ライフサイエンスコーパス: jejunum

1 sogastric tube that migrated to the proximal jejunum.

2 etastatic foci found in the brain, lung, and jejunum.

3 mping, and create exocrine drainage into the jejunum.

4 stinal length and function similar to normal jejunum.

5 NA-messenger RNA target relationships in the jejunum.

6 per cell (Th) 2-mediated inflammation in the jejunum.

7 onsistently higher viral levels than did the jejunum.

8 oup 1 animals had more severe lesions in the jejunum.

9 aKO and little changed (<20%) in the Pat-1KO jejunum.

10 amine and SP in both the shrew brainstem and jejunum.

11 neurotransmitters in both the brainstem and jejunum.

12 had more frequent and severe lesions in the jejunum.

13 s transmembrane conductance regulator in the jejunum.

14 -SEP in activating the thick CM in the human jejunum.

15 xocrine drainage is established to the donor jejunum.

16 d cells into the mucosa and submucosa of the jejunum.

17 ches of airway epithelia and in intact mouse jejunum.

18 s were not diminished in either the blood or jejunum.

19 thelium of the stomach, and the villi of the jejunum.

20 e transporter-2 and insulin receptor) in the jejunum.

21 t had no effect on J(ms)(NHE) across CFTR(-) jejunum.

22 N neointestine recapitulated those of native jejunum.

23 orption during steady-state perfusion of the jejunum.

24 tructural and dynamic features of the normal jejunum.

25 uctural and transporter properties of native jejunum.

26 ested 20 weeks postoperatively and in native jejunum.

27 the epithelia of the stomach, duodenum, and jejunum.

28 s in the heart, pancreas, spleen, liver, and jejunum.

29 tein expression in CD4(+) cells from MLNs or jejunum.

30 ppeared earlier in the colon compared to the jejunum.

31 tro using T84 cells and ex vivo using murine jejunum.

32 ileum and did not occur on infusion into the jejunum.

33 retion after a glucose bolus into the distal jejunum.

34 the colon but might also originate from the jejunum.

35 denum, and, to a lesser extent, the proximal jejunum.

36 mucosal samples from ten sites distal to the jejunum.

37 ic and uncoordinated was observed in Ano1 KO jejunum.

38 ammaH2AX formation in leukocytes, liver, and jejunum 40 min after CT, using preset parameters when co

39 In newborn swine jejunum, a high fat diet acutely induces a 7-fold increa

40 In jejunum, a similar correlation was observed only in grou

41 nsepithelial (22)Na(36)Cl flux across murine jejunum, a site of electroneutral NaCl absorption.

42 Na+-glucose cotransport was normal in the CF jejunum, absence of passive chloride absorption complete

43 terleukin-6 mRNA expression was increased in jejunum after 120 minutes of reperfusion (3.6-fold incre

44 actor-alpha mRNA expression were observed in jejunum after 30 and 120 minutes of reperfusion (P < 0.0

45 peptides were detected and sequenced in the jejunum after casein and WP ingestion, respectively.

46 The jejunum and ascending colon are the most common sites of

47 The jejunum and ascending colon were the most common sites o

48 e exhibit the expected MC hyperplasia in the jejunum and caecum and reject the adult worms from the s

49 eta) to GIT disease and viral replication in jejunum and colon collected at necropsy from 12 SIV-infe

50 We determined that the jejunum and colon of black bears do not harbor significa

51 atic increase in apoptosis in crypts of both jejunum and colon, and accelerated jejunal cell migratio

52 mal and distal parts of the duodenum, ileum, jejunum and colon, and the cecum.

53 the interleukin (IL)-6-JAK-STAT3 pathway in jejunum and colon, collected at necropsy, from 10 SIV-in

54 wall generally increased in the duodenum and jejunum and decreased in the ileum.

55 ctose absorption by approximately 75% in the jejunum and decreased the concentration of serum fructos

56 ea; they did not develop mastocytosis in the jejunum and had reduced ovalbumin-immunoglobulin E in th

57 sion of potential targets of mir-125a in rat jejunum and IEC-6 cells was determined using quantitativ

58 ase in heme oxygenase-1 messenger RNA in the jejunum and ileum 3 hrs following limb reperfusion, with

59 and protein levels, greater villus height in jejunum and ileum and crypt depth in ileum, compared to

60 TC mRNA levels were 4-fold higher in the jejunum and ileum compared to its levels in the duodenum

61 trations have been reported in the duodenum, jejunum and ileum of the small intestine, and in human i

