ライフサイエンスコーパス: Ancylostoma

1 Ancylostoma braziliense is most often implicated in derm

2 synthesized Acan1 and Nak1 peptides from the Ancylostoma caninum and Necator americanus hookworms and

3 cretory glands of the dog-infecting hookworm Ancylostoma caninum and the human-infecting hookworm Anc

4 e blood-feeding stage of the canine hookworm Ancylostoma caninum and vaccinated dogs with the purifie

5 en implicated in dermatological lesions, and Ancylostoma caninum has been associated with eosinophili

6 rized from soluble protein extracts of adult Ancylostoma caninum hookworms.

7 Vaccination of mice with either third-stage Ancylostoma caninum infective hookworm larvae (L3) or al

8 teins (NAPs) from the hematophagous nematode Ancylostoma caninum inhibit blood coagulation with picom

9 The hematophagous hookworm Ancylostoma caninum produces a family of small, disulfid

10 t in vitro, activated larvae of the hookworm Ancylostoma caninum released a 42-kDa protein, termed An

11 The dog hookworm Ancylostoma caninum secretes an astacin-like metalloprot

12 mino acids) anticoagulants from the hookworm Ancylostoma caninum termed AcAP (A. caninum anticoagulan

13 coprotein isolated from the canine hookworm (Ancylostoma caninum), binds to the I domain of CD11a and

14 coprotein isolated from the canine hookworm (Ancylostoma caninum), is a beta2 integrin antagonist tha

15 g protein isolated from the canine hookworm (Ancylostoma caninum).

16 otein secreted by infective hookworm larvae (Ancylostoma caninum).

17 thione S-transferase from the adult hookworm Ancylostoma caninum, and its possible role in parasite b

18 rush border membrane of the canine hookworm, Ancylostoma caninum, contains aspartic proteases (APR-1)

19 In the parasitic nematode Ancylostoma caninum, the dauer larval stage is the infec

20 ity to Ac-GST-1, a GST from the dog hookworm Ancylostoma caninum.

21 its homologue isolated from the dog hookworm Ancylostoma caninum.

22 IF), a glycoprotein produced by the hookworm Ancylostoma caninum.

23 l stages of both the human hookworm parasite Ancylostoma ceylanicum and the free-living nematode Caen

24 Hamsters were infected with the hookworm Ancylostoma ceylanicum and vaccinated with the recombina

25 two x-ray crystal structures of the hookworm Ancylostoma ceylanicum DAF-12 ligand binding domain in c

26 Here we describe the cloning of Ancylostoma ceylanicum excretory-secretory protein 2 (Ac

27 dworm Strongyloides stercoralis and hookworm Ancylostoma ceylanicum have highly dissimilar olfactory

28 linical sequelae (weight loss and anemia) of Ancylostoma ceylanicum hookworm infection in Syrian gold

29 th following oral infection with third-stage Ancylostoma ceylanicum hookworm larvae.

30 rotease inhibitor has been cloned from adult Ancylostoma ceylanicum hookworm RNA.

31 Unlike other hookworms, Ancylostoma ceylanicum infects both humans and other mam

32 Ancylostoma ceylanicum infects humans and animals, makin

33 The Ancylostoma ceylanicum Kunitz-type inhibitor (AceKI) is

34 node (MLN) cells from hamsters infected with Ancylostoma ceylanicum showed minimal proliferation in r

35 s been identified from the hookworm parasite Ancylostoma ceylanicum using reverse transcription PCR a

36 cator americanus, Ancylostoma duodenale, and Ancylostoma ceylanicum) infect humans.

37 ombinant Cry5B against the hookworm parasite Ancylostoma ceylanicum, a bloodfeeding gastrointestinal

38 oma caninum and the human-infecting hookworm Ancylostoma ceylanicum, and BmK1, the C-terminal domain

39 udy the impact of a human hookworm parasite, Ancylostoma ceylanicum, on cognition in hamsters in a co

40 ors in S. stercoralis and the human hookworm Ancylostoma ceylanicum, suggesting a critical role for d

41 closely related to human parasitic nematodes-Ancylostoma ceylanicum, Trichurismuris, and Ascarissuum-

42 ct retrovirus-like EVE in the human hookworm Ancylostoma ceylanicum, with an envelope protein genetic

43 ctor (MIF) has been cloned from the hookworm Ancylostoma ceylanicum.

44 ookworm infection using the hamster model of Ancylostoma ceylanicum.

45 n used to model infections with the hookworm Ancylostoma ceylanicum.

46 ed helminths Ascaris lumbricoides, hookworm (Ancylostoma duodenale and Necator americanus), Trichuris

47 lumbricoides, Trichuris trichiura, hookworm [Ancylostoma duodenale and Necator americanus], and Stron

48 ection with Plasmodium falciparum, hookworm (Ancylostoma duodenale and/or Necator americanus), Entamo

49 three hookworm species (Necator americanus, Ancylostoma duodenale, and Ancylostoma ceylanicum) infec

50 Ancylostoma eggs are morphologically indistinguishable,

51 anticoagulant virulence factors from related Ancylostoma hookworm species may have significant implic

52 larvae (L3) or alum-precipitated recombinant Ancylostoma secreted protein 1 from A. caninum (Ac-ASP-1

53 the most abundant L3 secreted antigens, the ancylostoma secreted proteins, ASP-1 and ASP-2.

54 ma caninum released a 42-kDa protein, termed Ancylostoma-secreted protein (ASP).

55 Ancylostoma-secreted protein 1 (ASP-1) is the major prot

56 Necator americanus Ancylostoma-secreted protein 2 (Na-ASP-2) is secreted by

57 ation with the recombinant fusion protein Ay-Ancylostoma-secreted protein 2 was analyzed in the Golde

58 ein (SmTAL1), SmTAL2, and Necator americanus Ancylostoma-secreted protein-2 (Na-ASP-2), following con

59 hogenesis-related (PR) proteins known as the Ancylostoma-secreted proteins (ASPs).

60 e major blood-feeding nematodes - hookworms (Ancylostoma spp. and Necator americanus) and the ruminan

61 asites, including Strongyloides stercoralis, Ancylostoma spp., and Necator americanus.

62 Giardia duodenalis, Cryptosporidium, Ancylostoma, Uncinaria, and Toxocara cati were shed.