ライフサイエンスコーパス: viper

1 n-Probe Aptima Combo 2 and BD ProbeTec using Viper.

2 ext of the envenomation caused by the Gaboon viper.

3 from the venom of the Vipera lebetina obtusa viper.

4 nits in venoms of related Asian and American vipers.

5 Envenoming by Echis saw scaled vipers and Bitis arietans puff adders is the leading cau

6 es, only vampire bats, boas, pythons and pit vipers are capable of detecting infrared radiation.

7 cetin" from the venom of West African gaboon viper, Bitis gabonica rhinoceros.

8 in, BomoTx, from the Brazilian lancehead pit viper (Bothrops moojeni).

9 those obtained using existing tools such as VIPER, but with the added benefit of being able to trace

10 leakeyi (Kenya), and from the sahara horned viper, Cerastes cerastes cerastes (Egypt) and the puff a

11 Pit vipers (Crotalinae) have a specific sensory system that

12 ding domain of the venom of the American pit viper, Crotalus molossus molossus as the targeting moiet

13 different from that of previously published viper CTLs.

14 rt the high-quality genome of the five-pacer viper, Deinagkistrodon acutus, and comparative analyses

15 The VIPER display was shown to effectively expose the range

16 This paper describes an evaluation of how VIPER displays the different scales and types of dataset

17 venom gland EST database for the saw-scaled viper, Echis ocellatus (Nigeria), using the gene ontolog

18 pressed in the venom gland of the saw scaled viper, Echis ocellatus.

19 fatal thrombotic complications in Russell's viper envenomation.

20 Importantly, in murine models, VIPER facilitates effective gene transfer to solid tumor

21 otein activity by enriched regulon analysis (VIPER), for accurate assessment of protein activity from

22 In vitro assays confirmed that VIPER-inferred protein activity outperformed mutational

23 se errors are exposed and explored using the VIPER interface and we evaluate the utility and usabilit

24 VIPER is composed of a polycation block for condensation

25 emonstrate that the region of A46 from which VIPER is derived represents the TLR4-specific inhibitory

26 VIPER may be downloaded free of charge at http://ncrr.pn

27 tide purified from the venom of Wagler's pit viper on the whole cell current response (I(GABA)) to ga

28 ed the behavior of 33 individuals to a model viper placed on their projected travel path.

29 TRPA1 orthologues from pit-bearing snakes (vipers, pythons and boas) are the most heat-sensitive ve

30 nstituent functionality of venoms from these vipers remains poorly understood.

31 h boid and crotaline snakes (pythons and pit vipers, respectively).

32 ur experimentally, with a description of how VIPER's display interface and functionality meet the cha

33 VIPER shows superior efficiencies compared to commercial

34 The VIPER software package is one of the key components of t

35 luster sequence conservation across all four viper species which were significantly different from th

36 es isolated (by PCR) from another saw-scaled viper species, E. pyramidum leakeyi (Kenya), and from th

37 , which can be performed on the automated BD Viper system.

38 dynamic lineage-specific expansion, and many viper TEs show brain-specific gene expression along with

39 n of this important group of venom toxins in vipers that are distributed throughout Africa, the Middl

40 We used VIPER to evaluate the functional relevance of genetic al

41 antigen can enhance defense against Russell viper venom (RVV) and determined whether such responses

42 e was then induced with the use of Russell's viper venom (RVV) and histamine.

43 An enzyme from Russell's viper venom (RVV) cleaves human factor V at Arg1018 and

44 Russell's viper venom (RVV) contains protein(s) that destabilize A

45 of coagulation factors V and X by Russell's viper venom (RVV) has been implicated in the development

46 showed that factor X activator of Russell's viper venom (RVV-X) contains six N-linked oligosaccharid

47 The X-activating protein from Russell's viper venom activates fXSt. Louis II completely but at a

48 aque disruption was triggered with Russell's viper venom and histamine.

49 ger) inducing plaque disruption with Russell viper venom and histamine.

50 Plaque rupture was triggered with Russell's viper venom and histamine.

51 markedly procoagulant in a modified Russell viper venom assay.

52 GDFX and was also activated by the Russell's viper venom at similar rate, but it cleaved the chromoge

53 peptide, was isolated from the Azemiops feae viper venom by combination of gel filtration and reverse

54 Because viper venom CTLs exhibit a high degree of sequence simil

55 degrees of sequence similarity to published viper venom CTLs.

56 Echistatin is a viper venom disintegrin containing RGD loop maintained b

57 Russell's viper venom factor X activator (RVV-X) triggers the casc

58 oresceinated antibody, and enzyme (Russell's viper venom factor X activator)-labeled antibody is allo

59 Factor X was activated with Russell's viper venom factor X activator, and single-chain unactiv

60 We characterized HUVEC GPIb using viper venom proteins: alboaggregins A and B, echicetin,

61 coagulable state, we have used the Russell's viper venom test (RVV) to show that red blood cells (RBC

62 rogram/mL) did not prolong a modified Russel viper venom time, suggesting no significant inhibition o

63 re and 48 hours after injection of Russell's viper venom, an endothelial toxin.

64 s, such as cyclic RGD peptides isolated from viper venom, may prove to be useful as anti-inflammatory

65 ation by the factor X activator from Russell viper venom, the mutants were characterized with respect

66 In conclusion, we report a new, potent viper venom-derived inhibitor of alpha2beta1 integrin, w

67 the ApoE(-/-) (-22.22+/-7.95%) and Russell's viper venom-injected (-10.37+/-17.60%) mice compared wit

68 0.54, R(12 weeks) 3.83+/-0.52) and Russell's viper venom-injected wild-type mice (R(1)=4.57+/-0.86).

69 the lethal effects of honeybee or Russell's viper venom.

70 factor, factors IXa and VIIIa, and Russell's viper venom.

71 ex or by a purified activator from Russell's viper venom.

72 are small non-enzymatic proteins present in viper venoms reported to modulate hemostasis of victims

73 Disintegrins are peptides found in viper venoms which bind to platelets through the glycopr

74 d a peptide fragment derived from A46 termed VIPER (Viral Inhibitory Peptide of TLR4), which specific

75 to mimic viral mechanisms of delivery called VIPER (virus-inspired polymer for endosomal release).

76 der to assist this process we are developing VIPER (Visual Pedigree Explorer), a software tool that i

77 om gland of the snake Bitis gabonica (Gaboon viper) was used for the first time to construct a unidir

78 ARHgamma), from the venom of the Malayan pit viper, was used to selectively cleave human factor X in

79 n), a cathelicidin from a South American pit viper, yielded fragments Ctn[1-14] and Ctn[15-34], which