ライフサイエンスコーパス: be augmented in

1 The expression of SHIP1 is augmented in 11betaHSD1(-/-) Mphi and contributes to

2 Preexisting rhEBNA-1-specific responses were augmented in 4/12 animals, and new epitopes were re

3 ndicate that functional immune responses can be augmented in a chronic viral infection, and provide r

4 synthesis and secretion of cellular Fn, and is augmented in a dose- and time-dependent manner by pla

5 pocampus and medial prefrontal cortex (mPFC) is augmented in a genetic mouse model of cognitive dysfu

6 for 5 to 7 days, HIV-1-specific cytotoxicity was augmented in a dose-dependent fashion (mean increase

7 IFN-gamma production was augmented in a nonantigen-specific manner by IL-12 i

8 onic acid release and COX2 expression, which were augmented in a Toll-like receptor 2 (TLR2)-dependen

9 d in the ABA-insensitive mutant, abi1-1, but was augmented in abi2-1.

10 mokine, LPS-induced CXC chemokine, and G-CSF were augmented in Adipo(-/-) versus wild-type mice.

11 Neutrophil regeneration was augmented in all cytokine protocols and combined PEG

12 tion of succinate, mitochondrial respiration was augmented in all groups, particularly in moderately-

13 ased locomotor and brief-rearing frequencies were augmented in all groups except trained controls, an

14 MSCs constitutively secrete PGE(2), which is augmented in allogeneic reactions.

15 autologous and allogeneic IgG concentrations were augmented in allograft recipients.

16 r stimulation, the phosphorylation of ERK1/2 was augmented in ALS microglia, and there was a mutual d

17 y, that spinal motor neuron regeneration can be augmented in an adult vertebrate by inhibiting Notch

18 giogenic response to myocardial ischemia can be augmented in animal models by gene transfer with the

19 Total IgE production was augmented in animals repeatedly exposed to A. fumiga

20 TCA3 mRNA levels are augmented in anticryptococcal DTH reactions at the s

21 l single-nephron GFR difference was found to be augmented in aquaporin-1 and Na/H exchanger-3 knockou

22 ases during oxidative stress, NPD1 synthesis is augmented in ARPE-19 cells.

23 vitro PKCdelta-Thr(505) autophosphorylation is augmented in assays performed with Src (which promote

24 We found that exosome production was augmented in asthmatic patients.

25 However, SDF-1alpha expression was augmented in bile ducts and oval cells in retrorsine

26 d during alloimmune response, and that P2X1R is augmented in both allogeneic and syngeneic transplant

27 baroreflex denervation, the increase in RSNA was augmented in both groups (control group more than in

28 Mitochondrial mean velocity and duty cycle were augmented in both anterograde and retrograde direct

29 aPP in human brains and that these complexes are augmented in brains from Alzheimer's cases, our data

30 es that had been engineered to lack Syk, and was augmented in cell lines that stably overexpressed Sy

31 t5 and the stimulation of cell growth by PRL are augmented in cells expressing the PRLR(S349A) mutant

32 cytosis, whereas Rab5-stimulated endocytosis is augmented in cells overexpressing a constitutively in

33 at baseline and after stimulation with cAMP was augmented in cells carrying mutations.

34 However, Ca2+ release was augmented in cells expressing mutant hRyR2 after RyR

35 st, LPA-elicited DNA synthesis and migration were augmented in cells expressing EGFR, EGFR(K721A), or

36 t peptide acylation, the effect of which may be augmented in certain instances with addition of CMCS.

37 RSNA and VE responses to hypoxia were augmented in CHF-sham and abolished in CHF-CBD anim

38 he effect of EPE on peanut SPT sensitization was augmented in children with a history of AD (OR, 1.97

39 The mechanisms by which sympathetic function is augmented in chronic heart failure (CHF) are not well

40 but the ACTH response to dexamethasone would be augmented, in concert with the enhanced cortisol resp

41 ntiation, whereas endothelial NOS expression was augmented in conditions of chronic NOS inhibition du

42 This behavior was augmented in corner flow regions of the flow chamber

43 tocin-induced diabetes, superoxide formation was augmented in coronary media and adventitia because o

44 ersus normal liver specimens, an effect that was augmented in cultured H4IIE cells versus isolated cu

45 icate that IL-1beta-mediated innate immunity is augmented in db/db mice both at the periphery and in

46 oung APP/PS1 or DBH (-/-) single mutant mice were augmented in DBH (-/-)/APP/PS1 double mutant mice.

