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1 smaller effect on nrd expression during DNA synthesis inhibition.
2 ry were similar to those produced by protein synthesis inhibition.
3 partial agonist activity as measured by DNA synthesis inhibition.
4 hormones, developmental signals, and protein synthesis inhibition.
5 observed appeared to be a consequence of DNA synthesis inhibition.
6 and hypertension in response to nitric oxide synthesis inhibition.
7 nvolved recovery from stress-induced protein synthesis inhibition.
8 uggest the presence of ER stress and protein synthesis inhibition.
9 cludes eIF2alpha phosphorylation and protein synthesis inhibition.
10 it down recapitulates the effects of protein synthesis inhibition.
11 nous mRNAs, leading to a strong host protein synthesis inhibition.
12 cell monolayers from ricin-mediated protein synthesis inhibition.
13 synthesis without an effect on host protein synthesis inhibition.
14 e from mechanisms unrelated to prostaglandin synthesis inhibition.
15 M breakdown, were ruled out as causes of RNA synthesis inhibition.
16 gardless of MHV-induced general host protein synthesis inhibition.
17 -6, during virus-induced severe host protein synthesis inhibition.
18 ring sustained hyperemia is unaffected by NO synthesis inhibition.
19 lcholine were not attenuated by nitric oxide synthesis inhibition.
20 of exercise, and this was not changed by NO synthesis inhibition.
21 induced COX-2 independently of prostaglandin synthesis inhibition.
22 use of blockers of ET-1 receptors and by NO synthesis inhibition.
23 duction of calreticulin mRNA resists protein synthesis inhibition.
24 culture and that did not increase during DNA synthesis inhibition.
28 ng hypothermia as the only cause for protein synthesis inhibition (active, 0.47 +/- 0.08 pmol/mg prot
29 e mature protein) that had identical protein synthesis inhibition activity as compared to native BD1.
32 sor and renal vasoconstrictor response to NO synthesis inhibition, although the natriuretic response
34 ypoxic ROS and contributed to global protein synthesis inhibition and adaptive ATF4-mediated gene exp
39 de the first evidence that placental protein synthesis inhibition and endoplasmic reticulum (ER) stre
40 lular pH and calcium manipulation on protein synthesis inhibition and energy failure due to anoxia/ag
41 olar macrophages with endogenous leukotriene synthesis inhibition and enhance this process in leukotr
42 factor alpha (TNF-alpha), the ability of RNA synthesis inhibition and NF-kappaB inactivation to sensi
43 summarize recent findings about triglyceride synthesis inhibition and prevention of progressive disea
44 ases the apoptotic threshold through protein synthesis inhibition and simultaneous production of cera
45 lls from forodesine-induced RNA- and protein-synthesis inhibition and stabilized and increased Mcl-1
46 ecifically discuss their role in the protein synthesis inhibition and the intrinsic pathway of apopto
47 minals show decreased sensitivity to protein synthesis inhibition, and resistance coincides with a de
48 ells in nude mice treated with C75 showed FA synthesis inhibition, apoptosis, and inhibition of tumor
50 on was correlated with the degree of protein synthesis inhibition as measured by autoradiography and
51 competed by an excess of IL-13 in a protein synthesis inhibition assay and confirmed by a clonogenic
52 neck cancer cells, as determined by protein synthesis inhibition assay and confirmed by clonogenic a
58 tein genes occurs in a background of protein synthesis inhibition, but in the course of diapause, a s
60 proposed model for the mechanism of protein synthesis inhibition by aminoglycosides that invokes a d
63 ion by bisindolylmaleimide (BIM) and protein synthesis inhibition by cycloheximide (CX) on basal and
64 DF is selectively inactivated during protein synthesis inhibition by cycloheximide and at a late stag
67 ic pathway activity and the magnitude of DNA synthesis inhibition by FAS inhibitors are increased in
71 (-5) mol/L) was measured before and after NO synthesis inhibition by nitro-L-arginine (LNA, 10(-4) mo
76 ts into the mode of action, drug uptake, DNA synthesis inhibition, cell cycle effects, and induction
78 revious studies have shown that nitric oxide synthesis inhibition corrects the hyporesponsiveness to
80 hat brief periods of global or local protein synthesis inhibition decrease the synaptic vesicles avai
81 transcriptional level, resulting in protein synthesis inhibition, decreased viral messenger RNA asso
82 Klf13 mRNA was resistant to de novo protein synthesis inhibition, demonstrating that Klf13 is a dire
83 correlate with TRAIL resistance, and protein synthesis inhibition did not sensitize the TRAIL-resista
84 increased biosynthetic activity, and protein synthesis inhibition downstream of mammalian target of r
85 reduction itself also attenuated the protein synthesis inhibition due to anoxia/aglycemia (to 55.6% o
87 E-BP1 occurs roughly concurrent with protein synthesis inhibition; during recovery from heat shock re
89 alternative interpretations are that protein synthesis inhibition facilitates extinction and that pos
90 s, cases have been reported in which protein synthesis inhibition failed to affect memory consolidati
91 zation of the medium exacerbated the protein synthesis inhibition following anoxia/aglycemia, and sig
94 ecifically and highly cytotoxic [50% protein synthesis inhibition (IC50) ranging from >0.1 to 13 ng/m
95 neither postsession inactivation nor protein synthesis inhibition impaired context-appropriate respon
97 otein expression and was overcome by protein synthesis inhibition in 50% of the resistant cell lines.
