ライフサイエンスコーパス: ileum

1 mpartments (stomach, duodenum, and jejunum + ileum).

2 ue which was involving muscular layer of the ileum.

3 rge (2.5 x 2.3 cm) pedunculated polyp in the ileum.

4 hich biopsy specimens were obtained from the ileum.

5 (15 g, 235 kJ) or saline to the duodenum or ileum.

6 er exposure resulted in organoids similar to ileum.

7 ormone convertase 1/3 gene expression in the ileum.

8 y means of the bile salt transporters of the ileum.

9 r-quadrant mass arising from the wall of the ileum.

10 mpaction of the distal- most fragment in the ileum.

11 el, and promotes colonization of the chicken ileum.

12 he duodenum and jejunum and decreased in the ileum.

13 more rapid response in the colon than in the ileum.

14 erexpressing HA-NHE3 and cGKII, and in mouse ileum.

15 ed the homeostatic amount of proIL-18 in the ileum.

16 small intestine and the circumference of the ileum.

17 e colon but not in the duodenum, jejunum, or ileum.

18 m receptor desensitization in the guinea pig ileum.

19 ion and IL-1beta and IL-18 production in the ileum.

20 ings affected mostly at jejunum and proximal ileum.

21 ble from both COS-7 cells and the guinea pig ileum.

22 A2) expressed on enterocytes in the terminal ileum.

23 patients, mainly seen at distal jejunum and ileum.

24 other had chronic ischemic ulceration in the ileum.

25 teins in cholinergic axons in the guinea pig ileum.

26 ge enteric duplication cyst arising from the ileum.

27 and reduced number of L cells in the distal ileum.

28 s, they are commonly seen in relation to the ileum.

29 tration changes in the duodenum, jejunum and ileum.

30 in expression was upregulated in jejunum and ileum.

31 titate the levels of amylase in the terminal ileum.

32 leum but only partially relaxed nNOS(S1412A) ileum.

33 segmentation were faster in the nNOS(S1412A) ileum.

34 al pain - an ectopic pancreas located in the ileum.

35 cated approximately 1.5 m distal to terminal ileum.

36 e and IFNgamma-producing immune cells in the ileum.

37 t of patients with CD affecting the terminal ileum.

38 er rates of healing in the colon than in the ileum.

39 cal site for stoma formation followed by the ileum (18, 10.8%).

40 nts with ileitis were higher than in control ileum (5.1% +/- 3.7 for P-selectin and 4.8% +/- 2.3 for

41 in the liver (98.3%), duodenum (97.8%), and ileum (89.7%), unconjugated bile acids comprised the lar

42 of patients had a histologic response in the ileum (95% CI 17.5-41.4).

43 of patients had a histologic response in the ileum (95% CI 19.1-52.2).

44 t and initiate tissue invasion of the distal ileum, a virulence process carried out by the type III s

45 T cells in human blood, colon, and terminal ileum acquired APC functions upon microbial activation i

46 nalyzed neutrophil infiltration of the mouse ileum after allo-HCT by in vivo myeloperoxidase imaging

47 CTX-induced disease in the ileum also led to increased concentrations of long-chain

48 tment x time, P < 0.05) such that glucose-to-ileum altered VAS-rated fullness, satisfaction, and thou

49 d significant DNA damage in the duodenum and ileum and apoptosis in the lungs of the RCO-treated mice

50 l biopsies (N = 236) collected from terminal ileum and ascending and sigmoid colons of children (medi

51 collected mucosal biopsies from the terminal ileum and ascending colon during surgery and post-operat

52 hared HIV-1 antibody clonal lineages between ileum and blood.

53 HDTA was found to be absorbed mainly in the ileum and Caco-2 cell monolayer through passive diffusio

54 stems and contributed to colonization of the ileum and caecum in the streptomycin-pretreated mouse mo

55 on induces cholecystokinin expression in the ileum and cecum by changing microbiota composition and m

56 nin (Cck) mRNA and protein expression in the ileum and cecum, as well as preproglucagon (Gcg) and neu

57 tide-1 (GLP-1)(+)/Peptide YY (PYY(-)) in the ileum and colon and GLP-1(-)/PYY(-) in the cecum.

58 nd upregulation of Fxr in duodenum, jejunum, ileum and colon in WD + PDX mice.

59 of Peptostreptococcaceae was higher in both ileum and colon of 13% CP group.

60 al integrity was compromised in the HS pigs (ileum and colon TER decreased; P<0.05).

