ライフサイエンスコーパス: ion permeability

1 a) polypeptide under conditions of increased ion permeability.

2 e stress, cell volume recovery, and membrane ion permeability.

3 logic range by regulated changes in membrane ion permeability.

4 ent, dog, monkey, and human origin; increase ion permeability across confluent cell monolayers; and p

5 for nonspecific disruption of viral bilayer ion permeability also identified a broad-spectrum antivi

6 Associated changes in cell membrane ion permeability and fluxes may provide the molecular ba

7 o causes secondary imbalances in sarcolemmic ion permeability and resting membrane potential, which m

8 pathways coupling changes in cell volume to ion permeability and secretion.

9 rgic signaling in the regulation of membrane ion permeability and suggest that CFTR potentiates ATP r

10 tropic receptors is reduced in ALS affecting ion permeability and the function of RNA-processing prot

11 elationship between cell volume and membrane ion permeability, and assess the possibility that cell s

12 er, detecting changes in membrane potential, ion permeability, and ion channel function.

13 el forming ability and channel lifetime, and ion permeability, as monitored by changes in single-chan

14 characterized the alterations in astrocytic ion permeability associated with exposure to this organo

15 ally when the function of the membrane as an ion-permeability barrier is compromised by agents such a

16 re, we report a mechanism for the control of ion permeability by WNK1.

17 This paper describes the ion permeability characteristics and the crystal structu

18 e temperature dependence of passive membrane ion permeability demonstrated that altered ion flux acro

19 may function in vivo, we used vesicle-based ion permeability, direct membrane association, and intri

20 btypes have evolved with different kinetics, ion permeability, expression patterns, and regulation by

21 ranes, but their effects on membrane passive ion permeability have not been systematically studied.

22 The changes in ion permeability, however, are quite different for Trp -

23 ors respond to ATP by stimulation of calcium ion permeability; however, it is unknown how P2X purinor

24 We propose that uncoupled ion permeabilities in metal ion transporters protect cel

25 ATP-gated P2X receptors display ion permeability increases within seconds of receptor ac

26 cytes, in which CsTx-1 and CT1-long increase ion permeability non-specifically.

27 odel for water and ion transport to quantify ion permeabilities of all pathways (apical, basolateral,

28 By providing a method to quantify all the ion permeabilities of respiratory epithelia, the model m

29 In fact, the ion permeabilities of the basolateral membrane and parac

30 brane selectivity means that they affect the ion permeability of both plasma and mitochondrial membra

31 Conventional antiarrhythmic drugs target the ion permeability of channels, but increasing evidence su

32 receptors stimulates a rapid increase in the ion permeability of liver cells.

33 This analysis demonstrates that the ion permeability of the NPCs is determined by the dimens

34 The remarkably high ion permeability of the NPCs is successfully measured by

35 technique, four individual RNAs increase the ion permeability of the plasma membrane of cultured huma

36 colloid-osmotic swelling due to an increased ion permeability of the plasma membrane.

37 hanges in membrane potential into changes in ion permeability or enzymatic activity.

38 mycin to K(+)-permeabilize the cells, low co-ion permeability, or reduced driving K(+) gradient, the

39 ability and introducing reversible selective ion permeability over previous multilayer film and cross

40 brane-spanning sequences that constitute the ion permeability pathway and thereby activate channel ga

41 TRIC) channels on SR as an essential counter-ion permeability pathway associated with rapid Ca(2+) re

42 e Ca(2+)-permeable ion channel with distinct ion permeability properties and unique coupled allosteri

43 stantial differences in the membrane passive ion permeability properties of phospholipid classes, sub

44 have substantive effects on membrane passive ion permeability properties.

45 of alpha7 and dramatically reducing divalent ion permeability relative to wild-type alpha7.

46 n permeabilities: The assumption of constant ion permeabilities resulted in a reasonable fit with exp

47 he importance of concentration dependence of ion permeabilities: The assumption of constant ion perme

48 For any constant set of transmembrane ion permeabilities, this set point of Vc was then determ

49 increases in volume are coupled to membrane ion permeability through a pathway involving (i) ATP eff

50 ing to the two leading mechanisms describing ion permeability through lipids.

51 ctivated currents (ICRAC) were identified by ion permeability, voltage dependence, and sensitivity to