Molecular genetics of congenital cataracts-Reference-Cited by-同舟云学术

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Molecular genetics of congenital cataracts

Published:2020-02 Issue: Volume:191 Page:107872
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Li Jinyu,Chen Xiangjun,Yan Yongbin,Yao Ke

Funder

National Natural Science Foundation of China

Zhejiang Province Key Research and Development

Medical science and technology project of Zhejiang Province

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference267 articles.

1. Aquaporin water channels--from atomic structure to clinical medicine;Agre;J. Physiol.,2002

2. Children with congenital and childhood cataract require frequent follow-up visits and examinations in general anaesthesia: considerations for the strain on families;Al-Bakri;Acta Ophthalmol.,2019

3. Novel recessive BFSP2 and PITX3 mutations: insights into mutational mechanisms from consanguineous populations;Aldahmesh;Genet. Med.,2011

4. Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genes;Aldahmesh;Genet. Med.,2012

5. Statins and risk of cataracts: a systematic review and meta-analysis of observational studies;Alves;Cardiovasc. Ther.,2018

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1. Truncation mutations of CRYGD gene in congenital cataracts cause protein aggregation by disrupting the structural stability of γD-crystallin;International Journal of Biological Macromolecules;2024-10

2. GBF1 deficiency causes cataracts in human and mouse;Human Genetics;2024-08-07

3. Surgical Outcomes of Children with Unilateral Congenital Cataract and Persistent Fetal Vasculature;Clinical Ophthalmology;2024-08

4. The role of cGAS/STING signaling in ophthalmological diseases;Biomedicine & Pharmacotherapy;2024-08

5. Quercetin-Loaded Nanocarriers as Effective Inhibitors for Copper Metal Ion-Induced γD-Crystallin Aggregation;Langmuir;2024-07-24

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