A cellular model for the investigation of Fuchs' endothelial corneal dystrophy. - Wikidata - awgldk - TriplyDB

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

http://www.wikidata.org/entity/Q34633206

about

Fuchs endothelial corneal dystrophy: current perspectives L450W and Q455K Col8a2 knock-in mouse models of Fuchs endothelial corneal dystrophy show distinct phenotypes and evidence for altered autophagy.Encoding Cell-Instructive Cues to PEG-Based Hydrogels via Triple Helical Peptide Assembly.Corneal dystrophies and genetics in the International Committee for Classification of Corneal Dystrophies era: a review.Extracellular Matrix and Integrin Expression Profiles in Fuchs Endothelial Corneal Dystrophy Cells and Tissue Model.NQO1 downregulation potentiates menadione-induced endothelial-mesenchymal transition during rosette formation in Fuchs endothelial corneal dystrophy.

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P2860

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

http://www.wikidata.org/entity/Q34633206

description

2011 nî lūn-bûn

@nan

2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年学术文章

@wuu

2011年学术文章

@zh-cn

2011年学术文章

@zh-hans

2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

@yue

name

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@ast

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@en

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@nl

type

label

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@ast

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@en

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@nl

prefLabel

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@ast

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@en

A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@nl

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J.EXER.2011.10.001

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Experimental Eye Research

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A cellular model for the investigation of Fuchs' endothelial corneal dystrophy.

@en

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Albert S Jun

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Christoph Engler

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Clare Kelliher

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Mario Matthaei

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Neeraj Vij

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Patrick J Stahl

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S Michael Yu

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Shukti Chakravarti

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Steve Mazur

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P2860

The alpha 2(VIII) collagen gene. A novel member of the short chain collagen family located on the human chromosome 1

Immunohistochemistry and electron microscopy of early-onset fuchs corneal dystrophy in three cases with the same L450W COL8A2 mutation

Sequence dependent conformational variations of collagen triple-helical structure

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

Differential protein expression in human corneal endothelial cells cultured from young and older donors

A comprehensive resource for integrating and displaying protein post-translational modifications.

Folding of peptide models of collagen and misfolding in disease.

Unfolded protein response in fuchs endothelial corneal dystrophy: a unifying pathogenic pathway?

The alpha1(VIII) and alpha2(VIII) collagen chains form two distinct homotrimeric proteins in vivo.

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.

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880-888

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