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dc.contributor.authorLavin, Thomas K.
dc.contributor.authorJin, Lei
dc.contributor.authorWickersham, Ian R.
dc.date.accessioned2021-10-12T16:01:51Z
dc.date.available2021-10-12T16:01:51Z
dc.date.issued2019-12
dc.date.submitted2019-07
dc.identifier.issn0891-0618
dc.identifier.urihttps://hdl.handle.net/1721.1/132925
dc.description.abstractMonosynaptic tracing using deletion-mutant rabies virus allows whole-brain mapping of neurons that are directly presynaptic to a targeted population of neurons. The most common and robust way of implementing it is to use Cre mouse lines in combination with Cre-dependent adeno-associated viral vectors for expression of the required genes in the targeted neurons before subsequent injection of the rabies virus. Here we present a step-by-step protocol for performing such experiments using first-generation (ΔG) rabies viral vectors.en_US
dc.description.sponsorshipNational Institute of Mental Health (Awards U01MH106018, U01MH114829, and U19MH114830)en_US
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.jchemneu.2019.101661en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceIan Wickershamen_US
dc.titleMonosynaptic tracing: a step-by-step protocolen_US
dc.typeArticleen_US
dc.identifier.citationLavin, Thomas K. et al. "Monosynaptic tracing: a step-by-step protocol." Journal of Chemical Neuroanatomy 102 (December 2019): 101661. © 2019 Elsevier B.V.en_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.relation.journalJournal of Chemical Neuroanatomyen_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.date.submission2019-08-14T19:49:21Z
mit.journal.volume102en_US
mit.metadata.statusCompleteen_US


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