ライフサイエンスコーパス: Dictyostelium

1 o cell speeds, and seen in Mouse T cells and Dictyostelium.

2 tes the RasC-mediated activation of TORC2 in Dictyostelium.

3 d is involved in developmental cell death in Dictyostelium.

4 tion leading to multicellular development in Dictyostelium.

5 n-based motility in cell-free systems and in Dictyostelium.

6 sis of the subunits' individual functions in Dictyostelium.

7 nant dynein fragments from budding yeast and Dictyostelium.

8 itical component for chemotaxis signaling in Dictyostelium.

9 ule during starvation-induced development of Dictyostelium.

10 16) identified in cells of the social amoeba Dictyostelium a G protein-coupled receptor (GPCR) that r

11 In Dictyostelium (a social amoeba), Toxoplasma gondii (the

12 In Dictyostelium, a basal chemotaxis pathway consisting of

13 protein, mediating inhibition of a conserved Dictyostelium AAA ATPase, p97, a homolog of the human tr

14 hat directly interact with the SH3 domain of Dictyostelium actin-binding protein 1 (dAbp1).

15 e carried out single cell transcriptomics on Dictyostelium aggregates.

16 ue, unbiased phenotypic chemotaxis-dependent Dictyostelium aggregation assay for high-throughput scre

17 e examine cell shape and movement in starved Dictyostelium amoebae during migration toward a chemoatt

18 Wildtype Dictyostelium amoebae feed on bacteria, but for decades

19 Dictyostelium amoebae represent an intriguing synthetic

20 actor-1 (DIF-1) is a polyketide that induces Dictyostelium amoebae to differentiate as prestalk cells

21 Starvation induces Dictyostelium amoebae to secrete cAMP, toward which othe

22 Diverse soil amoebas including Dictyostelium and Acanthamoeba can host intracellular ba

23 ated in survival during starvation in yeast, Dictyostelium and animals.

24 by pro-inflammatory mediators, chemotaxis of Dictyostelium and cell growth in Drosophila.

25 ionship is conserved in the simple eukaryote Dictyostelium and exploit this organism to define mechan

26 e (AMPK) has been proposed to play a role in Dictyostelium and human cytopathology in mitochondrial d

27 ies of both compounds were confirmed in both Dictyostelium and in human neutrophils in a directed EZ-

28 e observed for different chemoattractants in Dictyostelium and in human neutrophils, suggesting an ev

29 nd extend the reach of classical genetics in Dictyostelium and likely other systems as well.

30 AVE activation stops phosphorylation in both Dictyostelium and mammalian cells, implying that phospho

31 The genetic/molecular model Dictyostelium and mammalian phagocytes share mechanistic

32 yosin II localizes to the cleavage furrow in Dictyostelium and metazoan cells remains largely unknown

33 ression during development of wild-type (WT) Dictyostelium and mutant cells lacking ChdC, a Type III

34 In the social amoeba Dictyostelium and probably many other unicellular eukary

35 ediates O(2) regulation of the social amoeba Dictyostelium and the parasite Toxoplasma gondii The ful

36 rved F&H interactor was identified, GxcU (in Dictyostelium) and the Cdc42-GEF FGD1-related F-actin bi

37 as orthologue-specific degradation system in Dictyostelium, and further identification of the respons

38 show here that the inositol phospholipids of Dictyostelium are different, being highly enriched in an

39 We show that macropinocytic cups in Dictyostelium are organised around coincident intense pa

40 resistance in HR-deficient cells and present Dictyostelium as a convenient genetic model to character

41 ment the phenotypes, which further validates Dictyostelium as a model of the disease.

42 Using Dictyostelium as a model, we observe that a compression

43 Together, these data identify Dictyostelium as a novel model organism with the capacit

44 by prioritizing bacterial response genes in Dictyostelium as a novel model system for prokaryote-euk

45 Cell death in the model organism Dictyostelium, as studied in monolayers in vitro, can be

46 Dictyostelium biologists now face the widespread challen

47 for multicellular development of animals and Dictyostelium but are absent in plants and yeast.

48 TSET is non-essential in Dictyostelium, but may act in plasma membrane turnover,

49 utionize the field of functional genomics in Dictyostelium by greatly expanding the mutation spectrum

50 s of the alpha-actinin/spectrin subfamily of Dictyostelium calponin homology proteins.

