ライフサイエンスコーパス: Neurospora crassa

1 xual sporulation in the multicellular fungus Neurospora crassa.

2 sexual sporulation in the filamentous fungus Neurospora crassa.

3 st to control repetitive selfish elements in Neurospora crassa.

4 lue light responses in the filamentous fungi Neurospora crassa.

5 lass of small RNAs in the filamentous fungus Neurospora crassa.

6 protein complexes in the filamentous fungus Neurospora crassa.

7 in the adaptation of blue-light responses in Neurospora crassa.

8 egulator protein from the filamentous fungus Neurospora crassa.

9 f the RNAi pathway in the filamentous fungus Neurospora crassa.

10 idial germination in the filamentous fungus, Neurospora crassa.

11 ifungal peptide PAF26 using the model fungus Neurospora crassa.

12 derived from cosmid libraries of the fungus Neurospora crassa.

13 for most of the light-mediated processes in Neurospora crassa.

14 ement of genes encoding the core histones of Neurospora crassa.

15 sex pheromones of the heterothallic species Neurospora crassa.

16 o the RT of the Mauriceville retroplasmid of Neurospora crassa.

17 a wild population of the filamentous fungus Neurospora crassa.

18 ing the sre gene from the filamentous fungus Neurospora crassa.

19 quired for all known blue-light responses in Neurospora crassa.

20 ing regions and to predict gene structure in Neurospora crassa.

21 of 110 kDa) from Saccharomyces cerevisiae or Neurospora crassa.

22 little metabolized in the filamentous fungus Neurospora crassa.

23 nsible for all known cytosine methylation in Neurospora crassa.

24 e gene encoding subunit A of the V-ATPase of Neurospora crassa.

25 evisiae, Candida albicans, Mucor rouxii, and Neurospora crassa.

26 subunit, gna-3, from the filamentous fungus Neurospora crassa.

27 t-induced point mutation (RIP) in the fungus Neurospora crassa.

28 of the nuclear distribution protein RO11 of Neurospora crassa.

29 op-1, from the eukaryotic filamentous fungus Neurospora crassa.

30 recognize consensus GATA elements, exist in Neurospora crassa.

31 it sarcoplasmic reticulum and H+-ATPase from Neurospora crassa.

32 antage of genes controlled by methylation in Neurospora crassa.

33 dicted to be common in the ascomycete mould, Neurospora crassa.

34 ed as a component of the circadian system in Neurospora crassa.

35 and maintenance of regular hyphal growth in Neurospora crassa.

36 uring colony initiation in the fungal model, Neurospora crassa.

37 riod variation in single cell oscillators of Neurospora crassa.

38 on selection in the model filamentous fungus Neurospora crassa.

39 rmal hyphal growth in the filamentous fungus Neurospora crassa.

40 PAF26 has been characterized in detail using Neurospora crassa.

41 he deprotonation of nitroethane catalyzed by Neurospora crassa 2-nitropropane dioxygenase was investi

42 Catalytic turnover of Neurospora crassa 2-nitropropane dioxygenase with nitroe

43 al 1039 transcripts, contrasting with 117 in Neurospora crassa, a 14.3-fold difference.

44 In Neurospora crassa, a circadian rhythm of conidiation (as

45 In contrast, the histone modifications in Neurospora crassa, a convenient model organism for multi

46 In Neurospora crassa, a eukaryotic model system for studyin

47 f the roughly 100 dispersed 5S rRNA genes in Neurospora crassa, a methylated 5S rRNA pseudogene, Psi6

48 cell communication in the filamentous fungus Neurospora crassa, a simple and experimentally amenable

49 In Neurospora crassa, a single H3K9 methyltransferase compl

50 In Neurospora crassa, a transcription factor, WCC, activate

51 NcLPMO9C from Neurospora crassa acts both on cellulose and on non-cell

52 of the homolog in the filamentous ascomycete Neurospora crassa affects the circadian clock output, yi

53 In Neurospora crassa, all light responses depend on the Per

54 ubjected to repeat-induced point mutation in Neurospora crassa and A:T-rich repeated sequences in het

55 Highly similar proteins are encoded in Neurospora crassa and Aspergillus fumigatus.

56 ocarpus sp. (Chromista), and the ascomycetes Neurospora crassa and Aspergillus nidulans (Fungi), and

57 aken centre-stage over the last few decades--Neurospora crassa and Aspergillus nidulans.