61 At the end of the study, the ileum and colon were harvested, washed, and counted ex v

62 PrP(Sc) with time in the GI, except for the ileum and colon which showed sustained increases peaking

63 in the gastrointestinal (GI) tract (jejunum, ileum and colon).

64 colonization of beneficial bacteria in both ileum and colon, and improve gut barrier function.

65 blind sacs arising from the junction of the ileum and colon, are homologous to the cecum in mammals.

66 c evidence of ischemia/reperfusion injury in ileum and colon, but not in the lungs or kidneys.

67 In the ileum and colon, enteropathy was associated with increas

68 iscerofugal CART(+) neurons, enriched in the ileum and colon, modulated feeding and glucose metabolis

69 r mouse atlas include 5,068 neurons from the ileum and colon, revealing extraordinary neuron diversit

70 Pathogenesis is believed to occur in the ileum and colon, where the bacteria adhere and form a ro

71 ls were lower in PI-IBS D than in HC in both ileum and colon.

72 matory condition most commonly affecting the ileum and colon.

73 was present within the murine mucosa of both ileum and colon.

74 myenteric neurons were reduced by 27%-61% in ileum and colon.

75 seems to be more efficient and reliable for ileum and colon.

76 up 2) showed better results than Group 1 for ileum and colonic segments according to distension and c

77 glycaemic response which was specific to the ileum and did not occur on infusion into the jejunum.

78 Estimated mesors (rhythm-adjusted mean) of ileum and hepatic P-gp activity were higher in males as

79 Sepsis is a multiorgan disease affecting the ileum and jejunum (small intestine), liver, skeletal mus

80 In formula-fed animals, increases in ileum and jejunum villus height and crypt depth were obs

81 d to reduce C. jejuni colonization in cecum, ileum and jejunum, by more than one log CFU/g when compa

82 robial communities' compositions of terminal ileum and large intestine in 5 healthy individuals.

83 Plasma, ileum and liver concentrations of talinolol, a pure P-gp

84 Organ edema was increased in the ileum and liver in the HS/CR vs sham group, and MC-2 dec

85 es involved in linoleic acid metabolism: the ileum and lung had significant changes in the metabolism

86 imaging signal compared with that in control ileum and MBControl.

87 n increased IL-1beta and IL-18 production in ileum and NOX-2-dependent oxidative stress.

88 aging, and identify differences between the ileum and proximal/distal colon.

89 laparotomy for a perforation in the terminal ileum and recovered.

90 The reduction of ceramide levels in the ileum and serum in tempol- or antibiotic-treated mice fe

91 vely correlated with T cell expansion in the ileum and spleen.

92 d with reduced serum amyloid A expression in ileum and synovial tissue.

93 The ileum and the liver demonstrated significant changes in

94 on-like peptide-1 (GLP-1) is produced in the ileum and the nucleus of the solitary tract.

95 The terminal ileum and thoracic spinal cord (T(11)) were sampled for

96 of ileocolitis (inflammation of the terminal ileum and/or colon).

97 of the TIM-1 (stomach, duodenum, jejunum and ileum) and viscosity was measured with a dynamic rheomet

98 small intestine and measured in the terminal ileum, and can be readily quantitated by the existing te

99 Several EN subtypes in the duodenum, ileum, and colon are conserved between humans and mice b

100 and mucosal scraping samples from bronchus, ileum, and colon were collected approximately 164 days p

101 cART initiation (from the duodenum, jejunum, ileum, and colon), 3 months after cART initiation (from

102 n intestinal tissues, including the jejunum, ileum, and colon, but very few proliferating cells were

103 es ratio than the S-raised pigs at bronchus, ileum, and colon, respectively.

104 , had active Crohn's disease of the terminal ileum, and had not responded to at least 3 months of con

105 with skip lesions extending to the terminal ileum, and histology showing polymorph infiltration of t

106 ence intensity of HDTA in mice came from the ileum, and it was eliminated from the body through colon

107 emory) and non-CD4+ T leukocytes from blood, ileum, and rectum of 8 ART-suppressed HIV-positive subje

108 xpression is present in liver, lung, kidney, ileum, and some endocrine glands.

109 ver infection of B cells was not observed in ileum, and the entire lamina propria in sections of duod

110 y mediators-mostly in the colon, then in the ileum, and then in the duodenum.

