戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ate via the complex life cycle of the amoeba Dictyostelium discoideum.
2 densis to predation by the phagocytic amoeba Dictyostelium discoideum.
3 cell formation in the developmental cycle of Dictyostelium discoideum.
4  the mating-type locus of the model organism Dictyostelium discoideum.
5  model organisms, Caenorhabditis elegans and Dictyostelium discoideum.
6 dictyBase is the model organism database for Dictyostelium discoideum.
7 nt a protocol for the extraction of RNA from Dictyostelium discoideum.
8 y and cell adhesion during cell migration in Dictyostelium discoideum.
9 ial pathogens and for obtaining nutrients in Dictyostelium discoideum.
10 tracting DNA from cells of the social amoeba Dictyostelium discoideum.
11  controlling chemotaxis and cell adhesion in Dictyostelium discoideum.
12 hemotactic migration of the amoeboid form of Dictyostelium discoideum.
13 lated derivative of Pro-143 in the amebazoan Dictyostelium discoideum.
14 ed nematode species and from the slime mold, Dictyostelium discoideum.
15 orters present in apicomplexan parasites and Dictyostelium discoideum.
16 fflux or uptake systems in the social amoeba Dictyostelium discoideum.
17 rganism database (MOD) for the social amoeba Dictyostelium discoideum.
18 ilago maydis and spores of the social amoeba Dictyostelium discoideum.
19  to human DGK-theta, DGKA, was identified in Dictyostelium discoideum.
20  were able to visualize polyP extracted from Dictyostelium discoideum.
21  formation of the slug in the social amoebae Dictyostelium discoideum.
22 to isolate genes required for cytokinesis in Dictyostelium discoideum.
23  of bone resorption as well as the growth of Dictyostelium discoideum.
24 throughout the 24 h developmental program of Dictyostelium discoideum.
25  from P. vivax, P. knowlesi, P. berghei, and Dictyostelium discoideum.
26 omyces cerevisiae, Entamoeba histolytica and Dictyostelium discoideum.
27 al program of the simple eukaryotic organism Dictyostelium discoideum.
28 med during development of the social amoeba, Dictyostelium discoideum.
29 is thaliana, Mycobacterium tuberculosis, and Dictyostelium discoideum.
30 ld replicate within the unicellular organism Dictyostelium discoideum.
31 rganism size in the eukaryotic microorganism Dictyostelium discoideum.
32 -MHC) cells moving within the tight mound of Dictyostelium discoideum.
33 the first DNA transposon to be isolated from Dictyostelium discoideum.
34 lular development of the cellular slime mold Dictyostelium discoideum.
35 issimo (PiaA), involved in cAMP signaling in Dictyostelium discoideum.
36  marks a critical point in the life cycle of Dictyostelium discoideum.
37  measured in chemotaxing unicellular amoeba, Dictyostelium discoideum.
38 sion of social cheating in the social amoeba Dictyostelium discoideum.
39 arity is mainly studied in the social amoeba Dictyostelium discoideum.
40 h system is represented by the social amoeba Dictyostelium discoideum.
41 eukaryotic microbe (protist), the slime mold Dictyostelium discoideum.
42 on experiments on single cells of the amoeba Dictyostelium discoideum.
43 7C mutant of non-muscle myosin II motor from Dictyostelium discoideum.
44 three CHD orthologs (ChdA, ChdB and ChdC) in Dictyostelium discoideum.
45 odel organism database for the social amoeba Dictyostelium discoideum.
46 rward genetic approach in the model organism Dictyostelium discoideum.
47  through the social stage of an amoeba host, Dictyostelium discoideum.
48 diverse species including most metazoans and Dictyostelium discoideum.
49 he ampA gene has a role in cell migration in Dictyostelium discoideum.
50 y conserved between humans and the protozoan Dictyostelium discoideum.
51 red for normal chemotaxis and cytokinesis in Dictyostelium discoideum.
