ライフサイエンスコーパス: jejunal

1 Attenuation of collapsed jejunal (134 HU) and ileal (108 HU) loops was greater th

2 Expression levels of the jejunal Abcg5 (ATP-binding cassette transporter G5) and

3 effects of oleic acid and ricinoleic acid on jejunal absorption, steady-state jejunal perfusions were

4 umen perfusion catheter, we investigated the jejunal absorption, systemic availability, metabolism, a

5 Multiunit recordings of jejunal afferent activity were made using extracellular

6 Responses of rat jejunal afferent fibers were examined by electrophysiolo

7 SLIGRL-NH2 (0.001-1 mg kg-1, I.V.) increased jejunal afferent firing and intrajejunal pressure.

8 Colonic and jejunal afferent mechanosensory function was attenuated

9 s this issue, we examined the sensitivity of jejunal afferent nerves to a hexapeptide agonist of PAR2

10 te the contribution of the TRPV1 receptor to jejunal afferent sensitivity in the murine intestine.

11 t2 deficiency is associated with exaggerated jejunal afferent sensitivity to both mechanical and chem

12 The WT jejunal afferents responded to capsaicin with rapid incr

13 Moreover, PEDV infection altered plasma and jejunal amino acid profiles, and decreased the expressio

14 weeks after implantation, side-to-side cyst-jejunal anastomoses were fashioned in one cohort of rats

15 onstruction via either end-to-side Roux-en-Y jejunal anastomosis or direct duodenal anastomosis.

16 e ethanol-drinking group but less evident in jejunal and colonic LPLs compared with controls, suggest

17 Messenger RNA (mRNA) from jejunal and colonic mucosa was isolated, and transcript

18 h regard to the induction of swelling of the jejunal and colonic organoids.

19 (fibroblast-like cells) isolated from murine jejunal and colonic smooth muscle and/or mucosal tissues

20 Deletion of Gata6 and Gata4 resulted in a jejunal and duodenal phenotype that was nearly identical

21 MTX-ARG rats demonstrated greater jejunal and ileal bowel weight, greater ileal mucosal we

22 coli, the numbers of E. coli cells in their jejunal and ileal lavage fluid are significantly increas

23 HU) loops was greater than that of distended jejunal and ileal loops (P < .001).

24 was measured in the distended and collapsed jejunal and ileal loops and in the terminal ileum.

25 imals generated a dampened response, whereas jejunal and ileal LPLs from ethanol-drinking animals pro

26 Jejunal and ileal luminal BAs, portal blood BAs, and mes

27 les in adult human ileal mucus and adult pig jejunal and ileal mucus revealed no significant differen

28 crypt depths were increased in the duodenal-jejunal and ileal remnants of both genotypes.

29 ections, adaptation was analyzed in duodenal-jejunal and ileal segments from C57BL/6 Bax(+/+) (16, 48

30 Jejunal and ileal specimens from normal control dogs (n=

31 ted throughout the small intestinal tract in jejunal and ileal tissue from one pediatric intestinal t

32 Jejunal and ileal tissues were taken before harvesting,

33 Patients with jejunal and ileocecal NETs who were treated at the Moffi

34 In human jejunal and rat and guinea pig colonic segments, additio

35 l anomalies identified included omphalocele, jejunal, and ileal atresia with aberrant mesenteric bloo

36 n was high in the apical region of duodenal, jejunal, and ileal villus epithelial cells; low in absor

37 olitis, hyperplasia, diarrhea, and mistarget jejunal apical markers.

