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dc.contributor.authorZhao, Shengli
dc.contributor.authorTing, Jonathan Thomas
dc.contributor.authorAtallah, Hicham
dc.contributor.authorQiu, Li
dc.contributor.authorTan, Jie
dc.contributor.authorGloss, Bernd
dc.contributor.authorAugustine, George J.
dc.contributor.authorDeisseroth, Karl
dc.contributor.authorLuo, Minmin
dc.contributor.authorGraybiel, Ann M.
dc.contributor.authorFeng, Guoping
dc.date.accessioned2012-06-28T13:38:15Z
dc.date.available2012-06-28T13:38:15Z
dc.date.issued2011-10
dc.identifier.issn1548-7091
dc.identifier.issn1548-7105
dc.identifier.urihttp://hdl.handle.net/1721.1/71248
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 Channelrhodopsin2 (ChR2) under the control of cell-type specific promoter elements. We provide a detailed functional characterization of the newly established VGAT-ChR2-EYFP, ChAT-ChR2-EYFP, TPH2-ChR2-EYFP and Pvalb-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+ neuron subsets using blue light. This resource of cell type-specific ChR2 mouse lines will facilitate the precise mapping of neuronal connectivity and the dissection of the neural basis of behavior.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Ruth L. Kirschstein National Research Service award (F32MH084460))en_US
dc.description.sponsorshipNational Institute of Mental Health (U.S.) (RC1-MH088434)en_US
dc.description.sponsorshipBrain and Behavior Research Foundation (Young Investigator award)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191888/pdf/nihms-311754.pdf?tool=pmcentrezen_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.rights.urien_US
dc.sourcePubMed Centralen_US
dc.titleCell-type Specific Optogenetic Mice for Dissecting Neural Circuitry Functionen_US
dc.title.alternativeCell type–specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry functionen_US
dc.typeArticleen_US
dc.identifier.citationZhao, Shengli et al. "Cell type–specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry function." Nature Methods, 2011 ; 8(9): 745–752.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.approverFeng, Guoping
dc.contributor.mitauthorFeng, Guoping
dc.contributor.mitauthorAtallah, Hicham
dc.contributor.mitauthorTing, Jonathan Thomas
dc.contributor.mitauthorGraybiel, Ann M.
dc.relation.journalNature Methodsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsZhao, Shengli; Ting, Jonathan T.; Atallah, Hisham E.; Qiu, Li; Tan, Jie; Gloss, Bernd; Augustine, George J.; Deisseroth, Karl; Luo, Minmin; Graybiel, Ann M.; Feng, Guopingen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8021-277X
dc.identifier.orcidhttps://orcid.org/0000-0002-4326-7720
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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