51 tory subunit B56, encoded by psrA, modulates Dictyostelium cell differentiation through negatively af

52 P was not sufficient to induce cell death in Dictyostelium cell monolayers.

53 1evels of activated Rac in coronin-deficient Dictyostelium cells (corA(-)), which impacts myosin II a

54 Here we show that Dictyostelium cells accumulate extracellular polyphospha

55 When Dictyostelium cells are hyperosmotically stressed, STATc

56 Dictyostelium cells can move with both blebs and actin-d

57 cell squasher" to apply uniaxial pressure to Dictyostelium cells chemotaxing under soft agarose.

58 Dictyostelium cells disrupted in exonuclease I, a critic

59 Dictyostelium cells exchange signals to position special

60 criptomics, we identified a subpopulation of Dictyostelium cells experiencing spontaneous DNA damage.

61 Dictyostelium cells have to judge when sufficient cell d

62 Dictyostelium cells lacking the tumor suppressor PTEN sh

63 Consequently, Dictyostelium cells lacking WASH are unable to grow on m

64 Dictyostelium cells lacking WASP inappropriately activat

65 ence that the actin machinery of chemotactic Dictyostelium cells operates close to an oscillatory ins

66 Previously, we found that chemotaxing Dictyostelium cells preferentially bleb from concave reg

67 Thus, heterologous expression system in Dictyostelium cells provides mechanistic and functional

68 regation of a whole developing population of Dictyostelium cells splits into two.

69 We show that Dictyostelium cells switch from using predominantly pseu

70 n multiple signaling pathways [6] can direct Dictyostelium cells to either cathode or anode.

71 Developing Dictyostelium cells undergo highly efficient dedifferent

72 Dictyostelium cells were observed moving under agarose,

73 AprA also causes chemorepulsion of Dictyostelium cells, and CnrN is required for this proce

74 ee-dimensional forces exerted by chemotaxing Dictyostelium cells, and examined wild-type cells as wel

75 stem in which human PTEN-GFP is expressed in Dictyostelium cells, we identified mutations in the memb

76 s proliferation and causes chemorepulsion of Dictyostelium cells, yet AprA has little sequence simila

77 and is essential for efficient chemotaxis of Dictyostelium cells.

78 ated human PTEN and expressed the library in Dictyostelium cells.

79 entally in both wild-type and myosin II null Dictyostelium cells.

80 transcriptional events in individual living Dictyostelium cells.

81 AprA is a chemorepellent protein secreted by Dictyostelium cells.

82 f the same core set of around 80 proteins in Dictyostelium cells.

83 In neutrophils and Dictyostelium, chemoattractant gradients generate direct

84 ic pathways for chemotaxis and phagocytosis; Dictyostelium chemotax toward bacteria and phagocytose t

85 We quantified Dictyostelium chemotaxis towards live gram positive and

86 for PKBA and PKBR1 and thus heavily affects Dictyostelium chemotaxis.

87 a2 binding partner that directly couples the Dictyostelium cyclic AMP GPCR to Rap1.

88 anisms, such as humans and the social amoeba Dictyostelium (Dd).

89 ation is important for oxygen-sensing during Dictyostelium development and is mediated by a HIF-alpha

90 xylation of Skp1 contributes to O2-dependent Dictyostelium development, but full glycosylation at tha

91 We have trapped the catalytic domain of Dictyostelium (Dicty) myosin II in a weak actin-binding

92 and AcgA, both essential for sporulation in Dictyostelium, did not affect Polysphondylium sporulatio

93 that transcript variability emerging during Dictyostelium differentiation is driven predominantly by

94 Here we show that the Dictyostelium diguanylate cyclase, DgcA, produces c-di-G

95 Here we use the Dictyostelium diploid system to replace the essential Ar

96 lysine-265 (K265) of the myosin-2 motor from Dictyostelium discoideum (Dd) is proposed to be a key re

97 Here we consider Dictyostelium discoideum (Dd), a member of the Amoebazoa

98 direction sensing based on experiments using Dictyostelium discoideum (Dicty).