58 ased models were constructed to describe the Neurospora crassa and Drosophila melanogaster circadian

59 rgillus nidulans, Aspergillus fumigatus, and Neurospora crassa and expressed the genes as secreted pr

60 yed stage-specific expression and editing in Neurospora crassa and F. verticillioides Furthermore,F.

61 ATPases) isolated from vacuolar membranes of Neurospora crassa and from chromaffin granule membranes

62 f4, inhibits growth of the ascomycete fungi, Neurospora crassa and Fusarium graminearum, at micromola

63 mediated silencing in the filamentous fungus Neurospora crassa and identified a bromo-adjacent homolo

64 analyzed H3K27me3 in the filamentous fungus Neurospora crassa and in other Neurospora species.

65 he ascomycete fungi Fusarium graminearum and Neurospora crassa and induces accumulation of reactive o

66 The DEAD-box proteins CYT-19 in Neurospora crassa and Mss116p in Saccharomyces cerevisia

67 The DEAD-box proteins CYT-19 in Neurospora crassa and Mss116p in Saccharomyces cerevisia

68 ies of the starch-active PMOs from the fungi Neurospora crassa and Myceliophthora thermophila, NcAA13

69 In Neurospora crassa and other filamentous fungi, light-dep

70 wealth of sequence information available for Neurospora crassa and other fungi has greatly facilitate

71 Neurospora crassa and related heterothallic ascomycetes

72 At the het-c locus in Neurospora crassa and related species there is clear evi

73 Full-length constructs of the proteins of Neurospora crassa and Saccharomyces cerevisiae (ncVDAC a

74 In Neurospora crassa and Saccharomyces cerevisiae, efficien

75 In Neurospora crassa and Saccharomyces cerevisiae, the latt

76 Recent work in Neurospora crassa and Sclerotinia sclerotiorum has illum

77 ferase center (PTC) function was analyzed in Neurospora crassa and wheat germ translation extracts us

78 was initially inoculated with the mycelium (Neurospora crassa), and following the initial incubation

79 e TPP riboswitches in the filamentous fungus Neurospora crassa, and found that one activates and two

80 derstand the role of MAP kinase signaling in Neurospora crassa, and to identify downstream target gen

81 6p of Saccharomyces cerevisiae and CYT-19 of Neurospora crassa are ATP-dependent helicases that funct

82 ic MLEs and that of CMLE from the eukaryotic Neurospora crassa are completely different from that of

83 Filamentous fungi, such as Neurospora crassa, are very efficient in deconstructing

84 ons of the Saccharomyces cerevisiae CPA1 and Neurospora crassa arg-2 AAPs using translation extracts

85 frame (uORF) in the 5' leader segment of the Neurospora crassa arg-2 mRNA causes reduced initiation a

86 Neurospora crassa arg-2 mRNA contains an evolutionarily

87 The Neurospora crassa arg-2 uORF encodes the 24-residue argi

88 ces cerevisiae GCN4, S. cerevisiae CPA1, and Neurospora crassa arg-2, regulation by uORFs controls ex

89 Neurospora crassa ARG13 and Saccharomyces cerevisiae ARG

90 eatures using an in vivo tethering system in Neurospora crassa Artificial recruitment of the H3K9 met

91 Here, we use Neurospora crassa as a model filamentous fungus to inter

92 We use the filamentous fungus Neurospora crassa as a model to study the molecular mech

93 Using the cellulolytic fungus Neurospora crassa as a model, we identified a xylodextri

94 d Gzf3p), Penicillium chrysogenum (NREB) and Neurospora crassa (ASD4).

95 vels of aequorin expression were obtained in Neurospora crassa, Aspergillus niger and Aspergillus awa

96 structure of LAD from the filamentous fungus Neurospora crassa at 2.6 A resolution.

97 In the lowly bread mould, Neurospora crassa, biomolecular reactions involving the

98 lamentous fungi, such as the model eukaryote Neurospora crassa, but is absent from the genomes of bak

99 re essential for light-mediated responses in Neurospora crassa, but the molecular mechanisms underlyi

100 nted these issues in the microbial eukaryote Neurospora crassa by using a "reverse-ecology" populatio

101 r the structure of the ring of c subunits in Neurospora crassa by using data from the crystal structu

102 obium aromaticivorans oxygenase 2 (NOV2) and Neurospora crassa carotenoid oxygenase 1 (CAO1), using p

103 the reconstitution of NSP ubiquitylation in Neurospora crassa cell extracts.

