ライフサイエンスコーパス: discoideum

1 mplex life cycle of the amoeba Dictyostelium discoideum.

2 ologs (ChdA, ChdB and ChdC) in Dictyostelium discoideum.

3 database for the social amoeba Dictyostelium discoideum.

4 approach in the model organism Dictyostelium discoideum.

5 ocial stage of an amoeba host, Dictyostelium discoideum.

6 s including most metazoans and Dictyostelium discoideum.

7 as a role in cell migration in Dictyostelium discoideum.

8 smoregulation as well as cell motility of D. discoideum.

9 tween humans and the protozoan Dictyostelium discoideum.

10 es involved in resistance to predation by D. discoideum.

11 arly decreased resistance to predation by D. discoideum.

12 chemotaxis and cytokinesis in Dictyostelium discoideum.

13 ation by the phagocytic amoeba Dictyostelium discoideum.

14 ays of chemorepellent gradient sensing in D. discoideum.

15 in the developmental cycle of Dictyostelium discoideum.

16 ved between the yeast Pichia pastoris and D. discoideum.

17 pe locus of the model organism Dictyostelium discoideum.

18 ms, Caenorhabditis elegans and Dictyostelium discoideum.

19 ought after folic acid receptor, fAR1, in D. discoideum.

20 he model organism database for Dictyostelium discoideum.

21 for the extraction of RNA from Dictyostelium discoideum.

22 esion during cell migration in Dictyostelium discoideum.

23 and for obtaining nutrients in Dictyostelium discoideum.

24 or tyrosine kinase-like protein, VSK3, in D. discoideum.

25 at are affected by cisplatin treatment of D. discoideum.

26 rom cells of the social amoeba Dictyostelium discoideum.

27 hemotaxis and cell adhesion in Dictyostelium discoideum.

28 ration of the amoeboid form of Dictyostelium discoideum.

29 ve of Pro-143 in the amebazoan Dictyostelium discoideum.

30 specific function of volatile terpenes in D. discoideum.

31 of chimaerism experienced by the related D. discoideum.

32 ecies and from the slime mold, Dictyostelium discoideum.

33 in apicomplexan parasites and Dictyostelium discoideum.

34 reduced drug accumulation in transformed D. discoideum.

35 e systems in the social amoeba Dictyostelium discoideum.

36 se (MOD) for the social amoeba Dictyostelium discoideum.

37 nd spores of the social amoeba Dictyostelium discoideum.

38 theta, DGKA, was identified in Dictyostelium discoideum.

39 tant forms of PfCRT to acidic vesicles in D. discoideum.

40 nto cAMP, the primary chemoattractant for D. discoideum.

41 cell fusion during macrocyst formation in D. discoideum.

42 visualize polyP extracted from Dictyostelium discoideum.

43 cheating in the social amoeba Dictyostelium discoideum.

44 hemotaxing unicellular amoeba, Dictyostelium discoideum.

45 y studied in the social amoeba Dictyostelium discoideum.

46 of the yeast prion protein Sup35 (NM), in D. discoideum.

47 presented by the social amoeba Dictyostelium discoideum.

48 robe (protist), the slime mold Dictyostelium discoideum.

49 heterochromatin of the six chromosomes in D. discoideum.

50 on single cells of the amoeba Dictyostelium discoideum.

51 on-muscle myosin II motor from Dictyostelium discoideum.

52 Using the amoeba Dictyostelium discoideum, a model system for the study of chemotaxis,

53 Dictyostelium discoideum, a social slime mold that forms fruiting bodi

54 Dictyostelium discoideum, a social slime mold, is one of a few eukaryo

55 Dictyostelium discoideum, a soil-dwelling social amoeba, is a model fo

56 Dictyostelium discoideum, a unicellular organism capable of developing

57 bprocess of chemorepulsion, in Dictyostelium discoideum-a well characterized model eukaryotic system.

58 We show that, in Dictyostelium discoideum, activated forms of RasC prolong the time cou

59 of two of the five Argonaute proteins of D. discoideum, AgnA and AgnB, in DIRS-1 silencing.

60 molecules that mediate allorecognition in D. discoideum also control the integration of individual ce

61 When expressed in D. discoideum amoebae, AqpB-GFP fusion constructs localized

62 ny eukaryotic cells, including Dictyostelium discoideum amoebae, fibroblasts, and neutrophils, are ab

63 ss severe during growth within Dictyostelium discoideum amoebae, indicating that the requirement for

64 ound on the plasma membrane of Dictyostelium discoideum amoebae, was postulated previously to play a

65 nt protein stained the plasma membrane of D. discoideum amoebae.