38 Jejunal apoA-I synthesis and plasma apoA-I levels were i

39 At enteric phase CT enterography, jejunal attenuation is greater than ileal attenuation an

40 Furthermore, organ cultures of jejunal biopsies from 28 CD patients were set up to asse

41 Jejunal biopsies from volunteers challenged with Cryptos

42 es established from stem cells isolated from jejunal biopsies of six individuals with different ABO,

43 Jejunal biopsies showed an altered mucosal architecture

44 Proximal jejunal biopsies were obtained after the supplementation

45 cent to adherent organisms was observed in a jejunal biopsy from a volunteer who ingested the wild-ty

46 ody tests to determine if they could replace jejunal biopsy in patients with a high pretest probabili

47 We analyzed longitudinal jejunal biopsy samples from HIV-1-infected patients, dur

48 Evaluation of jejunal biopsy samples from long-term HIV-1-infected non

49 Jejunal biopsy specimens from patients with gluten-sensi

50 hemokines and cytokines in cell lysates from jejunal biopsy tissues were assayed by a 22-multiplex be

51 A full thickness jejunal biopsy was obtained from a 38-year-old insulin-d

52 Jejunal biopsy would be necessary in patients with disco

53 of the SMV, in the rare setting in which the jejunal branch is preserved, may also be managed by liga

54 Isolated involvement of the jejunal branch of the SMV may be managed by division of

55 2 primary branches of the SMV (the ileal and jejunal branches), with or without involvement of the ma

56 e randomly assigned to five groups: duodenal-jejunal bypass (DJB), jejunal resection (jejunectomy), i

57 iables of rats that had undergone a duodenal-jejunal bypass (DJB).

58 endoscopic implant that mimics the duodenal-jejunal bypass component of the Roux-en-Y gastric bypass

59 Duodenal-jejunal bypass group showed greater reductions in fastin

60 Duodenal-jejunal bypass improved insulin sensitivity and beta-cel

61 he safety and efficacy of 6 months' duodenal-jejunal bypass liner (DJBL) treatment in comparison with

62 safety of 12-month implantation of a duodeno-jejunal bypass liner (DJBL) with conventional medical ca

63 or the rapid antidiabetic effect of duodenal jejunal bypass surgery.

64 makes no more than a minimal contribution to jejunal Ca(2+) absorption at luminal concentrations prev

65 pression in peripheral blood CD4(+) T cells, jejunal CCR5(+) CD4(+) T cells exhibited significantly l

66 Jejunal CCR5(+) CD4(+) T cells exhibited the highest lev

67 arboxypeptidase cDNA was isolated from a pig jejunal cDNA library using an amplified homologous probe

68 s of both jejunum and colon, and accelerated jejunal cell migration.

69 e in vivo basal and prostaglandin-stimulated jejunal chloride secretion in normal subjects, CF hetero

70 d mean luminal [Cl(-)] of postprandial human jejunal chyme, and reflects contributions from both tran

71 ated an association between a suppression in jejunal circular muscle activity and a massive extravasa

72 of COX-2, we observed a decrease in in vitro jejunal circular muscle contractility and gastrointestin

73 tinal transit assessed in vivo motility, and jejunal circular muscle contractility was measured in vi

74 Jejunal circular muscle contractions were measured in an

75 Spontaneous and bethanechol-stimulated jejunal circular muscle contractions were measured in an

76 l muscularis and a functional suppression in jejunal circular muscle contractions.

77 rophils into the muscularis and also averted jejunal circular muscle dysfunction.

78 Leukocyte infiltration and in vitro jejunal circular muscle function were quantified in cont

79 el calcium currents were measured from human jejunal circular smooth muscle cells in response to incr

80 ensitive calcium channel is present in human jejunal circular smooth muscle cells.

81 Organ bath experiments were performed on jejunal circular smooth muscle strips.

82 on, gastric acid secretion, and cAMP-induced jejunal Cl- secretion.

83 ictures) were fewer in the duodenal than the jejunal cohort (7 patients [12%] vs 13 [35%]; P = .009).

84 Of patients with stricture, 5 of 9 in the jejunal cohort required percutaneous transhepatic access

85 The jejunal conduit was passed through a substernal route in

86 ssociated suppression of in vitro muscarinic jejunal contractility.

