Bruce E. Herring
Affiliations: | 2009-2015 | University of California, San Francisco, San Francisco, CA | |
| 2016- | University of Southern California, Los Angeles, CA, United States |
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"Bruce Herring"Mean distance: 13.05 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Aaron P. Fox | grad student | 2009 | Chicago | |
| (General anesthetics inhibit the neurotransmitter release machinery.) | ||||
| Roger A. Nicoll | post-doc | UCSF | ||
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Publications
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| Pushkin AN, Kay Y, Herring BE. (2023) Protein 4.1N plays a cell-type specific role in hippocampal glutamatergic synapse regulation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Rivera JF, Weng W, Huang H, et al. (2023) ATLAS: A rationally designed anterograde transsynaptic tracer. Biorxiv : the Preprint Server For Biology |
| Kay Y, Tsan L, Davis EA, et al. (2022) Schizophrenia-associated SAP97 mutations increase glutamatergic synapse strength in the dentate gyrus and impair contextual episodic memory in rats. Nature Communications. 13: 798 |
| Tian C, Paskus JD, Fingleton E, et al. (2021) Autism Spectrum Disorder/Intellectual Disability-associated mutations in Trio disrupt Neuroligin 1-mediated synaptogenesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Kay Y, Herring BE. (2021) An optogenetic method for investigating presynaptic molecular regulation. Scientific Reports. 11: 11329 |
| Paskus JD, Herring BE, Roche KW. (2020) Kalirin and Trio: RhoGEFs in Synaptic Transmission, Plasticity, and Complex Brain Disorders. Trends in Neurosciences. 43: 505-518 |
| Paskus JD, Tian C, Fingleton E, et al. (2019) Synaptic Kalirin-7 and Trio Interactomes Reveal a GEF Protein-Dependent Neuroligin-1 Mechanism of Action. Cell Reports. 29: 2944-2952.e5 |
| Rao S, Kay Y, Herring BE. (2019) Tiam1 is critical for glutamatergic synapse structure and function in the hippocampus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Tian C, Kay Y, Sadybekov A, et al. (2018) An Intellectual Disability-Related Missense Mutation in Rac1 Prevents LTP Induction. Frontiers in Molecular Neuroscience. 11: 223 |
| Sadybekov A, Tian C, Arnesano C, et al. (2017) An autism spectrum disorder-related de novo mutation hotspot discovered in the GEF1 domain of Trio. Nature Communications. 8: 601 |