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1 mease genes (opp1ABCDF), which encode an ABC oligopeptide transporter.
2 for their affinity for hPEPT1, an intestinal oligopeptide transporter.
3 he ORF YPR194C from S. cerevisiae encodes an oligopeptide transporter.
4 T-1) which appears to be associated with the oligopeptide transporter.
5 lute binding protein of the Escherichia coli oligopeptide transporter.
6                                          The oligopeptide transporter 1, PepT1, is a member of the Sl
7 tered the hfRPE cells via the sodium-coupled oligopeptide transporters 1 and 2 (SOPT1, SOPT2).
8 oem companion cell-localized Fe transporter, OLIGOPEPTIDE TRANSPORTER 3 (AtOPT3).
9 n contrast, inactivation of loci encoding an oligopeptide transporter, a purine repressor, and lantib
10 e include genes for amino acid transporters, oligopeptide transporters, and lantibiotic synthesis.
11 PA3934, which belongs to the family of small oligopeptide transporters; and PA5152-5155, which encode
12 BC transport systems originally annotated as oligopeptide transporters as candidate transporters for
13 he YSL1 and YSL3 proteins are members of the oligopeptide transporter family and are predicted to be
14                       Opt2p, a member of the oligopeptide transporter family, was also identified in
15 ransport by increasing membrane insertion of oligopeptide transporter from a preformed cytoplasmic po
16     Additionally, a gene encoding a putative oligopeptide transporter from YIM 93972 can restore the
17 resent evidence that AtOPT3, a member of the oligopeptide transporter gene family with significant si
18 ic carbohydrates, and in some cases putative oligopeptide transporter genes were also found to respon
19          The human intestinal proton-coupled oligopeptide transporter hPEPT1 has been implicated in t
20 he presence of a low affinity proton-coupled oligopeptide transporter in the liver lysosomal membrane
21                        We have identified an oligopeptide transporter in the yeast Saccharomyces cere
22                     The presence of multiple oligopeptide transporters in brain has generated conside
23 eport that OPT3, previously classified as an oligopeptide transporter, is a plasma membrane transport
24           We report here that an Arabidopsis oligopeptide transporter mutant, opt3-2, over-accumulate
25 is suggests that the putative C. trachomatis oligopeptide transporter OppABCDF (OppABCDF (Ct) ) encod
26 e Arabidopsis thaliana AtOPT3 belongs to the oligopeptide transporter (OPT) family, a relatively poor
27                      We have identified nine oligopeptide transporter (OPT) orthologs (AtOPT1 to AtOP
28 with glutathione, followed by uptake via the oligopeptide transporter Opt1.
29                     Qsp1 sensing requires an oligopeptide transporter, Opt1, and remarkably, cytoplas
30 rized a novel, neuron-specific, H(+)-coupled oligopeptide transporter (OPT3) from Caenorhabditis eleg
31  PepT2, which belong to the proton-dependent oligopeptide transporter, or POT family.
32 ive RNA PCRs established the presence of the oligopeptide transporter PEPT 1 in these pancreatic cell
33                                          The oligopeptide transporter (Pept-1), which is located in t
34 ent reciprocal relationship between the H(+)/oligopeptide transporter PepT1 and apical GLUT2, reflect
35                     Studies of the mammalian oligopeptide transporter PepT1 and the Na(+)- and K(+)-c
36                                          The oligopeptide transporter PepT1 expressed in inflamed col
37                         The human intestinal oligopeptide transporter (PEPT1) facilitates the absorpt
38                                           An oligopeptide transporter, PepT1, is transcriptionally up
39                           The proton-coupled oligopeptide transporters, PepT1 and PepT2, have been su
40   Both are substrates for the proton-coupled oligopeptide transporter PEPT2.
41 rg; L-KTP) administration in mice lacking an oligopeptide transporter, PEPT2.
42                           The proton-coupled oligopeptide transporter (POT) YdgR from Escherichia col
43 of TbGPR89 predicts unexpected similarity to oligopeptide transporters (POT), and when expressed in b
44                               Proton-coupled oligopeptide transporters (POTs) are of great pharmaceut
45                               Proton-coupled oligopeptide transporters (POTs) couple the inward trans
46 y with OPT1 and OPT2, two other H(+)-coupled oligopeptide transporters previously cloned from C. eleg
47 nsceptor CHL1/NRT1.1/NPF6.3 and four related oligopeptide transporters PTR1, 2, 4, and 5 into fluores
48                                          The oligopeptide transporters SOPT1 and SOPT2 mediate the up
49                             A sodium-coupled oligopeptide transporter (SOPT1) was described originall
50 fetal RPE cells express the newly discovered oligopeptide transporter SOPT2, and the transporter is i
51 al epithelial cells have identified a second oligopeptide transporter (SOPT2).
52  was coincidentally expressed with OPT-2, an oligopeptide transporter that is driven by a transmembra
53 e findings suggest that Chlamydia evolved an oligopeptide transporter to facilitate the acquisition o
54                      Genes encoding putative oligopeptide transporters were often coregulated with ad
55 ce uncovered a mutation in OPT3, encoding an oligopeptide transporter with a plant-specific role in m