about
Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataractsCRYBA4, 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 22qMethylation and carbamylation of human gamma-crystallinsAntagonistic action of Six3 and Prox1 at the gamma-crystallin promoterZebrafish--on the move towards ophthalmological researchRequirement for the c-Maf transcription factor in crystallin gene regulation and lens development.Evolution of graded refractive index in squid lenses.The structure of the cytoplasm of lens fibers as determined by conical tomography.Novel mutations in CRYGC are associated with congenital cataracts in Chinese families.Maternal experience with predation risk influences genome-wide embryonic gene expression in threespined sticklebacks (Gasterosteus aculeatus)Expression of transcription factors and crystallin proteins during rat lens regeneration.Cataract-causing αAG98R-crystallin mutant dissociates into monomers having chaperone activity.The congenital cataract-linked G61C mutation destabilizes γD-crystallin and promotes non-native aggregationAge-related changes in the water-soluble lens protein composition of Wistar and accelerated-senescence OXYS rats.The three-dimensional distribution of αA-crystalline in rat lenses and its possible relation to transparencyGene expression profiling elucidates a specific role for RARgamma in the retinoic acid-induced differentiation of F9 teratocarcinoma stem cellsCell-autonomous requirements for Dlg-1 for lens epithelial cell structure and fiber cell morphogenesis.Transcriptional analysis of a unique set of genes involved in Schistosoma mansoni female reproductive biologyCrystallins are regulated biomarkers for monitoring topical therapy of glaucomatous optic neuropathy.Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts.Overexpression of human γC-crystallin 5 bp duplication disrupts lens morphology in transgenic mice.Crystalline cataract caused by a heterozygous missense mutation in γD-crystallin (CRYGD).Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral stateThe unfolded protein response is activated in connexin 50 mutant mouse lenses.A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataractA mutation in the start codon of γ-crystallin D leads to nuclear cataracts in the Dahl SS/Jr-Ctr strain.Insights into the beaded filament of the eye lens.Synergistic transcription activation by Maf and Sox and their subnuclear localization are disrupted by a mutation in Maf that causes cataract.Evaluation of three canine gamma-crystallins (CRYGB, CRYGC, and CRYGS) as candidates for hereditary cataracts in the dachshund
P2860
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P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի նոյեմբերին 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
The crystallins: genes, proteins and diseases
@ast
The crystallins: genes, proteins and diseases
@en
The crystallins: genes, proteins and diseases
@nl
type
label
The crystallins: genes, proteins and diseases
@ast
The crystallins: genes, proteins and diseases
@en
The crystallins: genes, proteins and diseases
@nl
prefLabel
The crystallins: genes, proteins and diseases
@ast
The crystallins: genes, proteins and diseases
@en
The crystallins: genes, proteins and diseases
@nl
P1433
P1476
The crystallins: genes, proteins and diseases
@en
P2093
P304
P407
P577
1997-11-01T00:00:00Z