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1 induced expression of peptide transporter 1 (PEPT1).
2 etitively binding to the external surface of PepT1.
3 nsmembrane domain (TMD) topological model of PEPT1.
4 etitively binding to the external surface of PepT1.
5 H(2)O or with RNA encoding SGLT1, NKCC2, or PepT1.
6 edly, some dipeptides were not substrates of PEPT1.
7 tides could not bind to or be transported by PEPT1.
8 were unimpaired in macrophages deficient in PepT1, a peptide transporter previously implicated in MD
10 A 7-day rosiglitazone treatment increased PepT1 activity and prevented the 2-fold HFD-induced redu
12 betic drugs, rosiglitazone and metformin, on PepT1 activity/expression in a murine diet-induced obesi
14 taste receptors to coordinate regulation of PepT1 and apical GLUT2 reciprocally through a common ent
15 ip between the H(+)/oligopeptide transporter PepT1 and apical GLUT2, reflecting the fact that traffic
16 UT2, reflecting the fact that trafficking of PepT1 and GLUT2 to the apical membrane is inhibited and
20 lly target two peptide transporters (namely, PEPT1 and PEPT2) upregulated in several tumor cells.
21 e intestinal and renal peptide transporters (PEPT1 and PEPT2, respectively) from different animal spe
23 In mammals, peptide transport occurs via PepT1 and PepT2, which belong to the proton-dependent ol
27 intestinal H+-coupled peptide cotransporter PepT1 and recorded the dependence of transient charge mo
28 es of the mammalian oligopeptide transporter PepT1 and the Na(+)- and K(+)-coupled epithelial and neu
29 oth Xenopus laevis oocytes expressing rabbit PepT1 and through PepT1 in rat renal brush border membra
30 oth Xenopus Laevis oocytes expressing rabbit PepT1 and through PepT1 in rat renal brush border membra
31 that transport of the dipeptide Trp-Gly via PepT1 and transport of Na+ and K+ via EAAC1 across the o
34 This molecule is not translocated through PepT1 as measured both by direct HPLC analysis in PepT1-
35 This molecule is not translocated through PepT1 as measured both by direct HPLC analysis in PepT1-
36 ectrode voltage clamping revealed that R282E-PepT1 behaved as a peptide-gated non-selective cation ch
37 ort of protons and peptides of the wild-type PepT1 but also creates a peptide-gated cation channel in
41 intestinal H(+)-coupled peptide transporter PepT1, displays a broad substrate specificity and accept
42 amma agonist compensated for the HFD-induced PepT1 down-regulation, whereas metformin reversed rosigl
43 as measured both by direct HPLC analysis in PepT1-exp ressing oocytes and indirectly by its failure
46 as measured both by direct HPLC analysis in PepT1-expressing oocytes and indirectly by its failure t
48 stigated the long term leptin treatments, on PepT1 expression and activity in Caco2-BBE cells, and be
50 ts revealed that C rodentium induced colonic PepT1 expression and that, compared with their wild-type
53 he effects of pathogenic bacteria on colonic PepT1 expression together with its functional consequenc
54 chanism underlying the regulation of colonic PepT1 expression under pathologic conditions and reveal
56 e human intestinal oligopeptide transporter (PEPT1) facilitates the absorption of dipeptides, tripept
57 nd crypts samples, we found that ablation of PepT1 further directly or indirectly altered expression
58 arginine 282 with a glutamate residue (R282E-PepT1) gave a protein at the plasma membrane of Xenopus
61 Expression of the di/tripeptide transporter PepT1 has been observed in the colon under inflammatory
62 roton-coupled di- and tripeptide transporter PepT1 has been shown by site-directed mutagenesis to be
63 of 12 membrane-spanning domain transporters; PepT1 has proton/peptide cotransport activity and is sel
65 logic conditions and reveal a novel role for PepT1 in host defense via its capacity to modulate bacte
78 with previous data on the ion dependence of PepT1, it can therefore be concluded that peptide-evoked
79 the COOH terminus of a warm-adapted (rabbit) PEPT1, it conferred cold adaptation to the receiving pro
80 Ac-Phe-NH2 had a very weak interaction with PepT1 (Ki = 16.8+/-5.64 mM); neither Phe nor Phe-NH2 int
81 yr and Ac-Phe-Tyr-NH2 interacted weakly with PepT1 (Ki = 8.41+/-0.11 and 9.97+/-4.01 mM, respectively
85 ch activated PKC betaII and decreased apical PepT1 levels and absorption of the hydrolysis-resistant
86 ransport of VLPVPQK suggested involvement of PepT1 like transporters/SOPT2 while BCM 5, its hydrolyti
88 whether the KPV anti-inflammatory effect is PepT1-mediated in intestinal epithelian and immune cells
89 while GLUT5-mediated fructose transport and PepT1-mediated peptide transport were substantially redu
91 eptidyl peptidase IV and peptide transporter PepT1 messenger RNA levels were determined before and af
97 reverse trans-stimulation through expressed PepT1 of labelled peptid efflux induced by unlabelled pe
98 reverse trans-stimulation through expressed PepT1 of labelled peptide efflux induced by unlabelled p
100 The intestinal H(+)/peptide cotransporter 1 (PepT1) plays a major role in nitrogen supply to the body
102 al 3 membrane-spanning domains of intestinal PepT1 protein, with 3 additional N-terminal residues.
103 performed using cold KPV as a competitor for PepT1 radiolabelled substrate or using [(3)H]KPV to dete
105 In addition, peptide transport by R282E-PepT1 still induced depolarization as measured by microe
107 in contrast to the low-affinity transporter PepT1 that couples transport of one peptide to one H+.
108 (Chionodraco hamatus) peptide transporter 1 (PEPT1), the first transporter cloned from a vertebrate l
110 compared with their wild-type counterparts, PepT1 transgenic mice infected with C rodentium exhibite
113 tudies, rosiglitazone treatment up-regulated PepT1 transport activity with concomitant induction of S
114 diabetic drugs exert opposite effects on the PepT1 transport function probably through direct action
115 r results identify key features required for PEPT1 transport in contrast to most previously described
118 gether with their potential active uptake by PEPT1 transporter, intestinal permeability, and metaboli
119 illus width were measured, and expression of PepT1 was determined by Northern blotting, in situ hybri
120 parameters on extracellular pH (pHo), rabbit PepT1 was expressed in Xenopus laevis oocytes and used f
121 he wild type, the rate of transport by R282E-PepT1 was independent of the extracellular pH level, and
122 Slc15a1, a peptide transporter also known as Pept1, was predominantly present in peritubular myoid ce
123 the mammalian intestinal peptide transporter PepT1 were investigated, using the Xenopus laevis expres
124 nal peptide Phe-Tyr-NH2 also interacted with PepT1 with a relatively high affinity (Ki = 0.94+/-0.38
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