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1 in loner behavior in the model social amoeba Dictyostelium discoideum.
2 diverse species including most metazoans and Dictyostelium discoideum.
3 he ampA gene has a role in cell migration in Dictyostelium discoideum.
4 sesquiterpene and affects the development of Dictyostelium discoideum.
5 y conserved between humans and the protozoan Dictyostelium discoideum.
6 red for normal chemotaxis and cytokinesis in Dictyostelium discoideum.
7 densis to predation by the phagocytic amoeba Dictyostelium discoideum.
8 cell formation in the developmental cycle of Dictyostelium discoideum.
9  the mating-type locus of the model organism Dictyostelium discoideum.
10  model organisms, Caenorhabditis elegans and Dictyostelium discoideum.
11 dictyBase is the model organism database for Dictyostelium discoideum.
12 nt a protocol for the extraction of RNA from Dictyostelium discoideum.
13 y and cell adhesion during cell migration in Dictyostelium discoideum.
14 ial pathogens and for obtaining nutrients in Dictyostelium discoideum.
15 tracting DNA from cells of the social amoeba Dictyostelium discoideum.
16  controlling chemotaxis and cell adhesion in Dictyostelium discoideum.
17 hemotactic migration of the amoeboid form of Dictyostelium discoideum.
18 lated derivative of Pro-143 in the amebazoan Dictyostelium discoideum.
19 ed nematode species and from the slime mold, Dictyostelium discoideum.
20 orters present in apicomplexan parasites and Dictyostelium discoideum.
21 ate via the complex life cycle of the amoeba Dictyostelium discoideum.
22 rganism database (MOD) for the social amoeba Dictyostelium discoideum.
23 ilago maydis and spores of the social amoeba Dictyostelium discoideum.
24  to human DGK-theta, DGKA, was identified in Dictyostelium discoideum.
25  formation of the slug in the social amoebae Dictyostelium discoideum.
26  measured in chemotaxing unicellular amoeba, Dictyostelium discoideum.
27 to isolate genes required for cytokinesis in Dictyostelium discoideum.
28  of bone resorption as well as the growth of Dictyostelium discoideum.
29 throughout the 24 h developmental program of Dictyostelium discoideum.
30  from P. vivax, P. knowlesi, P. berghei, and Dictyostelium discoideum.
31 omyces cerevisiae, Entamoeba histolytica and Dictyostelium discoideum.
32 al program of the simple eukaryotic organism Dictyostelium discoideum.
33  through the social stage of an amoeba host, Dictyostelium discoideum.
34 med during development of the social amoeba, Dictyostelium discoideum.
35 is thaliana, Mycobacterium tuberculosis, and Dictyostelium discoideum.
36 ld replicate within the unicellular organism Dictyostelium discoideum.
37 rganism size in the eukaryotic microorganism Dictyostelium discoideum.
38 -MHC) cells moving within the tight mound of Dictyostelium discoideum.
39 fflux or uptake systems in the social amoeba Dictyostelium discoideum.
40  were able to visualize polyP extracted from Dictyostelium discoideum.
41 sion of social cheating in the social amoeba Dictyostelium discoideum.
42 arity is mainly studied in the social amoeba Dictyostelium discoideum.
43 d 'Cupid', was identified from the genome of Dictyostelium discoideum.
44 h system is represented by the social amoeba Dictyostelium discoideum.
45 eukaryotic microbe (protist), the slime mold Dictyostelium discoideum.
46 on experiments on single cells of the amoeba Dictyostelium discoideum.
47 7C mutant of non-muscle myosin II motor from Dictyostelium discoideum.
48 three CHD orthologs (ChdA, ChdB and ChdC) in Dictyostelium discoideum.
49 odel organism database for the social amoeba Dictyostelium discoideum.
50 rward genetic approach in the model organism Dictyostelium discoideum.