62 col, tissue injury and lipid peroxidation in jejunum and ileum were analyzed by histology and malondi

63 ompartments of the TIM-1 (stomach, duodenum, jejunum and ileum) and viscosity was measured with a dyn

64 compartment of the TIM-1 (stomach, duodenum, jejunum and ileum) at different times of digestion and a

65 submucosal neurons of the duodenum, but not jejunum and ileum, and in the areas of the DVC that regu

66 n in the total number of MSs absorbed in the jejunum and ileum, demonstrating that nonphagocytic proc

67 ted decreased FXR pathway expression in both jejunum and ileum, in association with increased gut per

68 Particularly noticed in sections of jejunum and ileum, the detection suggested the possibili

69 e (DR5, Bid, Puma, Noxa) were induced in the jejunum and ileum, which appeared to be the tissues most

70 crete concentration changes in the duodenum, jejunum and ileum.

71 ed an increase in numbers of Paneth cells in jejunum and ileum.

72 Pi-IIb protein expression was upregulated in jejunum and ileum.

73 id in 80% of patients, mainly seen at distal jejunum and ileum.

74 onization scores (square millimeters) in the jejunum and ileum; and clinical pathology parameters of

75 n in expression of both Mcpt-1 and -2 in the jejunum and increased tryptase expression, whereas Mcpt-

76 ppearance of villi until the proximal to mid jejunum and jejunal mucosal ulcerations.

77 e to protective effects of amifostine, while jejunum and lung showed only modest changes.

78 ry of mucosal injury required 28 days in the jejunum and more than 28 days in the ileum.

79 Piezo2 mRNA was expressed in human jejunum and mouse mucosa from all segments of the small

80 me of three endoderm-derived tissues, liver, jejunum and pancreas, using ultra-high throughput sequen

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

82 spots in the duodenum and ulcerations in the jejunum and proximal ileum covered by fibrin; histologic

83 These endoscopic findings affected mostly at jejunum and proximal ileum.

84 ention than does MR enterography in both the jejunum and the ileum and more accurately depicts endolu

85 t-like immunoreactivity, appear first in the jejunum and then in the ileum.

86 tions performed using either the duodenum or jejunum and with at least 2-year follow-up.

87 emical marker recovered within 3 days in the jejunum and within 7-14 days in the ileum; however, hist

88 and compare viral RNA and DNA in the small (jejunum) and large (colon) intestine of LTNPs.

89 blood, liver, mesenteric lymph nodes (MLNs), jejunum, and bronchoalveolar lavage (BAL) fluid of healt

90 Bile concentration varied in the duodenum, jejunum, and cecum of chicken intestine, and the inhibit

91 to bacteria in intestinal segments of ileum, jejunum, and colon was evaluated in an Ussing chamber.

92 n Apc(Min) mouse adenomas from the duodenum, jejunum, and colon.

93 fluid absorption processes are reduced in CF jejunum, and further studies revealed that this was due

94 Samples of the duodenum, jejunum, and ileum were also dissected from each animal

95 tire lamina propria in sections of duodenum, jejunum, and ileum were HuNoV-negative.

96 Segments of the duodenum, jejunum, and ileum were subjected to histological proces

97 mass spectrometry (QTOF-MS) in bone marrow, jejunum, and lung samples of amifostine-treated and sali

98 RED-4 was purified from monkey jejunum, and N-terminal peptide sequencing of putative R

99 ocal (myocardium, lungs, hepatic parenchyma, jejunum, and renal cortex/medulla) and potentially adver

100 lathrin-rich basolateral regions in neonatal jejunum are involved in IgG exocytosis and that MVBs fun

101 peak enhancement of the liver, pancreas, and jejunum are linearly related to that of the aorta.

102 mine whether myenteric ICC (ICC-MY) in human jejunum are pacemaker cells and whether these cells acti

103 was 2.6-fold greater in colon tissue than in jejunum, as assessed by quantitative PCR, with KChIP1 sh

104 was found in PC at the base of the crypts in jejunum at all stages of SIV infection as compared with

105 ed that all T1R members are expressed in rat jejunum at strategic locations including Paneth cells, S

106 n to increase in both the ileum and proximal jejunum at the onset of inflammation in SAMP1/YitFc mice

107 including changes in the citric acid cycle (jejunum), beta-alanine metabolism (skeletal muscle), and

108 ted increased RE content in the duodenum and jejunum but decreased RE content in the liver.

