The Human W42R γD-Crystallin Mutant Structure Provides a Link between Congenital and Age-related Cataracts

Structural and Biochemical Characterization of the Childhood Cataract-Associated R76S Mutant of Human γD-Crystallin

(2012) Fangling Ji et al.   BIOCHEMISTRY

Genetic analysis of adult-onset cataract in a city-based ophthalmic hospital

(2010) Ramachandran Vijaya et al.   CLINICAL GENETICS

A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family

(2010) Binbin Wang et al.   HUMAN MUTATION

A Single Destabilizing Mutation (F9S) Promotes Concerted Unfolding of an Entire Globular Domain in γS-Crystallin

(2010) Soojin Lee et al.   JOURNAL OF MOLECULAR BIOLOGY

Characterization of a Transient Unfolding Intermediate in a Core Mutant of γS-Crystallin

(2010) Bryon Mahler et al.   JOURNAL OF MOLECULAR BIOLOGY

The Structure of the Cataract-Causing P23T Mutant of Human γD-Crystallin Exhibits Distinctive Local Conformational and Dynamic Changes†,‡

(2009) Jinwon Jung et al.   BIOCHEMISTRY

Mechanism of the Very Efficient Quenching of Tryptophan Fluorescence in Human γD- and γS-Crystallins: The γ-Crystallin Fold May Have Evolved To Protect Tryptophan Residues from Ultraviolet Photodamage†

(2009) Jiejin Chen et al.   BIOCHEMISTRY

Hydrophobic Core Mutations Associated with Cataract Development in Mice Destabilize Human γD-Crystallin

(2009) Kate L. Moreau et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mechanism of the Efficient Tryptophan Fluorescence Quenching in Human γD-Crystallin Studied by Time-Resolved Fluorescence†

(2008) Jiejin Chen et al.   BIOCHEMISTRY

Congenital cataracts and their molecular genetics

(2007) J. Fielding Hejtmancik   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY