Wei Li, Ph.D.
Affiliations: | Neurobiology | University of Alabama, Birmingham, Birmingham, AL, United States |
Area:
BDNF, TRPC Channels, Hippocampus, MeCP2, Rett SyndromeGoogle:
"Wei Li"Mean distance: 14.93 (cluster 6) | S | N | B | C | P |
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Publications
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Medeiros D, Ayala-Baylon K, Egido-Betancourt H, et al. (2023) A small-molecule TrkB ligand improves dendritic spine phenotypes and atypical behaviors in female Rett syndrome mice. Biorxiv : the Preprint Server For Biology |
Li W, Pozzo-Miller L. (2019) Dysfunction of the corticostriatal pathway in autism spectrum disorders. Journal of Neuroscience Research |
Li W, Pozzo-Miller L. (2019) Differences in GluN2B-containing NMDA receptors result in distinct long-term plasticity at ipsilateral . contralateral cortico-striatal synapses. Eneuro |
Li W, Bellot-Saez A, Phillips ML, et al. (2017) A small-molecule TrkB ligand restores hippocampal synaptic plasticity and object location memory in Rett syndrome mice. Disease Models & Mechanisms. 10: 837-845 |
Li W, Xu X, Pozzo-Miller L. (2016) Excitatory synapses are stronger in the hippocampus of Rett syndrome mice due to altered synaptic trafficking of AMPA-type glutamate receptors. Proceedings of the National Academy of Sciences of the United States of America |
Calfa G, Li W, Rutherford JM, et al. (2015) Excitation/inhibition imbalance and impaired synaptic inhibition in hippocampal area CA3 of Mecp2 knockout mice. Hippocampus. 25: 159-68 |
Li W, Pozzo-Miller L. (2014) BDNF deregulation in Rett syndrome. Neuropharmacology. 76: 737-46 |
Chapleau CA, Lane J, Larimore J, et al. (2013) Recent Progress in Rett Syndrome and MeCP2 Dysfunction: Assessment of Potential Treatment Options. Future Neurology. 8 |
Leuner K, Li W, Amaral MD, et al. (2013) Hyperforin modulates dendritic spine morphology in hippocampal pyramidal neurons by activating Ca(2+) -permeable TRPC6 channels. Hippocampus. 23: 40-52 |
Li W, Pozzo-Miller L. (2012) Beyond Widespread Mecp2 Deletions to Model Rett Syndrome: Conditional Spatio-Temporal Knockout, Single-Point Mutations and Transgenic Rescue Mice. Autism-Open Access. 2012: 5 |