ライフサイエンスコーパス: nidulans

1 eterologous expression system in Aspergillus nidulans .

2 on (experimentally confirmed for Aspergillus nidulans).

3 og (PrpA) in a microbial system (Aspergillus nidulans).

4 ation of the cargo adapter HookA (Hook in A. nidulans).

5 bolism in the filamentous fungus Aspergillus nidulans.

6 an antibiotic not known to be produced by A. nidulans.

7 with U and C nucleotides, as in Aspergillus nidulans.

8 asexual development and conidiogenesis in A. nidulans.

9 d homologues of Bud4 and Axl2 in Aspergillus nidulans.

10 -fertilization and sexual reproduction in A. nidulans.

11 in-mediated nuclear migration in Aspergillus nidulans.

12 l for governing growth and development in A. nidulans.

13 developmental activator FlbC in Aspergillus nidulans.

14 icroscopy to monitor P-bodies in Aspergillus nidulans.

15 ation to take place in a timely manner in A. nidulans.

16 nuated by palB and pacC mutant strains of A. nidulans.

17 entral to nitrogen metabolism in Aspergillus nidulans.

18 al tip by using the model fungus Aspergillus nidulans.

19 mbrin (FimA) in hyphal growth in Aspergillus nidulans.

20 on of a stable axis of hyphal polarity in A. nidulans.

21 between asexual and sexual development in A. nidulans.

22 via homologous recombination in Aspergillus nidulans.

23 ed for polarity establishment in Aspergillus nidulans.

24 band purification, to transform Aspergillus nidulans.

25 ment and secondary metabolism in Aspergillus nidulans.

26 dary metabolite gene clusters in Aspergillus nidulans.

27 n the homothallic fungal species Aspergillus nidulans.

28 rnesol in the filamentous fungus Aspergillus nidulans.

29 olarity axis in the model fungus Aspergillus nidulans.

30 asexual to sexual spore ratio in Aspergillus nidulans.

31 d way, is nitrogen metabolism in Aspergillus nidulans.

32 also functional when VeA is expressed in A. nidulans.

33 controls splicing of the arginase mRNA in A. nidulans.

34 sexual development in the fungus Aspergillus nidulans.

35 or chromosomal DNA metabolism in Aspergillus nidulans.

36 aving a putative arginine riboswitch from A. nidulans.

37 gulates the G(2)/M transition in Aspergillus nidulans.

38 a compared with that which has evolved in A. nidulans.

39 nase from the filamentous fungus Aspergillus nidulans.

40 ve RGS proteins in the genome of Aspergillus nidulans.

41 rter from the filamentous fungus Aspergillus nidulans.

42 We find pinA to be an essential gene in A. nidulans.

43 w decades--Neurospora crassa and Aspergillus nidulans.

44 h is required for proper proliferation of A. nidulans.

45 lasm are regulated in the fungus Aspergillus nidulans.

46 eral filamentous fungi including Aspergillus nidulans.

47 ele of the gamma-tubulin gene of Aspergillus nidulans.

48 on critical for NIMA function in Aspergillus nidulans.

49 tanudG) at the nudG locus encoding LC8 in A. nidulans.

50 e control of mitotic spindle formation in A. nidulans.

51 play an important role in endocytosis in A. nidulans.

52 dissimilar to the non-oleaginous Aspergillus nidulans.

53 hosphatidylserine to the Spitzenkorper in A. nidulans.

54 ngal regulators VosA and VelB in Aspergillus nidulans.

55 activity is, thus, spatially regulated in A. nidulans.

56 th, while represses sexual development in A. nidulans.

57 fungisporin, not previously described in A. nidulans.

58 vement in the filamentous fungus Aspergillus nidulans.

59 and drives the sexual cycle in the fungus A. nidulans.

60 growth in the filamentous fungus Aspergillus nidulans.

61 cing system in the genetic model Aspergillus nidulans.

62 rs onto other wall components in Aspergillus nidulans.

63 oth Saccharomyces cerevisiae and Aspergillus nidulans.

64 d germination by interacting with VosA in A. nidulans.

