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1  principal canalicular multispecific organic anion transporter.
2 s an important function of the renal organic anion transporter.
3 th the putative functioning of pendrin as an anion transporter.
4 yeast pcCMT, STE14, and the mammalian band 3 anion transporter.
5 y its interaction with the classical organic anion transporter.
6 fectively limited to the "classical" organic anion transporter.
7  as well as 15-20% deficiency of band 3, the anion transporter.
8 is-catechol (3) functions as a transmembrane anion transporter.
9 st examples of pH-switchable nonelectrogenic anion transporters.
10 ll conserved family of genes that all encode anion transporters.
11 particular with mammalian organic cation and anion transporters.
12  selective inhibitors of other mitochondrial anion transporters.
13 prises both Cl(-) channels and H(+) -coupled anion transporters.
14 ns are a ubiquitous superfamily of secondary anion transporters.
15 ext of recent findings on the selectivity of anion transporters.
16 er hydrogen and halogen bond-based synthetic anion transporters.
17                                Human organic anion transporter 1 (hOAT1) belongs to a superfamily of
18                                Human organic anion transporter 1 (hOAT1) plays a critical role in the
19 ls transfected stably with the human organic anion transporter 1 (hOAT1), the hypothesis that hOAT1 c
20 ne stably transfected with the human organic anion transporter 1 (hOAT1).
21 n renal library and designated human organic anion transporter 1 (hOAT1).
22  anionic substrates, the human renal organic anion transporter 1 (hOATI) is capable of transporting t
23                                      Organic anion transporter 1 (OAT1) mediates the body disposition
24                                      Organic anion transporter 1 (OAT1), originally identified as NKT
25  kinetic interaction of ligands with organic anion transporter 1 (OAT1).
26  affected by the in vivo deletion of organic anion transporter 1 (Oat1, Slc22a6, originally NKT), a m
27 mportantly, both hOAT1 and rat renal organic anion transporter 1 (rROAT1) mediated saturable, probene
28 substrates for the renal basolateral organic anion transporter-1 (Oat1) from rat kidney.
29                             Notably, organic anion transporter-1 (OAT1) knockout mice expressed a sim
30                                      Organic anion transporter-1 (OAT1) mediates the body disposition
31                                      Organic anion transporter-1 (OAT1) mediates the body's dispositi
32 teroidal anti-inflammatory drugs) is organic anion transporter-1 (OAT1), originally identified as NKT
33 ulated in adenoma (Dra) or Slc26a6, putative anion transporter-1 (Pat-1).
34 -)/HCO(3)(-) exchangers, studies of putative anion transporter-1 knockout (KO) mice find little contr
35 O) mice find little contribution of putative anion transporter-1 to basal or cAMP-stimulated secretio
36 lls that were transfected with human organic anion transporter-1 were used.
37 e (Cyp7a1) and the Na(+)-independent organic anion transporter 2 (Oatp2).
38 major regulator of the Na+-dependent organic anion transporter 2.
39 und in the kidneys mediated by human organic anion transporter 3 (hOAT3) was hypothesized as a contri
40  a targeted disruption of the murine organic anion transporter 3 (Oat3) gene.
41          In this study, mice lacking organic anion transporter 3 (Oat3) had a 10 to 15% lower BP than
42  decrease in the expression level of organic anion transporter 3 (SLC22a8).
43                                Human organic anion transporter 4 (hOAT4) belongs to a superfamily of
44              The band 3 proteins function as anion transporters, acid base regulators, C02 transporte
45 t kinetics have been examined in erythrocyte anion transporter AE1 that has been chemically modified
46 e founding member of a unique gene family of anion transporters (ALMTs) that mediate the efflux of or
47 n the design of small-molecule transmembrane anion transporters and focuses on the progress so far in
48   Prestin is a member of the SLC26 family of anion transporters and is responsible for electromotilit
49 rstanding biological activities of synthetic anion transporters and potentially the uncoupling mechan
50 solute carrier (SLC) family 26, that encodes anion transporters and related proteins.
51 f many membrane proteins such as glucose and anion transporters and the erythropoietin receptor.
