ZFIN ID: ZDB-PERS-140211-2
Baraban, Scott
Email: Scott.Baraban@ucsf.edu
URL:
Affiliation: Baraban Lab
Address: University of California, San Francisco 521 Parnassus Ave., S380 San Francisco, CA 94143
Country: United States
Phone: 415/476-9473
Fax:
ORCID ID:


BIOGRAPHY AND RESEARCH INTERESTS


PUBLICATIONS
Moog, M., Baraban, S.C. (2022) Clemizole and Trazodone are Effective Antiseizure Treatments in a Zebrafish Model of STXBP1 Disorder. Epilepsia open. 7(3):504-511
Baraban, S.C. (2021) A zebrafish-centric approach to antiepileptic drug development. Disease models & mechanisms. 14(7)
Hadjiabadi, D., Lovett-Barron, M., Raikov, I.G., Sparks, F.T., Liao, Z., Baraban, S.C., Leskovec, J., Losonczy, A., Deisseroth, K., Soltesz, I. (2021) Maximally selective single-cell target for circuit control in epilepsy models. Neuron. 109(16):2556-2572.e6
Griffin, A., Carpenter, C., Liu, J., Paterno, R., Grone, B., Hamling, K., Moog, M., Dinday, M.T., Figueroa, F., Anvar, M., Ononuju, C., Qu, T., Baraban, S.C. (2021) Phenotypic analysis of catastrophic childhood epilepsy genes. Communications biology. 4:680
Liu, J., Salvati, K.A., Baraban, S.C. (2021) In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish. iScience. 24:102558
Banerji, R., Huynh, C., Figueroa, F., Dinday, M.T., Baraban, S.C., Patel, M. (2021) Enhancing glucose metabolism via gluconeogenesis is therapeutic in a zebrafish model of Dravet syndrome. Brain communications. 3:fcab004
Griffin, A., Anvar, M., Hamling, K., Baraban, S.C. (2020) Phenotype-Based Screening of Synthetic Cannabinoids in a Dravet Syndrome Zebrafish Model. Frontiers in pharmacology. 11:464
Burrows, D.R.W., Samarut, É., Liu, J., Baraban, S.C., Richardson, M.P., Meyer, M.P., Rosch, R.E. (2020) Imaging epilepsy in larval zebrafish. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 24:70-80
Liu, J., Baraban, S.C. (2019) Network Properties Revealed during Multi-Scale Calcium Imaging of Seizure Activity in Zebrafish. eNeuro. 6(1)
Griffin, A.L., Jaishankar, P., Grandjean, J.M., Olson, S.H., Renslo, A.R., Baraban, S.C. (2019) Zebrafish studies identify serotonin receptors mediating antiepileptic activity in Dravet syndrome. Brain communications. 1:fcz008
Griffin, A., Hamling, K.R., Hong, S., Anvar, M., Lee, L.P., Baraban, S.C. (2018) Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening. Frontiers in pharmacology. 9:573
Protas, M.E., Weh, E., Footz, T., Kasberger, J., Baraban, S.C., Levin, A.V., Katz, L.J., Ritch, R., Walter, M.A., Semina, E.V., Gould, D.B. (2017) Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma. Human molecular genetics. 26:3630-3638
Grone, B.P., Qu, T., Baraban, S.C. (2017) Behavioral Comorbidities and Drug Treatments in a Zebrafish scn1lab Model of Dravet Syndrome.. eNeuro. 4(4)
Griffin, A., Hamling, K.R., Knupp, K., Hong, S., Lee, L.P., Baraban, S.C. (2017) Clemizole and modulators of serotonin signalling suppress seizures in Dravet syndrome. Brain : a journal of neurology. 140(3):669-683
Hong, S., Lee, P., Baraban, S.C., Lee, L.P. (2016) A Novel Long-term, Multi-Channel and Non-invasive Electrophysiology Platform for Zebrafish. Scientific Reports. 6:28248
Kumar, M.G., Rowley, S., Fulton, R., Dinday, M.T., Baraban, S.C., Patel, M. (2016) Altered Glycolysis and Mitochondrial Respiration in a Zebrafish Model of Dravet Syndrome. eNeuro. 3(2):e0008-16
Grone, B.P., Marchese, M., Hamling, K.R., Kumar, M.G., Krasniak, C.S., Sicca, F., Santorelli, F.M., Patel, M., Baraban, S.C. (2016) Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish. PLoS One. 11:e0151148
Griffin, A., Krasniak, C., Baraban, S.C. (2016) Advancing epilepsy treatment through personalized genetic zebrafish models. Progress in brain research. 226:195-207
Dinday, M.T., Baraban, S.C. (2015) Large-Scale Phenotype-Based Antiepileptic Drug Screening in a Zebrafish Model of Dravet Syndrome(1,2,3). eNeuro. 2(4)
Grone, B.P., Baraban, S.C. (2015) Animal models in epilepsy research: legacies and new directions. Nature Neuroscience. 18:339-343
Baraban, S.C., Löscher, W. (2014) What new modeling approaches will help us identify promising drug treatments?. Advances in experimental medicine and biology. 813:283-94
Baraban, S.C. (2013) Forebrain electrophysiological recording in larval zebrafish. Journal of visualized experiments : JoVE. (71)
Baraban, S.C., Dinday, M.T., and Hortopan, G.A. (2013) Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment. Nature communications. 4:2410
Hunt, R.F., Hortopan, G.A., Gillespie, A., and Baraban, S.C. (2012) A novel zebrafish model of hyperthermia-induced seizures reveals a role for TRPV4 channels and NMDA-type glutamate receptors. Experimental neurology. 237(1):199-206
Chege, S.W., Hortopan, G.A., Dinday, M., and Baraban, S.C. (2012) Expression and function of KCNQ channels in larval zebrafish. Developmental Neurobiology. 72(2):186-98
Hortopan, G.A., and Baraban, S.C. (2011) Aberrant expression of genes necessary for neuronal development and notch signaling in an epileptic mind bomb zebrafish. Developmental Dynamics : an official publication of the American Association of Anatomists. 240(8):1964-76
Hortopan, G.A., Dinday, M.T., and Baraban, S.C. (2010) Spontaneous Seizures and Altered Gene Expression in GABA Signaling Pathways in a mind bomb Mutant Zebrafish. The Journal of neuroscience : the official journal of the Society for Neuroscience. 30(41):13718-13728
Hortopan, G.A., Dinday, M.T., and Baraban, S.C. (2010) Zebrafish as a model for studying genetic aspects of epilepsy. Disease models & mechanisms. 3(3-4):144-148
Baraban, S.C. (2007) Emerging epilepsy models: insights from mice, flies, worms and fish. Current Opinion in Neurology. 20(2):164-168

NON-ZEBRAFISH PUBLICATIONS