Best1 Shot Through the Eye—Structure, Functions and Clinical Implications of Bestrophin-1 Protein
Author:
Publisher
Informa UK Limited
Subject
Biotechnology
Link
http://www.tandfonline.com/doi/pdf/10.5504/BBEQ.2012.0124
Reference62 articles.
1. Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies
2. The mutation spectrum of the bestrophin protein - functional implications
3. ER-localized bestrophin 1 activates Ca2+-dependent ion channels TMEM16A and SK4 possibly by acting as a counterion channel
4. Clinical and Genetic Heterogeneity in Multifocal Vitelliform Dystrophy
5. The spectrum of ocular phenotypes caused by mutations in the BEST1 gene
Cited by 6 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. A novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy;BMC Ophthalmology;2022-12-16
2. Clinical reassessments and whole-exome sequencing uncover novel BEST1 mutation associated with bestrophinopathy phenotype;Ophthalmic Genetics;2021-11-09
3. Next generation sequencing identifies novel disease-associated BEST1 mutations in Bestrophinopathy patients;Scientific Reports;2018-07-05
4. Transepithelial resistance in human bestrophin-1 stably transfected Madin–Darby canine kidney cells;Biotechnology & Biotechnological Equipment;2014-12-10
5. Interaction of Bestrophin-1 with 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) in surface films;Colloids and Surfaces B: Biointerfaces;2014-10
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