111 Remarkably, a majority (82%) of the ileum anti-gp41 antibodies cross-reacted with commensal

112 Patients with CD of the ileum are characterized by reduced constitutive expressi

113 significantly increased Foxp3(+)Tregs in the ileum as early as day of life (DOL)1 but did not produce

114 cific host and microbe profiles identify the ileum as the primary inductive site for all forms of CD

115 aired antimicrobial factor expression in the ileum, as well as colonocyte apoptosis and microbiota-dr

116 F-beta1, alpha-SMA, TGR5, NTCP, OATP1a1, and ileum ASBT and decreased liver IL-10, FXR, CAR, VDR, BSE

117 stomach, antrum, corpus, duodenum, terminal ileum, ascending colon, and descending colon.

118 wed a dose-responsive GLP-1 secretion in the ileum at >/=200 mmol/L glucose.

119 ntestinal epithelial cells (IECs) within the ileum at steady state but was absent from the IECs of ge

120 of the TIM-1 (stomach, duodenum, jejunum and ileum) at different times of digestion and analysed in t

121 The dominant ileum B cell response was to Env gp41.

122 henomenon, we examined anti-HIV responses in ileum B cells using recombinant antibody technology and

123 29)-Lys-cholyl-insulin when infused into the ileum, B(1)-Phe-cholyl-insulin did cause a long lasting

124 CH4 was administered intraluminally into the ileum before 45 minutes mesenteric ischemia or before re

125 aluation of changes in HIV reservoir size in ileum biopsies and in peripheral blood in individuals sw

126 We obtained serum samples and terminal ileum biopsies from 47 patients with CD and 16 healthy i

127 normal were included, provided that terminal ileum biopsies had been performed.

128 on the HIV reservoir in peripheral blood and ileum biopsies in patients switching from boosted protea

129 We further show that FXR signalling in ileum biopsies of humans positively correlates with body

130 We analyzed blood and ileum biopsies to quantify episomal, total, and integrat

131 ere isolated from small bowel (i.e. terminal ileum) biopsies using EDTA/DTT and enzymatic release fol

132 22 and IFN-gamma mRNA levels in the terminal ileum but had limited effect on the GI fungal microbiome

133 ht junction protein organization only in the ileum but not in the colon of morphine treated WT animal

134 ed nNOS S1412 phosphorylation and relaxed WT ileum but only partially relaxed nNOS(S1412A) ileum.

135 In ex vivo tissue from the duodenum and ileum, but not the colon, 300 mmol/L glucose potently st

136 logical activity of released peptides on rat ileum by isolated organ bath from A1A1 (IC50=0.534-0.595

137 Colonization of the ileum by SFB induced changes in host gene expression and

138 We report a case of ectopic pancreas in the ileum causing obscure gastrointestinal bleeding and epis

139 d, including the stomach, duodenum, jejunum, ileum, cecum, appendix, colon and rectum.

140 mune activation were determined in duodenum, ileum, colon, and mesenteric lymph nodes.

141 vasion of the epithelium lining the terminal ileum, colon, and rectum by Shigella species.

142 munofluorescence), microbiota composition of ileum content (16S recombinant DNA massive sequencing),

143 (E2348/69) to induce infectious ileitis, and ileum contents were quantified by polymerase chain react

144 ed congestion of capillaries in the terminal ileum correlated with an increased bioavailability of lu

145 and ulcerations in the jejunum and proximal ileum covered by fibrin; histological report showed macr

146 al number of MSs absorbed in the jejunum and ileum, demonstrating that nonphagocytic processes (inclu

147 ly increased the fat-derived adiponectin and ileum-derived fibroblast growth factor (FGF) 15.

148 Fibroblast growth factor 19 (FGF19) is an ileum-derived metabolic hormone induced by bile salts up

149 hether glucose infused into the duodenum and ileum differentially alters appetite response, food inta

150 ed in increased Slc30a10 expression in mouse ileum epithelia.

151 ation and transcription patterns in terminal ileum epithelium, compared with controls.

152 hes infections by flagellar anchoring to the ileum epithelium.

