ライフサイエンスコーパス: Aspergillus nidulans

1 eveloped a heterologous expression system in Aspergillus nidulans .

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

3 xternal intron (experimentally confirmed for Aspergillus nidulans).

4 ns the cellular and metabolic development in Aspergillus nidulans.

5 plasmic dynein-mediated nuclear migration in Aspergillus nidulans.

6 the upstream developmental activator FlbC in Aspergillus nidulans.

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

8 activator central to nitrogen metabolism in Aspergillus nidulans.

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

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

11 target genes via homologous recombination in Aspergillus nidulans.

12 ction required for polarity establishment in Aspergillus nidulans.

13 ally without band purification, to transform Aspergillus nidulans.

14 ning development and secondary metabolism in Aspergillus nidulans.

15 everal secondary metabolite gene clusters in Aspergillus nidulans.

16 evelopment in the homothallic fungal species Aspergillus nidulans.

17 effect of farnesol in the filamentous fungus Aspergillus nidulans.

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

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

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

21 d represses sexual development in the fungus Aspergillus nidulans.

22 n required for chromosomal DNA metabolism in Aspergillus nidulans.

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

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

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

26 the nucleoplasm are regulated in the fungus Aspergillus nidulans.

27 duced by several filamentous fungi including Aspergillus nidulans.

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

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

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

31 tural and stereochemical specificity against Aspergillus nidulans.

32 phosphate nonrepressible acid phosphatase in Aspergillus nidulans.

33 Coccidioides immitis and the AnCHSC gene of Aspergillus nidulans.

34 lamentous fungi Cercospora nicotianae and in Aspergillus nidulans.

35 in germinating spores and growing hyphae of Aspergillus nidulans.

36 rough the mycelium of the filamentous fungus Aspergillus nidulans.

37 rtant for nuclear migration and viability in Aspergillus nidulans.

38 olved in determining nitrogen utilization in Aspergillus nidulans.

39 ellular structures in the filamentous fungus Aspergillus nidulans.

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

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

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

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

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

45 acC pathways of Saccharomyces cerevisiae and Aspergillus nidulans.

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

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

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

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

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

51 unction in vivo using the filamentous fungus Aspergillus nidulans.

52 rine transporter from the filamentous fungus Aspergillus nidulans.

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

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

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

56 zae but was dissimilar to the non-oleaginous 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 , a protein required for nuclear movement in Aspergillus nidulans [14].

67 The Aspergillus nidulans 7-TMD receptor PalH senses alkaline

68 In Aspergillus nidulans 86% of transcripts associate with i

69 In Aspergillus nidulans, a donor-disrupted stwintron (intro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 However, Aspergillus nidulans and vertebrate Nup2 also locate to

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

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

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

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

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

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

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

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

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

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

105 In Aspergillus nidulans, asexual development culminates in

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

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

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

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

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

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

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

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

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

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

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

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

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

119 s and demonstrate that the Raman signal from Aspergillus nidulans conidia originates in pigment molec

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

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

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

123 1 and SC4 from S.commune, rodA and dewA from Aspergillus nidulans, EAS from Neurospora crassa and ssg

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

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

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

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

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

129 The Aspergillus nidulans flbD gene encodes a protein with a

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

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

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

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

134 ), and the ascomycetes Neurospora crassa and Aspergillus nidulans (Fungi), and bring to light develop

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

136 The Aspergillus nidulans genome encodes 16 putative GPCRs, b

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

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

139 In Aspergillus nidulans, germinating conidia undergo multip

140 In Aspergillus nidulans, germinating conidia undergo multip

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

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

143 Aspergillus nidulans grows by apical extension of multin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

161 is by heterologous pathway reconstruction in Aspergillus nidulans identified the multicopper oxidase

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

163 med on single spores (conidia) of the fungus Aspergillus nidulans in order to establish a baseline me

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

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

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

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

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

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

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

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

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

173 Aspergillus nidulans is an ideal model to study nuclear

174 Aspergillus nidulans is an important experimental organi

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

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

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

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

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

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

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

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

183 leaching of calcium hydroxide from concrete, Aspergillus nidulans (MAD1445), a pH regulatory mutant,

184 Aspergillus nidulans matA encodes a critical regulator t

185 The Aspergillus nidulans mating type gene matA and the human

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

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

188 The Aspergillus nidulans mitochondrial COB group I intron en

189 During Aspergillus nidulans mitosis peripheral nuclear pore com

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

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

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

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

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

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

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

197 In Aspergillus nidulans, mutation of the transcriptional re

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

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

200 The Aspergillus nidulans NIMA kinase is essential for mitoti

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

202 431, present in transmembrane domains of the Aspergillus nidulans NrtA nitrate transporter protein we

203 In Aspergillus nidulans nuclear pore complexes (NPCs) under

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

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

206 Conidiophore morphogenesis in Aspergillus nidulans occurs in response to developmental

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

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

209 In Aspergillus nidulans, oxylipins are synthesized by the d

210 The Aspergillus nidulans PacC transcription factor mediates

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

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

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

214 PanK but exhibited significant similarity to Aspergillus nidulans PanK.

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

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

217 Aspergillus nidulans possesses two high-affinity nitrate

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

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

220 Aspergillus nidulans produces the polyketide toxin steri

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

222 The Aspergillus nidulans protein kinase NIMA regulates mitot

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

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

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

226 The Aspergillus nidulans proteome possesses a single formin,

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

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

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

230 Aspergillus nidulans rcoA encodes a member of the WD rep

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

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

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

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

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

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

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

238 with aspergillosis originally identified as Aspergillus nidulans (section Nidulantes) that are actua

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

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

241 Aspergillus nidulans shows both asexual and sexual repro

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

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

244 ated dynein activation in the model organism Aspergillus nidulans Specifically, we found that overexp

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

246 The Aspergillus nidulans stcL gene is predicted to encode a

247 Aspergillus nidulans steA encodes a protein with a homeo

248 Aspergillus nidulans strains bearing these mutations als

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

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

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

252 The model fungus Aspergillus nidulans synthesizes numerous secondary meta

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

254 However, Aspergillus nidulans TamA and the related Saccharomyces

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

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

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

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

259 In Aspergillus nidulans the global regulatory gene veA is n

260 In Aspergillus nidulans, the AcuK and AcuM transcription fa

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

262 In Aspergillus nidulans, the formin SEPA participates in tw

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

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

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

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

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

268 In Aspergillus nidulans, the N-myristoylation deficient swo

269 In Aspergillus nidulans, the principal transcription factor

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

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

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

273 In Aspergillus nidulans, the WCC and the phytochrome intera

274 functional expression of a mammalian NAT in Aspergillus nidulans Thus, our results provide a potenti

275 Tolerance of Aspergillus nidulans to alkalinity and elevated cation c

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

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

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

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

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

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

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

283 entation using heterologous RanBP genes from Aspergillus nidulans was successful, suggesting that the

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

285 Using Aspergillus nidulans, we demonstrate for the first time

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

287 ons affecting early-endosome distribution in Aspergillus nidulans, we identified the prp40A(L438*) mu

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

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

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

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

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

293 We have identified a similar system in Aspergillus nidulans, where Upf1 is required for the reg

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