104 In the filamentous fungus Neurospora crassa, cell fusion occurs during asexual spo

105 Here we identified Neurospora crassa centromeric DNA by chromatin immunopre

106 These data suggest that the Neurospora crassa circadian clock regulates an unknown t

107 present a comprehensive dynamic model of the Neurospora crassa circadian clock that incorporates its

108 In the Neurospora crassa circadian clock, a protein complex of

109 The Neurospora crassa circadian negative element FREQUENCY (

110 Neurospora crassa colonizes burnt grasslands and metabol

111 Neurospora crassa colonizes burnt grasslands in the wild

112 O system conserved between S. cerevisiae and Neurospora crassa compared with that which has evolved i

113 ues in subunit c of the vacuolar ATPase from Neurospora crassa conferred strong resistance to bafilom

114 In Neurospora crassa, constitutive heterochromatin is chara

115 dehydrogenase (CDH) isolated from the fungi Neurospora crassa, Corynascus thermophilus, and Myriococ

116 A Neurospora crassa cosmid library of 12,000 clones (at le

117 Cbk1p is most closely related to the Neurospora crassa Cot-1; Schizosaccharomyces pombe Orb6;

118 The 3D-solution structure of Neurospora crassa Cu(6)-metallothionein (NcMT) polypepti

119 used to profile circadian gene expression in Neurospora crassa cultures grown in constant darkness.

120 cilitated by both the S. cerevisiae CBP2 and Neurospora crassa CYT-18 protein cofactors.

121 The Neurospora crassa CYT-18 protein is a mitochondrial tyro

122 The Neurospora crassa CYT-18 protein, the mitochondrial tyro

123 s studies showed that one of these proteins, Neurospora crassa CYT-18, binds group I introns by using

124 The Neurospora crassa DEAD-box protein CYT-19 is a mitochond

125 sfolded group I intron ribozyme by CYT-19, a Neurospora crassa DEAD-box protein that functions as a g

126 ATPase, we have generated mutant strains of Neurospora crassa defective in six subunits, C, H, a, c,

127 Repeat-induced point (RIP) mutation in Neurospora crassa degrades transposable elements by targ

128 he at the position equivalent to Phe(281) of Neurospora crassa DIM-5 or Phe(1205) of human G9a allows

129 ously shown that a DNA methylation mutant of Neurospora crassa, dim-5 (defective in methylation), has

130 ications is generally unknown, in the fungus Neurospora crassa, DNA methylation acts genetically down

131 d condensed chromatin, "heterochromatin." In Neurospora crassa, DNA methylation depends on trimethyla

132 In Neurospora crassa, DNA sequence duplications are detecte

133 of a Moco-free eukaryotic NR from the fungus Neurospora crassa, documenting that Moco is necessary an

134 Ornithine decarboxylase (ODC) of the fungus Neurospora crassa, encoded by the spe-1 gene, catalyzes

135 The fl (fluffy) gene of Neurospora crassa encodes a binuclear zinc cluster prote

136 Here we show that in the model organism Neurospora crassa entrainment of the circadian clock, wh

137 Zymoseptoria tritici, Magnaporthe oryzae and Neurospora crassa, exhibited PAMP activity, inducing cel

138 tein purified from one of its natural hosts, Neurospora crassa, exists in a multimeric form and has t

139 erevisiae homologue, although it does have a Neurospora crassa expressed sequence tag homologue.

140 Notably, the only other NMO from Neurospora crassa for which biochemical evidence is avai

141 The hydrophobin EAS from the fungus Neurospora crassa forms functional amyloid fibrils calle

142 study explores the relative contributions of Neurospora crassa G alpha subunits, gna-1, gna-2, and gn

143 We have identified a Neurospora crassa gene called rca-1 (regulator of conidi

144 -cell communication and fusion in the fungus Neurospora crassa Genetically identical germinating spor

145 In the filamentous fungus Neurospora crassa, genetically identical asexual spores

146 Prior to initiation of this project, the Neurospora crassa genome assembly contained only 3 of th

147 The recent completion of the Neurospora crassa genome offers a resource for comparati

148 s to control selfish DNA, an analysis of the Neurospora crassa genome sequence reveals a complete abs

149 eport the analysis of a 36-kbp region of the Neurospora crassa genome, which contains homologs of two

