ライフサイエンスコーパス: microbiota composition

1 at of male patients, which were unrelated to microbiota composition.

2 ecies identity is the strongest predictor of microbiota composition.

3 diseases, driven by changes in diet and gut microbiota composition.

4 f breastfeeding as a key determinant of milk microbiota composition.

5 to be associated with changes in intestinal microbiota composition.

6 t association between antibiotic use and gut microbiota composition.

7 at variability was due to changes in the gut microbiota composition.

8 arguments linking Western diet to an altered microbiota composition.

9 oth the intestine and plasma via altered gut microbiota composition.

10 Many (58%) did not report an analysis of microbiota composition.

11 ade inflammation and specific changes in gut microbiota composition.

12 il proportion was the strongest predictor of microbiota composition.

13 es within the gut, profoundly influences gut microbiota composition.

14 highly variable and are associated with gut microbiota composition.

15 bacterial growth, which ultimately dictates microbiota composition.

16 energy balance, blood metabolomics and fecal microbiota composition.

17 duce gastric acid secretion and modulate gut microbiota composition.

18 owth of different bacteria, drive changes in microbiota composition.

19 ortant drivers of the early-life respiratory microbiota composition.

20 d, furthermore, altered the larva-associated microbiota composition.

21 ute to variation in marine mammal distal gut microbiota composition.

22 time antibiotic use after weaning, and fecal microbiota composition.

23 ions between H. pylori strain properties and microbiota composition.

24 y mass index is associated with neonatal gut microbiota composition.

25 ic population or carriage of the cagPAI with microbiota composition.

26 nses after oral immunization and affects the microbiota composition.

27 etary response was determined in part by gut microbiota composition.

28 ixed model, we estimated the heritability of microbiota composition.

29 pcidin induction is influenced by intestinal microbiota composition.

30 ut humoral response and to maintain a normal microbiota composition.

31 ediates intestinal homeostasis and regulates microbiota composition.

32 tes susceptibility to disease by controlling microbiota composition.

33 t the fate of this starch depends on the gut microbiota composition.

34 st inflammation associated cancer and normal microbiota composition.

35 seases are associated with complex shifts in microbiota composition.

36 n bacterial richness associated with altered microbiota composition.

37 NA gene sequencing was utilized to determine microbiota composition.

38 and is associated with both inflammation and microbiota composition.

39 with oral microbes) is associated with stool microbiota composition.

40 srupts longitudinal and lateral gradients in microbiota composition.

41 for 3 wk, after which they assumed a similar microbiota composition.

42 ted by wide interindividual heterogeneity in microbiota composition(1), probably due to population-wi

43 us, ultrafine particles ingestion alters gut microbiota composition, accompanied by increased atherog

44 Analyses from machine learning models of microbiota composition, across the study period, disting

45 Our findings suggest that microbiota composition affects disease outcome and may e

46 id not find significant differences in fecal microbiota composition among patients with different IBS

47 The microbiota composition analysis revealed higher abundanc

48 Fecal microbiota composition analysis was performed in a subco

49 In the subcohort of 42 children with fecal microbiota composition analysis, the children with short

50 hanges in gut permeability are linked to gut-microbiota composition and activity in alcohol-dependent

51 s with COPD and how they are associated with microbiota composition and airway neutrophil function.

52 ributes to the HFD-induced disruption of gut microbiota composition and alpha-defensin expression.

53 to determine the possible role of NT in gut microbiota composition and alpha-defensin gene expressio

54 n Rnf5(-/-) mice, coincides with altered gut microbiota composition and anti-tumor immunity to contro

55 e, a recently described regulator of colonic microbiota composition and biogeographical distribution,

56 of pathogen resistance, in turn, affect the microbiota composition and create an environment that ex

57 We hypothesized that the respiratory microbiota composition and development in infancy is aff

58 isease outcome and may explain links between microbiota composition and disease susceptibility.

59 Milk microbiota composition and diversity were associated wit

60 colonic segments in both CD and UC differ in microbiota composition and epigenetic profiles.

61 d the effects of IgA deficiency on human gut microbiota composition and evaluated the possibility tha

62 results provide insights into the human lung microbiota composition and function and their link to hu

63 Altered gut microbiota composition and function have been associated

64 lts indicate that the human gastrointestinal microbiota composition and function vary throughout the

65 anic compounds (VOCs), reflecting intestinal microbiota composition and function, allow for discrimin

66 studies to characterize natural variation in microbiota composition and function, identify important

67 We assessed the effects of FMT on microbiota composition and function, mucosal immune resp

68 leads to beneficial modifications of the gut microbiota composition and function.

