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1  gene when protein synthesis is inhibited by emetine.
2 by the translation inhibitors anisomycin and emetine.
3 he CTLs with the protein synthesis inhibitor emetine.
4                  In contrast, application of emetine 1 hr after LTP induction at the commissural-asso
5 eatment with the protein synthesis inhibitor emetine (1 microM) totally prevented the expression of g
6 al CSF, 44 +/- 10%; methysergide, 40 +/- 5%; emetine, 35 +/- 9%; and cycloheximide, 57 +/- 29%; all p
7                                              Emetine, a natural isoquinoline alkaloid with broad phar
8                          Bath application of emetine, a protein synthesis inhibitor, blocked eCB-LTD
9 opmentally down-regulated-8, suggesting that emetine accesses a previously undescribed cullin-indepen
10                               Unfortunately, emetine also induces a stress response that results in u
11  of serotonin (5-HT), the local perfusion of emetine, an inhibitor of protein synthesis, or a TAT-AS
12                                 In contrast, emetine, an inhibitor of the ribotoxic stress response,
13                           Also, injection of emetine and 5,6-dichlorobenzimidazole into Aplysia preve
14 eptide, and the protein synthesis inhibitors emetine and anisomycin.
15                  Our data suggest the use of emetine and cephaeline for investigating mechanisms of G
16 dicinal plant Psychotria ipecacuanha such as emetine and cephaeline possess a monoterpenoid-tetrahydr
17 monoterpenoid-isoquinoline alkaloids such as emetine and cephaeline, whose biosynthesis derives from
18 A synthesis, while the other two inhibitors, emetine and cycloheximide, blocked cell cycle progressio
19     An intermediate response was observed to emetine and cycloheximide, weak activators of JNK.
20 R-triggered FasL/Fas killing is inhibited by emetine and cyclosporin A, whereas IL-2-induced FasL/Fas
21                                  We identify emetine and its analog cephaeline as small molecules tha
22 ets also emerged, among them that methadone, emetine and loperamide (Imodium) may antagonize muscarin
23  because 5,6-dichlorobenzimidazole riboside, emetine, and brefeldin A inhibited the increase in Glu u
24           Surprisingly, cycloheximide (CHX), emetine, and verrucarin A were able to induce transcript
25 s method, we identify the bioactive alkaloid emetine as a selective inhibitor of the uncharacterized
26     Using this cell line, we have identified emetine as a specific inhibitor of HIF-2alpha protein st
27 site, Plasmodium falciparum, in complex with emetine at 3.2 A resolution.
28 eased 12-83% of emetine at pH 6.5 and 41-95% emetine at pH 5.5.
29            These prodrugs released 12-83% of emetine at pH 6.5 and 41-95% emetine at pH 5.5.
30 atic properties of the IpeGlu1 revealed that emetine biosynthesis branches off from N-deacetylisoipec
31 considered to be a part of the reactions for emetine biosynthesis, whereas its 1 beta(R)-epimer N-dea
32 hich was supposed to be the intermediate for emetine biosynthesis.
33 L-2-induced FasL/Fas killing is inhibited by emetine, but not by cyclosporin A.
34 cking the translocation of the ribosome with emetine could retain the puromycylated peptide on the ri
35 ine), whereas a protein synthesis inhibitor (emetine) decreased it by only 24%.
36 Experiments using the irreversible inhibitor emetine demonstrated that AKR.H-2(b) cells had to be met
37 itor (GSK2606414) or the translation blocker emetine did not prevent TDP-43 ubiquitylation and insolu
38                                    Moreover, emetine dissolves preformed SGs as it promotes the assem
39 is study examined the mode and energetics of emetine-DNA association.
40 future high-resolution structural studies of emetine-DNA interactions.
41 ated decay is inhibited by cycloheximide and emetine, drugs that stabilize polysomes, but is unaffect
42 lls were treated with cycloheximide (CHX) or emetine, expression levels were restored to those observ
43                             Hygromycin B and emetine failed to elevate ceramide levels or induce apop
44          Transcriptome analysis reveals that emetine globally regulates alternative splicing, includi
45 hibitors, such as anisomycin, cycloheximide, emetine, harringtonine, and puromycin, unlike several tr
46     The N-2' position of the natural product emetine has been derivatized to thiourea, urea, sulfonam
47 ge IC(50) ranging from 0.079 to 10 muM) than emetine (IC(50) ranging from 0.0237 to 0.0329 muM).
48                                              Emetine-induced HIF-2alpha down-regulation was confirmed
49 trand template blocked the time-dependent or emetine-induced instability but did not eliminate aphidi
50              Drugs that stabilize polysomes (emetine) inhibit the assembly of SGs, whereas drugs that
51                      Prolonged cell culture, emetine inhibition of lagging-strand synthesis, or slowi
52                                              Emetine interacts with the E-site of the ribosomal small
53                Selective injection of DRB or emetine into the presynaptic or postsynaptic neuron befo
54                                              Emetine is an anti-protozoan drug used in the treatment
55     In this approach, inhibition of NMD with emetine is complemented with inhibiting NMD by blocking
56 -yohimbenone and a formal synthesis of (+/-)-emetine is described.
57 composed of two copies of the P-gp substrate emetine, linked by tethers of varied composition.
58              An optimum distance between the emetine molecules of approximately 10 A was found to be
59 plication of the protein synthesis inhibitor emetine or cycloheximide 1 hr after MF LTP induction in
60 thysergide) or protein synthesis inhibitors (emetine or cycloheximide) were injected intrathecally in
61                These data support the use of emetine or structurally related compounds as useful lead
62                            Administration of emetine or the RNA synthesis inhibitor actinomycin-D bef
63              Pretreatment with methysergide, emetine, or cycloheximide attenuated or abolished phreni
64 rlay at neutral pH containing 1 microgram of emetine per ml and 20 micrograms of NaF per ml, resulted
65                   Anisomycin, cycloheximide, emetine, puromycin, and puromycin aminonucleoside, a neg
66      Without altering HIF-2alpha mRNA level, emetine rapidly and dramatically down-regulated HIF-2alp
67                                          The emetine-resistant protein, rpS14-EmRR, which contains tw
68 y IpeOMT2 and IpeOMT1 to form cephaeline and emetine, respectively.
69                             NAC treated with emetine retained approximately 40% of their capacity to
70 RNA and protein synthesis, actinomycin D and emetine, stimulate Glut4 translocation and glucose uptak
71  long isoform, which could be ameliorated by emetine, suggesting that the mutation induces nonsense-m
72 otein synthesis inhibitors cycloheximide and emetine to acute rat hippocampal slices have no effect o
73 ast to the pattern of initiation detected in emetine-treated cells, analysis of the short nascent str
74 ear the initiation region (IR) identified in emetine-treated cells.
75 osine phosphorylation and PI3K binding after emetine treatment to raise intracellular amino acids and
76       To overcome this, we have combined the emetine treatment with actinomycin D, which effectively
77 e (DeltaG = -7.13 kcal.mol(-1)), positioning emetine within the DNA minor groove and forming hydrogen
78 emain in the ribosome even in the absence of emetine, yet direct evidence for this has been lacking.