ライフサイエンスコーパス: be activated with

1 (FI)Ti(CH2SiMe3)2Me can be activated with 1 equiv of B(C6F5)3 at room temperatur

2 Paratyphi A O-specific polysaccharide (O-SP) was activated with 1-cyano-4-dimethylaminopyridinium tet

3 tide proved more potent when the lymphocytes were activated with 1 mM MnCl2; half-maximal inhibition

4 The CPs were activated with 1-cyano-4-dimethylaminopyridinium te

5 Cells were activated with 10 ng/ml LPS for various times where

6 When endothelial cells were activated with 100 units/ml of TNFalpha, neutrophil

7 lladium(0) dibenzylideneacetone (Pd(dba)(2)) is activated with 2-(di-tert-butylphosphino)biphenyl (Bu

8 Signaling was activated with 2-Amino-4-(3,4-(methylenedioxy)benzyl

9 When endothelial cells were activated with 2 units/ml of TNFalpha, the majority

10 The PMN were activated with 200 microg/ml of normal IgG or ANCA.

11 In addition, when platelets were activated with 2MeSADP under stirring conditions, a

12 a panel of synthetic GEF constructs that can be activated with a competitive ligand.

13 GNPs, such as sphere, shell or rod) that can be activated with a laser "switch".

14 sts and human adipose fibroblasts, which can be activated with a mixture of hormones to differentiate

15 e hydrolyzed by a stronger base but will not be activated with a weaker one.

16 ) epithelially expressed TGF-beta(1) may not be activated, with a consequent absence of expression of

17 rmationally distinct, low affinity state and is activated with a approximately 100-fold increase in a

18 flects a DNA damage checkpoint response that is activated with a direct contribution from dysfunction

19 ion of CFTR, and further inhibited when CFTR was activated with a cAMP-raising mixture (CKT).

20 ffect, and PLC activity in myocyte membranes was activated with a similar Ca2+ dependence.

21 When Prss31-null MCs were activated with a calcium ionophore or by their high

22 The radical reactions were activated with a readily available household compac

23 GIRK1/GIRK4 channels were activated with a similar efficacy by PtdIns(3,4)P(2

24 on of Pod1 and WT1, but not Tbx18 or NFATC1, is activated with all-trans-retinoic acid (RA) treatment

25 In contrast, when glycosidase-treated FV was activated with alpha-thrombin, the addition of the r

26 (UAG) codon with a suppressor tRNA that had been activated with (aminooxy)acetic acid.

27 On the other hand, phagocytic cells that are activated with an analogue of LPS that does not indu

28 When peritoneal macrophages are activated with an inflammatory stimulus (polymerized

29 , Pilrb(-/-) mice or mice in which PILRalpha was activated with an agonistic antibody showed improved

30 in a resting state or when alpha(IIb)beta(3) was activated with anti-LIBS6.

31 CD28- clones that were activated with anti-CD3 alone were not anergic to r

32 When peripheral T cells were activated with anti-CD3 and anti-CD28 Abs precoated

33 TDLN cells were activated with anti-CD3/anti-CD28 monoclonal antibo

34 cells to mature APCs or when endogenous APCs were activated with anti-CD40 Ab.

35 n tonsillar human B cell subpopulations that were activated with anti-IgM and anti-CD40 in the presen

36 the inner chamber produced ET-1 when T cells were activated with antigen or anti-CD3 antibody in the

37 ries indicated that a generic wound response is activated with any injury regardless of the regenerat

38 aising perfusion pressure and chemoreceptors were activated with aortic injections of sodium cyanide

39 and increased IFN-gamma expression when DCs were activated with AP.

40 cultured alveolar and peritoneal macrophages were activated with bacterial lipopolysaccharide in the

41 is substantially increased when calcineurin is activated with calmodulin and calcium.

42 Peripheral blood CD3+ lymphocytes were activated with CD3/CD28 beads and costimulated with

43 monocytes, primed with IFN-gamma and GM-CSF, were activated with CD40 ligand (CD40L) or TNF-alpha and

44 accharomyces cerevisiae, replication origins are activated with characteristic timing during S phase.

