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dc.contributor.authorDuszynski, Robert J.
dc.date.accessioned2009-05-04T19:48:36Z
dc.date.available2009-05-04T19:48:36Z
dc.date.issued2009
dc.identifier.urihttp://hdl.handle.net/10920/8296
dc.description1 broadsideen
dc.description.abstractCaenorhabditis elegans is a microscopic species of nematode that became a model organism for biological research in the 1970s The striated muscle cell within C. elegans is a highly ordered structure that contains actin and myosin filaments, anchoring structures, and regulatory proteins Uncoordinated (unc) mutations display phenotypes associated with hindered muscle structure unc-82 mutants display phenotypes such as slow movement and decreased presence and clumping of thick filaments at the ends of the muscle cells UNC-82 is a protein that is associated with myosin organization RW1596 strain of C. elegans contains a lethal myosin A mutation (myo-3) recovered by an extrachromosomal array of DNA called stEx30 One goal of the mutagenesis screen was to identify additional mutations in the unc-82 geneen
dc.description.sponsorshipKalamazoo College. Department of Biology. Diebold Symposium, 2009.en
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen
dc.publisherKalamazoo, Mich. : Kalamazoo College.
dc.relation.ispartofKalamazoo College Diebold Symposium Presentations Collectionen
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.en
dc.titleChemical mutagenesis of unc-82 and other muscle-affecting genes in Caenorhabditis elegansen
dc.typePresentationen


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  • Diebold Symposium Posters and Schedules [479]
    Poster and oral presentations by senior biology majors that include the results of their Senior Integrated Projects (SIPs) at the Diebold Symposium. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

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