The Glu228Ala polymorphism in the ligand-binding domain of death receptor 4 is not associated with rheumatoid arthritis

التفاصيل البيبلوغرافية
العنوان: The Glu228Ala polymorphism in the ligand-binding domain of death receptor 4 is not associated with rheumatoid arthritis
المؤلفون: U. Langsenlehner, H.-P. Brezinschek, Babak Yazdani-Biuki, W. Renner, Fürst F, Truschnig M, P. Krippl, Winfried Graninger, Kerstin Brickmann
المصدر: Annals of the Rheumatic Diseases. 67:1053-1054
بيانات النشر: BMJ, 2008.
سنة النشر: 2008
مصطلحات موضوعية: Male, musculoskeletal diseases, medicine.medical_specialty, Immunology, Inflammation, Polymorphism, Single Nucleotide, Receptors, Tumor Necrosis Factor, General Biochemistry, Genetics and Molecular Biology, Etanercept, Arthritis, Rheumatoid, Rheumatology, Internal medicine, Adalimumab, Animals, Humans, Immunology and Allergy, Medicine, Genetic Predisposition to Disease, skin and connective tissue diseases, Autoimmune disease, business.industry, medicine.disease, Infliximab, Receptors, TNF-Related Apoptosis-Inducing Ligand, Rheumatoid arthritis, Female, Tumor necrosis factor alpha, medicine.symptom, business, medicine.drug
الوصف: Rheumatoid arthritis (RA) is a chronic inflammatory disease resulting in inflammation of the synovial lining and destruction of the adjacent bone and cartilage. Although the initiating event of RA is still unknown, recent research has demonstrated the importance of the increased production of tumour necrosis factor (TNF) α in the perpetuation of the inflammatory process of this disease. Targeting this molecule with soluble receptors—that is, etanercept, or antibodies, like infliximab or adalimumab, a new class of highly effective antirheumatic drugs has been developed. Unfortunately, not all patients respond sufficiently to TNF blockade or become unresponsive, and therefore …
تدمد: 0003-4967
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e9e6f43484688fdf8259001e097558dTest
https://doi.org/10.1136/ard.2007.086124Test
رقم الانضمام: edsair.doi.dedup.....0e9e6f43484688fdf8259001e097558d
قاعدة البيانات: OpenAIRE