Functions of the intermediate filament cytoskeleton in the eye lens. - Wikidata - wikimedia - TriplyDB

Functions of the intermediate filament cytoskeleton in the eye lens.

Functions of the intermediate filament cytoskeleton in the eye lens.

http://www.wikidata.org/entity/Q37545190

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Planar cell polarity in the mammalian eye lens Order and disorder in intermediate filament proteins The specificity of the interaction between αB-crystallin and desmin filaments and its impact on filament aggregation and cell viability.Knockdown of a zebrafish aryl hydrocarbon receptor repressor (AHRRa) affects expression of genes related to photoreceptor development and hematopoiesis Intermediate filaments take the heat as stress proteins.Beta-1 integrin is important for the structural maintenance and homeostasis of differentiating fiber cells.Comparative quantification of plasma TDRD7 mRNA in cataract patients by real-time polymerase chain reaction Mutation screening and genotype phenotype correlation of α-crystallin, γ-crystallin and GJA8 gene in congenital cataract.L-type calcium channels play a critical role in maintaining lens transparency by regulating phosphorylation of aquaporin-0 and myosin light chain and expression of connexins Vimentin regulates activation of the NLRP3 inflammasome.Periaxin is required for hexagonal geometry and membrane organization of mature lens fibers Aquaporin-0 interacts with the FERM domain of ezrin/radixin/moesin proteins in the ocular lens.Nonlinear ionizing radiation-induced changes in eye lens cell proliferation, cyclin D1 expression and lens shape.Cytokinetic Failure-induced Tetraploidy Develops into Aneuploidy, Triggering Skin Aging in Phosphovimentin-deficient Mice.Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract.A dimensionless ordered pull-through model of the mammalian lens epithelium evidences scaling across species and explains the age-dependent changes in cell density in the human lens.Results of cataract surgery in renal transplantation and hemodialysis patients.Evolution of the vertebrate beaded filament protein, Bfsp2; comparing the in vitro assembly properties of a "tailed" zebrafish Bfsp2 to its "tailless" human orthologue Evolution of crystallins for a role in the vertebrate eye lens.Ankyrin-B in lens architecture and biomechanics: Just not tethering but more Hereditary pediatric cataract on the Arabian Peninsula.Foveolar Müller Cells of the Pied Flycatcher: Morphology and Distribution of Intermediate Filaments Regarding Cell Transparency "IF-pathies": a broad spectrum of intermediate filament-associated diseases.Pangolin genomes and the evolution of mammalian scales and immunity.Newborn mouse lens proteome and its alteration by lysine 6 mutant ubiquitin.Immunohistochemical characteristics of normal canine eyes.Comparative transcriptome analysis of epithelial and fiber cells in newborn mouse lenses with RNA sequencing.The molecular mechanisms underlying lens fiber elongation.Intermediate Filaments and the Plasma Membrane.Lessons from Animal Models of Cytoplasmic Intermediate Filament Proteins.Development. A new focus on RNA in the lens.Primary sequence contribution to the optical function of the eye lens.The oxidized thiol proteome in aging and cataractous mouse and human lens revealed by ICAT labeling.Quantum mechanism of light transmission by the intermediate filaments in some specialized optically transparent cells.Defect of mitotic vimentin phosphorylation causes microophthalmia and cataract via aneuploidy and senescence in lens epithelial cells.A novel p.G112E mutation in BFSP2 associated with autosomal dominant pulverulent cataract with sutural opacities.Stem Cell Isolation from Human Wharton's Jelly: A Study of Their Differentiation Ability into Lens Fiber Cells.Novel recessive BFSP2 and PITX3 mutations: insights into mutational mechanisms from consanguineous populations.Signaling and Gene Regulatory Networks in Mammalian Lens Development.A rim-and-spoke hypothesis to explain the biomechanical roles for cytoplasmic intermediate filament networks.

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Functions of the intermediate filament cytoskeleton in the eye lens.

http://www.wikidata.org/entity/Q37545190

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on July 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Functions of the intermediate filament cytoskeleton in the eye lens.

@en

Functions of the intermediate filament cytoskeleton in the eye lens.

@nl

type

label

Functions of the intermediate filament cytoskeleton in the eye lens.

@en

Functions of the intermediate filament cytoskeleton in the eye lens.

@nl

prefLabel

Functions of the intermediate filament cytoskeleton in the eye lens.

@en

Functions of the intermediate filament cytoskeleton in the eye lens.

@nl

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Journal of Clinical Investigation

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Functions of the intermediate filament cytoskeleton in the eye lens.

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Andrew Landsbury

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Qingjiong Zhang

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Ralf Dahm

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Roy A Quinlan

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Shuhua Song

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Yizhi Liu

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P2860

Radiocarbon dating of the human eye lens crystallines reveal proteins without carbon turnover throughout life

Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q

Synemin expression in developing normal and pathological human retina and lens

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA

The 'spectraplakins': cytoskeletal giants with characteristics of both spectrin and plakin families

A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy

A novel mutation in AlphaA-crystallin (CRYAA) caused autosomal dominant congenital cataract in a large Chinese family

Crystallin gene mutations in Indian families with inherited pediatric cataract

A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2

Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2

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1837-1848

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scholarly article

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10.1172/JCI38277

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7

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119

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19587458

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2701874

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