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1 m, other infectious bacteria, host and human gut flora.
2  calf IAP (cIAP) rapidly restores the normal gut flora.
3  out drug targets that may also affect human gut flora.
4 at their expansion is regulated by commensal gut flora.
5 acid degradation pathway is present in human gut flora.
6 extracts but at the same affected the normal gut flora.
7 ly caused by food sensitivity or a change in gut flora.
8  LRP5/6 in mediating immune tolerance to the gut flora.
9 er than indiscriminately eliminating natural gut flora.
10 ed in isolators and colonized with a defined gut flora.
11  appeared to be absent from the normal human gut flora.
12 be endogenously produced by normal microbial-gut flora.
13 sents a possibility of maintaining a healthy gut flora.
14 ncephalopathy is lactulose and alteration of gut flora.
15 ssex chickens possessing an acquired natural gut flora.
16  Hundreds of bacterial species make up human gut flora.
17 rRNAs distinct from those of common skin and gut flora.
18 ed that in competition with the normal mouse gut flora, an EHEC O157:H7 strain with a nonpolar deleti
19                                              Gut flora analyses have allowed gut microbiota signature
20  to inflammatory signals induced by both the gut flora and arthritis, Breg cells increase in number a
21                                    DCs sense gut flora and damaged epithelium via expression of C-typ
22            MS etiology is linked to both the gut flora and external environmental factors but this co
23 ve been shown to modulate the composition of gut flora and induce metabolic, neurochemical, and behav
24     Studies have shown that probiotics alter gut flora and lead to elaboration of flora metabolites t
25 enteritis and be associated with an abnormal gut flora and with food intolerance.
26                                              Gut flora appears to act as an important determinant in
27  human health, and alterations of the normal gut flora are associated with a variety of distinct dise
28 nged in the absence of TLR4, suggesting that gut flora associated with the graft may augment alloimmu
29 tedly enhances butyrate production by normal gut flora can influence the outcome of an E. coli O157 i
30 he clinical trial ChiCTR1800017404, that the gut flora characteristically differs among patients and
31 cently exhibited great prospect in modifying gut flora composition and regulating certain gene expres
32 ein-coupled receptors influenced by diet and gut flora composition.
33 and insulin resistance via modulation of the gut flora composition.
34           Although it is known that resident gut flora contribute to immune system function and homeo
35  is well recognized, components of the human gut flora critical for colonization resistance are not k
36 s Ib protein, MR1, which is required for the gut flora-dependent development of mucosa-associated inv
37          Discovery of a relationship between gut-flora-dependent metabolism of dietary phosphatidylch
38                                              Gut flora-depleted mice expressed lower levels of F4/80
39 with control BM monocytes, BM monocytes from gut flora-depleted mice had decreased migratory capacity
40 s of Lactobacillus, important members of the gut flora, differentially activate DC.
41                 In this study, we found that gut flora DNA (gfDNA) plays a major role in intestinal h
42  understand why, among the vast diversity of gut flora, enterococci are so well adapted to the modern
43 obacteria are important members of the human gut flora, especially in infants.
44 le MHC-related protein I (MR1), B cells, and gut flora for development and/or expansion, and they pre
45 nce supporting the role of altered commensal gut flora in human disease.
46 ce pointing to the role of altered commensal gut flora in such common conditions as irritable bowel s
47 ry input from innate immune responses to the gut flora in the establishment of oral tolerance.
48  oligonucleotide (CpG-B), can substitute for gut flora in the induction of neonatal immunoresponsiven
49 toimmunity, the particular role of commensal gut flora in the initiation of colitis, and the role of
50 rmed a critical role for dietary choline and gut flora in TMAO production, augmented macrophage chole
51 n is influenced by the presence of commensal gut flora, in particular increased colonization with seg
52  in LRP5/6(DeltaCD11c) mice by depleting the gut flora, indicating the importance of LRP5/6 in mediat
53          The loss of this bacterium from the gut flora is associated with an increased risk of hypero
54 rgrowth (SIBO) or other abnormalities in the gut flora is believed to contribute to the development o
55 Antibiotic-induced perturbation of the human gut flora is expected to play an important role in media
56 an aberrant T cell response directed against gut flora is sufficient to trigger IBD.
57             However, C3H mice with a limited gut flora (LF) were efficiently colonized at high levels
58   The induction of such cells in response to gut flora may be a mechanism protecting normal individua
59                               Alterations in gut flora may be important in the pathophysiology of the
60                       Evidence suggests that gut flora may play an important role in the pathophysiol
61 nsion and selection, known to require normal gut flora, may be driven through indirect effects of mic
62 whereby T1D induction can be circumvented by gut flora-mediated Th17 differentiation.
63                                              Gut flora modify primary bile acids to produce secondary
64  of human gut microbes with implications for gut flora modulations.
65 s well as provide the first insight into the gut flora of children affected with this debilitating di
66                        We then characterized gut flora of patients during onset of intestinal inflamm
67 nces and host genotype data from the Flemish Gut Flora Project (n = 2,223) and two German cohorts (Fo
68 ased cohorts including American Gut, Flemish Gut Flora Project and the extended TwinsUK cohort.
69 x method was successfully applied to Flemish Gut Flora Project cohort (n = 292) samples, leading to a
70 ataset (n = 282) and the independent Flemish Gut Flora Project population cohort (n = 2,345).
71 lence, antigenic, and non-homology with host/gut flora proteins.
72 c compounds, and fermentability by the human gut flora, SCFAs production, nitric oxide and cytokine e
73  humanity has experienced a depletion of the gut flora since diverging from Pan.
74       The second, found in bacteria from the gut flora such as Clostridioides difficile, salvages pre
75 ur findings demonstrate in neonatal mice how gut flora synergizes with poly(I:C) to elicit protective
76 intervention to affect this process - on the gut flora, the 'leaky' mucosal membrane and endotoxin co
77  required additional signals provided by the gut flora through TLR5 and MyD88 signaling.
78 lites derived from dietary tryptophan by the gut flora to activate AHR signaling in astrocytes and su
79 pithelial tight junctions, allowing resident gut flora to promote chronic increases in antimicrobial
80                     Among differences in the gut flora were increased abundances of Lactobacillus and
81 t change in the composition and diversity of gut flora when the pH of drinking water was altered.
82 AFLD because of its modulating effect on the gut flora, which can influence the gut-liver axis.
83 s exert highly selective effects on resident gut flora, which, in turn, lead to very specific alterat
84 mposition, diet had a preponderant impact on gut flora with some of the taxa being strongly associate