87 obestatin suppressed food intake, inhibited jejunal contraction, and decreased body-weight gain.

88 Spontaneous jejunal contractions were markedly suppressed in UP-LPS-

89 cence in situ hybridization was performed on jejunal cryosections with probes to detect formyl peptid

90 NKCC1 mRNA was found to be expressed in rat jejunal crypt but not villus cells.

91 imorphism in the extent of radiation-induced jejunal crypt cell apoptosis, with female mice having hi

92 rence in susceptibility to radiation-induced jejunal crypt cell apoptosis.

93 Jejunal crypt cell survival was decreased in those mice

94 id not appreciably alter radiation damage to jejunal crypt cells and tissue involved in the developme

95 Jejunal crypt cells undergo apoptosis in response to ion

96 Published human jejunal data (119 P(eff), 53 compounds) were analyzed by

97 Human jejunal digests after oral ingestion of casein and whey

98 terioration in his general condition, showed jejunal dilatation, intestinal intramural gas, portomese

99 unum of transgenics than wild-type mice, but jejunal disacharidase activities were not increased.

100 ollow up both Crohn disease patients without jejunal disease and in pediatric patients where nasogast

101 d to present a 67-year-old male patient with jejunal diverticulitis accompanying with abdominal pain

102 ral surgery department with the diagnosis of jejunal diverticulitis.

103 Jejunal diverticulosis is a rare, usually asymptomatic d

104 Duodenal, mid-jejunal effluents and plasma samples were collected at d

105 on average, a nearly 2-fold accumulation of jejunal endocannabinoids, whereas emulsions containing s

106 id revealed patchy infection of duodenal and jejunal enterocytes of 18 of 31 HuNoV-inoculated pigs wi

107 Intracellular pH was measured in jejunal enterocytes of wild-type mice and mice with disr

108 C1 Like 1 (NPC1L1) is a protein localized in jejunal enterocytes that is critical for intestinal chol

109 ption, was also dramatically up-regulated in jejunal enterocytes upon exposure to LXR agonists.

110 Studies in NCI-H716 cells and human jejunal enteroids engineered to make more enteroendocrin

111 of a pathogenic intestinal bacterium, human jejunal enteroids were cultured as monolayers in microen

112 TMs were extracted from colonic and jejunal epithelial cells and smooth muscle, and hTM isof

113 he major hTM isoforms present in colonic and jejunal epithelial cells are hTM5 and hTM4, whereas inte

114 -beta(1) are constitutively expressed in the jejunal epithelial compartment in uninfected mice and du

115 Here we show that primary intestinal (jejunal) epithelial cells express galactosylceramide, an

116 MCT feeding stimulated jejunal-epithelial thymic stromal lymphopoietin, Il25, a

117 FAK phosphorylation was increased in jejunal epithelium at the ulcer edge, and Ki-67 staining

118 aepithelial nematode Trichinella spiralis in jejunal epithelium from BALB/c mice.

119 thelial lining was not affected, whereas the jejunal epithelium was seriously damaged.

120 ralis induces changes in the proteome of the jejunal epithelium, including substantial up-regulation

121 nctionally distinct cell types of the murine jejunal epithelium.

122 ation; and feeding intolerance necessitating jejunal feeding (n = 8, 20%) due to delayed gastric empt

123 Enteral nutrition with gastric or jejunal feeding in healthy young men results in similar

124 Jejunal feeding is preferred instead of gastric feeding

125 teral nutrition as either gastric feeding or jejunal feeding on endocrine responses in vivo in humans

126 act of gastric feeding compared with that of jejunal feeding on postprandial circulating plasma gluco

127 Jejunal feeding resulted in higher peak plasma insulin c

128 e 2 (GLP-2) concentrations was greater after jejunal feeding than after gastric feeding, with higher

129 Studies on percutaneous jejunal feeding tubes demonstrate: high complication rat

130 on can also be iatrogenic from intracatheter jejunal feeding tubes, stent perforation, sclerotherapy,

131 nd GLP-2 concentrations being attained after jejunal feeding.

