1 present in orthologs of animals or cellular
slime molds.
2 ous media or plasmodial shuttle streaming in
slime molds.
3 matid and apicomplexan parasites, algae, and
slime molds.
4 aryotes including animals, plants, fungi and
slime molds.
5 , trypanosomes, Giardia, ciliates, alga, and
slime molds [
3-8].
6 are different from the waves observed during
slime mold aggregation that depend on diffusible morphog
7 ns are also present in zebrafish, nematodes,
slime mold and plants.
8 lants, chlorophyte green algae, demosponges,
slime molds and brown algae.
9 orly understood feature of organisms such as
slime molds and fungi.
10 gesting a phylogenetic link between cellular
slime molds and true fungi.
11 ority of eukaryotes (fungi, plants, animals,
slime mold,
and euglena) synthesize Asn-linked glycans (
12 mans was shown to interact with macrophages,
slime molds,
and amoebae in a similar manner, suggesting
13 matid and apicomplexan parasites, algae, and
slime molds,
and have also been found in the bacterium A
14 ental responses in bacteria, Archaea, fungi,
slime molds,
and plants.
15 und in eukaryotic organisms including fungi,
slime molds,
and plants.
16 bees, multiple queen-founding ants, cellular
slime molds,
and social bacteria).
17 xin sequences present in animals, fungi, and
slime molds began prior to the divergence of these taxa.
18 ad are closely related to pks genes from the
slime mold Dictyostelium and eubacteria.
19 consistent with the behavior of the cellular
slime mold Dictyostelium discodeum, which switches from
20 cular system, the slug stage of the cellular
slime mold Dictyostelium discoideum (Dd).
21 the rep B and rep D genes from the cellular
slime mold Dictyostelium discoideum .
22 The cellular
slime mold Dictyostelium discoideum has long been recogn
23 The cellular
slime mold Dictyostelium discoideum is a widely used mod
24 The cellular
slime mold Dictyostelium discoideum is an attractive sys
25 In the development of the cellular
slime mold Dictyostelium discoideum there is a stage in
26 Our findings identified the
slime mold Dictyostelium discoideum's CISD proteins as t
27 sely related to the annexin homologue of the
slime mold Dictyostelium discoideum, suggesting a phylog
28 he multicellular development of the cellular
slime mold Dictyostelium discoideum.
29 ified in a eukaryotic microbe (protist), the
slime mold Dictyostelium discoideum.
30 tical for proper development in the cellular
slime mold Dictyostelium.
31 tion relationships of dynein in the cellular
slime mold Dictyostelium.
32 In particular, the
slime-mold Dictyostelium, the protozoan Trichomonas vagi
33 udding yeast (Saccharomyces cerevisiae), two
slime molds (
Dictyostelium discoideum and Physarum polyc
34 The cellular
slime mold,
Dictyostelium discoideum is a non-metazoan o
35 Because the cellular
slime mold,
Dictyostelium discoideum, is a genetically t
36 tantly related nematode species and from the
slime mold,
Dictyostelium discoideum.
37 s in this region to nematode talin, cellular
slime mold filopodin, and an Sla2 homolog from nematode.
38 ribed also in non-metazoan organisms such as
slime molds,
fungi and plants.
39 Plasmodial
slime molds grow as networks and use flexible, undiffere
40 New evidence from a primitive
slime mold,
however, suggests that alpha- and beta-caten
41 Cellular
slime molds,
including the well-studied Dictyostelium di
42 Dictyostelium discoideum, a social
slime mold,
is one of a few eukaryotes known to possess
43 Cellular
slime molds of the genus Polysphondylium periodically re
44 We show that the brainless
slime mold Physarum polycephalum constructs a form of sp
45 The
slime mold Physarum polycephalum grows as a random netwo
46 endonuclease, a homing endonuclease from the
slime mold Physarum polycephalum, is a small enzyme (2 x
47 ase, an intron-encoded endonuclease from the
slime mold Physarum polycephalum, is a small enzyme (2 x
48 Nuclei in G2 phase of the
slime mold Physarum polycephalum, when transplanted, by
49 apply the method to the mitochondrion of the
slime mold Physarum polycephalum.
50 is encoded by a group I intron found in the
slime mold Physarum polycephalum.
51 In the cellular
slime mold Polysphondylium spherical masses of cells are
52 ansition from one symmetry to another in the
slime mold Polysphondylium, we developed a genetic scree
53 in D. discoideum with 5'-editing in another
slime mold,
Polysphondylium pallidum, suggests organism-
54 Dictyostelium discoideum, the social
slime mold,
possesses a PPK activity (DdPPK1) with seque
55 equency concentric pacemaker activity by the
slime mold'
s scroll-wave tip.
56 In yeast and
slime mold,
some retrotransposons are associated with tR
57 ns include the metazoan talins, the cellular
slime mold talin homologues TalA and TalB, fungal Sla2p,
58 Dictyostelium discoideum, a social
slime mold that forms fruiting bodies with spores, depen
59 We suggest that in all cellular
slime molds the existence of loners could resolve the ap
60 periments confirm peristalsis is used by the
slime mold to drive internal cytoplasmic flows.
61 mplest phospholipids, is found in cells from
slime mold to humans and has a largely unknown function.
62 ity commonly used in robotics--requiring the
slime mold to reach a chemoattractive goal behind a U-sh
63 This mechanism allows the
slime mold to solve the U-shaped trap problem--a classic
64 dentified in organisms ranging from cellular
slime mold to vertebrates, including plants, fungi, nema
65 arily conserved in eukaryotic organisms from
slime molds to humans, JAK-STAT signaling appears to be
66 e found in a wide variety of organisms, from
slime molds to humans.
67 hting immune cells in organisms ranging from
slime molds to mammals.
68 on of sugar beet plants by the endoparasitic
slime-mold vector Polymyxa betae.