ライフサイエンスコーパス: discoideum

1 identified from the genome of Dictyostelium discoideum.

2 presented by the social amoeba Dictyostelium discoideum.

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

4 heterochromatin of the six chromosomes in D. discoideum.

5 on single cells of the amoeba Dictyostelium discoideum.

6 on-muscle myosin II motor from Dictyostelium discoideum.

7 r development, and ecological dynamics in D. discoideum.

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

9 database for the social amoeba Dictyostelium discoideum.

10 approach in the model organism Dictyostelium discoideum.

11 s including most metazoans and Dictyostelium discoideum.

12 as a role in cell migration in Dictyostelium discoideum.

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

14 tween humans and the protozoan Dictyostelium discoideum.

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

16 arly decreased resistance to predation by D. discoideum.

17 chemotaxis and cytokinesis in Dictyostelium discoideum.

18 and affects the development of Dictyostelium discoideum.

19 ation by the phagocytic amoeba Dictyostelium discoideum.

20 ays of chemorepellent gradient sensing in D. discoideum.

21 in the developmental cycle of Dictyostelium discoideum.

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

23 pe locus of the model organism Dictyostelium discoideum.

24 ms, Caenorhabditis elegans and Dictyostelium discoideum.

25 he model organism database for Dictyostelium discoideum.

26 for the extraction of RNA from Dictyostelium discoideum.

27 esion during cell migration in Dictyostelium discoideum.

28 and for obtaining nutrients in Dictyostelium discoideum.

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

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

31 rom cells of the social amoeba Dictyostelium discoideum.

32 hemotaxis and cell adhesion in Dictyostelium discoideum.

33 ration of the amoeboid form of Dictyostelium discoideum.

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

35 le from the volatile bouquet of wild type D. discoideum.

36 of chimaerism experienced by the related D. discoideum.

37 ecies and from the slime mold, Dictyostelium discoideum.

38 in apicomplexan parasites and Dictyostelium discoideum.

39 reduced drug accumulation in transformed D. discoideum.

40 mplex life cycle of the amoeba Dictyostelium discoideum.

41 hemotaxing unicellular amoeba, Dictyostelium discoideum.

42 ior in the model social amoeba Dictyostelium discoideum.

43 ocial stage of an amoeba host, Dictyostelium discoideum.

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

45 specific function of volatile terpenes in D. discoideum.

46 e systems in the social amoeba Dictyostelium discoideum.

47 visualize polyP extracted from Dictyostelium discoideum.

48 cheating in the social amoeba Dictyostelium discoideum.

49 y studied in the social amoeba Dictyostelium discoideum.

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

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

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

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

54 Dictyostelium discoideum, a unicellular organism capable of developing

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

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

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

58 Unlike described for yeast, D. discoideum allows for an unconditional deletion of the s

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

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

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

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

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

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

65 Dictyostelium discoideum amoebas coordinate aggregation and morphogene

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

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

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

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

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

71 me acidification and lysosome activity in D. discoideum and macrophages and reduced early endosomal m

72 Conversely, treatment of D. discoideum and macrophages with recombinant yeast exopol

73 lar polyphosphate and reduced survival in D. discoideum and macrophages, and this was reversed by the

74 ed E. coli survival after phagocytosis by D. discoideum and macrophages.

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

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

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

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

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

80 Likewise, Dictyostelium discoideum and Saccharomyces cerevisiae can perform cyto

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

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

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

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

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

86 from the cellular slime mold, Dictyostelium discoideum, and the protozoan parasite, Toxoplasma gondi

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

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

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

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

91 Dictyostelium discoideum are social amoebas that propagate as unicellu

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

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

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

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

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

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

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

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

104 echanism of oligomerisation in Dictyostelium discoideum CAP.

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

106 Proliferating Dictyostelium discoideum cells accumulate extracellular polyphosphate.

107 Chemotaxing Dictyostelium discoideum cells adapt their morphology and migration sp

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

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

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

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

112 Dictyostelium discoideum cells lacking PTEN exhibited impaired migrati

113 gocytosed M. smegmatis or M. tuberculosis D. discoideum cells lacking the putative polyphosphate rece

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

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

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

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

118 In multinucleated Dictyostelium discoideum cells, each centrosome organizes a radial MT

119 t varies across cell types: in Dictyostelium discoideum cells, it is mediated by biochemical signalin

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

121 llective behavior of migrating Dictyostelium discoideum cells.

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

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

124 n network in experiments using Dictyostelium discoideum cells.

125 e of oversized, multinucleated Dictyostelium discoideum cells.

126 nsport within the cytoplasm of Dictyostelium discoideum cells: the anomalous non-linear scaling of th

127 phorylation in social amoebae (Dictyostelium discoideum) cells.

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

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

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

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

132 nsible for osmoregulation, the Dictyostelium discoideum contractile vacuole.

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

134 The social amoebae Dictyostelium discoideum cooperate by forming multicellular aggregates

135 Here, we show that the amoeba Dictyostelium discoideum coordinates Ras and Rac activity using the mu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 Dictyostelium discoideum expresses multiple G alpha subunits but only

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

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

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

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

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

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

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

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

168 The Dictyostelium discoideum genome encodes five proteins that share weak

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

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

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

172 ase and potency for inhibiting Dictyostelium discoideum growth.

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

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

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

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

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

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

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

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

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

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

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

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

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

186 In Dictyostelium discoideum, increased intracellular pH through undefined

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

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

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

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

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

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

193 Dictyostelium discoideum is a model system for studying many important

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

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

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

197 Dictyostelium discoideum is a useful model for studying mechanisms of

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

199 The eukaryote Dictyostelium discoideum is amenable to numerous genetic manipulations

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

216 modification pathway exists in Dictyostelium discoideum, model of the evolutionary superfamily Amoebo

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

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

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

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

221 ium solani myosin-1, human myosin-1c, and D. discoideum myosin isoforms 1B, 1E, and 2.

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

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

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

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

226 survival after phagocytosis by Dictyostelium discoideum or human macrophages.

227 ely better survival after phagocytosis by D. discoideum or macrophages.

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

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

230 the mycetozoan model organism Dictyostelium discoideum Our results show that phenamacril potently (I

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

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

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

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

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

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

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

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

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

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

241 nicellular phagocytic organism Dictyostelium discoideum reveal that, like OCRL, the Dictyostelium OCR

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

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

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

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

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

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

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

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

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

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

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

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

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

255 In Dictyostelium discoideum, small GTPase methylation occurs seconds afte

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

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

258 using genome sequences from 67 Dictyostelium discoideum strains.

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

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

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

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

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

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

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

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

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

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 R-E test in the model organism Dictyostelium discoideum to demonstrate that Dync1li1 is an essential

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

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

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

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

275 athways, such as those used by Dictyostelium discoideum to move toward cAMP, use a G protein-coupled

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

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

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

279 Dictyostelium discoideum transformed with mutant PfCRT expresses key f

280 more primitive model organism Dictyostelium discoideum using a microfluidic chip design.

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

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

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

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

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

286 Examining these proteins in D. discoideum, we find that, like OCRL, Dd5P4 acts at well-

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 ped diversity of natural products made by D. discoideum, which may have diverse roles in its developm

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

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

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

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