ライフサイエンスコーパス: proximal small intestine

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1 on the rate of delivery of nutrients to the proximal small intestine.

2 rated faster-than-normal transit through the proximal small intestine.

3 t not other cholesterol transporters, in the proximal small intestine.

4 rily Na(+)/H(+) exchanger 3) activity in the proximal small intestine.

5 immunodominant peptides concentrated in the proximal small intestine.

6 and in absorptive enterocytes located in the proximal small intestine.

7 nvolved in the clearing of reovirus from the proximal small intestine.

8 ried out microarray studies in the colon and proximal small intestine.

9 The RetDN/+ proximal small intestine also had severe hypoganglionosi

10 ly more intestinal tumors, especially in the proximal small intestine and colon, and some of these tu

11 peptide produced by K cells of the mammalian proximal small intestine and is a potent stimulant of in

12 beta-galactosidase activity initiated in the proximal small intestine and spread cranially and caudal

13 he duration of infection, including both the proximal small intestine and the colon.

14 CCK cells are concentrated in the proximal small intestine, and hormone is secreted into t

15 Isolating the proximal small intestine, and in particular its luminal

16 ated mice is preferentially delivered to the proximal small intestine as a precursor to fecal excreti

17 the distal gut inhibits transit through the proximal small intestine as the ileal brake.

18 In this group, mucosal blood flow to the proximal small intestine but not to the ileum returned t

19 ated endocannabinoid mobilization in the rat proximal small intestine by altering enzymatic activitie

20 llous differentiated epithelial cells of the proximal small intestine, decreases in expression in the

21 c crypts, and were highest in numbers in the proximal small intestine, decreasing in frequency in a g

22 tinal lesions (one/two calves tested) in the proximal small intestine (duodenum and jejunum) of Gn ca

23 G is removed by FcRn-expressing cells in the proximal small intestine (duodenum and jejunum); remaini

24 stine but are somewhat less effective in the proximal small intestine (especially the clinically impo

25 ross the apical brush-border membrane of the proximal small intestine established by the loss-of-func

26 RECENT FINDINGS: Recently, the proximal small intestine has gained attention for its un

27 dose-dependent morphological changes in the proximal small intestine (i.e., duodenum), including wid

28 ounts for their enhanced colonization of the proximal small intestine in an animal model of cholera.

29 acids, a prevalent constituent of the human proximal small intestine, increase intracellular c-di-GM

30 sulting from passage from the stomach to the proximal small intestine induce the functional effect of

31 This segment of proximal small intestine is innervated by the gastroduod

32 Uroguanylin propeptide expression is high in proximal small intestine, low in stomach and distal smal

33 atic protein secretion when infused into the proximal small intestine of conscious rats.

34 igen was also detected in the jejunum of the proximal small intestine of one of two calves tested by

35 logic examination showed mild lesions in the proximal small intestine of only one pig (1/7).

36 ed by immunofluorescent (IF) staining in the proximal small intestine of the WT-PEC-inoculated pigs,

37 gnificant (125)I-STa-binding occurred in the proximal small intestines of GC-C KO and WT mice.

38 tes folate transport into enterocytes in the proximal small intestine; pcft loss-of-function mutation

39 al BaP doses result in adenocarcinoma of the proximal small intestine (PSI) in Cyp1a1(-/-) mice; Cyp1

40 by lipolytic enzymes in the stomach and the proximal small intestine, releasing fatty acids and mono

41 Sensing of dietary triacylglycerol in the proximal small intestine results in physiological, hormo

42 eflect efficient detoxication of oral BaP in proximal small intestine such that significant amounts o

43 -type of enteroendocrine cell located in the proximal small intestine that produces glucose-dependent

44 Side-to-side anastomosis of TESI to proximal small intestine was performed or omitted.

45 The velocity through the proximal small intestine was significantly higher in cir

46 carotid artery, as well as enterocytes from proximal small intestine, were obtained at 1.5 hrs after

47 undant on apical enterocyte membranes in the proximal small intestine, where it facilitates FA uptake

48 Uroguanylin mRNA is most prominent in proximal small intestine, whereas guanylin mRNA is predo

49 y has a strict axial gradient-highest in the proximal small intestine with no expression in the colon

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