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1.	PDF 573_etd Altered Purkinje cell pacemaking underlies motor deficits in mouse models of cerebellar ataxia Davis, Forrest 2010 \| Dissertation \| Detailed record - Similar records
2.	PDF Rakela.Benjamin.2017 Astrocytic modulation of excitatory neuronal signaling in a mouse model of rett syndrome Rakela, Benjamin Astrocyte-mediated processes are important for maintaining neuronal homeostasis and proper synaptic transmission. Recent work from the Mandel lab has implicated astrocyte [...] 2017 \| Thesis \| Detailed record - Similar records
3.	PDF 586_etd Contribution of GABA [beta] receptors to acute ethanol sensitivity and as a pharmacotherapeutic target Holstein, Sarah E. 2008 \| Thesis \| Detailed record - Similar records
4.	PDF 2993_etd Deregulated gene expression in the brain of Rett syndrome patients and MeCP2-null mice Deng, Vivianne W. 2005 \| Dissertation \| Detailed record - Similar records
5.	PDF 665_etd Determining the cellular basis of a neurodevelopmental disease: MeCP2 dysfunction in glia and neurons Lioy-Ryan, Daniel T. 2011 \| Dissertation \| Detailed record - Similar records
6.	PDF 2760_etd Initial sensitivity and tolerance to the ataxic effects of ethanol in selectively bred hot and cold mice Schafer, Gwen L. 1995 \| Thesis \| Detailed record - Similar records
7.	PDF ResearchWeek.2020.Prewitt.Austin Plantarflexor muscle fatigue in people with multiple sclerosis impairs standing balance Prewitt, Austin ; McBarron, Grace ; Horak, Fay ; Arpan, Ishu People with Multiple Sclerosis (PwMS) experience fatigue differently than those without MS due to weakness, ataxia, and spasticity. This fatigue can play a role in balanc [...] 2020 \| Abstract \| Detailed record - Similar records
8.	PDF 3246_etd Single-channel properties of episodic ataxia type 1 (EA-1) mutations in the human voltage-gated potassium channels (hKv1.1) Liu, Zhaoping 2001 \| Thesis \| Detailed record - Similar records
9.	PDF ResearchWeek.2023.Yung.John Targeted RNA editing in brainstem alleviates respiratory dysfunction in a mouse model of rett syndrome Sinnamon, John R. ; Jacobson, Michael E. ; Yung, John F. ; Fisk, Jenna R.[...] Rett syndrome is a neurological disease due to loss-of-function mutations in the transcription factor, Methyl CpG binding protein 2 (MECP2). Because overexpression of end [...] 2023-09-13 \| Abstract \| Detailed record - Similar records

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