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Titlebook: Activating and Inhibitory Immunoglobulin-like Receptors; Max D. Cooper,Toshiyuki Takai,Jeffrey V. Ravetch Conference proceedings 2001 Spri

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發(fā)表于 2025-3-21 17:04:00 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Activating and Inhibitory Immunoglobulin-like Receptors
影響因子2023Max D. Cooper,Toshiyuki Takai,Jeffrey V. Ravetch
視頻videohttp://file.papertrans.cn/145/144152/144152.mp4
圖書封面Titlebook: Activating and Inhibitory Immunoglobulin-like Receptors;  Max D. Cooper,Toshiyuki Takai,Jeffrey V. Ravetch Conference proceedings 2001 Spri
影響因子A remarkable spectrum of novel immunoreceptors sharing related immunoglobulin-like domains and signaling potential has been identified in recent years. These receptors have attracted widespread interest because they resemble the TCR, BCR, and FcR complexes in their ability to serve as activating or inhibitory receptors on the cells that bear them. Moreover, they are well positioned to affect both innate and adaptive immunity. The full range of ligands for these new receptor families is still not known, and understanding of their physiological roles is far from complete. This volume is the first attempt to summarize and highlight all known aspects of immunoglobulin-like receptors, providing a topical overview of the roles and characteristic features of the immunoglobulin-like receptors and related molecules in the immune system. Researchers in immunology, molecular biology, cell biology, clinical medicine, and pharmacology will find this book invaluable.
Pindex Conference proceedings 2001
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cent years. These receptors have attracted widespread interest because they resemble the TCR, BCR, and FcR complexes in their ability to serve as activating or inhibitory receptors on the cells that bear them. Moreover, they are well positioned to affect both innate and adaptive immunity. The full r
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https://doi.org/10.1007/978-981-97-2724-7long to an ancient ancestral lineage of related Ig-like receptor families. A phylogenetic analysis, employing primary amino acid sequences and three-dimensional protein structures of the PIR homologs and their relatives, suggests a common ancestry for the PIR and Fc receptor families.
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https://doi.org/10.1007/978-3-030-50228-7lasmic tail and a charged amino acid in its transmembrane region, which is characteristic of an activatory receptor. Additionally, the translation starts at a different codon, if compared to other family members.
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https://doi.org/10.1007/978-3-030-50228-7y, gp49 molecules are also upregulated in the context of murine cytomegalovirus infection. Furthermore, the gp49 molecules do not appear to display allelic polymorphism, suggesting a unique functional role for gp49 molecules in regulating NK cells long after initial stimuli.
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