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1 e ILFs (organized lymphoid aggregates with a follicle-associated epithelium).
2 ganized lymphoid tissues and the specialized follicle-associated epithelium.
3 c lpfC mutant did not destroy M cells of the follicle-associated epithelium.
4 gh the specialized epithelial M cells of the follicle-associated epithelium.
5 NCE in ILF was concentrated just beneath the follicle-associated epithelium, a pattern of polarizatio
6 involves cooperation between M cells of the follicle-associated epithelium and DCs of the subepithel
7 ulation of intraepithelial DN DCs within the follicle-associated epithelium and demonstrate a predomi
8 a small subpopulation of enterocytes in the follicle-associated epithelium and in goblet cell mucins
9 cell-derived LT and TNF, the development of follicle-associated epithelium and M cells in PP was com
11 ce by adhering selectively to M cells in the follicle-associated epithelium and then exploiting M cel
13 mucosa, specialized M cells of the lymphoid follicle-associated epithelium conduct vesicular transpo
15 lar interactions that occur in and under the follicle-associated epithelium could greatly facilitate
16 th the mucosal absorptive epithelium and the follicle-associated epithelium covering the lymphoid tis
17 the dome regions of PPs upon invasion of the follicle associated epithelium (FAE) by an enteric patho
18 her antigen-sampling M cells, present in the follicle-associated epithelium (FAE) above organized con
19 pha-linked galactose were found to label the follicle-associated epithelium (FAE) almost exclusively.
20 in the intestinal epithelium, including the follicle-associated epithelium (FAE) and microfold (M) c
22 l intestine, EHEC adhesion was restricted to follicle-associated epithelium (FAE) of ileal Peyer's pa
24 ted to organized lymphoid tissues across the follicle-associated epithelium (FAE) of Peyer's patches.
26 r were preferably taken up by M cells in the follicle-associated epithelium (FAE) region of Peyer's p
28 e mucosal immune responses, are covered by a follicle-associated epithelium (FAE) specialized for the
29 phoid follicles are covered by a specialized follicle-associated epithelium (FAE) that contains M cel
30 truction and loss of adjacent regions of the follicle-associated epithelium (FAE), although the condi
33 expression of IFN-lambda mRNA was higher in follicle-associated epithelium of animals that had clear
34 type 1 Lang (T1L) adheres to M cells in the follicle-associated epithelium of mouse intestine and ex
35 and nonstructural proteins were localized to follicle-associated epithelium of the dorsal soft palate
38 mRNA was dramatically expressed only by the follicle-associated epithelium overlying the SED, while
39 a specialized epithelium residing within the follicle-associated epithelium that covers mucosal induc
40 follicles, B cells home sequentially to the follicle-associated epithelium, the follicular dendritic
41 , an antigen-sampling cell type found in the follicle-associated epithelium, transcytosis of fluoresc
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