109 ted Na(+) absorption (J(ms)(NHE)) in CFTR(+) jejunum but had no effect on J(ms)(NHE) across CFTR(-) j

110 rising induction of genes normally silent in jejunum but highly expressed in ileum, specifically thos

111 factors, is highly expressed in duodenum and jejunum but is nearly undetectable in distal ileum of ad

112 uction of villus epithelial cells in CFTR(+) jejunum but no changes in CFTR(-) epithelium after intra

113 ptive enterocyte genes normally expressed in jejunum but not in ileum, including those for the antici

114 ion in the mucosal layer of rat duodenum and jejunum but not in the serosal layer from the same intes

115 of MEPE inhibits phosphate absorption in the jejunum but not the duodenum.

116 tion of WT H. hepaticus in cecum, colon, and jejunum but only transient colonization of H. hepaticus

117 -)-epicatechin is apparently absorbed in the jejunum but with substantial interindividual differences

118 n the duodenal bulb and the post-anastomotic jejunum, but limited data exists regarding their signifi

119 At P0, slow-wave activity was present in the jejunum, but neural responses were poorly developed.

120 EGFP expression in the duodenum and proximal jejunum, but not in the ileum and colon.

121 f such extensions were found in the proximal jejunum, but only a few were present in the terminal ile

122 otective effect was not as pronounced in the jejunum, but the percentage of damaged villi was still r

123 d more commonly originated proximally in the jejunum, but the velocity of migration did not differ.

124 ntrol jejunum, control ileum, and GATA4 null jejunum by gene array analysis revealed that GATA4 null

125 e C. jejuni colonization in cecum, ileum and jejunum, by more than one log CFU/g when compared to the

126 250 with human insulin into the lumen of rat jejunum caused a decrease in blood glucose levels that w

127 cDNAs, RED-1 to RED-6, were identified in a jejunum cDNA library; the deduced RED peptides exhibited

128 cell levels, were higher in the duodenum and jejunum, compared with the colon.

129 Adult and neonatal jejunum contain a viable population of cells that shows

130 e global gene expression profiles of control jejunum, control ileum, and GATA4 null jejunum by gene a

131 to modify albumin clearances in duodenum and jejunum could be accounted for by local increases in vas

132 nd eosin staining to investigate macroscopic jejunum damage were performed.

133 leen, inguinal LN, mesenteric LN, colon, and jejunum directly correlated with the plasma virus level.

134 analysis to determine leukocyte, liver, and jejunum DNA damage and hematoxylin and eosin staining to

135 egradative functions after weaning, when the jejunum does not express FcRn or transport IgG.

136 upper intestinal compartments (duodenum and jejunum) ending with D(h) = 110 +/- 20 nm and a smaller

137 Indeed, we found that jejunum eosinophils expressed remarkably high levels of

138 feeding tube placement into the duodenum or jejunum (erythromycin group, 13 of 14 patients or 93% vs

139 ic mice overexpressing human PSTI within the jejunum (FABPi(-1178 to +28) hPSTI construct) showed no

140 Nanogold-labeled Fc (Au-Fc) in neonatal rat jejunum, focusing on later aspects of transport by chasi

141 bowel via a catheter placed in the proximal jejunum for optimal distention and better depiction of i

142 used for 3 hours, before harvest of proximal jejunum for SGLT1 analysis with Western blotting and qua

143 hypothesized that by excluding duodenum and jejunum from nutrient transit, this procedure may reduce

144 Before weaning, the jejunum functions primarily in IgG transport and exhibit

145 Each ICC-MY in human jejunum generates spontaneous pacemaker activity that ac

146 ted with that of Th17 cells, with duodenum > jejunum > ileum > colon.

147 of lactose intake (p < 0.05), with improved jejunum histology (p < 0.0001).

148 rom different intestinal segments (duodenal, jejunum, ileal, and colon) of a single donor.

149 gestive compartments (stomach, duodenum, and jejunum + ileum).

150 al samples were collected from the duodenum, jejunum, ileum (small intestine) and colon at six weeks

151 6, Fiaf and upregulation of Fxr in duodenum, jejunum, ileum and colon in WD + PDX mice.

152 sues within the gastrointestinal (GI) tract (jejunum, ileum and colon).

153 d proliferation in epithelial cells from the jejunum, ileum and colon.

154 iverted through a gallbladder anastomosis to jejunum, ileum or duodenum (sham control).

