Please use this identifier to cite or link to this item: https://doi.org/10.1038/nmeth.1668
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dc.titleCell type-specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry function
dc.contributor.authorZhao, S.
dc.contributor.authorTing, J.T.
dc.contributor.authorAtallah, H.E.
dc.contributor.authorQiu, L.
dc.contributor.authorTan, J.
dc.contributor.authorGloss, B.
dc.contributor.authorAugustine, G.J.
dc.contributor.authorDeisseroth, K.
dc.contributor.authorLuo, M.
dc.contributor.authorGraybiel, A.M.
dc.contributor.authorFeng, G.
dc.date.accessioned2016-10-19T08:44:11Z
dc.date.available2016-10-19T08:44:11Z
dc.date.issued2011-09
dc.identifier.citationZhao, S., Ting, J.T., Atallah, H.E., Qiu, L., Tan, J., Gloss, B., Augustine, G.J., Deisseroth, K., Luo, M., Graybiel, A.M., Feng, G. (2011-09). Cell type-specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry function. Nature Methods 8 (9) : 745-755. ScholarBank@NUS Repository. https://doi.org/10.1038/nmeth.1668
dc.identifier.issn15487091
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/128698
dc.description.abstractOptogenetic methods have emerged as powerful tools for dissecting neural circuit connectivity, function and dysfunction. We used a bacterial artificial chromosome (BAC) transgenic strategy to express the H134R variant of channelrhodopsin-2, ChR2(H134R), under the control of cell type-specific promoter elements. We performed an extensive functional characterization of the newly established VGAT-ChR2(H134R)-EYFP, ChAT-ChR2(H134R)-EYFP, Tph2-ChR2(H134R)-EYFP and Pvalb(H134R)-ChR2-EYFP BAC transgenic mouse lines and demonstrate the utility of these lines for precisely controlling action-potential firing of GABAergic, cholinergic, serotonergic and parvalbumin-expressing neuron subsets using blue light. This resource of cell type-specific ChR2(H134R) mouse lines will facilitate the precise mapping of neuronal connectivity and the dissection of the neural basis of behavior. © 2011 Nature America, Inc. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1038/nmeth.1668
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1038/nmeth.1668
dc.description.sourcetitleNature Methods
dc.description.volume8
dc.description.issue9
dc.description.page745-755
dc.identifier.isiut000294439100011
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