52 uman pathogen Pseudomonas aeruginosa infects Dictyostelium discoideum, a genetically tractable eukary
53                             Using the amoeba Dictyostelium discoideum, a model system for the study o
54                                              Dictyostelium discoideum, a social slime mold that forms
55                                              Dictyostelium discoideum, a social slime mold, is one of
56                                              Dictyostelium discoideum, a soil-dwelling social amoeba,
57                                              Dictyostelium discoideum, a unicellular organism capable
58 , the first subprocess of chemorepulsion, in Dictyostelium discoideum-a well characterized model euka
59                             We show that, in Dictyostelium discoideum, activated forms of RasC prolon
60                              The csA gene in Dictyostelium discoideum acts as a single-gene greenbear
61 olated a constitutively active mutant of the Dictyostelium discoideum adenylyl cyclase harboring a si
62 ss VII unconventional myosin (DdMVII) in the Dictyostelium discoideum amoeba, which is a model for ph
63 tracellular signals is remarkably similar in Dictyostelium discoideum amoebae and mammalian leukocyte
64                                           In Dictyostelium discoideum amoebae and mammalian leukocyte
65                          Uniform exposure of Dictyostelium discoideum amoebae as well as mammalian le
66                      The ability of prespore Dictyostelium discoideum amoebae to undergo redifferenti
67             Many eukaryotic cells, including Dictyostelium discoideum amoebae, fibroblasts, and neutr
68  family was less severe during growth within Dictyostelium discoideum amoebae, indicating that the re
69 otein gp130, found on the plasma membrane of Dictyostelium discoideum amoebae, was postulated previou
70  40,000 actin filament severing protein from Dictyostelium discoideum amoebae, we have identified a m
71                           On food depletion, Dictyostelium discoideum amoebas collect into aggregates
72                                              Dictyostelium discoideum amoebas coordinate aggregation
73                          In highly polarized Dictyostelium discoideum amoebas, membrane-associated be
74                                              Dictyostelium discoideum (Amoebidae) secretes cell-lysin
75 nzyme A (CoA)-binding protein (ACBP; AcbA in Dictyostelium discoideum), an unconventionally secreted
76 ut only a approximately 1-2 mM IC(50) versus Dictyostelium discoideum and a human cell line, indicati
77  DIRS-1 is the most abundant retroelement in Dictyostelium discoideum and constitutes the pericentrom
78 seudopod-dominated migration of the amoeboid Dictyostelium discoideum and for the lamellipod-driven m
79  pneumophila is grown within the soil amoeba Dictyostelium discoideum and how D. discoideum genetics
80                            Investigations in Dictyostelium discoideum and neutrophils have establishe
81 ukaryotic cells, including amoeboid cells of Dictyostelium discoideum and neutrophils, respond to che
82  in the well-characterized chemotactic cells Dictyostelium discoideum and neutrophils, signaling to t
83 (Saccharomyces cerevisiae), two slime molds (Dictyostelium discoideum and Physarum polycephalum), and
84 ms that control multicellular development in Dictyostelium discoideum and reconstruct how some of the
85  integrated, high quality data and tools for Dictyostelium discoideum and related species.
