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1 nse to EAAC1-mediated Na+ cotransport and K+ countertransport.
2 l competition between similar molecules, and countertransport.
3 it with three sodium ions and a proton, and countertransporting a potassium ion via an elevator mech
6 t NHA genes may contribute to sodium-lithium countertransport activity and salt homeostasis in humans
10 plasm is known to be indirectly linked to H+ countertransport and, hence, stromal pH and photosynthet
12 wed that ORP5 and ORP8 could mediate PI4P/PS countertransport between the ER and the PM, thus deliver
13 ion and release as a consequence of the H(+) countertransport by VMAT that accompanies vesicular upta
14 A related question is whether P4-ATPases countertransport ions or other substrates in the opposit
16 current and the concentration of analyte and countertransporting ions and is found to correspond well
17 on flow beside the well-known inverse proton countertransport occurring in active Ca(2+) transport.
18 nosomes preloaded with tyrosine demonstrated countertransport of 10 microM [3H]tyrosine, indicating c
20 e net flux and complete a transport cycle by countertransport of K+, ASCT-1 mediates only homo- and h
22 l glutamate transport is achieved by the co-/countertransport of Na(+) and other ions down their conc
23 exchangers catalyze the electrically silent countertransport of Na+ and H+, controlling the transmem
28 atp1-mediated uptake is energized by efflux (countertransport) of intracellular reduced glutathione (
29 er affinity for the neurotransmitter and the countertransported potassium ion than outward- or inward
30 ontrols studies are consistent with an anion countertransport process using a relay mechanism and a k
31 e becomes competitive toward F and Britton's countertransport property disappears with these activato
32 he K(+) ion, which is believed to serve as a countertransport substrate for SERT, was the most effect
34 so showed that no charged substrate is being countertransported, thereby distinguishing the P4-ATPase