ライフサイエンスコーパス: volume-sensitive

1 n 185 is surrounded by other residues and is volume sensitive.

2 Taken together, these findings indicate that volume-sensitive activation of PI 3-kinase and the gener

3 We conclude that bestrophins are volume sensitive and that they could play a novel role i

4 is concluded that activity of the beta-cell volume-sensitive anion channel can be modulated by chang

5 lular adenine nucleotides on activity of the volume-sensitive anion channel in single, isolated rat p

6 s were used to investigate the expression of volume-sensitive anion channels in acinar cells isolated

7 an absolute requirement for the activity of volume-sensitive anion channels in rat lacrimal gland ac

8 ments in DCFS precluded glutamate release by volume-sensitive anion channels, P2X7 purinergic recepto

9 A volume-sensitive anion conductance was observed when cel

10 ory activity and may involve activation of a volume-sensitive anion conductance.

11 Volume-sensitive anion conductances were observed in bot

12 dynamic changes in cell volume, resulting in volume-sensitive channel activation, and efflux of cytos

13 Our observations indicate that volume-sensitive channel may constitute a previously unc

14 t p38 negatively modulates the set point for volume-sensitive channel opening.

15 The effect of noradrenaline on the volume-sensitive chloride current (I(Cl(swell))) was stu

16 been implicated in several tissues as a cell-volume-sensitive Cl(-) channel.

17 It is concluded that the volume-sensitive Cl- conductance in ROS 17/2.8 cells is

18 The effects of arachidonic acid upon the volume-sensitive Cl- current present in cultured osteobl

19 The volume-sensitive conductance was permeable to Na(+) appr

20 Of these two volume-sensitive conductances, L-alanine elicited a spec

21 ibited by wortmannin or LY294002 and because volume-sensitive current activation was inhibited by int

22 ermine possible molecular candidates for the volume-sensitive current.

23 ivator, MEK-6, which substantially inhibited volume-sensitive currents.

24 e that H2O2 strongly up-regulates astrocytic volume-sensitive EAA release via a CaMKII-dependent mech

25 The volume-sensitive glutamine transport process features ch

26 These findings indicate that volume-sensitive increases in p60(c-src) and/or related

27 ast five distinct Cl- channels; a ClCO-like, volume-sensitive, inward rectifying, Ca2+-activated and

28 of hepatocytes and other epithelia activates volume-sensitive ion channels that facilitate fluid and

29 motic gradients and cellular volume requires volume-sensitive ion channels.

30 eads to fluid and electrolyte efflux through volume-sensitive K(+) and Cl(-) channels.

31 Volume-sensitive K+ influxes in high potassium-containin

32 n a volume-dependent manner and so regulates volume-sensitive K+ transport.

33 A Cl(-)/volume-sensitive kinase has been proposed to coordinatel

34 integral component of the long-sought "Cl(-)/volume-sensitive kinase" of the cation-Cl(-) cotransport

35 plicating it as (one of) the long-sought Cl-/volume-sensitive kinase(s).

36 represent an important target for modifying volume-sensitive liver functions.

37 To determine whether IK1 underwent volume-sensitive localization, we expressed a green fluo

38 A key component of the volume-sensitive machinery, the transient receptor poten

39 er (VSOR) anion channel, also referred to as volume-sensitive organic osmolyte-anion channel (VSOAC),

40 sed as a molecular candidate responsible for volume-sensitive osmolyte and anion channels (VSOACs) in

41 Short ClC3 isoform (sClC3) functions as a volume-sensitive outwardly rectifying anion channel (VSO

42 tween endogenous ClC-3 expression and native volume-sensitive outwardly rectifying anion channels (VS

43 is increase does not stem from activation of volume-sensitive P2 receptors.

44 ) examine differences in perceived "at-risk" volume-sensitive populations, including end-stage renal

45 ose of these studies was to evaluate whether volume-sensitive tyrosine kinases mediate cell volume in