Functional characterization of a human aquaporin 0 mutation that leads to a congenital dominant lens cataract

Medicine & Life Sciences

• aquaporin 0 100%
• Lenses 51%
• Cataract 50%
• Cell Membrane 39%
• Oocytes 38%
• Sequence Deletion 31%
• Mutation 30%
• Mutant Proteins 29%
• Water 27%
• Autosomal Dominant Cataract 23%
• Permeability 23%
• trimethyloxamine 20%
• Water Movements 20%
• Fluorescence Resonance Energy Transfer 18%
• Reading Frames 17%
• Aquaporins 17%
• Nonsense Codon 15%
• Dimethyl Sulfoxide 15%
• Cultured Cells 11%
• Nucleotides 10%
• Necrosis 10%
• Epithelium 10%
• Cell Death 10%
• Membranes 8%
• Proteins 4%