66 On food depletion, Dictyostelium discoideum amoebas collect into aggregates, which first

67 Dictyostelium discoideum amoebas coordinate aggregation and morphogene

68 binding protein (ACBP; AcbA in Dictyostelium discoideum), an unconventionally secreted protein, is de

69 oximately 1-2 mM IC(50) versus Dictyostelium discoideum and a human cell line, indicating selective a

70 most abundant retroelement in Dictyostelium discoideum and constitutes the pericentromeric heterochr

71 ated migration of the amoeboid Dictyostelium discoideum and for the lamellipod-driven migration of hu

72 lism genes confer cisplatin resistance in D. discoideum and in human cells, raised interest in the re

73 Investigations in Dictyostelium discoideum and neutrophils have established that pleckst

74 haracterized chemotactic cells Dictyostelium discoideum and neutrophils, signaling to the cytoskeleto

75 are fundamentally different from those in D. discoideum and neutrophils.

76 D. discoideum and other species that use cAMP to aggregate

77 l multicellular development in Dictyostelium discoideum and reconstruct how some of these mechanisms

78 igh quality data and tools for Dictyostelium discoideum and related species.

79 Likewise, Dictyostelium discoideum and Saccharomyces cerevisiae can perform cyto

80 residues follows myosin II in Dictyostelium discoideum) and the water molecule that spans this salt

81 unction within macrophages and Dictyostelium discoideum, and for intrapulmonary proliferation in mice

82 gans, Acathamoeba castellanii, Dictyostelium discoideum, and Galleria mellonella have provided means

83 he genome of the social amoeba Dictyostelium discoideum, and show, with the use of heterologous expre

84 ed Acanthamoeba castellanii or Dictyostelium discoideum, and the intracellular growth defect was comp

85 In Dictyostelium discoideum, AprA and CfaD are secreted proteins that inh

86 In Dictyostelium discoideum, AprA is a secreted protein that inhibits pro

87 Yet, data on D. discoideum AQPs is almost absent.

88 Despite cloning of two putative D. discoideum AQPs, WacA, and AqpA, water permeability has

89 Dictyostelium discoideum are social amoebas that propagate as unicellu

90 a, Vermamoeba vermiformis and Dictyostellium discoideum) are permissive to M. bovis infection and tha

91 ds, including the well-studied Dictyostelium discoideum, are amoebae whose life cycle includes both a

92 charomyces pombe and DnmA from Dictyostelium discoideum, are strongly stimulated by prior queuosine (

93 ell as the results of decades of study of D. discoideum as a model for development, allow us to explo

94 Using Dictyostelium discoideum as a model host, we have identified a virulen

95 Despite widespread interest in Dictyostelium discoideum as a model system, almost no molecular data e

96 -editing occurs at all predicted sites in D. discoideum as evidenced by changes in the sequences of i

97 Predation by D. discoideum, assessed by uptake and digestion of Klebsiel

98 tion limits the potential for cheating in D. discoideum because defecting on prestalk cell production

99 Dictyostelium discoideum belongs to a group of multicellular life form

100 ignal transduction pathways in Dictyostelium discoideum but Galpha subunit-effector interactions have

101 homologues, PkbA and PkbR1, in Dictyostelium discoideum by phosphorylation of activation loops (ALs)

102 sms: Saccharomyces cerevisiae, Dictyostelium discoideum, Caenorhabditis elegans, Drosophila melanogas

103 ted sequence identity with the Dictyostelium discoideum cAMP receptor cAR1 and the Aspergillus nidula

104 ng cells of the social amoebae Dictyostelium discoideum can aggregate and develop into multicellular

105 stance phenotype conferred on transformed D. discoideum can be reversed by the channel-blocking agent

106 echanism of oligomerisation in Dictyostelium discoideum CAP.