51 uman pathogen Pseudomonas aeruginosa infects Dictyostelium discoideum, a genetically tractable eukary
52                             Using the amoeba Dictyostelium discoideum, a model system for the study o
53                                              Dictyostelium discoideum, a social slime mold that forms
54                                              Dictyostelium discoideum, a social slime mold, is one of
55                                              Dictyostelium discoideum, a soil-dwelling social amoeba,
56                                              Dictyostelium discoideum, a unicellular organism capable
57 , the first subprocess of chemorepulsion, in Dictyostelium discoideum-a well characterized model euka
58                             We show that, in Dictyostelium discoideum, activated forms of RasC prolon
59                              The csA gene in Dictyostelium discoideum acts as a single-gene greenbear
60 olated a constitutively active mutant of the Dictyostelium discoideum adenylyl cyclase harboring a si
61 tracellular signals is remarkably similar in Dictyostelium discoideum amoebae and mammalian leukocyte
62                                           In Dictyostelium discoideum amoebae and mammalian leukocyte
63                          Uniform exposure of Dictyostelium discoideum amoebae as well as mammalian le
64                      The ability of prespore Dictyostelium discoideum amoebae to undergo redifferenti
65             Many eukaryotic cells, including Dictyostelium discoideum amoebae, fibroblasts, and neutr
66  family was less severe during growth within Dictyostelium discoideum amoebae, indicating that the re
67 otein gp130, found on the plasma membrane of Dictyostelium discoideum amoebae, was postulated previou
68  40,000 actin filament severing protein from Dictyostelium discoideum amoebae, we have identified a m
69                           On food depletion, Dictyostelium discoideum amoebas collect into aggregates
70                                              Dictyostelium discoideum amoebas coordinate aggregation
71                          In highly polarized Dictyostelium discoideum amoebas, membrane-associated be
72 nzyme A (CoA)-binding protein (ACBP; AcbA in Dictyostelium discoideum), an unconventionally secreted
73 ut only a approximately 1-2 mM IC(50) versus Dictyostelium discoideum and a human cell line, indicati
74  DIRS-1 is the most abundant retroelement in Dictyostelium discoideum and constitutes the pericentrom
75 seudopod-dominated migration of the amoeboid Dictyostelium discoideum and for the lamellipod-driven m
76  pneumophila is grown within the soil amoeba Dictyostelium discoideum and how D. discoideum genetics
77                            Investigations in Dictyostelium discoideum and neutrophils have establishe
78 ukaryotic cells, including amoeboid cells of Dictyostelium discoideum and neutrophils, respond to che
79  in the well-characterized chemotactic cells Dictyostelium discoideum and neutrophils, signaling to t
80 ms that control multicellular development in Dictyostelium discoideum and reconstruct how some of the
81  integrated, high quality data and tools for Dictyostelium discoideum and related species.
82                                    Likewise, Dictyostelium discoideum and Saccharomyces cerevisiae ca
83 F-actin assay detects the same proteins from Dictyostelium discoideum and with approximately the same
84 e numbering of residues follows myosin II in Dictyostelium discoideum) and the water molecule that sp
85 s biological function within macrophages and Dictyostelium discoideum, and for intrapulmonary prolife
86 orhabditis elegans, Acathamoeba castellanii, Dictyostelium discoideum, and Galleria mellonella have p
87              As L. pneumophila replicates in Dictyostelium discoideum, and macroautophagy genes have
88              Gene knockout studies in yeast, Dictyostelium discoideum, and mammalian cells have begun
89 ated gene in the genome of the social amoeba Dictyostelium discoideum, and show, with the use of hete
90 ous structures of S1 (from chicken skeletal, Dictyostelium discoideum, and smooth muscle myosins), in
91 n phytate-loaded Acanthamoeba castellanii or Dictyostelium discoideum, and the intracellular growth d
92 PHD homologues from the cellular slime mold, Dictyostelium discoideum, and the protozoan parasite, To
93                                           In Dictyostelium discoideum, AprA and CfaD are secreted pro
94                                           In Dictyostelium discoideum, AprA is a secreted protein tha
95 roportions of prespore and prestalk cells in Dictyostelium discoideum are regulated so that they are
96                                              Dictyostelium discoideum are social amoebas that propaga
97 ular slime molds, including the well-studied Dictyostelium discoideum, are amoebae whose life cycle i
98 from Schizosaccharomyces pombe and DnmA from Dictyostelium discoideum, are strongly stimulated by pri
99                                        Using Dictyostelium discoideum as a model host, we have identi
100               Despite widespread interest in Dictyostelium discoideum as a model system, almost no mo
101                                              Dictyostelium discoideum belongs to a group of multicell
102 of different signal transduction pathways in Dictyostelium discoideum but Galpha subunit-effector int
103 inase B (PKB) homologues, PkbA and PkbR1, in Dictyostelium discoideum by phosphorylation of activatio
104 n model organisms: Saccharomyces cerevisiae, Dictyostelium discoideum, Caenorhabditis elegans, Drosop
105 4, shares limited sequence identity with the Dictyostelium discoideum cAMP receptor cAR1 and the Aspe
106      Free-living cells of the social amoebae Dictyostelium discoideum can aggregate and develop into
107 underlie the mechanism of oligomerisation in Dictyostelium discoideum CAP.