132 of 51 patients who underwent a supercharged jejunal flap for total esophageal reconstruction between

133 n the stomach is unavailable, a supercharged jejunal flap may reestablish alimentary tract continuity

134 The discovery of the jejunal folylpoly-gamma-carboxypeptidase gene provides a

135 Jejunal folylpoly-gamma-glutamate carboxypeptidase hydro

136 rostate-specific membrane antigen and to the jejunal folylpoly-gamma-glutamate carboxypeptidase.

137 hat exhibit several aspects of physiological jejunal function and that survive to form luminal struct

138 data demonstrate that GATA4 is essential for jejunal function including fat and cholesterol absorptio

139 ctor GATA4 has been implicated in regulating jejunal gene expression, the contribution of GATA4 in co

140 oncept data for engineering patient-specific jejunal grafts for children with intestinal failure, ult

141 of contrast material to the skin in 11 (4%), jejunal hematomas in five (2%), and intussusceptions in

142 apture microdissection and gammadelta TCR(+) jejunal IELs purified by flow cytometry disclosed that t

143 al tissues, including the colorectal, cecal, jejunal, ileal, duodenal, and cecal tonsil tissues.

144 introduced a TNM staging classification for jejunal-ileal (midgut) neuroendocrine tumors (NETs).

145 85% of the small intestine and regulates the jejunal-ileal gradient in absorptive enterocyte gene exp

146 of Gata4 is critical for the maintenance of jejunal-ileal homeostasis in the adult small intestine i

147 ional signal required for the maintenance of jejunal-ileal identities in the adult mouse small intest

148 ge of the patients was 43 years, the average jejunal-ileal length was 23 cm, and the average length o

149 Forty-five TPN-dependent adults with a jejunal-ileal remnant < or = 50 cm and a portion of colo

150 We identified 691 patients with jejunal-ileocecal NETs.

151 meostasis between commensal bacteria and the jejunal immune system.

152 acteristics of this inhibition are: 1) local jejunal inflammation induced by T. spiralis systemically

153 Dietary sodium restriction also increased jejunal interstitial fluid cGMP and fluid absorption.

154 unctionally distinct cell types of the mouse jejunal intestinal epithelium and that miRNAs respond to

155 uercetin sophoroside in the plasma following jejunal introduction of the sophoroside; we found deriva

156 motic leaks and strictures, marginal ulcers, jejunal ischemia, small bowel obstruction, internal hern

157 o draw comparisons between human colonic and jejunal ischemia-reperfusion sequelae in a human in vivo

158 Native jejunal (J) and non-anastomosed (N-N) and anastomosed (A

159 We compared the results of jejunal (JBx) and ileal (IBx) biopsies after bowel trans

160 The duodenum and duodenal-jejunal junction are often malpositioned in children wit

161 t runs parallel to the gut from the duodenal-jejunal junction to the cloaca.

162 ce and position of the duodenum and duodenal-jejunal junction were recorded.

163 The duodenum and duodenal-jejunal junction were visualized on anteroposterior spot

164 s was investigated using an in vivo isolated jejunal loop model of intestinal ischemia-reperfusion.

165 ed stomach, proximal efferent loop, oversewn jejunal loop, and distal jejunojejunal anastomosis were

166 unidirectional efflux (absorption) from the jejunal loop.

167 labeled glucose transport were determined in jejunal loops and in mice following apelin gavage.

168 ux through the gastric epithelial barrier in jejunal loops and in vivo following oral glucose adminis

169 Distended jejunal loops had significantly greater attenuation than

170 ly disease, particularly at the level of the jejunal loops.

171 t and consumption were assayed using ex vivo jejunal loops.

172 v-specific MHC class I restricted CTL in the jejunal LP.