86                                    Likewise, Dictyostelium discoideum and Saccharomyces cerevisiae ca
87 F-actin assay detects the same proteins from Dictyostelium discoideum and with approximately the same
88 e numbering of residues follows myosin II in Dictyostelium discoideum) and the water molecule that sp
89 s biological function within macrophages and Dictyostelium discoideum, and for intrapulmonary prolife
90 orhabditis elegans, Acathamoeba castellanii, Dictyostelium discoideum, and Galleria mellonella have p
91              As L. pneumophila replicates in Dictyostelium discoideum, and macroautophagy genes have
92              Gene knockout studies in yeast, Dictyostelium discoideum, and mammalian cells have begun
93 ated gene in the genome of the social amoeba Dictyostelium discoideum, and show, with the use of hete
94 ous structures of S1 (from chicken skeletal, Dictyostelium discoideum, and smooth muscle myosins), in
95 n phytate-loaded Acanthamoeba castellanii or Dictyostelium discoideum, and the intracellular growth d
96                                           In Dictyostelium discoideum, AprA and CfaD are secreted pro
97                                           In Dictyostelium discoideum, AprA is a secreted protein tha
98 many of the essential developmental genes in Dictyostelium discoideum are known to depend on PKA acti
99 roportions of prespore and prestalk cells in Dictyostelium discoideum are regulated so that they are
100                                              Dictyostelium discoideum are social amoebas that propaga
101 ular slime molds, including the well-studied Dictyostelium discoideum, are amoebae whose life cycle i
102 from Schizosaccharomyces pombe and DnmA from Dictyostelium discoideum, are strongly stimulated by pri
103                                        Using Dictyostelium discoideum as a model host, we have identi
104               Despite widespread interest in Dictyostelium discoideum as a model system, almost no mo
105                                              Dictyostelium discoideum belongs to a group of multicell
106 of different signal transduction pathways in Dictyostelium discoideum but Galpha subunit-effector int
107  cAR1, the major chemoattractant receptor of Dictyostelium discoideum by a strategy that is independe
108 inase B (PKB) homologues, PkbA and PkbR1, in Dictyostelium discoideum by phosphorylation of activatio
109 n model organisms: Saccharomyces cerevisiae, Dictyostelium discoideum, Caenorhabditis elegans, Drosop
110 4, shares limited sequence identity with the Dictyostelium discoideum cAMP receptor cAR1 and the Aspe
111      Free-living cells of the social amoebae Dictyostelium discoideum can aggregate and develop into
112 underlie the mechanism of oligomerisation in Dictyostelium discoideum CAP.
113           Farmer clones of the social amoeba Dictyostelium discoideum carry bacteria to seed out new
114                                           In Dictyostelium discoideum, cell density is monitored by l
115                                  Chemotaxing Dictyostelium discoideum cells adapt their morphology an
116                                     Starving Dictyostelium discoideum cells aggregate to form dendrit
117 ne signal AprA, which is produced by growing Dictyostelium discoideum cells and inhibits their prolif
118 oteins (G-proteins) was visualized in living Dictyostelium discoideum cells by monitoring fluorescenc
119  intracellular transport are investigated in Dictyostelium discoideum cells by single particle tracki
120                  Upon starvation, individual Dictyostelium discoideum cells enter a developmental pro
121 antify the directional biases in chemotactic Dictyostelium discoideum cells in a flow chamber with al
122                                              Dictyostelium discoideum cells lacking PTEN exhibited im
123 ne the nature of this response, we subjected Dictyostelium discoideum cells to measurable temporal an
124 emonstrate here that M. marinum grows within Dictyostelium discoideum cells, allowing the genetic ana
125 ion of adenylyl cyclase (ACA) at the back of Dictyostelium discoideum cells, an essential determinant
126 e early stages of cytokinesis, in rounded-up Dictyostelium discoideum cells, the small G-protein Rap1
127 front and back, respectively, of chemotaxing Dictyostelium discoideum cells.
128  is required for the efficient chemotaxis of Dictyostelium discoideum cells.
129 elay on the collective behavior of migrating Dictyostelium discoideum cells.
130 served in bacterial cellulose synthases, the Dictyostelium discoideum cellulose synthase, and other p
131 died the role of the adenylyl cyclase ACA in Dictyostelium discoideum chemotaxis and streaming.
132 high-resolution HAPPY map of chromosome 6 of Dictyostelium discoideum consisting of 300 sequence-tagg
133                                The genome of Dictyostelium discoideum contains six genes encoding pro
134 rganelle responsible for osmoregulation, the Dictyostelium discoideum contractile vacuole.
135                                 Two TCs from Dictyostelium discoideum converted farnesyl diphosphate
136                           The social amoebae Dictyostelium discoideum cooperate by forming multicellu
137       In this study, we investigated whether Dictyostelium discoideum could serve as an alternate hos
138                                           In Dictyostelium discoideum counting factor (CF), a secrete
139 scovered in a genetic suppressor screen of a Dictyostelium discoideum cytokinesis-deficient mutant ce
140 lysine-265 (K265) of the myosin-2 motor from Dictyostelium discoideum (Dd) is proposed to be a key re
141               The fluorescence properties of Dictyostelium discoideum (Dd) myosin II constructs conta
142 report periodic movements during erection of Dictyostelium discoideum (Dd) sorocarps.
