ライフサイエンスコーパス: ileum

1 ripheral blood and within the gut (colon and ileum).

2 hich biopsy specimens were obtained from the ileum.

3 small intestine and the circumference of the ileum.

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

5 m receptor desensitization in the guinea pig ileum.

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

7 ings affected mostly at jejunum and proximal ileum.

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

9 A2) expressed on enterocytes in the terminal ileum.

10 patients, mainly seen at distal jejunum and ileum.

11 other had chronic ischemic ulceration in the ileum.

12 teins in cholinergic axons in the guinea pig ileum.

13 ge enteric duplication cyst arising from the ileum.

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

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

16 and histopathology in TcdA-challenged mouse ileum.

17 and decreased the burden of parasites in the ileum.

18 , with only minor expression observed in the ileum.

19 , evaluated in 37 patients) for the terminal ileum.

20 d by the nuclear bile acid receptor, FXR, in ileum.

21 -containing compounds that left the terminal ileum.

22 endoscopically confirmed CD of the terminal ileum.

23 ed secretion and epithelial injury in rabbit ileum.

24 leased when bile acids are taken up into the ileum.

25 (15 g, 235 kJ) or saline to the duodenum or ileum.

26 se in numbers of Paneth cells in jejunum and ileum.

27 d delivery of F.IX to Peyer's patches in the ileum.

28 Th1-driven granulomatous inflammation in the ileum.

29 ereas the median HIV RNA level peaked in the ileum.

30 orated into the nuclei of crypt cells of the ileum.

31 utyrate was present in the cecum but not the ileum.

32 itute alternative stable states of the human ileum.

33 the pathology of Salmonella infection in the ileum.

34 ation of pSTAT3+ neutrophils in the affected ileum.

35 duodenum is less damaged than the jejunum or ileum.

36 er exposure resulted in organoids similar to ileum.

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

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

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

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

41 el, and promotes colonization of the chicken ileum.

42 he duodenum and jejunum and decreased in the ileum.

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

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

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

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

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

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

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

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

51 ype that was nearly identical to that in the ileum after deletion of Gata6 alone, revealing common fu

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

53 The intrinsic factor (IF) vitamin B(12) ileum anchored receptor, cubilin, mediates endocytotic u

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

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

56 he mRNA and peptide levels highest in distal ileum and below detection in duodenum.

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

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

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

60 ort-chain fatty acids (SCFAs) present in the ileum and cecum of streptomycin-treated mice and untreat

61 complex bacterial populations inhabiting the ileum and cecum of TLR- and MyD88-deficient mice.

62 at transduction with rAd5 was highest in the ileum and colon among all intestinal segments.

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

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

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

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

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

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

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

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

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

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

73 ration in epithelial cells from the jejunum, ileum and colon.

74 recipients had higher grades of GVHD in the ileum and colon.

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

76 ood-borne pathogen that colonizes the distal ileum and colon.

77 matory condition most commonly affecting the ileum and colon.

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

79 levels, greater villus height in jejunum and ileum and crypt depth in ileum, compared to MTX animals.

80 1).We obtained 291 biopsy samples from graft ileum and date-matched DSA assay reports.

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

82 rally related to disease in the small bowel (ileum and jejenum).

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

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

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

86 MR enterography in both the jejunum and the ileum and more accurately depicts endoluminal abnormalit

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

88 Biopsy specimens from the colon and ileum and peripheral blood samples were collected from c

89 tly increased epithelial permeability of the ileum and reduced expression of the tight junction prote

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

91 healthy human cecum compared to the terminal ileum and sigmoid colon, whereas T(H)1 and T(H)2 cells d

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

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

94 trains was reduced, especially in the distal ileum and the cecum in experimental cirrhosis with BT (e

95 ll antimicrobials was most pronounced in the ileum and the coecum.