107 er clones of the social amoeba Dictyostelium discoideum carry bacteria to seed out new food populatio

108 Chemotaxing Dictyostelium discoideum cells adapt their morphology and migration sp

109 , which is produced by growing Dictyostelium discoideum cells and inhibits their proliferation, also

110 transport are investigated in Dictyostelium discoideum cells by single particle tracking of fluoresc

111 Upon starvation, individual Dictyostelium discoideum cells enter a developmental program that lead

112 ectional biases in chemotactic Dictyostelium discoideum cells in a flow chamber with alternating chem

113 Dictyostelium discoideum cells lacking PTEN exhibited impaired migrati

114 We find that as migrating D. discoideum cells round up to enter cytokinesis, PI(3,4,5

115 of this response, we subjected Dictyostelium discoideum cells to measurable temporal and spatial chem

116 th classes of RNR genes were expressed in D. discoideum cells, although the class I transcripts were

117 l cyclase (ACA) at the back of Dictyostelium discoideum cells, an essential determinant of their abil

118 en imaging rapid morphological changes in D. discoideum cells, as well as improved contrast and resol

119 of cytokinesis, in rounded-up Dictyostelium discoideum cells, the small G-protein Rap1 is activated

120 cloned a novel AQP, AqpB, from amoeboidal D. discoideum cells.

121 T-transformed, hematin-free vesicles from D. discoideum cells.

122 llective behavior of migrating Dictyostelium discoideum cells.

123 ies of the diiron-oxo/radical cofactor of D. discoideum class I RNR are similar to those of the mamma

124 Inhibition of D. discoideum class I RNR by hydroxyurea resulted in a 90%

125 The amino acid sequence of the D. discoideum class I RNR is similar to other eukaryotic RN

126 holderia inhibit the growth of non-farmer D. discoideum clones that could exploit the farmers' crops.

127 nsible for osmoregulation, the Dictyostelium discoideum contractile vacuole.

128 Two TCs from Dictyostelium discoideum converted farnesyl diphosphate into (2S,3R,6S

129 The social amoebae Dictyostelium discoideum cooperate by forming multicellular aggregates

130 65) of the myosin-2 motor from Dictyostelium discoideum (Dd) is proposed to be a key residue in an al

131 The fluorescence properties of Dictyostelium discoideum (Dd) myosin II constructs containing a single

132 Here we consider Dictyostelium discoideum (Dd), a member of the Amoebazoa outgroup of M

133 age of the cellular slime mold Dictyostelium discoideum (Dd).

134 gelation factor (ABP-120) from Dictyostelium discoideum (ddFLN5) by NMR spectroscopy to provide a bas

135 ly regulated Na-H exchanger in Dictyostelium discoideum (DdNHE1) localizes to the leading edge of pol

136 re, we demonstrate that peroxidase A from D. discoideum (DdPoxA) is a stable, monomeric, glycosylated

137 that class I is the principal RNR during D. discoideum development and growth and is important for s

138 face cAMP receptors throughout Dictyostelium discoideum development, controlling chemotaxis and morph

139 component of the cAMP export mechanism in D. discoideum development.

140 s, including the social amoeba Dictyostelium discoideum, development is often marked by dynamic morph

141 Dictyostelium discoideum DgcA synthesized c-di-GMP in a GTP-dependent

142 zymes, such as PDE for cAMP in Dictyostelium discoideum (Dicty) and BAR1 for mating factor alpha in S

143 We have engineered a mutant of Dictyostelium discoideum (Dicty) myosin II that contains the same fast

144 ing based on experiments using Dictyostelium discoideum (Dicty).

145 The simple eukaryote Dictyostelium discoideum displays chemotactic locomotion in stages of

146 The social amoeba Dictyostelium discoideum diverged from the line leading to animals sho

147 Orthologues of Hem1 in Dictyostelium discoideum, Drosophila melanogaster, and Caenorhabditis

148 liana, Caenorhabditis elegans, Dictyostelium discoideum, Drosophila melanogaster, Saccharomyces cerev

149 turally occurring genotypes of Dictyostelium discoideum during the formation of chimeric fruiting bod

150 ectly observe the structure of Dictyostelium discoideum dynein dimers on microtubules at near-physiol

151 In vitro activities of putative D. discoideum editing enzymes are consistent with the obser

152 s, including the social amoeba Dictyostelium discoideum, encode both a class I and a class II RNR.