173 entrations of sugars similar to those in the jejunal lumen immediately after a meal, is severalfold g

174 m, fascia, explant and donor liver bile, and jejunal lumen in 77 liver transplantations, and we monit

175 Jejunal luminal BA levels were similar between animals w

176 increased Hsp25 and Hsp72, but not Hsc73, in jejunal lymphocytes and epithelial cells.

177 levels of peripheral blood eosinophilia and jejunal mastocytosis occurred in wild-type and IgE-defic

178 Thus, the ability of a jejunal MC to reversibly alter its tryptase expression d

179 ring the recovery phase of the inflammation, jejunal MCs cease expressing mMCP-2 and then express var

180 the helminth-induced inflammation, when the jejunal MCs move from the submucosa to the tips of the v

181 In noninfected mice, most jejunal MCs reside in the submucosa and express mMCP-6 a

182 from the jejunum supports the view that many jejunal MCs translocate to the spleen during the recover

183 g this translocation process, some senescent jejunal MCs undergo nuclear segmentation.

184 was studied by extracellular recordings from jejunal mesenteric afferent bundles and patch clamp reco

185 nnervation was examined in the external ear, jejunal mesenteric arterioles, superficial epigastric, f

186 cell depletion, such as dysregulation of the jejunal microenvironment after SIV infection, likely acc

187 somewhat lower than, that observed in human jejunal microsomes (7.4-15.4), which may reflect the pre

188 ne gastric mucin (pPGM) and purified porcine jejunal mucin (pPJM).

189 ated to be somewhat lower than that of human jejunal mucosa (1.14 and 3.67 ml/min/g of cells, respect

190 ) mice, eosinophils are not recruited to the jejunal mucosa after infection and are not present in th

191 nd mast cells were markedly increased in the jejunal mucosa during primary infections with S. venezue

192 luated the regulation of CYP3A5 in liver and jejunal mucosa from white donors.

193 lyposis occurs in the remaining duodenal and jejunal mucosa in the majority of patients after surgica

194 Using in vivo microscopy to image jejunal mucosa of GFP gammadelta T-cell transgenic mice,

195 rhesus enteric alpha-defensins (REDs) in the jejunal mucosa of rhesus macaques during all stages of S

196 rs that gliadin is not directly toxic to GSE jejunal mucosa per se, but rather toxicity requires the

197 The response of the jejunal mucosa to a known cathartic provides observation

198 No abnormality of jejunal mucosa was detected histologically in five patie

199 1c/123(-) CD13(+) CD14(-) macrophages in the jejunal mucosa were infected, albeit at lower levels tha

200 induced differential growth of duodenal and jejunal mucosa.

201 ry is based primarily on in vitro studies of jejunal mucosa.

202 er edge, and Ki-67 staining was unchanged in jejunal mucosa.

203 detected two cytosolic beta-glucosidases in jejunal mucosa.

204 PCR revealed the presence of Ca(v)beta(3) in jejunal mucosa; Western blotting and immunocytochemistry

205 Here we construct autologous jejunal mucosal grafts using biomaterials from pediatric

206 Jejunal mucosal mass was 30% greater with MCTs plus LCTs

207 le proteases that are readily seen in mature jejunal mucosal MC that also are induced by the infectio

208 villi until the proximal to mid jejunum and jejunal mucosal ulcerations.

209 wo times lower than the viscosity of the pig jejunal mucus (P < 0.05).

210 that microstructural organisation of native, jejunal mucus depends on its spatial location in the int

211 mean Stokes-Einstein viscosity of the piglet jejunal mucus was approx. two times lower than the visco

212 at would sum with responses of ICC in intact jejunal muscle strips.

213 iptase-polymerase chain reaction (RT-PCR) in jejunal muscle, whereas 5-HT(1A), 5-HT(1D), and 5-HT(2C)

214 f Ca(2+) transients in ICC-DMP within intact jejunal muscles expressing a genetically encoded Ca(2+)

215 ave amplitude, however, were noted in intact jejunal muscles that were not observed in ICC.