153 nowledge, cells isolated from human terminal ileum exposed ex vivo to the wild-type S. Typhi strain w

154 to quantify which neurons in the guinea pig ileum expressed alpha-synuclein, cysteine string protein

155 nNOS(S1412A) ileum expressed less phosphodiesterase-5 and was more se

156 l to terminal ileum transit and 10% terminal ileum filling also decreased as small bowel transit time

157 ng, maximal intestinal filling, 10% terminal ileum filling, duodenal to terminal ileum transit, cecal

158 In ileum, formula diet induced significant up-regulation of

159 -hydroxylase mRNA levels were induced, while ileum FXR target genes were suppressed in DKO mice compa

160 um G2 lesion, 7 ileum G2 lesions, 2 terminal ileum G1 lesions, 1 pancreas G2 lesion, and 1 gallbladde

161 d graded as follows: 1 duodenum G2 lesion, 7 ileum G2 lesions, 2 terminal ileum G1 lesions, 1 pancrea

162 med distal gallbladder bile diversion to the ileum (GB-IL(dist)), that emulates the altered bile flow

163 Bile diversion to the ileum (GB-IL) has strikingly similar metabolic and satia

164 Compared to the blood, the ileum had higher levels of HIV DNA and RNA in both CD4+

165 ogical activity of pancreatic enzymes in the ileum has been studied in healthy volunteers but not qua

166 Ileum heat shock protein 70 expression increased (P<0.05

167 resent a case of a patient with strangulated ileum herniated through the foramen of Winslow.

168 After delivering MSs to the jejunum or ileum, high concentrations of polystyrene were detected

169 stress agent in epithelial cells of the rat ileum (IEC-18) were determined.

170 Bile diversion to the ileum improves glucose homeostasis via an intestinal Fxr

171 ucoside conjugates were not recovered in the ileum in agreement with their absorption in the upper GI

172 , designed to deliver the drug to the distal ileum in patients with IgA nephropathy.

173 computed tomography scan revealed a loop of ileum in the lesser sac.

174 d FXR pathway expression in both jejunum and ileum, in association with increased gut permeability th

175 Glucose infusion to the ileum increased GLP-1 and PYY secretion, suppressed aspe

176 Gene expression analysis of the liver and ileum indicated alterations in several steps of bile aci

177 t ZnO NPs reduce fluid accumulation in mouse ileum induced by the cholera toxin (CT) protein.

178 ld stimulation (EFS) of wild-type (WT) mouse ileum induced nNOS S1412 phosphorylation that was blocke

179 Thus, MHC class II expression by IECs in the ileum initiates lethal GVHD, and blockade of IL-12/23p40

180 colic intussusception is the invagination of ileum into the colon.

181 on (IT), a surgical relocation of the distal ileum into the proximal jejunum, on FXR and LXRs in rats

182 Ectopic pancreas in the ileum is a rare and often an incidental finding.

183 ide with pH-modified release in the terminal ileum is not effective.

184 Histomorphometric analyses of ileum, jejunum and Peyer's patches were carried out, to

185 The specific metabolic changes in the ileum, jejunum, liver, skeletal muscle, and lung have no

186 Eighteen hours later, ileum, jejunum, medial gastrocnemius skeletal muscle, li

187 d 426 genes co-regulated with ENHO in liver, ileum, kidney medulla, and lung.

188 composition of bacterial communities in the ileum (Lactobacillus species became the most abundant) a

189 mote inflammation in both adipose tissue and ileum, leading to insulin resistance and impaired glucos

190 l sampling device positioned at the terminal ileum level.

191 ompromised mice, duodenum-like organoids and ileum-like organoids retained their regional identity, d

192 Patients with diseased terminal ileum longer than 40 cm or abdominal abscesses were excl

193 in patients with limited (diseased terminal ileum <40 cm), non-stricturing, ileocaecal Crohn's disea

194 i feeding resulted in a 3.9-fold increase in ileum lumen H(2)O(2).

195 id not affect secretory IgA release into the ileum lumen or mucosal leukocyte subsets.

196 ameter) were actively absorbed in the distal ileum mediated by interactions with the apical sodium bi

197 Lymphocytes isolated from ileum, mesenteric lymph nodes (MLN), spleen and thymus w

198 cell recruitment, and cytokine expression in ileum, mesenteric lymph nodes, and spleen.

199 Adding BEOs changed the host ileum microbial population by increasing the numbers of

200 ccelerated and the meal reached the terminal ileum more rapidly.

201 pecific circadian changes were found in P-gp ileum mRNA and protein levels, circadian amplitudes bein

202 Ex-vivo bioluminescence recordings of ileum mucosae from transgenic mice revealed endogenous c

203 =2), stomach (n=5), duodenum (n=1), terminal ileum (n=5), and rectum (n=1).

204 This was supported by increased ileum Na(+)/K(+) ATPase activity in HS pigs.

205 al specimens from sigmoid colon and terminal ileum of 19 INR and 20 IR in addition to 20 HIV negative

206 y converse, pDCs accumulated in the terminal ileum of ART-naive HIV individuals compared with control

207 nd dopamine transporter are deficient in the ileum of Cdnf (-/-) mice.

