Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/13/9/945/1612916/ddh110.pdf
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1. Dysregulation of Autophagy Occurs During Congenital Cataract Development in βA3ΔG91 Mice;Investigative Opthalmology & Visual Science;2024-04-01
2. Multifunctional Proteins and Alternative Translation: Functional Diversification of BetaA3/A1-Crystallin Via Leaky Ribosomal Scanning;Essentials in Ophthalmology;2024
3. Endoplasmic Reticulum Stress and the Lysosomal Pathway Play Crucial Roles in the Progression of βB2-Crystallin Mutation-Induced Congenital Cataracts in Mice;Investigative Opthalmology & Visual Science;2023-04-27
4. Lens-specific βA3/A1-conditional knockout mice: Phenotypic characteristics and calpain activation causing protein degradation and insolubilization;PLOS ONE;2023-03-29
5. Generation of Lens Progenitor Cells and Lentoid Bodies from Pluripotent Stem Cells: Novel Tools for Human Lens Development and Ocular Disease Etiology;Cells;2022-11-06
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