69 t dysfunction, including modification of gut microbiota composition and higher local inflammatory rea

70 Paneth cells are critical in maintaining gut microbiota composition and homeostasis by releasing anti

71 Alterations in microbiota composition and host responses to the microbi

72 enetically distinct strain influence the gut microbiota composition and immune key markers in mice.

73 Antibiotics alter microbiota composition and increase infection susceptibi

74 Fecal microbiota composition and inferred function, fecal SCFA

75 this study was to detect the changes in gut microbiota composition and inflammatory cytokines produc

76 udies have established a primary role of the microbiota composition and intestinal permeability in su

77 ore germination rate in the colon depends on microbiota composition and its level of disruption by an

78 olatile organic compounds (VOCs) reflect the microbiota composition and may provide insight into meta

79 ttle is known about the consequences for gut microbiota composition and metabolic activity and for la

80 lammation, which correlates with altered gut microbiota composition and metabolic syndrome, both pres

81 , and the potential of modulating intestinal microbiota composition and metabolism as a novel therape

82 major regulators of inflammation, infection, microbiota composition and metabolism(1).

83 wel disease (IBD) is associated with altered microbiota composition and metabolism, but it is unclear

84 xpression in the ileum and cecum by changing microbiota composition and metabolism.

85 We further investigate the gut microbiota composition and microbiota-metabolite relatio

86 een associated with long-term changes in gut microbiota composition and more recently also with chang

87 ce of environmental and lifestyle factors on microbiota composition and pancreatic autoimmunity.

88 defensins expressed by Paneth cells, control microbiota composition and play a key role in intestinal

89 ota interactions, we mapped loci controlling microbiota composition and prioritized candidate genes.

90 ith a broad spectrum antibiotic modifies gut microbiota composition and promotes anti-inflammatory re

91 luence S. mutans colonization, tooth biofilm microbiota composition and risk of dental caries in Swed

92 immune cell profiling, complemented with gut microbiota composition and routine clinical chemistry.

93 ant starch type 4 (RS4) enriched diet on gut microbiota composition and short-chain fatty acid (SCFA)

94 sm, and we examined correlations between gut microbiota composition and signaling pathways.

95 etween dietary phenolic compounds (PCs), gut microbiota composition and targeted faecal metabolites w

96 g and bacterial cell sorting to evaluate gut microbiota composition and taxa-specific antibody coatin

97 splaying despair behavior, we found that the microbiota composition and the metabolic signature drama

98 ucosal immune system through modification of microbiota composition and their interactions with the h

99 targets for CH4 mitigation at the levels of microbiota composition and transcriptional regulation.

100 re also believed to act as modulators of the microbiota composition and, consequently, as agents that

101 e were variable shifts in faecal and mucosal microbiota composition and, in some patients, changes in

102 try, and biochemical assays to determine the microbiota compositions and the physiological and metabo

103 in subcutaneous white fat, 3) change the gut microbiota composition, and 4) prevent and reverse obesi

104 Plasma corticosterone, microbiota composition, and cecal short-chain fatty acid

105 nent alterations in anti-commensal immunity, microbiota composition, and chronic inflammation, which

106 uding to what extent crop plants impact soil microbiota composition, and how changes in microbiota co

107 Stroke alters the gut microbiota composition, and in turn, microbiota dysbiosi

108 ions and serum vitamin K concentrations, gut microbiota composition, and inflammation.Fecal and serum

109 t the hypothesis that a distortion in normal microbiota composition, and not an enrichment of potenti

110 and serum menaquinone concentrations, fecal microbiota composition, and plasma and fecal cytokine co

111 ation between feeding strategies, intestinal microbiota composition, and the development of NEC.We pe

112 The indoor dust microbiota composition appears to be a definable, reprod

113 Changes in immunological processes and microbiota composition are accentuated in obese asthma p

114 Alterations in gut microbiota composition are associated with metabolic syn

115 ling caused by antibiotic-induced changes in microbiota composition are dependent on the synthesis of

116 Shifts in commensal microbiota composition are emerging as a hallmark of gas

117 ce indicate that MHC-mediated differences in microbiota composition are sufficient to explain suscept

118 ary antibiotic therapy, but their effects on microbiota composition are undetermined.

119 l microbiota composition, and how changes in microbiota composition arising from cultivation affect c

120 ocus on the increasing evidence defining the microbiota composition as a key determinant of immunity

121 men, sIgAd subjects displayed an altered gut microbiota composition as compared to healthy controls.

