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Publications by Si Quan Zhu
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
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Truncated Human βB1-Crystallin Shows Altered Structural Properties and Interaction With Human βA3-Crystallin
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Dual Roles for Prox1 in the Regulation of the Chicken βB1-Crystallin Promoter
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
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
The Congenital Cataract-Linked A2V Mutation Impairs Tetramer Formation and Promotes Aggregation of βB2-Crystallin
PLoS ONE
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Dense Nuclear Cataract Caused by the γB-Crystallin S11R Point Mutation
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
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Oligomerization and Phase Transitions in Aqueous Solutions of Native and Truncated Human βB1-Crystallin†
Biochemistry
Biochemistry
A Novel P20R Mutation in the Alpha-B Crystallin Gene Causes Autosomal Dominant Congenital Posterior Polar Cataracts in a Chinese Family
BMC Ophthalmology
Medicine
Ophthalmology
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
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
