ライフサイエンスコーパス: Plasmodium chabaudi

1 sistant to infection with the rodent malaria Plasmodium chabaudi.

2 wise lethal blood-stage malaria of the genus Plasmodium chabaudi.

3 ses in mice infected with erythrocytic-stage Plasmodium chabaudi.

4 re we show that after infection of mice with Plasmodium chabaudi, a c-Kit(hi) progenitor subset posit

5 els of beta S globin are well-protected from Plasmodium chabaudi adami and partially protected agains

6 Plasmodium chabaudi adami causes a nonlethal infection i

7 ice were immunized with purified recombinant Plasmodium chabaudi AMA-1 (PcAMA-1) and/or the 42-kDa C-

8 ctions between two rodent malaria parasites, Plasmodium chabaudi and P. yoelii.

9 socosms'' - i.e. mice infected with malaria (Plasmodium chabaudi) and nematodes (Nippostrongylus bras

10 latelets during the ascending parasitemia in Plasmodium chabaudi- and Plasmodium berghei-infected mic

11 Plasmodium berghei and Plasmodium chabaudi are widely used model malaria specie

12 sed the nonlethal malaria infection model of Plasmodium chabaudi AS in combination with the gastroint

13 Plasmodium chabaudi AS infection during early pregnancy

14 We investigated this question for Plasmodium chabaudi AS infection in C57BL/6 mice.

15 intain long-term protective immunity against Plasmodium chabaudi AS malaria.

16 erythropoiesis, A/J mice were infected with Plasmodium chabaudi AS, treated with intravenous ferric

17 his study, the roles of IFN-gamma and TNF in Plasmodium chabaudi AS-induced fetal loss in mice were d

18 ized (gdx) C57BL/6 mice were inoculated with Plasmodium chabaudi AS-infected erythrocytes, and the re

19 ice, similar to our previous observations in Plasmodium chabaudi AS-infected mice.

20 verity and parasitemia in mice infected with Plasmodium chabaudi AS.

21 enesis of malaria during pregnancy using the Plasmodium chabaudi AS/C57BL/6 mouse model.

22 etitive suppression of an avirulent clone of Plasmodium chabaudi (AS) by a virulent clone (AJ) in imm

23 Immunization with Plasmodium chabaudi by mosquito bite under chloroquine c

24 oplast genome of the rodent malaria parasite Plasmodium chabaudi chabaudi (Pcc) isolate CB was charac

25 Blood-stage Plasmodium chabaudi chabaudi AS infection requires cell-

26 rus (HIV) transgenic mice were infected with Plasmodium chabaudi chabaudi clone AS.

27 ned "strains" of the rodent malaria parasite Plasmodium chabaudi chabaudi in mice.

28 The rodent malaria parasite Plasmodium chabaudi chabaudi shares many features with h

29 virus Ankara vectors encoding AMA1 from the Plasmodium chabaudi chabaudi strain AS.

30 ransmission of serially blood passaged (SBP) Plasmodium chabaudi chabaudi to interrogate regulation o

31 gmodontis) and noncerebral malaria (clone AS Plasmodium chabaudi chabaudi), we quantified disease sev

32 to clear a primary erythrocytic infection of Plasmodium chabaudi chabaudi.

33 acid synthesis (FAS) in Tmem development in Plasmodium chabaudi chronic mouse malaria infection.

34 ed at peak parasitemia during infection with Plasmodium chabaudi Concentrations of the closely relate

35 hly purified antigen on the malaria parasite Plasmodium chabaudi evolving in laboratory mice.

36 with experimental data in mice infected with Plasmodium chabaudi, finding that dying mice trace a lar

37 ng early infection with the malaria parasite Plasmodium chabaudi, implying that another MYD88-depende

38 We examine the rodent malaria Plasmodium chabaudi in laboratory mice, a parasite-host

39 ocytic stages of the rodent-malaria parasite Plasmodium chabaudi in vivo.

40 these CD4 T cell responses in the spleens of Plasmodium chabaudi-infected mice.

41 During Plasmodium chabaudi infection in mice, a population of C

42 Blood-stage Plasmodium chabaudi infections are suppressed by antibod

43 uppress the parasitemia of acute blood-stage Plasmodium chabaudi malaria by an antibody- or T-cell-de

44 of splenic gammadelta T cells during chronic Plasmodium chabaudi malaria.

45 We outline here the parallels between the Plasmodium chabaudi mouse model of malaria and human mal

46 Using the Plasmodium chabaudi mouse model of malaria and immunizat

47 Artemisinin- and artesunate-resistant Plasmodium chabaudi mutants, AS-ART and AS-ATN, were pre

48 viously that chronic exposure to blood-stage Plasmodium chabaudi offers the best protection from para

49 e now report that the time course shows that Plasmodium chabaudi parasitemia in NADPH oxidase KO (p47

50 The production of NO during descending Plasmodium chabaudi parasitemia, a period when parasites

51 s an important fitness-determining trait and Plasmodium chabaudi parasites adjust their sex allocatio

52 ng infection of the HIV-transgenic mice with PLASMODIUM: chabaudi parasites.

53 rasitic disease and lymphomagenesis, we used Plasmodium chabaudi (Pc) to produce chronic malaria infe

54 e have reported that isolated, permeabilized Plasmodium chabaudi, releases Ca(2+) upon addition of ex

55 Infection of MIF knockout mice with Plasmodium chabaudi resulted in less severe anemia, impr

56 ne expression profiles in mice infected with Plasmodium chabaudi revealed and validated similar respo

57 o real data from mice infected with a single Plasmodium chabaudi strain, we estimate that transmissio

58 f two strains of the rodent malaria parasite Plasmodium chabaudi that differ in virulence.

59 for the merozoite surface protein (MSP)-1 of Plasmodium chabaudi to show that activated T cells gener

60 Using the rodent model of malaria, Plasmodium chabaudi, we show that individual CIR protein

61 -term artificial selection for resistance in Plasmodium chabaudi, we tested resilience of WP against

62 zed red blood cells from the rodent parasite Plasmodium chabaudi with seco-cyclopropyl pyrrolo indole