150 When isolated from Neurospora crassa, H(+)-ATPase is a 600 kDa hexamer of i

151 In the fungus Neurospora crassa, H3K9me3 and 5mC are catalyzed, respec

152 Neurospora crassa has been a model organism for the stud

153 Neurospora crassa has been for decades a principal model

154 rupts post-transcriptional gene silencing in Neurospora crassa has been found to affect the homologue

155 The filamentous fungus Neurospora crassa has been shown to be missing homologs

156 Neurospora crassa has been utilized as a model organism

157 The eukaryotic filamentous fungus Neurospora crassa has proven to be a dependable model sy

158 Neurospora crassa has the highest mutation rate and muta

159 i in general other than the model ascomycete Neurospora crassa--has been neglected, leaving this type

160 Mammals and the fungus Neurospora crassa have about 2-3% of cytosines methylate

161 ental mechanisms in Aspergillus nidulans and Neurospora crassa have been intensively studied, leading

162 e control and function of DNA methylation in Neurospora crassa have led to a greater understanding of

163 Genetics studies of Neurospora crassa have revealed that a DNA methyltransfe

164 ccharomyces pombe and the filamentous fungus Neurospora crassa have served as important model systems

165 an RdRP component of the quelling pathway in Neurospora crassa, have rapidly diverged in evolution at

166 and disiRNA locus DNA methylation (DLDM) in Neurospora crassa Here we show that the conserved exonuc

167 In Neurospora crassa, het-c is one of 11 het loci.

168 In the filamentous fungus Neurospora crassa, HET-C regulates a conserved programme

169 The small heat shock protein of Neurospora crassa, Hsp30, when employed in affinity chro

170 H(+)-ATPases (V-ATPase), inhibited growth of Neurospora crassa in medium adjusted to alkaline pH.

171 We used time-lapse live-cell imaging of Neurospora crassa in microfluidic environments to show h

172 n X-ray crystal structures of an enzyme from Neurospora crassa in the resting state and of a copper(I

173 ng a genetic screen of the ascomycete fungus Neurospora crassa, in which dynein is nonessential.

174 During sexual development, Neurospora crassa inactivates genes in duplicated DNA se

175 The circadian system of Neurospora crassa includes a molecular feedback loop tha

176 The biological clock of Neurospora crassa includes interconnected transcriptiona

177 laser scanning microscopy that a LPMO (from Neurospora crassa) introduces carboxyl groups primarily

178 Neurospora crassa is a central organism in the history o

179 Neurospora crassa is a heterothallic filamentous fungus

180 The filamentous fungus Neurospora crassa is a model laboratory organism, but in

181 The conidiation rhythm in the fungus Neurospora crassa is a model system for investigating th

182 The transcription factor CYS3 of Neurospora crassa is a positive regulator of the sulfur

183 The eukaryotic model organism Neurospora crassa is an excellent system to study evolut

184 This hyphal type in Neurospora crassa is being used as a model for studies o

185 The model filamentous fungus Neurospora crassa is capable of utilizing a variety of c

186 at heterochromatin in the filamentous fungus Neurospora crassa is marked by cytosine methylation dire

187 The nop-1 gene from Neurospora crassa is predicted to encode a seven-helix p

188 tion of the quinic acid (qa) gene cluster of Neurospora crassa is proposed.

189 The fluffy (fl) gene of Neurospora crassa is required for asexual sporulation an

190 n transcription/translation feedback loop in Neurospora crassa is the protein FREQUENCY (FRQ), shown

191 A model filamentous fungus, Neurospora crassa, is a multinucleate system used to elu

192 that PERIOD-4 (PRD-4), the CHK-2 ortholog of Neurospora crassa, is part of a signaling pathway that i

193 In Neurospora crassa, light promotes the interaction of WCC

194 xamined secretion in a temperature-sensitive Neurospora crassa mcb mutant that shows a loss of growth

195 ent studies showed that the splicing of some Neurospora crassa mitochondrial group I introns addition

196 The bifunctional Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

197 One such protein, the Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

198 rystal structure of a C-terminally truncated Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

199 The Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

200 The Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

201 The Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

202 hage T4 td intron to test the ability of the Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

203 The Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

204 Moreover, expression of Neurospora crassa MMM1, which naturally lacks a long N-t

205 We have isolated hundreds of Neurospora crassa mutants, known as ropy, that are defec

206 studies on the Schizosaccharomyces pombe and Neurospora crassa Nbp2p orthologues and the high conserv

207 with the corresponding dicer-like genes from Neurospora crassa [Ncdcl-1 (50.5%); Ncdcl-2 (38.0%)] and

208 g the motility of a fast fungal kinesin from Neurospora crassa (NcKin).