99 In this study, PKAR and PDE from Dictyostelium discoideum (RD and RegA, respectively) wer

100 On food depletion, Dictyostelium discoideum amoebas collect into aggregates

101 Dictyostelium discoideum amoebas coordinate aggregation

102 DIRS-1 is the most abundant retroelement in Dictyostelium discoideum and constitutes the pericentrom

103 seudopod-dominated migration of the amoeboid Dictyostelium discoideum and for the lamellipod-driven m

104 Farmer clones of the social amoeba Dictyostelium discoideum carry bacteria to seed out new

105 Proliferating Dictyostelium discoideum cells accumulate extracellular

106 Chemotaxing Dictyostelium discoideum cells adapt their morphology an

107 intracellular transport are investigated in Dictyostelium discoideum cells by single particle tracki

108 antify the directional biases in chemotactic Dictyostelium discoideum cells in a flow chamber with al

109 In multinucleated Dictyostelium discoideum cells, each centrosome organize

110 y establishment varies across cell types: in Dictyostelium discoideum cells, it is mediated by bioche

111 e early stages of cytokinesis, in rounded-up Dictyostelium discoideum cells, the small G-protein Rap1

112 entral membrane of oversized, multinucleated Dictyostelium discoideum cells.

113 elay on the collective behavior of migrating Dictyostelium discoideum cells.

114 ce of the actin network in experiments using Dictyostelium discoideum cells.

115 d material transport within the cytoplasm of Dictyostelium discoideum cells: the anomalous non-linear

116 Two TCs from Dictyostelium discoideum converted farnesyl diphosphate

117 The social amoebae Dictyostelium discoideum cooperate by forming multicellu

118 Here, we show that the amoeba Dictyostelium discoideum coordinates Ras and Rac activit

119 d for cell surface cAMP receptors throughout Dictyostelium discoideum development, controlling chemot

120 Dictyostelium discoideum DgcA synthesized c-di-GMP in a

121 The simple eukaryote Dictyostelium discoideum displays chemotactic locomotion

122 roscopy we directly observe the structure of Dictyostelium discoideum dynein dimers on microtubules a

123 Dictyostelium discoideum encodes one Thg1 and three TLPs

124 In the Dictyostelium discoideum farming symbiosis, certain amoe

125 The amoeba Dictyostelium discoideum feeds on, and is colonized by,

126 melanogaster, Schizosaccharomyces pombe and Dictyostelium discoideum for methylation of the Geobacte

127 The Dictyostelium discoideum genome encodes five proteins th

128 Here we show that the model organism Dictyostelium discoideum has evolved to normally encode

129 The model organism Dictyostelium discoideum has greatly facilitated our und

130 Using bioinformatics tools, we show that Dictyostelium discoideum has the highest content of prio

131 The life cycle of the social amoeba Dictyostelium discoideum includes a multicellular stage

132 The social amoeba Dictyostelium discoideum integrates into a multicellular

133 ion-induced aggregation of the social amoeba Dictyostelium discoideum into a multicellular slug is kn

134 The social amoeba Dictyostelium discoideum is a professional phagocyte tha

135 The social amoeba Dictyostelium discoideum is a widely used model organism

136 Dictyostelium discoideum is an amoebozoa that exists in

137 es were explored for cellular ion imaging in Dictyostelium discoideum live cells but spontaneous dye

138 min G (ForG) from the professional phagocyte Dictyostelium discoideum localizes to endocytic cups.

139 Dictyostelium discoideum MyoB is a class I myosin involv

140 and have poor survival after phagocytosis by Dictyostelium discoideum or human macrophages.

141 m species, and the mycetozoan model organism Dictyostelium discoideum Our results show that phenamacr

142 ulticellular slug stage of the social amoeba Dictyostelium discoideum produce ETs upon stimulation wi

143 ew research indicates that the social amoeba Dictyostelium discoideum recognizes distinctions between

144 ides and the unicellular phagocytic organism Dictyostelium discoideum reveal that, like OCRL, the Dic

145 Here we show that Dictyostelium discoideum Roco4 is a suitable model to st

146 Experiments on the social amoeba Dictyostelium discoideum show that the origins of lineag

147 The excitable cells of Dictyostelium discoideum show traveling waves of signali

148 interactions using genome sequences from 67 Dictyostelium discoideum strains.

