ライフサイエンスコーパス: be strongly activated

1 nless p85-associated PI 3-kinase or p70(s6k) are strongly activated.

2 lpha, and several INF-alpha-stimulated genes was strongly activated.

3 t at these concentrations, p42/44 MAP kinase was strongly activated.

4 -AG production, although both phospholipases were strongly activated.

5 or necrosis factor alpha and interleukin-10, are strongly activated after MPLA stimulation despite we

6 ally of cyclins B1 and B4, whose translation is strongly activated after meiosis I.

7 The c-Jun-N-terminal kinase (JNK) pathway is strongly activated after partial hepatectomy (PH), bu

8 Here we show that TRPV3 is strongly activated and sensitized by carvacrol, thymo

9 osed to transient ischaemic insults, calpain was strongly activated, and the AMPAR current density an

10 t, several enzymes involved in fat synthesis were strongly activated, and microvesicular fat accumula

11 The Kir6.2 + SUR1 currents are strongly activated at pH 5.9-6.5 even in the presenc

12 ivated in prospective neural plate, while it is strongly activated at the neural plate border, a regi

13 h feedback regulation of the light reactions was strongly activated at low light, but returned to wil

14 However, when a PN is strongly activated, back-propagating action potential

15 : at low stimulus drift speeds, both domains were strongly activated, but activity fell off in high s

16 that the alpha(1)-receptors of the mouse LC are strongly activated by 6FNE and serve to potently inh

17 Y1073E and Y1073Q are strongly activated by free magnesium to the same ext

18 Nmb neurons are chemoreceptors because they are strongly activated by hypercapnia and express high l

19 d protein modification by ISG15 (ISGylation) are strongly activated by interferon, genotoxic stress,

20 d protein modification by ISG15 (ISGylation) are strongly activated by interferon, genotoxic stress,

21 d protein modification by ISG15 (ISGylation) are strongly activated by interferons.

22 We find that K(B) channels are strongly activated by MgATP (but not ATP(4)(-)) with

23 In vivo recorded L-ITCcs are strongly activated by noxious stimuli, such as hindp

24 1 ATPase and chromatin remodeling activities are strongly activated by Parp1 and its substrate NAD an

25 mally respond only to central visual stimuli are strongly activated by peripheral stimuli.

26 ition to being intrinsically photosensitive, are strongly activated by rods and cones, and display a

27 fibres in the respiratory tract of the mouse are strongly activated by serotonin.

28 to four Escherichia coli genes/operons that are strongly activated by the accumulation of self-produ

29 ed that while somatodendritic K(v)7 channels are strongly activated by the backpropagating action pot

30 olyadenylated nuclear RNA promoter, known to be strongly activated by a viral transactivator, Rta.

31 Twenty-seven genes were found to be strongly activated by CrfA accumulation.

32 Expressed in oocytes, wild-type channels can be strongly activated by either hypotonicity or exposure

33 nation for the observation that the MEKs can be strongly activated by ionizing radiation and only wea

34 tachykinins substance P and neurokinin A) to be strongly activated by LP within the sheep PT.

35 alkylator, N-ethylmaleimide, was observed to be strongly activated by transient external Ca(2+) remov

36 rate that TREK-1 is resistant to hypoxia and is strongly activated by arachidonic acid even at low P(

37 the fibroblast growth factor-4 (FGF-4) gene is strongly activated by B-Myb in HeLa cells and it can

38 at a 0.8-kb fragment of the siamois promoter is strongly activated by beta-catenin.

39 bsLSD is strongly activated by cations, particularly potassium

40 sporter: Cl--dependent uptake of 86Rb+ which is strongly activated by cell swelling and weakly sensit

41 ion within the largest intron showed that it is strongly activated by Egr2 expression in reporter ass

42 The wild-type enzyme is strongly activated by fructose-1,6-bisphosphate and w

43 tiation factor 2 (MD-2) LPS receptor complex is strongly activated by hexa-acylated lipid A and poorl

44 Focal adhesion kinase (FAK) is strongly activated by integrins and growth factors an

45 now shown that the RAF/ERK signaling pathway is strongly activated by ionizing radiation.

