ライフサイエンスコーパス: right shift

1 cence, or Ca(2+) responses between left- and right-shifted beta-cells.

2 iabetic and nondiabetic subjects, implying a right shifted but parallel dose-response curve.

3 voltage dependence of F1304Q inactivation is right-shifted by 26 +/- 2 mV.

4 Dose-response curves were right-shifted by aging (twice the dose was required to a

5 The voltage sensitivity of hSlo was right-shifted by approximately 16 mV.

6 Right-shifted [Ca2+]i dependence of secretion explains c

7 KCNQ2(I205V) has a right-shifted conductance-to-voltage relationship, sugge

8 tention-related, are improved over a broader/right-shifted dose range.

9 Activation of G proteins by PTA(2) is right-shifted from binding of the ligand to receptor, a

10 rent (voltage) (I (V)) relations indicated a right-shifted G (V) relationship for R669C and for R669C

11 eft-hemisphere-biasing genetic influence, a "right-shift" genotype that is lost in nonright handers,

12 relate to global biodiversity policy; human rights; shifting human geography; inclusion, diversity,

13 The LV pressure-volume curves demonstrated a right shift in control PCO animals, whereas the (-)-epic

14 lutamate resulted in reduced responses and a right shift in dose response, indicating that receptor p

15 left hemisphere correlated with the left-to-right shift in handedness.

16 to increasing prepulse intensities showed a right shift in the BN relative to the WKY.

17 f tamoxifen with the pore was supported by a right shift in the concentration-response curve for tetr

18 with this drug cocktail showed a significant right shift in the ED50 for opioid-mediated analgesia, w

19 gradation of the DOR/MOR heteromer after the right shift in the ED50 had occurred, or blocking signal

20 a severely impaired channel function with a right shift in the voltage dependence of activation, a r

21 This indicates that a right-shift in [Ca2+]i dependence of insulin secretion,

22 slets to the same levels as WT, indicating a right-shift in [Ca2+]i dependence of secretion.

23 of channel palmitoylation and a significant right-shift in channel half maximal voltage for activati

24 ws by approximately 10-fold a time-dependent right-shift in V0.5 values ("run-down"); (3) speeds macr

25 ouble-knockout mice and potency of BuTAC was right-shifted in M4(-/-) as compared with wild-type and

26 buloglomerular feedback function curves were right-shifted, indicating reduced sensitivity in the sub

27 ey exclude the simplest formulations of the 'right-shift' model of Annett and the 'dextral/chance' mo

28 We observed a correlation between the right shift of tension activation threshold and the loss

29 helix with a charged residue (Y75E) causes a right shift of the activation curve ("stiff" phenotype)

30 This produces a right shift of the concentration-response relationship f

31 ygous null mice have latent myasthenia and a right shift of the force-stimulus relation, without evid

32 tion experiments, all the analogues caused a right shift of the glucagon-stimulated adenylate cyclase

33 n experiments, all of the analogues caused a right shift of the glucagon-stimulated adenylate cyclase

34 lations suggested that the interface-induced right shift of the localized states for unpaired Fe d el

35 I(Kr) that has a primary effect of causing a right shift of V(1/2) for inactivation, we then examined

36 We found right-shifted oxyhemoglobin dissociation curves, with pH

37 turation (shallow maturation), rather than a right-shifted pattern (lagged maturation), was implicate

38 the dose-response curve for this action was right-shifted relative to working memory, as seen with s

39 ating or inactivating mutation were left- or right-shifted, respectively.

40 the VSD from Ci-VSP (Ci-VSD) is dramatically right shifted, so that at 0 mV it presumably populates t

41 edly less than wild-type (WT) InsP(3)R-1 and right shifted some approximately 15-fold when the concen

42 The ability to right-shift the oxygen dissociation curve was retained a

43 RA-2 at 100 nM right-shifted the KCa3.1 concentration-response curve fo

44 KE right-shifted the left ventricular end-diastolic pressur

45 ine for beta2AR binding sites and expectedly right-shifted the terbutaline dose-response curve to 8 +

46 , suppressed the sodium current density, and right-shifted the V1/2 of the inactivation curve, of hin

47 l opening solely in the presence of KCNE1 by right-shifting the voltage dependence of activation.

48 Replacing the gating ring also right-shifts the conductance-voltage relation, decreases

49 pected rise in basal metabolic demands and a right-shifted thermal window, which aids in maintaining

50 dtype curve, whereas the declining phase was right-shifted toward lower affinity.

51 By pooling information on left-right shifts underlying whole-brain structure, we deconv

52 Right shift, V . a/Q . , and right-left shunt were deriv

53 nduced increased tau(inact) and restored the right-shifted voltage at half-activation (V(1/2)) induce

54 isradipine-insensitive ICa (ICa-ins) with a right-shifted voltage dependence compared to that in con

55 estingly, Qand SRCa2+ release also displayed right-shifted voltage dependence in fibres expressing EG

56 nserved charge pair mutant D451E exhibited a right-shifted voltage dependence, indicating an increase

57 right of that in placebo-pelleted rats; this right shift was blocked by RVM lidocaine.

58 en ancestral alleles are favored by gBGC and right-shifted when derived alleles are favored by gBGC.

59 was observed with ADP in that the ratio was right-shifted with respect to total [fS1].