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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

Genetic susceptibility to autoimmune thyroid disease: past, present, and future

http://www.wikidata.org/entity/Q34171280

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The role of thyrotrophin receptor antibody assays in graves' disease Vitamin D and chronic hepatitis C: effects on success rate and prevention of side effects associated with pegylated interferon-α and ribavirin Fetal microchimeric cells in autoimmune thyroid diseases: harmful, beneficial or innocent for the thyroid gland?Autoimmune and neoplastic thyroid diseases associated with hepatitis C chronic infection Atopy and autoimmune thyroid diseases: melatonin can be useful?The ontology of genetic susceptibility factors (OGSF) and its application in modeling genetic susceptibility to vaccine adverse events Novel associations for hypothyroidism include known autoimmune risk loci Prevalence of anti-Neu5Gc antibodies in patients with hypothyroidism.Association of BTG2, CYR61, ZFP36, and SCD gene polymorphisms with Graves' disease and ophthalmopathy.Polymorphisms in the TNFA and IL6 genes represent risk factors for autoimmune thyroid disease Fetal microchimeric cells in blood of women with an autoimmune thyroid disease.mRNA-Seq reveals novel molecular mechanisms and a robust fingerprint in Graves' disease.Autoimmune thyroid diseases in children.Thyrotropin receptor and CD40 mediate interleukin-8 expression in fibrocytes: implications for thyroid-associated ophthalmopathy (an American Ophthalmological Society thesis)Graves' disease in monozygotic twins - a case report.Replication of association of nine susceptibility loci with Graves' disease in the Chinese Han population Comparative Study of Alterations in Tri-iodothyronine (T3) and Thyroxine (T4) Hormone Levels in Breast and Ovarian Cancer.Cutting edge: the etiology of autoimmune thyroid diseases.Novel variant of thyroglobulin promoter triggers thyroid autoimmunity through an epigenetic interferon alpha-modulated mechanism.Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies Genetic factors of autoimmune thyroid diseases in Japanese Delineating the autoimmune mechanisms in Graves' disease New genetic insights from autoimmune thyroid disease.Selective IgA deficiency in autoimmune diseases Prevalence of unknown thyroid disorders in a Sardinian cohort Differences in Gene-Gene Interactions in Graves' Disease Patients Stratified by Age of Onset.Association of Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4) Gene Polymorphisms with Autoimmune Thyroid Disease in Children and Adults: Case-Control Study.Fetal microchimeric cells in blood and thyroid glands of women with an autoimmune thyroid disease.Genetic profiling in Graves' disease: further evidence for lack of a distinct genetic contribution to Graves' ophthalmopathy.Shared Genetic Basis for Type 1 Diabetes, Islet Autoantibodies, and Autoantibodies Associated With Other Immune-Mediated Diseases in Families With Type 1 Diabetes CTLA-4 gene polymorphisms and their influence on predisposition to autoimmune thyroid diseases (Graves' disease and Hashimoto's thyroiditis).CD40 Expression in Fibrocytes Is Induced by TSH: Potential Synergistic Immune Activation.Genetics of autoimmune thyroid disease in the Lebanese population.Indices of thyroid epidemiology Autoimmune thyroid disease in rheumatoid arthritis: a global perspective The pathophysiology of thyroid eye disease: implications for immunotherapy.Associations of autoantibodies, autoimmune risk alleles, and clinical diagnoses from the electronic medical records in rheumatoid arthritis cases and non-rheumatoid arthritis controls.Genetic and epigenetic mechanisms in thyroid autoimmunity.Association between age at diagnosis of Graves' disease and variants in genes involved in immune response Association between the IL1B (-511), IL1B (+3954), IL1RN (VNTR) polymorphisms and Graves' disease risk: a meta-analysis of 11 case-control studies.

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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

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2010 nî lūn-bûn

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2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2010年の論文

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2010年論文

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2010年論文

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2010年论文

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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

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Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

Recurring mutations found by sequencing an acute myeloid leukemia genome

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity: back to the future

A haplotype map of the human genome

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

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