Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
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Corneal dystrophiesProteoglycan form and function: A comprehensive nomenclature of proteoglycansThe IC3D classification of the corneal dystrophiesRole of integrins in the periodontal ligament: organizers and facilitatorsRole of Decorin Core Protein in Collagen Organisation in Congenital Stromal Corneal Dystrophy (CSCD)LRRCE: a leucine-rich repeat cysteine capping motif unique to the chordate lineageExtracellular matrix molecules: potential targets in pharmacotherapy.Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness.Pathophysiological Significance of Dermatan Sulfate Proteoglycans Revealed by Human Genetic Disorders.Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.Chromosome abnormalities and the genetics of congenital corneal opacification.Molecular description of eye defects in the zebrafish Pax6b mutant, sunrise, reveals a Pax6b-dependent genetic network in the developing anterior chamber.Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12Current gene discovery strategies for ocular conditionsPathophysiological mechanisms of autosomal dominant congenital stromal corneal dystrophy: C-terminal-truncated decorin results in abnormal matrix assembly and altered expression of small leucine-rich proteoglycansCollagen V is a dominant regulator of collagen fibrillogenesis: dysfunctional regulation of structure and function in a corneal-stroma-specific Col5a1-null mouse model.The small leucine-rich repeat proteoglycans in tissue repair and atherosclerosisBiological functions of the small leucine-rich proteoglycans: from genetics to signal transduction.Mechanisms of trophoblast migration, endometrial angiogenesis in preeclampsia: The role of decorin.Specific requirement of Gli transcription factors in Hedgehog-mediated intestinal development.Intracellularly-retained decorin lacking the C-terminal ear repeat causes ER stress: a cell-based etiological mechanism for congenital stromal corneal dystrophy.Congenital corneal opacities: a review with a focus on genetics.The molecular basis of corneal transparency.Genetics of anterior and stromal corneal dystrophies.Genetic evidence for the coordinated regulation of collagen fibrillogenesis in the cornea by decorin and biglycanComparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology.Glycoproteomics Reveals Decorin Peptides With Anti-Myostatin Activity in Human Atrial FibrillationSmall leucine rich proteoglycan family regulates multiple signalling pathways in neural development and maintenance.Collagens and proteoglycans of the cornea: importance in transparency and visual disorders.Small leucine-rich repeat proteoglycans in corneal inflammation and wound healing.Lumican Peptides: Rational Design Targeting ALK5/TGFBRI.The integrin needle in the stromal haystack: emerging role in corneal physiology and pathology.Development of myotendinous-like junctions that anchor cardiac valves requires fibromodulin and lumican.Focus on molecules: decorin.A novel decorin gene mutation in congenital hereditary stromal dystrophy: a Korean family.Absence of the dermatan sulfate chain of decorin does not affect mouse development.Fibromodulin regulates collagen fibrillogenesis during peripheral corneal development.Genes encoding proteoglycans are associated with the risk of anterior cruciate ligament ruptures.Bilateral cloudy cornea: is the usual suspect congenital hereditary endothelial dystrophy or stromal dystrophy?Clinical characteristics in patients with interstitial deletions of chromosome region 12q21-q22 and identification of a critical region associated with keratosis pilaris.
P2860
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P2860
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
description
2005 nî lūn-bûn
@nan
2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@ast
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@en
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@nl
type
label
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@ast
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@en
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@nl
prefLabel
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@ast
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@en
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@nl
P2093
P356
P1476
Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene
@en
P2093
Cecilie Bredrup
Eyvind Rødahl
Helge Boman
Jacek Majewski
Per M Knappskog
P356
10.1167/IOVS.04-0804
P407
P577
2005-02-01T00:00:00Z