ライフサイエンスコーパス: ion permeability

1 ced these functional effects on paracellular ion permeability.

2 a) polypeptide under conditions of increased ion permeability.

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

4 logic range by regulated changes in membrane ion permeability.

5 s in transepithelial voltage, resistance, or ion permeabilities.

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

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

8 te the molecular bases for hCLDN-9 selective ion permeability and binding by CpE, and provide mechani

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

10 ading to an elevation of astrocytic membrane ion permeability and gap junction activity, with a conse

11 demonstrate that shell properties influence ion permeability and leverages the integration of experi

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

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

14 ds that control important properties such as ion permeability and selectivity as well as inactivation

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

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

17 ed with a milder phenotype, retained partial ion permeability and was the only mutant capable of cons

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

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

20 mutations disrupt subcellular localization, ion permeability, and selectivity, which contribute to t

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

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

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

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

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

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

27 The gradual shift of relative ion permeability did not correlate with the channel acti

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

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

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

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

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

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

34 Ion permeability in these membranes spans five orders of

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

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

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

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

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

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

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

42 ng ion conductance microscopy to measure the ion permeability of GO films and evaluate its relationsh

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

44 transmembrane domains in such a way that the ion permeability of the latter and the affinity for neur

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

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

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

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

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

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

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

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

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

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

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

56 have substantive effects on membrane passive ion permeability properties.

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

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

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

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

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

62 Tracking selective ion permeability through ion channels, however, remains

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

64 ovide information critical for understanding ion permeability through the outer cell surface of S-lay

65 PLD2 mechanosensitivity combines with TREK-1 ion permeability to elicit a mechanically evoked respons

66 th improved photocurrents and more selective ion permeability using an automated multifaceted fluores

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

68 N-chlorination reduces membrane polarity and ion permeability, while C-chlorination has an opposite e