CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model
about
Secondary glaucoma in CAPN5-associated neovascular inflammatory vitreoretinopathy.Calpain-5 Expression in the Retina Localizes to Photoreceptor Synapses.Calpain research for drug discovery: challenges and potential.Small-angle X-ray scattering of calpain-5 reveals a highly open conformation among calpains.Two Novel CAPN5 Variants Associated with Mild and Severe Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy Phenotypes.Calpain-5 gene expression in the mouse eye and brain.An anti-CAPN5 intracellular antibody acts as an inhibitor of CAPN5-mediated neuronal degeneration.Therapeutic drug repositioning using personalized proteomics of liquid biopsies.A novel de novo CAPN5 mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay.
P2860
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P2860
CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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name
CAPN5 mutation in hereditary u ...... inflammation in a mouse model
@ast
CAPN5 mutation in hereditary u ...... inflammation in a mouse model
@en
type
label
CAPN5 mutation in hereditary u ...... inflammation in a mouse model
@ast
CAPN5 mutation in hereditary u ...... inflammation in a mouse model
@en
prefLabel
CAPN5 mutation in hereditary u ...... inflammation in a mouse model
@ast
CAPN5 mutation in hereditary u ...... inflammation in a mouse model
@en
P2093
P2860
P356
P1476
CAPN5 mutation in hereditary u ...... inflammation in a mouse model
@en
P2093
Alexander G Bassuk
Chyuan-Sheng Lin
Diana Coglan
MaryAnn Mahajan
Stephen H Tsang
Vinit B Mahajan
Wen-Hsuan Wu
P2860
P304
P356
10.1093/HMG/DDV189
P577
2015-05-20T00:00:00Z