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- A New Locus for Autosomal Dominant Congenital Cataracts Maps to Chromosome 3
- New Phenotype Associated with an Arg116cys Mutation in the CRYAA Gene Nuclear Cataract, Iris Coloboma, and Microphthalmia
- Lens A-Crystallin: JOSEPH HORWITZ, MICHAEL P
- Ageing and Vision: Structure, Stability and Function of Lens Crystallins Hans Bloemendala, Wilfried De Jonga, Rainer Jaenickeb,C, Nicolette H
- Review Alpha-Crystallin
- Differential Expression Patterns of Crystallin Genes During Ocular Development of Olive Flounder (Paralichthys Olivaceus)
- Human Alpha-Crystallin-III Isolation and Characterization of Protein from Normal Infant Lenses and Old Lens Peripheries
- βA1-Crystallin Regulates Glucose Metabolism and Mitochondrial
- The Eye Lens Chaperone -Crystallin Forms Defined Globular Assemblies
- The Human Crystallin Gene Families Graeme Wistow
- Cgmp Via PKG Activates 26S Proteasomes and Enhances Degradation of Proteins, Including Ones That Cause Neurodegenerative Diseases
- Differentially Expressed Genes Identified by Cross-Species Microarray in the Blind Cavefish Astyanax
- How Complexity Originates: • Explore Related Articles • Search Keywords the Evolution of Animal Eyes
- CRYAA Nucleotide Variants to a Complex Presentation of Anterior Segment Dysgenesis Andrey V
- Structure of the Crysta II I Ns
- Human/Mouse Alphaa Crystallin/CRYAA Antibody Antigen Affinity-Purified Polyclonal Goat Igg Catalog Number: AF4848
- Increased Expression of Αa-Crystallin in Human Diabetic Eye
- Investigation of Crystallin Genes in Familial Cataract, and Report of Two
- Cell Death Triggered by a Novel Mutation in the Alphaa-Crystallin Gene Underlies Autosomal Dominant Cataract Linked to Chromosome 21Q
- Cataract-Associated New Mutants S175G/H181Q of Βb2-Crystallin and P24S/S31G of Γd-Crystallin Are Involved in Protein Aggregation by Structural Changes
- GCAP1, Rab6, and HSP27: Novel Autoantibody Targets in Cancer-Associated Retinopathy and Autoimmune Retinopathy
- Biophysical Investigation of the Cataract Associated Mutant, E107A
- Gamma C Crystallin (CRYGC) Mouse Monoclonal Antibody [Clone ID: OTI1D6] Product Data
- (CRYGD) Associated with Autosomal Dominant "Coral-Like" Cataract Linked to Chromosome 2Q Donna S
- Therapeutic Potential of -Crystallins in Retinal Neurodegenerative Diseases
- Gamma C Crystallin (CRYGC) Mouse Monoclonal Antibody [Clone ID: OTI1E3] Product Data
- Gamma-S Crystallin Gene (CRYGS)
- A Comprehensive Analysis of the Expression of Crystallins in Mouse Retina Jinghua Xi Washington University School of Medicine in St
- Circadian Proteome Changes in Photoreceptor Outer Segments
- Rhodopsin Retinitis Pigmentosa: an in Vitro Study of the Cellular Fate of Wild
- Catalysis of Cataract-Associated Human Γd Crystallin Aggregation Via Dynamic Disulfide Exchange
- Novel Mutations in CRYGC Are Associated with Congenital
- A Novel Human Crygdmutation in a Juvenile Autosomal Dominant Cataract
- Etv Transcription Factors Functionally Diverge from Their Upstream FGF
- Crystallin Gene Mutations in Indian Families with Inherited Pediatric Cataract
- Preferential Interaction of Alpha Crystallin with Denatured Forms of Gamma Crystallin
- U-Crystallin Is a Mammalian Homologue Of
- Gamma-D Crystallin Gene
- A Nonsense Mutation of CRYGC Associated with Autosomal Dominant Congenital Nuclear Cataracts and Microcornea in a Chinese Pedigree
- Overexpression of Human C-Crystallin 5 Bp Duplication Disrupts Lens
- Novel Mutations in the Γ-Crystallin Genes Cause Autosomal Dominant
- A New A1-Crystallin Splice Junction Mutation in Autosomal Dominant
- Dense Nuclear Cataract Caused by the B-Crystallin S11R Point Mutation
- Phosphate Lipids in the Retinal Pigment Epithelium Implicate