Shunan Liu
Affiliations: | 2012- | Neurology | University of Texas Southwestern Medical Center, Dallas, TX, United States |
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Publications
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| Jaramillo TC, Xuan Z, Reimers JM, et al. (2020) Early restoration of expression in knockout mice prevents core ASD-like behavioural phenotypes. Eneuro |
| Speed HE, Kouser M, Xuan Z, et al. (2019) Apparent Genetic Rescue of Adult Exon 21 Insertion Mutation Mice Tempered by Appropriate Control Experiments. Eneuro |
| Escamilla CO, Filonova I, Walker AK, et al. (2017) Kctd13 deletion reduces synaptic transmission via increased RhoA. Nature |
| Jaramillo TC, Escamilla CO, Liu S, et al. (2017) Genetic background effects in Neuroligin-3 mutant mice: Minimal behavioral abnormalities on C57 background. Autism Research : Official Journal of the International Society For Autism Research |
| Jaramillo TC, Speed HE, Xuan Z, et al. (2016) Novel Shank3 mutant exhibits behaviors with face validity for autism and altered striatal and hippocampal function. Autism Research : Official Journal of the International Society For Autism Research |
| Jaramillo TC, Speed HE, Xuan Z, et al. (2015) Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism. Autism Research : Official Journal of the International Society For Autism Research |
| Espinosa F, Xuan Z, Liu S, et al. (2015) Neuroligin 1 modulates striatal glutamatergic neurotransmission in a pathway and NMDAR subunit-specific manner. Frontiers in Synaptic Neuroscience. 7: 11 |
| Speed HE, Kouser M, Xuan Z, et al. (2015) Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 9648-65 |
| Jaramillo TC, Liu S, Pettersen A, et al. (2014) Autism-related neuroligin-3 mutation alters social behavior and spatial learning. Autism Research : Official Journal of the International Society For Autism Research. 7: 264-72 |
| Kouser M, Speed HE, Dewey CM, et al. (2013) Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 18448-68 |