52  on prestin, a member of the SLC26 family of anion transporters and utilizes the electric energy avai
53 cholate cotransporter, multispecific organic anion transporter, and P-glycoprotein) were also determi
54                                Transmembrane anion transporters (anionophores) have potential for new
55 e also provide evidence that the most potent anion transporters are able to induce apoptosis in human
56                             Notably the best anion transporters are highly selective for transport of
57    ABA binds specifically to Band 3 (the RBC anion transporter), as determined by labeling of RBC mem
58                                 Further, the anion transporter band 3 was implicated as the counterio
59  the erythrocyte membrane; these include the anion transporter (band 3: Diego and Wright antigens), t
60 ts interaction with ankyrin and adducin, the anion transporter, band 3 (AE1), contributes prominently
61 or a high beta-carotene diet on aging of the anion transporter, band 3, in lymphocytes and brain.
62 olase to the N-terminus of human erythrocyte anion transporter, band 3, inhibits enzyme activity.
63 ciparum and Sendai virus, and along with the anion transporter, band 3, may contribute to the mechani
64  tyrosine phosphorylation of the erythrocyte anion transporter, band 3, triggers membrane destabiliza
65                                              Anion transporters based on small molecules have receive
66 al, and comparisons with GlpT show that both anion transporters bind substrates within equivalent dom
67                  We previously localized the anion transporter ClC-3 to polymorphonuclear leukocytes
68 hly motile PMN functions, suggested that the anion transporters, ClC-3 and ICl(swell), are involved i
69 1) and the canalicular multispecific organic anion transporter (cMOAT or MRP2) are ATP-binding casset
70  (MRP) and canalicular multispecific organic anion transporter (cMOAT) are closely related mammalian
71  the liver canalicular multispecific organic anion transporter (cMOAT) protein.
72 (MRP)1 and canalicular multispecific organic anion transporter (cMOAT)/MRP2 are ATP-binding cassette
73 strate for canalicular multispecific organic anion transporter [cMOAT]).
74 ve been identified such as the multispecific anion transporter, cMOAT, bile acid transporters, ion-mo
75            These results identify an organic anion transporter composed of a putative seven-helix TM
76  series of easy-to-make fluorinated tripodal anion transporters containing urea and thiourea groups h
77 hese coupled (stoichiometric) and uncoupled (anion) transporter currents is poorly understood, transp
78  as a target in the development of synthetic anion transporters despite natural fluoride transport ch
79  acid binding proteins (L-FABP), and organic anion transporters--determine the distribution, accumula
80                                Pendrin is an anion transporter encoded by the PDS/Pds gene.
81 sport proteins that includes the rat sulfate-anion transporter (encoded by Sat-1; 29% amino acid sequ
82 ndependently correlated with hepatic organic anion transporter expression.
83 endrin and prestin both belong to a distinct anion transporter family called solute carrier protein 2
84 ember 1 (Slc10a1) and solute carrier organic anion transporter family member (Slco) 1a1 and 1b2, resp
85 ight chain (FTL), and solute carrier organic anion transporter family member 2B1 (SLCO2B1), in the bl
86 brane protein prestin, a member of the SLC26 anion transporter family, is responsible for the voltage
87 otein, prestin, which evolved from the SLC26 anion transporter family, underlies the OHC's voltage-de
88 ucture-function relationships of the organic anion transporter family.
89 ucture-function relationships of the organic anion transporter family.
90 of organic anions by a member of the organic anion transporter family.
91 nous molecular motors evolved from the SLC26 anion transporter family.
92  development of small-molecule lipid-bilayer anion transporters for potential future use in channel r
93 the presence of distinctly different organic anion transporters for the efflux of VPA at the parenchy
94                                          CLC anion transporters form dimers that function either as C
95 previously cloned a cDNA encoding an organic anion transporter from mouse kidney (mOAT).
96                      These cells had organic anion transporter function.
97 vement and morphology of PMNs lacking normal anion transporter function.
98 m on chloride anions suggests that selective anion transporters function as important components of t
99          Although recessive mutations in the anion transporter gene SLC26A4 are known to be responsib
100 associated with polymorphisms in the organic anion transporter gene SLCO1B1 (P = 2.1 x 10(-11)).
