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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                           The gating defects left-shifted and increased the window currents, resultin
6 peptide positive allosteric ligands produced left-shifts and peptide concentration-response augmentat
7 alpha(1C) + beta(3), the prepulse produced a left shift ( approximately 40 mV) of the activation curv
8 d conductance-voltage relations for mSlo are left-shifted at free Ca(2+) concentrations >or=1 microm.
9 e was lower in patients than controls, and a left-shifting axis of symmetry was associated with bette
10 ll differentiation potential was retained in left-shifted band-stage neutrophils but lost in neutroph
11 s from the bone marrow into the circulation (left shift, band forms).
12  In contrast, the Y301A receptor displayed a left-shifted, but overall reduced, chemotaxis response t
13 NA overflow and vasoconstriction for MV were left-shifted compared to MA; (iii) the P2X receptor anta
14 ogenous gonadotropin-releasing hormone and a left-shifted dose-response curve for gonadotropin-releas
15 expressed alone with the former exhibiting a left shift in activation midpoint when expressed alone o
16  in deaths (>98%) occurred, but with a large left shift in age of onset among residual deaths.
17 y V445M due to both a slower recovery (10 mV left shift in beta(V)) and an accelerated entry rate (1.
18  singly and in various combinations caused a left shift in Ca(2+) response compared with wild type re
19 Ca(2+), but not Na(+), current and induced a left shift in E(rev).
20    Blood smears revealed thrombocytopenia, a left shift in neutrophils (in some cases degenerating),
21 69 +/- 0.43 mN; P < 0.001) and a significant left shift in PE dosage-response curve.
22 ons containing T226M conductance displayed a left shift in rheobase relative to control.
23 low deactivation was accompanied by a slight left shift in the activation-voltage relationship, slowe
24 pendent P2X(7)R activation as indicated by a left shift in the ATP dose-response relationship.
25 1), resulting in an approximately 2.8 mmol/L left shift in the beta-cell glucose threshold.
26 modulation alters CaV1.3 activity, causing a left shift in the current-voltage relationship and stron
27 ne at doses below K1/2 (the dose causing 50% left shift in the current-voltage relationship) are addi
28               PFTalpha did, however, cause a left shift in the dexamethasone dose response curve by i
29 of eotaxin to cultures resulted in a 40-fold left shift in the dose response to Ag.
30  concentrations of glucocorticoids, due to a left shift in the dose-response curve, and by saturating
31 fect in the absence of PKA but abolished the left shift in the dose-response relation elicited by PKA
32 the presence of PKA, there was a significant left shift in the dose-response relation such that 10(-1
33          In the presence of PKA, there was a left shift in the dose-response relation.
34 .009; units in pu) and peak location, with a left shift in the histogram.
35 r pollution exposures were associated with a left shift in the lower tails of the IFN-gamma and ICAM-
36  the progesterone trajectory showed that its left shift in the luteal phase (e.g., earlier rise in pr
37              However, 24, 25-D3 inhibits the left shift in the peak current-voltage relationship medi
38                                   However, a left shift in the sensitivity of exocytosis to Ca(2+) wa
39 unction on IKS channel gating by producing a left shift in the voltage dependence of activation.
40 its by attenuating the beta1-subunit-induced left shift in the voltage for half-maximal activation.
41 p for glucose-induced [ATP]pm generation was left shifted in alpha-cells compared to beta-cells.
42  values, with only few exceptions of overall left shifts in distribution.
43  A similar depolarized resting potential and left-shift in rheobase was observed for CA1 hippocampal
44  in after-hyperpolarization amplitudes and a left-shift in the frequency-current relationships.
45 on was found for the effect of modulation on left-shift in the GABA EC50 value; furthermore, the same
46 gh levels of methemoglobin associated with a left-shift in the oxygen dissociation curve, profound as
47 sus membrane potential (Vm) curves were more left-shifted in cerebral versus cremaster VSMCs as cytop
48 mined by stop flow pressure measurements was left-shifted in NKCC2A-/- compared with wild-type mice,
49 tractions by isoproterenol was significantly left-shifted in the presence of glycine.
50 nt at positive membrane potentials, but also left-shifted its voltage dependence and slowed inactivat
51                              CMPI produced a left shift of the ACh concentration-response curve witho
52                                            A left shift of the diastolic pressure-volume curves witho
53 ; yet, gamma-2 causes a much more pronounced left shift of the dose-response relationship by increasi
54 component feedback loop that causes a stable left shift of the glucose concentration-reactive oxygen
55 focal application of acetylcholine induced a left shift of the input/output curve and persistent firi
56 ing 6 h of passive hyperventilation: (i) the left shift of the VE-PET,CO2 relationship is due to alka
57 nclude high fever, relative bradycardia, and left shift of WBCs.
58                                              Left shift of white blood cells was more common in Salmo
59    Lateral motion was similarly simulated by left shifting of the raw projection datasets in a return
60 atio) combinations, the inhibitory curve was left-shifted onto that of the more potent variant in the
61 lter sodium channel current density, but did left shift steady-state parameters of activation and ina
62 bition of K(ATP) channel activity (NP(o)) is left-shifted such that the concentration of ATP producin
63 ncreased the Ca(2+) sensitivity of force and left shifted the I(11)/I(10)-pCa relationship, indicatin
64 lated the 3alpha:2beta receptor and acted by left shifting the ACh concentration-response relationshi
65 ar saline, lowered the current amplitude and left-shifted the reversal potential, consistent with a n
66 methylscopolamine ([(3)H]NMS) binding to M1, left-shifting the ACh Ki approximately 19-fold at 10 muM
67  of NS1619-like BK openers, Cym04 reversibly left-shifts the half-activation voltage of Slo1 BK chann
68 t GLP-1(9-36)(amide) reverses the persistent left shift, thereby normalizing persistent overproductio
69                                     Parallel left shifts (versus MI) were observed in pressure-volume
70 mbrane BK(Ca) when associated with BK-beta1 (left-shifted voltage dependence of activation, V(1/2) =
71 cs resembling those of rat Ca(V)1.2 but with left-shifted voltage sensitivity for activation and inac
72                         The magnitude of the left shift was linearly correlated with intracellular li
73  In addition, the site frequency spectrum is left-shifted when ancestral alleles are favored by gBGC
74 mitment and found that SDS hematopoiesis was left-shifted with selective loss of granulocyte-monocyte