ライフサイエンスコーパス: Leishmania mexicana

1 two human parasites; Trypanosoma brucei and Leishmania mexicana.

2 n vivo responses to cutaneous infection with Leishmania mexicana.

3 primitive trypanosomatid pathogen of humans, Leishmania mexicana.

4 gues from the eukaryotic protozoan parasite, Leishmania mexicana.

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

6 ic parasites including Trypanosoma cruzi and Leishmania mexicana.

7 transporter genes in the parasitic protozoan Leishmania mexicana.

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

9 -protection against cutaneous lesion-causing Leishmania mexicana.

10 Leishmania mexicana amastigotes are particularly rich in

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

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

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

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

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

16 1 substrate calcein AM were examined in both Leishmania mexicana and L. enriettii LeMDR1 -/- and over

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

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

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

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

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

22 Leishmania mexicana are parasitic protozoa that express

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

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

25 The structures of Leishmania mexicana cofactor-independent phosphoglycerat

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

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

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

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

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

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

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

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

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

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

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

37 Leishmania mexicana has a large family of cyclin-depende

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

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

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

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

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

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

44 Leishmania mexicana infections in C57BL/6 mice are assoc

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

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

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

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

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

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

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

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

53 In Leishmania mexicana parasites, a unique glucose transpor

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

55 Leishmania mexicana promastigotes with an MPK2 deletion

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

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

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

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

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

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

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

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