208 iNKT markers (Il4, Il15) were upregulated in ileum of CS-delivered mice.

209 upregulated in the spleen, liver, colon, and ileum of GVHD mice.

210 ileal bacteria with genes upregulated in the ileum of healthy or CMA colonized mice identified a clos

211 d microbiota could also be isolated from the ileum of HIV-1 uninfected individuals.

212 decreased in IMFs isolated from the inflamed ileum of IBD patients indicating that Tpl2 function in I

213 neutrophil granulocytes (neutrophils) in the ileum of mice developing GVHD.

214 docrine cell progenitors are abnormal in the ileum of patients with irritable bowel syndrome (IBS), a

215 Biopsy specimens from the terminal ileum of patients with ulcerative colitis (n = 20), CD (

216 ximin alters the bacterial population in the ileum of rats, leading to a relative abundance of Lactob

217 eas, liver, kidney, esophagus, duodenum, and ileum of RCO-treated mice.

218 sis was enhanced in the pancreas, colon, and ileum of Rpl12 haplosufficient mice.

219 marily in the kidney and ear (outside of the ileum of the GI) offering significant scope for specific

220 e been reported in the duodenum, jejunum and ileum of the small intestine, and in human intestinal tu

221 Intestinal tissues from the ileum of wild-type mice injected with a vector expressin

222 om) were delivered locally to the jejunum or ileum or by oral administration to young male rats.

223 Eosinophils were not increased in ileum or colon samples.

224 CDAI) of 220-450, with mucosal ulcers in the ileum or colon, or both, and a Crohn's Disease Endoscopi

225 hrough a gallbladder anastomosis to jejunum, ileum or duodenum (sham control).

226 We employed mouse primary ileum organoids to investigate the transcriptional effec

227 < 0.01 villus height, p < 0.04 crypt depth; ileum p < 0.001 villus height, p < 0.002 crypt depth).

228 ly, DCA reduced C. perfringens invasion into ileum (P < 0.05) without altering the bacterial ileal lu

229 gulate the density of microfold (M) cells in ileum Peyer's patch (PP) follicle-associated epithelia (

230 In the ileum, pigs fed hLZ-milk had significantly lower express

231 orter (IBAT) protein expressed in the distal ileum plays a key role in the enterohepatic circulation

232 articipant A despite extensive sampling from ileum, rectum, lymph nodes, bone marrow, CSF, circulatin

233 n between mucosal Teff cells and CBAs in the ileum regulate intestinal immune homeostasis.

234 monocyte differentiation into the colon and ileum-resident macrophages revealed the graduated acquis

235 We find that only bile diversion to the ileum results in physiologic changes similar to RYGB, in

236 ssion of tight junction (TJ) proteins in the ileum revealed claudin 3 and occludin expression to be i

237 nd fat-1 mice were chronically fed EtOH, and ileum RNA-seq and bioinformatic analyses were performed.

238 d cell death at the crypt bottom in inflamed ileum samples.

239 volving infusion of natural insulin into the ileum showed either nil absorption or absorption of a sm

240 of CD3(+) T cells and Foxp3(+) Tregs in the ileum significantly decreased in pups with NEC, compared

241 proportion of Clostridium_sensu_stricto_1 in ileum significantly decreased, whereas Escherichia-Shige

242 s were collected from the duodenum, jejunum, ileum (small intestine) and colon at six weeks post-term

243 Here we examined the ileum-specific effects of reducing CLR on TxA ileitis by

244 ere collected at weeks 0, 8, and 44 from the ileum, splenic flexure, and rectum (18 biopsy samples fr

245 gallbladder bile is diverted to the proximal ileum, termed GB-IL(prox), also improves glucose control

246 and effector memory cells were higher in the ileum than blood.

247 ircumferential lesion involving the terminal ileum that acted as a leading point to an ileo-ileal int

248 1 as an IFNgamma-regulated gene in the mouse ileum that controls gut A. muciniphila levels.