153 Dictyostelium discoideum encodes one Thg1 and three TLPs (DdiTLP2, Ddi

154 ed vesicles from mutant-PfCRT-transformed D. discoideum exhibit features of the CQR phenotype, consis

155 The amoeba Dictyostelium discoideum expresses a simple complement of MyTH/FERM my

156 Dictyostelium discoideum expresses multiple G alpha subunits but only

157 e results change our understanding of the D. discoideum farming symbiosis by establishing that the ba

158 In the Dictyostelium discoideum farming symbiosis, certain amoebas (termed "f

159 The amoeba Dictyostelium discoideum feeds on, and is colonized by, diverse bacter

160 shown that a little-studied component of D. discoideum fitness--the loner cells that do not particip

161 Schizosaccharomyces pombe and Dictyostelium discoideum for methylation of the Geobacter tRNA-Asp and

162 Dictyostelium discoideum form groups of approximately 2 x 10(4) cells.

163 We show that the non-metazoan Dictyostelium discoideum forms a polarized epithelium that is essentia

164 In the social amoeba Dictyostelium discoideum, four signaling pathways act synergistically

165 The Dictyostelium discoideum genome encodes five proteins that share weak

166 D. discoideum, given its utility in molecular genetic studi

167 D. discoideum grows as a unicellular organism when food is

168 FPPS from Leishmania major, in Dictyostelium discoideum growth inhibition, in gammadelta T cell activ

169 ase and potency for inhibiting Dictyostelium discoideum growth.

170 we show that the social amoeba Dictyostelium discoideum has a primitive farming symbiosis that includ

171 e show that the model organism Dictyostelium discoideum has evolved to normally encode long polygluta

172 The model organism Dictyostelium discoideum has greatly facilitated our understanding of

173 nformatics tools, we show that Dictyostelium discoideum has the highest content of prion-like protein

174 Dictyostelium discoideum has two talins, TalA and TalB, which have dis

175 Our data suggest that D. discoideum has undergone specific adaptations that incre

176 at control the developmental programme of D. discoideum, highlighting the central role of cAMP in the

177 KrsB interacts genetically with another D. discoideum Hippo/MST homolog, KrsA, but the two genes ar

178 The D. discoideum htt(-)-mutant failed to undergo both K(+)-fac

179 teins remain soluble and are innocuous to D. discoideum, in contrast to other organisms, where they f

180 the model developmental system Dictyostelium discoideum, in which Ca(2+) plays a role in receptor-reg

181 on occurs in the social amoeba Dictyostelium discoideum, in which some cells die to form a stalk that

182 ife cycle of the social amoeba Dictyostelium discoideum includes a multicellular stage in which not n

183 PtdInsP(3)-binding proteins in Dictyostelium discoideum, including five pleckstrin homology (PH) doma

184 In Dictyostelium discoideum, increased intracellular pH through undefined

185 main and the evidence for TPS function in D. discoideum indicate that the TPS genes mediate lineage-s

186 behavior of the model organism Dictyostelium discoideum indicate the biocompatibility of the function

187 advantage in the amoebal host Dictyostelium discoideum, indicating that the protein family may modul

188 ith starvation, the amoebae of Dictyostelium discoideum initiate a developmental process that begins

189 The social amoeba Dictyostelium discoideum integrates into a multicellular organism when

190 gregation of the social amoeba Dictyostelium discoideum into a multicellular slug is known to result

191 Dictyostelium discoideum is a model system for studying many important

192 The microbial soil amoeba Dictyostelium discoideum is a model system for the study of social evo

193 Our results demonstrate that D. discoideum is a powerful model organism to study the evo

194 The social amoeba Dictyostelium discoideum is a professional phagocyte that chases bacte

195 Dictyostelium discoideum is a useful model for studying mechanisms of

196 The social amoeba Dictyostelium discoideum is a widely used model organism for studying

197 The eukaryote Dictyostelium discoideum is amenable to numerous genetic manipulations

198 Dictyostelium discoideum is an amoebozoa that exists in both a free-li

199 Dictyostelium discoideum is an excellent system in which to study deve

200 psulation of prespore cells of Dictyostelium discoideum is controlled by several intercellular signal

201 he genome of the social amoeba Dictyostelium discoideum is known to have a very high density of micro

202 ort that a Cdk8 homologue from Dictyostelium discoideum is localized in the nucleus where it forms pa

203 D. discoideum is rapidly becoming a model system of choice

204 The social amoeba, Dictyostelium discoideum, is known to use peptides to trigger sporulat

205 te and define social interactions between D. discoideum isolates, thus providing a conceptual framewo

206 Although D. discoideum lacks a cadherin homolog, we identify an alph

207 xpand and disperse geographically via the D. discoideum life cycle.

