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Article

A novel RIPK4–IRF6 connection is required to prevent epithelial fusions characteristic for popliteal pterygium syndromes

28 Nov 2014

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25430793
DOI: 10.1038/cdd.2014.191

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A novel RIPK4–IRF6 connection is required to prevent epithelial fusions characteristic for popliteal pterygium syndromesPMID 25430793Read ↗

Receptor-interacting Protein Kinase 4 and Interferon Regulatory Factor 6 Function as a Signaling Axis to Regulate Keratinocyte DifferentiationSemantic proximity Read ↗

Unravelling the molecular tapestry of pterygium: insights into genes for diagnostic and therapeutic innovationsSemantic proximity Read ↗

Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders.Semantic proximity Read ↗

Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome.Semantic proximity Read ↗

Van der Woude and Popliteal Pterygium Syndromes: Broad intrafamilial variability in a three generation family with mutation in IRF6.Semantic proximity Read ↗

Variable phenotypic manifestation of IRF6 mutations in the Van der Woude syndrome and popliteal pterygium syndrome: implications for genetic counseling.Semantic proximity Read ↗

RIPK4 regulates cell–cell adhesion in epidermal development and homeostasisSemantic proximity Read ↗

Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus.Semantic proximity Read ↗

Transcriptome Analysis of Pterygium and Pinguecula Reveals Evidence of Genomic Instability Associated with Chronic InflammationSemantic proximity Read ↗

Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and MaintenanceSemantic proximity Read ↗

Mechanisms and biomarker candidates in pterygium developmentSemantic proximity Read ↗

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