143                             Here we consider Dictyostelium discoideum (Dd), a member of the Amoebazoa
144 m, the slug stage of the cellular slime mold Dictyostelium discoideum (Dd).
145 repeat of the gelation factor (ABP-120) from Dictyostelium discoideum (ddFLN5) by NMR spectroscopy to
146  developmentally regulated Na-H exchanger in Dictyostelium discoideum (DdNHE1) localizes to the leadi
147 d for cell surface cAMP receptors throughout Dictyostelium discoideum development, controlling chemot
148 In many systems, including the social amoeba Dictyostelium discoideum, development is often marked by
149                                              Dictyostelium discoideum DgcA synthesized c-di-GMP in a
150 l-degrading enzymes, such as PDE for cAMP in Dictyostelium discoideum (Dicty) and BAR1 for mating fac
151               We have engineered a mutant of Dictyostelium discoideum (Dicty) myosin II that contains
152 direction sensing based on experiments using Dictyostelium discoideum (Dicty).
153                         The simple eukaryote Dictyostelium discoideum displays chemotactic locomotion
154                            The social amoeba Dictyostelium discoideum diverged from the line leading
155 Disruption of the PI 3-phosphatase, PTEN, in Dictyostelium discoideum dramatically prolonged and broa
156                       Orthologues of Hem1 in Dictyostelium discoideum, Drosophila melanogaster, and C
157 rabidopsis thaliana, Caenorhabditis elegans, Dictyostelium discoideum, Drosophila melanogaster, Sacch
158  success of naturally occurring genotypes of Dictyostelium discoideum during the formation of chimeri
159 roscopy we directly observe the structure of Dictyostelium discoideum dynein dimers on microtubules a
160 some eukaryotes, including the social amoeba Dictyostelium discoideum, encode both a class I and a cl
161                                              Dictyostelium discoideum encodes one Thg1 and three TLPs
162                                   The amoeba Dictyostelium discoideum expresses a simple complement o
163                                              Dictyostelium discoideum expresses multiple G alpha subu
164                                       In the Dictyostelium discoideum farming symbiosis, certain amoe
165                                   The amoeba Dictyostelium discoideum feeds on, and is colonized by,
166  melanogaster, Schizosaccharomyces pombe and Dictyostelium discoideum for methylation of the Geobacte
167                                              Dictyostelium discoideum form groups of approximately 2
168                             The non-metazoan Dictyostelium discoideum forms a multicellular, differen
169                We show that the non-metazoan Dictyostelium discoideum forms a polarized epithelium th
170                         In the social amoeba Dictyostelium discoideum, four signaling pathways act sy
171  counting factor (CF), regulates the size of Dictyostelium discoideum fruiting bodies in part by regu
172                         We have identified a Dictyostelium discoideum gene encoding a serine/threonin
173  another member of the PRKX gene family (the Dictyostelium discoideum gene KAPC-DICDI) also plays a r
174                          We have disrupted a Dictyostelium discoideum gene, helC, which encodes helic
175                                          The Dictyostelium discoideum genome encodes five proteins th
176  an expressed FPPS from Leishmania major, in Dictyostelium discoideum growth inhibition, in gammadelt
177 ting FDP synthase and potency for inhibiting Dictyostelium discoideum growth.
