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1 gulation of the immune response to commensal intestinal bacteria.
2 tor-kappaB, are involved in the detection of intestinal bacteria.
3 s of oligosaccharides fermented by different intestinal bacteria.
4 Mucolytic potential is widespread among intestinal bacteria.
5 on of small-molecule metabolites produced by intestinal bacteria.
6 the host immune system in the gut and in the intestinal bacteria.
7 ding changes the composition and behavior of intestinal bacteria.
8 ngle epitope, which act together to regulate intestinal bacteria.
9 motherapy and immunotherapy is influenced by intestinal bacteria.
10 to the anaerobic growth requirements of most intestinal bacteria.
11 W and PflD, which are widespread among human intestinal bacteria.
12 al stimulation that can functionally replace intestinal bacteria.
13 atory agent cyclophosphamide (CTX) relies on intestinal bacteria.
14 enteropathy and the prevalence of pathogenic intestinal bacteria.
15 s.IMPORTANCE Butyrate is a lipid produced by intestinal bacteria.
16 utualistic relationship between the host and intestinal bacteria.
17 uld be attenuated in the complete absence of intestinal bacteria.
18 s an exaggerated immune response directed at intestinal bacteria.
19 promotes colonic neurogenesis, regulated by intestinal bacteria.
20 fense that protects against dissemination of intestinal bacteria.
21 lin or to different commensal and pathogenic intestinal bacteria.
22 on of IgM and complement-mediated control of intestinal bacteria.
23 e suggests a connection between diet and the intestinal bacteria.
24 tory IgA (SIgA) is found in association with intestinal bacteria.
25 IgT coated most intestinal bacteria.
26 ce points to the various mechanisms by which intestinal bacteria act on distal tumors and how to harn
29 y be due to excessive hydrogen production by intestinal bacteria altering the partial pressure of nit
30 ently, the O-protease OpeRATOR, derived from intestinal bacteria and expressed in Escherichia coli, h
32 n part, by the interaction between commensal intestinal bacteria and gut-associated lymphoid tissue (
33 cells, and the interrelationship between the intestinal bacteria and Tfh cell responses in the gut.
34 ng the complex interactions between resident intestinal bacteria and the immune system could improve
36 at host innate immune signaling can modulate intestinal bacteria and ultimately the host's susceptibi
37 ulting in tissue infiltration of 'symbiotic' intestinal bacteria and viruses that essentially become
38 tyrate, a short-chain fatty acid produced by intestinal bacteria, and lipoteichoic acid, a cell wall
39 of principles governing the localization of intestinal bacteria, and spatial relationships between b
43 inant daidzein metabolites produced by human intestinal bacteria are equol and O-desmethylangolensin.
49 bacteriophage (phages) to eliminate targeted intestinal bacteria as an alternative to a broad-spectru
50 Enterococcus faecalis strains are resident intestinal bacteria associated with invasive infections,
51 ealed that neomycin altered the abundance of intestinal bacteria bearing gamma-d-glutamyl-meso-diamin
52 resent a major nutrient source, not just for intestinal bacteria but also for microorganisms that occ
54 matic activity leads to growth inhibition of intestinal bacteria by causing local tryptophan depletio
55 hat commensal fungi can functionally replace intestinal bacteria by conferring protection against inj
56 is a short-chain fatty acid produced by the intestinal bacteria by the fermentation of nondigestible
57 how a marked proportion of oxygen-sensitive intestinal bacteria can be transmitted between individua
62 is or defective host defense toward invasive intestinal bacteria can result in chronic inflammation.
