92 (2014). WB, ICC/IF ; Mouse . PubMed: 24937429
  • Ortiz-Virumbrales M  et al. Dystonia type 6 gene product Thap1: identification of a 50 kDa DNA-binding species in neuronal nuclear fractions. Acta Neuropathol Commun 2:139 (2014). WB ; Mouse, Human . PubMed: 25231164
  • Cho JA  et al. 4-phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell models. PLoS One 9:e110086 (2014). WB . PubMed: 25379658
  • Puglisi F  et al. Torsin A Localization in the Mouse Cerebellar Synaptic Circuitry. PLoS One 8:e68063 (2013). WB . PubMed: 23840813
  • Yokoi F  et al. Pre-synaptic release deficits in a DYT1 dystonia mouse model. PLoS One 8:e72491 (2013). WB ; Mouse . PubMed: 23967309
  • Yokoi F  et al. Improved motor performance in Dyt1 ?GAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-out. Behav Brain Res 230:389-98 (2012). WB ; Mouse . PubMed: 22391119
  • Gordon KL  et al. The ubiquitin ligase F-box/G-domain protein 1 promotes the degradation of the disease-linked protein torsinA through the ubiquitin-proteasome pathway and macroautophagy. Neuroscience 224:160-71 (2012). WB . PubMed: 22917612
  • Bode N  et al. DYT1 knock-in mice are not sensitized against mitochondrial complex-II inhibition. PLoS One 7:e42644 (2012). WB . PubMed: 22880064
  • Sciamanna G  et al. Developmental profile of the aberrant dopamine D2 receptor response in striatal cholinergic interneurons in DYT1 dystonia. PLoS One 6:e24261 (2011). IHC-P ; Mouse . PubMed: 21912682
  • Kim CE  et al. A molecular mechanism underlying the neural-specific defect in torsinA mutant mice. Proc Natl Acad Sci U S A 107:9861-6 (2010). WB, ICC/IF ; Mouse . PubMed: 20457914
  • Cao S  et al. Chemical enhancement of torsinA function in cell and animal models of torsion dystonia. Dis Model Mech 3:386-96 (2010). WB ; Mouse . PubMed: 20223934
  • Yokoi F  et al. Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce. J Biochem 148:459-66 (2010). WB ; Mouse . PubMed: 20627944
  • Napolitano F  et al. Dopamine D2 receptor dysfunction is rescued by adenosine A2A receptor antagonism in a model of DYT1 dystonia. Neurobiol Dis 38:434-45 (2010). WB ; Mouse . PubMed: 20227500
  • Granata A  et al. The Dystonia-associated Protein TorsinA Modulates Synaptic Vesicle Recycling. J Biol Chem 283:7568-79 (2008). ICC/IF ; Human . PubMed: 18167355

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