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Article

Analysis of Genes Associated With Monogenic Primary Immunodeficiency Identifies Rare Variants in XIAP in Patients With Crohn’s Disease

5 Mar 2018

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Share to Autoimmune and Inflammatory Disorders Research
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 29501442
DOI: 10.1053/j.gastro.2018.02.028

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Related research

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Analysis of Genes Associated With Monogenic Primary Immunodeficiency Identifies Rare Variants in XIAP in Patients With Crohn’s DiseasePMID 29501442Read ↗

XIAP variants in male Crohn's disease.Semantic proximity Read ↗

Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study.Semantic proximity Read ↗

A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case reportSemantic proximity Read ↗

An overview of germline variations in genes of primary immunodeficiences through integrative analysis of ClinVar, HGMD® and dbSNP databases.Semantic proximity Read ↗

How genetic testing can lead to targeted management of XIAP deficiency-related inflammatory bowel disease.Semantic proximity Read ↗

Identification of Variants in Genes Associated with Single-gene Inflammatory Bowel Disease by Whole-exome Sequencing.Semantic proximity Read ↗

Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.Semantic proximity Read ↗

X-linked inhibitor of apoptosis protein deficiency complicated with Crohn's disease-like enterocolitis and Takayasu arteritis: A case report.Semantic proximity Read ↗

Novel XIAP mutation causing enhanced spontaneous apoptosis and disturbed NOD2 signalling in a patient with atypical adult-onset Crohn's disease.Semantic proximity Read ↗

Phenotype, genotype, treatment, and survival outcomes in patients with X-linked inhibitor of apoptosis deficiency.Semantic proximity Read ↗

Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease.Semantic proximity Read ↗

Primary Immunodeficiencies and Inflammatory Disease: A Growing Genetic Intersection.Semantic proximity Read ↗

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