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Titlebook: Cytokines and Joint Injury; Wim B. Berg,Pierre Miossec Book 2004 Springer Basel AG 2004 Arthritis.bone.cytokine.cytokines.diseases.inflamm

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書目名稱Cytokines and Joint Injury
編輯Wim B. Berg,Pierre Miossec
視頻videohttp://file.papertrans.cn/243/242642/242642.mp4
概述Gives a balanced view on central cytokines and joint pathology.International authorship
叢書名稱Progress in Inflammation Research
圖書封面Titlebook: Cytokines and Joint Injury;  Wim B. Berg,Pierre Miossec Book 2004 Springer Basel AG 2004 Arthritis.bone.cytokine.cytokines.diseases.inflamm
描述The purpose of this volume in the Progress in Inflammation Research series is to provide the biomedical and clinical researcher with a state-of-the-art insight in the role of cytokines in joint inflammation and joint destruction. This is of relevance for better understanding of key processes in diseases such as rheumatoid arthritis (RA) and osteoarthritis (OA). Apart from the impact of old and novel cytokines on joint tissues, the various chapters address the issue of targeted therapy with biological response modifiers and future interventions with carefully designed inhibitors. Spe- cial attention is given to elements of synovial cell activation, cell-cell interaction, cytokine interplay as well as mechanisms of cartilage destruction and bone erosion. In addition to an outline of the role of established cytokines, such as TNF, IL-l and IL-6, new information is given on the novel cytokines IL-15, IL-17 and IL-18 and their positioning in the complex cytokine interplay. Cytokine regulation of destructive enzymes, RANKL, the endogenous inhibitor OPG and their crucial roles as central players in joint erosion are highlighted. Together, the chapters provide a complete and balanced view
出版日期Book 2004
關(guān)鍵詞Arthritis; bone; cytokine; cytokines; diseases; inflammation; joint; necrosis; osteoarthritis; pathology; prot
版次1
doihttps://doi.org/10.1007/978-3-0348-7883-8
isbn_softcover978-3-0348-9609-2
isbn_ebook978-3-0348-7883-8Series ISSN 1422-7746 Series E-ISSN 2296-4525
issn_series 1422-7746
copyrightSpringer Basel AG 2004
The information of publication is updating

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Robert J. Klaassen MD,Nancy L. Young PhD historical approach to the definition of TNFα as a therapeutic target that has heralded three blockbuster drugs and consolidated the future of ‘biodrugs’ as an important sector of future pharmaceutical products.
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Jochen H. O. Hoffmann,Alexander H. Enkd immunocompetent cells into the extravascular space. IL-1 is also an angiogenic factor and plays a role in tumor metastasis and blood vessel supply [.]. Mice lacking IL-1 receptors fail to develop proliferative lesions of vascular smooth muscle cells in mechanically injured arteries. In humans with
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Current IgG Products and Future Perspectiveshe human. An important distinction between these two molecules is that pro-IL-1β is biologically inactive, whereas both pro-IL-lα and mature IL-lα exhibit full receptor binding activity. In addition, to its biologic effects following receptor binding, pro-IL-lα exerts other functions inside cells [.
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