155 sion were investigated in the liver, spleen, jejunum, ileum, and cecal tonsils in newly hatched chick

156 d before cART initiation (from the duodenum, jejunum, ileum, and colon), 3 months after cART initiati

157 o found in intestinal tissues, including the jejunum, ileum, and colon, but very few proliferating ce

158 PET/CT visualized the primary tumor region (jejunum, ileum, and pancreas, respectively) not identifi

159 ation parameters in four intestinal regions (jejunum, ileum, cecum, and colon) of outbred Swiss Webst

160 t examined, including the stomach, duodenum, jejunum, ileum, cecum, appendix, colon and rectum.

161 ressed in neural and nonneural layers of the jejunum, ileum, colon, and cecum and in HT-29, T-84, T98

162 s expressed in epithelial cells of duodenum, jejunum, ileum, stomach, cecum, colon, and kidney proxim

163 senteric nerve bundle supplying a segment of jejunum in anaesthetized adult rats.

164 agnosis in three cases, was localized in the jejunum in four cases and in the duodenum in one case.

165 CD4(+) T cells from peripheral blood and the jejunum in rhesus macaques, revealing distinct expressio

166 th showing contrast enhancement and adjacent jejunum in the left middle quadrant, increased density o

167 ulated by taste receptors using perfused rat jejunum in vivo.

168 ignificant changes in gene expression in the jejunum, including genes expressed by intestinal epithel

169 ed expansion of connective tissue MCs in the jejunum, increased serum IL-4 levels, and systemic anaph

170 phages (LPM) were isolated from normal human jejunum, infected with HCMV, and studied for their cytok

171 Glucose absorption in rat jejunum involves Ca(2+)- and PKC betaII-dependent insert

172 d (iv) the relative "leakiness" of the human jejunum is not so different from that observed in a numb

173 oreover, profound and selective depletion of jejunum lamina propria CD4(+) T cells occurred in neonat

174 eron or tumor necrosis factor alpha from the jejunum lamina propria were quantified in all macaques.

175 rption, metabolism and clearance organs (the jejunum, liver and kidney) were evaluated, along with sk

176 odest induction of IP-10 and MIG mRNA in the jejunum, liver, and spleen.

177 The specific metabolic changes in the ileum, jejunum, liver, skeletal muscle, and lung have not previ

178 gene array analysis revealed that GATA4 null jejunum lost expression of 53% of the jejunal-specific g

179 Eighteen hours later, ileum, jejunum, medial gastrocnemius skeletal muscle, liver, an

180 In both peripheral blood and the jejunum, memory CD4(+) T cells expressed higher levels o

181 These contractions in the jejunum migrated orally to the antrum (retrograde perist

182 can resolve differences between gastric and jejunum mucins.

183 Jejunum mucosal pressure increased 5-HT release and shor

184 5), the gastric pouch (n = 5), the oversewn jejunum (n = 2), and the distal anastomosis (n = 1).

185 tation deep into muscle bundles of the human jejunum, necessary for motor patterns underlying mixing.

186 and increased Tgfbeta mRNA expression in the jejunum; numbers of CD103(+) dendritic cells in MLNs wer

187 In contrast, in the jejunum of a knockout mouse model of cystic fibrosis (CF

188 In the jejunum of C3-deficient mice the cytokine ratio between

189 0.009), and 85% (p = 0.007), whereas in the jejunum of cecal ligation and puncture mice sodium-depen

190 l peptide (Camp) gene was upregulated in the jejunum of HC diet-protected rats, and CAMP(+) cells col

191 of the presence of bioactive peptides in the jejunum of healthy humans who ingested casein.

192 tecture was observed in the submucosa of the jejunum of human patients, cows, and sheep supported wit

193 of the formation of peptides present in the jejunum of humans who ingested casein or whey proteins b

194 downregulation of miR-16 and miR-103 in the jejunum of IBS-D patients correlating with symptoms.

195 s in the gut microbiome were observed in the jejunum of infected animals on day 5.

196 dicates direct effects of heat stress on the jejunum of mammals already at moderately elevated ambien

197 e of the JCI, Clayburgh et al. show that, in jejunum of mice injected with anti-CD3 or with TNF, flui

198 ressed at significantly higher levels in the jejunum of Muc2(-/-) mice fed the isocaloric diet or alc

199 lon of all group 1 and 2 macaques and in the jejunum of only group 1 macaques compared to controls.

200 nificantly in colon of groups 1 and 2 and in jejunum of only group 1 macaques compared with controls.

201 t proteins along the crypt-villi axis in the jejunum of PepT1 KO mice.

