Weihl, Conrad C <br/><br/>
Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice.  [electronic resource] 

 -  Human molecular genetics  Apr 2007 
 - 919-28 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddm037  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Animals<br/>Cell Cycle Proteins--genetics<br/>Gene Expression<br/>Inclusion Bodies--metabolism<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Transgenic<br/>Muscle Weakness--genetics<br/>Muscle, Skeletal--metabolism<br/>Mutant Proteins--genetics<br/>Myositis, Inclusion Body--genetics<br/>Organ Specificity<br/>Proteasome Endopeptidase Complex--physiology<br/>Sarcolemma--ultrastructure<br/>Ubiquitin--metabolism<br/>Valosin Containing Protein