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1 application to the phage-infected bacterial lawn.
2 ks inscribed as they move through an E. coli lawn.
3 ans starts to vacate the pathogenic bacteria lawn.
4 indicated by plaque formation in a bacterial lawn.
5 , also failed to produce plaques on a mutant lawn.
6 cula of 10(5)-10(6) cells per plate formed a lawn.
7 ofilm matrix as they move through a Yersinia lawn.
8 nd generated the largest plaques on the slyD lawn.
9 mutants of phi X174 were isolated on a slyD lawn.
10 these amoebae and leave an intact bacterial lawn.
11 with best growth on membranes over "helper" lawns.
12 nifera) appeared to migrate more easily into lawns.
13 thodologies, with emission rates greatest in lawns.
14 igration, forming large plaques on bacterial lawns.
15 bacteria and form plaques in their bacterial lawns.
16 lopment and display slow growth on bacterial lawns.
17 Solitary foragers move slowly on a bacterial lawn and disperse across it, while social foragers move
20 er, we create well-defined replicates of the lawn and quantitatively study the population expansion o
21 utant, which does not aggregate on bacterial lawns and arrests as loose mounds on nitrocellulose filt
22 face flows (primarily from overirrigation of lawns and ornamental plants) harbor FIB at concentration
23 uburban neighborhoods (e.g., from forests to lawns and ornamental plants) increase the distribution o
25 types (evergreen trees, deciduous trees and lawn) and (ii) different ages (constructed 10, approxima
26 had a specific swarm rate reduction on prey lawns, and thus reduced fitness, compared to an isogenic
27 the dominant lawn fluxes, and the fact that lawns are unlikely to dry out, climate warming may subst
30 y clear circular zones of lysis on bacterial lawns at the site of gamma phage inoculation after incub
31 of sensory neurons to inhibit P. aeruginosa lawn avoidance behaviour through inhibition of the neuro
35 one and in combination was evaluated against lawn biofilms of bioluminescent strains of Staphylococcu
38 nts do not aggregate in plaques on bacterial lawns, but they do proceed further in development on nit
39 teria, form visible lesions within bacterial lawns (called plaques), which are employed ubiquitously
50 uipped with a three-way catalytic converter, lawn equipment, utility vehicles, urban buses, semitruck
51 ubwatersheds of the Mississippi River in St. Lawn fertilizer and pet waste dominated N and P inputs,
53 rong temperature sensitivity of the dominant lawn fluxes, and the fact that lawns are unlikely to dry
56 ental phosphorylation of an NDC80 molecular "lawn," in which the NDC80-MT bonds reorganize dynamicall
57 microtopographical subunits (sedge-dominated lawns, interhummocks and hummocks) within an aapa mire i
58 at do form when cells are grown on bacterial lawns lack the one- and two-dimensional symmetries so ap
61 ere more likely than controls to have used a lawn mower or brush cutter in the two weeks before the i
62 ak of primary pneumonic tularemia implicates lawn mowing and brush cutting as risk factors for this i
64 entiation involving the formation of a dense lawn of aerial hyphae that grow away from the colony sur
65 often visualized as plaques, or holes, in a lawn of bacteria on an agar-filled Petri dish; however,
66 s of a synthetic sensor kinase that allows a lawn of bacteria to function as a biological film, such
69 myces coelicolor involves the formation of a lawn of hair-like aerial hyphae on the colony surface th
73 (OS-Seq), in which we modify the immobilized lawn of oligonucleotide primers of a next-generation DNA
77 s die with similar kinetics when placed on a lawn of S. typhimurium for a relatively short time (3-5
79 ngless or armadillo mutant embryos secrete a lawn of ventral denticles; armadillo mutants also exhibi
81 ragments should be able to form plaques on a lawn of wild-type Escherichia coli (i.e., lacking supF).
83 -containing cells on solid medium containing lawns of bacteria of the same (plasmid-containing) strai
84 We found that for N2 worms grown on mixed lawns of bacteria, Salmonella enterica serovar Typhimuri
87 multiple life cycles of amoebae grown on the lawns of other bacteria, thus demonstrating a stable rel
88 we allowed Caenorhabditis elegans to feed on lawns of P. aeruginosa PAO1 grown on high and low phosph
90 rnema jollieti nematodes cultivated on mixed lawns of X. bovienii expressing green or DsRed fluoresce
91 ill able to predate when directly applied to lawns of YFP-labelled prey bacteria, showing that flagel
92 imensional propagation of viruses through a "lawn" of receptive hosts, commonly called plaque growth,
93 ork variants, an initially undifferentiated 'lawn' of receivers is engineered to form a bullseye patt
94 ent P. aeruginosa strains, the bacteria form lawns on these plates with amoebae embedded in them.
96 cted by whether the upland being invaded was lawn or wooded, but the marsh-edge plant communities tha
97 The carbohydrate is present in bacterial lawns prior to addition of nematodes, indicating that bi
99 n a spatially heterogeneous Escherichia coli lawn serves as an experimental model system to study pop
102 of this source by studying decomposition in lawns, street gutters, and catch basins during two winte
105 nclude typical ecosystems in suburban yards: lawn, trees, water reservoirs, and a vegetable garden; t
106 tap water that was used to supply water to a lawn water slide on which the child had played extensive
109 on showed improved robustness when bacterial lawns were tested with high- and low-density inoculum us
110 retained the ability to grow as a confluent lawn, while seven grew only as single colonies around Hb
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