209 4-oxidizing family AA9 LPMOs from the fungus Neurospora crassa, NcLPMO9A (NCU02240), NcLPMO9C (NCU029

210 is study, we have characterized an LPMO from Neurospora crassa (NcLPMO9C; also known as NCU02916 and

211 We demonstrate that an LPMO from Neurospora crassa, NcLPMO9C, indeed degrades various hem

212 In Neurospora crassa, negative feedback is executed by a co

213 ning sensors, such as BarA and TorS; and the Neurospora crassa Nik-1 (Os-1) sensor that contains a ta

214 1 shows a significant sequence similarity to Neurospora crassa NIT2.

215 owed the highest degree of similarity to the Neurospora crassa nrc-1, Schizosaccharomyces pombe byr2

216 Most 5-methylcytosine in Neurospora crassa occurs in A:T-rich sequences high in T

217 In this study, we show that the Neurospora crassa osmosensing MAPK pathway, essential fo

218 Using the model filamentous fungus, Neurospora crassa, our microfluidic system enabled direc

219 s that are expressed in mycelial cultures of Neurospora crassa over the course of the circadian day,

220 In Neurospora crassa, pairing of homologous DNA segments is

221 on initiation factor, is clock controlled in Neurospora crassa, peaking during the subjective day.

222 agnets are small modules engineered from the Neurospora crassa photoreceptor Vivid by orthogonalizing

223 The Neurospora crassa photoreceptor Vivid tunes blue-light r

224 The filamentous fungus Neurospora crassa played a central role in the developme

225 viously reported that the filamentous fungus Neurospora crassa possesses a Galpha protein, GNA-1, tha

226 Neurospora crassa possesses this pathway, termed the thy

227 Genomes with good genetic maps, such as Neurospora crassa, provide a means for reducing ambiguit

228 to RNA-directed RNA polymerase (RdRP) and to Neurospora crassa QDE-1, two proteins implicated in post

229 h the previously determined apo structure of Neurospora crassa QDE2 revealed that the PIWI domain has

230 ted asexual spores in the filamentous fungus Neurospora crassa rcd-1 alleles are highly polymorphic a

231 uding the Saccharomyces cerevisiae Tup1p and Neurospora crassa RCO1.

232 We show that the model cellulolytic fungus Neurospora crassa relies on a high-affinity cellodextrin

233 Using Neurospora crassa repeat-induced point mutation (RIP) as

234 analysis of how the model filamentous fungus Neurospora crassa responds to the three main cell wall p

235 estigating the introns of the model organism Neurospora crassa revealed a different organization at t

236 he genome sequence of the filamentous fungus Neurospora crassa reveals a gene number very much higher

237 FEX KOs in three eukaryotic model organisms, Neurospora crassa, Saccharomyces cerevisiae, and Candida

238 tic studies of Schizosaccharomyces pombe and Neurospora crassa show that these types of enzymes are i

239 central component of the circadian clock in Neurospora crassa, shows daily cycles that are exquisite

240 ntly found that NOP-1, a membrane protein of Neurospora crassa, shows homology to haloarchaeal rhodop

241 Neurospora crassa sports features of heterochromatin fou

242 cell extracts derived from MacroD-deficient Neurospora crassa strain exhibit a major reduction in th

243 e polymorphisms (SNPs) between the reference Neurospora crassa strain Oak Ridge and the Mauriceville

244 implement our algorithm on a real dataset of Neurospora crassa strains, using the genetic and geograp

245 th an MTS derived from S. cerevisiae OXA1 or Neurospora crassa SU9, both coding for hydrophobic mitoc

246 n Mss116 and the related protein Cyt-19 from Neurospora crassa suggest that these proteins form a sub

247 Studies with the Neurospora crassa synthetase (CYT-18 protein) showed tha

248 ral potential new PMO families in the fungus Neurospora crassa that are likely to be active on novel

249 tions among the circadian clock mutations of Neurospora crassa that indicate possible physical intera

250 me-mediated TER 3'-end cleavage mechanism in Neurospora crassa that is distinct from that found speci

251 critical component of the circadian clock of Neurospora crassa that regulates the abundance of its co