45 amage response (DDR) cell signalling network is activated, with checkpoint kinase 1 (Chk1) activation

46 ative- and Ag85B-specific CD4(+) T cells had been activated with coinfected DCs compared to Mtb-infec

47 MSCs were activated with concanavalin A (ConA), a Toll-like r

48 To explore this process, pDCs were activated with CpG oligodeoxyribonucleotides, which

49 The detoxified polysaccharides were activated with cyanogen bromide (CNBr) or with 1-cy

50 n a cell is determined by the number of NLRs being activated, with each NLR initiating its own inflam

51 positive IgG over endothelial cells that had been activated with either 2 units/ml or 100 units/ml of

52 s expression, four areas of the gerbil brain are activated with ejaculation, i.e., the posterodorsal

53 ary microvascular endothelial cells (HMVECs) were activated with endotoxin or buffer, HNA-3a+ or HNA-

54 When the Erk pathway is activated with epidermal growth factor, the concentra

55 estrogen receptor (DeltaRaf-1:ER), which can be activated with estradiol.

56 They can be activated with excess AlCl3 to form cationic olefin m

57 of factor IX binding, the chimeric proteins were activated with factor XIIa and tested for their cap

58 r not treated with JNK inhibitor (SP600125), were activated with FGF-2/heparin sulfate (HS) or TGF-be

59 surface-engineered such that the electrodes were activated with fibronectin to mediate cell attachme

60 cells from volunteers expressing HLA-B*57:01 are activated with flucloxacillin when dendritic cells p

61 Neutrophils were activated with fMLP, normal IgG, or ANCA IgG.

62 G proteins in an extract of brain membranes were activated with GDP and AlF4- and deactivated in the

63 When PMNLs were activated with granulocyte macrophage-colony-stimul

64 Mitogen-activated protein (MAP) kinases are activated with great specificity by MAP/ERK kinases

65 Cs, respectively), provided the latter cells are activated with growth factors.

66 its remained bound to the membrane when they were activated with guanosine 5'-(3-O-thio)triphosphate

67 When murine gastric macrophages were activated with H. pylori, supraphysiologic levels o

68 cam, cyt P40 1A2, and myoglobin in the array were activated with H2O2 to metabolize BP to genotoxic m

69 Ca2+ stimulation was also observed when sAC was activated with HCO3-, was independent of calmodulin,

70 nsient receptor potential (TRP) ion channels are activated with high sensitivity by either cold or ho

71 in common with other group III mGluR that it is activated with higher potency and efficacy by L-SOP.

72 This process was amplified when cells were activated with hydrogen peroxide.

73 is was able to replicate in macrophages that were activated with IFN-gamma after infection (postactiv

74 replicate in primary murine macrophages that were activated with IFN-gamma.

75 ondrial oxidative phosphorylation when cells were activated with IL-12 plus IL-18.

76 /-) cells was unaffected when effector cells were activated with IL-12, and thyroids expressed predom

77 onor IFN-gamma(+/+) and IFN-gamma(-/-) cells were activated with IL-12.

78 ion, RA synovial fibroblasts and macrophages were activated with IL-17 and examined for the expressio

79 s (PLHV) are common porcine viruses that may be activated with immunosuppression for xenotransplantat

80 g acute SIV infection, circulating platelets were activated with increased surface expression of P-se

81 is not regulated by FBP, but the other LDHs are activated with increasing sensitivity in the followi

82 In contrast, p70(S6K) was activated with increasing glucose concentration (bet

83 Although vascular endothelium can be activated with inflammatory cytokines to express func

84 cultures of human mucosal mesenchymal cells were activated with interleukin (IL)-1 beta, IL-6, and t

85 Clonal populations of uNK cells were activated with interleukin-12 (IL-12) and IL-15, an

86 LPTs were activated with interleukin-2 or via CD3, CD2, and C

87 Accordingly, recipient T cells were activated with intravenous (IV) injections of 10(6)

88 initiation of Na(+)-glucose cotransport, Akt is activated with kinetics that parallel those of ezrin

89 In vivo, this pathway may be activated with larger rectal distensions, leading to

90 If lymphocytes alone were activated with lectins and their supernatants added

91 n specific groups of neurons, which can then be activated with light - has only been around for six y

92 This work shows that existing membranes can be activated with lipidated coiled coil forming peptides

93 RAW264.7 (or primary peritoneal macrophages) was activated with lipopolysaccharide in the absence or

94 In other slices, synapses were activated with low-frequency control stimulation or

95 3 beta) to cultures of human PBMCs that have been activated with LPS or PHA results in a significant

96 Cultured microglia were activated with LPS and then incubated at 33 or 37 d

97 When the human mu transgenic spleen cells were activated with LPS before transfer, they no longer

98 Neurons, heat-sensitized by expressing TRPV1 are activated with magnetic field application.

99 rojecting to the medial SDA, PdPN, and MeApd were activated with mating.