108           Farmer clones of the social amoeba Dictyostelium discoideum carry bacteria to seed out new
109                                           In Dictyostelium discoideum, cell density is monitored by l
110                                Proliferating Dictyostelium discoideum cells accumulate extracellular
111                                  Chemotaxing Dictyostelium discoideum cells adapt their morphology an
112                                     Starving Dictyostelium discoideum cells aggregate to form dendrit
113 ne signal AprA, which is produced by growing Dictyostelium discoideum cells and inhibits their prolif
114 oteins (G-proteins) was visualized in living Dictyostelium discoideum cells by monitoring fluorescenc
115  intracellular transport are investigated in Dictyostelium discoideum cells by single particle tracki
116                  Upon starvation, individual Dictyostelium discoideum cells enter a developmental pro
117 antify the directional biases in chemotactic Dictyostelium discoideum cells in a flow chamber with al
118                                              Dictyostelium discoideum cells lacking PTEN exhibited im
119 ne the nature of this response, we subjected Dictyostelium discoideum cells to measurable temporal an
120 emonstrate here that M. marinum grows within Dictyostelium discoideum cells, allowing the genetic ana
121 ion of adenylyl cyclase (ACA) at the back of Dictyostelium discoideum cells, an essential determinant
122                            In multinucleated Dictyostelium discoideum cells, each centrosome organize
123 y establishment varies across cell types: in Dictyostelium discoideum cells, it is mediated by bioche
124 e early stages of cytokinesis, in rounded-up Dictyostelium discoideum cells, the small G-protein Rap1
125 ce of the actin network in experiments using Dictyostelium discoideum cells.
126 front and back, respectively, of chemotaxing Dictyostelium discoideum cells.
127  is required for the efficient chemotaxis of Dictyostelium discoideum cells.
128 entral membrane of oversized, multinucleated Dictyostelium discoideum cells.
129 elay on the collective behavior of migrating Dictyostelium discoideum cells.
130 d material transport within the cytoplasm of Dictyostelium discoideum cells: the anomalous non-linear
131 C2 in AKT phosphorylation in social amoebae (Dictyostelium discoideum) cells.
132 served in bacterial cellulose synthases, the Dictyostelium discoideum cellulose synthase, and other p
133 died the role of the adenylyl cyclase ACA in Dictyostelium discoideum chemotaxis and streaming.
134 high-resolution HAPPY map of chromosome 6 of Dictyostelium discoideum consisting of 300 sequence-tagg
135                                The genome of Dictyostelium discoideum contains six genes encoding pro
136 rganelle responsible for osmoregulation, the Dictyostelium discoideum contractile vacuole.
137                                 Two TCs from Dictyostelium discoideum converted farnesyl diphosphate
138                           The social amoebae Dictyostelium discoideum cooperate by forming multicellu
139                Here, we show that the amoeba Dictyostelium discoideum coordinates Ras and Rac activit
140       In this study, we investigated whether Dictyostelium discoideum could serve as an alternate hos
141                                           In Dictyostelium discoideum counting factor (CF), a secrete
142 scovered in a genetic suppressor screen of a Dictyostelium discoideum cytokinesis-deficient mutant ce
143 lysine-265 (K265) of the myosin-2 motor from Dictyostelium discoideum (Dd) is proposed to be a key re
144               The fluorescence properties of Dictyostelium discoideum (Dd) myosin II constructs conta
145 report periodic movements during erection of Dictyostelium discoideum (Dd) sorocarps.
146                             Here we consider Dictyostelium discoideum (Dd), a member of the Amoebazoa
147 m, the slug stage of the cellular slime mold Dictyostelium discoideum (Dd).
148 repeat of the gelation factor (ABP-120) from Dictyostelium discoideum (ddFLN5) by NMR spectroscopy to
149  developmentally regulated Na-H exchanger in Dictyostelium discoideum (DdNHE1) localizes to the leadi
150 d for cell surface cAMP receptors throughout Dictyostelium discoideum development, controlling chemot
151 In many systems, including the social amoeba Dictyostelium discoideum, development is often marked by
152                                              Dictyostelium discoideum DgcA synthesized c-di-GMP in a
153 l-degrading enzymes, such as PDE for cAMP in Dictyostelium discoideum (Dicty) and BAR1 for mating fac
154               We have engineered a mutant of Dictyostelium discoideum (Dicty) myosin II that contains
155 direction sensing based on experiments using Dictyostelium discoideum (Dicty).
