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AHR promoter variant modulates its transcription and downstream effectors by allele-specific AHR-SP1 interaction functioning as a genetic marker for vitiligo.
- Published in:
- Scientific Reports, 2015, p. 13542, doi. 10.1038/srep13542
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- Publication type:
- Article
A nationwide survey of Aicardi–Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study.
- Published in:
- Rheumatology, 2014, v. 53, n. 3, p. 448, doi. 10.1093/rheumatology/ket372
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- Publication type:
- Article
Rothmund–Thomson syndrome—a single case report with systemic muscular atrophy, multiple organ fibrosis and pulmonary cachexia.
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- Rheumatology, 2012, v. 51, n. 11, p. 2109, doi. 10.1093/rheumatology/kes143
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- Publication type:
- Article
Confirmation of association of the macrophage migration inhibitory factor gene with systemic sclerosis in a large European population.
- Published in:
- Rheumatology, 2011, v. 50, n. 11, p. 1976, doi. 10.1093/rheumatology/ker259
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- Publication type:
- Article
Comment on: Low TNF-induced NF-κB and p38 phosphorylation levels in leucocytes in tumour necrosis factor receptor-associated periodic syndrome.
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- Rheumatology, 2011, v. 50, n. 8, p. 1525, doi. 10.1093/rheumatology/ker145
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- Publication type:
- Article
Comment on: Low TNF-induced NF-κB and p38 phosphorylation levels in leucocytes in tumour necrosis factor receptor-associated periodic syndrome: reply.
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- Rheumatology, 2011, v. 50, n. 8, p. 1526, doi. 10.1093/rheumatology/ker167
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- Publication type:
- Article
Comment on: Familial Mediterranean fever caused by homozygous E148Q mutation complicated by Budd–Chiari syndrome and polyarteritis nodosa: reply.
- Published in:
- 2011
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- Publication type:
- Letter
Comment on: Familial Mediterranean fever caused by homozygous E148Q mutation complicated by Budd–Chiari syndrome and polyarteritis nodosa.
- Published in:
- 2011
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- Publication type:
- Letter
A Japanese case of familial Mediterranean fever presenting diffuse bone marrow uptake of FDG-PET and high levels of neutrophil membrane CD64 expression.
- Published in:
- Rheumatology, 2011, v. 50, n. 6, p. 1171, doi. 10.1093/rheumatology/ker012
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- Publication type:
- Article
Familial Mediterranean fever caused by homozygous E148Q mutation complicated by Budd–Chiari syndrome and polyarteritis nodosa.
- Published in:
- Rheumatology, 2011, v. 50, n. 3, p. 624, doi. 10.1093/rheumatology/keq405
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- Publication type:
- Article
Study of the association between human leukocyte antigens ( HLA) and pemphigus vulgaris in Brazilian patients.
- Published in:
- International Journal of Dermatology, 2017, v. 56, n. 5, p. 557, doi. 10.1111/ijd.13577
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- Publication type:
- Article
Multiple Sclerosis: It Is Our Turn to Attack.
- Published in:
- Journal of Stem Cells, 2017, v. 12, n. 2, p. 81
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- Publication type:
- Article
Familial Risks between Pernicious Anemia and Other Autoimmune Diseases in the Population of Sweden.
- Published in:
- Autoimmune Diseases (2090-0422), 2021, v. 2021, p. 1, doi. 10.1155/2021/8815297
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- Publication type:
- Article
Inflammatory disorders associated with trisomy 8‐myelodysplastic syndromes: French retrospective case‐control study.
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- European Journal of Haematology, 2019, v. 102, n. 1, p. 63, doi. 10.1111/ejh.13174
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- Publication type:
- Article
Analysis of cell surface and intranuclear markers on non-stimulated human PBMC using mass cytometry.
- Published in:
- PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0194593
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- Publication type:
- Article
Identification and in silico analysis of functional SNPs of human TAGAP protein: A comprehensive study.