65 323 to 592 for A. flavus, 131 to 143 for A. nidulans, 366 to 520 for A. niger, 330 to 462 for A. ter

66 The Aspergillus nidulans 7-TMD receptor PalH senses alkaline pH, subsequ

67 echanism for NUDF (LIS1/Pac1) of Aspergillus nidulans, a key component of the dynein pathway, has not

68 In Aspergillus nidulans, a strain carrying a deletion of the clr-2 homo

69 rgillus species (A. flavus, A. fumigatus, A. nidulans, A. niger, A. terreus, A. ustus, and A. versico

70 ates of Aspergillus fumigatus, A. flavus, A. nidulans, A. niger, and A. terreus to caspofungin (MICs

71 ve structural annotation improvements for A. nidulans, A. oryzae and A. fumigatus genomes based on re

72 r, A. terreus, A. versicolor, A. glaucus, A. nidulans, A. ustus, and A. sydowii.

73 carried highly expressed active Aspergillus nidulans acetylesterases localized to the apoplast and h

74 n by binding to two sites in the Aspergillus nidulans AflR promoter region, a C6 transcription factor

75 A. fumigatus uap1 gene with the Aspergillus nidulans alcA promoter, revealed that uap1 is essential

76 PG species is decreased in both Aspergillus nidulans and A. fumigatus ppo mutants, implicating Ppo a

77 ted with the production of eicosanoids in A. nidulans and Aspergillus fumigatus provides new insights

78 ntire published literature about Aspergillus nidulans and Aspergillus fumigatus, and this annotation

79 ctures of C-terminally truncated Aspergillus nidulans and Coccidioides posadasii mtTyrRSs.

80 Fur proteins of the model fungus Aspergillus nidulans and discovered novel functions and specificitie

81 al roles of the Pin1 orthologue, PINA, in A. nidulans and evaluate the relevance of the interaction o

82 hat C-terminal domains of the full-length A. nidulans and Geobacillus stearothermophilus synthetases

83 measure tip growth rates in germlings of A. nidulans and in multinucleate hyphal tip cells, and we u

84 naling was conserved in the genetic model A. nidulans and mediated by NapA, a homolog of AP-1-like bZ

85 condary metabolite background in Aspergillus nidulans and minimize the rediscovery of compounds and p

86 Developmental mechanisms in Aspergillus nidulans and Neurospora crassa have been intensively stu

87 abilities of the mitochondrial genomes in A. nidulans and P. anserina.

88 omologous to the AREA protein of Aspergillus nidulans and related transcription factors involved in n

89 protein initially identified in Aspergillus nidulans and shown to be phosphorylated by Plk1 , plays

90 al of these organisms, including Aspergillus nidulans and the human pathogens Coccidioides posadasii

91 However, Aspergillus nidulans and vertebrate Nup2 also locate to chromatin du

92 ulatable promoter, transferring them into A. nidulans , and expressing them.

93 e sequence of the model organism Aspergillus nidulans, and a comparative study with Aspergillus fumig

94 s of A. fumigatus, A. flavus, A. terreus, A. nidulans, and A. oryzae for domains conserved in NRPS pr

95 We engineered ZmLOX3 into wild-type A. nidulans, and into a DeltappoAC strain that was reduced

96 In Ustilago maydis, Aspergillus nidulans, and Saccharomyces cerevisiae fluorescently lab

97 Here we show that Aspergillus nidulans, another model fungus, does not require an RDRP

98 biosynthesis in the model fungus Aspergillus nidulans are discussed in depth.

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

100 Here we identified FhipA in Aspergillus nidulans as a key player for HookA (A. nidulans Hook) fu

101 VezA, a vezatin-like protein in Aspergillus nidulans, as a factor critical for early endosome distri

102 In Aspergillus nidulans, asexual development culminates in the formatio

103 accharide-degrading enzymes from Aspergillus nidulans, Aspergillus fumigatus, and Neurospora crassa a

104 rgillus granulosus, Aspergillus (Emericella) nidulans, Aspergillus niger, Aspergillus restrictus, Asp

105 s flavus, Aspergillus fumigatus, Aspergillus nidulans, Aspergillus niger, Aspergillus terreus, Asperg

106 or four key Aspergillus species: Aspergillus nidulans, Aspergillus oryzae, Aspergillus fumigatus and

107 We successfully expressed Aspergillus nidulans aspyridone synthetase (ApdA) from an engineered

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

109 In the filamentous fungus Aspergillus nidulans BrlA triggers the central developmental pathway

110 terologous markers that are selectable in A. nidulans but do not direct integration at any site in th

111 lation of sexual development, not only in A. nidulans, but also in the phylogenetically unrelated fun

112 genus as genomic analysis indicates that A. nidulans, but not A. fumigatus or A. oryzae, has lost a

