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Kevin Foust grad student Ohio State
G. Andrew Mickley grad student Baldwin-Wallace College
Amy Lovett-Racke grad student 2016- Ohio State
Caryl E. Sortwell grad student 2007-2013 University of Cincinnati
 (Impact of Pleiotrophin Gene Therapy in 6-hydroxydopamine and AAV Alpha-synuclein Rodent Models of Parkinson's Disease.)
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Publications

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Gombash SE, Lee PW, Sawdai E, et al. (2022) Vitamin D as a Risk Factor for Multiple Sclerosis: Immunoregulatory or Neuroprotective? Frontiers in Neurology. 13: 796933
Fischer DL, Manfredsson FP, Kemp CJ, et al. (2017) Subthalamic Nucleus Deep Brain Stimulation Does Not Modify the Functional Deficits or Axonopathy Induced by Nigrostriatal α-Synuclein Overexpression. Scientific Reports. 7: 16356
Gombash SE, Cowley CJ, Fitzgerald JA, et al. (2017) Systemic gene delivery transduces the enteric nervous system of guinea pigs and cynomolgus macaques. Gene Therapy
Fischer DL, Gombash SE, Kemp CJ, et al. (2016) Viral Vector-Based Modeling of Neurodegenerative Disorders: Parkinson's Disease. Methods in Molecular Biology (Clifton, N.J.). 1382: 367-82
Gombash SE, Foust KD. (2016) Systemic Gene Therapy for Targeting the CNS. Methods in Molecular Biology (Clifton, N.J.). 1382: 231-7
Gombash SE, Fitzgerald JA, Cowley CJ, et al. (2016) 619. AAV9 Transduction Is Similar in Adult and Aged Mouse Brains Following Intraparenchymal Injection Molecular Therapy. 24: S245
Gombash SE, Cowley CJ, Fitzgerald JA, et al. (2016) 612. Systemic AAV Injection in Guinea Pigs and Non-Human Primates Targets the Enteric Nervous System Molecular Therapy. 24: S242-S243
Iyer CC, McGovern VL, Murray JD, et al. (2015) Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA. Human Molecular Genetics
Gombash SE, Cowley CJ, Fitzgerald JA, et al. (2015) SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice. Human Molecular Genetics
McGovern VL, Iyer CC, Arnold WD, et al. (2015) SMN expression is required in motor neurons to rescue electrophysiological deficits in the SMNΔ7 mouse model of SMA. Human Molecular Genetics. 24: 5524-41
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