100 s are inactive at low temperatures, they can be activated with microwave irradiation.

101 us studies have shown that the cloned Kir6.2 is activated with mild acidification but inhibited with

102 n in the presence of Ca2+: when the receptor was activated with monoclonal antibody (8A2) or when the

103 e severe granulomatous EAT when spleen cells were activated with MTg and anti-IL-2R mAb in the presen

104 Cells were activated with N-formyl-Met-Leu-Phe, and the temper

105 itu silylated nucleobase, thioglycosides can be activated with NIS/HOTf to give nucleosides in high y

106 istent with the conclusion that PARP and p53 are activated with nonoverlapping kinetics during apopto

107 alpha-Adrenergic receptors were activated with noradrenaline (NA) after blocking be

108 cted in the medium when 10(6) neutrophils/ml were activated with opsonized zymosan (OZ), more than 50

109 d cytotoxicity to >90% only when neutrophils were activated with OZ due in part to inhibition of myel

110 ther, these findings suggest that granzyme C is activated with persistent antigenic stimulation, prov

111 ed by polymorphonuclear leukocytes that have been activated with phorbol-12-myristate 13-acetate or r

112 leven unsystematically selected blood donors were activated with phorbol ester and recombinant interl

113 tes and the chondrosarcoma cell line SW-1353 were activated with poly(I-C) of different molecular wei

114 and non-alpha7 subunit-containing nAChRs and were activated with pressure applications of acetylcholi

115 Each extracted drive was activated with pulses at a single time scale or comm

116 ion of the OX(1) sensor demonstrated that it was activated with rank order of potency orexin A > orex

117 teric constraints, allowing the potential to be activated with receptor engagement.

118 Factor X was activated with Russell's viper venom factor X activa

119 ake of MKK was enhanced when quiescent cells were activated with serum-phorbol 12-myristate 13-acetat

120 ay is present in cultured hRPE cells and can be activated with sFasL or by upregulation of FasL and F

121 The data indicate that the P2Y2 receptor is activated with similar potencies by ATP and UTP but n

122 Thirty-nine CD4+ clones were activated with SMX-NO and found to proliferate and

123 The appropriate tertiary benzylic alcohols are activated with SOCl(2) or concentrated HCl and then

124 der typical microscopic illumination but can be activated with stronger pulses of UV light.

125 However, regenerative NMDA conductances can be activated with stronger stimulation.

126 vating transcription factor 6, and eIF2alpha were activated with subsequent overexpression of CCAAT/e

127 Our simulations predict that when EGFR is activated with TGF-alpha, receptor activation is bias

128 s within an individual's repertoire that can be activated with the beta-lactam hapten and/or an imbal

129 Substituted pyridines can also be activated, with the rates of C-H activation depending

130 ce of human platelets before and after their being activated with the thrombin receptor agonist pepti

131 Bone morphogenetic protein (BMP) signaling was activated with the ectopic chondrogenic cells and ch

132 IML and medial gray of T13-L2, respectively, was activated with the UG reflex.

133 ammalian target of rapamycin (mTOR) pathways were activated with the addition of SiNPs.

134 -76(-/-)) or heterozygous (SLP-76(+/-)) mice were activated with the GPVI agonist convulxin, and surf

135 The suppressor tRNAs were activated with the unnatural aspartic acid analogue

136 rted to develop when presensitized CD4 cells were activated with their target Ag during polarization

137 lly related bis(pinacolato)diboron could not be activated with this fluoride methodology.

138 s, monocytes, and monocytoid dendritic cells were activated with TLR-4, TLR-7, and TLR-8 agonists.

139 microvascular endothelial cells (BMVEC) that are activated with TNF-alpha, IL-1beta, or recombinant e

140 Recombinant human neutrophil procollagenase was activated with trypsin or APMA.

141 to human aortic endothelial cells, which had been activated with tumor necrosis factor-alpha to up-re

142 et microvascular endothelial cell monolayers were activated with tumor necrosis factor-alpha (TNF-alp

143 n endothelial cell (HUVEC) monolayers, which were activated with tumor necrosis factor-alpha.

144 rotection, antigen immunomodulatory pathways were activated with upregulation of STAT1 and CASP3 and

145 Because caspase-8 was activated with UV treatment alone, we believe that U

146 Platelets are activated with various agonists that allow them to a