ライフサイエンスコーパス: Aspergillus nidulans

1 eveloped a heterologous expression system in Aspergillus nidulans .

2 xternal intron (experimentally confirmed for Aspergillus nidulans).

3 e PARP homolog (PrpA) in a microbial system (Aspergillus nidulans).

4 activator central to nitrogen metabolism in Aspergillus nidulans.

5 growing hyphal tip by using the model fungus Aspergillus nidulans.

6 ActA) and fimbrin (FimA) in hyphal growth in Aspergillus nidulans.

7 target genes via homologous recombination in Aspergillus nidulans.

8 ction required for polarity establishment in Aspergillus nidulans.

9 ally without band purification, to transform Aspergillus nidulans.

10 ning development and secondary metabolism in Aspergillus nidulans.

11 everal secondary metabolite gene clusters in Aspergillus nidulans.

12 evelopment in the homothallic fungal species Aspergillus nidulans.

13 effect of farnesol in the filamentous fungus Aspergillus nidulans.

14 f a stable polarity axis in the model fungus Aspergillus nidulans.

15 balance of asexual to sexual spore ratio in Aspergillus nidulans.

16 ise and rapid way, is nitrogen metabolism in Aspergillus nidulans.

17 d represses sexual development in the fungus Aspergillus nidulans.

18 n required for chromosomal DNA metabolism in Aspergillus nidulans.

19 nase that regulates the G(2)/M transition in Aspergillus nidulans.

20 rine transporter from the filamentous fungus Aspergillus nidulans.

21 A (NIMA) kinase from the filamentous fungus Aspergillus nidulans.

22 oding putative RGS proteins in the genome of Aspergillus nidulans.

23 the last few decades--Neurospora crassa and Aspergillus nidulans.

24 the nucleoplasm are regulated in the fungus Aspergillus nidulans.

25 duced by several filamentous fungi including Aspergillus nidulans.

26 ensitive allele of the gamma-tubulin gene of Aspergillus nidulans.

27 gion, a region critical for NIMA function in Aspergillus nidulans.

28 e to the essential mitotic regulator NIMA of Aspergillus nidulans.

29 tural and stereochemical specificity against Aspergillus nidulans.

30 phosphate nonrepressible acid phosphatase in Aspergillus nidulans.

31 Coccidioides immitis and the AnCHSC gene of Aspergillus nidulans.

32 lamentous fungi Cercospora nicotianae and in Aspergillus nidulans.

33 in germinating spores and growing hyphae of Aspergillus nidulans.

34 rough the mycelium of the filamentous fungus Aspergillus nidulans.

35 rtant for nuclear migration and viability in Aspergillus nidulans.

36 olved in determining nitrogen utilization in Aspergillus nidulans.

37 ellular structures in the filamentous fungus Aspergillus nidulans.

38 almodulin (CaM)-regulated protein kinases in Aspergillus nidulans.

39 endent upon activation of the NIMA kinase in Aspergillus nidulans.

40 gh tyrosine phosphorylation of NIMX(cdc2) in Aspergillus nidulans.

41 ino-n-butyrate (GABA) permease of the fungus Aspergillus nidulans.

42 in; ST) production by the filamentous fungus Aspergillus nidulans.

43 acC pathways of Saccharomyces cerevisiae and Aspergillus nidulans.

44 hat mediates pH-dependent gene expression in Aspergillus nidulans.

45 ogy to the laccase encoded by the yA gene of Aspergillus nidulans.

46 F, a component of the pH response pathway in Aspergillus nidulans.

47 y related to the mitotic regulator, NIMA, of Aspergillus nidulans.

48 tudying the heat-sensitive bimD6 mutation of Aspergillus nidulans.

49 zae but was dissimilar to the non-oleaginous Aspergillus nidulans.

50 unction in vivo using the filamentous fungus Aspergillus nidulans.

51 the class I myosin heavy chain gene myoA of Aspergillus nidulans.

52 g of the telomeres of the filamentous fungus,Aspergillus nidulans.

53 ase (CaMK) has been shown to be essential in Aspergillus nidulans.

54 and shown to be required for this process in Aspergillus nidulans.

55 itiation of the sexual reproductive cycle in Aspergillus nidulans.

56 id replicator and transformation enhancer in Aspergillus nidulans.

57 F-kB like fungal regulators VosA and VelB in Aspergillus nidulans.

58 endosome movement in the filamentous fungus Aspergillus nidulans.

