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1 nems 4-7 with beta-lactamases (TEM-1, SHV-1, Amp-C) were characterized by electrospray ionization mas
2 M), or cyclo[Asp(5)-/Glu(5)-/Asp(5)(Gly(5'))-Amp(8)] (19, K(i) = 1.3 nM; 22, K(i) = 3.3 nM; and 23, K
3 mino-3-(7-methoxy-4-coumaryl)propionic acid (Amp) or L- or D-2-amino-3-(6,7-dimethoxy-4-coumaryl)prop
4 ate that in vervet monkey striatum, an acute Amp or MeAmp drug dosage produces extensive striatal dop
5 /kg, i.m., 4 h apart) of either amphetamine (Amp), n = 3, or methamphetamine (MeAmp), n = 3.
6 ene for CMS 514A derived from an amphiploid (Amp H. angustifolius/P 21, 2n = 68).
7 here the beta-lactam antibiotics ampicillin (Amp) and amoxicillin (Amx) are linked to a monofunctiona
8 bp integrons added resistance to ampicillin (Amp) and chloramphenicol (Cm), and the 1,600-bp integron
9 imals were then given water with ampicillin (Amp; 5 g/liter) ad libitum.
10 implicit time (IT) Z-score, mfERG amplitude (Amp) Z-score, sex, diabetes duration, diabetes type, blo
11                  At 1-2 weeks postdrug, both Amp and MeAmp exposure effected similar decreases (60-70
12 ntegron; the beta-lactamase gene, conferring Amp resistance in the 1,200-bp integron; and the aadA an
13                       Since both the donors (Amp(s)-Tet(r)) and recipients (Amp(r)-Tet(s)) were resis
14 b) Adp has a larger Stokes shift than either Amp or Lys(Mca) and thus has less chance of self-quenchi
15 ecies such as Staphylococcus aureus, and Ent-Amp exhibits low cytotoxicity against human T84 intestin
16 obactin-antibiotic conjugates, hereafter Ent-Amp/Amx, where the beta-lactam antibiotics ampicillin (A
17                                Moreover, Ent-Amp and Ent-Amx selectively kill E. coli CFT073 co-cultu
18 me-kill kinetic studies demonstrate that Ent-Amp/Amx kill this strain more rapidly at 10-fold lower c
19 ctively, for St Spc Su Tet; 0.95 and 1.0 for Amp Cm St Spc Su Tet; and 1.0 and 0.99 for Gen Kan St Sp
20                        The C227-11-infected, Amp-treated C57BL/6 mice exhibited both morbidity and mo
21                                    The mfERG Amp, mfERG IT, SBP, and sex were together predictive of
22 used to calculate the maximum IT and minimum Amp Z-scores for each zone.
23  demonstrated that the shorter side chain of Amp or Adp was better tolerated by MMP-1 and MMP-2.
24 els, and in 100 uninfected persons by use of Amp-RT, an ultrasensitive RT assay.
25 eks, by 25% at 10-12 weeks and by 16% in one Amp-treated subject at 32 weeks.
26 pcDNA-89 or with the plasmid backbone pcDNAI/Amp (pcDNA) and then challenged 2 weeks later with eithe
27 ed sequences were C6-(Gly-Pro-Hyp)5-Gly-Pro-[Amp/Adp]-Gly-Pro-Gln-Gly approximately Leu-Arg-Gly-Gln-L
28 h the donors (Amp(s)-Tet(r)) and recipients (Amp(r)-Tet(s)) were resistant to erythromycin, the trans
29 ined in significantly higher yields than the Amp-containing fTHPs, (b) Adp has a larger Stokes shift
30 for uropathogenic E. coli CFT073 relative to Amp/Amx, and time-kill kinetic studies demonstrate that
31    Of the 50 clinical samples, 38 (76%) were Amp-RT positive, while all uninfected controls were nega
32 titutions in this series, such as those with Amp (25, 26), Orn (27), or IAmp (29) at position 7, were

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