156                         The simple eukaryote Dictyostelium discoideum displays chemotactic locomotion
157                            The social amoeba Dictyostelium discoideum diverged from the line leading
158 Disruption of the PI 3-phosphatase, PTEN, in Dictyostelium discoideum dramatically prolonged and broa
159                       Orthologues of Hem1 in Dictyostelium discoideum, Drosophila melanogaster, and C
160 rabidopsis thaliana, Caenorhabditis elegans, Dictyostelium discoideum, Drosophila melanogaster, Sacch
161  success of naturally occurring genotypes of Dictyostelium discoideum during the formation of chimeri
162 roscopy we directly observe the structure of Dictyostelium discoideum dynein dimers on microtubules a
163 some eukaryotes, including the social amoeba Dictyostelium discoideum, encode both a class I and a cl
164                                              Dictyostelium discoideum encodes one Thg1 and three TLPs
165                                   The amoeba Dictyostelium discoideum expresses a simple complement o
166                                              Dictyostelium discoideum expresses multiple G alpha subu
167                                       In the Dictyostelium discoideum farming symbiosis, certain amoe
168                                   The amoeba Dictyostelium discoideum feeds on, and is colonized by,
169  melanogaster, Schizosaccharomyces pombe and Dictyostelium discoideum for methylation of the Geobacte
170                                              Dictyostelium discoideum form groups of approximately 2
171                             The non-metazoan Dictyostelium discoideum forms a multicellular, differen
172                We show that the non-metazoan Dictyostelium discoideum forms a polarized epithelium th
173                         In the social amoeba Dictyostelium discoideum, four signaling pathways act sy
174  counting factor (CF), regulates the size of Dictyostelium discoideum fruiting bodies in part by regu
175  another member of the PRKX gene family (the Dictyostelium discoideum gene KAPC-DICDI) also plays a r
176                                          The Dictyostelium discoideum genome encodes five proteins th
177  an expressed FPPS from Leishmania major, in Dictyostelium discoideum growth inhibition, in gammadelt
178 ting FDP synthase and potency for inhibiting Dictyostelium discoideum growth.
179          Here we show that the social amoeba Dictyostelium discoideum has a primitive farming symbios
180 s cerevisiae, Schizosaccharomyces pombe, and Dictyostelium discoideum has allowed us to tentatively d
181         Here we show that the model organism Dictyostelium discoideum has evolved to normally encode
182                           The model organism Dictyostelium discoideum has greatly facilitated our und
183                                              Dictyostelium discoideum has proven a useful system for
184     Using bioinformatics tools, we show that Dictyostelium discoideum has the highest content of prio
185                                              Dictyostelium discoideum has two talins, TalA and TalB,
186 in 2 of severin, the gelsolin homologue from Dictyostelium discoideum, has been determined by multipl
187 cro-organisms Prototheca wickerhamii (I) and Dictyostelium discoideum (II) have been determined by ch
188 T ortholog in the model developmental system Dictyostelium discoideum, in which Ca(2+) plays a role i
189 t of cooperation occurs in the social amoeba Dictyostelium discoideum, in which some cells die to for
190          The life cycle of the social amoeba Dictyostelium discoideum includes a multicellular stage
191 fied multiple PtdInsP(3)-binding proteins in Dictyostelium discoideum, including five pleckstrin homo
192                                           In Dictyostelium discoideum, increased intracellular pH thr
193 tudies of the behavior of the model organism Dictyostelium discoideum indicate the biocompatibility o
194 layed a growth advantage in the amoebal host Dictyostelium discoideum, indicating that the protein fa
195 n confronted with starvation, the amoebae of Dictyostelium discoideum initiate a developmental proces
196                            The social amoeba Dictyostelium discoideum integrates into a multicellular
197 ion-induced aggregation of the social amoeba Dictyostelium discoideum into a multicellular slug is kn
198                                              Dictyostelium discoideum is a model system for studying
199                    The microbial soil amoeba Dictyostelium discoideum is a model system for the study
200                     The cellular slime mold, Dictyostelium discoideum is a non-metazoan organism, yet
201                                              Dictyostelium discoideum is a powerful and genetically t
202                            The social amoeba Dictyostelium discoideum is a professional phagocyte tha
203                                              Dictyostelium discoideum is a useful model for studying
204                            The social amoeba Dictyostelium discoideum is a widely used model organism
205                      The cellular slime mold Dictyostelium discoideum is a widely used model system f
206                                The eukaryote Dictyostelium discoideum is amenable to numerous genetic
207 ature of development in the simple eukaryote Dictyostelium discoideum is an aggregative transition fr
208                                              Dictyostelium discoideum is an amoebozoa that exists in
209                                              Dictyostelium discoideum is an excellent system in which
210 e terminal stage of spore differentiation in Dictyostelium discoideum is an important example of deve
211           Encapsulation of prespore cells of Dictyostelium discoideum is controlled by several interc
212              The genome of the social amoeba Dictyostelium discoideum is known to have a very high de
213   Here, we report that a Cdk8 homologue from Dictyostelium discoideum is localized in the nucleus whe
214                                Chemotaxis in Dictyostelium discoideum is mediated by G protein-couple
215             Because the cellular slime mold, Dictyostelium discoideum, is a genetically tractable mod
216                           The social amoeba, Dictyostelium discoideum, is known to use peptides to tr
217                           The social amoeba, Dictyostelium discoideum, is widely used as a simple mod
218 es were explored for cellular ion imaging in Dictyostelium discoideum live cells but spontaneous dye
219 min G (ForG) from the professional phagocyte Dictyostelium discoideum localizes to endocytic cups.