59 hyphal tip growth in the filamentous fungus Aspergillus nidulans.

60 c gene-silencing system in the genetic model Aspergillus nidulans.

61 Galf monomers onto other wall components in Aspergillus nidulans.

62 growth of both Saccharomyces cerevisiae and Aspergillus nidulans.

63 condary metabolism in the filamentous fungus Aspergillus nidulans.

64 o 3' tagging with U and C nucleotides, as in Aspergillus nidulans.

65 characterized homologues of Bud4 and Axl2 in Aspergillus nidulans.

66 plasmic dynein-mediated nuclear migration in Aspergillus nidulans.

67 the upstream developmental activator FlbC in Aspergillus nidulans.

68 uorescence microscopy to monitor P-bodies in Aspergillus nidulans.

69 , a protein required for nuclear movement in Aspergillus nidulans [14].

70 The Aspergillus nidulans 7-TMD receptor PalH senses alkaline

71 In Aspergillus nidulans 86% of transcripts associate with i

72 iously showed that in the filamentous fungus Aspergillus nidulans, a GFP-tagged cytoplasmic dynein he

73 In the filamentous fungus Aspergillus nidulans, a heterotrimeric G protein alpha-s

74 targeting mechanism for NUDF (LIS1/Pac1) of Aspergillus nidulans, a key component of the dynein path

75 In Aspergillus nidulans, a strain carrying a deletion of th

76 gal susceptibility testing of 35 isolates of Aspergillus nidulans, A. terreus, Bipolaris hawaiiensis,

77 genic plants carried highly expressed active Aspergillus nidulans acetylesterases localized to the ap

78 The nudF gene of the filamentous fungus Aspergillus nidulans acts in the cytoplasmic dynein/dyna

79 The Aspergillus nidulans aflR gene is found within a 60 kb g

80 SM production by binding to two sites in the Aspergillus nidulans AflR promoter region, a C6 transcri

81 moter of the A. fumigatus uap1 gene with the Aspergillus nidulans alcA promoter, revealed that uap1 i

82 roduction of PG species is decreased in both Aspergillus nidulans and A. fumigatus ppo mutants, impli

83 T), a toxic secondary metabolite produced by Aspergillus nidulans and an aflatoxin (AF) precursor in

84 iew of the entire published literature about Aspergillus nidulans and Aspergillus fumigatus, and this

85 crystal structures of C-terminally truncated Aspergillus nidulans and Coccidioides posadasii mtTyrRSs

86 terised all Fur proteins of the model fungus Aspergillus nidulans and discovered novel functions and

87 ologies to the cytosolic protein ASPND1 from Aspergillus nidulans and fibrinogen binding protein from

88 utations of the mipA, gamma-tubulin, gene of Aspergillus nidulans and have created strains carrying t

89 educe the secondary metabolite background in Aspergillus nidulans and minimize the rediscovery of com

90 The filamentous fungi Aspergillus nidulans and Neurospora crassa and the yeast

91 Developmental mechanisms in Aspergillus nidulans and Neurospora crassa have been int

92 dynein is required for nuclear migration in Aspergillus nidulans and other fungi.

93 ATA-factor homologous to the AREA protein of Aspergillus nidulans and related transcription factors i

94 C), a 42 kDa protein initially identified in Aspergillus nidulans and shown to be phosphorylated by P

95 s from several of these organisms, including Aspergillus nidulans and the human pathogens Coccidioide

96 However, Aspergillus nidulans and vertebrate Nup2 also locate to

97 usly expressed in both a filamentous fungus (Aspergillus nidulans) and in a methylotrophic yeast (Pic

98 rt the genome sequence of the model organism Aspergillus nidulans, and a comparative study with Asper

99 is, Kluyveromyces lactis, Neurospora crassa, Aspergillus nidulans, and A. flavus.

100 can synthase activity from Candida albicans, Aspergillus nidulans, and Cryptococcus neoformans by rib

101 In Ustilago maydis, Aspergillus nidulans, and Saccharomyces cerevisiae fluor

102 essential for progression through mitosis in Aspergillus nidulans, and there is evidence for a simila

103 Here we show that Aspergillus nidulans, another model fungus, does not req

104 gmatocystin biosynthesis in the model fungus Aspergillus nidulans are discussed in depth.

105 Hyphal tip cells of the fungus Aspergillus nidulans are useful for studying long-range

106 Here we identified FhipA in Aspergillus nidulans as a key player for HookA (A. nidul

107 including other Aspergillus genomes (such as Aspergillus nidulans) as they become available.