70 t of progenitor cell responses to pathogenic intestinal bacteria could provide a measure of predispos
71 TMAO is produced by hepatic processing of intestinal bacteria-derived trimethylamine (TMA) followi
77 tively, these data demonstrate that resident intestinal bacteria enhance the stability of beta-cateni
78 unication system where compounds produced by intestinal bacteria, especially short-chain fatty acids,
80 rmfree or colonized with a limited number of intestinal bacteria failed to develop inflammatory bowel
82 d to a considerable interest in manipulating intestinal bacteria for therapeutic benefit, and trials
84 rier in Rd8 mice led to the translocation of intestinal bacteria from the lower gastrointestinal (GI)
86 , and to microbial products derived from the intestinal bacteria, has resulted in a distinctive local
91 IgA coating uniquely identifies colitogenic intestinal bacteria in a mouse model of microbiota-drive
92 to equol and O-desmethylangolensin (ODMA) by intestinal bacteria in approximately 30-50% and 80-90% o
94 bacillus plantarum and its interactions with intestinal bacteria in mice undergoing switches between
96 microbiota, focusing on the role of resident intestinal bacteria in the development of immune respons
97 scuss the roles of known and novel commensal intestinal bacteria in the pathogenesis of inflammatory
98 Dysregulated immune responses to commensal intestinal bacteria, including Escherichia coli, contrib
99 gated whether oral inoculation with specific intestinal bacteria increased colon inflammation in the
100 sion, these results support the concept that intestinal bacteria induce endogenous signals that play
101 ring the fermentation of fiber by endogenous intestinal bacteria, induces mitochondrial function-depe
103 Our results suggest that translocation of intestinal bacteria into liver may be involved as a one
106 ses vs controls, we found that reactivity to intestinal bacteria is a normal property of the human CD
108 innate immune inflammatory response against intestinal bacteria is sufficient to induce colon cancer
111 tyrate, a short-chain fatty acid produced by intestinal bacteria, lipoteichoic acid, a cell wall comp
114 accumulating to support the hypothesis that intestinal bacteria not only exchange resistance genes a
115 nce elicitor of systemic immune responses to intestinal bacteria observed in a loss-of-tolerance mode
117 ing of the impact of translocating commensal intestinal bacteria on mucosal-associated T cell respons
118 eview examines the influence of signals from intestinal bacteria on the homeostasis of the mammalian
121 ed that stress promotes the translocation of intestinal bacteria or their toxins into the systemic co
123 rapidly respond to commensal and pathogenic intestinal bacteria, parasites and food components by po
124 a selective force in the evolution of their intestinal bacteria, particularly by increasing the prev
126 ation after antibiotic-mediated depletion of intestinal bacteria prevents colitis and influenza, thus
130 robiota.IMPORTANCE Recent data indicate that intestinal bacteria promote intestinal infection of seve
132 ead to exaggerated inflammatory responses to intestinal bacteria, raising the possibility that defect
133 verse IS elements insert into the genomes of intestinal bacteria regardless of human host lifestyle.
134 ggravate chronic inflammation via effects on intestinal bacteria regulating gut permeability to visce
137 chain fatty acids (SCFA) are metabolites of intestinal bacteria resulting from fermentation of dieta
139 tem targets non-self rather than self, these intestinal bacteria should be considered foreign and the
140 n probiotics, nutritional components and the intestinal bacteria should be considered when examining
141 ses against a panel of taxonomically diverse intestinal bacteria species in sera from TN-10 participa
142 ponses influence host health, yet only a few intestinal bacteria species that induce cognate adaptive
143 entage of them become colonized by resistant intestinal bacteria such as extended-spectrum beta-lacta
144 ns that are highly specific for target Ag on intestinal bacteria, suggesting that an aberrant T cell
145 ry bowel disease, is attributed, in part, to intestinal bacteria that may initiate and perpetuate muc
146 overactive immunity to a subset of resident intestinal bacteria that mediate multiple inflammatory c
147 MIA phenotypes in offspring require maternal intestinal bacteria that promote TH17 cell differentiati
148 e contact at birth with maternal vaginal and intestinal bacteria, the authors proposed that this coul
149 s review, we explore a more sinister side of intestinal bacteria; their role as traffickers in antibi
151 New evidence has implicated the lack of intestinal bacteria to be responsible for the degradatio
153 ta indicate that enteric viruses can utilize intestinal bacteria to promote viral replication and pat
154 ve identified molecular cues propagated from intestinal bacteria to the brain that can affect neurolo
155 a, which may contribute to the adaptation of intestinal bacteria to the mucosal environment in health
156 ot clear how LACC1 balances defenses against intestinal bacteria vs intestinal inflammation or what c
158 at colonization of GF mice with a variety of intestinal bacteria was capable of reducing T1D in MyD88
159 oxidative derivative of choline produced by intestinal bacteria, was positively associated with rect
160 erplay between the mucosal immune system and intestinal bacteria, we investigated the role of MIF in
163 n of SAAs from meat to sulfide production by intestinal bacteria with use of both a model culture sys
164 utrient release acts as a source of fuel for intestinal bacteria, with implications for gut inflammat