46 This enzyme is strongly activated by K+ and similar monovalent catio

47 The susAC is strongly activated by manganese, but has low activity

48 oter, which contains only a single CArG box, is strongly activated by myocardin.

49 ne kinase with molecular mass 50-60 kDa that is strongly activated by N, N'-dimethylsphingosine and s

50 ngipain Rs, especially the 95-kDa form which is strongly activated by phospholipids, could occur in p

51 that Hoxa-10 expression in the adult uterus is strongly activated by progesterone.

52 IRP1 is strongly activated by silencing and genetic mutation

53 mall subset of CD8+ T cells (CD8+CD18bright) is strongly activated by the combination of IL-12 and IL

54 Herein, we demonstrate that DNMT1 is strongly activated by the human polyomavirus BKV larg

55 of the Saccharomyces cerevisiae MT gene CUP1 is strongly activated by the superoxide anion generator

56 at the VEGF promoter of nontransformed cells is strongly activated by the tumor microenvironment poin

57 al peptide, to the FERM domain of talin, and is strongly activated by this interaction.

58 MEK6 is strongly activated by UV, anisomycin, and osmotic sho

59 lamic parafascicular nucleus (Pf) in monkeys is strongly activated by vagus nerve afferents.

60 luciferase reporter gene into Jurkat T cells was strongly activated by a combination of human neutrop

61 We found that JNK was strongly activated by antigen cross-linking in a mou

62 CICD was strongly activated by both TNF and lymphotoxin-beta

63 The cerebellar vermis was strongly activated by capsaicin, whereas light brush

64 The pgp2/mdr1b promoter was strongly activated by co-transfected wild type Sp1 b

65 U.1 and IRF-1 or with PU.1 and ICSBP, but it was strongly activated by co-transfection with PU.1, IRF

66 r assays revealed that the Ca(V)3.2 promoter was strongly activated by Egr1 overexpression in vitro a

67 M H(2)O(2) but not by 8 micro M H(2)O(2) and was strongly activated by either t-buOOH or, in a contro

68 While UCP1 was strongly activated by free fatty acids, no stimulato

69 In addition, we found that rPLD2 was strongly activated by Galpha(q)Q209L and phorbol est

70 On the contrary, Pyk2, which was strongly activated by IGF-I, was critical for IGF-IR

71 We found that rostral ACC was strongly activated by infrequent threat-related dist

72 We also observed that p38delta was strongly activated by MKK3 and MKK6, while p38alpha

73 Unexpectedly, Nox3 was strongly activated by NOXO1 in the absence of NOXA1

74 A 2.3-kb promoter fragment was strongly activated by phenylephrine and endothelin-1

75 The channels responsible were strongly activated by 10(-7) M Ca(2+), and 10(-6) M

76 Both phenotypes were strongly activated by arachidonic acid, membrane st

77 TRPA1 channels were strongly activated by hypochlorite and hydrogen per

78 These neurons were strongly activated by hypoxia (10-15% O(2); 30 s) o

79 and both type A and type B horizontal cells were strongly activated by KA.

80 paB and AP-1, two transcription factors that were strongly activated by LPA in ovarian cancer cell li

81 their mechanical sensitivity, such that they were strongly activated by mechanical stimuli that initi

82 XCR1(+) DC were strongly activated by polyinosinic-polycytidylic ac

83 - than in response to L2-infected cells, MdM were strongly activated by serovar L2 infection, indicat

84 The 13 pS channels were strongly activated by the calmodulin inhibitors cal

85 s regulated by the E2F transcription factors were strongly activated by the IE86 protein.