108 discovery of VezA, a vezatin-like protein in Aspergillus nidulans, as a factor critical for early end

109 t a DeltafluG mutation results in a block in Aspergillus nidulans asexual sporulation and that overex

110 In Aspergillus nidulans, asexual development culminates in

111 coding polysaccharide-degrading enzymes from Aspergillus nidulans, Aspergillus fumigatus, and Neurosp

112 m Aspergillus flavus, Aspergillus fumigatus, Aspergillus nidulans, Aspergillus niger, Aspergillus ter

113 literature for four key Aspergillus species: Aspergillus nidulans, Aspergillus oryzae, Aspergillus fu

114 We successfully expressed Aspergillus nidulans aspyridone synthetase (ApdA) from a

115 The dormant spores of Aspergillus nidulans become competent for growth and nuc

116 CDC16, and CDC23, APC contained a homolog of Aspergillus nidulans BIME, a protein essential for anaph

117 In the filamentous fungus Aspergillus nidulans, both cytoplasmic dynein and NUDF,

118 In the filamentous fungus Aspergillus nidulans BrlA triggers the central developme

119 a PanK cDNA clone from the eukaryotic fungus Aspergillus nidulans by functional complementation of a

120 It is possible to cause G2 arrest in Aspergillus nidulans by inactivating either p34cdc2 or N

121 imG, the major protein phosphatase 1 gene in Aspergillus nidulans, causes multiple cell cycle and hyp

122 We find that Aspergillus nidulans cells, which are unable to satisfy

123 ion of the nuclear pore complex (NPC) during Aspergillus nidulans closed mitosis, a systematic analys

124 Similar results are obtained on Aspergillus nidulans comparing Conrad versus Fgenesh.

125 The filamentous fungus Aspergillus nidulans contains a cluster of 25 genes that

126 In the filamentous fungus Aspergillus nidulans, cytokinesis/septation is triggered

127 In Aspergillus nidulans, cytoplasmic dynein and NUDF/LIS1 a

128 Structures have been reported for Aspergillus nidulans DHQS (AnDHQS) in complexes with a r

129 a mitochondrial intron-encoded protein from Aspergillus nidulans directly facilitates splicing in vi

130 1 and SC4 from S.commune, rodA and dewA from Aspergillus nidulans, EAS from Neurospora crassa and ssg

131 the mitochondrial apocytochrome b gene from Aspergillus nidulans encodes a bi-functional maturase pr

132 The AnCOB group I intron from Aspergillus nidulans encodes a homing DNA endonuclease c

133 The tinA gene of Aspergillus nidulans encodes a protein that interacts wi

134 from static late endosomes in order to study Aspergillus nidulans endosomal traffic.

135 on of a 237 residue deacetylase (AnCDA) from Aspergillus nidulans FGSC A4.

136 The Aspergillus nidulans flbD gene encodes a protein with a

137 We have developed a genetic screen in Aspergillus nidulans for negative regulators of fungal S

138 cultivation media of the filamentous fungus Aspergillus nidulans for the study of the cyclic tetrape

139 The NUDF protein of the filamentous fungus Aspergillus nidulans functions in the cytoplasmic dynein

140 Here, we analyzed in the filamentous fungus Aspergillus nidulans functions of the only LIC and two L

141 me mechanism that is after activation of the Aspergillus nidulans G2 cyclin-dependent kinase, NIMXCDC

142 The Aspergillus nidulans genome encodes 16 putative GPCRs, b

143 ergillus nidulans, intensive analyses of the Aspergillus nidulans genome have been carried out and ni

144 A physical map of the 31-megabase Aspergillus nidulans genome is reported, in which 94% of

145 In Aspergillus nidulans, germinating conidia undergo multip

146 In Aspergillus nidulans, germinating conidia undergo multip

147 In the filamentous fungus Aspergillus nidulans, germination of an asexual conidios

148 telium discoideum cAMP receptor cAR1 and the Aspergillus nidulans GPCR protein GprH and also shares s

149 Aspergillus nidulans grows by apical extension of multin

150 The filamentous fungus Aspergillus nidulans grows by polarized extension of hyp

151 f secondary metabolite (SM) gene clusters in Aspergillus nidulans has been shown to occur through clu