- Published in:
- PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0188143
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- Publication type:
- Article
Polymorphism in Exon 2 of CD1 Genes in Southwest of Iran.
- Published in:
- Iranian Journal of Public Health, 2013, v. 42, n. 7, p. 775
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- Publication type:
- Article
Pemphigus Vulgaris Activity Score and Assessment of Convergent Validity.
- Published in:
- Acta Medica Iranica, 2013, v. 51, n. 4, p. 224
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- Publication type:
- Article
Familial implications of autoimmune disease: Recurrence risks of alopecia areata and associated conditions in first‐degree relatives.
- Published in:
- Journal of Genetic Counseling, 2020, v. 29, n. 1, p. 35, doi. 10.1002/jgc4.1178
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- Publication type:
- Article
A single nucleotide polymorphism rs9468925 of MHC region is associated with clinical features of generalized vitiligo in Chinese Han population.
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- Journal of the European Academy of Dermatology & Venereology, 2012, v. 26, n. 9, p. 1137, doi. 10.1111/j.1468-3083.2011.04259.x
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- Publication type:
- Article
B-Cell Infiltrates Induce Endosteal Bone Formation in Inflammatory Arthritis.
- Published in:
- Journal of Bone & Mineral Research, 2008, v. 23, n. 10, p. 1650, doi. 10.1359/jbmr.080508
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- Publication type:
- Article
Ig-like transcript 4 as a cellular receptor for soluble complement fragment C4d.
- Published in:
- FASEB Journal, 2016, v. 30, n. 4, p. 1492, doi. 10.1096/fj.15-275594
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- Publication type:
- Article
Epigenetics in Rheumatology Research.
- Published in:
- International Journal of Advances in Rheumatology, 2011, v. 9, n. 1, p. 17
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- Publication type:
- Article
Genetic Polymorphisms in Juvenile Idiopathic Arthritis: Effects on Disease and Therapy.
- Published in:
- International Journal of Advances in Rheumatology, 2010, v. 8, n. 1, p. 8
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- Publication type:
- Article
Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases.
- Published in:
- 2001
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- Publication type:
- journal article
Neonatal beta-cell apoptosis: a trigger for autoimmune diabetes?
- Published in:
- 2000
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- Publication type:
- journal article
Interleukin-2-330T/G and Interleukin-10-1082A/G Genetic Polymorphisms and B-Cell Non-Hodgkin Lymphoma.
- Published in:
- Turkish Journal of Hematology, 2018, v. 35, n. 4, p. 301, doi. 10.4274/tjh.2018.0189
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- Publication type:
- Article
CTLA-4 A49G polymorphism and autoimmune blood disease: A comment.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population.
- Published in:
- BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-81
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- Publication type:
- Article
How Promiscuity Promotes Tolerance: The Case of Myasthenia Gravis.
- Published in:
- Annals of the New York Academy of Sciences, 2008, v. 1132, p. 157, doi. 10.1196/annals.1405.026
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- Publication type:
- Article
Genetics of autoimmune diseases — disorders of immune homeostasis.
- Published in:
- Nature Reviews Genetics, 2006, v. 7, n. 12, p. 917, doi. 10.1038/nrg1944
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- Publication type:
- Article
Congenic strains displaying similar clinical phenotype of arthritis represent different immunologic models of inflammation.
- Published in:
- Genes & Immunity, 2008, v. 9, n. 7, p. 591, doi. 10.1038/gene.2008.54
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- Publication type:
- Article
A polymorphic variant of the gene coding desmoglein 1, the target autoantigen of pemphigus foliaceus, is associated with the disease.
- Published in:
- Genes & Immunity, 2001, v. 2, n. 1, p. 41, doi. 10.1038/sj.gene.6363718
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- Publication type:
- Article
Comment on "Relationship between the IL12B (rs3212227) gene polymorphism and susceptibility to multiple autoimmune diseases: a meta-analysis".
