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Article

Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis

21 Sept 2018

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Share to Dermatology and Skin Diseases
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Share to Psoriasis: Treatment and Pathogenesis

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30248356
DOI: 10.1016/j.jaci.2018.09.002

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitisPMID 30248356Read ↗

Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease.Semantic proximity Read ↗

Germline hypomorphic CARD11 mutations in severe atopic diseaseSemantic proximity Read ↗

Gain-of-Function Mutation of Card14 Leads to Spontaneous Psoriasis-like Skin Inflammation through Enhanced Keratinocyte Response to IL-17ASemantic proximity Read ↗

Clinical and Genetic Heterogeneity of CARD14 Mutations in Psoriatic Skin DiseaseSemantic proximity Read ↗

Psoriasis mutations disrupt CARD14 autoinhibition promoting BCL10-MALT1-dependent NF-κB activation.Semantic proximity Read ↗

CARD14-Mediated Activation of Paracaspase MALT1 in Keratinocytes: Implications for Psoriasis.Semantic proximity Read ↗

PSORS2 is due to mutations in CARD14.Semantic proximity Read ↗

Activating CARD14 Mutations Are Associated with Generalized Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis Vulgaris.Semantic proximity Read ↗

CARD14 alterations in Tunisian patients with psoriasis and further characterization in European cohorts.Semantic proximity Read ↗

Novel CARD11 Mutations in Human Cutaneous Squamous Cell Carcinoma Lead to Aberrant NF-κB Regulation.Semantic proximity Read ↗

Novel role for caspase recruitment domain family member 14 and its genetic variant rs11652075 in skin filaggrin homeostasis.Semantic proximity Read ↗

Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation.Semantic proximity Read ↗

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