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1  fruit flies, nematodes, carpenter ants, and slime mold.
2 otility and phagocytosis in animal cells and slime molds.
3  of heart muscle to the self-organization of slime molds.
4 ous media or plasmodial shuttle streaming in slime molds.
5  present in orthologs of animals or cellular slime molds.
6 matid and apicomplexan parasites, algae, and slime molds.
7 aryotes including animals, plants, fungi and slime molds.
8 ubstances affect the exploration behavior of slime molds; (2) Nutritive and adverse substances both s
9 , trypanosomes, Giardia, ciliates, alga, and slime molds [3-8].
10 are different from the waves observed during slime mold aggregation that depend on diffusible morphog
11 ns are also present in zebrafish, nematodes, slime mold and plants.
12 lants, chlorophyte green algae, demosponges, slime molds and brown algae.
13 s explain how network-forming organisms like slime molds and fungi thrive in complex environments.
14 orly understood feature of organisms such as slime molds and fungi.
15 gesting a phylogenetic link between cellular slime molds and true fungi.
16 ority of eukaryotes (fungi, plants, animals, slime mold, and euglena) synthesize Asn-linked glycans (
17 mans was shown to interact with macrophages, slime molds, and amoebae in a similar manner, suggesting
18 matid and apicomplexan parasites, algae, and slime molds, and have also been found in the bacterium A
19 er social insects to include immune systems, slime molds, and microbiomes.
20 ental responses in bacteria, Archaea, fungi, slime molds, and plants.
21 und in eukaryotic organisms including fungi, slime molds, and plants.
22 bees, multiple queen-founding ants, cellular slime molds, and social bacteria).
23 restingly, simple organisms such as cellular slime mold appear exclusively on one branch, bilaterians
24 ells into a migratory slug phase in cellular slime molds at times of starvation.
25 xtract the network topology and followed the slime molds before and after fusion.
26 xin sequences present in animals, fungi, and slime molds began prior to the divergence of these taxa.
27                   Our results show that: (1) slime molds build sparse networks with thin veins in a n
28          Our data shows that a single-celled slime mold can control its gene expression in a region-s
29                                     A single slime mold can precipitate up to a gram of HACC over the
30 spiration comes from Physarum, a unicellular slime mold capable of solving the traveling salesman and
31 s in a nutritive or adverse environment; (2) slime molds construct long, efficient and resilient netw
32                        Dictyostelid cellular slime molds (dictyostelids) are key components of soil m
33 ad are closely related to pks genes from the slime mold Dictyostelium and eubacteria.
34 consistent with the behavior of the cellular slime mold Dictyostelium discodeum, which switches from
35 cular system, the slug stage of the cellular slime mold Dictyostelium discoideum (Dd).
36  the rep B and rep D genes from the cellular slime mold Dictyostelium discoideum .
37                                 The cellular slime mold Dictyostelium discoideum has long been recogn
38                                 The cellular slime mold Dictyostelium discoideum is a widely used mod
39                                 The cellular slime mold Dictyostelium discoideum is an attractive sys
40           In the development of the cellular slime mold Dictyostelium discoideum there is a stage in
41                  Our findings identified the slime mold Dictyostelium discoideum's CISD proteins as t
42 sely related to the annexin homologue of the slime mold Dictyostelium discoideum, suggesting a phylog
43  CBM8 family member (CBM8), DdCBM8, from the slime mold Dictyostelium discoideum, which was identifie
44 iscoban Naegleria gruberi and the amoebozoan slime mold Dictyostelium discoideum.
45 ified in a eukaryotic microbe (protist), the slime mold Dictyostelium discoideum.
46 he multicellular development of the cellular slime mold Dictyostelium discoideum.
47 tical for proper development in the cellular slime mold Dictyostelium.
48 tion relationships of dynein in the cellular slime mold Dictyostelium.
49                           In particular, the slime-mold Dictyostelium, the protozoan Trichomonas vagi
50 udding yeast (Saccharomyces cerevisiae), two slime molds (Dictyostelium discoideum and Physarum polyc
51                                 The cellular slime mold, Dictyostelium discoideum is a non-metazoan o
52  studies on PHD homologues from the cellular slime mold, Dictyostelium discoideum, and the protozoan
53                         Because the cellular slime mold, Dictyostelium discoideum, is a genetically t
54 tantly related nematode species and from the slime mold, Dictyostelium discoideum.
55 ehavior coaggregate, cross-signaling impacts slime-mold diversity across spatiotemporal scales.