101 hitectures, while the study of transmembrane anion transporters has flourished from almost nothing in
102                                Human organic anion transporter hOAT1 belongs to a superfamily of orga
103                                Human organic anion transporter hOAT1 plays critical roles in the body
104                            The human organic anion transporter (hOAT1) is a key component in the rena
105 n the functional maturation of human organic anion transporter hOAT4.
106                   In contrast to the organic anion transporters identified to date, a transport activ
107 mbrane-associated protein; cMOAT, an organic anion transporter implicated in multidrug resistance; an
108 e studies indicate that pendrin is an apical anion transporter in intercalated cells of CCDs and has
109        Prodigiosin is one of the most potent anion transporters in lipid bilayer membranes reported t
110     The molecular identity and regulation of anion transporters in PTs is unknown.
111                                      Organic anion transporters in the kidney proximal tubule play an
112 rect evidence implicating one of the organic anion transporters in the uptake of a mercuric conjugate
113 d circumstantial evidence implicates organic anion transporters in these processes.
114 ed in the presence of probenecid, an organic anion transporter inhibitor.
115  Clcn3(-/-) PMNs and human PMNs treated with anion transporter inhibitors demonstrated impaired chemo
116 (2)17betaG indicates that it is a lipophilic anion transporter involved in phase III (cellular extrus
117    Prestin, a member of the SLC26A family of anion transporters, is a polytopic membrane protein foun
118       This conductance is independent of the anion transporter mechanism.
119                    Ci-Slc26aalpha acts as an anion transporter, mediating the electrogenic exchange o
120 ional modification of a mouse kidney organic anion transporter (mOAT), in a mammalian cell system, CO
121 protein (P-gp) and the multispecific organic anion transporter (MOAT), the liver-specific homologue o
122 rt in COS-7 cells expressing a mouse organic anion transporter (mOAT1), suggesting an important role
123        In vivo studies implicate the organic anion transporter (OAT) family as a pivotal component of
124 ent of the contributions of specific organic anion transporter (OAT) family members to detoxification
125 clude two "drug" transporters of the organic anion transporter (OAT) family: OAT1 (SLC22A6, originall
126 le cells by the basolateral membrane organic anion transporters (Oat) 1 and Oat3.
127                                Renal organic anion transporters (OAT) are known to mediate the excret
128                                      Organic anion transporters (OAT) play essential roles in the bod
129                                  The organic anion transporters OAT1 (SLC22A6) and OAT3 (SLC22A8) hav
130                                  The organic anion transporters OAT1 (SLC22A6, originally identified
131 cation transporters (OCT2 and OCT3), organic anion transporter (OAT1), and monoamine transporters wer
132                                  The organic anion transporter OAT4 (SLC22A11) and organic anion tran
133  and transport function of olfactory organic anion transporter, Oat6, in comparison with the more bro
134                                      Organic anion transporters (OATs) and organic cation transporter
135                                      Organic anion transporters (OATs) are believed to mediate the ce
136                                      Organic anion transporters (Oats) are located in the barrier epi
137 ty acid binding proteins (FABPs) and organic anion transporters (OATs) have been identified as import
138                       Studies of the organic anion transporters (Oats) have focused mainly on their i
139    Given the selective expression of organic anion transporters (OATs) in renal proximal tubular cell
140 he proximal tubule-specific drug and organic anion transporters (OATs) OAT1 (SLC22a6) and OAT3 (SLC22
141                                      Organic anion transporters (OATs) play a critical role in the ha
142                                      Organic anion transporters (OATs) play a pivotal role in the cle
143 e cloning of multiple genes encoding organic anion transporters (OATs), the study of organic anion se
144 creted by the recently characterized organic anion transporters (OATs), which are expressed in proxim
145                                      Organic anion transporters (OATs, SLC21) are important in the ex
146                                      Organic anion transporters (OATs, SLC22) interact with a remarka
147 in which, in common with other mitochondrial anion transporters of known sequence and function, displ
148 amilies, most notably the organic cation and anion transporters of the solute carrier family (SLC22),
149 s suggest that GmN70 and LjN70 are inorganic anion transporters of the symbiosome membrane with enhan
150 orted that expression of the epithelial cell anion transporter pendrin is markedly increased in respo
151                                              Anion transporters play a vital role in cellular process
152                                      Organic anion transporters play an essential role in eliminating
153 t associations were with SNPs in the organic anion transporter polypeptide, SLCO1B1.