202 h mir-125a-overexpressing IEC-6 cells and in jejunum of resected rats, confirming Mcl-1 as a previous

203 iral capsid antigen was also detected in the jejunum of the proximal small intestine of one of two ca

204 ng and blunting of villi in the duodenum and jejunum of the TC-PEC-inoculated pigs, in contrast to mo

205 ulated active transport of phosphate only in jejunum of wild-type mice, though NaPi-IIb protein expre

206 shortening and blunting in the duodenum and jejunum of WT-PEC-inoculated pigs.

207 n the proximal small intestine (duodenum and jejunum) of Gn calves, with lesions similar to, but less

208 ed folds were seen in either the duodenum or jejunum on VCE.

209 cation of the distal ileum into the proximal jejunum, on FXR and LXRs in rats.

210 m to 5 microm) were delivered locally to the jejunum or ileum or by oral administration to young male

211 After delivering MSs to the jejunum or ileum, high concentrations of polystyrene wer

212 h time the duodenum is less damaged than the jejunum or ileum.

213 s differentially expressed between liver and jejunum or pancreas.

214 Mild (duodenum and jejunum) or no (ileum) villous atrophy was observed in h

215 ession in the colon but not in the duodenum, jejunum, or ileum.

216 -sectional diameters in duodenum (P = .143), jejunum (P < .001), and ileum (P < .001).

217 cose uptake into enterocytes of duodenum and jejunum (P < 0.001).

218 f mural features in the duodenum (P = .003), jejunum (P = .024), and ileum (P = .01) and a trend towa

219 the stomach (P = .013), duodenum (P = .006), jejunum (P = .029), and ileum (P = .140) in group 1 comp

220 e observed in comparison to sow-fed animals (jejunum, p < 0.01 villus height, p < 0.04 crypt depth; i

221 In the jejunum, PepT1 is particularly enriched in the well-diff

222 SGLT1 component of glucose absorption in rat jejunum perfused with 75 mM glucose.

223 ther miR-190b expression levels in colon and jejunum positively correlated with tissue viral loads.

224 co-transporter, NKCC1, of stimulated CFTR(+) jejunum prevented maximal volume reduction of villus epi

225 cond endogenous ligand of the Apelin peptide jejunum receptor highly expressed in the kidney, further

226 In duct-to-jejunum reconstruction, enterotomy was performed first u

227 ce demonstrated modest Dra expression in the jejunum relative to large intestine.

228 emulsion increased endocannabinoid levels in jejunum, relative to animals that received either minera

229 n the proximal small intestine (duodenum and jejunum); remaining proteins are absorbed and degraded b

230 ma, that preferentially infect the cecum and jejunum, respectively.

231 messenger RNA has been silenced in liver and jejunum resulting in decreased plasma levels of apolipop

232 Ussing chamber analysis of jejunum revealed that Na+/H+ exchanger-mediated Na+ abso

233 In situ zymography of the proximal jejunum reveals increased gelatinase activity in the int

234 mosis was performed in 473 (81%) and duct-to-jejunum Roux limb in 111 (19%) biliary reconstructions.

235 reement values were detected in duodenum and jejunum scores.

236 rker implanted into the surface of the mouse jejunum, serving as a fiducial marker for precise radiat

237 these tissues and also in stomach fundus and jejunum showed evidence for similar short-range structur

238 fferentiated crypt cells isolated from mouse jejunum showed higher CD98 levels and lower levels of mm

239 ared to healthy volunteers or UC patients in jejunum, sigmoid colon, rectum, and descending colon can

240 e in the upper small intestine (duodenum and jejunum), similar to the NLV BEC strains.

241 metabolism of valine/leucine/isoleucine; the jejunum, skeletal muscle, and liver had significant chan

242 a multiorgan disease affecting the ileum and jejunum (small intestine), liver, skeletal muscle, and l

243 Most of the sequences found in jejunum, some of them not previously described, were als

244 In contrast to leukocytes, the liver and jejunum still showed evidence of DNA damage 3 d after CT

245 nteric afferents supplying segments of mouse jejunum taken from wild-type (WT) and TRPV1 knockout (TR

246 pp4 were all substantially higher in the rat jejunum than in colonic mucosa by a mean (SE) factor of

247 of the CCK(1) gene in both the duodenum and jejunum than the other strains.

