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1 mum, devoid of inner membranes embedded in a mucus layer.
2 the mucosal lining, and the thickness of the mucus layer.
3 at are secreted by epithelial cells into the mucus layer.
4 dvantage for penetrating the viscous stomach mucus layer.
5 tes enhanced the retention in the intestinal mucus layer.
6 lls and abundantly secreted into the surface mucus layer.
7 cin denaturation and microbial access to the mucus layer.
8 r subdiffusive virions to traverse through a mucus layer.
9 tiating the retention of bacteria within the mucus layer.
10 ucin-degrading bacterium that resides in the mucus layer.
11 the main components of the gastrointestinal mucus layer.
12 wim through and colonize the viscous gastric mucus layer.
13 tract are in intimate contact with the outer mucus layer.
14 and limiting the association of VRE with the mucus layer.
15 ng the protection provided by the intestinal mucus layer.
16 ersistence of H. pylori in the human gastric mucus layer.
17 an "expanded" rather than more concentrated mucus layer, a prediction confirmed by electron microsco
18 development of NEC: reducing bacteria in the mucus layer, administering probiotic treatment, and bloc
19 d model of the glycocalyx layer, or adhesive mucus layer (AML), covered by mucus gel (luminal mucus l
23 7BL/6 mice wherein V. cholerae colonizes the mucus layer and forms microcolonies in the crypts of the
24 underscored by decreased thickness of the OE mucus layer and increased numbers of immune cells within
26 ual intercourse, allows virions to cross the mucus layer and reach the epithelium in a short timefram
27 a are physically separated from villi by the mucus layer and their numbers controlled by mucus-embedd
28 ound in mucin, a component of the intestinal mucus layer and thus one of the prime adherence targets
29 ntraluminal digestive enzymes, the unstirred mucus layer, and a systemic ischemic-reperfusion injury.
31 We investigated the roles of the intestinal mucus layer, and in particular Muc2, in development of e
34 d barrier properties of the adherent gastric mucus layer are normally maintained by building-block st
35 achieved in part by the presence of a dense mucus layer at the epithelial surface and by the product
36 nteractions among the intestinal microbiota, mucus layer, bile acids, and mucosal immune responses, r
37 Entamoeba histolytica (Eh) colonizes the mucus layer by binding of the parasite's surface galacto
39 s capable of dissolving the inner protective mucus layer by specific cleavages in the MUC2 mucin and
43 s on the relative mucin concentration of the mucus layer compared with that of the periciliary layer;
48 ; and CF secretion osmotic pressures predict mucus layer-dependent osmotic compression of the pericil
49 obes may affect goblet cell dynamics and the mucus layer directly via the local release of bioactive
50 n in the colonic mucosa was mirrorred in the mucus layer fecal colonocytes isolated from AOM rat stoo
52 dent microbiome is dependent on a protective mucus layer generated by goblet cells, impairment of whi
53 pure frictional coupling with the overlying mucus layer; hence, ciliary mixing most likely accelerat
56 fails to explain the formation of a distinct mucus layer in health or why mucus clearance fails in di
61 y member of communities in the outer (loose) mucus layer, in the cecum and colon, starting at day 1 p
64 ypothesis that growth of MRSA in the colonic mucus layer is required for establishment of intestinal
66 as analyzed, considering that the intestinal mucus layer is the first defense against enteric pathoge
67 crypt regeneration, and also replenished the mucus layer, leading to amelioration of C. rodentium- an
68 s comprehensive insight into the dynamics of mucus layer maturation upon bacterial colonization of ge
70 of functions in pathogen resistance such as mucus layer modifications and hydration, tight junction
75 ty member of mixed bacterial biofilms in the mucus layer of the streptomycin-treated mouse intestine.
77 ed fluid secretion mechanically disrupts the mucus layer or that toxins interfere with innate mucosal
79 disease (IBD) are associated with a reduced mucus layer, potentially leading to dysbiosis associated
80 ng mucins, which are major components of the mucus layer protecting many epithelial surfaces, are clu
86 s (IEC-Cosmc(-/y)) resulted in a compromised mucus layer, spontaneous microbe-dependent inflammation,
87 , for example, is lined by a firmly adherent mucus layer that is typically devoid of bacteria, follow
89 imarily as single cells dispersed within the mucus layer that overlies the mouse cecal epithelium.
90 epithelial surface is protected by an inner mucus layer that the commensal microflora cannot penetra
91 tected by a highly viscoelastic and adhesive mucus layer that traps most foreign particles, including
92 ay surface liquid (ASL) consisting of both a mucus layer that traps, kills, and inactivates bacteria
94 oatings that allow them to rapidly penetrate mucus layers through openings in the mucus mesh at rates
96 stribution of inert nanoparticles within the mucus layers using an efficient replica exchange Monte C
97 s layer (AML), covered by mucus gel (luminal mucus layer) using a polymer lattice model and stochasti
98 duct exteriorization whereas the role of the mucus layer was tested via the enteral administration of
100 l exhibited lower FAS levels and a decreased mucus layer, which could be restored with insulin treatm
101 e show that the small intestine has a porous mucus layer, which permitted the uptake of MUC2 by antig
102 ella propel bacteria through urine and along mucus layers, while type 1 fimbriae allow bacteria to ad
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