86 Interestingly, several long noncoding RNAs were strongly activated by this mechanism.

87 interneurons (transverse interneurons) that are strongly activated during both fictive flexion refle

88 identify a group of spinal interneurons that are strongly activated during fictive flexion reflex but

89 during sleep, indicating that these neurons are strongly activated during nonREM and/or REM sleep st

90 ic limb motor patterns, although these cells are strongly activated during the ipsilateral hip flexor

91 r gene activity driven by the Grp78 promoter is strongly activated during early embryonic heart devel

92 We previously showed that Cdk5 is strongly activated during stress fiber formation and

93 tudy we showed that the reconstituted K(ATP) was strongly activated during hypercapnia and intracellu

94 rescent protein (GFP) to detect neurons that were strongly activated during associative learning, in

95 port, we have shown that the GADD45 promoter is strongly activated following expression of wild-type

96 12L or alpha qQ209L, although these proteins were strongly activated following expression of constitu

97 ctivated protein kinase kinase (MAPK kinase) are strongly activated in Schwann cells by glial growth

98 normal mice in an age-dependent manner, and is strongly activated in 5XFAD transgenic mouse model an

99 STAT3 is strongly activated in cyst-lining epithelial cells in

100 find that TGFbeta/BMP/SMAD pathway signaling is strongly activated in luminal and suprabasal cells of

101 PKCtheta is strongly activated in most GISTs and hence may serve,

102 Similarly, PI 3-kinase is strongly activated in neu, TGFalpha and heregulin/NDF

103 The FA pathway is strongly activated in response to both agents.

104 pathway for IgE switching in the mouse that is strongly activated in retroviral infection but weakly

105 181 nucleotide long RNA whose transcription is strongly activated in somatic nuclei after their inje

106 The tumor suppressor P19(ARF) is strongly activated in the nerves of these mice and, e

107 he secreted frizzled related protein, Sfrp2, was strongly activated in all Pax2b-expressing cells.

108 VCAM-1 mRNA formation was strongly activated in animals treated with ET, TNF-a

109 al raphe nucleus serotonergic neurons in cat was strongly activated in association with oral-buccal m

110 Under diabetogenic conditions, MST1 was strongly activated in beta cells in human and mouse

111 In contrast, RhoA was strongly activated in cells bound to type I collagen

112 sed during reprogramming, the hTERT promoter was strongly activated in class II cells and was further

113 t time, demonstrated that the hTERT promoter was strongly activated in discrete steps, revealing a cr

114 -promoting genes analyzed, TWIST1 expression was strongly activated in response to MMSET.

115 yielded little signal when glycosylated but was strongly activated in the absence of its glycosylati

116 n tomographic scanning, the occipital cortex was strongly activated in the congenitally blind and ear

117 The Vg-DefA transgene was strongly activated in the fat body by a blood meal.

118 Furthermore, the SPDS2 promoter was strongly activated in the nematode-induced syncytia,

119 signal-regulated protein kinase 1/2 (Erk1/2) were strongly activated in As-transformed p53lowHBECs.

120 gene expression driven by the grp94 promoter was strongly activated not only in spontaneous but also

121 is greatly reduced when the stress response is strongly activated, presumably to ensure maximum acti

122 contrast to WI38, both cSrc and MAPK in VA13 were strongly activated regardless of FGF stimulation or

123 Complement alternative pathway was strongly activated, resulting in the deposition of C

124 ion from G (+*) back onto the A-T base pairs is strongly activated, so charge recombination from G (o

125 If CD4(+)CD25(+high) regulatory cells were strongly activated, they maintained suppressive eff

126 strongly inhibited, whereas Slo2.2 currents are strongly activated through GqPCR stimulation.

127 gly, ISG15 expression and protein ISGylation are strongly activated upon viral and bacterial infectio

128 This signalling module is strongly activated upon mucosal injury to promote hea

129 dings show that individual neurons in cortex are strongly activated when engaged in appropriate tasks

130 In contrast, STAT3 was strongly activated when the cells were treated with

131 Fork-head box class-O 1 (FOXO1) was strongly activated, which was confirmed in vitro and