47 We found that alphaSKA is augmented in DCM compared with healthy controls, 43.1

48 jection of the NO donor diethylamine-NONOate were augmented in eNOS-/- and nNOS-/-, eNOS-/- mice but

49 pathetic stimulation is not reduced, but may be augmented in exercising muscle of healthy older human

50 Accordingly, collagen deposition was augmented in GK rats, which was reversed by atrasent

51 med to determine whether capillary branching was augmented in glomeruli with ARB-induced regression o

52 nd that, like CL biosynthesis, CL remodeling is augmented in growth conditions requiring mitochondria

53 ogenic responsiveness to beta-AR stimulation is augmented in habitually exercising adults.

54 cts on SERCA of reactive oxygen species that are augmented in HC.

55 The plateau and NO-dependent vasodilatation were augmented in HC with arginase inhibition (92+/-2, 6

56 As was the case in the cell lines, p21 mRNA was augmented in heart, lung, liver, and spleen 7 days a

57 aradoxically when filling pressure increases is augmented in HFrEF.

58 Here we found that CRH expression is augmented in hippocampus of middle-aged CES rats, and

59 bsence epilepsy, interictal beta/gamma power is augmented in homozygous stargazer (stg/stg) but not h

60 Further, Nox1, Nox2, and Nox4 protein levels were augmented in human AMs from alcoholic patients comp

61 onal Ca2+ channels in vascular smooth muscle is augmented in hypertension was tested in basilar arter

62 on of Stat5, proliferative responses to IL-2 were augmented in IL-4-cultured cells, and activation of

63 uclear vesicles of strial marginal cells and is augmented in inner hair cells vs. outer hair cells.

64 ch as platelet spreading and clot retraction is augmented in Jam-A-deficient platelets.

65 pulmonary vascular resistance induced by CPB is augmented in lambs with increased pulmonary blood flo

66 inhibition of neutrophil ROS and NETs by Ent was augmented in Lcn2-deficient neutrophils compared wit

67 e that occurs in response to a challenge may be augmented in lesioned rats.

68 tes T-cell homeostasis, and its availability is augmented in lymphopenic hosts.

69 ion of L-arginine (L-Arg) into L-citrulline, was augmented in lysates of MPhis stimulated in the pres

70 -associated growth arrest, as its expression is augmented in many terminally differentiating cells.

71 transcription factor, the activity of which is augmented in many tumour types.

72 imilarly, RD-induced photoreceptor apoptosis was augmented in mice carrying hypomorphic mutations of

73 es have shown that liver expression of G-CSF was augmented in mice challenged by inflammatory stimuli

74 r activity was increased and glycogen levels were augmented in mice and cells after activation of the

75 The TNF-alpha-induced activation of JNK1 is augmented in Miz1-deficient mouse embryonic fibroblas

76 In agreement, we observed that BMP signaling is augmented in models of muscle growth.

77 cell apoptosis, and inflammasome activation were augmented in NLRX1-deficient animals.

78 responses to ozone, a common air pollutant, are augmented in obese individuals.

79 a BMA-specific manner (PPD-driven IFN-gamma was augmented in only two of eight MF individuals and on

80 esized that the CTL response to MART-1 might be augmented in part by T cell encounters with peptides

81 Because CGRP release is augmented in pathophysiological conditions, such as s

82 osartan, acetylcholine-mediated vasodilation was augmented in patients (44+/-5% to 58+/-4% reduction

83 poptosis after exposure to Zn2+ or Cd2+ that was augmented in presence Cr6+, whereas the onset of apo

84 13-dependent lysophosphatidic acid receptors was augmented in R7BP-expressing cells.

85 ation are blunted and P2X-mediated responses are augmented in rats with HF owing to large MIs.

86 agonist D-Ala-Tyr-Gly-NMePhe-Gly-OH (DAMGO) is augmented in rats sustaining dopamine depletions.

87 a stressor (footshock) is CRF dependent and is augmented in rats that self-administered cocaine unde

88 entral pallidum levels of extracellular GABA was augmented in rats extinguished from cocaine self-adm

89 oad-induced increase in RNA pol III activity is augmented in Rb-deficient hearts.

90 that improvements for a remote system could be augmented in reality, with haptic feedback, size redu

91 Consistent with these data, GVHD was augmented in recipients of B7-H3(-/-) Treg-depleted

92 ing and postprandial energy expenditure (EE) is augmented in regularly exercising compared with seden

93 However, Mekk2(-/-) T-cell proliferation was augmented in response to anti-CD3 monoclonal antibod

94 TMEM reactivity in (naive) old mice was augmented in response to polyclonal but not to allog

95 The effect on INS-1 cells was augmented in response to suppression of CACT.

96 -kappaB-regulated genes, cyclin D1 and IL-6, were augmented in response to mechanical strain.