208 ed for cellular ion imaging in Dictyostelium discoideum live cells but spontaneous dye loss resulted

209 rom the professional phagocyte Dictyostelium discoideum localizes to endocytic cups.

210 In Dictyostelium discoideum, loss of SCAR is compensated by WASP moving t

211 we show that WASH coats mature Dictyostelium discoideum lysosomes and is essential for exocytosis of

212 a genetic interaction between Dictyostelium discoideum mek1, smkA (named for its role in the suppres

213 ng member), Homo sapiens RNF4, Dictyostelium discoideum MIP1 and Saccharomyces cerevisiae Slx5-Slx8.

214 We show that D. discoideum mitochondria exhibit membrane potential-depen

215 el of the contraction phase of Dictyostelium discoideum motility with an emphasis on the adhesive pro

216 The structures of the D. discoideum motor domain (S1dC) S236A mutant protein in c

217 Dictyostelium discoideum MyoB is a class I myosin involved in the form

218 One such residue is Ser236 (Dictyostelium discoideum myosin II numbering) which was proposed to be

219 e show that in the nonmetazoan Dictyostelium discoideum, myosin II localizes apically in tip epitheli

220 associated Burkholderia isolates colonize D. discoideum nonfarmers and infectiously endow them with f

221 The social stage of Dictylostelium discoideum occurs when the amoebae run out of their bact

222 The crawling motion of Dictyostelium discoideum on substrata involves a number of coordinated

223 lls, including neutrophils and Dictyostelium discoideum, orient and move directionally in very shallo

224 analysis revealed that cAMP signalling in D. discoideum originated from a second messenger role in am

225 n this study we identified the Dictyostelium discoideum ortholog of the adaptor protein AP180 and cha

226 rize mutations in the putative Dictyostelium discoideum orthologues of budding yeast genes that are i

227 only partially restored aggregation of a D. discoideum pdsA-null mutant, but was more effective at r

228 The eukaryote D. discoideum possesses a homolog of PPK1.

229 We report here that mutants of D. discoideum PPK1 (DdPPK1) have reduced levels of poly P a

230 Remarkably, another PPK in Dictyostelium discoideum (PPK2) is an actin-related protein (Arp) comp

231 lug stage of the social amoeba Dictyostelium discoideum produce ETs upon stimulation with bacteria or

232 Thus, D. discoideum provides a novel, high-throughput model syste

233 that, in contrast to observations made in D discoideum, PTEN-null Jurkat T cells exhibited potent ch

234 this study, PKAR and PDE from Dictyostelium discoideum (RD and RegA, respectively) were used as a mo

235 dicates that the social amoeba Dictyostelium discoideum recognizes distinctions between Gram(-) and G

236 ediction for the social amoeba Dictyostelium discoideum; relatedness in natural wild groups is so hig

237 entiation in the social amoeba Dictyostelium discoideum relies on a sequence of events that is indepe

238 Targeted disruption of the gene in D. discoideum resulted in cells that were unable to regulat

239 ement of volatile terpenes in cultures of D. discoideum revealed essentially no emission at an early

240 Transcriptional profiling of D. discoideum revealed sets of genes whose expression is en

241 such as Ciona intestinalis and Dictyostelium discoideum, revealed the presence of membrane-linked end

242 Here we show that Dictyostelium discoideum Roco4 is a suitable model to study the struct

243 ings identified the slime mold Dictyostelium discoideum's CISD proteins as the closest to the ancient

244 sapiens, Arabidopsis thaliana, Dictyostelium discoideum, Saccharomyces cerevisiae, Escherichia coli a

245 We show that, unexpectedly, Dictyostelium discoideum SCAR knockouts could still spread, migrate, a

246 he "turbine wave." Herein we argue that a D. discoideum scroll or concentric wave territory containin

247 inase, a globular protein from Dictyostelium discoideum, serve as two illustrative examples.

248 Although intravesicular pH levels in D. discoideum show small acidic changes with the expression

249 periments on the social amoeba Dictyostelium discoideum show that the origins of lineage bias in this

250 The excitable cells of Dictyostelium discoideum show traveling waves of signaling and generat

251 terologous expression, all nine TPSs from D. discoideum showed sesquiterpene synthase activities.

