| P50 | author | Frank van de Veerdonk | Q92689750 |
| P2093 | author name string | Steven M Holland | |
| | Elise M N Ferre | |
| | Michail S Lionakis | |
| | Muthulekha Swamydas | |
| | Mukil Natarajan | |
| | Lindsey B Rosen | |
| | Ofer Zimmerman | |
| P2860 | cites work | Inhibition of Stat1-mediated gene activation by PIAS1 | Q24310082 |
| | An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains | Q24313206 |
| | Transcriptional regulation by STAT1 and STAT2 in the interferon JAK-STAT pathway | Q24622379 |
| | Deletional tolerance mediated by extrathymic Aire-expressing cells | Q24652952 |
| | Inborn errors of human STAT1: allelic heterogeneity governs the diversity of immunological and infectious phenotypes | Q26825342 |
| | Redefined clinical features and diagnostic criteria in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy | Q27333247 |
| | Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases | Q28116288 |
| | Interferon activation of the transcription factor Stat91 involves dimerization through SH2-phosphotyrosyl peptide interactions | Q28118180 |
| | Projection of an immunological self shadow within the thymus by the aire protein | Q28207164 |
| | A Novel Heterozygous Mutation in the STAT1 SH2 Domain Causes Chronic Mucocutaneous Candidiasis, Atypically Diverse Infections, Autoimmunity, and Impaired Cytokine Regulation | Q30841541 |
| | Chronic mucocutaneous candidiasis in APECED or thymoma patients correlates with autoimmunity to Th17-associated cytokines | Q33348588 |
| | Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I | Q33656182 |
| | STAT1 mutations in autosomal dominant chronic mucocutaneous candidiasis | Q34196284 |
| | Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype | Q34523567 |
| | A novel form of human STAT1 deficiency impairing early but not late responses to interferons | Q34541567 |
| | Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis | Q35144610 |
| | Immune tolerance. Regulatory T cells generated early in life play a distinct role in maintaining self-tolerance | Q36455565 |
| | Mechanisms of an autoimmunity syndrome in mice caused by a dominant mutation in Aire | Q36540892 |
| | Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome | Q36901678 |
| | Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genes | Q36960285 |
| | Signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations and disseminated coccidioidomycosis and histoplasmosis | Q37101568 |
| | Refractory disseminated coccidioidomycosis and mycobacteriosis in interferon-gamma receptor 1 deficiency | Q37314463 |
| | Aire | Q37419376 |
| | Functional interaction of AIRE with PIAS1 in transcriptional regulation | Q40034953 |
| | Ruxolitinib reverses dysregulated T helper cell responses and controls autoimmunity caused by a novel signal transducer and activator of transcription 1 (STAT1) gain-of-function mutation. | Q40352195 |
| | Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations | Q40379041 |
| | Aire Inhibits the Generation of a Perinatal Population of Interleukin-17A-Producing γδ T Cells to Promote Immunologic Tolerance. | Q40449499 |
| | Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. | Q40479586 |
| | Chronic mucocutaneous candidiasis associated with an SH2 domain gain-of-function mutation that enhances STAT1 phosphorylation | Q40765767 |
| | AIRE-Deficient Patients Harbor Unique High-Affinity Disease-Ameliorating Autoantibodies | Q41819064 |
| | Aire Enforces Immune Tolerance by Directing Autoreactive T Cells into the Regulatory T Cell Lineage | Q41982942 |
| | Recurrent herpes simplex virus infection in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy associated with L29P and IVS9-1G>C compound heterozygous autoimmune regulator gene mutations | Q45403313 |
| | Determination of human anticytokine autoantibody profiles using a particle-based approach. | Q50520646 |
| | A novel mutation of the autoimmune regulator gene in an Italian kindred with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy, acting in a dominant fashion and strongly cosegregating with hypothyroid autoimmune thyroiditis. | Q55035365 |
| | Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene. | Q55042744 |
| | Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. | Q55057090 |
| | Interferon-gamma receptor 2 expression as the deciding factor in human T, B, and myeloid cell proliferation or death | Q77338031 |
| P304 | page(s) | 820 | |
| P577 | publication date | 2017-07-14 | |
| P1433 | published in | Frontiers in Immunology | Q27723748 |
| P1476 | title | Autoimmune Regulator Deficiency Results in a Decrease in STAT1 Levels in Human Monocytes | |
| P478 | volume | 8 | |