ライフサイエンスコーパス: haematobium

1 ew advances that will deepen knowledge of S. haematobium.

2 nown to exhibit activity against Schistosoma haematobium.

3 um that are coinfected with S. mansoni or S. haematobium.

4 red with Schistosoma mansoni and Schistosoma haematobium.

5 parasitic trematode blood fluke Schistosoma haematobium.

6 ure of acetylcholinesterase from Schistosoma haematobium.

7 h endemic Schistosoma mansoni or Schistosoma haematobium.

8 h either Wuchereria bancrofti or Schistosoma haematobium.

9 educes morbidity is proposed for Schistosoma haematobium, a parasite of major public health importanc

10 Schistosoma haematobium, a parasitic flatworm that infects more than

11 species and cloned the complete gene for S. haematobium AChE.

12 tterns of recognition of defined Schistosoma haematobium adult worm antigens by serum antibodies from

13 aused by the parasitic trematode Schistosoma haematobium, affects over 112 million people worldwide.

14 indicate a diversity of lesions caused by S. haematobium and a dynamic evolution of the genital lesio

15 ted with Schistosoma mansoni and Schistosoma haematobium and considers the practical implications of

16 erative to search for new drug targets in S. haematobium and other schistosomes.

17 -1 gene (Mta1) product in the survival of S. haematobium and productive infection in the host.

18 ecimens to determine the seroprevalence of S haematobium and S mansoni by ELISA and immunoblot analys

19 The literature search identified Schistosoma haematobium and Schistosoma mansoni surveys done in, res

20 vides a global insight into the kinome of S. haematobium and should assist the repurposing or discove

21 the AChE from the human parasite Schistosoma haematobium and succeeded in expressing functional recom

22 Hybridisation between S haematobium and the cattle schistosome S bovis had a put

23 ution of Schistosoma mansoni and Schistosoma haematobium and the incidence of schistosomiasis in area

24 water exposure was limited to Lake Malawi; S haematobium antibodies were found in 135 of 141 (96%) se

25 he most comprehensive characterization of S. haematobium antigens to date and describes novel antigen

26 verrini, Clonorchis sinensis and Schistosoma haematobium are classified as Group 1 biological carcino

27 errini, Clonorchis sinensis, and Schistosoma haematobium are classified as group 1 biological carcino

28 Most kinases of S. haematobium are very similar to those of its congener, S

29 ts, Schistosoma japonicum, S. mansoni and S. haematobium, are blood flukes that have complex life cyc

30 To study the mechanisms of S. haematobium-bacterial urinary tract coinfections, we com

31 The blood fluke Schistosoma haematobium causes urogenital schistosomiasis, a neglect

32 rvention for reducing the transmission of S. haematobium [corrected] is an economically attractive st

33 show that genital infection with Schistosoma haematobium [corrected] may increase the risk for HIV in

34 y between 10% and 70% of WSH for reducing S. haematobium [corrected] transmission, our model predicte

35 Schistosoma haematobium egg excretion rates showed a median reductio

36 Thus, S. haematobium eggs express IPSE homologs that appear to pe

37 A single bladder exposure to S. haematobium eggs triggers interleukin-4 (IL-4) productio

38 o bacterial UTI despite prior exposure to S. haematobium eggs.

39 eripheral blood of children residing in a S. haematobium-endemic area and in the peripheral blood, sp

40 Women aged 15-35 years living in an S. haematobium-endemic area in Madagascar underwent pelvic

41 Venous blood from 72 Schistosoma haematobium-exposed participants was cultured with schis

42 zed by pooled serum samples from Schistosoma haematobium-exposed Zimbabweans were determined by 2-dim

43 tosomiasis due to infection with Schistosoma haematobium following recreational water exposure at Cap

44 Features of the S. haematobium genome that are conserved among platyhelmint

45 snails, which are capable of transmitting S haematobium-group schistosomes.

46 Chronic infection with S. haematobium has been linked with bladder cancer and incr

47 d (3) the use of animal models to explore S. haematobium-host interactions.

