ライフサイエンスコーパス: membrane resistance

1 cause of both uphill transport and increased membrane resistance.

2 erning signal dissipation through changes in membrane resistance.

3 d instead likely mediated by lowering of the membrane resistance.

4 s in spontaneous IPSCs (sIPSCs), sEPSCs, and membrane resistance.

5 t decrease in spontaneous AP firing rate and membrane resistance.

6 microM), with a concomitant net decrease in membrane resistance.

7 iring rate but as a secondary action reduces membrane resistance.

8 eus resulted in depolarization and increased membrane resistance.

9 ns by inducing depolarization and increasing membrane resistance.

10 rization and hence a decrease in basolateral membrane resistance.

11 llular resistivity, membrane capacitance, or membrane resistance.

12 eover, it did not produce sizable changes in membrane resistance.

13 cells a hyperpolarization and a reduction of membrane resistance.

14 able phase of the action potential with high membrane resistance.

15 le for these cannabinoid-produced changes in membrane resistances.

16 urons and a relative decrease in the somatic membrane resistance (0.7-8.1 M omega) was detected durin

17 sport resistance for P(m)>1 cm s(-1) whereas membrane resistance accounts for 50-75% of total transpo

18 e appears to depend upon both an increase in membrane resistance and a decrease in total cell surface

19 increased spike duration, and reductions in membrane resistance and amplitude of the Ih current.

20 ride was associated with a decrease in ileal membrane resistance and an increase in inducible nitric

21 ne excitability, as indexed by a decrease in membrane resistance and an increase in the stimulus thre

22 ane region includes local models for passive membrane resistance and capacitance, nonlinear active so

23 on/dehydration induces reversible changes of membrane resistance and effective capacitance.

24 n its resting membrane properties, including membrane resistance and potential.

25 tic potential integration by influencing the membrane resistance and resting membrane potential.

26 filaments have to be bundled to overcome the membrane resistance and that the filopodial length is li

27 The neutral salt is used to reduce membrane resistance and to ensure reversibility of the s

28 ere also associated with a small increase in membrane resistance, and in voltage-clamp recordings ore

29 s of membrane potential, severe reduction of membrane resistance, and influx of Na+, Ca2+, Cl- and wa

30 ntial (RMP), spontaneous AP firing rate, and membrane resistance are cyclically regulated as a functi

31 llate cells, a voltage-dependent increase in membrane resistance at sub-threshold voltages mediated b

32 ance of the nerve cell and by increasing its membrane resistance, but little is known about the latte

33 eurons (7.8 +/- 0.6 mV; n = 16), reduced the membrane resistance by 33 +/- 3%, and could convert the

34 rectification and steady-state components of membrane resistance by 37 and 38 %, respectively, in 66

35 dels was accompanied with decreased specific membrane resistance by approximately 25% and efficacy of

36 No differences were found in the membrane resistance, capacitance, or kinetic and voltage

37 Neither membrane resistance changes nor spine density changes we

38 hannels in S-D muscle produced high specific membrane resistance, comparable to similarly treated con

39 olarized resting potentials and an increased membrane resistance compared with age-matched control ce

40 to L-glutamate without significant change in membrane resistance, consistent with the well-establishe

41 Over the next 2 weeks, membrane resistance decreased and resting membrane poten

42 partial depolarization, to about -40 mV; the membrane resistance decreased by only 37%.

43 onstrates for the first time that increasing membrane resistance decreases the efficiency of this res

44 ined depolarization up to -27 mV and reduced membrane resistance (EC50 140-170 pm).

45 Ang II depolarized and increased membrane resistance equally in both TNs (n = 8) and PNs

46 ee Hb due to transport resistances including membrane resistance, extra- and intra-cellular resistanc

47 a passive current-voltage relationship, low membrane resistance, high capacitance, and dye-coupling

48 e contrast is due to the decrease in tip and membrane resistance, in the vicinity of the pore opening

49 Also, the membrane resistance increased quite strongly at high pol

50 On average, the membrane resistance is 14 times lower and the effective

51 er of G-protein trimers required to overcome membrane resistance is 3 to 5, within a contact zone bet

52 1) for 10-45% Hct, respectively, below which membrane resistance is more significant and above which

53 d depend on the number of bundled filaments, membrane resistance, lamellipodial protrusion rate, and

54 take by intracellular hemoglobin or a unique membrane resistance mechanism.

55 The phasic membrane resistance modulation in relation to the gill r

56 Gram-negative bacteria utilize dual membrane resistance nodulation division-type efflux syst

57 In contrast, a decreased membrane resistance of DCN granule cells (multisensory i

58 This strategy exploits the change in the membrane resistance of the powered system, comprising a

59 In contrast, the resting potential and membrane resistance of the recorded cells remained uncha

60 P>0.05) in T-type current kinetics or in the membrane resistance of the thalamic cells between the tw

61 ing voltage clamp, we found that the passive membrane resistance of VS cells was reduced during fligh

62 ough strophanthidin did not alter either the membrane resistance or the Na(+) reversal potential, the

63 ated inhibitory postsynaptic potentials, the membrane resistance, or the holding current, whereas it

64 se effects on resting membrane potential and membrane resistance persisted in the presence of TTX.

65 n ORNs (4.4 +/- 0.4 pF) and a lower apparent membrane resistance (R(m)) (160 +/- 11 MOmega versus 664

66 increased the ratio of apical-to-basolateral membrane resistance (R:(A)/R:(B)).

67 T, excitability is determined by the resting membrane resistance, R(m).

68 larized, with spontaneous AP firing rate and membrane resistance remaining stable.

69 in fibres of young HSA(LR) mice, the resting membrane resistance (Rm) at -90 mV is only slightly larg

70 resting membrane potential (Vm), IK,ADO, and membrane resistance (Rm) in rabbit isolated AV nodal myo

71 e inexcitable despite resting potentials and membrane resistances similar to those of control denerva

72 ices taken from MeA-trained birds had higher membrane resistances than did cells from water-trained c

73 ime constant is attributed to an increase in membrane resistance; the increase in input resistance ap

74 The upper limit of resting membrane resistance, then, is 6 GOmega.

75 In addition, a more limited decrease in membrane resistance upon reduction of extracellular calc

76 n transfected cells was 43.7 +/- 13.8 pF and membrane resistance was 458 +/- 123 Mohms.

77 Additionally, membrane resistance was found to be an important factor

78 n = 18) and PNs (-48 +/- 1 mV, n = 23) while membrane resistance was significantly higher in TNs.

79 Apical and basolateral membrane resistances were determined by nonlinear curve-

80 Image contrast also becomes independent of membrane resistance when an electrical shunt is used, al