戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 rpH abolished the receptor-binding activity (hemagglutinating ability) of MrpH but allowed normal fim
2              Anti-Hs Fab did not inhibit the hemagglutinating activities of several heterologous S. g
3    A recombinant BgGal (rBgGal) demonstrated hemagglutinating activity against rabbit erythrocytes, w
4 ed and were similar to native lectin in both hemagglutinating activity and high-affinity binding to l
5                       The co-localization of hemagglutinating activity and host range determinants on
6 sess a mrkD1C allele that is associated with hemagglutinating activity but does not bind to either ty
7 ontrast, two S. gordonii strains that lacked hemagglutinating activity did not react with anti-Hs ant
8                                 The relative hemagglutinating activity of berries from Synsepalum dul
9                                          The hemagglutinating activity of heated SBA was measured by
10 anti-DL1 serum and anti-Hs Fab inhibited the hemagglutinating activity of strain DL1, and the inhibit
11       These enzymes are also involved in the hemagglutinating activity of the organisms.
12 BA aggregation was proportionally related to hemagglutinating activity reduction.
13          FVJ, diluted by one half, displayed hemagglutinating activity whilst VJ did not display any
14 ulture supernatants from both samples showed hemagglutinating activity with mouse erythrocytes.
15 ating activity whilst VJ did not display any hemagglutinating activity.
16 n other strains of this species that possess hemagglutinating activity.
17 mutant, strain D102, that specifically lacks hemagglutinating activity.
18                                         Both hemagglutinating and collagen-binding activities were as
19                          The antibodies were hemagglutinating and cytotoxic antibodies.
20 on in addition to a significant reduction in hemagglutinating and hemolysin activities.
21                                  Because the hemagglutinating and hemolytic potentials of mutant stra
22    The henipavirus G glycoproteins lack both hemagglutinating and neuraminidase activities and, inste
23 of which are commonly found in pigs, porcine hemagglutinating encephalomyelitis remains one of the le
24 ip with bovine coronavirus (BCV) and porcine hemagglutinating encephalomyelitis virus (mammalian grou
25                                      Porcine hemagglutinating encephalomyelitis virus (PHEV) is a bet
26  (BCoV)-its presumptive ancestor-and porcine hemagglutinating encephalomyelitis virus (PHEV).
27 preserving the SA-dependent cell binding and hemagglutinating functions of the virion.
28 to determine the similarity of these pili to hemagglutinating, HifA- and HifE-containing pili express
29 id-based influenza virus assembly assay, and hemagglutinating material from the supernatants of such
30 populations constituted ca. 20% of the total hemagglutinating particle population in which these noni
31 cluded total physical particles (measured as hemagglutinating particles [HAPs]) with their subsumed b
32                               Phase-variable hemagglutinating pili are expressed by many H. influenza
33         The HMW1 and HMW2 proteins, Hia, and hemagglutinating pili are important adherence factors in
34 ical H. influenzae isolates and suggest that hemagglutinating pili may play a larger role in H. influ
35 tructures that were shorter and thicker than hemagglutinating pili of the respiratory strains AAr176
36 hich encodes the major structural subunit of hemagglutinating pili, and hifE, which encodes the tip a
37 enes that code for HifA- and HifE-containing hemagglutinating pili, epithelial cell adherence exhibit
38 Hi adherence to epithelial cells mediated by hemagglutinating pili, Hia, HMW1, HMW2, and Hap and epit
39 , and hifE, which encodes the tip adhesin of hemagglutinating pili, were detected by PCR from six and
40 if genes; Hap, Hia, and HMW1/2 adhesins; and hemagglutinating pili.
41 ese strains is not mediated by expression of hemagglutinating pili.
42 components, including the neurotoxin BoNT/A, hemagglutinating protein HA17/A, and non-toxic non-hemag
43                                          The hemagglutinating protein HA33 from Clostridium botulinum
44 lutinating protein HA17/A, and non-toxic non-hemagglutinating protein NTNHA/A, suggests that most of
45 in, nonhemagglutinin subunit and a family of hemagglutinating proteins.
46  blood cells, nor could they be enriched for hemagglutinating variants.
47                                              Hemagglutinating virus of Japan (HVJ)-liposome technique
48 nt DiI and then treated with fusion-inducing hemagglutinating virus of Japan (HVJ).
49                       The fusion proteins of hemagglutinating virus of Japan (HVJ; also Sendai virus)
50 ype IL-1ra gene by intracoronary infusion of Hemagglutinating Virus of Japan liposome and were hetero
51         Rat hearts were infused ex vivo with Hemagglutinating Virus of Japan-liposome complex contain
52 nsfected with the human VEGF(165) gene using hemagglutinating virus of Japan-liposome with >95% trans
53 ontrol plasmid by intra-coronary infusion of Hemagglutinating Virus of Japan-liposome, and transplant
54 th human HSP72 by intra-coronary infusion of Hemagglutinating Virus of Japan-liposome, resulting in g