ライフサイエンスコーパス: hemagglutinating

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 anti-DL1 serum and anti-Hs Fab inhibited the hemagglutinating activity of strain DL1, and the inhibit

9 These enzymes are also involved in the hemagglutinating activity of the organisms.

10 FVJ, diluted by one half, displayed hemagglutinating activity whilst VJ did not display any

11 ulture supernatants from both samples showed hemagglutinating activity with mouse erythrocytes.

12 ating activity whilst VJ did not display any hemagglutinating activity.

13 n other strains of this species that possess hemagglutinating activity.

14 mutant, strain D102, that specifically lacks hemagglutinating activity.

15 Both hemagglutinating and collagen-binding activities were as

16 The antibodies were hemagglutinating and cytotoxic antibodies.

17 on in addition to a significant reduction in hemagglutinating and hemolysin activities.

18 Because the hemagglutinating and hemolytic potentials of mutant stra

19 The henipavirus G glycoproteins lack both hemagglutinating and neuraminidase activities and, inste

20 ip with bovine coronavirus (BCV) and porcine hemagglutinating encephalomyelitis virus (mammalian grou

21 preserving the SA-dependent cell binding and hemagglutinating functions of the virion.

22 to determine the similarity of these pili to hemagglutinating, HifA- and HifE-containing pili express

23 id-based influenza virus assembly assay, and hemagglutinating material from the supernatants of such

24 populations constituted ca. 20% of the total hemagglutinating particle population in which these noni

25 cluded total physical particles (measured as hemagglutinating particles [HAPs]) with their subsumed b

26 Phase-variable hemagglutinating pili are expressed by many H. influenza

27 The HMW1 and HMW2 proteins, Hia, and hemagglutinating pili are important adherence factors in

28 ical H. influenzae isolates and suggest that hemagglutinating pili may play a larger role in H. influ

29 tructures that were shorter and thicker than hemagglutinating pili of the respiratory strains AAr176

30 hich encodes the major structural subunit of hemagglutinating pili, and hifE, which encodes the tip a

31 enes that code for HifA- and HifE-containing hemagglutinating pili, epithelial cell adherence exhibit

32 Hi adherence to epithelial cells mediated by hemagglutinating pili, Hia, HMW1, HMW2, and Hap and epit

33 , and hifE, which encodes the tip adhesin of hemagglutinating pili, were detected by PCR from six and

34 if genes; Hap, Hia, and HMW1/2 adhesins; and hemagglutinating pili.

35 ese strains is not mediated by expression of hemagglutinating pili.

36 components, including the neurotoxin BoNT/A, hemagglutinating protein HA17/A, and non-toxic non-hemag

37 The hemagglutinating protein HA33 from Clostridium botulinum

38 lutinating protein HA17/A, and non-toxic non-hemagglutinating protein NTNHA/A, suggests that most of

39 in, nonhemagglutinin subunit and a family of hemagglutinating proteins.

40 blood cells, nor could they be enriched for hemagglutinating variants.

41 Hemagglutinating virus of Japan (HVJ)-liposome technique

42 nt DiI and then treated with fusion-inducing hemagglutinating virus of Japan (HVJ).

43 The fusion proteins of hemagglutinating virus of Japan (HVJ; also Sendai virus)

44 ype IL-1ra gene by intracoronary infusion of Hemagglutinating Virus of Japan liposome and were hetero

45 Rat hearts were infused ex vivo with Hemagglutinating Virus of Japan-liposome complex contain

46 nsfected with the human VEGF(165) gene using hemagglutinating virus of Japan-liposome with >95% trans

47 ontrol plasmid by intra-coronary infusion of Hemagglutinating Virus of Japan-liposome, and transplant

48 th human HSP72 by intra-coronary infusion of Hemagglutinating Virus of Japan-liposome, resulting in g