by the fluorescence resonance energy transfer (FRET) technique. FRET data.Structural changes occurring in these mutants, as reported earlier, could be the underlying cause for the decreased interaction with αB may contribute to development of congenital cataract
T5P C-crystallin mutation is associated with Coppock-like cataract, one of the autosomal dominant co...
Human γS-crystallin is an important component of the human eye lens nucleus and cortex. The mutation...
Alpha-crystallin, a major component of the eye lens cytoplasm, is a large multimer formed from two m...
BACKGROUND: Mutation in αA-crystallin contributes to the development of congenital cataract in human...
BACKGROUND: Mutations of human αA-crystallin cause congenital cataract by protein aggregation. How m...
Mutations of human αA-crystallin cause congenital cataract by protein aggregation. How mutations of ...
Mutation of the glycine 98 residue to arginine in αA-crystallin has been shown to cause preseni...
Mutations in the human γD-crystallin gene have been linked to several types of congenital cataracts....
Abstract β/γ-Crystallins are predominant structural proteins in the cytoplasm of lens fiber cells an...
Purpose: The objective of this study is to understand the molecular basis of cataract that develops ...
BACKGROUND: Human γS-crystallin is an important component of the human eye lens nucleus and cortex. ...
AbstractCongenital hereditary cataract, which is mainly caused by the deposition of crystallins in l...
AbstractTo test the hypothesis that α-crystallin chaperone activity plays a central role in maintena...
AbstractCataract is a common cause of childhood blindness worldwide. α-crystallin, which is comprise...
PURPOSE. Many forms of congenital hereditary cataract are associated with mutations in the crystalli...
T5P C-crystallin mutation is associated with Coppock-like cataract, one of the autosomal dominant co...
Human γS-crystallin is an important component of the human eye lens nucleus and cortex. The mutation...
Alpha-crystallin, a major component of the eye lens cytoplasm, is a large multimer formed from two m...
BACKGROUND: Mutation in αA-crystallin contributes to the development of congenital cataract in human...
BACKGROUND: Mutations of human αA-crystallin cause congenital cataract by protein aggregation. How m...
Mutations of human αA-crystallin cause congenital cataract by protein aggregation. How mutations of ...
Mutation of the glycine 98 residue to arginine in αA-crystallin has been shown to cause preseni...
Mutations in the human γD-crystallin gene have been linked to several types of congenital cataracts....
Abstract β/γ-Crystallins are predominant structural proteins in the cytoplasm of lens fiber cells an...
Purpose: The objective of this study is to understand the molecular basis of cataract that develops ...
BACKGROUND: Human γS-crystallin is an important component of the human eye lens nucleus and cortex. ...
AbstractCongenital hereditary cataract, which is mainly caused by the deposition of crystallins in l...
AbstractTo test the hypothesis that α-crystallin chaperone activity plays a central role in maintena...
AbstractCataract is a common cause of childhood blindness worldwide. α-crystallin, which is comprise...
PURPOSE. Many forms of congenital hereditary cataract are associated with mutations in the crystalli...
T5P C-crystallin mutation is associated with Coppock-like cataract, one of the autosomal dominant co...
Human γS-crystallin is an important component of the human eye lens nucleus and cortex. The mutation...
Alpha-crystallin, a major component of the eye lens cytoplasm, is a large multimer formed from two m...
DOI
Add to ORKG