Proteomic insight into the pathogenesis of CAPN5-vitreoretinopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-44031-7.pdf
Reference58 articles.
1. Mahajan, V. B. et al. Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration. PLoS Genet 8, e1003001, https://doi.org/10.1371/journal.pgen.1003001 (2012).
2. Velez, G., Bassuk, A. G., Colgan, D., Tsang, S. H. & Mahajan, V. B. Therapeutic drug repositioning using personalized proteomics of liquid biopsies. JCI Insight 2, https://doi.org/10.1172/jci.insight.97818 (2017).
3. Schaefer, K. et al. Calpain-5 gene expression in the mouse eye and brain. BMC Res Notes 10, 602, https://doi.org/10.1186/s13104-017-2927-8 (2017).
4. Schaefer, K. A. et al. Calpain-5 Expression in the Retina Localizes to Photoreceptor Synapses. Invest Ophthalmol Vis Sci 57, 2509–2521, https://doi.org/10.1167/iovs.15-18680 (2016).
5. Wert, K. J. et al. CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model. Hum Mol Genet 24, 4584–4598, https://doi.org/10.1093/hmg/ddv189 (2015).
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