99 host protein synthesis, whereas host protein synthesis inhibition in SARS-CoV-mt-infected cells was n
101 study was to examine the effects of protein synthesis inhibition in the intermediate cerebellum on t
102 ate the beneficial effects of thromboxane A2 synthesis inhibition in the setting of ischemia-reperfus
103 DCs display an unusual resistance to protein synthesis inhibition induced in response to cytosolic ds
108 extinction and that postreactivation protein synthesis inhibition leads to an inability to retrieve t
109 NO synthase blockade and acute prostaglandin synthesis inhibition led to the equalization of GFR, ERP
110 ns were sought with these parameters and DNA synthesis inhibition measured ex vivo by [3H]thymidine i
111 with superimposition of acute prostaglandin synthesis inhibition (meclofenamate, 10 mg/kg IV), renal
113 atosis in alcohol-fed mice, but only de novo synthesis inhibition, not sphingomyelin hydrolysis, impr
115 viability was greatly preserved when protein synthesis inhibition occurred after peroxide induction.
116 s of both effects are rapid, with fatty acid synthesis inhibition occurring within 30 min and DNA syn
117 s inhibition occurring within 30 min and DNA synthesis inhibition occurring within 90 min of drug exp
118 arrest at the G0/G1 phase, inhibition of DNA synthesis, inhibition of cyclin D and cyclin E promoter
119 amined the effects of pharmacologic ceramide synthesis inhibition on hepatic PLIN2 expression, steato
120 n accumulation, azithromycin-induced protein synthesis inhibition, oprM (encoding the outer-membrane
123 ensitive electrode, that was abolished by NO synthesis inhibition, or endothelium removal, and reduce
124 -3 activation was also attenuated by protein synthesis inhibition, p53 deficiency, or Bax deficiency,
125 ruption of original consolidation by protein synthesis inhibition (PSI) begun shortly after training.
127 ed to examine the impact of systemic protein synthesis inhibition (PSI) on the reconsolidation of a c
128 I-labeled ligand binding competition and DNA synthesis inhibition revealed that IGFBP-3 was a more po
133 e-activated cell sorting analyses showed DNA synthesis inhibition uniformly throughout the S phase af
134 , were studied in vitro by examining protein synthesis inhibition using Vero monkey kidney cells and
136 The DNA-binding domain essential for DNA synthesis inhibition was mapped to within 42 amino acid
139 op1-mediated DNA single-strand breaks or DNA synthesis inhibition were observed after 1 h exposure to
140 noid signaling, or by 2-arachidonoylglycerol synthesis inhibition, which impairs postsynaptic endocan
141 )O(2) from elevating Nrf2 protein level, RNA synthesis inhibition with actinomycin D failed to do so.
142 he next experiment examined the effect of NE synthesis inhibition with bis(4-methyl-1-homopiperazinyl
144 holesterolemic patients before and during NO synthesis inhibition with N(G)-monomethyl-L-arginine (4
145 ience can be disrupted; by contrast, protein synthesis inhibition without prior reminding commonly do
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