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The Ubr2 gene is expressed in skeletal muscle atrophying as a result of hind limb suspension, but not Merg1a expression alone

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Skeletal muscle (SKM) atrophy is a potentially debilitating condition induced by muscle disuse, denervation, many disease states, and aging. The ubiquitin proteasome pathway (UPP) contributes greatly to the protein loss suffered in muscle atrophy. The MERG1a K+ channel is known to induce UPP activit...

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Bibliographic Details
Main Authors: Gregory H. Hockerman (Author), Nicole M. Dethrow (Author), Sohaib Hameed (Author), Maureen Doran (Author), Christine Jaeger (Author), Wen-Horng Wang (Author), Amber L. Pond (Author)
Format: Book
Published: PAGEPress Publications, 2014-09-01T00:00:00Z.
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3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
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