122 ularly important for predicting steady-state microbiota composition as it imposes significant restric

123 ome was within-patient change in respiratory microbiota composition (assessed by Bray-Curtis index) b

124 Microbiota composition, assessed by 16S rRNA gene amplic

125 Distinct alterations of gut morphology and microbiota composition associated with reduction of circ

126 Though we find no major differences in microbiota composition associated with wAnga infection,

127 The microbiota composition at one week of life is associated

128 he quantity and source of dietary protein on microbiota composition, bacterial metabolite production,

129 ad4(+/-)/Sptbn1(+/-)) to identify changes in microbiota composition before development of colon tumor

130 als, and cheese contributed to shifts within microbiota composition (beta-diversity).

131 The change in microbiota composition between baseline and week 48 was

132 e show by modeling differences in house dust microbiota composition between farm and non-farm homes o

133 Differences in fecal microbiota composition between groups were analyzed by m

134 ifferences in the small intestinal and fecal microbiota composition between mice housed on clean bedd

135 terial strains and incorporates variation in microbiota composition between people, while also allowi

136 tly different microbiota, and segregation of microbiota composition between periodontitis and health

137 he use of microarrays.HPDs did not alter the microbiota composition, but induced a shift in bacterial

138 fferent time points after infection to study microbiota composition by 16 S rRNA amplicon sequencing

139 Analysis of fecal microbiota composition by 16S ribosomal RNA gene sequenc

140 Secondary end points were safety and microbiota composition by phylogenetic microarray in fec

141 microbiota and revealed that differences in microbiota composition can be associated with inflammato

142 Reciprocally, microbiota composition can influence the efficacy and to

143 iet became the most important determinant of microbiota composition; cessation of breastfeeding, rath

144 We discuss how shifts in the microbiota composition change host susceptibility to inf

145 of this study were to examine how the faecal microbiota composition changed before, during and after

146 We also found that CB0313.1 modulated gut microbiota composition, characterized by a decreased rat

147 gnizes flagellin, have an altered intestinal microbiota composition compared with wild-type mice; the

148 Ten years ago, we discovered that microbiota composition controls intestinal T cell homeos

149 rac distances, P = .027) of the variation in microbiota composition could be explained by the GFD.

150 i et al. (2017) show that RegIIIbeta impacts microbiota composition, decreasing vitamin B6 production

151 Here we show that gut microbiota composition depends on interactions between h

152 copic findings of Pap smears and the vaginal microbiota composition determined by next generation seq

153 In this study, we investigated if the fecal microbiota composition, determined by a high throughput

154 Despite distinct strain differences in gut microbiota composition, diet had a preponderant impact o

155 many factors that determine the human colon microbiota composition, diet is an important one because

156 One year after surgery, the fecal microbiota composition differed between CD patients (n =

157 therapy had independent and rapid effects on microbiota composition distinct from other stressor-indu

158 yet the role of the immune system in shaping microbiota composition during an organism's life span ha

159 tential for modulating diet, sanitation, and microbiota composition during antibiotics.

160 We explored variation in Tibetan macaque gut microbiota composition during winter and spring seasons.

161 Microbiota composition (dysbiosis) was evaluated by Pyro

162 roof of concept that a HD-5 fragment shifted microbiota composition (e.g., increases of Akkermansia s

163 tions of each of these factors on intestinal microbiota composition following VSG prior to substantia

164 s can be used to obtain predicted changes in microbiota composition for improved health.

165 The role of the fecal microbiota composition for the postoperative disease cou

166 d to estimate and separate the effect of gut microbiota composition from that of nutrient intake on V

167 e determined relative and absolute bacterial microbiota compositions from six distinct cultivars duri

168 Larval survival, growth, microbiota composition, gene expression profiles and dis

169 ons between breastfeeding and nasopharyngeal microbiota composition had disappeared.

170 es are not clear; modification of intestinal microbiota composition has been reported to reflect anim

171 f a posteriori-derived dietary patterns, and microbiota composition has not been adequately studied,

172 Perturbations in intestinal microbiota composition have been associated with a varie

173 Microbiota compositions have great implications in human

174 Host diet is known to alter microbiota composition, implying that dietary treatments

175 aronia berries on vascular function and gut microbiota composition in a healthy population.

176 the associations between usual diet and gut microbiota composition in a large sample of healthy Fren

177 The phylogenetic microbiota composition in asthmatics patients' homes was

178 omponent, abolished rhythmicity in the fecal microbiota composition in both genders.

179 mation, increased adiposity, and altered gut microbiota composition in both male and female mice, alt

180 pplication as a prebiotic for regulating gut microbiota composition in diabetic patients.

