Christian L. Lorson
Affiliations: | University of Missouri - Columbia, Columbia, MO, United States |
Area:
Microbiology Biology, Neuroscience Biology, Molecular Biology, GeneticsGoogle:
"Christian Lorson"Children
Sign in to add trainee| Virginia Mattis | grad student | University of Missouri (Neurotree) | |
| Travis Baughan | grad student | 2008 | University of Missouri - Columbia |
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Publications
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| Comley LH, Kline RA, Thomson AK, et al. (2022) Motor Unit Recovery Following Smn Restoration in Mouse Models of Spinal Muscular Atrophy. Human Molecular Genetics |
| Dumas SA, Villalón E, Bergman EM, et al. (2022) A combinatorial approach increases SMN level in SMA model mice. Human Molecular Genetics |
| Tang Z, Hegde S, Zhao J, et al. (2022) CRISPR-mediated Enzyme Fragment Complementation Assay for Quantification of the Stability of Splice Isoforms. Chembiochem : a European Journal of Chemical Biology |
| Smith CE, Lorson MA, Ricardez Hernandez SM, et al. (2021) The Ighmbp2D564N mouse model is the first SMARD1 model to demonstrate respiratory defects. Human Molecular Genetics |
| Shababi M, Smith CE, Ricardez Hernandez SM, et al. (2021) Defining the optimal dose and therapeutic window in SMA with respiratory distress type I model mice, FVB/NJ- . Molecular Therapy. Methods & Clinical Development. 23: 23-32 |
| McCormack NM, Villalón E, Viollet C, et al. (2021) Survival motor neuron deficiency slows myoblast fusion through reduced myomaker and myomixer expression. Journal of Cachexia, Sarcopenia and Muscle |
| Rietz A, Hodgetts KJ, Lusic H, et al. (2021) Short-duration splice promoting compound enables a tunable mouse model of spinal muscular atrophy. Life Science Alliance. 4 |
| Kaifer KA, Villalón E, Smith CE, et al. (2020) AAV9-DOK7 gene therapy reduces disease severity in Smn SMA model mice. Biochemical and Biophysical Research Communications. 530: 107-114 |
| Osman EY, Van Alstyne M, Yen PF, et al. (2020) Minor snRNA gene delivery improves the loss of proprioceptive synapses on SMA motor neurons. Jci Insight |
| Shababi M, Smith CE, Kacher M, et al. (2019) Development of a novel severe mouse model of spinal muscular atrophy with respiratory distress type 1: FVB-nmd. Biochemical and Biophysical Research Communications |