113 tion during transformation is possible in A. nidulans, but the frequency of correct gene targeting is

114 Conidiation induction in A. nidulans by another microbial redox-active secondary met

115 Therefore SVs arrive at the apex of A. nidulans by anterograde transport involving cooperation

116 This indicates that A. nidulans cells ensure accurate mitotic NPC segregation t

117 We find that Aspergillus nidulans cells, which are unable to satisfy the SAC, ina

118 Here, we have identified the A. nidulans CLIP-170 homologue, CLIPA.

119 uclear pore complex (NPC) during Aspergillus nidulans closed mitosis, a systematic analysis of nuclea

120 binding affinities within the cell during A. nidulans' closed mitosis, analogous to what occurs durin

121 nism by which the NPC is regulated during A. nidulans' closed mitosis.

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

123 Mutations that disrupt tagging, including A. nidulans cutA and a newly characterized gene, cutB, reta

124 In the filamentous fungus Aspergillus nidulans, cytokinesis/septation is triggered by the sept

125 In Aspergillus nidulans, cytoplasmic dynein and NUDF/LIS1 are found at

126 tructures have been reported for Aspergillus nidulans DHQS (AnDHQS) in complexes with a range of liga

127 The A. nidulans disordered protein Spa18(Mto2) and the centroso

128 ation suggest that PrpA acts early in the A. nidulans DNA damage response.

129 we demonstrate that SepB functions in the A. nidulans DNA damage response.

130 on-transfer and repair kinetics of Anacystis nidulans DNA photolyase with dimeric and pentameric olig

131 Because A. nidulans does not secrete detectable amounts of farnesol

132 In A. nidulans, dynein is not apparently required for mitotic

133 The AnCOB group I intron from Aspergillus nidulans encodes a homing DNA endonuclease called I-AniI

134 The tinA gene of Aspergillus nidulans encodes a protein that interacts with the NIMA

135 Aspergillus nidulans (teleomorph: Emericella nidulans) endogenous oxylipins, called psi factor, serve

136 late endosomes in order to study Aspergillus nidulans endosomal traffic.

137 These data also reveal that A. nidulans exhibits a remarkable spatial regulation of mic

138 residue deacetylase (AnCDA) from Aspergillus nidulans FGSC A4.

139 lated Aspergillus species, A.fumigatus and A.nidulans, finding 89% of the exons and predicting 74% of

140 ve developed a genetic screen in Aspergillus nidulans for negative regulators of fungal SM gene clust

141 We have used A. nidulans for our method development and validation due t

142 herefore, an essential function exists in A. nidulans for the Pho85-like kinase pair PHOA and PHOB, w

143 media of the filamentous fungus Aspergillus nidulans for the study of the cyclic tetrapeptide nidula

144 w here that loss of either FhipA or FtsA (A. nidulans FTS homologue) disrupts HookA-early endosome as

145 rotein of the filamentous fungus Aspergillus nidulans functions in the cytoplasmic dynein pathway.

146 alyzed in the filamentous fungus Aspergillus nidulans functions of the only LIC and two LCs, RobA (Ro

147 polar growth and nuclear distribution in A. nidulans, functions not yet described for its homologs.

148 . terreus; one isolate each of A. flavus, A. nidulans, Fusarium moniliforme, and F. solani; and two i

149 We propose that GpgA is the only A. nidulans G gamma-subunit and is required for normal vege

150 One mutation, an unprecedented finding in A. nidulans genetics, resulted from an insertion of an endo

151 The Aspergillus nidulans genome encodes 16 putative GPCRs, but only a fe

152 ulans, intensive analyses of the Aspergillus nidulans genome have been carried out and nine genes (gp

153 Analysis of the A. nidulans genome identified a single gene named gpgA enco

154 not direct integration at any site in the A. nidulans genome.

155 Wild-type A. nidulans germinated on porcine corneas and produced hyph

156 ideum cAMP receptor cAR1 and the Aspergillus nidulans GPCR protein GprH and also shares structural si

157 The filamentous fungus Aspergillus nidulans grows by polarized extension of hyphal tips.

158 metabolite (SM) gene clusters in Aspergillus nidulans has been shown to occur through cluster-specifi

159 The filamentous fungus Aspergillus nidulans has previously been found to produce two merote

160 In this study the genetic model organism, A. nidulans, has been used to investigate the regulation an

161 we identified a mutation in the Aspergillus nidulans heavy chain tail domain, nudA(F208V), which cau

162 pathway, we utilized an advanced Aspergillus nidulans heterologous system for the expression of the P

163 We also demonstrate that the single A. nidulans histone H2A gene contains the C-terminal SQE mo

164 We have identified the A. nidulans homolog (nkuA) of the human KU70 gene that is e

165 combined with mutations in scaANBS1, the A. nidulans homolog of NBS1.