181 al and non-redundant role in controlling gut microbiota composition in humans and that secretory IgA

182 e reasons underlying striking differences in microbiota composition in independently evolved, yet fun

183 phimurium infection is strongly modulated by microbiota composition in individual lines.

184 A comparison of root and gut microbiota composition in multiple host species belongin

185 and higher Firmicutes, resembling changes in microbiota composition in nonalcoholic steatohepatitis (

186 benefits or harmful consequences of the gut microbiota composition in regard to wound healing are ne

187 whether urbanization is associated with the microbiota composition in the infants' body and early im

188 idified water differentially changed the gut microbiota composition in these mice.

189 High fat feeding altered gut microbiota composition including enrichment of Acinetoba

190 also been implicated as determinants of the microbiota composition, including exclusion of pathogens

191 lulose-based diet had similar changes in gut microbiota composition, indicating that diet can modify

192 roved endothelial function and modulated gut microbiota composition, indicating that regular aronia c

193 We investigated whether specific microbiota compositions influence immune responses to gl

194 Host immunity shapes intestinal microbiota composition, influencing health and disease.

195 tasis by controlling host defense responses, microbiota composition, intestinal inflammation and tiss

196 Gut microbiota composition is a contributing factor to the s

197 microbiota variability, and its influence on microbiota composition is an active area of investigatio

198 Nasopharyngeal microbiota composition is associated with delayed RSV cl

199 However, what shapes microbiota composition is not clear, in particular the r

200 and dermis, demonstrating that the change in microbiota composition is related to the presence of MCT

201 Overall, gut microbiota composition is strongly associated with breas

202 Patterns of spatial variation in microbiota composition may help explain Staphylococcus a

203 al consortia to individuals with compromised microbiota composition may reduce inter-patient transmis

204 utrient intake, food-related behavior, fecal microbiota composition, microbial fermentation, and gast

205 Differences in microbiota composition might influence the response to a

206 Lastly, we found that neither microbiota composition nor diversity were associated wit

207 The greatest shifts in microbiota composition occurred between stem cell infusi

208 could also affect the dynamic changes in the microbiota composition occurring during pregnancy.

209 In this study, we examined the microbiota composition of allo-HSCT recipients to identi

210 At this time point, the microbiota composition of CD patients was associated wit

211 The fecal microbiota composition of CD patients, analyzed by GA-ma

212 16S rRNA gene sequencing to investigate the microbiota composition of each periodontal group evaluat

213 Data on perinatal pet ownership, WB, and the microbiota composition of faecal samples of the infants

214 We characterized baseline microbiota composition of fecal samples at 6 months of a

215 80 degrees C had only limited effects on the microbiota composition of human feces.

216 ed the influence of long-term storage on the microbiota composition of human stool samples collected

217 ative real-time PCR and immunofluorescence), microbiota composition of ileum content (16S recombinant

218 A large interpersonal variation in the skin microbiota composition of patients hospitalized with cel

219 Changes in the microbiota composition of patients with FGIDs are genera

220 Microbiota composition of post-UC samples was different

221 Secondly, the fecal microbiota composition of the African swine fever (ASF)

222 us 2, explained significant variation in gut microbiota composition of the infants.

223 We also analyzed the microbiota composition of the recipients and their genet

224 impact of initial alpha-diversity and fecal microbiota composition on beta-diversity instability upo

225 diet, sleep patterns, physical activity, and microbiota composition on microglia biology and consider

226 imary objective was to determine if baseline microbiota composition or diversity was associated with

227 Although imbalances in gut microbiota composition, or "dysbiosis," are associated w

228 tion without affecting disease severity, gut microbiota composition, or gut permeability.

229 opmental block caused by Rag deficiency), in microbiota composition, or minor differences in the gene

230 omal RNA gene amplicon sequencing to profile microbiota composition over a 12-mo period in 49 partici

231 dataset, individuality was a major driver of microbiota composition (P = 0.002) and was more pronounc

232 erythromycin caused a significant change in microbiota composition (p=0.03 [by analysis of similarit

233 estinal tract is regulated by the intestinal microbiota composition, particularly the presence of seg

234 Our findings suggest that microbiota composition, perhaps Clostridium spp., contri

235 ire and examined in relation to overall oral microbiota composition (PERMANOVA analysis), and to spec

236 nd adipose tissue insulin sensitivity, fecal microbiota composition, plasma and fecal SCFA, energy ex

237 e previously showed differences in mucus gut microbiota composition preceded colitis-induced inflamma

238 nd used 16S rRNA sequencing to determine gut microbiota composition pretransplantation and post-trans

239 ranscript levels, metabolite levels, and gut microbiota composition, provide a framework for understa

240 Bowel decontamination led to redistributed microbiota composition, reduced proinflammatory activati

241 We report that altering the microbiota composition reduces CRC in APC(Min/+)MSH2(-/-

242 fecal anti-flagellin IgA and alterations in microbiota composition, reduces fecal flagellin concentr

243 t cold exposure leads to marked shift of the microbiota composition, referred to as cold microbiota.