152 We addressed the question of whether Aspergillus nidulans has more than one cyclin-dependent

153 The filamentous fungus Aspergillus nidulans has previously been found to produc

154 Recent work with the filamentous fungus Aspergillus nidulans has provided new insights into the

155 system, derived from the filamentous fungus Aspergillus nidulans, has previously been used successfu

156 Here, we identified a mutation in the Aspergillus nidulans heavy chain tail domain, nudA(F208V

157 the melanin pathway, we utilized an advanced Aspergillus nidulans heterologous system for the express

158 interactions between klpA1, a deletion of an Aspergillus nidulans homolog of pkl1, and mutations in t

159 nal characterization and localization of the Aspergillus nidulans homolog of the axial bud site marke

160 We have cloned the Aspergillus nidulans homologue (pyroA) of this highly co

161 Cleavage of Rim1p, like that of its Aspergillus nidulans homologue PacC, is stimulated under

162 uivocal evidence that the filamentous fungus Aspergillus nidulans houses both peroxisomal and mitocho

163 the model fungi Saccharomyces cerevisiae and Aspergillus nidulans However, the roles of myosins in th

164 ully introduced into Colombia-0 plants three Aspergillus nidulans hydrolases, beta-xylosidase/alpha-a

165 Using Aspergillus nidulans hyphae, we show that late Golgi cis

166 oxygen species (ROS) in the apical region of Aspergillus nidulans hyphae.

167 design and apply a DNA expression array for Aspergillus nidulans in combination with legacy data to

168 ectly, we have generated isogenic strains of Aspergillus nidulans in which one or both of the catalas

169 In the filamentous fungus Aspergillus nidulans, inactivation of cytoplasmic dynein

170 o determine the products of eight NR-PKSs of Aspergillus nidulans, including seven novel compounds, a

171 Previous studies in Aspergillus nidulans indicate that a Pho85-like kinase,

172 ured intensities sampled from actual data on Aspergillus nidulans indicate that using hybridization i

173 nalling mechanisms in the filamentous fungus Aspergillus nidulans, intensive analyses of the Aspergil

174 Interestingly, the NIMA kinase of Aspergillus nidulans interacts with two nuclear pore com

175 ges during mitosis, which in vertebrates and Aspergillus nidulans involves movement of Nup2 from NPCs

176 The archetypal nudC gene from Aspergillus nidulans is a member of the nud gene family

177 Aspergillus nidulans is an ideal model to study nuclear

178 Aspergillus nidulans is an important experimental organi

179 The single class I myosin (MYOA) of Aspergillus nidulans is essential for hyphal growth.

180 The ST biosynthetic pathway in Aspergillus nidulans is estimated to involve at least 15

181 ment (conidiation) in the filamentous fungus Aspergillus nidulans is governed by orchestrated gene ex

182 Conidiation in Aspergillus nidulans is induced by exposure to red light

183 e growth signaling in the filamentous fungus Aspergillus nidulans is primarily mediated by the hetero

184 Nitrogen metabolism in Aspergillus nidulans is regulated by AREA, a member of t

185 cence microscopy that KlpA-a kinesin-14 from Aspergillus nidulans-is a context-dependent bidirectiona

186 color, five Aspergillus calidoustus, and two Aspergillus nidulans isolates and two isolates identifie

187 tifungal effect on Aspergillus fumigatus and Aspergillus nidulans; it increased the antifungal activi

188 Aspergillus nidulans matA encodes a critical regulator t

189 The Aspergillus nidulans mating type gene matA and the human

190 A gamma-tubulin mutation in Aspergillus nidulans, mipA-D159, causes failure of inact

191 A cold-sensitive gamma-tubulin allele of Aspergillus nidulans, mipAD159, causes defects in mitoti

192 The Aspergillus nidulans mitochondrial COB group I intron en

193 During Aspergillus nidulans mitosis peripheral nuclear pore com

194 ganizing regions (NORs) from nucleoli during Aspergillus nidulans mitosis.

195 We find that the Aspergillus nidulans Mlp1 NPC protein has previously unr

196 observed in previous studies using MdpC from Aspergillus nidulans (monodictyphenone biosynthetic gene

197 ure of the isolated C-terminal domain of the Aspergillus nidulans mt TyrRS, which is closely related

198 In the filamentous fungus, Aspergillus nidulans, multiple rounds of nuclear divisio

199 phox)(-/-) mice infected with pH-insensitive Aspergillus nidulans mutants despite a paucity of fungal

200 reened a collection of temperature-sensitive Aspergillus nidulans mutants for swollen cells.

