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- 17Β-Estradiol Delivered in Eye Drops: Evidence of Impact on Protein Networks and Associated Biological Processes in the Rat Retina Through Quantitative Proteomics
- Whole-Transcriptome Analysis of Fully Viable Energy Efficient Glycolytic
- Microarray Analysis of Iris Gene Expression in Mice with Mutations Influencing Pigmentation
- ODF 1.0 Headerlines= 9 Model= Gene List COLUMN NAMES:Feature Description COLUMN TYPES:String String Float COLUMN DESCS:Name of the Description of the Gene
- Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
- The Human Crystallin Gene Families Graeme Wistow
- CRYAA Nucleotide Variants to a Complex Presentation of Anterior Segment Dysgenesis Andrey V
- Partial Duplication of the CRYBB1-CRYBA4 Locus Is Associated with Autosomal Dominant Congenital Cataract
- Investigation of Crystallin Genes in Familial Cataract, and Report of Two
- A Novel Mutation in CRYBB2 Responsible for Inherited Coronary
- Proteomic Analysis of the Aqueous Humour in Eyes with Pseudoexfoliation Syndrome Amelie Botling Taube,1,2 Anne Konzer,3 Albert Alm,1 Jonas Bergquist 3
- Cataract-Associated New Mutants S175G/H181Q of Βb2-Crystallin and P24S/S31G of Γd-Crystallin Are Involved in Protein Aggregation by Structural Changes
- Evolution and Molecular Mechanisms of Photoreceptor Transmutation in Reptiles
- Long-Term Neuroprotective Effects of NT-4–Engineered Mesenchymal Stem Cells Injected Intravitreally in a Mouse Model of Acute Retinal Injury
- The Genetic Landscape of Crystallins in Congenital Cataract Vanita Berry1,2* , Alex Ionides2, Nikolas Pontikos1,2, Michalis Georgiou1,2, Jing Yu4, Louise A
- Abstract Book Table of Contents Table of Contents 3
- CRYBB1) Associated with Autosomal Recessive Nuclear Pulverulent Cataract
- Novel Mutations in CRYGC Are Associated with Congenital