Autoimmune polyendocrinopathy syndrome type 1 (APS1) and AIRE gene: new views on molecular basis of autoimmunity.
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Summary
Identification of the AIRE gene, detailed characterization of molecular pathogenesis of human APS1 as well as analyses of mouse models carrying targeted interruption of Aire gene have provided new views on the understanding of molecular background of autoimmunity.
- Type
- article
- Published
- 2005-01-01
- Cited by
- 124
- References
- 45
- Access
- Open access
- OpenAlex
- https://openalex.org/W16290093
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:12369840
Keywords
Nomination, Political science, Advertising, Business, Computer science
References
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- A signature motif in transcriptional co-activators mediates binding to nuclear receptors
- The SAND domain structure defines a novel DNA-binding fold in transcriptional regulation
- Development of Autoimmunity against Transcriptionally Unrepressed Target Antigen in the Thymus of Aire-Deficient Mice1
- Two different cytochrome P450 enzymes are the adrenal antigens in autoimmune polyendocrine syndrome type I and Addison's disease.
- Identification by molecular cloning of an autoantigen associated with Addison's disease as steroid 17 alpha-hydroxylase.
- Autoimmune regulator induced changes in the gene expression profile of human monocyte-dendritic cell-lineage.
- Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED
- Aire regulates negative selection of organ-specific T cells
- The PHD finger: implications for chromatin-mediated transcriptional regulation.
- Self-representation in the thymus: an extended view
- AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype.
- The cellular mechanism of Aire control of T cell tolerance.
- RNA and protein expression of the murine autoimmune regulator gene (Aire) in normal, RelB‐deficient and in NOD mouse
- Positional cloning of the APECED gene
- Autoantibodies to cytochrome P450 enzymes P450scc, P450c17, and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease.
- Analysis of antibody reactivity against cysteine sulfinic acid decarboxylase, a pyridoxal phosphate-dependent enzyme, in endocrine autoimmune disease.
- 21-Hydroxylase, a major autoantigen in idiopathic Addison's disease.
- Subcellular Localization of the Autoimmune Regulator Protein
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- CRITICAL ROLE OF SUPEROXIDE PRODUCTION IN THE PATHOGENESIS OF AUTOIMMUNE DIABETES
- Estudio molecular de los genes CDKN1B y CITED2 en mujeres con falla ovárica prematura idiopática
- Functional and cellular analysis of autoimmune regulator (AIRE) protein
- Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy
- Mulibrey nanism: Characterization of hypogonadism, infertility and tumors
- Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy: known and novel aspects of the syndrome
- Roles of zinc and zinc signaling in immunity: zinc as an intracellular signaling molecule.
- Autoimmune polyglandular syndrome type 1 in Saudi children.
- Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy (APECED) in Sicily: confirmation that R203X is the peculiar AIRE gene mutation
- Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune Phenotype1
- Aire deficiency results in decreased expression of CCR4 and CCR7 ligands and in delayed migration of CD4+ thymocytes
- FROM DISEASE TO THE GENE - Identification of arthritis-regulating loci in rats
- Phenotypic and functional analysis of the mesenchymal stromal cell compartment in the thymus
- Cellular immune responses to low density lipoprotein in atherosclerosis
- Control of Central and Peripheral Tolerance by Aire
- Effector mechanisms of the autoimmune syndrome in the murine model of Autoimmune Polyglandular Syndrome Type 1
- Autoimmune Regulator protein interaction with DNA-dependent protein kinase and its role in apoptosis
- Mucocutaneous candidiasis and autoimmunity against cytokines in APECED and thymoma patients: Clinical and pathogenetic implications
- A paucity of colonic enteroendocrine and/or enterochromaffin cells characterizes a subset of patients with chronic unexplained diarrhea/malabsorption
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