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1 rly in embryogenesis, P1 is silent, while P2 is strongly activated.
2 nless p85-associated PI 3-kinase or p70(s6k) are strongly activated.
3 t at these concentrations, p42/44 MAP kinase was strongly activated.
4 lpha, and several INF-alpha-stimulated genes was strongly activated.
5 -AG production, although both phospholipases were strongly activated.
6 or necrosis factor alpha and interleukin-10, are strongly activated after MPLA stimulation despite we
7 ally of cyclins B1 and B4, whose translation is strongly activated after meiosis I.
8    The c-Jun-N-terminal kinase (JNK) pathway is strongly activated after partial hepatectomy (PH), bu
9                      We show that MAIT cells are strongly activated and represent the major T cell so
10                      Here we show that TRPV3 is strongly activated and sensitized by carvacrol, thymo
11 osed to transient ischaemic insults, calpain was strongly activated, and the AMPAR current density an
12 t, several enzymes involved in fat synthesis were strongly activated, and microvesicular fat accumula
13                   The Kir6.2 + SUR1 currents are strongly activated at pH 5.9-6.5 even in the presenc
14 ivated in prospective neural plate, while it is strongly activated at the neural plate border, a regi
15 h feedback regulation of the light reactions was strongly activated at low light, but returned to wil
16 ost projection neurons, whereas interneurons were strongly activated at a latency preceding that foun
17                           However, when a PN is strongly activated, back-propagating action potential
18 : at low stimulus drift speeds, both domains were strongly activated, but activity fell off in high s
19  that the alpha(1)-receptors of the mouse LC are strongly activated by 6FNE and serve to potently inh
20 howed several temporal cortical regions that are strongly activated by bodies.
21                            Y1073E and Y1073Q are strongly activated by free magnesium to the same ext
22  Nmb neurons are chemoreceptors because they are strongly activated by hypercapnia and express high l
23                    Extrastriate visual areas are strongly activated by image symmetry.
24 d protein modification by ISG15 (ISGylation) are strongly activated by interferon, genotoxic stress,
25 d protein modification by ISG15 (ISGylation) are strongly activated by interferon, genotoxic stress,
26 d protein modification by ISG15 (ISGylation) are strongly activated by interferons.
27                   We find that K(B) channels are strongly activated by MgATP (but not ATP(4)(-)) with
28                     In vivo recorded L-ITCcs are strongly activated by noxious stimuli, such as hindp
29 1 ATPase and chromatin remodeling activities are strongly activated by Parp1 and its substrate NAD an
30 mally respond only to central visual stimuli are strongly activated by peripheral stimuli.
31 hat the USV-suppressing Amg(C/M-PAG) neurons are strongly activated by predator cues or during social
32 ition to being intrinsically photosensitive, are strongly activated by rods and cones, and display a
33 formation, and their hippocampal projections are strongly activated by salient environmental inputs i
34 fibres in the respiratory tract of the mouse are strongly activated by serotonin.
35  to four Escherichia coli genes/operons that are strongly activated by the accumulation of self-produ
36 ed that while somatodendritic K(v)7 channels are strongly activated by the backpropagating action pot
37 olyadenylated nuclear RNA promoter, known to be strongly activated by a viral transactivator, Rta.
38             Twenty-seven genes were found to be strongly activated by CrfA accumulation.
39 Expressed in oocytes, wild-type channels can be strongly activated by either hypotonicity or exposure
40 nation for the observation that the MEKs can be strongly activated by ionizing radiation and only wea
41 tachykinins substance P and neurokinin A) to be strongly activated by LP within the sheep PT.
42 alkylator, N-ethylmaleimide, was observed to be strongly activated by transient external Ca(2+) remov
43 rate that TREK-1 is resistant to hypoxia and is strongly activated by arachidonic acid even at low P(
44  the fibroblast growth factor-4 (FGF-4) gene is strongly activated by B-Myb in HeLa cells and it can
45 at a 0.8-kb fragment of the siamois promoter is strongly activated by beta-catenin.
46                                        bsLSD is strongly activated by cations, particularly potassium
47 sporter: Cl--dependent uptake of 86Rb+ which is strongly activated by cell swelling and weakly sensit
48 ion within the largest intron showed that it is strongly activated by Egr2 expression in reporter ass
49                         The wild-type enzyme is strongly activated by fructose-1,6-bisphosphate and w
50 tiation factor 2 (MD-2) LPS receptor complex is strongly activated by hexa-acylated lipid A and poorl
51                 One glomerulus in particular is strongly activated by human odour but responds weakly
52                  Focal adhesion kinase (FAK) is strongly activated by integrins and growth factors an
53 now shown that the RAF/ERK signaling pathway is strongly activated by ionizing radiation.
