ライフサイエンスコーパス: jejunum

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

2 mping, and create exocrine drainage into the jejunum.

3 stinal length and function similar to normal jejunum.

4 NA-messenger RNA target relationships in the jejunum.

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

6 onsistently higher viral levels than did the jejunum.

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

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

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

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

11 neurotransmitters in both the brainstem and jejunum.

12 had more frequent and severe lesions in the jejunum.

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

14 xocrine drainage is established to the donor jejunum.

15 ches of airway epithelia and in intact mouse jejunum.

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

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

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

19 ppeared earlier in the colon compared to the jejunum.

20 N neointestine recapitulated those of native jejunum.

21 orption during steady-state perfusion of the jejunum.

22 tructural and dynamic features of the normal jejunum.

23 uctural and transporter properties of native jejunum.

24 ested 20 weeks postoperatively and in native jejunum.

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

26 eased throughout the entire thickness of the jejunum.

27 the mucosal and serosal compartments of the jejunum.

28 serosal afferent neurones supplying the rat jejunum.

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

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

31 retion after a glucose bolus into the distal jejunum.

32 the colon but might also originate from the jejunum.

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

34 mucosal samples from ten sites distal to the jejunum.

35 ic and uncoordinated was observed in Ano1 KO jejunum.

36 sogastric tube that migrated to the proximal jejunum.

37 creased biliary recovery of (3)H-TC from the jejunum (3.4-fold) and ileum (1.7-fold), but did not enh

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 (Caco2-BBE, T84, and HT29-Cl.19A) and human jejunum and colon biopsy specimens.

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

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 GI tract lymphocytes were harvested from the jejunum and ileum of 4 euthanized SIVmac-infected rhesus

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 tivity characterizes crypt epithelium in the jejunum and ileum, but not in other epithelia of the dig

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

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

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

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

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

72 he upper half of the intestinal villi of the jejunum and ileum.

73 ayer of the canine proximal colon, duodenum, jejunum and ileum.

74 myenteric neurons and glia of the duodenum, jejunum and ileum.

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

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

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

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

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

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

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

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

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

84 Although MCs from the jejunum and spleen of noninfected mice failed to express

85 s and highest constitutive expression in the jejunum and spleen.

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

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

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

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

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

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

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

93 ression in enterocytes of duodenum, proximal jejunum, and cecum.

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

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

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

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

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

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

100 ed in villus cell populations from duodenum, jejunum, and ileum.

101 istal colon), with lower levels in duodenum, jejunum, and ileum.

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

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

104 A segment of jejunum (approximately 13 cm) was mounted into a three c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 erneurons, secretomotor or motor neurons) in jejunum, but not colon; A2aR is also found in other neur

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

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

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

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

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

129 250 with human insulin into the lumen of rat jejunum caused a decrease in blood glucose levels that w

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

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

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

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

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

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

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

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

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

139 nophils and MCs after their expansion in the jejunum during a helminth infection.

140 eased 5-HT from BON cells or from guinea pig jejunum during neural blockade with tetrodotoxin.

141 phils undergoing apoptosis were found in the jejunum during the resolution phase of the infection, ev

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

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

144 The MCs in the jejunum expressed mMCP-9 before any mMCP-9-containing ce

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

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

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

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

149 Fourteen SSISs were constructed in the jejunum, four in the ileum, and three with ileum overlap

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

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

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

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

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

155 6, Fiaf and upregulation of Fxr in duodenum, jejunum, ileum and colon in WD + PDX mice.

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

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

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

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

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

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

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

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

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

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

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

167 er constructs were anastomosed to the native jejunum in a side-to-side fashion.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

184 can resolve differences between gastric and jejunum mucins.

185 Jejunum mucosal pressure increased 5-HT release and shor

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

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

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

189 c, inflammatory, or ischemic necrosis of the jejunum, occurs in developing countries but is rare in d

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

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

192 0.009), and 85% (p = 0.007), whereas in the jejunum of cecal ligation and puncture mice sodium-depen

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

214 s differentially expressed between liver and jejunum or pancreas.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

243 s as these cells began to disappear from the jejunum supports the view that many jejunal MCs transloc

244 y the difference between visceral (liver and jejunum) surface Pco2 and PaCO2 during UHS.

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 that regeneration was more pronounced in the jejunum than in the ileum.

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

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

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

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

252 (1) infusing fluid into the oral end of the jejunum; the ejected fluid was diverted via a cannula fr

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

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

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

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

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

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

259 ions of the small intestine (i.e., duodenum, jejunum, upper ileum, and lower ileum) and the large int

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

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

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

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

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

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

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 of CD4 T cells in the lamina propria of the jejunum was observed.

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

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

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

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 In the jejunum, wet weight, protein mass, and villus height wer

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

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

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

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

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

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

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

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

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

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

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

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