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1 aborate maze-like patterns on the surface of mucosal epithelial cells.
2 rum are intracellular bacterial pathogens of mucosal epithelial cells.
3 well defined how HIV-1 infects CD4-negative mucosal epithelial cells.
4 r for HIV-1 envelope (Env) interactions with mucosal epithelial cells.
5 envelope glycoprotein (Env) interaction with mucosal epithelial cells.
6 coprotein expressed on the apical surface of mucosal epithelial cells.
7 nscytosed by the pIgA receptor (pIgR) across mucosal epithelial cells.
8 atively regulates DeltaNp73 transcription in mucosal epithelial cells.
9 coupled prostaglandin receptors expressed by mucosal epithelial cells.
10 ptor (pIgR) mediates transport of IgA across mucosal epithelial cells.
11 at are associated with increased invasion of mucosal epithelial cells.
12 fection may be facilitated by replication in mucosal epithelial cells.
13 extent by transcription of the PIGR gene in mucosal epithelial cells.
14 ing small molecule therapeutics and genes to mucosal epithelial cells.
15 and novel VCAM-1 expression by cutaneous and mucosal epithelial cells.
16 host defense, transporting antibodies across mucosal epithelial cells.
17 ponsible for specific interaction with human mucosal epithelial cells.
18 t had no effect on the growth rate of normal mucosal epithelial cells.
19 type ranging from professional phagocytes to mucosal epithelial cells.
20 shed by specific binding to the cilia of the mucosal epithelial cells.
21 d cytotoxic effects marked by exfoliation of mucosal epithelial cells.
22 ytotoxin causes vacuolation of primary human mucosal epithelial cells.
23 ve significantly higher MHC II expression on mucosal epithelial cells.
24 for the radiation-induced depletion of oral mucosal epithelial cells.
25 king their attachment to or penetration into mucosal epithelial cells, a common site of exposure to v
26 d by tropic binding to the apical surface of mucosal epithelial cells and cells lining gastric pits.
29 istry data showed that IL-32 was detected in mucosal epithelial cells and inflammatory cells in the l
30 ciated epithelial chemokine), is secreted by mucosal epithelial cells and is found in saliva and in b
31 complex (MHC) II is dynamically expressed on mucosal epithelial cells and is induced in response to i
33 of IgA antibodies is to transport IgA across mucosal epithelial cells and not, as in the case of the
35 s act globally, IFN-lambdas primarily target mucosal epithelial cells and protect them against the fr
36 s can prevent virus entry and replication in mucosal epithelial cells and therefore virus shedding.
37 ral to gammaherpesvirus persistence, whereas mucosal epithelial cells are considered nonessential.
42 since C. albicans is closely associated with mucosal epithelial cells as a commensal, we sought to id
43 s on glycoproteins decorating the surface of mucosal epithelial cells as receptors for the virus hema
44 tor-1 (SDF-1) is constitutively expressed by mucosal epithelial cells at sites of HIV transmission an
45 er was unable to pass from the lumen between mucosal epithelial cells, because the presence of an int
46 e of genital herpes, infects oral or genital mucosal epithelial cells before infecting the peripheral
50 eptors (GRP-R) are not normally expressed by mucosal epithelial cells except for those lining the gas
57 itis was characterized by moderate to marked mucosal epithelial cell hyperplasia with mild monocytic
58 to the polymeric immunoglobulin receptor on mucosal epithelial cells, IgA antibodies can bind to rec
59 n Bak was reduced compared to that of normal mucosal epithelial cells in 27 of 30 (90%) carcinomas an
60 mmensal organisms have a role in stimulating mucosal epithelial cells in maintaining the barrier that
62 des new findings regarding the role of local mucosal epithelial cells in the initiation of ocular all
64 membrane of chlamydiae that are involved in mucosal epithelial cell infection must clearly be identi
65 SIgA is transported across glandular and mucosal epithelial cells into external secretions by the
66 suggest that HIV-mediated TSLP production by mucosal epithelial cells is a critical trigger for DC-me
67 tachment, biofilm formation, and invasion of mucosal epithelial cells is a new genetic cause of menin
68 bacterium, efficient colonization of genital mucosal epithelial cells is crucial to the infectious pr
70 helial subtypes, that we compared to 141,367 mucosal epithelial cells (n = 29 patients; 18 CD, 11 con
72 f mitochondrial structures in the intestinal mucosal epithelial cells of mice and in Caco-2 cells.
73 i.e., FGFR4 and betaKlotho) are expressed in mucosal epithelial cells of the gallbladder and small in
74 le of TLR signaling in immune defense of the mucosal epithelial cells of the lower female genital tra
78 linaclotide: it activates GC-C expressed on mucosal epithelial cells, resulting in the production an
79 OSR) using tissue-engineered cultivated oral mucosal epithelial cell sheets (COMECS) is a promising n
80 found in intestinal capillaries and between mucosal epithelial cells, suggesting that the microvascu
82 cationic antimicrobial peptides, secreted by mucosal epithelial cells that regulate adaptive immune f
83 to the intensity observed in adjacent normal mucosal epithelial cells, the intensity of Bcl-X immunos
85 to keratinocytes and heterotypic adhesion of mucosal epithelial cells to E-cadherin-negative intestin
86 tely understood, it is known that CT induces mucosal epithelial cells to produce the proinflammatory
87 We report that HIV induces human genital mucosal epithelial cells to produce thymic stromal lymph
88 mucin-galectin interaction in four different mucosal epithelial cell types using competitive carbohyd
89 lates mitochondrial respiration in two human mucosal epithelial cell types: insulin-insensitive corne
90 e body by transporting them directly through mucosal epithelial cells, using the same mechanism that
91 osal signaling is inactivated by uptake into mucosal epithelial cells, which are mediated by an integ