252 In the fungus Neurospora crassa, the blue light photoreceptor(s) and s

253 In Neurospora crassa, the circadian clock generates daily r

254 In Neurospora crassa, the circadian clock transcriptionally

255 In Neurospora crassa, the frq, wc-1, and wc-2 genes encode

256 lletotrichum graminicola, the model organism Neurospora crassa, the human pathogen Sporothrix schenck

257 In the filamentous fungus Neurospora crassa, the IME2 homolog (ime-2) is not requi

258 In Neurospora crassa, the interactions between products of

259 e cloned and characterized the dim-2 gene of Neurospora crassa, the only eukaryotic gene currently kn

260 Among natural accessions of Neurospora crassa, there is significant variation in clo

261 In Neurospora crassa, three allelic specificities at the he

262 haromyces pombe, and one filamentous fungus, Neurospora crassa-three species that arguably are not re

263 (Hi-C) with wild-type and mutant strains of Neurospora crassa to gain insight into the role of heter

264 f the widely studied circadian oscillator of Neurospora crassa to inactivation of the frq gene.

265 therefore used the model filamentous fungus Neurospora crassa to search for uncharacterized transcri

266 uction of the NPS6 ortholog from the saprobe Neurospora crassa to the Deltanps6 strain of C. heterost

267 acultative and constitutive heterochromatin, Neurospora crassa, to explore possible interactions betw

268 During meiosis in the filamentous fungus Neurospora crassa, unpaired genes are identified and sil

269 In Neurospora crassa, unpaired genes are silenced by a mech

270 This system, derived from genes in Neurospora crassa, uses the transcriptional activator QF

271 We initially identified TER from Neurospora crassa using a novel deep-sequencing-based ap

272 We have successfully applied BiFC in Neurospora crassa using two genes involved in meiotic si

273 Neurospora crassa utilizes DNA methylation to inhibit tr

274 ite-directed mutagenesis at sites throughout Neurospora crassa VDAC (naturally devoid of cysteine) we

275 In Neurospora crassa, VIVID (VVD), a small LOV domain conta

276 y, the ncd-2 gene encoding for the enzyme in Neurospora crassa was cloned, expressed in Escherichia c

277 The complex from Neurospora crassa was composed of Tob55-Sam50, Tob38-Sam

278 A heterologous expression method in Neurospora crassa was developed as a step toward connect

279 In this research, the urease-positive fungus Neurospora crassa was investigated for the biomineraliza

280 gene encoding a novel GATA factor, ASD4, of Neurospora crassa was isolated and demonstrated to posse

281 tation, the conidiation rhythm of the fungus Neurospora crassa was monitored in constant darkness dur

282 ble complete genome of a filamentous fungus (Neurospora crassa) was released.

283 a conserved glucose homeostatic process, in Neurospora crassa We find that glycogen synthase (gsn) m

284 of the clock in the circadian model organism Neurospora crassa We show that, in a ras2-deficient stra

285 tween H3S10p, H3K9me, and DNA methylation in Neurospora crassa, we built and tested mutants of the pu

286 rward genetic approach in the model organism Neurospora crassa, we identified two alleles of a gene,

287 by allelic differences at the het-c locus of Neurospora crassa, we isolated mutants that suppressed p

288 lear movement in the model ascomycete fungus Neurospora crassa, we show that genetic diversity is mai

289 Different PMOs isolated from Neurospora crassa were found to generate oxidized cellod

290 lopsis (formerly Mortierella) ramanniana and Neurospora crassa were introduced into maize using an em

291 y are acutely active in the meiotic cells of Neurospora crassa, where they evaluate the mutual identi

292 In this study, we employed LPMO9C from Neurospora crassa, which is active toward cellulose and

293 g regulation by a fungal TPP riboswitch from Neurospora crassa, which is mostly located in a large in

294 salinarium Bat, Azotobacter vinelandii NIFL, Neurospora crassa White Collar-1, Escherichia coli Aer,

295 In Neurospora crassa, white collar 1 (WC-1), a transcriptio

296 ithin a 7 kb sequence that is not present in Neurospora crassa wild-type 74 A mtDNA.

297 ithin a 7 kb sequence that is not present in Neurospora crassa wild-type 74A mtDNA.

298 eacetylase 1 (HDA1) mutant (hda-1) strain of Neurospora crassa with inactivated histone deacetylase 1

299 of sequence data from the filamentous fungus Neurospora crassa with the complete genome sequence of S

300 in single cells of the model fungal system, Neurospora crassa, with droplet microfluidics and the us