54                                  This enzyme is strongly activated by K+ and similar monovalent catio
55                                    The susAC is strongly activated by manganese, but has low activity
56 oter, which contains only a single CArG box, is strongly activated by myocardin.
57 ne kinase with molecular mass 50-60 kDa that is strongly activated by N, N'-dimethylsphingosine and s
58 ngipain Rs, especially the 95-kDa form which is strongly activated by phospholipids, could occur in p
59  that Hoxa-10 expression in the adult uterus is strongly activated by progesterone.
60 oughout the first postnatal week in rats, M1 is strongly activated by self-generated forelimb movemen
61                                         IRP1 is strongly activated by silencing and genetic mutation
62                                           LP is strongly activated by specific sensory signals relaye
63                                     Thus, LS is strongly activated by SPW-Rs and may convey hippocamp
64 mall subset of CD8+ T cells (CD8+CD18bright) is strongly activated by the combination of IL-12 and IL
65            Herein, we demonstrate that DNMT1 is strongly activated by the human polyomavirus BKV larg
66 of the Saccharomyces cerevisiae MT gene CUP1 is strongly activated by the superoxide anion generator
67 at the VEGF promoter of nontransformed cells is strongly activated by the tumor microenvironment poin
68 al peptide, to the FERM domain of talin, and is strongly activated by this interaction.
69                                         MEK6 is strongly activated by UV, anisomycin, and osmotic sho
70 lamic parafascicular nucleus (Pf) in monkeys is strongly activated by vagus nerve afferents.
71 luciferase reporter gene into Jurkat T cells was strongly activated by a combination of human neutrop
72                            We found that JNK was strongly activated by antigen cross-linking in a mou
73                                         CICD was strongly activated by both TNF and lymphotoxin-beta
74                        The cerebellar vermis was strongly activated by capsaicin, whereas light brush
75                      The pgp2/mdr1b promoter was strongly activated by co-transfected wild type Sp1 b
76 U.1 and IRF-1 or with PU.1 and ICSBP, but it was strongly activated by co-transfection with PU.1, IRF
77 r assays revealed that the Ca(V)3.2 promoter was strongly activated by Egr1 overexpression in vitro a
78 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
79                                   While UCP1 was strongly activated by free fatty acids, no stimulato
80             In addition, we found that rPLD2 was strongly activated by Galpha(q)Q209L and phorbol est
81                 On the contrary, Pyk2, which was strongly activated by IGF-I, was critical for IGF-IR
82                    We found that rostral ACC was strongly activated by infrequent threat-related dist
83               We also observed that p38delta was strongly activated by MKK3 and MKK6, while p38alpha
84                           Unexpectedly, Nox3 was strongly activated by NOXO1 in the absence of NOXA1
85                   A 2.3-kb promoter fragment was strongly activated by phenylephrine and endothelin-1
86                     The channels responsible were strongly activated by 10(-7) M Ca(2+), and 10(-6) M
87                              Both phenotypes were strongly activated by arachidonic acid, membrane st
88                               TRPA1 channels were strongly activated by hypochlorite and hydrogen per
89                                These neurons were strongly activated by hypoxia (10-15% O(2); 30 s) o
90  and both type A and type B horizontal cells were strongly activated by KA.
91 paB and AP-1, two transcription factors that were strongly activated by LPA in ovarian cancer cell li
92 their mechanical sensitivity, such that they were strongly activated by mechanical stimuli that initi
93 CeA neurons expressing both MOR and PKCdelta were strongly activated by naltrexone, and selectively i
94                                   XCR1(+) DC were strongly activated by polyinosinic-polycytidylic ac
95 - than in response to L2-infected cells, MdM were strongly activated by serovar L2 infection, indicat
96                           The 13 pS channels were strongly activated by the calmodulin inhibitors cal
97 s regulated by the E2F transcription factors were strongly activated by the IE86 protein.