178          Here we show that the social amoeba Dictyostelium discoideum has a primitive farming symbios
179 s cerevisiae, Schizosaccharomyces pombe, and Dictyostelium discoideum has allowed us to tentatively d
180         Here we show that the model organism Dictyostelium discoideum has evolved to normally encode
181                           The model organism Dictyostelium discoideum has greatly facilitated our und
182                                              Dictyostelium discoideum has proven a useful system for
183     Using bioinformatics tools, we show that Dictyostelium discoideum has the highest content of prio
184                                              Dictyostelium discoideum has two talins, TalA and TalB,
185 in 2 of severin, the gelsolin homologue from Dictyostelium discoideum, has been determined by multipl
186 cro-organisms Prototheca wickerhamii (I) and Dictyostelium discoideum (II) have been determined by ch
187 T ortholog in the model developmental system Dictyostelium discoideum, in which Ca(2+) plays a role i
188 t of cooperation occurs in the social amoeba Dictyostelium discoideum, in which some cells die to for
189          The life cycle of the social amoeba Dictyostelium discoideum includes a multicellular stage
190 fied multiple PtdInsP(3)-binding proteins in Dictyostelium discoideum, including five pleckstrin homo
191                                           In Dictyostelium discoideum, increased intracellular pH thr
192 tudies of the behavior of the model organism Dictyostelium discoideum indicate the biocompatibility o
193 layed a growth advantage in the amoebal host Dictyostelium discoideum, indicating that the protein fa
194 n confronted with starvation, the amoebae of Dictyostelium discoideum initiate a developmental proces
195                            The social amoeba Dictyostelium discoideum integrates into a multicellular
196 ion-induced aggregation of the social amoeba Dictyostelium discoideum into a multicellular slug is kn
197                                              Dictyostelium discoideum is a model system for studying
198                    The microbial soil amoeba Dictyostelium discoideum is a model system for the study
199                     The cellular slime mold, Dictyostelium discoideum is a non-metazoan organism, yet
200                                              Dictyostelium discoideum is a powerful and genetically t
201                            The social amoeba Dictyostelium discoideum is a professional phagocyte tha
202                                              Dictyostelium discoideum is a useful model for studying
203                            The social amoeba Dictyostelium discoideum is a widely used model organism
204                      The cellular slime mold Dictyostelium discoideum is a widely used model system f
205                                The eukaryote Dictyostelium discoideum is amenable to numerous genetic
206 ature of development in the simple eukaryote Dictyostelium discoideum is an aggregative transition fr
207                                              Dictyostelium discoideum is an amoebozoa that exists in
208                      The cellular slime mold Dictyostelium discoideum is an attractive system for stu
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 mechanical model of the contraction phase of Dictyostelium discoideum motility with an emphasis on th
227                                              Dictyostelium discoideum MyoB is a class I myosin involv
228 rt here the structure of the motor domain of Dictyostelium discoideum myosin II both in its nucleotid
229 structures of the truncated myosin head from Dictyostelium discoideum myosin II complexed with dinitr
230                  One such residue is Ser236 (Dictyostelium discoideum myosin II numbering) which was
231 nt-ADP and beryllium fluoride complexed with Dictyostelium discoideum myosin motor domain (S1dC) at 1
232                                           In Dictyostelium discoideum, myosin II filament assembly is
233              We show that in the nonmetazoan Dictyostelium discoideum, myosin II localizes apically i
234  complete sequence of a retrotransposon from Dictyostelium discoideum , named skipper , was obtained
235                                The 14,955-bp Dictyostelium discoideum nuclear plasmid Ddp5 contains s
236                   The specific disruption in Dictyostelium discoideum of the sphingosine-1-phosphate
237                       The crawling motion of Dictyostelium discoideum on substrata involves a number
238 Chemotactic cells, including neutrophils and Dictyostelium discoideum, orient and move directionally
239              In this study we identified the Dictyostelium discoideum ortholog of the adaptor protein
240 y, we characterize mutations in the putative Dictyostelium discoideum orthologues of budding yeast ge
241                   Remarkably, another PPK in Dictyostelium discoideum (PPK2) is an actin-related prot
242                        In the mound stage of Dictyostelium discoideum, pre-stalk cells sort and form
243 ulticellular slug stage of the social amoeba Dictyostelium discoideum produce ETs upon stimulation wi
244 tain a domain with similarity to that of the Dictyostelium discoideum protein discoidin I.
