The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation. [electronic resource]
Producer: 20160624Description: 1281-94 p. digitalISSN:- 1090-0535
- Age Factors
- Animals
- Apoptosis
- Darkness
- Female
- G-Protein-Coupled Receptor Kinase 1 -- deficiency
- Gene Expression Regulation
- Glial Fibrillary Acidic Protein -- genetics
- In Situ Nick-End Labeling
- Male
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Mutation
- Nerve Tissue Proteins -- genetics
- Phenotype
- Photic Stimulation
- Photoreceptor Cells, Vertebrate -- metabolism
- Retinal Degeneration -- genetics
- Signal Transduction
- Species Specificity
- Zonula Occludens-1 Protein -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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