Molecular and developmental mechanisms of anterior segment dysgenesis.
about
Equine Multiple Congenital Ocular Anomalies maps to a 4.9 megabase interval on horse chromosome 6Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment diseaseA novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomalyA novel histopathologic finding in the Descemet's membrane of a patient with Peters Anomaly: a case-report and literature reviewThe Genetics and the Genomics of Primary Congenital GlaucomaExtracellular matrix in the trabecular meshwork: intraocular pressure regulation and dysregulation in glaucomaProgenitors for the corneal endothelium and trabecular meshwork: a potential source for personalized stem cell therapy in corneal endothelial diseases and glaucomaZebrafish foxc1a drives appendage-specific neural circuit development.Mutations in POMGNT1 cause non-syndromic retinitis pigmentosaMissed case of Axenfeld-Rieger syndrome: a case reportAP-2alpha knockout mice exhibit optic cup patterning defects and failure of optic stalk morphogenesisMutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment DysgenesisFOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1Anterior segment dysgenesis associated with Williams-Beuren syndrome: a case report and review of the literature.Type II Peter's anomaly with histopathological proof: a case reportGenetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation in mouse.Rodent models of glaucoma.Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutationsAnterior segment dysgenesis and early-onset glaucoma in nee mice with mutation of Sh3pxd2bThree periods of one and a half decade of ischemic stroke susceptibility gene research: lessons we have learnedChromosome abnormalities and the genetics of congenital corneal opacification.Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucomaGenetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacityAnalysis of copy number variation using whole genome exon-focused array CGH in Korean patients with primary congenital glaucomaLoss of Msx2 function down-regulates the FoxE3 expression and results in anterior segment dysgenesis resembling Peters anomaly.Analysis of FOXD3 sequence variation in human ocular disease.Using genetic mouse models to gain insight into glaucoma: Past results and future possibilities.PITX2 and FOXC1 spectrum of mutations in ocular syndromesGenetics of anterior segment dysgenesis disorders.Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma.Impaired ADAMTS9 secretion: A potential mechanism for eye defects in Peters Plus Syndrome.Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.Neural crest derivatives in ocular development: discerning the eye of the stormFoxc1 and Foxc2 in the Neural Crest Are Required for Ocular Anterior Segment Development.The genetics of ocular disorders: insights from the zebrafish.Genomics and anterior segment dysgenesis: a review.The Trabecular Meshwork: A Basic Review of Form and FunctionA novel mouse model of anterior segment dysgenesis (ASD): conditional deletion of Tsc1 disrupts ciliary body and iris developmentThe zebrafish eye-a paradigm for investigating human ocular genetics.Major review: Molecular genetics of primary open-angle glaucoma.
P2860
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P2860
Molecular and developmental mechanisms of anterior segment dysgenesis.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Molecular and developmental mechanisms of anterior segment dysgenesis.
@en
type
label
Molecular and developmental mechanisms of anterior segment dysgenesis.
@en
prefLabel
Molecular and developmental mechanisms of anterior segment dysgenesis.
@en
P2860
P356
P1433
P1476
Molecular and developmental mechanisms of anterior segment dysgenesis
@en
P2093
P2860
P2888
P304
P356
10.1038/SJ.EYE.6702852
P577
2007-10-01T00:00:00Z