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

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

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

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

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

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

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

103 neurons of the duodenum, but not jejunum and ileum, and in the areas of the DVC that regulate food in

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

105 isualized the primary tumor region (jejunum, ileum, and pancreas, respectively) not identified on CT

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

107 IL-17A-producing cells in the lung, terminal ileum, and spleen.

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

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

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

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

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

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

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

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

116 doscopic biopsy specimens from the duodenum, ileum, ascending colon, and rectum.

117 d 5-HT(7) agonist properties in a guinea pig ileum assay but blocked 5-HT-mediated cAMP accumulation

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

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

120 ting that epithelial COX-2 expression in the ileum attenuates bacteremia following CLP.

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 After a meal, FGF19 is secreted from the ileum; binds to a hepatic membrane receptor complex, FGF

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

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

127 22 and IFN-gamma mRNA levels in the terminal ileum but had limited effect on the GI fungal microbiome

128 tor-15 and BA transporters, was lower in the ileum but higher in the gallbladders of Cftr-/- mice, co

129 a marked accumulation of worm ova within the ileum but impaired fecal egg excretion compared with inf

130 CFAs, showed that formate was present in the ileum but low or not detectable in the cecum while butyr

131 tly impaired enterocyte proliferation in the ileum but not colon in newborn but not adult mice and in

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

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

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

135 liver, midpancreas, midkidneys, and terminal ileum-by using two five-point scales.

136 gastrointestinal cancer (8 gastric cancer, 1 ileum cancer, 13 colorectal cancer).

137 ibuted to the absorptive epithelial cells in ileum, cecum, and colon along with TRPV6.

138 ts of complete (organ plus luminal contents) ileum, cecum, and colon of MMP7-null and wild-type mice

139 ver 7 days), and epithelial infection in the ileum, cecum, and colon.

140 The mutant was outcompeted in the ileum, cecum, and midcolon, suggesting that Lpf contribu

141 ences in the metabolic state of the terminal ileum, cecum, and sigmoid colon.

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

143 developed granulomatous inflammation of the ileum, characterized by an increased expression of Th1-r

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

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

146 ight in jejunum and ileum and crypt depth in ileum, compared to MTX animals.

147 lation of PrP(Sc) was observed in the distal ileum, confined to follicles and/or the enteric nervous

148 In ileum, deletion of Gata6 caused a decrease in crypt cell

149 In contrast to ileum, deletion of Gata6 caused an increase in numbers o

150 RS4C in protein extracts of MMP-7-null mouse ileum demonstrates the in vivo requirement for intracell

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

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

153 dizing divisions, were observed during adult ileum development in the mosquito Culex pipiens.

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

155 one to innumerable polyps in the colorectum, ileum, duodenum, stomach, and/or esophagus, with 24 subj

156 zed genome-wide DNA methylation in the mouse ileum during chronic inflammation, aging, and cancer.

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

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

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

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

161 occludens-1, occludin, and claudin-1 in the ileum following CLP.

162 Digesta were collected from the terminal ileum for a period of 8 h by using a nasoileal tube in 6

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

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

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

166 hat of Th17 cells, with duodenum > jejunum > ileum > colon.

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

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

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

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

171 vity of phosphorylated MYPT1 in telokin-null ileum homogenates was restored to nonphosphorylated MYPT

172 our major chicken tissues: cecal tonsil (C), ileum (I), liver (L), and spleen (S) were used for compa

173 t were either healthy, or that had CD in the ileum (ICD) or colon (CCD).

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

175 n the small bowel crypt, most notably in the ileum in comparison to other sites along the gastrointes

176 es demonstrated their ability to home to the ileum in infected animals and protect Ccr2(-/-) mice, wh

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

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

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

180 that the response to McN-A-343 in the mouse ileum included a non-M(3) muscarinic receptor component.

