Association of functional polymorphisms related to the transcriptional level of FOXP3 with prognosis of autoimmune thyroid diseases. - Wikidata - awgldk - TriplyDB

Association of functional polymorphisms related to the transcriptional level of FOXP3 with prognosis of autoimmune thyroid diseases.

Association of functional polymorphisms related to the transcriptional level of FOXP3 with prognosis of autoimmune thyroid diseases.

http://www.wikidata.org/entity/Q53295920

about

Hypothyroidism among pediatric patients with type 1 diabetes mellitus, from patients' characteristics to disease severity Regulatory T Cell and Forkhead Box Protein 3 as Modulators of Immune Homeostasis Hashimoto's Thyroiditis: From Genes to the Disease.Dissecting the role of the FOXP3 gene in the joint genetic susceptibility to autoimmune thyroiditis and diabetes: a genetic and functional analysis Disturbances of modulating molecules (FOXP3, CTLA-4/CD28/B7, and CD40/CD40L) mRNA expressions in the orbital tissue from patients with severe graves' ophthalmopathy The relationship between skewed X chromosome inactivation and the prognosis of Graves' and Hashimoto's diseases.Association between functional polymorphisms of Foxp3 gene and the occurrence of unexplained recurrent spontaneous abortion in a Chinese Han population.Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome.Genetic factors of autoimmune thyroid diseases in Japanese Investigation of FOXP3 genetic variations at positions -2383 C/T and IVS9+459 T/C in southern Iranian patients with lung carcinoma.Male gender bias in autism and pediatric autoimmunity Immunogenetics of autoimmune thyroid diseases: A comprehensive review.Associations of FoxP3 gene polymorphisms with severe recurrent respiratory papillomatosis in Korean patients.The dual role of the X-linked FoxP3 gene in human cancers Genetic polymorphism in FOXP3 gene: imbalance in regulatory T-cell role and development of human diseases.Association of Foxp3 Polymorphism With Allograft Outcome in Kidney Transplantation Association between FOXP3 polymorphisms and susceptibility to autoimmune diseases: A meta-analysis.Nonsegmental vitiligo and autoimmune mechanism.FOXP3 genetic variant and risk of acute coronary syndrome in Chinese Han population.The serum level of transforming growth factor beta1 and its association with Foxp3 gene polymorphism in Iranian women with recurrent spontaneous abortion.Association between FOXP3 polymorphisms and vitiligo in a Han Chinese population.Role of Foxp3 gene in maternal susceptibility to pre-eclampsia - a study from South India.Foxp3 promoter polymorphism (rs3761548) in breast cancer progression: a study from India.Association of aplastic anemia and FoxP3 gene polymorphisms in Koreans.The role of regulatory T cells and genes involved in their differentiation in pathogenesis of selected inflammatory and neoplastic skin diseases. Part III: Polymorphisms of genes involved in Tregs' activation and function.Role of the T and B lymphocytes in pathogenesis of autoimmune thyroid diseases.Analysis of chosen polymorphisms in FoxP3 gene in children and adolescents with autoimmune thyroid diseases.The IL15 +96522 A>T functional polymorphism is related to the differentiation of Th17 cells and the severity of Hashimoto's disease.Association between functional SIRT1 polymorphisms and the clinical characteristics of patients with autoimmune thyroid disease.Significant association between FOXP3 gene polymorphism and steroid-resistant acute rejection in living donor liver transplantation.The functional polymorphisms of VDR, GC and CYP2R1 are involved in the pathogenesis of autoimmune thyroid diseases.The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto's Thyroiditis.The synergic effects of CTLA-4/Foxp3-related genotypes and chromosomal aberrations on the risk of recurrent spontaneous abortion among a Chinese Han population.Nivolumab-induced thyroid dysfunction lacking antithyroid antibody is frequently evoked in Japanese patients with malignant melanoma.Associations between autoimmune thyroid disease prognosis and functional polymorphisms of susceptibility genes, CTLA4, PTPN22, CD40, FCRL3, and ZFAT, previously revealed in genome-wide association studies Novel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto's thyroiditis The -> and -> in the Gene Are Associated With Viral Load and Liver Enzyme Levels in Patients With Chronic Viral Liver Diseases

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P2860

Association of functional polymorphisms related to the transcriptional level of FOXP3 with prognosis of autoimmune thyroid diseases.

http://www.wikidata.org/entity/Q53295920

description

2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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2010年學術文章

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name

Association of functional poly ...... f autoimmune thyroid diseases.

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Association of functional poly ...... f autoimmune thyroid diseases.

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type

label

Association of functional poly ...... f autoimmune thyroid diseases.

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Association of functional poly ...... f autoimmune thyroid diseases.

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Association of functional poly ...... f autoimmune thyroid diseases.

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Association of functional poly ...... f autoimmune thyroid diseases.

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Clinical and Experimental Immunology

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Association of functional poly ...... f autoimmune thyroid diseases.

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K Tatsumi

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M Morita

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M Watanabe

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P2860

FOXP3 controls regulatory T cell function through cooperation with NFAT

Crucial role of FOXP3 in the development and function of human CD25+CD4+ regulatory T cells

Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population.

A functional polymorphism in the promoter/enhancer region of the FOXP3/Scurfin gene associated with type 1 diabetes.

Association of serum antithyroid antibodies with lymphocytic infiltration of the thyroid gland: studies of seventy autopsied cases.

Yin-Yang 1 activates interleukin-4 gene expression in T cells.

Independent involvement of CD8+ CD25+ cells and thyroid autoantibodies in disease severity of Hashimoto's disease.

Ex vivo generated regulatory T cells modulate experimental autoimmune myasthenia gravis.

Intron-1 rs3761548 is related to the defective transcription of Foxp3 in psoriasis through abrogating E47/c-Myb binding.

The regulatory T cell gene FOXP3 and genetic susceptibility to thyroid autoimmunity: an association analysis in Caucasian and Japanese cohorts.

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