201 In Aspergillus nidulans, mutation of the transcriptional re

202 ave identified a novel cluster suppressor in Aspergillus nidulans, MvlA (modulator of veA loss).

203 Nase P and a partially purified RNase P from Aspergillus nidulans mycelia succeeded in cleaving a put

204 The Aspergillus nidulans NIMA kinase is essential for mitoti

205 The Aspergillus nidulans NIMX(CDC2) protein kinase has been

206 431, present in transmembrane domains of the Aspergillus nidulans NrtA nitrate transporter protein we

207 In Aspergillus nidulans nuclear pore complexes (NPCs) under

208 In Aspergillus nidulans, nuclear distribution gene C (nudC)

209 In Aspergillus nidulans, NUDF (a LIS1 homolog) functions in

210 Conidiophore morphogenesis in Aspergillus nidulans occurs in response to developmental

211 Cytokinesis (septation) in the fungus Aspergillus nidulans occurs through the formation of a t

212 uence was isolated from a genomic library of Aspergillus nidulans on the basis of its ability to enha

213 We find that the Aspergillus nidulans orthologue of the p25 subunit of dy

214 In Aspergillus nidulans, oxylipins are synthesized by the d

215 The Aspergillus nidulans PacC transcription factor mediates

216 In response to alkaline ambient pH, the Aspergillus nidulans PacC transcription factor mediating

217 The zinc finger regions of the Aspergillus nidulans PacC transcription factor, mediatin

218 e we have investigated the importance of the Aspergillus nidulans PacC-mediated pH response in the pa

219 PanK but exhibited significant similarity to Aspergillus nidulans PanK.

220 elated PHOA cyclin-dependent kinase (CDK) of Aspergillus nidulans plays no role in regulation of enzy

221 The filamentous fungus Aspergillus nidulans possesses both asexual and sexual r

222 Aspergillus nidulans possesses two high-affinity nitrate

223 The AREA DNA binding domain, from Aspergillus nidulans, possesses a single Cys2-Cys2 zinc

224 w study has found that strains of the fungus Aspergillus nidulans produce more of their spores sexual

225 Aspergillus nidulans produces the polyketide toxin steri

226 onsisting of the E. coli hph gene flanked by Aspergillus nidulans promoter and terminator sequences.

227 The Aspergillus nidulans protein kinase NIMA regulates mitot

228 The Aspergillus nidulans protein NIMA (never in mitosis, gen

229 NIMA-related kinase 6) is a homologue of the Aspergillus nidulans protein NIMA (never in mitosis, gen

230 BBER1 encodes a protein with homology to the Aspergillus nidulans protein NUDC that has similarity to

231 The Aspergillus nidulans proteome possesses a single formin,

232 nd validate a three-dimensional model of the Aspergillus nidulans purine-cytosine/H(+) FcyB symporter

233 activator protein for quinate catabolism in Aspergillus nidulans, QUTA, is derived from the pentafun

234 In Aspergillus nidulans, RabO(RAB1) resides in the Golgi, R

235 Aspergillus nidulans rcoA encodes a member of the WD rep

236 an antifungal plant defense protein, against Aspergillus nidulans requires the activity of a heterotr

237 tion (conidiation) in the filamentous fungus Aspergillus nidulans requires the early developmental ac

238 f the spermidine synthase gene in the fungus Aspergillus nidulans results in a strain, deltaspdA, whi

239 Studies in U. maydis and Aspergillus nidulans reveal a complex interplay of the m

240 flbA encodes an Aspergillus nidulans RGS (regulator of G protein signali

241 Here, we report the reconstruction of the Aspergillus nidulans salt stress-controlling MAP kinase

242 EST sequences from other eukaryotes such as Aspergillus nidulans, Schizosaccharomyces pombe, Brugia

243 The AnCOB group I intron from Aspergillus nidulans self-splices, providing the Mg2+ co

244 The Aspergillus nidulans sepI(+) gene has been implicated in

245 Aspergillus nidulans shows both asexual and sexual repro

246 a single amino acid substitution within the Aspergillus nidulans SONBnNup98 NPC protein (nucleoporin

247 In the filamentous fungus Aspergillus nidulans SPBs and septum-associated MTOCs we

248 is work, we investigated the contribution of Aspergillus nidulans sphingolipid Delta8-desaturase (Sde

