Significance of optineurin mutations in glaucoma and other diseases-Reference-Cited by-同舟云学术

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Significance of optineurin mutations in glaucoma and other diseases

Published:2016-11 Issue: Volume:55 Page:149-181
ISSN:1350-9462
Container-title:Progress in Retinal and Eye Research
language:en
Short-container-title:Progress in Retinal and Eye Research

Author:

Minegishi Yuriko,Nakayama Mao,Iejima Daisuke,Kawase Kazuhide,Iwata Takeshi^ORCID

Funder

Japanese Ministry of Health, Labour and Welfare

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Elsevier BV

Subject

Sensory Systems,Ophthalmology

Reference180 articles.

1. Human TBK1: a gatekeeper of neuroinflammation;Ahmad;Trends Mol. Med.,2016

2. Microsatellite analysis of the GLC1B locus on chromosome 2 points to NCK2 as a new candidate gene for normal tension glaucoma;Akiyama;Br. J. Ophthalmol,2008

3. Optineurin suppression causes neuronal cell death via NF-kappaB pathway;Akizuki;J. Neurochem.,2013

4. Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone;Albagha;Nat. Genet.,2010

5. Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma;Alward;Am. J. Ophthalmol.,2003

Cited by 95 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Age-related effects of optineurin deficiency in the mouse eye;Vision Research;2024-11

2. TGF-β2/OPTN/FOXC1/miR-200axis regulates intraocular pressure dynamics in trabecular meshwork cells;2024-06-06

3. Exploring the Genetic Landscape of Childhood Glaucoma;Children;2024-04-09

4. Optineurin-facilitated axonal mitochondria delivery promotes neuroprotection and axon regeneration;2024-04-03

5. Molecular genetics of inherited normal tension glaucoma;Indian Journal of Ophthalmology;2024-02-23

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