149 ost is a "farmer" clone of the social amoeba Dictyostelium discoideum that carries and disperses bact

150 ady present in mycetozoan eukaryotes such as Dictyostelium discoideum This social amoeba kills bacter

151 emical mutagenesis in the social soil amoeba Dictyostelium discoideum Through genome sequencing, we s

152 sed this CRISPR-E test in the model organism Dictyostelium discoideum to demonstrate that Dync1li1 is

153 show that PIP(3) is not only unnecessary for Dictyostelium discoideum to migrate toward folate, but a

154 transduction pathways, such as those used by Dictyostelium discoideum to move toward cAMP, use a G pr

155 Dictyostelium discoideum transformed with mutant PfCRT e

156 nserved in the more primitive model organism Dictyostelium discoideum using a microfluidic chip desig

157 The social amoeba Dictyostelium discoideum was selected for functional stu

158 mediated signaling network for chemotaxis in Dictyostelium discoideum We identified a negative regula

159 o used for communication in the social ameba Dictyostelium discoideum when the solitary cells aggrega

160 Our findings identified the slime mold Dictyostelium discoideum's CISD proteins as the closest

161 C2 in AKT phosphorylation in social amoebae (Dictyostelium discoideum) cells.

162 Dictyostelium discoideum, a soil-dwelling social amoeba,

163 n phytate-loaded Acanthamoeba castellanii or Dictyostelium discoideum, and the intracellular growth d

164 PHD homologues from the cellular slime mold, Dictyostelium discoideum, and the protozoan parasite, To

165 In Dictyostelium discoideum, AprA and CfaD are secreted pro

166 In Dictyostelium discoideum, AprA is a secreted protein tha

167 ular slime molds, including the well-studied Dictyostelium discoideum, are amoebae whose life cycle i

168 from Schizosaccharomyces pombe and DnmA from Dictyostelium discoideum, are strongly stimulated by pri

169 n model organisms: Saccharomyces cerevisiae, Dictyostelium discoideum, Caenorhabditis elegans, Drosop

170 In many systems, including the social amoeba Dictyostelium discoideum, development is often marked by

171 some eukaryotes, including the social amoeba Dictyostelium discoideum, encode both a class I and a cl

172 In the social amoeba Dictyostelium discoideum, four signaling pathways act sy

173 T ortholog in the model developmental system Dictyostelium discoideum, in which Ca(2+) plays a role i

174 In Dictyostelium discoideum, loss of SCAR is compensated by

175 is three-step modification pathway exists in Dictyostelium discoideum, model of the evolutionary supe

176 We show that in the nonmetazoan Dictyostelium discoideum, myosin II localizes apically i

177 ins from Homo sapiens, Arabidopsis thaliana, Dictyostelium discoideum, Saccharomyces cerevisiae, Esch

178 In an unrelated protist, Dictyostelium discoideum, Skp1 hydroxyproline is modifie

179 In the social amoeba Dictyostelium discoideum, starvation-triggered multicell

180 d in cheating behaviors in the social amoeba Dictyostelium discoideum, testing whether these genes ex

181 ate spore encapsulation in the social amoeba Dictyostelium discoideum, the metabolic profile and othe

182 Here we employ a simple eukaryote, Dictyostelium discoideum, to demonstrate distinct effect

183 Using a forward genetic screen in Dictyostelium discoideum, we identified the Ste20 kinase

184 Using the social amoeba Dictyostelium discoideum, we provide a possible explanat

185 ine repeats from the single-celled eukaryote Dictyostelium discoideum, which also has a multicellular

186 We test this evolutionary hypothesis in Dictyostelium discoideum, which forms multicellular frui

187 fflux or uptake systems in the social amoeba Dictyostelium discoideum.

188 were able to visualize polyP extracted from Dictyostelium discoideum.

189 sion of social cheating in the social amoeba Dictyostelium discoideum.

190 arity is mainly studied in the social amoeba Dictyostelium discoideum.

191 d 'Cupid', was identified from the genome of Dictyostelium discoideum.

192 h system is represented by the social amoeba Dictyostelium discoideum.

193 eukaryotic microbe (protist), the slime mold Dictyostelium discoideum.

194 on experiments on single cells of the amoeba Dictyostelium discoideum.

195 7C mutant of non-muscle myosin II motor from Dictyostelium discoideum.

196 three CHD orthologs (ChdA, ChdB and ChdC) in Dictyostelium discoideum.

197 odel organism database for the social amoeba Dictyostelium discoideum.

198 rward genetic approach in the model organism Dictyostelium discoideum.

199 sesquiterpene and affects the development of Dictyostelium discoideum.

200 diverse species including most metazoans and Dictyostelium discoideum.

201 he ampA gene has a role in cell migration in Dictyostelium discoideum.

202 ate via the complex life cycle of the amoeba Dictyostelium discoideum.

203 measured in chemotaxing unicellular amoeba, Dictyostelium discoideum.

