ライフサイエンスコーパス: right shift

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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