56  we characterize the network organization of slime molds exploring homogeneous neutral, nutritive and
57 s in this region to nematode talin, cellular slime mold filopodin, and an Sla2 homolog from nematode.
58  ACC (HACC) precipitated by the cosmopolitan slime mold Fuligo septica (L.) F.H. Wigg.
59 ribed also in non-metazoan organisms such as slime molds, fungi and plants.
60 orter and more centralized networks; and (3) slime molds fuse rapidly and establish multiple connecti
61    However, some eukaryotic protists such as slime molds generate diverse and complex structures whil
62                                   Plasmodial slime molds grow as networks and use flexible, undiffere
63 ciation imparts the extreme stability of the slime mold HACC by inhibiting loss of H(2)O and subseque
64                New evidence from a primitive slime mold, however, suggests that alpha- and beta-caten
65                                     Cellular slime molds, including the well-studied Dictyostelium di
66           Dictyostelium discoideum, a social slime mold, is one of a few eukaryotes known to possess
67                   Our results also show that slime molds migrate at a rate governed by the substrate
68                  Our study demonstrates that slime mold networks evolve continuously via pruning and
69                                          How slime molds networks are built and fuse to allow for eff
70                                     Cellular slime molds of the genus Polysphondylium periodically re
71                                More broadly, slime molds offer the extraordinary opportunity to explo
72                   We show that the brainless slime mold Physarum polycephalum constructs a form of sp
73 contrast to other unicellular organisms, the slime mold Physarum polycephalum forms a giant network-s
74                                          The slime mold Physarum polycephalum grows as a random netwo
75 formed spatial transcriptome analysis of the slime mold Physarum polycephalum in the plasmodium state
76                                The acellular slime mold Physarum polycephalum provides an excellent m
77     We here follow how the giant unicellular slime mold Physarum polycephalum responds to a nutrient
78                              Among them, the slime mold Physarum polycephalum, a giant single cell, i
79 endonuclease, a homing endonuclease from the slime mold Physarum polycephalum, is a small enzyme (2 x
80 ase, an intron-encoded endonuclease from the slime mold Physarum polycephalum, is a small enzyme (2 x
81 sion of signals among decentralized units in slime mold Physarum polycephalum, we introduce a combina
82                    Nuclei in G2 phase of the slime mold Physarum polycephalum, when transplanted, by
83 apply the method to the mitochondrion of the slime mold Physarum polycephalum.
84  is encoded by a group I intron found in the slime mold Physarum polycephalum.
85 ere, we report a remarkable exception in the slime mold Physarum polycephalum.
86 fungi to single-celled organisms such as the slime mold Physarum polycephalum.
87 prevent the formation of pseudopods; and (3) Slime mold placed in an adverse environment preferential
88                              In the cellular slime mold Polysphondylium spherical masses of cells are
89 ansition from one symmetry to another in the slime mold Polysphondylium, we developed a genetic scree
90  in D. discoideum with 5'-editing in another slime mold, Polysphondylium pallidum, suggests organism-
91         Dictyostelium discoideum, the social slime mold, possesses a PPK activity (DdPPK1) with seque
92 equency concentric pacemaker activity by the slime mold's scroll-wave tip.
93 oration dynamics, the migration rate and the slime mold shape.
94                                 In yeast and slime mold, some retrotransposons are associated with tR
95 o-scale collective systems, including social slime mold, spermatozoa vortex arrays, and Quincke rolle
96 ns include the metazoan talins, the cellular slime mold talin homologues TalA and TalB, fungal Sla2p,
97           Dictyostelium discoideum, a social slime mold that forms fruiting bodies with spores, depen
98              We suggest that in all cellular slime molds the existence of loners could resolve the ap
99 ncept applies to real-world systems, such as slime molds, the actin cytoskeleton, and human organizat
100 periments confirm peristalsis is used by the slime mold to drive internal cytoplasmic flows.
101 mplest phospholipids, is found in cells from slime mold to humans and has a largely unknown function.
102 ity commonly used in robotics--requiring the slime mold to reach a chemoattractive goal behind a U-sh
103                    This mechanism allows the slime mold to solve the U-shaped trap problem--a classic
104 dentified in organisms ranging from cellular slime mold to vertebrates, including plants, fungi, nema
105 arily conserved in eukaryotic organisms from slime molds to humans, JAK-STAT signaling appears to be
106 e found in a wide variety of organisms, from slime molds to humans.
107  a paradigm in cell signaling conserved from slime molds to mammals.
108 hting immune cells in organisms ranging from slime molds to mammals.
109 on of sugar beet plants by the endoparasitic slime-mold vector Polymyxa betae.

 
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