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1 t phenotype (REP) in the free-living amoeba, Acanthamoeba castellanii.
2 intracellular growth in the unicellular host Acanthamoeba castellanii.
3 on of antifungal drugs in the human pathogen Acanthamoeba castellanii.
4 nea and Cbu.L1951 from lower eukaryotes like Acanthamoeba castellanii.
5 ic cell line U937 and the environmental host Acanthamoeba castellanii.
6 hamsters resistant to corneal infection with Acanthamoeba castellanii.
7 red for full virulence in the protozoan host Acanthamoeba castellanii.
8 viously for this fungus with macrophages and Acanthamoeba castellanii.
9 a genes necessary for survival in the amoeba Acanthamoeba castellanii.
10 r steroids could affect the pathogenicity of Acanthamoeba castellanii.
11 could not replicate within a protozoan host, Acanthamoeba castellanii.
12 ntial protozoan host, the water-borne amoeba Acanthamoeba castellanii.
13 nd structural characterization of CYP51 from Acanthamoeba castellanii.
14 L. pneumophila virulence in the amoeban host Acanthamoeba castellanii.
15           Infection of EpiCorneal cells with Acanthamoeba castellanii 50493 and A. polyphaga 50372 le
16 r intracellular growth in the protozoan host Acanthamoeba castellanii, a well-established important e
17                                 Among these, Acanthamoeba castellanii, A. polyphaga, and A. hatchetti
18 tected by certain individual assays included Acanthamoeba castellanii, Acanthamoeba culbertsoni, and
19 at five FLA species (Acanthamoeba polyphaga, Acanthamoeba castellanii, Acanthamoeba lenticulata, Verm
20 single-headed monomeric myosin I isozymes of Acanthamoeba castellanii (AMIs)-AMIA, AMIB, and AMIC-are
21 decreased by nearly 3 orders of magnitude in Acanthamoeba castellanii amoebae and nearly 2 orders of
22 with the P450 gene products we identified in Acanthamoeba castellanii, an amoeba host for many giant
23 atest overall inhibition for all isolates of Acanthamoeba castellanii and Acanthamoeba polyphaga test
24  against two potentially pathogenic species, Acanthamoeba castellanii and Acanthamoeba polyphaga, and
25 umophila promotes intracellular infection of Acanthamoeba castellanii and Hartmannella vermiformis, t
26 cells, including macrophages and the amoebae Acanthamoeba castellanii and Hartmannella vermiformis.
27                      Following encystment in Acanthamoeba castellanii and reversion of cysts to amoeb
28 copy and three-dimensional reconstruction of Acanthamoeba castellanii and Saccharomyces cerevisiae Ar
29  actin purified from rabbit skeletal muscle, Acanthamoeba castellanii, and Saccharomyces cerevisiae i
30 e activities of the myosin I isoenzymes from Acanthamoeba castellanii are greatly increased by phosph
31       Pathogenic free-living amoebae such as Acanthamoeba castellanii are present in soil and water w
32                                        Using Acanthamoeba castellanii as a FLA host, the priming effe
33 nisms revealed a predation strategy in which Acanthamoeba castellanii assemble L. monocytogenes in ag
34   The Arp2/3 complex was first purified from Acanthamoeba castellanii by profilin affinity chromatogr
35 ization mode in CYP51 from a human pathogen, Acanthamoeba castellanii CYP51 (AcCYP51).
36 ir L. pneumophila growth in the amoebal host Acanthamoeba castellanii, demonstrating a host-specific
37 sent study was designed to determine whether Acanthamoeba castellanii derived from an infected human
38     This clade B marseillevirus was found in Acanthamoeba castellanii from a composting soil sample i
39                             For example, the Acanthamoeba castellanii homolog directly regulates 5S R
40                 Pathogenic mycobacteria lyse Acanthamoeba castellanii in an Esx-1-dependent manner.
41 coded Stx efficiently kills the bacteriovore Acanthamoeba castellanii in co-culture.
42 n intracellular multiplication in the amoeba Acanthamoeba castellanii, indicating that certain dotA/B
43 la was also phagocytosed more efficiently by Acanthamoeba castellanii, indicating that the process is
44 stinct hosts, the mutants were evaluated for Acanthamoeba castellanii invasion.
45                                              Acanthamoeba castellanii is a ubiquitous free-living amo
46             Myosin I heavy chain kinase from Acanthamoeba castellanii is activated in vitro by autoph
47                                              Acanthamoeba castellanii is an amoeba that inhabits soil
48 MS), we demonstrate that the major sterol of Acanthamoeba castellanii is ergosterol and identify nove
49 f the TATA box binding protein (TBP) gene in Acanthamoeba castellanii is regulated by TATA box bindin
50                  The opportunistic pathogen, Acanthamoeba castellanii is the causative agent for the
51 ila grown in one of its environmental hosts, Acanthamoeba castellanii, is phenotypically different fr
52            Here we report that the eukaryote Acanthamoeba castellanii lacks the G(-1) identity elemen
53           The animals were then infected via Acanthamoeba castellanii-laden contact lenses.
54                                              Acanthamoeba castellanii mannose-binding protein (MBP) m
55       We describe a quantitative analysis of Acanthamoeba castellanii myosin II rod domain images col
56 catalytic motor domain of the heavy chain of Acanthamoeba castellanii myosin-2 and the phosphomimetic
57                                          The Acanthamoeba castellanii myosin-Is were the first unconv
58    Infection in murine macrophages, amoebae (Acanthamoeba castellanii), nematodes (Caenorhabditis ele
59 eplicated less efficiently in phytate-loaded Acanthamoeba castellanii or Dictyostelium discoideum, an
60 in this group, which is capable of infecting Acanthamoeba castellanii Pacmanvirus A23 has a linear co
61 closest homolog in Pandoraviruses and 10% in Acanthamoeba castellanii probably through horizontal gen
62  examined possible mechanisms to explain why Acanthamoeba castellanii remains restricted to the corne
63 pstream elements of the exceptionally strong Acanthamoeba castellanii ribosomal RNA core promoter, to
64             In the small, free-living amoeba Acanthamoeba castellanii, rRNA transcription requires, i
65  of L. pneumophila by the free-living amoeba Acanthamoeba castellanii shows many similarities to the
66        We discovered that the enzyme target [Acanthamoeba castellanii sterol 14alpha-demethylase (AcC
67 rowth in HL-60-derived human macrophages and Acanthamoeba castellanii, the lvh system was found to be
68 f amino acids from the natural host organism Acanthamoeba castellanii to Legionella pneumophila under
69                                              Acanthamoeba castellanii transcription initiation factor
70 ft] were tested for their efficacies against Acanthamoeba castellanii trophozoites and cysts by using
71                                         When Acanthamoeba castellanii trophozoites are grown in methy
72                                              Acanthamoeba castellanii trophozoites were grown in pept
73 , has been purified to near homogeneity from Acanthamoeba castellanii using standard techniques.
74                                              Acanthamoeba castellanii were exposed to varying strengt
75 -2006 keratitis outbreak and trophozoites of Acanthamoeba castellanii were inoculated into commercial
76 legionellae for their capacity to parasitize Acanthamoeba castellanii Whereas the mutant behaved norm
77 that Cn is phagocytosed by and replicates in Acanthamoeba castellanii, which leads to death of amoeba
78 le to multiply within the free-living amoeba Acanthamoeba castellanii yet was able to kill HL-60-deri
79 panosoma cruzi and the eukaryote crown group Acanthamoeba castellanii yielded two distinct alpha prot