220                                           In Dictyostelium discoideum, loss of SCAR is compensated by
221 6-sulfate and Man-6-P methyl ester) found on Dictyostelium discoideum lysosomal enzymes.
222 6-sulfate and Man-6-P methyl ester) found on Dictyostelium discoideum lysosomal enzymes: the amino-te
223 n this paper, we show that WASH coats mature Dictyostelium discoideum lysosomes and is essential for
224 , we discerned a genetic interaction between Dictyostelium discoideum mek1, smkA (named for its role
225 x8-Rfp (founding member), Homo sapiens RNF4, Dictyostelium discoideum MIP1 and Saccharomyces cerevisi
226 is three-step modification pathway exists in Dictyostelium discoideum, model of the evolutionary supe
227 mechanical model of the contraction phase of Dictyostelium discoideum motility with an emphasis on th
228                                              Dictyostelium discoideum MyoB is a class I myosin involv
229 rt here the structure of the motor domain of Dictyostelium discoideum myosin II both in its nucleotid
230 structures of the truncated myosin head from Dictyostelium discoideum myosin II complexed with dinitr
231                  One such residue is Ser236 (Dictyostelium discoideum myosin II numbering) which was
232                                           In Dictyostelium discoideum, myosin II filament assembly is
233              We show that in the nonmetazoan Dictyostelium discoideum, myosin II localizes apically i
234                   The specific disruption in Dictyostelium discoideum of the sphingosine-1-phosphate
235                       The crawling motion of Dictyostelium discoideum on substrata involves a number
236 and have poor survival after phagocytosis by Dictyostelium discoideum or human macrophages.
237 Chemotactic cells, including neutrophils and Dictyostelium discoideum, orient and move directionally
238              In this study we identified the Dictyostelium discoideum ortholog of the adaptor protein
239 y, we characterize mutations in the putative Dictyostelium discoideum orthologues of budding yeast ge
240 m species, and the mycetozoan model organism Dictyostelium discoideum Our results show that phenamacr
241                   Remarkably, another PPK in Dictyostelium discoideum (PPK2) is an actin-related prot
242 ulticellular slug stage of the social amoeba Dictyostelium discoideum produce ETs upon stimulation wi
243 tain a domain with similarity to that of the Dictyostelium discoideum protein discoidin I.
244                 The eukaryotic microorganism Dictyostelium discoideum provides a unique experimental
245             In this study, PKAR and PDE from Dictyostelium discoideum (RD and RegA, respectively) wer
246 ew research indicates that the social amoeba Dictyostelium discoideum recognizes distinctions between
247 onfirm this prediction for the social amoeba Dictyostelium discoideum; relatedness in natural wild gr
248  that dedifferentiation in the social amoeba Dictyostelium discoideum relies on a sequence of events
249 ides and the unicellular phagocytic organism Dictyostelium discoideum reveal that, like OCRL, the Dic
250 ke cellulose, such as Ciona intestinalis and Dictyostelium discoideum, revealed the presence of membr
251                            Here we show that Dictyostelium discoideum Roco4 is a suitable model to st
252       Our findings identified the slime mold Dictyostelium discoideum's CISD proteins as the closest
253 ins from Homo sapiens, Arabidopsis thaliana, Dictyostelium discoideum, Saccharomyces cerevisiae, Esch
254                  We show that, unexpectedly, Dictyostelium discoideum SCAR knockouts could still spre
255 s of UMP/CMP kinase, a globular protein from Dictyostelium discoideum, serve as two illustrative exam
256             Experiments on the social amoeba Dictyostelium discoideum show that the origins of lineag
257                       The excitable cells of Dictyostelium discoideum show traveling waves of signali
258 alba x Populus tremula, corn (Zea mays), and Dictyostelium discoideum showed that cyanobacteria share
259                     In an unrelated protist, Dictyostelium discoideum, Skp1 hydroxyproline is modifie
260                                           In Dictyostelium discoideum, small GTPase methylation occur
261                         In the social amoeba Dictyostelium discoideum, starvation-triggered multicell
262  interactions using genome sequences from 67 Dictyostelium discoideum strains.