166 rization and localization of the Aspergillus nidulans homolog of the axial bud site marker Bud3.

167 e have investigated the role of CdhA, the A. nidulans homologue of the APC/C activator protein Cdh1,

168 illus nidulans as a key player for HookA (A. nidulans Hook) function via a genome-wide screen for mut

169 ence that the filamentous fungus Aspergillus nidulans houses both peroxisomal and mitochondrial beta-

170 ngi Saccharomyces cerevisiae and Aspergillus nidulans However, the roles of myosins in the growth and

171 ced into Colombia-0 plants three Aspergillus nidulans hydrolases, beta-xylosidase/alpha-arabinosidase

172 Using Aspergillus nidulans hyphae, we show that late Golgi cisternae under

173 es (ROS) in the apical region of Aspergillus nidulans hyphae.

174 host-defense pathway, the pathogenesis of A. nidulans in CGD cannot be explained.

175 apply a DNA expression array for Aspergillus nidulans in combination with legacy data to form a compr

176 standing of invasive infections caused by A. nidulans in the CGD patient and is intended to direct fu

177 Using A. nidulans in vivo microscopy, we show that HypA(Trs120) c

178 the products of eight NR-PKSs of Aspergillus nidulans, including seven novel compounds, as well as th

179 Previous studies in Aspergillus nidulans indicate that a Pho85-like kinase, PHOA, does n

180 anisms in the filamentous fungus Aspergillus nidulans, intensive analyses of the Aspergillus nidulans

181 nterestingly, the NIMA kinase of Aspergillus nidulans interacts with two nuclear pore complex (NPC) p

182 s required for mitotic NPC inheritance in A. nidulans Interestingly, the role of Nup2 during mitotic

183 itosis, which in vertebrates and Aspergillus nidulans involves movement of Nup2 from NPCs to the chro

184 silencing is not a significant aspect of A. nidulans IRT-RNA silencing.

185 The archetypal nudC gene from Aspergillus nidulans is a member of the nud gene family that is invo

186 Aspergillus nidulans is an ideal model to study nuclear migration an

187 Aspergillus nidulans is an important experimental organism, and it i

188 ation) in the filamentous fungus Aspergillus nidulans is governed by orchestrated gene expression.

189 l and positively regulates NIMA function, A. nidulans is most sensitive to a reduction in PINA concen

190 el depicting regulation of conidiation in A. nidulans is presented.

191 naling in the filamentous fungus Aspergillus nidulans is primarily mediated by the heterotrimeric G-p

192 Interestingly, Aspergillus (Emericella) nidulans is the second most encountered mold in CGD pati

193 copy that KlpA-a kinesin-14 from Aspergillus nidulans-is a context-dependent bidirectional motor.

194 Aspergillus calidoustus, and two Aspergillus nidulans isolates and two isolates identified as Aspergi

195 ect on Aspergillus fumigatus and Aspergillus nidulans; it increased the antifungal activity of PMNs f

196 ole, 0.25 (95%); voriconazole, 1 (98.1%); A. nidulans, itraconazole, 1 (95%); posaconazole, 1 (97.7%)

197 cus, and sterigmatocystin biosynthesis in A. nidulans, led to the cloning of 17 genes responsible for

198 ine immunity contributes significantly to A. nidulans lethality.

199 Aspergillus nidulans matA encodes a critical regulator that is a fun

200 The Aspergillus nidulans mating type gene matA and the human SRY (Sex-De

201 ssembly under control of NIMA and Cdk1 in A. nidulans may represent a new mechanism for regulating cl

202 e a complete biosynthetic pathway for the A. nidulans meroterpenoids.

203 A gamma-tubulin mutation in Aspergillus nidulans, mipA-D159, causes failure of inactivation of t

204 ensitive gamma-tubulin allele of Aspergillus nidulans, mipAD159, causes defects in mitotic and cell c

205 The Aspergillus nidulans mitochondrial COB group I intron encodes a bi-f

206 ramatic changes in NPC composition during A. nidulans mitosis and provides insight into how NPC disas

207 During Aspergillus nidulans mitosis peripheral nuclear pore complex (NPC) p

208 ions (NORs) from nucleoli during Aspergillus nidulans mitosis.

