Sofia B. Lizarraga
Affiliations: | University of South Carolina, Columbia, SC |
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"Sofia Lizarraga"Mean distance: 14.83 (cluster 46) | S | N | B | C | P |
Parents
Sign in to add mentor| Yixian Zheng | grad student | 2003 | Johns Hopkins | |
| (Regulation of spindle assembly by the Ran pathway.) | ||||
| Chris A. Walsh | post-doc | Harvard Medical School | ||
| Eric Morrow | post-doc | 2010-2014 | Brown | |
| (Tenure-track Assistant Professor at University of South Carolina Columbia as of 2015) | ||||
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Publications
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| Ghate PS, Vacharasin JM, Ward JA, et al. (2023) The Warburg micro syndrome protein RAB3GAP1 modulates neuronal morphogenesis and interacts with axon elongation end ER-Golgi trafficking factors. Neurobiology of Disease. 106215 |
| Ritchie FD, Lizarraga SB. (2023) The role of histone methyltransferases in neurocognitive disorders associated with brain size abnormalities. Frontiers in Neuroscience. 17: 989109 |
| Leung CS, Rosenzweig S, Yoon B, et al. (2023) Dysregulation of the chromatin environment leads to differential alternative splicing as a mechanism of disease in a human model of autism spectrum disorder. Human Molecular Genetics |
| Cheon S, Culver AM, Bagnell AM, et al. (2022) Counteracting epigenetic mechanisms regulate the structural development of neuronal circuitry in human neurons. Molecular Psychiatry |
| Lizarraga SB, Ma L, Maguire AM, et al. (2021) Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13 |
| Chukwurah E, Osmundsen A, Davis SW, et al. (2019) All Together Now: Modeling the Interaction of Neural With Non-neural Systems Using Organoid Models. Frontiers in Neuroscience. 13: 582 |
| Xu M, Ouyang Q, Gong J, et al. (2017) Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome. Eneuro. 4 |
| Hollingsworth EW, Vaughn JE, Orack JC, et al. (2017) iPhemap: an atlas of phenotype to genotype relationships of human iPSC models of neurological diseases. Embo Molecular Medicine |
| Ouyang Q, Nakayama T, Baytas O, et al. (2016) Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features. Proceedings of the National Academy of Sciences of the United States of America |
| Morrow EM, Lizarraga SB, Ouyang Q. (2015) REMOVED: Novel endosomal mechanisms in human axonal growth mediated by Christianson syndrome protein NHE6. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 20 |