Maxwell, Megan <br/><br/>
Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype.  [electronic resource] 

 -  Molecular and cellular biology  Aug 2003 
 - 5947-57 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0270-7306 
<br/><br/><label>Standard No.: </label>10.1128/MCB.23.16.5947-5957.2003  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Blotting, Northern<br/>Blotting, Western<br/>Cell Movement<br/>Cerebral Cortex--pathology<br/>Disease Models, Animal<br/>Fibroblasts--metabolism<br/>Green Fluorescent Proteins<br/>Hepatocytes--pathology<br/>Integrases--metabolism<br/>Liver--metabolism<br/>Luminescent Proteins--metabolism<br/>Membrane Proteins--genetics<br/>Mice<br/>Mice, Knockout<br/>Mice, Transgenic<br/>Microscopy, Electron<br/>Microscopy, Fluorescence<br/>Molecular Sequence Data<br/>Mutation<br/>Neurons--metabolism<br/>Peroxisomes--metabolism<br/>Phenotype<br/>Plasmids--metabolism<br/>Protein Biosynthesis<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Transcription, Genetic<br/>Viral Proteins--metabolism<br/>Zellweger Syndrome--genetics