Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12 - Wikidata - awgldk - TriplyDB

Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12

Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12

http://www.wikidata.org/entity/Q35156016

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Regulation of corneal stroma extracellular matrix assembly Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy.Molecular description of eye defects in the zebrafish Pax6b mutant, sunrise, reveals a Pax6b-dependent genetic network in the developing anterior chamber.Transcriptomic Analysis of Cultured Corneal Endothelial Cells as a Validation for Their Use in Cell Replacement Therapy.Small leucine-rich repeat proteoglycans in corneal inflammation and wound healing.Long intergenic non-coding RNA GALMD3 in chicken Marek's disease.Posterior amorphous corneal dystrophy caused by a de novo deletion.

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P2860

Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12

http://www.wikidata.org/entity/Q35156016

description

2014 nî lūn-bûn

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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

@yue

2014年論文

@zh-hant

2014年論文

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2014年論文

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2014年論文

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2014年论文

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Posterior amorphous corneal dy ...... proteoglycans on chromosome 12

@ast

Posterior amorphous corneal dy ...... proteoglycans on chromosome 12

@en

type

label

Posterior amorphous corneal dy ...... proteoglycans on chromosome 12

@ast

Posterior amorphous corneal dy ...... proteoglycans on chromosome 12

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prefLabel

Posterior amorphous corneal dy ...... proteoglycans on chromosome 12

@ast

Posterior amorphous corneal dy ...... proteoglycans on chromosome 12

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Posterior amorphous corneal dy ...... proteoglycans on chromosome 12

@en

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Anthony J Aldave

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Derek J Le

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George O D Rosenwasser

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Michelle J Kim

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Ricardo F Frausto

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Tina Bui

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P2860

Mutations in KERA, encoding keratocan, cause cornea plana

Lumican regulates collagen fibril assembly: skin fragility and corneal opacity in the absence of lumican

Matrix proteoglycans: from molecular design to cellular function

Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene

Keratocan, a cornea-specific keratan sulfate proteoglycan, is regulated by lumican

A comprehensive collection of experimentally validated primers for Polymerase Chain Reaction quantitation of murine transcript abundance.

A PCR primer bank for quantitative gene expression analysis.

PrimerBank: a resource of human and mouse PCR primer pairs for gene expression detection and quantification.

Copy number variation in human health, disease, and evolution.

Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.

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scholarly article

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posterior amorphous corneal dystrophy

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3997350

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