Pak, Joseph S <br/><br/>
The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation.  [electronic resource] 

 -  Molecular vision  2015 
 - 1281-94 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-0535 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age Factors<br/>Animals<br/>Apoptosis<br/>Darkness<br/>Female<br/>G-Protein-Coupled Receptor Kinase 1--deficiency<br/>Gene Expression Regulation<br/>Glial Fibrillary Acidic Protein--genetics<br/>In Situ Nick-End Labeling<br/>Male<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Knockout<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Phenotype<br/>Photic Stimulation<br/>Photoreceptor Cells, Vertebrate--metabolism<br/>Retinal Degeneration--genetics<br/>Signal Transduction<br/>Species Specificity<br/>Zonula Occludens-1 Protein--genetics