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Publications by Norman L. Hawes
Dense Nuclear Cataract Caused by the γB-Crystallin S11R Point Mutation
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Related publications
A Novel Mutation in CRYBB1 Associated With Congenital Cataract-Microcornea Syndrome: The p.Ser129Arg Mutation Destabilizes the βB1/βA3-crystallin Heteromer but Not the βB1-crystallin Homomer
Human Mutation
Genetics
The Congenital Cataract-Linked A2V Mutation Impairs Tetramer Formation and Promotes Aggregation of βB2-Crystallin
PLoS ONE
Multidisciplinary
Cataract Mutation P20S of αB-crystallin Impairs Chaperone Activity of αA-crystallin and Induces Apoptosis of Human Lens Epithelial Cells
Biochimica et Biophysica Acta - Molecular Basis of Disease
Molecular Medicine
Molecular Biology
A Novel Mutation (F71L) in αA-Crystallin With Defective Chaperone-Like Function Associated With Age-Related Cataract
Biochimica et Biophysica Acta - Molecular Basis of Disease
Molecular Medicine
Molecular Biology
αA-Crystallin–Derived Mini-Chaperone Modulates Stability and Function of Cataract Causing αAG98R-Crystallin
PLoS ONE
Multidisciplinary
Dyskeratosis Congenita Caused by a Novel TERT Point Mutation in Siblings With Pancytopenia and Exudative Retinopathy
Pediatric Blood and Cancer
Oncology
Child Health
Hematology
Perinatology
Medicine
Pediatrics
Lens Crystallin Modifications and Cataract in Transgenic Mice Overexpressing Acylpeptide Hydrolase
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Deamidation of Human γS-Crystallin Increases Attractive Protein Interactions: Implications for Cataract
Biochemistry
Biochemistry
Unique Presentation of Congenital Cataract Concurrent With Microcornea, Microphthalmia Plus Posterior Capsule Defect in Monozygotic Twins Caused by a Novel GJA8 Mutation
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