98   Interestingly, several long noncoding RNAs were strongly activated by this mechanism.
99    In both expert and novice mice, VIP cells were strongly activated by whisker stimuli and goal-dire
100  interneurons (transverse interneurons) that are strongly activated during both fictive flexion refle
101 identify a group of spinal interneurons that are strongly activated during fictive flexion reflex but
102  during sleep, indicating that these neurons are strongly activated during nonREM and/or REM sleep st
103 ic limb motor patterns, although these cells are strongly activated during the ipsilateral hip flexor
104           It is clear that adaptive immunity is strongly activated during asymptomatic infection, but
105 r gene activity driven by the Grp78 promoter is strongly activated during early embryonic heart devel
106               We previously showed that Cdk5 is strongly activated during stress fiber formation and
107 he insula, the middle cingulate cortex (MCC) was strongly activated during both action observation an
108 tudy we showed that the reconstituted K(ATP) was strongly activated during hypercapnia and intracellu
109                          This opioid circuit was strongly activated during sugar consumption, which w
110 rescent protein (GFP) to detect neurons that were strongly activated during associative learning, in
111 port, we have shown that the GADD45 promoter is strongly activated following expression of wild-type
112 12L or alpha qQ209L, although these proteins were strongly activated following expression of constitu
113 ctivated protein kinase kinase (MAPK kinase) are strongly activated in Schwann cells by glial growth
114  normal mice in an age-dependent manner, and is strongly activated in 5XFAD transgenic mouse model an
115                                        STAT3 is strongly activated in cyst-lining epithelial cells in
116 find that TGFbeta/BMP/SMAD pathway signaling is strongly activated in luminal and suprabasal cells of
117     In the present study, we found that mTOR is strongly activated in microglia following excitatory
118                                     PKCtheta is strongly activated in most GISTs and hence may serve,
119                       Similarly, PI 3-kinase is strongly activated in neu, TGFalpha and heregulin/NDF
120                               The FA pathway is strongly activated in response to both agents.
121  pathway for IgE switching in the mouse that is strongly activated in retroviral infection but weakly
122  181 nucleotide long RNA whose transcription is strongly activated in somatic nuclei after their inje
123                The tumor suppressor P19(ARF) is strongly activated in the nerves of these mice and, e
124 he secreted frizzled related protein, Sfrp2, was strongly activated in all Pax2b-expressing cells.
125                        VCAM-1 mRNA formation was strongly activated in animals treated with ET, TNF-a
126 al raphe nucleus serotonergic neurons in cat was strongly activated in association with oral-buccal m
127          Under diabetogenic conditions, MST1 was strongly activated in beta cells in human and mouse
128                            In contrast, RhoA was strongly activated in cells bound to type I collagen
129 sed during reprogramming, the hTERT promoter was strongly activated in class II cells and was further
130 t time, demonstrated that the hTERT promoter was strongly activated in discrete steps, revealing a cr
131 -promoting genes analyzed, TWIST1 expression was strongly activated in response to MMSET.
132  yielded little signal when glycosylated but was strongly activated in the absence of its glycosylati
133 n tomographic scanning, the occipital cortex was strongly activated in the congenitally blind and ear
134                        The Vg-DefA transgene was strongly activated in the fat body by a blood meal.
135              Furthermore, the SPDS2 promoter was strongly activated in the nematode-induced syncytia,
136 signal-regulated protein kinase 1/2 (Erk1/2) were strongly activated in As-transformed p53lowHBECs.
137 iated with defense and programmed cell death were strongly activated, including a suite of 22 PATHOGE
138 gene expression driven by the grp94 promoter was strongly activated not only in spontaneous but also
139  is greatly reduced when the stress response is strongly activated, presumably to ensure maximum acti
140 contrast to WI38, both cSrc and MAPK in VA13 were strongly activated regardless of FGF stimulation or
141               Complement alternative pathway was strongly activated, resulting in the deposition of C
142 ion from G (+*) back onto the A-T base pairs is strongly activated, so charge recombination from G (o
143        If CD4(+)CD25(+high) regulatory cells were strongly activated, they maintained suppressive eff
144  strongly inhibited, whereas Slo2.2 currents are strongly activated through GqPCR stimulation.
145 gly, ISG15 expression and protein ISGylation are strongly activated upon viral and bacterial infectio
146                       This signalling module is strongly activated upon mucosal injury to promote hea
147 dings show that individual neurons in cortex are strongly activated when engaged in appropriate tasks
148  type in the Drosophila visual system (LT52) is strongly activated when flies groom their heads.
149                           In contrast, STAT3 was strongly activated when the cells were treated with
150              Fork-head box class-O 1 (FOXO1) was strongly activated, which was confirmed in vitro and

 
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