Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4

Medicine & Life Sciences

• Stargardt disease 3 100%
• Fatty Acids 41%
• Pathology 30%
• Mutation 27%
• Skin 26%
• Lipofuscin 19%
• Lipids 12%
• Mouse Elovl4 protein 12%
• Epidermis 9%
• Mass Spectrometry 8%
• Messenger RNA 8%
• Nuclease Protection Assays 8%
• High Pressure Liquid Chromatography 7%
• Alleles 7%
• Genetic Models 5%
• Southern Blotting 5%
• Base Pairing 4%
• Point Mutation 4%
• Postpartum Period 4%
• Retina 4%
• Permeability 4%
• Exons 4%
• Genes 3%
• Genotype 3%
• Amino Acids 3%
• Phenotype 2%
• DNA 2%