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pubmed-article:8274768pubmed:abstractTextFetal suprachiasmatic nucleus (SCN) tissue transplanted into the third ventricle of hamsters bearing complete SCN lesions restores the circadian locomotor rhythm with a period that depends exclusively on the genetically determined period of the tissue donor. If the host is only partially lesioned and thus retains rhythmicity with its own genetically determined period, an implant from an animal of a different genotype can induce a second rhythm with a period determined by the donor genotype. Both rhythms can be present simultaneously in the record of such a "temporal chimera," interacting only superficially (i.e., not at the level of the pacemaker). Our data support the interpretation that under such circumstances the graft is able to capture part of the locomotor output of the circadian system, but does not make functional connections with the host SCN pacemaking system.lld:pubmed
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pubmed-article:8274768pubmed:paginationS93-8lld:pubmed
pubmed-article:8274768pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:8274768pubmed:year1993lld:pubmed
pubmed-article:8274768pubmed:articleTitleMutant circadian period as a marker of suprachiasmatic nucleus function.lld:pubmed
pubmed-article:8274768pubmed:affiliationDepartment of Biology, University of Virginia, Charlottesville 22901.lld:pubmed
pubmed-article:8274768pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8274768pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:8274768pubmed:publicationTypeReviewlld:pubmed