245                 The eukaryotic microorganism Dictyostelium discoideum provides a unique experimental
246             In this study, PKAR and PDE from Dictyostelium discoideum (RD and RegA, respectively) wer
247 ew research indicates that the social amoeba Dictyostelium discoideum recognizes distinctions between
248 onfirm this prediction for the social amoeba Dictyostelium discoideum; relatedness in natural wild gr
249  that dedifferentiation in the social amoeba Dictyostelium discoideum relies on a sequence of events
250 ke cellulose, such as Ciona intestinalis and Dictyostelium discoideum, revealed the presence of membr
251 s study, we analyzed the function of a novel Dictyostelium discoideum Rho family protein (RacC).
252                            Here we show that Dictyostelium discoideum Roco4 is a suitable model to st
253       Our findings identified the slime mold Dictyostelium discoideum's CISD proteins as the closest
254 ins from Homo sapiens, Arabidopsis thaliana, Dictyostelium discoideum, Saccharomyces cerevisiae, Esch
255                  We show that, unexpectedly, Dictyostelium discoideum SCAR knockouts could still spre
256 s of UMP/CMP kinase, a globular protein from Dictyostelium discoideum, serve as two illustrative exam
257             Experiments on the social amoeba Dictyostelium discoideum show that the origins of lineag
258                       The excitable cells of Dictyostelium discoideum show traveling waves of signali
259 alba x Populus tremula, corn (Zea mays), and Dictyostelium discoideum showed that cyanobacteria share
260                     In an unrelated protist, Dictyostelium discoideum, Skp1 hydroxyproline is modifie
261                                           In Dictyostelium discoideum, small GTPase methylation occur
262                         In the social amoeba Dictyostelium discoideum, starvation-triggered multicell
263 d to the annexin homologue of the slime mold Dictyostelium discoideum, suggesting a phylogenetic link
264 d in cheating behaviors in the social amoeba Dictyostelium discoideum, testing whether these genes ex
265 featured in this review is one discovered in Dictyostelium discoideum that becomes an actin-like fibe
266 ost is a "farmer" clone of the social amoeba Dictyostelium discoideum that carries and disperses bact
267   We have identified a new protein kinase in Dictyostelium discoideum that carries the same conserved
268 nt an NMR analysis of the isolated MTBD from Dictyostelium discoideum that demonstrates the coiled-co
269 e identified an Elmo-like protein, ElmoA, in Dictyostelium discoideum that unexpectedly functions as
270 ystem for performing interaction genetics in Dictyostelium discoideum that uses a cDNA library comple
271  a non-linear model for cAMP oscillations in Dictyostelium discoideum, the cell-cycle data for Saccha
272 ate spore encapsulation in the social amoeba Dictyostelium discoideum, the metabolic profile and othe
273                                              Dictyostelium discoideum, the social slime mold, possess
274 ady present in mycetozoan eukaryotes such as Dictyostelium discoideum This social amoeba kills bacter
275 emical mutagenesis in the social soil amoeba Dictyostelium discoideum Through genome sequencing, we s
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                    In this paper, we exploit Dictyostelium discoideum to uncover a novel role for PAR
279           Here we employ a simple eukaryote, Dictyostelium discoideum, to demonstrate distinct effect
280                                              Dictyostelium discoideum transformed with mutant PfCRT e
281 ed state previously reported for the similar Dictyostelium discoideum UMP/CMP kinase reveals the conf
282                                              Dictyostelium discoideum uses G protein-mediated signal
283 regulated 34 kDa actin-bundling protein from Dictyostelium discoideum was found to contribute to the
284                            The social amoeba Dictyostelium discoideum was selected for functional stu
285 mediated signaling network for chemotaxis in Dictyostelium discoideum We identified a negative regula
286 ard genetic screen for chemotaxis mutants in Dictyostelium discoideum, we identified a loss-of-functi
287            Using a forward genetic screen in Dictyostelium discoideum, we identified the Ste20 kinase
288                      Using the social amoeba Dictyostelium discoideum, we provide a possible explanat
289  acceleration was increased until amoebae of Dictyostelium discoideum were "stalled" or no longer abl
290                   The mass-dense granules of Dictyostelium discoideum were shown to contain large amo
291 o used for communication in the social ameba Dictyostelium discoideum when the solitary cells aggrega
292     We have characterized the mntA gene from Dictyostelium discoideum which encodes the beta-1,4-mann
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

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top