48 Using the example of Schistosoma haematobium in Africa, this article illustrates how ecoz

49 cted Bulinus globosus, the snail vector of S haematobium in Malawi, were found at Cape Maclear and ot

50 S. haematobium-infected children and adolescents with bladd

51 S. haematobium-infected children with bladder pathology had

52 A greater percentage of B cells from S. haematobium-infected donors expressed cytoplasmic interl

53 resulted in less IL-10(+) T cells in the S. haematobium-infected group, while levels of FoxP3(+) reg

54 re was a lack of treatment effects in the S. haematobium-infected group; however, the small sample si

55 lished study, which included 163 Schistosoma haematobium-infected individuals and 183 matched healthy

56 A Nigerian cohort of 168 Schistosoma haematobium-infected individuals and 192 healthy control

57 anemic children with documented Schistosoma haematobium infection (n = 224 for AGP, CRP, SF, sTfR, a

58 ctions in the prevalence and intensity of S. haematobium infection 1 year after treatment were, howev

59 with observed field patterns of Schistosoma haematobium infection and antibody responses, including

60 y that evaluates the relationship between S. haematobium infection and associated morbidity in childr

61 otherapy can have a substantial impact on S. haematobium infection and its associated morbidity in ch

62 osed to increased TNF-alpha production to S. haematobium infection are more likely to develop an exag

63 d the efficacy of mefloquine IPTp against S. haematobium infection in pregnant women.

64 S haematobium infection is highly prevalent among expatria

65 ether bladder pathology in human Schistosoma haematobium infection is related to the balance of Th17

66 ws promising activity against concomitant S. haematobium infection leading to an important reduction

67 Pregnant women with S. haematobium infection presenting at 2 antenatal health c

68 complex biological processes that connect S. haematobium infection to bladder carcinogenesis.

69 Schistosoma haematobium infection was positively associated with IgE

70 At baseline, higher intensities of S. haematobium infection were observed in children with ane

71 en with different intensities of Schistosoma haematobium infection.

72 alent in cases with low-intensity urinary S. haematobium infection.

73 afebrile malaria, hookworm, and Schistosoma haematobium infection.

74 e risk of undernutrition and intensity of S. haematobium infection.

75 Schistosoma mansoni (and rarely Schistosoma haematobium) intestinal infection is also not very commo

76 ract morbidity in areas in which Schistosoma haematobium is endemic.

77 Comparative genomics for S. haematobium is feasible, given the sequencing of multipl

78 Among the schistosomes, Schistosoma haematobium is responsible for the most infections, whic

79 Schistosoma haematobium is responsible for two-thirds of the world's

80 schistosomiasis, infection with Schistosoma haematobium, is linked to increased risk for the develop

81 nital schistosomiasis, caused by Schistosoma haematobium, is the most prevalent form of schistosomias

82 nth species and others that are unique to S. haematobium may provide novel diagnostic and drug target

83 ng anti-IL-10 added to PBMC from Schistosoma haematobium patients' enhanced adult worm (SWAP)- or egg

84 esearch into human coinfections (Schistosoma haematobium-Plasmodium falciparum versus Schistosoma man

85 were recruited from areas where Schistosoma haematobium (S.h) infections were high or low endemic.

86 Despite S. haematobium's importance, relevant research has lagged.

87 2 patients showed infection with Schistosoma haematobium, S haematobium-Schistosoma bovis hybrids, an

88 velers returned from Mali with a Schistosoma haematobium-Schistosoma bovis hybrid infection, confirme

89 ed infection with Schistosoma haematobium, S haematobium-Schistosoma bovis hybrids, and S bovis.

90 t completely inhibited by CCDs, as well as S haematobium soluble egg antigen.

91 derivatives that kill both S. mansoni and S. haematobium, the two species responsible for >99% of sch

92 is context, we defined here the kinome of S. haematobium using a refined bioinformatic pipeline.

93 are orthologs of M-IPSE, from egg cDNA of S. haematobium Using PCR and immunodetection, we confirmed

94 million people are infected with Schistosoma haematobium, with the most intense infections in childre

95 ciated with increasing levels of Schistosoma haematobium worm IgG1, with adolescents with optical den

96 Urogenital schistosomiasis, Schistosoma haematobium worm infection, afflicts millions of people

97 eproducibly recovered significantly fewer S. haematobium worms and eggs from Mta1-/- mice than wild-t

98 ponse is stimulated by the death of adult S. haematobium worms and reduces worm fecundity.

99 ract coinfection by bacteria and Schistosoma haematobium worms, the etiologic agent of urogenital sch