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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 otaxis, and role in Salmonella targeting the follicle-associated epithelium.
5 gh the specialized epithelial M cells of the follicle-associated epithelium.
6 NCE in ILF was concentrated just beneath the follicle-associated epithelium, a pattern of polarizatio
7  involves cooperation between M cells of the follicle-associated epithelium and DCs of the subepithel
8 ulation of intraepithelial DN DCs within the follicle-associated epithelium and demonstrate a predomi
9  a small subpopulation of enterocytes in the follicle-associated epithelium and in goblet cell mucins
10  cell-derived LT and TNF, the development of follicle-associated epithelium and M cells in PP was com
11 virus-sized microparticles bound only to the follicle-associated epithelium and M cells.
12 ce by adhering selectively to M cells in the follicle-associated epithelium and then exploiting M cel
13       Organogenesis of Peyer's patches (PP), follicle-associated epithelium, and M cells is impaired
14  mucosa, specialized M cells of the lymphoid follicle-associated epithelium conduct vesicular transpo
15                                 Cells in the follicle-associated epithelium contained both sigma1 and
16 lar interactions that occur in and under the follicle-associated epithelium could greatly facilitate
17 th the mucosal absorptive epithelium and the follicle-associated epithelium covering the lymphoid tis
18 the dome regions of PPs upon invasion of the follicle associated epithelium (FAE) by an enteric patho
19 her antigen-sampling M cells, present in the follicle-associated epithelium (FAE) above organized con
20 pha-linked galactose were found to label the follicle-associated epithelium (FAE) almost exclusively.
21  in the intestinal epithelium, including the follicle-associated epithelium (FAE) and microfold (M) c
22 e scarcity and small sizes of ILFs and their follicle-associated epithelium (FAE) impeded the charact
23                                              Follicle-associated epithelium (FAE) in the intestinal P
24                                     Instead, follicle-associated epithelium (FAE) M cell differentiat
25 l intestine, EHEC adhesion was restricted to follicle-associated epithelium (FAE) of ileal Peyer's pa
26            Transport of antigens through the follicle-associated epithelium (FAE) of Peyer's patch (P
27 ted to organized lymphoid tissues across the follicle-associated epithelium (FAE) of Peyer's patches.
28                                          The follicle-associated epithelium (FAE) plays key roles in
29 r were preferably taken up by M cells in the follicle-associated epithelium (FAE) region of Peyer's p
30                                          The follicle-associated epithelium (FAE) secretes chemokines
31 e mucosal immune responses, are covered by a follicle-associated epithelium (FAE) specialized for the
32 phoid follicles are covered by a specialized follicle-associated epithelium (FAE) that contains M cel
33 truction and loss of adjacent regions of the follicle-associated epithelium (FAE), although the condi
34 ut epithelium via microfold cells lining the follicle-associated epithelium (FAE).
35        Preferential uptake of latex beads by follicle-associated epithelium indicates that the presen
36 id tissue to bacteria transported across the follicle associated epithelium into the subepithelial do
37                    At later time points, the follicle-associated epithelium of animals infected with
38  expression of IFN-lambda mRNA was higher in follicle-associated epithelium of animals that had clear
39 tes directional electric fields (EFs) in the follicle-associated epithelium of mouse cecum.
40  type 1 Lang (T1L) adheres to M cells in the follicle-associated epithelium of mouse intestine and ex
41 and nonstructural proteins were localized to follicle-associated epithelium of the dorsal soft palate
42 the isogenic rpoS mutant did not destroy the follicle-associated epithelium of the GALT.
43             This study demonstrates that the follicle-associated epithelium of the rabbit conjunctiva
44  mRNA was dramatically expressed only by the follicle-associated epithelium overlying the SED, while
45 a specialized epithelium residing within the follicle-associated epithelium that covers mucosal induc
46  follicles, B cells home sequentially to the follicle-associated epithelium, the follicular dendritic
47 , an antigen-sampling cell type found in the follicle-associated epithelium, transcytosis of fluoresc
48                               M cells in the follicle-associated epithelium transport foreign macromo