209 of the NPC is dramatically changed during A. nidulans' mitosis.

210 We find that the Aspergillus nidulans Mlp1 NPC protein has previously unrealized mito

211 previous studies using MdpC from Aspergillus nidulans (monodictyphenone biosynthetic gene cluster).

212 solated C-terminal domain of the Aspergillus nidulans mt TyrRS, which is closely related to but small

213 ice infected with pH-insensitive Aspergillus nidulans mutants despite a paucity of fungal growth.

214 marginally altered phenotypes observed in A. nidulans mutants indicate the presence of effective comp

215 wild-type isolate (A83), loss-of-function A. nidulans mutants of the palB (B7) or pacC (C6309) genes,

216 ed a novel cluster suppressor in Aspergillus nidulans, MvlA (modulator of veA loss).

217 partially purified RNase P from Aspergillus nidulans mycelia succeeded in cleaving a putative argini

218 in transmembrane domains of the Aspergillus nidulans NrtA nitrate transporter protein were altered i

219 In Aspergillus nidulans nuclear pore complexes (NPCs) undergo partial m

220 In Aspergillus nidulans, nuclear distribution gene C (nudC) has been im

221 In Aspergillus nidulans, NUDF (a LIS1 homolog) functions in the dynein

222 ort that the FluG-mediated conidiation in A. nidulans occurs via derepression.

223 We find that the Aspergillus nidulans orthologue of the p25 subunit of dynactin is cr

224 CGD) is Aspergillus fumigatus followed by A. nidulans; other aspergilli rarely cause the disease.

225 We additionally explored whether A. nidulans oxylipins affect seed LOX gene expression durin

226 In Aspergillus nidulans, oxylipins are synthesized by the dioxygenase e

227 The Aspergillus nidulans PacC transcription factor mediates gene regulat

228 vestigated the importance of the Aspergillus nidulans PacC-mediated pH response in the pathogenesis o

229 enhance virulence, demonstrating that the A. nidulans pH-responsive transcription factor PacC plays a

230 , in neutropenic mice, elimination of the A. nidulans pH-responsive transcription factor PacC, blocki

231 cyclin-dependent kinase (CDK) of Aspergillus nidulans plays no role in regulation of enzymes involved

232 Moreover, A. nidulans possesses a second likely ceramide synthase tha

233 The filamentous fungus Aspergillus nidulans possesses both asexual and sexual reproductive

234 ZmLOX3) could substitute functionally for A. nidulans ppo genes.

235 Here, we report the identification of A. nidulans ppoA, encoding a putative fatty acid dioxygenas

236 found that strains of the fungus Aspergillus nidulans produce more of their spores sexually in enviro

237 Aspergillus nidulans produces the polyketide toxin sterigmatocystin

238 The Aspergillus nidulans protein NIMA (never in mitosis, gene A) is a pr

239 kinase 6) is a homologue of the Aspergillus nidulans protein NIMA (never in mitosis, gene A).

240 s a protein with homology to the Aspergillus nidulans protein NUDC that has similarity to protein cha

241 Therefore, in A. nidulans, proteins encoded by the smo genes likely have

242 The Aspergillus nidulans proteome possesses a single formin, SepA, which

243 a three-dimensional model of the Aspergillus nidulans purine-cytosine/H(+) FcyB symporter.

244 In Aspergillus nidulans, RabO(RAB1) resides in the Golgi, RabE(RAB11) l

245 (2014) describe important new findings in A. nidulans regarding the role of EBA, the master regulator

246 ation) in the filamentous fungus Aspergillus nidulans requires the early developmental activator fluG

247 Studies in U. maydis and Aspergillus nidulans reveal a complex interplay of the motor protein

248 n of the 27 polyketide synthases (PKS) in A. nidulans revealed that one highly reduced PKS (HR-PKS, A

249 quencing of Aspergillus species including A. nidulans reveals that the products of many of the second

250 The A. nidulans rtfA gene product accumulates in nuclei.

251 Since no known A. nidulans secondary metabolites could be produced by two

252 Here, we show that in A. nidulans several SPB outer plaque proteins also locate t

253 developed procedures for deleting entire A. nidulans SM clusters.

254 Although comparable to S. pombe eMTOCs, A. nidulans sMTOCS are permanent septum-associated structur

255 ino acid substitution within the Aspergillus nidulans SONBnNup98 NPC protein (nucleoporin).

