ライフサイエンスコーパス: Leishmania mexicana

1 n analogy to the enzyme in the crystals from Leishmania mexicana.

2 -protection against cutaneous lesion-causing Leishmania mexicana.

3 n vivo responses to cutaneous infection with Leishmania mexicana.

4 primitive trypanosomatid pathogen of humans, Leishmania mexicana.

5 gues from the eukaryotic protozoan parasite, Leishmania mexicana.

6 ypanosoma brucei, Trypanosoma congolense and Leishmania mexicana.

7 n vivo, ICOS-/- mice were infected s.c. with Leishmania mexicana.

8 two human parasites; Trypanosoma brucei and Leishmania mexicana.

9 ic parasites including Trypanosoma cruzi and Leishmania mexicana.

10 transporter genes in the parasitic protozoan Leishmania mexicana.

11 mmetric localisation in the related parasite Leishmania mexicana.

12 y application to captured videomicroscopy of Leishmania mexicana, a parasitic monoflagellate of the f

13 Leishmania mexicana amastigotes are particularly rich in

14 the past, ultrastructural investigations of Leishmania mexicana amastigotes revealed structures that

15 n 3 and 6 days after a blood feed containing Leishmania mexicana amastigotes.

16 ellular integrity of the macrophage parasite Leishmania mexicana amazonensis from intraphagolysosomal

17 Virulent and avirulent clones of Leishmania mexicana amazonensis promastigotes or amastig

18 hat inhibit the growth of Trypanosoma cruzi, Leishmania mexicana amazonensis, and Pneumocystis carini

19 in that is an essential virulence factor for Leishmania mexicana and can be targeted by small-molecul

20 1 substrate calcein AM were examined in both Leishmania mexicana and L. enriettii LeMDR1 -/- and over

21 nes exhibited excellent potency against both Leishmania mexicana and Leishmania donovani parasites wi

22 a brucei (T. brucei), Trypanosoma cruzi, and Leishmania mexicana and that protein farnesyltransferase

23 recursors, the arginase gene was cloned from Leishmania mexicana, and Deltaarg null mutants were crea

24 es of Trypanosoma brucei, Trypanosoma cruzi, Leishmania mexicana, and human GAPDH's provided details

25 w World Leishmania (Leishmania braziliensis, Leishmania mexicana, and Leishmania donovani).

26 llular organisms including Leishmania major, Leishmania mexicana, and Listeria monocytogenes.

27 Leishmania mexicana are parasitic protozoa that express

28 anosomatids T. brucei, Trypanosoma cruzi and Leishmania mexicana are quite similar to each other, and

29 the flagellum of the kinetoplastid parasite Leishmania mexicana, but the mechanism for targeting thi

30 The structures of Leishmania mexicana cofactor-independent phosphoglycerat

31 sis associated with infection by Leishmania (Leishmania mexicana complex and L. donovani) has been es

32 at maintenance of Leishmania infections with Leishmania mexicana complex parasites (Leishmania amazon

33 lex (P8 PGLC) is a glyconjugate expressed by Leishmania mexicana complex parasites.

34 l for protection against Leishmania pifanoi (Leishmania mexicana complex).

35 gluconeogenesis by generating the respective Leishmania mexicana Deltagk, Deltapepck, and Deltappdk n

36 K, TOR1, IFT88, IFT139, IFT140, and RAB5A in Leishmania mexicana, demonstrating a significant improve

37 pathogens such as Listeria monocytogenes and Leishmania mexicana did not induce the soluble inhibitor

38 The cpb genes of Leishmania mexicana encode stage-regulated, cathepsin L-

39 The genome of Leishmania mexicana encompasses a cluster of three gluco

40 C3H mice infected with Leishmania mexicana fail to develop a protective Th1 res

41 crystal structures of human, T. brucei, and Leishmania mexicana glyceraldehyde-3-phosphate dehydroge

42 The ternary complex structure of Leishmania mexicana GPDH (LmGPDH) with dihydroxyacetone

43 Leishmania mexicana has a large family of cyclin-depende

44 neous leishmaniasis caused by infection with Leishmania mexicana has been reported from Texas and Okl

45 Previous studies in Leishmania mexicana have identified the cytoskeletal pro

46 ckouts of L. donovani HSP78 (LdHSP78+/-) and Leishmania mexicana HSP78 (LmxHSP78+/-) were generated u

47 Recent data suggest that Leishmania mexicana ICP plays an important role in host-

48 ase (GAPDH) from the trypanosomatid parasite Leishmania mexicana in a new crystal form has been deter

49 orter null mutant of the parasitic protozoan Leishmania mexicana, in which three linked glucose trans

50 Here we analyse the inocula from Leishmania mexicana-infected Lutzomyia longipalpis sand

51 h upon activation in vitro as well as during Leishmania mexicana infection.

52 ls that express CXCR3 from one allele during Leishmania mexicana infection.

53 Leishmania mexicana infections in C57BL/6 mice are assoc

54 Leishmania mexicana is a protozoan parasite of the order

55 Infection of C57BL/6 (B6) mice with Leishmania mexicana is associated with a minimal immune

56 ynamics analysis of the pyruvate kinase from Leishmania mexicana is presented in the absence and pres

57 roscopy to image swimming cells of different Leishmania mexicana life cycle stages in three dimension

58 nown function had expression patterns in the Leishmania mexicana life cycle suggesting their involvem

59 ort X-ray structures of pyruvate kinase from Leishmania mexicana (LmPYK) that are trapped in differen

60 In contrast, Ilg and colleagues showed that Leishmania mexicana LPG2 mutants retained virulence for

61 braziliensis (n = 7), L. panamensis (n = 5), Leishmania mexicana (n = 1), Leishmania infantum (n = 3)

62 eral steps of the infectious cycle but, with Leishmania mexicana, no effect on virulence was found.

63 een the microtubule axoneme structure of the Leishmania mexicana parasite infecting a macrophage and

64 red for chronic disease in C57BL/6 mice with Leishmania mexicana parasite infection.

65 In Leishmania mexicana parasites, a unique glucose transpor

66 ions of macrophages by promastigote forms of Leishmania mexicana pifanoi induce the production of sup

67 inome-wide gene deletion and gene tagging in Leishmania mexicana promastigotes to define protein kina

68 Leishmania mexicana promastigotes with an MPK2 deletion

69 oteophosphoglycans from Leishmania major and Leishmania mexicana proteophosphoglycans has been develo

70 ase of mice caused by the protozoan parasite Leishmania mexicana requires interleukin-10 (IL-10) and

71 By generating profilin knockout and knockin Leishmania mexicana strains, we show that profilin is im

72 a intimate that parasite-encoded arginase of Leishmania mexicana subverts macrophage microbicidal act

73 r tropical pathogens, Trypanosoma brucei and Leishmania mexicana, the causative agents of African sle

74 We have shown that Leishmania mexicana undergoes large changes in morpholog

75 mutants for the crk1 Cdc2-Related Kinase of Leishmania mexicana was attempted using targeted gene di

76 The cutaneous growth of Leishmania mexicana was measured in STAT6-deficient mice

77 functional annotation community resource for Leishmania mexicana, where deletion mutant growth in vit

78 In murine infection, Leishmania mexicana, which lives intracellularly in host