216 copGFP(+) cells from jejunal muscles were Kit(+) and free of contaminating ce

217 tochemistry for neutrophils was performed in jejunal muscularis whole mounts.

218 ) decreased neutrophil infiltration into the jejunal muscularis; and (3) prevented SITx-induced suppr

219 A1R is expressed in jejunal myenteric neurons and colonic submucosal neurons

220 tion of reactive oxygen species (ROS) in the jejunal myenteric plexi and phosphorylation (p) of mitog

221 nic myocytes possess densities twice that of jejunal myocytes.

222 v4-like immunoreactivity was less evident in jejunal myocytes.

223 of the KChIP family in isolated colonic and jejunal myocytes.

224 At laparotomy, extensive jejunal necrosis required bowel resection, jejunostomy,

225 In conclusion, neurons in Remak's juxta-jejunal nerve appear to regulate gut motility.

226 alpha-MD-G-stimulated jejunal NHE3 activity was defective in NHERF2-/- mice an

227 te alpha-methyl-D-Glu (alpha-MD-G) activated jejunal NHE3; this process required Akt and NHERF2.

228 No intact casein was detected in the jejunal nor in the in vitro samples taken during the int

229 Additionally, jejunal nutrient sensing and leptin action are demonstra

230 In contrast, jejunal nutrient sensing inhibits glucose production and

231 fined; intestinal absorption was assessed by jejunal or ileal perfusion studies.

232 on of hemorrhagic luminal fluid in duodenal, jejunal, or ileal loops treated for 6 h with purified CP

233 Indeed, seeding of jejunal organoids onto either type of scaffold reliably

234 ed treatment algorithms for NETs of ileal or jejunal origin and of pancreatic origin are presented.

235 In both models jejunal perfusion was used to assess absorption.

236 eic acid on jejunal absorption, steady-state jejunal perfusions were performed in healthy volunteers.

237 The study aimed to predict effective human jejunal permeability (P(eff)) using a biophysical model

238 The biophysical model predicted human jejunal permeability data within the experimental uncert

239 on, the contribution of GATA4 in controlling jejunal physiology has not been addressed.

240 Eligible participants had jejunal placement of a percutaneous gastrojejunostomy tu

241 Jejunal polyp-free survival after duodenectomy differed

242 is including maximal Spigelman stage (SS) of jejunal polyposis (neo-SS).

243 Jejunal polyposis is advanced in 1 in 5 patients, but ra

244 Endoscopic management of jejunal polyposis seems feasible but has proven difficul

245 Jejunal polyposis was advanced in 21% (neo- SS III or IV

246 operatively, 38/64 (59%) were diagnosed with jejunal polyposis, with median time to diagnosis of 55 m

247 ermine time to diagnosis of duodenal bulb or jejunal polyps, length of follow up, and severity of pol

248 In vitro mouse colonic and jejunal preparations with attached splanchnic and mesent

249 59 duodenal reconstructions and 37 Roux-en-Y jejunal reconstructions.

250 n routes in bronchoalveolar lavage fluid and jejunal, rectal, and vaginal tissue samples.

251 five groups: duodenal-jejunal bypass (DJB), jejunal resection (jejunectomy), ileal resection (ileect

252 Both DJB and jejunal resection normalized SI in diabetic rats as show

253 At laparotomy, rats had jejunal sacs filled with (glucose + alanine), glucose, g

254 protein expression levels were increased in jejunal samples following C. parvum infection and were a

255 Jejunal samples from macaques before and after Cryptospo

256 ile beta-lactoglobulin was found in one hour-jejunal samples in agreement with the in vitro digestion

257 exposed to 10 mmol/L theophylline to induce jejunal secretion.

258 Immunohistochemistry of jejunal sections with a rabbit polyclonal Ab to Xenopus

259 ducing cells compared with the corresponding jejunal segment of controls.