244 Further, the changes in intestinal microbiota composition related to the improvement of thi

245 in weight loss and shifts in the intestinal microbiota composition relative to sham-operated mice.

246 Nasal microbiota composition remained relatively stable despit

247 Restoration and maintenance of a healthy gut microbiota composition requires effective therapies to r

248 The analysis of the microbiota composition revealed a decrease of the relati

249 le Positive Breast Cancer (TPBC) tissues for microbiota composition revealed significant differences

250 Analysis of fecal microbiota composition showed an increase in bacterial r

251 These results suggest the gut microbiota composition significantly affects the bioavai

252 onas aeruginosa, erythromycin did not change microbiota composition significantly.

253 in nutrients on VFM appears to depend on gut microbiota composition, specific gut microbes may affect

254 (median age, 35 d) were divisible into three microbiota composition states (NGM1-3).

255 atory machinery of the host and the resident microbiota composition, such that disturbances in one tr

256 neficial" influence of older siblings on the microbiota composition suggests that this microbiota may

257 ittle is known about specific changes in the microbiota composition that cause phenotypic differences

258 ach geographic locale displayed a unique gut-microbiota composition that could not be fully explained

259 to pathological bone loss, while changes in microbiota composition that prevent, or reverse, bone lo

260 In addition to alterations in gut microbiota composition, the metabolic potential of gut m

261 enotypic shift was accompanied by changes in microbiota composition: the genus Burkholderia was speci

262 acteristics at sites of infection will shape microbiota composition through exerting selective pressu

263 Identifying differences in microbiota composition through the use of 16S rRNA gene

264 sted for confounding factors, we found fecal microbiota composition to be associated with development

265 Strategies to use changes in microbiota composition to effect health improvements req

266 use of nutritional strategies to program the microbiota composition to favor a more beneficial bacter

267 es as the similarity of their home bacterial microbiota composition to that of farm homes increases.

268 on by regulating macrophage polarization and microbiota composition under homeostatic conditions and

269 y, we show that CRTAM expression affects gut microbiota composition under homeostatic conditions.

270 olling Th17 activity and that changes in the microbiota composition upon Giardia infection partially

271 bwe, we determined the association of sputum microbiota composition (using 16S ribosomal RNA V4 gene

272 er (25% vs 17%), an association with the gut microbiota composition was almost undetectable.

273 Microbiota composition was analysed by a combination of

274 Fecal and rectal biopsy-associated microbiota composition was analyzed by 16S ribosomal DNA

275 Gut microbiota composition was analyzed in fecal samples and

276 ausative pathogen, and explored whether skin microbiota composition was associated with clinical outc

277 Microbiota composition was characterized using 16S ribos

278 Microbiota composition was considerably different betwee

279 Microbiota composition was determined by 16S rRNA gene s

280 Microbiota composition was determined in 167 participant

281 Microbiota composition was determined using 16S ribosoma

282 Gut microbiota composition was determined via 16S rRNA seque

283 The basal microbiota composition was distinct between genotypes, a

284 The cecal microbiota composition was drastically modified in the K

285 Gut microbiota composition was established through sequencin

286 Microbiota composition was heterogeneous, but there was

287 The gastric microbiota composition was highly variable between indiv

288 While baseline microbiota composition was not predictive of weight loss

289 Further analysis of microbiota composition was performed at the genus level.

290 ere examined for basal phenotypes, including microbiota composition; we also analyzed responses to pa

291 etabolic disease and inflammation, and fecal microbiota composition were assessed.

292 ression in the hippocampus and shifts in the microbiota composition were normalized by the enriched d

293 Dietary habits affect gut microbiota composition, whereas endotoxins produced by G

294 Analysis revealed significant segregation of microbiota compositions which was validated by Beta dive

295 l permeability and changes in the intestinal microbiota composition, which contribute to the developm

296 ciated with significantly altered intestinal microbiota composition, which was linked to an impaired

297 tribution, HF diet also drastically affected microbiota composition with a profile characterized by t

298 system changes were associated with altered microbiota composition with notable increases in intesti

299 tify features and determinants of human milk microbiota composition, with potential implications for

300 ection accelerated the rate of change in gut microbiota composition within individuals for periods of