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1 late that replicates in the amoeboflagellate Naegleria.
2 cillaene, and difficidin) in the presence of Naegleria.
3              In subsequent transfers, axenic Naegleria amebas and, later, tissue cultures (monkey kid
4 ween Pseudomonas fluorescens and the protist Naegleria americana.
5                   Previous studies show that Naegleria amoebae express a divergent alpha-tubulin duri
6 tubulin during mitosis, and we now show that Naegleria amoebae express a second mitotic alpha- and tw
7                                              Naegleria amoebae lack a cytoplasmic microtubule cytoske
8 ike nearly all other known eukaryotic cells, Naegleria amoebae lack interphase microtubules; this sug
9                          We demonstrate that Naegleria, an amoeba from the Heterolobosea-an evolution
10  small subunit rRNA precursor of the protist Naegleria andersoni.
11 t origin for these processes and establishes Naegleria as a natural model system for studying microtu
12 o build distinct microtubule networks: while Naegleria builds flagella from conserved tubulins during
13 y, and molecular perturbations, we show that Naegleria encodes conserved actin nucleators and builds
14                                The genome of Naegleria encodes homologues of mammalian DNA methyltran
15                  Our study demonstrates that Naegleria enhances plant health by predating on pathogen
16   Population dynamics tracking revealed that Naegleria enriched Bacillus populations, leading to a po
17            In contrast, the amoeboflagellate Naegleria expresses distinct tubulin genes to build dist
18  other known pathogenic free-living amoebas (Naegleria fowleri and Acanthamoeba species), drug discov
19                                              Naegleria fowleri associated with biofilm and biological
20                                              Naegleria fowleri causes an acute and rapidly fatal cent
21                                              Naegleria fowleri causes an uncommon but deadly disease
22 ation from a boy who had died of undiagnosed Naegleria fowleri infection.
23                       The free-living amoeba Naegleria fowleri is a causative agent of primary amoebi
24                                              Naegleria fowleri is a climate-sensitive, thermophilic a
25                                              Naegleria fowleri is a climate-sensitive, thermophilic a
26      Developing drugs for brain infection by Naegleria fowleri is an unmet medical need.
27 amoebic meningoencephalitis (PAM) induced by Naegleria fowleri is extremely lethal, with mortality ra
28                                              Naegleria fowleri is the causative agent of primary amoe
29                                              Naegleria fowleri is the protozoan pathogen that causes
30 s (PAM) is a human brain infection caused by Naegleria fowleri with a 97% mortality rate.
31                         Infections caused by Naegleria fowleri, Acanthamoeba spp., and Balamuthia man
32                 Free-living amoebae, such as Naegleria fowleri, Acanthamoeba spp., and Vermamoeba spp
33 amoeba species, Balamuthia mandrillaris, and Naegleria fowleri, are known to cause infections of the
34 litis (PAM), caused by the free-living ameba Naegleria fowleri, has historically been associated with
35 ubulin homologs of the "brain-eating amoeba" Naegleria fowleri, making them potential drug targets.
36                                              Naegleria fowleri, the causative agent of primary amebic
37 genus comprises the notorious human pathogen Naegleria fowleri, the causative agent of the rare but f
38 caused by the thermophilic free-living ameba Naegleria fowleri.
39 Pi-PFK of the mitochondriate heterolobosean, Naegleria fowleri.
40 al condition caused by the free-living ameba Naegleria fowleri.
41                                          The Naegleria genome facilitates substantially broader phylo
42                                          The Naegleria genome, analyzed in the context of other proti
43 P1 CKK domain (HsCKK) with a CKK domain from Naegleria gruberi (NgCKK), which lacks minus-end specifi
44  different eukaryotic lineages: the discoban Naegleria gruberi and the amoebozoan slime mold Dictyost
45             The free-living amoeboflagellate Naegleria gruberi belongs to a varied and ubiquitous pro
46                                              Naegleria gruberi is a unicellular eukaryote whose evolu
47 nase I of the single-celled amoeboflagellate Naegleria gruberi is the only eukaryotic thiaminase I to
48  The genome sequence of the amoeboflagellate Naegleria gruberi reported by Fritz-Laylin et al. reveal
49                                              Naegleria gruberi RNA ligase (NgrRnl) exemplifies a fami
50                                              Naegleria gruberi RNA ligase (NgrRnl) exemplifies the Rn
51 d the activity of the mouse TET1 (mTET1) and Naegleria gruberi TET (nTET) oxygenases with DNA substra
52  of a TET-like (5m)C oxygenase (NgTET1) from Naegleria gruberi, a single-celled protist evolutionaril
53 and TET1 from mouse and their homologue from Naegleria gruberi, the full-length protein NgTET1, are d
54 f life, from mammals to the amoeboflagellate Naegleria gruberi.
55 uding in the heterolobosean amoeboflagellate Naegleria gruberi.
56 elta24 sterol reductase from the soil amoeba Naegleria gruberi.
57 NiV), and show its unique adaptations to its Naegleria host using fluorescence in situ hybridization,
58              NiV has acquired genes from its Naegleria host, which code for heat shock proteins and a
59            The diversity of RGS domains from Naegleria in particular, which has the largest complemen
60 les of selected pathogenic and nonpathogenic Naegleria in vitro using an untargeted metabolomics appr
61                                Additionally, Naegleria increases SynCom biofilm biomass by 2.44 times
62 ed for infection of Willaertia magna but not Naegleria lovaniensis, suggesting that Cas2 promotes inf
63 is also critical for infection of the amoeba Naegleria lovaniensis.
64  Ectocarpus, Emiliania, Euglena, Micromonas, Naegleria, Nephroselmis, Paramecium, Pavlova, Phaeodacty
65 ments, we find that the SynCom together with Naegleria provided significantly greater suppression of
66 h as Clostridium, Cryptococcus, Candida, and Naegleria, reported in one or more of the wetlands asses
67  sexually, many amoebae (e.g., Acanthamoeba, Naegleria) reproduce asexually and therefore, according
68 f the 15,727 protein-coding genes encoded by Naegleria's 41 Mb nuclear genome indicates a capacity fo
69  quantitative light microscopy, we find that Naegleria's mitotic spindle is a distinctive barrel-like
70           Similar to those of other species, Naegleria's spindle is twisted, and its length increases
71      Here, we examine how two soil protists (Naegleria sp. and Cercomonas sp.) affect the pathogen Ra
72     Notably, NiV infection was lethal to all Naegleria species tested, including the human pathogen N
73 ., 21 were Hartmannella vermiformis, 13 were Naegleria spp., and one was Vanella spp.
74 entify previously unknown Ggamma subunits in Naegleria, suggesting that the trimeric version was alre
75             Like mammalian Tet proteins, the Naegleria Tet-like protein, NgTet1, acts on 5-methylcyto
76 dy biochemically and structurally one of the Naegleria Tet-like proteins (NgTet1), which shares signi
77                                              Naegleria therefore represents a powerful system to prob
78 ted during only one process, suggesting that Naegleria uses distinct component pools to specialize it
79       Outside of these groups lies the genus Naegleria, which shared a common ancestor with humans >1