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1  suggesting that the sea urchin protein is a Na+/HCO3- cotransporter.
2       Potassium (K+) had no affinity for the Na+:HCO3- cotransporter.
3 we propose that NBC-1 is the proximal tubule Na+:HCO3- cotransporter.
4 of Vm that is characteristic of electrogenic Na+-HCO3- cotransporters.
5 -like events and mediated by an electrogenic Na(+)/HCO3 (-) cotransporter.
6 enal enteroid model showed that electrogenic Na(+)/HCO3(-) cotransporter 1 might be a target in the i
7 brane conductance regulator and electrogenic Na(+)/HCO3(-) cotransporter 1.
8        The most similar human protein is the Na+/HCO3- cotransporter-2 (NBC2), which has 53% identity
9 orters includes Cl- -HCO3- exchangers, three Na+/HCO3- cotransporters, a K+/HCO3- cotransporter, and
10                                          The Na+:HCO3- cotransporter activity was assayed as the Na+
11 nsporters such as CFTR, Na/Pi cotransporter, Na/HCO3 cotransporter and Trp (calcium) channels.
12 re activity, are mediated by an electrogenic Na(+)/HCO3- cotransporter, and are more tightly coupled
13                   This is characteristic for Na+/HCO3- cotransporters, but not for anion exchangers,
14                                          The Na+:HCO3- cotransporter could also function in Na+:OH- c
15 change in CFTR-dependent HCO3 (-) efflux nor Na(+) /HCO3 (-) cotransporter-dependent HCO3 (-) influx
16 ransporter known: the renal 1:3 electrogenic Na+/HCO3- cotransporter from the salamander Ambystoma ti
17 n Cl-/HCO3- exchanger and the electroneutral Na+/HCO3- cotransporter, have crucial roles in regulatin
18 ssical mechanism of HCO3 (-) uptake involves Na(+)/HCO3 (-) cotransporters, here we demonstrate that
19                                     The NBC1 Na+/HCO3- cotransporter is expressed in many tissues, in
20 tered HCO3- is reabsorbed by an electrogenic Na/HCO3 cotransporter located at the basolateral membran
21 olving basolateral HCO3(-) entry through the Na(+)-HCO3(-) cotransporter (NBC) NBCe1-B, and luminal H
22 s heterologously expressing the electrogenic Na+-HCO3- cotransporter (NBC), AQP1 and carbonic anhydra
23 nctional properties of a cloned human kidney Na+:HCO3- cotransporter (NBC-1) were studied in cultured
24                                          The Na+-HCO3- cotransporter NBC1 is located exclusively on t
25 increasing the activities of the basolateral Na(+) -HCO3(-) cotransporter (NBC1) and apical Cl(-) /HC
26                          In the electrogenic Na(+)-HCO3(-) cotransporter NBCe1-A, EL-3 is the largest
27 ocytes of mice deficient in the electrogenic Na(+)/HCO3(-) cotransporter NBCe1.
28  to arise from operation of the electrogenic Na+ -HCO3- cotransporter NBCe1.
29 the anion exchanger AE1 and the electrogenic Na/HCO3 cotransporter NBCe1-A, enhancing transport.
30                             The electrogenic Na+-HCO3- cotransporter (NBCe1) plays a central role in
31 (AE2); approximately 50% to the electrogenic Na/HCO3 cotransporter (NBCe1) from salamander, rat, and
32 ical and functional interactions between the Na(+),HCO3(-) cotransporter NBCn1 (slc4a7) and the Ca(2+
33 cterized by compensatory upregulation of the Na(+)/HCO3(-) cotransporter NBCn1.
34 ied two novel variants of the electroneutral Na(+)/HCO3- cotransporter NBCn1, one full-length startin
35 pproximately 73% to mammalian electroneutral Na/HCO3 cotransporters (NBCn1); 71% to mouse NCBE; and 4
36 oning of three variants of an electroneutral Na+/HCO3- cotransporter, NBCn1, from rat smooth muscle.
37 at the basolateral membrane, mediated by the Na+-HCO3- cotransporter, pNBC1, and exit at the luminal

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