249 At emergency laparotomy, a herniated loop of ileum that had become strangulated at its entry to the l

250 In the ileum, the density of the general population and nitrerg

251 ticularly noticed in sections of jejunum and ileum, the detection suggested the possibility of direct

252 In the ileum, the proportion of intraepithelial lymphocytes and

253 mparing the microbial signatures between the ileum, the rectum, and fecal samples indicates that at t

254 In the ileum, this response was independent of osmotic influenc

255 wild-type Teff cells upregulated Mdr1 in the ileum, those lacking Mdr1 displayed mucosal dysfunction

256 presented with granulomatous nodulae in the ileum, thus reflecting an intestinal sarcoid manifestati

257 lower in inflamed mucosal samples (terminal ileum (TI) and duodenum) of children with CD, but higher

258 rentiation in a region-specific manner, with ileum tissue being influenced the most.

259 ctum, caecum, and sigmoid colon and terminal ileum tissue samples at 22 months.

260 After 5 days, distal ileum tissue was collected, homogenized, and protein ext

261 iciency was assessed by lysozyme staining of ileum tissues and lysozyme activity in fecal samples.

262 ormed immunohistochemical analyses of distal ileum tissues from 6-8 patients with Crohn's disease (CD

263 Distal ileum tissues from patients with CD had lower levels of

264 and did not receive rapamycin (controls), in ileum tissues from rats or mice given rapamycin, and in

265 reduction in Na(+)/H(+) exchange activity in ileum tissues from these mice.

266 Distal ileum tissues were collected from mice; IECs and enteroi

267 Levels of IFNL were highest in ileum tissues with severe inflammation.

268 bile acid-responsive genes in the intestinal ileum to augment insulin sensitivity and of cholesterol

269 Vibrio cholerae colonizes the human terminal ileum to cause cholera, and the arthropod intestine and

270 ted the xenobiotic transporter, Mdr1, in the ileum to maintain homeostasis in the presence of bile ac

271 m the bile duct to the midjejunum or the mid-ileum to match the modified bile delivery in the gut occ

272 nipulate fatty acid sensing machinery in the ileum to regulate glucose homeostasis.

273 showed ulcerative lesions from the terminal ileum to the ascending colon with a non-specific histo-p

274 Duodenal to terminal ileum transit and 10% terminal ileum filling also decrea

275 terminal ileum filling, duodenal to terminal ileum transit, cecal filling initiation, and ileocecal v

276 and thoughts of food compared with saline-to-ileum (Tukey's post hoc, P < 0.05); decreased ad libitum

277 with normalized permeability selectively in ileum (up-regulated claudin-1 and occludin) and a signif

278 eceptors, as well as the guinea pig isolated ileum, using the full agonist CP55940 as a positive cont

279 rmine the membrane protein expression in the ileum, VE-cadherin, occludin, and claudin-3, Western blo

280 induced contractions in isolated guinea pig ileum via CB1 receptors (pEC50, 6.0 +/- 0.4).

281 ession and reduced apoptosis in the terminal ileum via Fas-associated protein with death domain prote

282 us bacteria (SFB), a gut microbe residing on ileum villi and PP FAE that mediates resistance to STm i

283 sham group, and MC-2 decreased edema in the ileum vs the HS/CR group.

284 The ileum was imaged with clinical-grade dual P- and E-selec

285 T-cell infiltration into the ileum was increased; epithelial proliferation was decrea

286 independent port access to the duodenum and ileum was inserted, and position was confirmed by X-ray.

287 The loop of ileum was reduced but was nonviable, which had to be res

288 expression of tight junction proteins in the ileum was significantly decreased.

289 nous nitrogen and AA flows at the end of the ileum was studied.

290 y reduced intestinal IRI (P < 0.001): In the ileum, we observed a more than 8-fold decrease in injure

291 Samples of the duodenum, jejunum, and ileum were also dissected from each animal to evaluate t

292 injury and lipid peroxidation in jejunum and ileum were analyzed by histology and malondialdehyde (MD

293 ropria in sections of duodenum, jejunum, and ileum were HuNoV-negative.

294 Segments of the duodenum, jejunum, and ileum were subjected to histological processing for morp

295 es, and prevention of edema formation in the ileum when administered with CR following HS.

296 expression was predominantly observed in the ileum where bacterial density appeared highest.

297 A major site of BA action is the terminal ileum, where enterocytes actively reuptake BAs and expre

298 bust IL-17A production was restricted to the ileum, where SFB makes direct contact with the epitheliu

299 eptor-induced contractions in the guinea pig ileum, which are down-regulated after chronic, but not a

300 iet initiation, the intervillous zone of the ileum-which is usually described as free of bacteria-bec

301 C increased the % of Foxp3(+) T cells in the ileum while decreasing the percentage of cells in the ML