Sequence analysis of betaA3, betaB3, and betaA4 crystallins completes the identification of the major proteins in young human lens
about
Detection of protein-protein interactions among lens crystallins in a mammalian two-hybrid system assayCell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21qDomain interaction sites of human lens betaB2-crystallinCRYBA4, a novel human cataract gene, is also involved in microphthalmiaA nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese familyA nonsense mutation in CRYBB1 associated with autosomal dominant cataract linked to human chromosome 22qModifications of human betaA1/betaA3-crystallins include S-methylation, glutathiolation, and truncationLaser light-scattering evidence for an altered association of beta B1-crystallin deamidated in the connecting peptideThe X-ray crystal structure of human gamma S-crystallin C-terminal domainBiophysical Properties of γC-Crystallin in Human and Mouse Eye Lens: The Role of Molecular DipolesThe Human W42R D-Crystallin Mutant Structure Provides a Link between Congenital and Age-related CataractsNuclear Magnetic Resonance Structure of a Major Lens Protein, Human γC-Crystallin: Role of the Dipole Moment in Protein SolubilityFunctions of crystallins in and out of lens: roles in elongated and post-mitotic cellsLens β-crystallins: the role of deamidation and related modifications in aging and cataract.Quantitative measurement of deamidation in lens betaB2-crystallin and peptides by direct electrospray injection and fragmentation in a Fourier transform mass spectrometerIsolation and characterization of betaA3-crystallin associated proteinase from alpha-crystallin fraction of human lenses.Expressed sequence tag analysis of guinea pig (Cavia porcellus) eye tissues for NEIBank.Age-dependent deamidation of lifelong proteins in the human lens.Techniques for accurate protein identification in shotgun proteomic studies of human, mouse, bovine, and chicken lensesbeta-Strand interactions at the domain interface critical for the stability of human lens gammaD-crystallinFormation of amyloid fibrils in vitro from partially unfolded intermediates of human gammaC-crystallin.A missense mutation in CRYBA4 associated with congenital cataract and microcornea.βB1-crystallin: thermodynamic profiles of molecular interactions.Association of high myopia with crystallin beta A4 (CRYBA4) gene polymorphisms in the linkage-identified MYP6 locus.A serine-type protease activity of human lens βA3-crystallin is responsible for its autodegradation.A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family.Acetylation of Gly1 and Lys2 promotes aggregation of human γD-crystallin.Human and monkey lenses cultured with calcium ionophore form alphaB-crystallin lacking the C-terminal lysine, a prominent feature of some human cataracts.α- and β-crystallins modulate the head group order of human lens membranes during aging.A missense mutation in CRYBB2 leads to progressive congenital membranous cataract by impacting the solubility and function of βB2-crystallin.Wild-type human γD-crystallin promotes aggregation of its oxidation-mimicking, misfolding-prone W42Q mutant.CRYβA3/A1-Crystallin Knockout Develops Nuclear Cataract and Causes Impaired Lysosomal Cargo Clearance and Calpain Activation.A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts.iTRAQ-Based Proteomics Investigation of Aqueous Humor from Patients with Coats' Disease.A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree.Genetic and epigenetic mechanisms of gene regulation during lens development.Formation of amyloid fibrils in vitro by human gammaD-crystallin and its isolated domains.Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.Contributions of hydrophobic domain interface interactions to the folding and stability of human gammaD-crystallin.A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract
P2860
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P2860
Sequence analysis of betaA3, betaB3, and betaA4 crystallins completes the identification of the major proteins in young human lens
description
1997 nî lūn-bûn
@nan
1997 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Sequence analysis of betaA3, b ...... r proteins in young human lens
@ast
Sequence analysis of betaA3, b ...... r proteins in young human lens
@en
Sequence analysis of betaA3, b ...... r proteins in young human lens
@en-gb
Sequence analysis of betaA3, b ...... r proteins in young human lens
@nl
type
label
Sequence analysis of betaA3, b ...... r proteins in young human lens
@ast
Sequence analysis of betaA3, b ...... r proteins in young human lens
@en
Sequence analysis of betaA3, b ...... r proteins in young human lens
@en-gb
Sequence analysis of betaA3, b ...... r proteins in young human lens
@nl
prefLabel
Sequence analysis of betaA3, b ...... r proteins in young human lens
@ast
Sequence analysis of betaA3, b ...... r proteins in young human lens
@en
Sequence analysis of betaA3, b ...... r proteins in young human lens
@en-gb
Sequence analysis of betaA3, b ...... r proteins in young human lens
@nl
P2093
P2860
P921
P3181
P356
P1476
Sequence analysis of betaA3, b ...... r proteins in young human lens
@en
P2093
T R Shearer
P2860
P304
P3181
P356
10.1074/JBC.272.4.2268
P407
P577
1997-01-24T00:00:00Z