263 d in cheating behaviors in the social amoeba Dictyostelium discoideum, testing whether these genes ex
264 featured in this review is one discovered in Dictyostelium discoideum that becomes an actin-like fibe
265 ost is a "farmer" clone of the social amoeba Dictyostelium discoideum that carries and disperses bact
266   We have identified a new protein kinase in Dictyostelium discoideum that carries the same conserved
267 nt an NMR analysis of the isolated MTBD from Dictyostelium discoideum that demonstrates the coiled-co
268 e identified an Elmo-like protein, ElmoA, in Dictyostelium discoideum that unexpectedly functions as
269 ystem for performing interaction genetics in Dictyostelium discoideum that uses a cDNA library comple
270  a non-linear model for cAMP oscillations in Dictyostelium discoideum, the cell-cycle data for Saccha
271 ate spore encapsulation in the social amoeba Dictyostelium discoideum, the metabolic profile and othe
272                                              Dictyostelium discoideum, the social slime mold, possess
273 ady present in mycetozoan eukaryotes such as Dictyostelium discoideum This social amoeba kills bacter
274 emical mutagenesis in the social soil amoeba Dictyostelium discoideum Through genome sequencing, we s
275 sed this CRISPR-E test in the model organism Dictyostelium discoideum to demonstrate that Dync1li1 is
276                          A genetic screen in Dictyostelium discoideum to identify redundant pathways
277 show that PIP(3) is not only unnecessary for Dictyostelium discoideum to migrate toward folate, but a
278 transduction pathways, such as those used by Dictyostelium discoideum to move toward cAMP, use a G pr
279                    In this paper, we exploit Dictyostelium discoideum to uncover a novel role for PAR
280           Here we employ a simple eukaryote, Dictyostelium discoideum, to demonstrate distinct effect
281                                              Dictyostelium discoideum transformed with mutant PfCRT e
282 ed state previously reported for the similar Dictyostelium discoideum UMP/CMP kinase reveals the conf
283                                              Dictyostelium discoideum uses G protein-mediated signal
284 nserved in the more primitive model organism Dictyostelium discoideum using a microfluidic chip desig
285                            The social amoeba Dictyostelium discoideum was selected for functional stu
286 mediated signaling network for chemotaxis in Dictyostelium discoideum We identified a negative regula
287 ard genetic screen for chemotaxis mutants in Dictyostelium discoideum, we identified a loss-of-functi
288            Using a forward genetic screen in Dictyostelium discoideum, we identified the Ste20 kinase
289                      Using the social amoeba Dictyostelium discoideum, we provide a possible explanat
290  acceleration was increased until amoebae of Dictyostelium discoideum were "stalled" or no longer abl
291                   The mass-dense granules of Dictyostelium discoideum were shown to contain large amo
292 o used for communication in the social ameba Dictyostelium discoideum when the solitary cells aggrega
293 tion can be manipulated in the social amoeba Dictyostelium discoideum, which allows us to test and co
294 ine repeats from the single-celled eukaryote Dictyostelium discoideum, which also has a multicellular
295 served in other social organisms, especially Dictyostelium discoideum, which depend on diffusible mor
296      We test this evolutionary hypothesis in Dictyostelium discoideum, which forms multicellular frui
297 ndria (FMT), a homologue of the CluA gene of Dictyostelium discoideum, which is involved in the corre
298 GP) is a developmentally regulated enzyme in Dictyostelium discoideum, which is involved in trehalose
299 gets of the inhibitor (EC(50) >/= 50 muM) in Dictyostelium discoideum, while the strongest interactan
300  at the nucleotide-binding site of wild-type Dictyostelium discoideum (WT) myosin and a construct con

 
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