- Published in:
- Modern Rheumatology, 2017, v. 27, n. 1, p. 178, doi. 10.3109/14397595.2016.1170751
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- Publication type:
- Article
Response to the comment on "Relationship between the IL12B (rs3212227) gene polymorphism and susceptibility to multiple autoimmune diseases: A meta-analysis".
- Published in:
- Modern Rheumatology, 2017, v. 27, n. 1, p. 180, doi. 10.1080/14397595.2016.1205779
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- Publication type:
- Article
Influence of thiopurine S‐methyltransferase polymorphisms in mercaptopurine pharmacokinetics in healthy volunteers.
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- Basic & Clinical Pharmacology & Toxicology, 2019, v. 124, n. 4, p. 449, doi. 10.1111/bcpt.13153
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- Publication type:
- Article
A microRNA sponge, LINC02193, promotes neutrophil activation by upregulating ICAM1 and is correlated with ANCA-associated vasculitis.
- Published in:
- Rheumatology, 2024, v. 63, n. 8, p. 2295, doi. 10.1093/rheumatology/kead605
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- Publication type:
- Article
Parental autoimmunity and offspring risks of rheumatic diseases: a nationwide population-based study.
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- Rheumatology, 2024, v. 63, n. 8, p. 2189, doi. 10.1093/rheumatology/kead562
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- Publication type:
- Article
Kidney disease in eosinophilic granulomatosis with polyangiitis: expect the unexpected.
- Published in:
- 2021
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- Publication type:
- Editorial
Current and future advances in genetic testing in systemic autoinflammatory diseases.
- Published in:
- Rheumatology, 2019, v. 58, p. vi44, doi. 10.1093/rheumatology/kez294
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- Publication type:
- Article
PR3-ANCA-associated vasculitis is associated with a specific motif in the peptide-binding cleft of HLA-DP molecules.
- Published in:
- Rheumatology, 2019, v. 58, n. 11, p. 1942, doi. 10.1093/rheumatology/kez111
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- Publication type:
- Article
Family history of systemic lupus erythematosus and risk of autoimmune disease: Nationwide Cohort Study in Denmark 1977-2013.
- Published in:
- Rheumatology, 2017, v. 56, n. 6, p. 957, doi. 10.1093/rheumatology/kex005
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- Publication type:
- Article
Familial aggregation of rheumatoid arthritis and co-aggregation of autoimmune diseases in affected families: a nationwide population-based study.
- Published in:
- Rheumatology, 2017, v. 56, n. 6, p. 928, doi. 10.1093/rheumatology/kew500
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- Publication type:
- Article
Epigenetics and Autoimmune Thyroid Diseases.
- Published in:
- Frontiers in Endocrinology, 2017, p. 1, doi. 10.3389/fendo.2017.00149
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- Publication type:
- Article
A switch-variant model integrates the functions of an autoimmune variant of the phosphatase PTPN22.
- Published in:
- Science Signaling, 2018, v. 11, n. 526, p. 1, doi. 10.1126/scisignal.aat0936
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- Publication type:
- Article
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations.
- Published in:
- Genome Medicine, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13073-018-0604-8
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- Publication type:
- Article
Strong Similarities in Turkish and European Patients Diagnosed with APECED Syndrome.
- Published in:
- Turkish Journal of Endocrinology & Metabolism, 2015, v. 19, n. 3, p. 89, doi. 10.4274/tjem.2987
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- Publication type:
- Article
Give GWAS a Chance.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Sulfotyrosine Recognition as Marker for Druggable Sites in the Extracellular Space.
- Published in:
- International Journal of Molecular Sciences, 2011, v. 12, n. 6, p. 3740, doi. 10.3390/ijms12063740
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- Publication type:
- Article
MiR-146a G/C rs2910164 variation in South African Indian and Caucasian patients with psoriatic arthritis.
- Published in:
- BMC Medical Genetics, 2018, v. 19, p. 1, doi. 10.1186/s12881-018-0565-1
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- Publication type:
- Article