248 In the jejunum, the density of the nitrergic subpopulation was

249 In the duodenum and jejunum, the HFD promoted a decreased in the proportion

250 In the jejunum, the primary and secondary initiation sites were

251 bsent for infusion of the conjugate into the jejunum, these results were taken as evidence that B(1)-

252 ange, and was markedly elevated in colon and jejunum throughout SIV infection.

253 An anastomosis of the remaining jejunum to the colon can allow PN to be stopped.

254 signals through its receptor (Apelin peptide jejunum) to exert singular inotropic/vasotropic actions

255 ty), and the conduit used (recipient duct or jejunum) to reconstruct the biliary tree.

256 th of functional intestine, particularly the jejunum, to promote nutritional independence(2).

257 black bear GMB communities in the colon and jejunum, two functionally distinct regions of the gastro

258 Ramp distension of the jejunum up to 60 mmHg induced biphasic increases in affe

259 nd the myenteric neurons of the duodenum and jejunum using a diaminobenzidine reaction.

260 s WT PEC caused mild to severe (duodenum and jejunum) villous atrophy and fusion.

261 formula-fed animals, increases in ileum and jejunum villus height and crypt depth were observed in c

262 The jejunum was also exteriorized to quantify the flux of ro

263 eding tube placement into either duodenum or jejunum was confirmed in all 18 patients with a pH step-

264 A segment of jejunum was exteriorized and an MA network was superfuse

265 py an extensive polyposis of the stomach and jejunum was found.

266 Jejunum was harvested for microRNA microarrays, laser ca

267 going pancreaticoduodenectomy, 6 cm colon or jejunum was isolated and exposed to 60 minutes ischemia

268 nding cassette transporter A1 (ABCA1) in the jejunum was markedly elevated in the ACAT2(-/-) mice, ir

269 ssive" components of glucose absorption, rat jejunum was perfused with 50 mM glucose under conditions

270 When rat jejunum was perfused with 75 mM glucose, Ca(2+)-deplete

271 modynamics while the microvasculature of the jejunum was studied with in vivo intravital microscopy.

272 pancreaticoduodenectomy, an isolated part of jejunum was subjected to IR.

273 ell distribution, and gene expression in the jejunum were analyzed.

274 anastomosed to native bowel [AN]) and native jejunum were harvested serially (3-56 weeks postoperativ

275 ralateral from the injury, heart, spleen and jejunum were lower with ubiquitin.

276 senteric lymph node (MLN) CD4(+) T cells and jejunum were monitored.

277 Segments of jejunum were mounted in Ussing chambers to measure mucos

278 Segments of jejunum were mounted in Ussing chambers, and short circu

279 Phasic contractions of the jejunum were observed after icv-injection of morphine.

280 peak enhancement of the liver, pancreas, and jejunum were positively and linearly correlated with the

281 copGFP(+) ICC from the jejunum were purified by a fluorescence-activated cell s

282 hancement of the aorta, liver, pancreas, and jejunum were recorded and correlated with the time to pe

283 IP/PROB, the mean values of VH and CD of the jejunum were significantly higher than the ones from gro

284 Transmural sections of jejunum were stained with fluorescein isothiocyanate-con

285 m either whole mucosa or epithelium of mouse jejunum were stained with Hoechst 33342 and propidium io

286 Segments of jejunum were suspended in an organ bath, and responses t

287 Segments of jejunum were suspended in organ baths, and smooth muscle

288 stinal disease and resection of duodenum and jejunum, where vitamin D is absorbed.

289 iferating memory CD4(+) T cells than did the jejunum, whereas markers of cell activation were compara

290 ding was caused by an ulcus Dieulafoy in the jejunum which was stopped by clipping.

291 weeks induced intestinal inflammation in the jejunum, which is characterized by an increased number o

292 enteroendocrine cells (EECs) in the duodenum/jejunum, which regulate events important for fat digesti

293 B that circumvents the duodenum and proximal jejunum while leaving the stomach unperturbed rapidly im

294 GLT-1 and GLUT2 were unaffected in LEPR-B-KO jejunum, while GLUT5-mediated fructose transport and Pep

295 easured during steady state perfusion of the jejunum with a balanced electrolyte solution.

296 peak enhancement of the liver, pancreas, and jejunum with respect to the time to peak aortic enhancem

297 induced intestinal mucositis in the proximal jejunum with villous atrophy, accumulation of damaged DN

298 isolated infusions of duodenum and proximal jejunum, with a blunted effect distally; topography matc

299 increase in active transport of phosphate in jejunum, without changing paracellular fluxes.

300 ion of this lengthened intestine into normal jejunum would preserve this gain in intestinal length an