ライフサイエンスコーパス: left shift

1 treatment but not subjects with a neutrophil left shift.

2 WT, whereas mutations at position 2456 were left shifted.

3 in current levels exceeding Emax(ACh) and a left-shifted ACh concentration-response relationship.

4 clamp in the two small groups showed both a left shift and a lower maximal response in the NM group

5 peptide positive allosteric ligands produced left-shifts and peptide concentration-response augmentat

6 alpha(1C) + beta(3), the prepulse produced a left shift ( approximately 40 mV) of the activation curv

7 d conductance-voltage relations for mSlo are left-shifted at free Ca(2+) concentrations >or=1 microm.

8 ll differentiation potential was retained in left-shifted band-stage neutrophils but lost in neutroph

9 s from the bone marrow into the circulation (left shift, band forms).

10 In contrast, the Y301A receptor displayed a left-shifted, but overall reduced, chemotaxis response t

11 NA overflow and vasoconstriction for MV were left-shifted compared to MA; (iii) the P2X receptor anta

12 ogenous gonadotropin-releasing hormone and a left-shifted dose-response curve for gonadotropin-releas

13 in deaths (>98%) occurred, but with a large left shift in age of onset among residual deaths.

14 y V445M due to both a slower recovery (10 mV left shift in beta(V)) and an accelerated entry rate (1.

15 singly and in various combinations caused a left shift in Ca(2+) response compared with wild type re

16 Ca(2+), but not Na(+), current and induced a left shift in E(rev).

17 Blood smears revealed thrombocytopenia, a left shift in neutrophils (in some cases degenerating),

18 69 +/- 0.43 mN; P < 0.001) and a significant left shift in PE dosage-response curve.

19 low deactivation was accompanied by a slight left shift in the activation-voltage relationship, slowe

20 pendent P2X(7)R activation as indicated by a left shift in the ATP dose-response relationship.

21 1), resulting in an approximately 2.8 mmol/L left shift in the beta-cell glucose threshold.

22 modulation alters CaV1.3 activity, causing a left shift in the current-voltage relationship and stron

23 ne at doses below K1/2 (the dose causing 50% left shift in the current-voltage relationship) are addi

24 PFTalpha did, however, cause a left shift in the dexamethasone dose response curve by i

25 of eotaxin to cultures resulted in a 40-fold left shift in the dose response to Ag.

26 concentrations of glucocorticoids, due to a left shift in the dose-response curve, and by saturating

27 fect in the absence of PKA but abolished the left shift in the dose-response relation elicited by PKA

28 the presence of PKA, there was a significant left shift in the dose-response relation such that 10(-1

29 In the presence of PKA, there was a left shift in the dose-response relation.

30 .009; units in pu) and peak location, with a left shift in the histogram.

31 r pollution exposures were associated with a left shift in the lower tails of the IFN-gamma and ICAM-

32 However, 24, 25-D3 inhibits the left shift in the peak current-voltage relationship medi

33 However, a left shift in the sensitivity of exocytosis to Ca(2+) wa

34 unction on IKS channel gating by producing a left shift in the voltage dependence of activation.

35 p for glucose-induced [ATP]pm generation was left shifted in alpha-cells compared to beta-cells.

36 in after-hyperpolarization amplitudes and a left-shift in the frequency-current relationships.

37 on was found for the effect of modulation on left-shift in the GABA EC50 value; furthermore, the same

38 gh levels of methemoglobin associated with a left-shift in the oxygen dissociation curve, profound as

39 sus membrane potential (Vm) curves were more left-shifted in cerebral versus cremaster VSMCs as cytop

40 mined by stop flow pressure measurements was left-shifted in NKCC2A-/- compared with wild-type mice,

41 tractions by isoproterenol was significantly left-shifted in the presence of glycine.

42 nt at positive membrane potentials, but also left-shifted its voltage dependence and slowed inactivat

43 CMPI produced a left shift of the ACh concentration-response curve witho

44 A left shift of the diastolic pressure-volume curves witho

45 component feedback loop that causes a stable left shift of the glucose concentration-reactive oxygen

46 focal application of acetylcholine induced a left shift of the input/output curve and persistent firi

47 ing 6 h of passive hyperventilation: (i) the left shift of the VE-PET,CO2 relationship is due to alka

48 nclude high fever, relative bradycardia, and left shift of WBCs.

49 Left shift of white blood cells was more common in Salmo

50 Lateral motion was similarly simulated by left shifting of the raw projection datasets in a return

51 atio) combinations, the inhibitory curve was left-shifted onto that of the more potent variant in the

52 lter sodium channel current density, but did left shift steady-state parameters of activation and ina

53 bition of K(ATP) channel activity (NP(o)) is left-shifted such that the concentration of ATP producin

54 lated the 3alpha:2beta receptor and acted by left shifting the ACh concentration-response relationshi

55 methylscopolamine ([(3)H]NMS) binding to M1, left-shifting the ACh Ki approximately 19-fold at 10 muM

56 of NS1619-like BK openers, Cym04 reversibly left-shifts the half-activation voltage of Slo1 BK chann

57 t GLP-1(9-36)(amide) reverses the persistent left shift, thereby normalizing persistent overproductio

58 Parallel left shifts (versus MI) were observed in pressure-volume

59 The magnitude of the left shift was linearly correlated with intracellular li

60 In addition, the site frequency spectrum is left-shifted when ancestral alleles are favored by gBGC