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1 Cal PA-XFS expressed significantly less PA-X than Cal wi
2 Cal WT, but not Cal PA-XFS, induced degradation of host
3 Cal- modulin was found to interact strongly with the cyt
5 in the Neolithic ( approximately 4,000-7,000 Cal y B.P.) and continues through the Iron/Roman period
6 PA from the pH1N1 virus A/California/04/09 (Cal) strongly enhances activity of an otherwise avian po
7 ly different Ca2+ indicators, such as OGB-1, Cal-590 can be readily used for simultaneous multicolor
8 se component or NS1 of A/California/04/2009 (Cal) and found that PA has a significant impact on the e
9 ex of the pH1N1 strain A/California/04/2009 (Cal) is highly active in mammalian 293T cells, despite t
10 nd after receiving the A/California/04/2009 (Cal/09) vaccine between October 2009 and January 2010.
12 t of neurons that stain for calbindin D-28K (Cal), a calcium-binding protein involved in regulating n
13 roximately 11,550 yBP ( approximately 13,390 Cal years) at "El Fin del Mundo," an archaeological site
18 by DI virus, ferrets formed high levels of A/Cal-specific serum haemagglutination-inhibiting antibodi
19 d in nasal washes following infection with A/Cal, consistent with its amelioration of clinical diseas
21 sed BSO+AUR-induced cell killing in FaDu and Cal-27 cells, while catalase and selenium supplementatio
27 vival compared to either drug alone in FaDu, Cal-27 and SCC-25 HNSCC cells in vitro and in vivo in Ca
28 BSO+AUR also significantly sensitized FaDu, Cal-27, SCC-25 and SQ20B cells to cell killing induced b
29 n the dLGN that were also immunoreactive for Cal varied from less than 40% to over 80%, indicating th
30 elial cell monolayers with supernatants from Cal-stimulated mast cells resulted in upregulation of th
33 nstrated considerable susceptibility to H1N1 Cal/04/09 infection, whereas FluMist-vaccinated mice had
35 ween the pandemic A/California/04/09 (H1N1) (Cal/09) virus and another H1N1 strain, A/Puerto Rico/8/3
36 influenza A virus, A/California/04/09 (H1N1, Cal), containing mutations at the frameshift motif in th
38 tis serovars D (UW-3/Cx), E (Bour), or F (IC-Cal-3) or Chlamydia muridarum strain Nigg II using CpG-1
39 and neutralizing antibodies were produced in Cal PA-XFS-infected mice than in Cal WT-infected mice, d
40 ing the presence of unidentified residues in Cal PB2 that are required for efficient growth at low te
41 produced in Cal PA-XFS-infected mice than in Cal WT-infected mice, despite the lower level of virus r
43 d the red-shifted fluorescent Ca2+ indicator Cal-590 for deep tissue experiments in the mouse cortex
44 conclude that the red-shifted Ca2+ indicator Cal-590 is well suited for in vivo two-photon Ca2+ imagi
49 have implications for future satellite lidar Cal/Val efforts, because planned satellite lidars measur
53 at least 5 years old, and had Medicaid (Medi-Cal in California), Medicare, private, or no insurance w
57 cipating in the state Medicaid program (Medi-Cal) to charge customers who present a Medicare card amo
60 that, despite the relatively low affinity of Cal-590 for Ca2+ (Kd=561 nM), single-action potential-ev
61 complexes containing various combinations of Cal and avian influenza virus A/chicken/Nanchang/3-120/0
62 also demonstrated that, while the growth of Cal PA-XFS was attenuated in the lungs of infected anima
64 led neuron and the surrounding population of Cal-590-labeled cells were recorded simultaneously on tw
65 nea pig model to understand which segment of Cal/09 virus conferred transmissibility to the poorly tr
66 with the acetoxymethyl (AM) ester version of Cal-590, combined two-photon imaging and cell-attached r
69 fferent viruses (recombinant wild-type [rWT] Cal/09 and the 66N and 66S viruses) did not result in si
70 a A virus A/California/7/2009 (H1N1) strain (Cal) were protected from a lethal challenge with the het
71 We present a dual-protein switch system, Cal-Light, that translates neuronal-activity-mediated ca
76 (Nan) by reporter gene assay indicates that Cal PA, but not PB2, is a major contributing factor to h
77 tured neurons and brain slices, we show that Cal-Light drives expression of the reporter EGFP with hi
78 eterogeneous in nature and also suggest that Cal content may be a critical feature of the pathway by
79 d by the empirical relationship given by the Cal Tech group, but the strength of these should be redu
80 y demonstrates that PB1-F2 expression by the Cal/09 virus modulates the immune response to infection
83 The data showed that the M segment of the Cal/09 virus promoted aerosol transmissibility to recomb
85 who received either the NJ/76 vaccine or the Cal/09 vaccine experienced a robust boost in HA stalk-re
86 ng site-directed mutagenesis showed that the Cal PA residues 85I, 186S, and 336M contribute to enhanc
89 ical target may be systematically related to Cal content in the geniculo-extrastriate projection.
90 ve addressed this question by generating two Cal/09 viruses with productive PB1-F2 open reading frame
94 ouble-labeling techniques to examine whether Cal content characterizes all or a subset of neurons mak
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