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1 n shown recently to be a divalent amphoteric cation transporter.
2 tter norepinephrine (NE) via an Oct3 organic cation transporter.
3 -type ATPase with its putative function as a cation transporter.
4 T mainly functions as a polyspecific organic cation transporter.
5 assign a new function to the CorA family of cation transporters.
6 ical role in binding of substrate to organic cation transporters.
7 luding choline acetyltransferase and organic cation transporters.
8 ns predicted the substrates of these organic cation transporters.
9 lium is non-vesicular and occurs via organic cation transporters.
10 ubstrate specificity between the two organic cation transporters.
11 e important in the function of this group of cation transporters.
12 rectal and other cancers bearing appropriate cation transporters.
13 ransported into cells through BA and organic cation transporters.
14 onserved family of divalent transition metal cation transporters.
15 hypothesis that genetic variation in organic cation transporter 1 (OCT1) affects the response to the
16 t reduced transport of metformin via organic cation transporter 1 (OCT1) could increase metformin con
23 ism (SNP) mapping to intron 1 of the organic cation transporter 1 (OCTN1; SLC22A4) gene was associate
24 tly the clinical importance of human organic cation transporters 1 (hOCT1/SLC22A1) and 2 (hOCT2/SLC22
25 mpound is an excellent substrate for organic cation transporters 1 and 2, also designated SLC22A1 and
26 is an excellent substrate for human organic cation transporters 1-3 (hOCT1-3) and the multidrug and
27 attributed to the presence of human organic cation transporter-1 (hOCT1) single nucleotide polymorph
28 ess two point mutations of the human organic cation transporter-1 (hOCT1), R488M and G465R, have been
29 n-regulation of SLC22A1 encoding the organic cation transporter-1 (OCT1) may affect the response of h
30 nd expression of the molecular human organic cation transporter-1 (RR, 1.79; P = .038) as the only in
31 oration in tubule membrane function (organic cation transporter-1 transport activity) was observed du
32 evidence for a critical role of the organic cation transporter 2 (OCT2) in satellite glial cells in
34 e Golgi pool of D1DR is dependent on organic cation transporter 2 (OCT2), a dopamine transporter, pro
35 ere found to be potent inhibitors of organic cation transporter 2 (OCT2), which contributes to the ce
37 t, and muscle carnitine transporter [organic cation transporter 2 (OCTN2)] messenger RNA and protein
38 s transporter, known as OCTN2 (novel organic cation transporter 2), is expressed in most tissues and
39 pe of solute carriers and identified organic cation transporter 3 (OCT3) (SLC22A3) as a critical tran
40 we show that Ru265 is transported by organic cation transporter 3 (OCT3) and taken up more effectivel
48 T, PQ(+) is also a substrate for the organic cation transporter 3 (Oct3, Slc22a3), which is abundantl
49 transporter 2 (VMAT2) together with organic cation transporter 3 and monoamine oxidase type B, two k
52 selectively and highly express OCT3 (organic cation transporter-3), a polyspecific drug transporter i
53 3-PHOSPHATE DEHYDROGENASE (PvGAPC1), ORGANIC CATION TRANSPORTER 4 (PvOCT4), and GLUTATHIONE S-TRANSFE
54 entified in the ZIP, HMA and CDF families of cation transporters, although only few are characterized
56 o1, Cyp2d2, Cyp2d4, Nqo2, as well as organic cation transporters and organic anion transporters Slc22
57 ted that includes alignments of the analyzed cation transporters and their chromosomal locations.