260 -)-epicatechin was perfused into an isolated jejunal segment together with antipyrine as a marker for

261 Rat jejunal segment was subjected to ischemia for 30 minutes

262 engthening device was inserted into isolated jejunal segments in pigs, and fully expanded over 8 days

263 Jejunal segments isolated from Trichinella spiralis-infe

264 To evaluate cytotoxicity, jejunal segments of the anesthetized rat were exposed to

265 re made from mesenteric afferents from mouse jejunal segments perfused in vitro.

266 tochemistry for neutrophils was performed in jejunal segments.

267 transcriptomes from the associated tissues (jejunal smooth muscle, colonic smooth muscle, and coloni

268 Jejunal SOCS (SOCS-1, -2, -3, and cytokine-inducible SH2

269 GH, but not IGF-I, induced jejunal SOCS-2 mRNA.

270 4 null jejunum lost expression of 53% of the jejunal-specific gene set and gained expression of 47% o

271 (mMCP) 9, essentially all of the MCs in the jejunal submucosa and spleen of T. spiralis-infected mic

272 transcript and protein were observed in the jejunal submucosa of Trichinella spiralis-infected BALB/

273 A3R IR occurs in 57% of substance P-positive jejunal submucosal neurons (putative intrinsic primary a

274 Jejunal sucrase activity (in U/cm) was significantly gre

275 dication that heat stress may directly alter jejunal tight junction proteins suggesting an impaired i

276 Rats were euthanized to harvest jejunal tissue for histology and cytokine profiles by EL

277 rs cyclin D1 and cyclin D2 were decreased in jejunal tissue in septic transgenic mice.

278 used rises in short circuit current from rat jejunal tissue mounted in a Ussing chamber and rounding

279 cuit current and potential difference in rat jejunal tissue mounted in Ussing chambers.

280 of ACSL5 and disrupted splicing of ZDHHC6 in jejunal tissue of affected Kelpies.

281 we studied SP mRNA and protein expression in jejunal tissue samples of patients with AIDS with natura

282 reduced STa-provoked anion secretion in pig jejunal tissue, and fluid retention and cGMP levels in S

283 antitative PCR indicated that in colonic and jejunal tissue, Kv4.3 transcripts demonstrate greater re

284 Here we use electron tomography to make jejunal transcytosis visible directly in space and time,

285 upon nutritional rehabilitation with either jejunal tube feedings or parenteral nutrition until weig

286 Continued evaluation of endoscopic jejunal tube placement methods and associated clinical o

287 ings as compared with bedside self-migrating jejunal tubes in patients with severe acute pancreatitis

288 tion, lymphangioma) were identified, but two jejunal tumors were not detected in a patient with poor

289 infarction developed refractory duodenal and jejunal variceal bleeding as a result of diffuse viscera

290 2; middle colic vein (MCV), in 29; and first jejunal vein (FJV), in 36.

291 Jejunal villar epithelial and hepatocellular necrosis we

292 m, whereas apoptosis was clearly observed in jejunal villi and crypts, (42 times more M30 positivity

293 ice exhibited a 2-fold increase in length of jejunal villi and have normal growth on a normal diet bu

294 Capillaries in jejunal villi can absorb nutrients at rates several hund

295 Individuals with CD, defined as duodenal or jejunal villous atrophy (stage 3 Marsh score), were matc

296 Intracellular pH (pH(i)) of intact jejunal villous epithelium was measured by ratiometric m

297 itative reverse transcriptase-PCR studies of jejunal villus epithelium recovered from germ-free trans

298 c epithelial lining, but extensive damage in jejunal villus tips after 60 minutes ischemia.

299 at GATA4 plays a pivotal role in determining jejunal vs ileal identity.

300 Anti-CD3 mAb increased jejunal wt/l ratios by more than 50% at 3 hours, returni