Associated Papers
Mimicking oxidative damage in γS-crystallin with site-specific incorporation of 5-hydroxytryptophan.
Seo Y et al.
Biophysical Reports, 2026
41548873 (PubMed )
Supplement: mmc2.pdf
Human γS-Crystallin Mutation F10_Y11delinsLN in the First Greek Key Pair Destabilizes and Impairs Tight Packing Causing Cortical Lamellar Cataract.
Vendra VPR et al.
International Journal of Molecular Sciences, 2023
A novel missense mutation of CRYBA1 in a northern Chinese family with inherited coronary cataract with blue punctate opacities.
Ni SH et al.
European Journal of Ophthalmology, 2022
Chemical Properties Determine Solubility and Stability in βγ-Crystallins of the Eye Lens.
Rocha MA et al.
Chembiochem : a European Journal of Chemical Biology, 2021
A Molecular Dynamics Perspective To Identify Precursors to Aggregation in Human γS-Crystallin Unravels the Mechanism of Childhood Cataracts.
Bari KJ et al.
The Journal of Physical Chemistry. B, 2019
Conformational dynamics study on human γS-crystallin as an efficient route to childhood blindness.
Bari KJ et al.
Biochemical and Biophysical Research Communications, 2019
Sequence specific 1H, 13C and 15N resonance assignments of the C-terminal domain of human γS-crystallin.
Bari KJ et al.
Biomolecular Nmr Assignments, 2019
A novel missense mutation of CRYGS underlies congenital cataract in a Chinese family.
Zhang T et al.
Gene, 2018
Sequence specific 1H, 13C and 15N resonance assignments of a cataract-related variant G57W of human γS-crystallin.
Bari KJ et al.
Biomolecular Nmr Assignments, 2018
Multiple Aggregation Pathways in Human γS-Crystallin and Its Aggregation-Prone G18V Variant.
Roskamp KW et al.
Investigative Ophthalmology & Visual Science, 2017
Structural study of the G57W mutant of human gamma-S-crystallin, associated with congenital cataract.
Khan I et al.
Molecular Vision, 2016
A G57W Mutation of CRYGS Associated with Autosomal Dominant Pulverulent Cataracts in a Chinese Family.
Yang Z et al.
Ophthalmic Genetics, 2015
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