256 In the filamentous fungus Aspergillus nidulans SPBs and septum-associated MTOCs were described

257 investigated the contribution of Aspergillus nidulans sphingolipid Delta8-desaturase (SdeA), sphingol

258 P-body formation is disrupted in A. nidulans strains deleted for Edc3, an enhancer of decapp

259 In vitro growth kinetics were similar for A. nidulans strains in liquid medium at pH 6.0 (P = 0.24) a

260 f scarified porcine or human corneas with A. nidulans strains maintained in buffered medium until his

261 ces apoptotic-like cell death in Aspergillus nidulans, suggesting that this molecule has multiple and

262 Here we demonstrate that the Aspergillus nidulans Sur2 homolog BasA is also required for phytosph

263 e show that the nearly essential Aspergillus nidulans syntaxin PepA(Pep12) , present in all endocytic

264 The model fungus Aspergillus nidulans synthesizes numerous secondary metabolites, inc

265 drial morphology and function in Aspergillus nidulans, systematic characterization was carried out.

266 However, Aspergillus nidulans TamA and the related Saccharomyces cerevisiae D

267 In the fungus Aspergillus nidulans (teleomorph: Emericella nidulans) endogenous ox

268 fect on cellular physiology and ageing in A. nidulans than that of their homologs in another fungus P

269 tfA, a transcription factor from Aspergillus nidulans that contains a related double zinc finger, is

270 oteins in the filamentous fungus Aspergillus nidulans that possess an NPFxD motif, which signals for

271 For example, in Aspergillus nidulans the entire pathway for the production of sterig

272 In Aspergillus nidulans the global regulatory gene veA is necessary for

273 In Aspergillus nidulans, the AcuK and AcuM transcription factors form a

274 fusions of four SAC proteins in Aspergillus nidulans, the homologs of Mad2, Mps1, Bub1/BubR1 and Bub

275 in the model filamentous fungus Aspergillus nidulans, the molecular mechanisms underlying the develo

276 In the filamentous fungus Aspergillus nidulans, the multisubunit motor complex cytoplasmic dyn

277 In Aspergillus nidulans, the N-myristoylation deficient swoF1 mutant wa

278 Tolerance of Aspergillus nidulans to alkalinity and elevated cation concentration

279 e the UapA purine transporter of Aspergillus nidulans to investigate the role of cargo oligomerizatio

280 sponse of the filamentous fungus Aspergillus nidulans to the presence of high and low glucose concent

281 ar localization signal (NLS) motif in the A. nidulans VeA amino acid sequence and demonstrated its fu

282 ion can be fully complemented by Aspergillus nidulans VeA, which can physically interact with AfuVelB

283 aired in a farnesol-dependent manner when A. nidulans was co-cultivated with C. albicans.

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

285 Using the filamentous fungus Aspergillus nidulans we found that hitchhiking is mediated by a nove

286 Using Aspergillus nidulans, we demonstrate for the first time that septal

287 +end-binding proteins (+TIPS) in Aspergillus nidulans, we find that MTs are regulated to depolymerize

288 on of the pathway metabolite scytalone in A. nidulans, we provided chemical evidence that the Pfma cl

289 Using Aspergillus nidulans, we show that AP-2 has a clathrin-independent e

290 hyphae of the filamentous fungus Aspergillus nidulans, we show that three morphologically and functio

291 s on the pH regulatory system of Aspergillus nidulans, where a novel signal transduction (pal) pathwa

292 ows that the filamentous fungus, Aspergillus nidulans, which has a closed mitosis, does not maintain

293 exploits the filamentous fungus Aspergillus nidulans, which has many of the advantages of yeast mole

294 a second and specific RGS-Galpha pair in A. nidulans, which may govern upstream regulation of fungal

295 n, and will then juxtapose N. crassa with A. nidulans, which, as will be described below, provides an

296 ated from the filamentous fungus Aspergillus nidulans, whose mycelium is made of multinucleate cells.

297 Fungal strains included an A. nidulans wild-type isolate (A83), loss-of-function A. ni

298 bination deficient (nkuADelta) strains of A. nidulans with fusion PCR products results in high freque

299 a methyl-accepting substrate in Aspergillus nidulans with various assays, including in vivo S-adenos

300 stigation focuses on clathrin in Aspergillus nidulans, with the aim of understanding its role in memb