204 through the social stage of an amoeba host, Dictyostelium discoideum.

205 in loner behavior in the model social amoeba Dictyostelium discoideum.

206 ress currently stores the data from over 800 Dictyostelium experiments and is embedded within a gener

207 ymes thus appear to mediate the synthesis of Dictyostelium extracellular polyphosphate, which is used

208 ostelids, including Dictyostelium purpureum, Dictyostelium fasciculatum and Polysphondylium pallidum.

209 e heterodimers complex in vivo with DGAP1, a Dictyostelium GAP protein.

210 We identify a Dictyostelium gene showing rapid transcriptional oscilla

211 ates the addition of the final two sugars in Dictyostelium, generating Galalpha1, 3Galalpha1,3Fucalph

212 We find that Dictyostelium genes are demarcated precisely at their 5'

213 ocytosis of bacteria induced upregulation of Dictyostelium genes encoding the copper uptake transport

214 rocal linking with dictyBase-a repository of Dictyostelium genomic data.

215 in Dictyostelium, whereas human H-Ras and a Dictyostelium H-Ras homologue (RasC) are refractory to u

216 gnaling during large-scale endocytosis in WT Dictyostelium has been, for the most part, attributed to

217 We also show that Dictyostelium has the capacity to suppress aggregation o

218 Dictyostelium histones are modified in response to DNA d

219 nability of c-di-GMP to induce cell death in Dictyostelium HMX44A cells and DH1 cells upon pharmacolo

220 ional myosin 7 (DdMyo7) in the social amoeba Dictyostelium However, the exact roles of these MyTH4-FE

221 e quiescence of organisms such as yeasts and Dictyostelium in response to nutritional starvation and

222 raid as a synthetic biological framework for Dictyostelium, including a library of 250 DNA parts and

223 Studies in Dictyostelium indicate that TSET is a heterohexamer, wit

224 hydroxyproline by a pentasaccharide that, in Dictyostelium, influences Skp1 structure to favor assemb

225 GbpC is a multidomain Roco protein in Dictyostelium, involved in transduction of intracellular

226 y distinguish IqgC from other members of the Dictyostelium IQGAP family and call for repositioning of

227 d complementation assays in live cells, that Dictyostelium IQGAP-related protein IqgC interacts with

228 stinct but structurally compatible glycan in Dictyostelium is a remarkable case of convergent evoluti

229 expulsion by the contractile vacuole (CV) in Dictyostelium is carried out by a giant kiss-and-run foc

230 Dictyostelium is the only nonmetazoan with functionally

231 nism for interaction with the environment in Dictyostelium is unknown and thus, we explore different

232 mediated cytofission, originally observed in Dictyostelium, is relevant to human biology--where it se

233 Dictyostelium lacking P2XA receptors showed impaired reg

234 Dictyostelium lacks HIFalpha, and P4H1 modifies a differ

235 We propose that Dictyostelium loners-cells that do not join the multicel

236 Using the Dictyostelium model system, we show that the three Diaph

237 ACA produces the cAMP pulses that coordinate Dictyostelium morphogenetic cell movement and is highly

238 trate active nucleosome repositioning during Dictyostelium multicellular development, establish an in

239 Our results suggest that Dictyostelium multicellular sporulation was a likely ada

240 By characterizing a Dictyostelium mutant defective in chemotactic responses,

241 This phenomenon was also observed in a Dictyostelium mutant lacking MidA (C2orf56/PRO1853/Ndufa

242 Now we show that PH domains occur in all Dictyostelium myosin 1s and that the BH sites of Myo1A,

243 tions of BH sites affect localization of all Dictyostelium myosin 1s.

244 The tail of Dictyostelium myosin IB (DMIB) also contains a BH site.

245 muscle myosin, beta-cardiac myosin (CMIIB), Dictyostelium myosin II (DdMII), and nonmuscle myosin II

246 We labeled a Cys-lite Dictyostelium myosin II motor domain with donor and acce

247 ns to resolve a structural transition in the Dictyostelium myosin II relay helix during the actin-act

248 spin label (BSL) bound stereospecifically to Dictyostelium myosin II, we determined with high resolut

249 Using mathematical modeling for Dictyostelium myosin II, we predict that myosin II mecha

250 two sequentially divergent IQ motifs of the Dictyostelium myosin-1C.