97 Ductus relaxation and cAMP generation were augmented in response to selective EP receptor agon

98 e levels of IFN-gamma, but not IL-2 or IL-4, were augmented in response to viral antigen, and this sp

99 signal-regulated kinase 1/2 phosphorylation are augmented in RSK2 knockout fibroblasts.

100 successful, that the basic visualization has been augmented in several ways to enhance protein viewin

101 ce, 2) vasopressin-triggered Ca2+ transients are augmented in smooth muscle cells from resistance art

102 ation domains in beta-catenin whose function is augmented in specific association with LEF-1.

103 with IkappaB kinase (IKK), and IKK activity is augmented in stable cell lines overexpressing TRE17,

104 L-21 induced STAT1 phosphorylation, and this was augmented in Stat3-deficient CD4(+) T cells.

105 orylation of STAT5 and STAT1, but not STAT4, is augmented in T cells activated into Th1 cells with PH

106 es of activity bout duration and bout number are augmented in TASK-3 mutants well beyond that seen in

107 sLTs evoked by passive cutaneous anaphylaxis was augmented in TG mice.

108 al translocations to the c-myc oncogene also are augmented in the combined absence of Ku70 and ligase

109 ans models and, notably, nuclear TFEB levels are augmented in the livers of mice subjected to dietary

110 Remarkably, these effects are augmented in the NF-kappaB dependent ABC-like subgro

111 to identify specific genes whose expressions are augmented in the SSC-enriched Thy1(+) germ cell frac

112 suggest that this cardiomyocyte turnover can be augmented in the adult mammalian heart by redeploymen

113 itamin D analogs and calcimimetic agents may be augmented in the future by agents that alter the stab

114 s (DCs) phagocytosing killed tumor cells can be augmented in the presence of antitumor monoclonal ant

115 gnaling in the liver so that gluconeogenesis is augmented in the IUGR rat.

116 The dehalogenation ability of wild-type Mb is augmented in the peroxidase-like Mb mutants (F43H/H64

117 ffinity is independent of GTP hydrolysis and is augmented in the presence of BCAAs.

118 KLF6 phosphorylation is augmented in the presence of GSK3beta based on in vit

119 in TFII-I, to the initiation region of HIV-1 is augmented in the presence of Rel p50 and Rel p52 homo

120 D8 T-cell expansion in allogeneic recipients was augmented in the absence of IFN-gamma.

121 This interaction was augmented in the amino- and carboxyl-terminal direct

122 High-gamma activity was augmented in the left temporal/frontal lobe regions,

123 D1s showed GA-binding activity in vitro that was augmented in the presence of GhSLR1a, GhSLR1b, or ri

124 UB cell epithelialization was augmented in the presence of MM cell-derived conditi

125 tion of purified yeast Hsp90 ATPase activity was augmented in the presence of NQO1 and abrogated by 5

126 iac muscle promoters and Myocd_v1's activity was augmented in the presence of the cardiac transcripti

127 ssion of proinflammatory cytokines and IL-10 was augmented in the skin of DC-IL10R(-/-) mice after ha

128 In contrast, interleukin-10 expression was augmented in the TNF-alpha-neutralized mice.

129 ivity and subsequent phosphorylation of STMN were augmented in the absence of JNK activation, indicat

130 lls demonstrated that mucosal Th17 responses were augmented in the absence of T-bet, and we have demo

131 GPR55 levels were augmented in the adipose tissue of obese subjects a

132 f R5 HIV-1 infection, and this up-regulation is augmented in tissues coinfected with R5 HIV-1.

133 ivity was reduced by alcohol in TLR4, but it was augmented in TLR2- plus TLR4-stimulated cells.

134 rotein zero, PMP22, and myelin basic protein is augmented in TrJ nerves.

135 We now show that Lmo2 expression is augmented in tumour endothelium such as mouse thymoma

136 following antigen receptor cross-linking can be augmented in vitro by ligation of cell surface CD22,

137 Human NK cell activity can be augmented in vitro by stimulation with IL-2 or IL-12,

138 ization can be rescued when PI3K/Akt cascade is augmented in vitro or in PIKE(-/-)PTEN(-/-) double-kn

139 KCNQ2/3 channel activity is augmented in vivo by phosphatidylinositol 4,5-bisphos

140 be here that activator binding to a promoter is augmented in vivo by the effects of two other determi

141 Endogenous SA content was augmented in whitefly-infested plants upon Agrobacte

142 Furthermore, NFAT activity could be augmented in wild-type effector T cells by inhibition