249 The Aspergillus nidulans stcL gene is predicted to encode a

250 Aspergillus nidulans steA encodes a protein with a homeo

251 Aspergillus nidulans strains bearing these mutations als

252 The Aspergillus nidulans Stunted protein (StuAp) regulates m

253 tingly, induces apoptotic-like cell death in Aspergillus nidulans, suggesting that this molecule has

254 Here we demonstrate that the Aspergillus nidulans Sur2 homolog BasA is also required

255 We show that the nearly essential Aspergillus nidulans syntaxin PepA(Pep12) , present in a

256 The model fungus Aspergillus nidulans synthesizes numerous secondary meta

257 of mitochondrial morphology and function in Aspergillus nidulans, systematic characterization was ca

258 However, Aspergillus nidulans TamA and the related Saccharomyces

259 In the fungus Aspergillus nidulans (teleomorph: Emericella nidulans) e

260 dings that MtfA, a transcription factor from Aspergillus nidulans that contains a related double zinc

261 earch for proteins in the filamentous fungus Aspergillus nidulans that possess an NPFxD motif, which

262 For example, in Aspergillus nidulans the entire pathway for the producti

263 In Aspergillus nidulans the global regulatory gene veA is n

264 In Aspergillus nidulans, the AcuK and AcuM transcription fa

265 In the filamentous fungus Aspergillus nidulans, the dynein HC is localized to the

266 In Aspergillus nidulans, the formin SEPA participates in tw

267 cent protein fusions of four SAC proteins in Aspergillus nidulans, the homologs of Mad2, Mps1, Bub1/B

268 In Aspergillus nidulans, the LIS1 homolog, NUDF, and cytopl

269 When applied to a sample of invertase from Aspergillus nidulans, the method indicated that all of t

270 ocystin (ST) in the model filamentous fungus Aspergillus nidulans, the molecular mechanisms underlyin

271 In the filamentous fungus Aspergillus nidulans, the multisubunit motor complex cyt

272 In Aspergillus nidulans, the N-myristoylation deficient swo

273 In Aspergillus nidulans, the principal transcription factor

274 In the Ascomycete fungus Aspergillus nidulans, the ratio of conidia (asexual spor

275 rein, we show that in the filamentous fungus Aspergillus nidulans, the septin AspB is important for c

276 In Aspergillus nidulans, the uvsB gene encodes a member of

277 Tolerance of Aspergillus nidulans to alkalinity and elevated cation c

278 Here, we use the UapA purine transporter of Aspergillus nidulans to investigate the role of cargo ol

279 riptional response of the filamentous fungus Aspergillus nidulans to the presence of high and low glu

280 I (TOP1) gene was cloned and sequenced from Aspergillus nidulans using the polymerase chain reaction

281 In Aspergillus nidulans, uvsB and uvsD belong to the same e

282 A null mutation can be fully complemented by Aspergillus nidulans VeA, which can physically interact

283 The crnA nitrate transporter from Aspergillus nidulans was identified as belonging to the

284 inity nitrate transporter from the eukaryote Aspergillus nidulans was isolated and characterized.

285 nt of the mitochondrial genome of the fungus Aspergillus nidulans was sequenced and shown to contain

286 Using the filamentous fungus Aspergillus nidulans we found that hitchhiking is mediat

287 Using Aspergillus nidulans, we demonstrate for the first time

288 tracking MT +end-binding proteins (+TIPS) in Aspergillus nidulans, we find that MTs are regulated to

289 cytoplasmic dynein in the filamentous fungus Aspergillus nidulans, we replaced the gene for the cytop

290 he ambient pH signal transduction pathway in Aspergillus nidulans, we report the characterization of

291 Using Aspergillus nidulans, we show that AP-2 has a clathrin-i

292 y polarized hyphae of the filamentous fungus Aspergillus nidulans, we show that three morphologically

293 Here we focus on the pH regulatory system of Aspergillus nidulans, where a novel signal transduction

294 the zinc-finger transcription factor PacC of Aspergillus nidulans, which activates alkaline pH-induce

295 new study shows that the filamentous fungus, Aspergillus nidulans, which has a closed mitosis, does n

296 This screen exploits the filamentous fungus Aspergillus nidulans, which has many of the advantages o

297 The NUDF protein of Aspergillus nidulans, which is required for nuclear migr

298 ein was isolated from the filamentous fungus Aspergillus nidulans, whose mycelium is made of multinuc

299 did not find a methyl-accepting substrate in Aspergillus nidulans with various assays, including in v

300 This investigation focuses on clathrin in Aspergillus nidulans, with the aim of understanding its