251 tic properties of the alpha-kinase domain of Dictyostelium myosin-II heavy chain kinase-A (termed A-C

252 Disruption of Dictyostelium Ndufaf5 leads to CI deficiency and defects

253 elium discoideum reveal that, like OCRL, the Dictyostelium OCRL orthologue Dd5P4 binds two proteins c

254 ed that c-di-GMP could trigger cell death in Dictyostelium only in the presence of the DIF-1 polyketi

255 AVE phosphorylation does not require ERK2 in Dictyostelium or mammalian cells.

256 s been, for the most part, attributed to the Dictyostelium ortholog of human RasGAP NF1, in commonly

257 Here, we demonstrate RasG, the Dictyostelium orthologue of K-Ras, is targeted for degra

258 In Dictyostelium, oscillatory actin foci interact with sign

259 Dictyostelium p21-activated kinase B (PakB) phosphorylat

260 there is limited functional redundancy among Dictyostelium P2X receptors.

261 Loss of the Dictyostelium polyphosphate kinase DdPpk1 causes intrace

262 Pathological mutations were recreated in the Dictyostelium protein and expressed in the mutant backgr

263 gh basal and poststimulus phosphorylation of Dictyostelium protein kinase B (PKB) kinase family membe

264 We have previously shown that the Dictyostelium protein phosphatase 2A regulatory subunit

265 Dictyostelium provides an ideal system to examine the ex

266 For two of these taxa, the amoebozoan Dictyostelium purpureum and the jakobid Andalucia incarc

267 up to host multiple Dictyostelids, including Dictyostelium purpureum, Dictyostelium fasciculatum and

268 es of CP knockdown, overexpression of V-1 in Dictyostelium reduced the size of pseudopodia and the co

269 generation sequencing based inquiries by the Dictyostelium research community.

270 Here, we show that a Dictyostelium Rho GTPase, RacE, and a guanine nucleotide

271 ch inhibitors, we mutated the active site of Dictyostelium Roco4 kinase to resemble LRRK2.

272 te that the C-terminal acidic domain of most Dictyostelium SCAR is basally phosphorylated at four ser

273 Under defined conditions, individual Dictyostelium secrete chemoattractants, migrate, and agg

274 By analogy to Dictyostelium Skp1, the mechanism may involve regulation

275 n can prolyl hydroxylate both Toxoplasma and Dictyostelium Skp1s.

276 The Dictyostelium stalk always forms at the organizing tip,

277 Studies in mammalian cells and Dictyostelium suggest that WASH functions primarily in a

278 In mammals and now in Dictyostelium, the hydrocarbon chains of inositol phosph

279 In Dictyostelium, the mechanoenzyme myosin II and the actin

280 In the early chemotaxis studies in Dictyostelium, the rictor's ortholog has been identified

281 In Dictyostelium, this system tunes myosin II accumulation

282 y validated as necessary for the response of Dictyostelium to Gram-negative bacteria.

283 Here we exploit the model Dictyostelium to identify site-specific histone ADP-ribo

284 Here, we exploit the genetic versatility of Dictyostelium to investigate the effects of physiologica

285 In Dictyostelium, TORC2 functions at the front of migrating

286 egulates multiple physiological processes as Dictyostelium transitions from a group of unicellular am

287 myosin 10 (Myo10) in mammalian cells and of Dictyostelium unconventional myosin 7 (DdMyo7) in the so

288 Accumulated Cu(I) in Dictyostelium was monitored using a copper biosensor bac

289 We report that, in Dictyostelium, WASH is also required for the lysosomal d

290 Using Dictyostelium, we demonstrate that WASH drives protein s

291 Using a tractable model system, Dictyostelium, we show that decanoic acid can decrease m

292 r modification is found in the social amoeba Dictyostelium, where it regulates SCF assembly and O2-de

293 ergoes polyubiquitin-mediated degradation in Dictyostelium, whereas human H-Ras and a Dictyostelium H

294 monstrate conservation of these phenomena in Dictyostelium which has three single-copy H3 variant gen

295 ogical significance of this CP antagonist in Dictyostelium, which expresses a V-1 homolog that we sho

296 We have identified protein NE81 in Dictyostelium, which has properties that justify its den

297 l resistance induces bleb-driven movement in Dictyostelium, which is chemotactic and controlled throu

298 A primary example is the social amoeba Dictyostelium, which migrates to the source of traveling

299 Global stimulation of Dictyostelium with different chemoattractants elicits mu

300 developmental self-organisation is shown by Dictyostelium, with cells segregating into two major fat