ライフサイエンスコーパス: Neurospora crassa

1 st to control repetitive selfish elements in Neurospora crassa.

2 lue light responses in the filamentous fungi Neurospora crassa.

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

4 protein complexes in the filamentous fungus Neurospora crassa.

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

6 egulator protein from the filamentous fungus Neurospora crassa.

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

8 idial germination in the filamentous fungus, Neurospora crassa.

9 derived from cosmid libraries of the fungus Neurospora crassa.

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

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

12 sex pheromones of the heterothallic species Neurospora crassa.

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

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

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

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

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

18 little metabolized in the filamentous fungus Neurospora crassa.

19 nsible for all known cytosine methylation in Neurospora crassa.

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

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

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

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

24 of the nuclear distribution protein RO11 of Neurospora crassa.

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

26 recognize consensus GATA elements, exist in Neurospora crassa.

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

28 antage of genes controlled by methylation in Neurospora crassa.

29 ine kinase Nik-1 from the filamentous fungus Neurospora crassa.

30 the anx14 gene of the filamentous ascomycete Neurospora crassa.

31 metabolism is a highly regulated process in Neurospora crassa.

32 ein alpha subunits in the filamentous fungus Neurospora crassa.

33 hymidine kinase gene ( tk ) was expressed in 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 on selection in the model filamentous fungus Neurospora crassa.

38 rmal hyphal growth in the filamentous fungus Neurospora crassa.

39 PAF26 has been characterized in detail using Neurospora crassa.

40 xual sporulation in the multicellular fungus Neurospora crassa.

41 sexual sporulation in the filamentous fungus Neurospora crassa.

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

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

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

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

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

47 In Neurospora crassa, a eukaryotic model system for studyin

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

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

50 In Neurospora crassa, a single H3K9 methyltransferase compl

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

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

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

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

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

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

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

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

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

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

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

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

69 Neurospora crassa and related heterothallic ascomycetes

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

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

72 In Neurospora crassa and Saccharomyces cerevisiae, efficien

73 In Neurospora crassa and Saccharomyces cerevisiae, the latt

74 Recent work in Neurospora crassa and Sclerotinia sclerotiorum has illum

75 and dewA from Aspergillus nidulans, EAS from Neurospora crassa and ssgA from Metarhizium anisopliae)

76 e filamentous fungi Aspergillus nidulans and Neurospora crassa and the yeast Saccharomyces cerevisiae

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

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

85 Neurospora crassa arg-2 mRNA contains an evolutionarily

86 reading frame (uORF) in the 5'-leader of the Neurospora crassa arg-2 mRNA was reconstituted in a homo

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 ae, S. carlsbergensis, Kluyveromyces lactis, Neurospora crassa, Aspergillus nidulans, and A. flavus.

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

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

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

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

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

101 requently mutated during the sexual cycle in Neurospora crassa by a process named repeat-induced poin

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

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

104 The Neurospora crassa catabolic enzyme, arginase (L-arginine

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

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

107 Here we identified Neurospora crassa centromeric DNA by chromatin immunopre

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

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

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

111 The Neurospora crassa circadian negative element FREQUENCY (

112 Neurospora crassa colonizes burnt grasslands and metabol

113 Neurospora crassa colonizes burnt grasslands in the wild

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

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

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

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

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

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

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

130 In Neurospora crassa, DNA sequence duplications are detecte

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

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

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

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

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

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

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

138 Neurospora crassa fluffy (fl) mutants are unable to prod

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

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

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

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

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

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

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

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

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

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

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

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

151 Neurospora crassa has been a model organism for the stud

152 Neurospora crassa has been for decades a principal model

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

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

155 Neurospora crassa has been utilized as a model organism

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

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

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

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

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

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

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

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

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

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

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

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

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

169 tor of vacuolar ATPases, inhibited growth of Neurospora crassa in medium adjusted to pH 7 or above.

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

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

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

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

174 The biological clock of Neurospora crassa includes interconnected transcriptiona

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

176 Neurospora crassa is a central organism in the history o

177 Neurospora crassa is a heterothallic filamentous fungus

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

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

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

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

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

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

184 Macroconidiation in Neurospora crassa is influenced by a number of environme

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

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

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

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

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

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

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

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

193 The bifunctional Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

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

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

196 The Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

197 The Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

198 The Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

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

200 The Neurospora crassa mitochondrial tyrosyl-tRNA synthetase

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

202 nsertional mutagenesis approach, a series of Neurospora crassa mutants affected in the ability to con

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

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

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

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

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

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

209 The aab1 gene maps on linkage group III of Neurospora crassa near the trp-1 locus.

210 a conserved amino-terminal domain within the Neurospora crassa negative regulator sulfur controller-2

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

212 1 shows a significant sequence similarity to Neurospora crassa NIT2.

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

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

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

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

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

218 In Neurospora crassa, pairing of homologous DNA segments is

219 The Neurospora crassa photoreceptor Vivid tunes blue-light r

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

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

222 Neurospora crassa possesses this pathway, termed the thy

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

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

225 uding the Saccharomyces cerevisiae Tup1p and Neurospora crassa RCO1.

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

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

228 In Neurospora crassa, repeated sequences are silenced by re

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

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

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

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

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

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

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

236 Neurospora crassa sports features of heterochromatin fou

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

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

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

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

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

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

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

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

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

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

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

248 In Neurospora crassa, the circadian clock generates daily r

249 In Neurospora crassa, the circadian clock transcriptionally

250 In Neurospora crassa, the expression of the nit-3 gene (nit

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

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

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

254 In Neurospora crassa, the interactions between products of

255 In Neurospora crassa, the major nitrogen regulatory protein

256 In Neurospora crassa, the mitochondrial arginine biosynthet

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

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

259 In Neurospora crassa, three allelic specificities at the he

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

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

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

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

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

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

266 f tigA from Aspergillus niger and erp38 from Neurospora crassa, two novel members of the PDI superfam

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

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

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

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

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

272 Neurospora crassa utilizes DNA methylation to inhibit tr

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

274 d to introduce single cysteine residues into Neurospora crassa VDAC (naturally lacks cysteine).

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

276 ntromere region of linkage group (LG) VII of Neurospora crassa was cloned previously from a yeast art

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

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

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

280 development) gene of the filamentous fingus Neurospora crassa was identified as a gene expressed pre

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

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

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

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

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

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

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