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

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

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

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

185 t that epithelial expression of COX-2 in the ileum is a critical modulator of tight junction protein

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

187 ssed with GATA4 but also is expressed in the ileum; its function in the mature small intestine is unk

188 e proximal and distal parts of the duodenum, ileum, jejunum and colon, and the cecum.

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

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

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

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

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

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

200 -induced relaxation of force in telokin-null ileum muscle was reduced but not correlated with a chang

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

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

203 being marked by H3K27 trimethylation in the ileum of adult wild-type mice.

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

205 ssential for MDX metabolism, uniquely in the ileum of CD patients.

206 in and beta-arrestin immunoreactivity in the ileum of guinea pigs rendered tolerant by chronic admini

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

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

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

210 surface of epithelial cells in the terminal ileum of mice with Th17 cells but are absent from mice t

211 hat NF-kappaB signaling was inhibited in the ileum of Min/+ mice receiving long-term treatment with c

212 cant decrease in enterocyte apoptosis in the ileum of MTX-ARG rats (vs MTX) was accompanied by decrea

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

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

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

216 We found that the microbiota in the ileum of untreated mice differed greatly from that of th

217 of enterocyte shedding by C parvum-infected ileum on barrier function ex vivo with Ussing chambers.

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

219 No inflammatory lesions were observed in the ileum or colon during infection.

220 liferation was detected in IEC-6 cells or in ileum or colon from wild-type, TLR4-mutant, or TLR4(-/-)

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

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

223 < 0.01 villus height, p < 0.04 crypt depth; ileum p < 0.001 villus height, p < 0.002 crypt depth).

224 xperimental conditions close to those of the ileum (pH 8, 37 degrees C), with rather low binding affi

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

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

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

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

229 bowel (median, 314 v 206 mm; P < .0001), and ileum removed (median, 83 v 63 mm; P = .003), and the ar

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

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

232 d four gastrointestinal (GI) sites (terminal ileum, right colon, left colon, and sigmoid colon).

233 tinaldehyde dehydrogenase (RALDH) enzymes in ileum samples, DCs, and IECs by real-time polymerase cha

234 ies, an appendicovesicostomy or reconfigured ileum segment is a reasonable method to achieve continen

235 ro analysis of active phosphate transport in ileum segments isolated from wild-type or Npt2b(-/-) mic

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

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

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

239 ed a contraction of beta-escin-permeabilized ileum SM at constant pCa 6.3 (EC(50) = 2 microm), which

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

241 ization of rAd5 encoding HIV-1 gp140B to the ileum stimulated potent CD8(+) T-cell responses in the i

242 In ileum subjected to long-term celecoxib treatment, we not

243 after direct surgical introduction into the ileum than after oral gavage, with rAd5 showing greater

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

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

246 1 as an IFNgamma-regulated gene in the mouse ileum that controls gut A. muciniphila levels.

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

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

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

250 In the ileum, the proportion of intraepithelial lymphocytes and

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

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

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

254 s oxygen into the otherwise anaerobic distal ileum, thus driving the transition from one microbial co

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 more, the direct injection of rAd41-Env into ileum together with intramuscular rAd5-Env boosting incr

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

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

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

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

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

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

276 ASBT reclaims bile acids from the distal ileum via active sodium co-transport, in a multistep pro

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

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

279 The total nitrogen that passed the terminal ileum was 39.3 mg/g native digesta dry matter.

280 roblast growth factor 15 (FGF15) mRNA in the ileum was decreased 70% in PPd10 versus controls, wherea

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

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

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

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

285 Image acceptability for the kidneys and ileum was significantly greater than that for the liver

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

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

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

289 Blood and tissue samples from the ileum were collected after 3 days of treatment.

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

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

292 ne carrier, identified previously in situ in ileum, were demonstrated for the first time.

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

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

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

296 inal grafts consisted of a 150-cm segment of ileum, whereas the liver transplant was completed using

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

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

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

300 ot-spot" or high-risk area for cancer in the ileum.With risk that increases with age and high possibi