154                                  Rat organic anion transporter polypeptide1 (Oatp1) is known to trans
155 sociated protein 2 (Mrp2, Abcc2), an organic anion transporter present in the apical membrane of hepa
156 ssociated protein 2 (Mrp2/Abcc2), an organic anion transporter present in the apical membrane of hepa
157 inocytes expressed the organic anion organic anion transporter protein (OATP) 2B1 transporter.
158 urocholate cotransporter protein and organic anion transporter protein 1.
159 ely taken up by a sodium-independent organic anion transporter protein-1B1 (OATP1B1) exclusively expr
160               The molecular identity of this anion transporter remains unknown.
161  GLUT1, the glucose transporter; SLC4A1, the anion transporter; RhAG, the Rh-associated glycoprotein;
162  GLUT1, the glucose transporter; SLC4A1, the anion transporter; RhAG, the Rh-associated glycoprotein;
163                              The rat organic anion transporter, rOAT3, mediates the transport of orga
164 ansport of organic anions by the rat organic anion transporter, rOAT3.
165 the STAS domain from the SulP/SLC26 putative anion transporter Rv1739c of Mycobacterium tuberculosis.
166 tile prestin orthologs, while functioning as anion transporters, should be much less sensitive to mem
167 l as organic cation transporters and organic anion transporters Slc22a1 (Oct1), Slc22a2 (Oct2), Slc22
168 deled, based on structural data from related anion transporters (SLC26Dg and UraA), to have a 7 + 7 i
169 Recent studies have implicated roles for the anion transporter, SLC4A1, and the Rh-associated glycopr
170 ed STAS domains of the ubiquitous SulP/SLC26 anion transporter superfamily have until recently remain
171 stin', the molecule is a member of the SLC26 anion transporter superfamily.
172 by URAT1 (SLC22A12), a member of the organic anion transporter superfamily.
173 f SLC26A7 was inhibited by all inhibitors of anion transporters tested, 4,4'-diisothiocyanostilbene-2
174   We conclude that NaDC-1 is an electrogenic anion transporter that accepts either Na+ or Li+ as coup
175                    These results identify an anion transporter that functions in stomatal opening and
176   Human MRP4 (ABCC4, MOAT-B) is a lipophilic anion transporter that is able to confer resistance to n
177      We conclude that MRP8 is an amphipathic anion transporter that is able to efflux cAMP and cGMP a
178             Slc26a9 is a recently identified anion transporter that is abundantly expressed in gastri
179                                    ClC-3, an anion transporter that is primarily found in intracellul
180       oatp1 is an hepatic sinusoidal organic anion transporter that mediates uptake of various struct
181 he expression of rOat2 (Slc22a7), an organic anion transporter that regulates, in part, the transfer
182 amily of putative membrane-localized sulfate/anion transporters that contain a sulfate transporter do
183   Prestin is a member of the SLC26 family of anion transporters that is responsible for outer hair ce
184       In this report, we introduce synthetic anion transporters that operate with chalcogen bonds.
185           The mechanisms that target organic anion transporters to different domains of the ileal ent
186                           The application of anion transporters to the potential future treatment of
187 late cotransporter and multispecific organic anion transporter were more profoundly diminished.
188   SLC26A9 is a member of the SLC26 family of anion transporters, which is expressed at high levels in
189 er hOAT1 belongs to a superfamily of organic anion transporters, which play critical roles in the bod
190  (hOAT1) belongs to a superfamily of organic anion transporters, which play critical roles in the bod
191 es for the canalicular multispecific organic anion transporter whose activity has recently been assoc
192 e solute carrier 26 (SLC26) transporters are anion transporters with diverse substrate specificity.
193 related to MRP, cMOAT, and the yeast organic anion transporter YCF1.

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