Lyst mutation in mice recapitulates iris defects of human exfoliation syndrome

Keyphrases

• Iris Defect 100%
• Pseudoexfoliation Syndrome 100%
• Mutant Mice 100%
• Transillumination Defects 40%
• Histological Analysis 20%
• Risk Factors 20%
• Protein-protein Interaction 20%
• C57BL 20%
• Insults 20%
• Increased Intraocular Pressure 20%
• Human Eye 20%
• Sequence Analysis 20%
• Optic Nerve Damage 20%
• Histologic 20%
• Genetic Background 20%
• Leucine 20%
• Anatomic 20%
• LOXL1 Gene 20%
• Pigment Dispersion 20%
• Iris pigment Epithelium 20%
• Ocular Features 20%
• Multi-feature 20%
• Molecular Genetic Analysis 20%
• Case-control Association Study 20%
• Clinical Genetics 20%
• Mutant Strains 20%
• Iris Transillumination Defects 20%
• Sawtooth 20%
• WD40 Domain 20%
• Slit Lamp Examination 20%

Medicine and Dentistry

• Iris 100%
• Transillumination 100%
• Pseudoexfoliation 100%
• Allele 33%
• Intraocular Pressure 33%
• Optic Nerve Lesion 33%
• Genetic Background 33%
• Genetic Analysis 33%
• Sequence Analysis 33%
• WD Repeat 33%
• Human Genetics 33%
• Slit Lamp Microscopy 33%
• Protein Sequencing 33%
• Iris Pigment Epithelium 33%
• Pigmentation 33%
• Genetic Association 33%
• Isoleucine 33%

Neuroscience

• Iris 100%
• Intraocular Pressure 33%
• Optic Nerve 33%
• Protein Sequencing 33%
• Isoleucine 33%
• WD Repeat 33%
• Pigmentation 33%
• Nerve Injury 33%