Titlebook: ;

purulent

書目名稱Gut-Associated Lymphoid Tissues影響因子(影響力)




書目名稱Gut-Associated Lymphoid Tissues影響因子(影響力)學科排名




書目名稱Gut-Associated Lymphoid Tissues網(wǎng)絡(luò)公開度




書目名稱Gut-Associated Lymphoid Tissues網(wǎng)絡(luò)公開度學科排名




書目名稱Gut-Associated Lymphoid Tissues被引頻次




書目名稱Gut-Associated Lymphoid Tissues被引頻次學科排名




書目名稱Gut-Associated Lymphoid Tissues年度引用




書目名稱Gut-Associated Lymphoid Tissues年度引用學科排名




書目名稱Gut-Associated Lymphoid Tissues讀者反饋




書目名稱Gut-Associated Lymphoid Tissues讀者反饋學科排名

打谷工具

注意到

Gerrit Krupski-Berdien MD,Volkmar Nicolas MDboth types of lymphoid organs. In the adult, a similar population of cells, termed lymphoid tissue inducer-like cells (LTi-like cells), supports the formation of organized gut-associated lymphoid tissue (GALT) in the intestine, including both isolated lymphoid follicles (ILFs) and cryptopatches (CPs

浪費物質(zhì)

The Treatment of Pulmonary Atresiahis process is their adhesion to microvascular endothelium and subsequent diapedesis into a target tissue. Naive and effector/memory T and B cells possess distinct repertoires of traffic molecules that restrict their ability to interact with specialized microvessels in different anatomic compartment

Crayon

Victor H. Frankel,James W. Pughde-ranging impact on host immunity and physiology. One adaptation following intestinal colonisation is increased production and secretion of polyspecific intestinal IgA. In contrast to the strong mucosal immune response to bacterial colonisation, the systemic immune system remains ignorant of these

euphoria

euphoria

美學

Osteotomy: General Concepts and Indications,mmune responses are critical for preventing invasion by pathogens. In this chapter, we review structural studies that have illuminated various aspects of mucosal immunity. Crystal structures of IgA1-Fc and IgA-binding fragments of the polymeric immunoglobulin receptor and FcαRI, combined with models

Measured

規(guī)范要多

Molecular Networks Orchestrating GALT Development,estration. Mesenteric lymph nodes (LNs) and Peyer’s patches (PPs) are localized in proximity to mucosal surfaces, and their development is coordinated by a series of temporally and spatially regulated molecular events involving the collaboration between hematopoietic, mesenchymal, and, for PPs, epit