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8. Diverse Mechanisms Lead to Common Dysfunction of Striatal Cholinergic Interneurons in Distinct Genetic Mouse Models of Dystonia. Eskow Jaunarajs KL; Scarduzio M; Ehrlich ME; McMahon LL; Standaert DG J Neurosci; 2019 Sep; 39(36):7195-7205. PubMed ID: 31320448 [TBL] [Abstract][Full Text] [Related]
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10. Function of dopamine transporter is compromised in DYT1 transgenic animal model in vivo. Hewett J; Johanson P; Sharma N; Standaert D; Balcioglu A J Neurochem; 2010 Apr; 113(1):228-35. PubMed ID: 20132487 [TBL] [Abstract][Full Text] [Related]
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15. Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia. Song CH; Fan X; Exeter CJ; Hess EJ; Jinnah HA Neurobiol Dis; 2012 Oct; 48(1):66-78. PubMed ID: 22659308 [TBL] [Abstract][Full Text] [Related]
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19. Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons. Pappas SS; Darr K; Holley SM; Cepeda C; Mabrouk OS; Wong JM; LeWitt TM; Paudel R; Houlden H; Kennedy RT; Levine MS; Dauer WT Elife; 2015 Jun; 4():e08352. PubMed ID: 26052670 [TBL] [Abstract][Full Text] [Related]
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