Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0).
about
Lipid-protein interactions in double-layered two-dimensional AQP0 crystals.Functional characterization of a human aquaporin 0 mutation that leads to a congenital dominant lens cataract.Functional expression of aquaporins in embryonic, postnatal, and adult mouse lensesDiffusion of glycerol through Escherichia coli aquaglyceroporin GlpF.PKC putative phosphorylation site Ser235 is required for MIP/AQP0 translocation to the plasma membrane.Transgenic expression of AQP1 in the fiber cells of AQP0 knockout mouse: effects on lens transparency.Physiological role of aquaporin 5 in salivary glands.Noncanonical binding of calmodulin to aquaporin-0: implications for channel regulation.MIP/Aquaporin 0 represents a direct transcriptional target of PITX3 in the developing lens.Molecular genetics of age-related cataract.Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataractIdentification and functional analysis of GJA8 mutation in a Chinese family with autosomal dominant perinuclear cataracts.Aquaporins: a water channel family.Developmental genetics in ophthalmology.A novel nonsense mutation in the MIP gene linked to congenital posterior polar cataracts in a Chinese family.AKAP2 anchors PKA with aquaporin-0 to support ocular lens transparency.MALDI Imaging Mass Spectrometry Spatially Maps Age-Related Deamidation and Truncation of Human Lens Aquaporin-0.Functions of aquaporins in the eyeMolecular basis of pH and Ca2+ regulation of aquaporin water permeability.Aquaporins: a promising target for drug development.Phosphorylation determines the calmodulin-mediated Ca2+ response and water permeability of AQP0A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.Congenital cataracts and their molecular geneticsThe G18V CRYGS mutation associated with human cataracts increases gammaS-crystallin sensitivity to thermal and chemical stressStructural insights into eukaryotic aquaporin regulation.Evidence of clinical and genetic heterogeneity in autosomal dominant congenital cerulean cataracts.Aquaporin Protein-Protein Interactions.Aquaporin 0 Modulates Lens Gap Junctions in the Presence of Lens-Specific Beaded Filament Proteins.Identification of mutations in HSF4 in dogs of three different breeds with hereditary cataracts.
P2860
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P2860
Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0).
description
2000 nî lūn-bûn
@nan
2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Congenital progressive polymor ...... otein of the lens, MIP (AQP0).
@ast
Congenital progressive polymor ...... otein of the lens, MIP (AQP0).
@en
type
label
Congenital progressive polymor ...... otein of the lens, MIP (AQP0).
@ast
Congenital progressive polymor ...... otein of the lens, MIP (AQP0).
@en
prefLabel
Congenital progressive polymor ...... otein of the lens, MIP (AQP0).
@ast
Congenital progressive polymor ...... otein of the lens, MIP (AQP0).
@en
P2093
P2860
P356
P1476
Congenital progressive polymor ...... otein of the lens, MIP (AQP0).
@en
P2093
P2860
P304
P356
10.1136/BJO.84.12.1376
P407
P577
2000-12-01T00:00:00Z