ライフサイエンスコーパス: Brugia malayi

1 of a metalloprotease from the filarial worm Brugia malayi.

2 ss in the important human parasitic nematode Brugia malayi.

3 ainst the Wolbachia-dependent model filaria, Brugia malayi.

4 e tropical parasites Onchocerca volvulus and Brugia malayi.

5 r chronic exposure to the nematode parasite, Brugia malayi.

6 en developed for the human filarial parasite Brugia malayi.

7 a nematode model with the filarial parasite, Brugia malayi.

8 parasitic nematodes Wuchereria bancrofti and Brugia malayi.

9 gy to identify candidate vaccine antigens of Brugia malayi.

10 quisition in the parasitic filarial nematode Brugia malayi.

11 C. elegans and the human-parasitic nematode Brugia malayi.

12 rial nematodes, including Brugia pahangi and Brugia malayi.

13 nematode parasites Wuchereria bancrofti and Brugia malayi.

14 interleukin-4 (IL-4) in host defense against Brugia malayi.

15 ability to combat infection by the nematode Brugia malayi.

16 nematode parasites Wuchereria bancrofti and Brugia malayi.

17 in two nematodes; Caenorhabditis elegans and Brugia malayi.

18 ge larvae (L3) or live microfilariae (Mf) of Brugia malayi, a causative agent of human lymphatic fila

19 has been isolated from the filarial nematode Brugia malayi, a causative agent of human lymphatic fila

20 of almost all the major mammalian stages of Brugia malayi, a causative agent of lymphatic filariasis

21 ertaken the first study of heme transport in Brugia malayi, a causative agent of lymphatic filariasis

22 nts generated from MF patients, filarial Ag (Brugia malayi adult Ag (BmA))-stimulated supernatants fr

23 basophils released histamine in response to Brugia malayi Ag (BmAg).

24 Brugian filariasis (caused by the nematodes Brugia malayi and B. timori) is an important cause of di

25 During our investigations into the course of Brugia malayi and Brugia pahangi infections in immunodef

26 Extracts of Brugia malayi and Onchocerca volvulus, which contain Wol

27 e (Mb) genome of the human filarial parasite Brugia malayi and predict approximately 11,500 protein c

28 ical to the MIFs from the parasitic nematode Brugia malayi, and 22-35% identical to mammalian MIFs.

29 cells were exposed to microfilariae (mf) of Brugia malayi, and their phenotypic and functional chara

30 enomes to that of another filarial parasite, Brugia malayi, and to those of several other nematodes,

31 duals (n = 11) were stimulated in vitro with Brugia malayi antigen (BMA) or mycobacterial purified pr

32 association between ratios of polyclonal to Brugia malayi antigen (BmAg)-specific IgE (range, 14:1 t

33 (-/-) mice were first immunized with soluble Brugia malayi antigens and then inoculated intravenously

34 d secondary murine and human infections with Brugia malayi are characterized by substantial increases

35 s brenneri, using Pristionchus pacificus and Brugia malayi as outgroups, and identified numerous oper

36 chocerca volvulus, Wuchereria bancrofti, and Brugia malayi available, new drug targets have been iden

37 on passive transfer, led to the clearance of Brugia malayi (Bm) microfilariae (mf) from infected jird

38 nce tag, from the distantly related parasite Brugia malayi (Bm-her-1).

39 response to live, infective-stage larvae of Brugia malayi but not to microfilariae of this parasite.

40 rgillus nidulans, Schizosaccharomyces pombe, Brugia malayi, Caenorhabditis elegans, Trypanosoma cruzi

41 uble extracts of the human filarial parasite Brugia malayi can induce potent inflammatory responses,

42 Infection with the parasitic helminth Brugia malayi can result in development of a severe asth

43 sponding genes in Caenorhabditis elegans and Brugia malayi contained a cysteine codon in place of TGA

44 la melanogaster, Caenorhabditis elegans, and Brugia malayi EST sequences.

45 behaviour towards host cues when exposed to Brugia malayi filarial parasites.

46 The filarial nematode gene Bmgmf for Brugia malayi glia maturation factor contains six predic

47 Brugia malayi GMF (BmGMF) is also related to a large fam

48 The human filarial parasite Brugia malayi harbors an endosymbiotic bacterium Wolbach

49 e heme; however, the human filarial parasite Brugia malayi has acquired a bacterial gene encoding fer

50 sponse to the infective-stage larvae (L3) of Brugia malayi has not been well-characterized in vivo (b

51 he genomic environment of a newly identified Brugia malayi Hox6-8 ortholog (Bm-ant-1) revealed that i

52 ilarial Ag (MfAg) from the filarial parasite Brugia malayi in the presence of APCs.

53 We have shown that live microfilariae of Brugia malayi induce caspase-dependent apoptosis in huma

54 immune responses were assayed in a group of Brugia malayi-infected rhesus monkeys.

55 luated the contributions of T and B cells in Brugia malayi infection by utilizing knockout mice on a

56 after treatment with diethylcarbamazine for Brugia malayi infection, and recorded the severity of an

57 uired for host protection in mouse models of Brugia malayi infection.

58 A cDNA clone isolated from a Brugia malayi infective-stage larva expression library e

59 Together, these results suggest that Brugia malayi mf employ mechanisms of metabolic modulati

60 Brugia malayi microfilariae and adults were exposed in v

61 Blood-borne Brugia malayi microfilariae survived for significantly l

62 tics and anti-Wolbachia efficacy in a murine Brugia malayi model of minocycline versus doxycycline.

63 We have isolated and sequenced a Brugia malayi nematode 3.4-kb genomic DNA fragment and i

64 del of alternative activation in which adult Brugia malayi nematodes are implanted surgically in the

65 bitor of NO synthase abrogated resistance to Brugia malayi, one of the causative agents of human lymp

66 interactions between the infective stage of Brugia malayi--one of the extracellular parasites respon

67 termine, via preclinical infection models of Brugia malayi or Onchocerca ochengi that elevated exposu

68 nsoni ova, larvae from the filarial helminth Brugia malayi, or CFA.

69 IL4Ralpha(-/-) mice elicited by the nematode Brugia malayi, or via intraperitoneal thioglycollate inj

70 ells (PEC) from mice transplanted with adult Brugia malayi parasites suppress the proliferation of ly

71 a donovani, Toxoplasma gondii) and helminth (Brugia malayi) parasites were examined, each of which pr

72 ocheilonema viteae, Onchocerca volvulus, and Brugia malayi, strongly supporting the concept that the

73 ympahtic filariasis is the nematode parasite Brugia malayi that requires a competent mosquito vector

74 cation of binding protein(s) of the helminth Brugia malayi to CaGC and the ability of binding complex

75 The resistance of the human parasite Brugia malayi to the antiparasitic activity of cyclospor

76 pod Drosophila melanogaster and the nematode Brugia malayi, together with the partial genome sequenci

77 e, C. remanei, C. brenneri, C. japonica, and Brugia malayi using some of the best-performing gene-fin

78 e infective-stage larvae or microfilariae of Brugia malayi, we found significant impairment of both T

79 our research on the human nematode parasite Brugia malayi, which causes elephantiasis.

80 t the filarial nematodes responsible for LF (Brugia malayi, Wuchereria bancrofti) or onchocerciasis (