252 In an unrelated protist, Dictyostelium discoideum, Skp1 hydroxyproline is modified by five suga

253 In Dictyostelium discoideum, small GTPase methylation occurs seconds afte

254 Burkholderia inside and outside colonized D. discoideum spores after fruiting body formation; this ob

255 In the social amoeba Dictyostelium discoideum, starvation-triggered multicellular developme

256 ogenomic approach we have determined that D. discoideum TalA/B and the animal talins are related by d

257 behaviors in the social amoeba Dictyostelium discoideum, testing whether these genes experience rapid

258 is review is one discovered in Dictyostelium discoideum that becomes an actin-like fiber concurrent w

259 er" clone of the social amoeba Dictyostelium discoideum that carries and disperses bacteria during it

260 tified a new protein kinase in Dictyostelium discoideum that carries the same conserved class of "alp

261 ysis of the isolated MTBD from Dictyostelium discoideum that demonstrates the coiled-coil beta(+) reg

262 We have identified a gene, dimA, in D. discoideum that has two contrasting effects.

263 n Elmo-like protein, ElmoA, in Dictyostelium discoideum that unexpectedly functions as a negative reg

264 model for cAMP oscillations in Dictyostelium discoideum, the cell-cycle data for Saccharomyces cerevi

265 psulation in the social amoeba Dictyostelium discoideum, the metabolic profile and other potential fu

266 In D. discoideum, the receptor was found on intracellular memb

267 Dictyostelium discoideum, the social slime mold, possesses a PPK activ

268 mycetozoan eukaryotes such as Dictyostelium discoideum This social amoeba kills bacteria via phagocy

269 esis in the social soil amoeba Dictyostelium discoideum Through genome sequencing, we successfully id

270 part of a regulatory network that allows D. discoideum to elicit specific cellular responses to diff

271 mutation of lysine 76 (e.g. K76T) enable D. discoideum to expel chloroquine.

272 A genetic screen in Dictyostelium discoideum to identify redundant pathways revealed a gen

273 3) is not only unnecessary for Dictyostelium discoideum to migrate toward folate, but actively inhibi

274 In this paper, we exploit Dictyostelium discoideum to uncover a novel role for PARylation in reg

275 we employ a simple eukaryote, Dictyostelium discoideum, to demonstrate distinct effects of loss of I

276 We found that expression of most D. discoideum TPS genes was induced during development.

277 mechanism shows structural specificity as D. discoideum transformants that expel chloroquine do not e

278 Dictyostelium discoideum transformed with mutant PfCRT expresses key f

279 he closed state based on the structure of D. discoideum UMP/CMP kinase aids to rationalize the substr

280 ously reported for the similar Dictyostelium discoideum UMP/CMP kinase reveals the conformational cha

281 Dictyostelium discoideum uses G protein-mediated signal transduction f

282 Mutant PfCRT-transformed D. discoideum vesicles show features of the CQR phenotype,

283 ct on the PfCRT-mediated CQR phenotype of D. discoideum vesicles.

284 The social amoeba Dictyostelium discoideum was selected for functional study of the iden

285 D. discoideum WASH causes filamentous actin (F-actin) patch

286 ling network for chemotaxis in Dictyostelium discoideum We identified a negative regulator of Ras sig

287 reen for chemotaxis mutants in Dictyostelium discoideum, we identified a loss-of-function mutation, d

288 ng a forward genetic screen in Dictyostelium discoideum, we identified the Ste20 kinase KrsB, a homol

289 Using the social amoeba Dictyostelium discoideum, we provide a possible explanation for the co

290 late multicellular development stages of D. discoideum when migrating slugs differentiate into fruit

291 munication in the social ameba Dictyostelium discoideum when the solitary cells aggregate to form mul

292 ect on the accumulation of chloroquine by D. discoideum, whereas forms of PfCRT carrying a key charge

293 nipulated in the social amoeba Dictyostelium discoideum, which allows us to test and confirm the two

294 om the single-celled eukaryote Dictyostelium discoideum, which also has a multicellular stage.

295 his evolutionary hypothesis in Dictyostelium discoideum, which forms multicellular fruiting bodies by

296 hibitor (EC(50) >/= 50 muM) in Dictyostelium discoideum, while the strongest interactant was found to

297 Transformed D. discoideum will be useful for further studies of the chl

298 A comparison of 5'-editing in D. discoideum with 5'-editing in another slime mold, Polysp

299 a previously unrecognized PPK (DdPPK2) in D. discoideum with the sequences and properties of actin-re

300 tide-binding site of wild-type Dictyostelium discoideum (WT) myosin and a construct containing a sing