59 , Glc-Pt 1 exploits both glucose and organic cation transporters, both widely overexpressed in cancer
60 ate in subsequent experiments that the metal cation transporter CNNM4 regulates growth by induction o
61 rse cellular processes, although how various cation transporters collaborate to maintain a suitable K
62 ber 1 (SLC11A1; formerly NRAMP1), a divalent cation transporter crucial to host defense against certa
65 te Carrier DmSLC22A, a member of the organic cation transporter family, enhances olfactory memory exp
67 for Cd2+ transport we tested putative plant cation transporters for Cd2+ uptake activity by expressi
73 icated homology to integral membrane organic cation transporters; hence, we designate this gene ORCTL
75 ) were recently identified as a subfamily of cation transporters; however, no plant CCXs have been fu
76 f genes encodes electroneutral Cl--dependent cation transporters (i.e., Na-Cl, K-Cl, Na-K-2Cl cotrans
78 transporter (PMAT) is a polyspecific organic cation transporter in the solute carrier 29 (SLC29) fami
79 To understand the diversity and role of H(+)/cation transporters in controlling plant ion levels, ano
85 constructs suggest that a functional organic cation transporter is encoded by the larger open reading
86 Although functional results also point to a cation transporter, its molecular identity remains uncer
87 eir involvement in the regulation of ATPase, cation transporter, kinase and UDP-glycosyltransferases
90 d the transcriptional regulators of divalent cation transporters MerR and PsaR in vitro and in vivo.
92 ever, no valid biomarker for hepatic organic cation transporter (OCT) 1 has been described to date.
93 ultidrug transporters, including the organic cation transporter (OCT) 2, is influenced by the structu
95 resembles the pharmacophore of known organic cation transporter (OCT) inhibitors and reduced oxalipla
96 organic anion transporter (OAT) and organic cation transporter (OCT) may be used to evaluate their r
101 substrate spectrum and synergy with organic cation transporters OCT1 and OCT2 remain incompletely un
102 distinct from the previously cloned organic cation transporters (OCT1, OCT2, NKT, NLT, RST, and OCTN
107 polymorphisms (SNPs) mapping to the organic cation transporter (OCTN) genes, SLC22A4 and SLC22A5, wa
113 ransporters for 5-HT in brain [i.e., organic cation transporters (OCTs) and plasma membrane monoamine
118 rganic anion transporters (OATs) and organic cation transporters (OCTs) mediate the flux of xenobioti
120 ic cations that rely on polyspecific organic cation transporters (OCTs) to traverse cell membranes.
121 e the Oats share close homology with organic cation transporters (Octs), it is possible that Oats int
128 s to previously cloned rat and human organic cation transporters, organic cation transport kinetics d
131 Arabidopsis thaliana , different families of cation transporters play pivotal roles in Zn homeostasis
132 Together, these data suggest that monovalent cation transporters play some role in C. perfringens spo
133 gdoms of life and constitute a wide range of cation transporters, primarily for H(+), Na(+), K(+), Ca
134 potential biomarkers for OCT1 and additional cation transporters (renal OCT2, MATE1, and MATE2K).
135 We also studied the expression of SKC1, a cation transporter reported by others as a major source
136 transport into plant cells is a low-affinity cation transporter represented by the wheat protein LCT1
142 ter of a divalent metal transporter/divalent cation transporter/solute carrier 11 group A member 2 or
144 ins, GerO and GerQ, homologous to monovalent cation transporters suggested to have roles in the germi
147 c11a1 (formerly Nramp1) is a proton/divalent cation transporter that regulates cation homeostasis in
148 PMAT, SLC29A4) is a new polyspecific organic cation transporter that transports a wide variety of org
149 Plant HKT proteins comprise a family of cation transporters together with prokaryotic KtrB, TrkH
150 tance, impaired uptake through human organic cation transporter type 1 (hOCT1) (gene SLC22A1) has bee
151 e demonstrate that expression of the organic cation transporter type 3 (OCT3, SLC22A3), which also tr
153 Originally described as a monoamine/organic cation transporter, we found that both human and mouse E
154 rA (UvrABC endonuclease), and ctpV (putative cation transporter) were obtained from macrophage-grown
155 22a1 encodes for a hepatic and renal organic cation transporter which may be important for the uptake
156 PMAT can function as a polyspecific organic cation transporter, which may play a role in organic cat