1 OD600) data of Aspergillus fumigatus growth (
filamentous fungus).
2 and those of several pathogenic yeasts and a
filamentous fungus.
3 ation of the first Ste12 protein from a true
filamentous fungus.
4 ole in apical transport of mitochondria in a
filamentous fungus.
5 ted in septin bundles in growing hyphae of a
filamentous fungus.
6 nt small interfering RNAs (disiRNAs) in this
filamentous fungus.
7 degradation mechanisms used by a ubiquitous
filamentous fungus.
8 n-binding protein fimbrin in live cells of a
filamentous fungus.
9 ave been cloned and sequenced from the model
filamentous fungus A. nidulans.
10 mRNA levels in response to ER stress in the
filamentous fungus A. oryzae cells.
11 We demonstrated in a
filamentous fungus,
a budding yeast, and a mammalian epi
12 nd secondary metabolite, aflatoxin B1 in the
filamentous fungus and an important plant pathogen, Aspe
13 Fusarium graminearum is a
filamentous fungus and causes the devastating and econom
14 nonribosomal peptide, by taking genes from a
filamentous fungus and directing their efficient express
15 s show that HDC1 has multiple functions in a
filamentous fungus and is required for full virulence of
16 h's postulates for a true dsRNA virus from a
filamentous fungus and the description of a definitive f
17 We solved the structure of Dfg5 from a
filamentous fungus and used in crystallo glycan fragment
18 Resting conidia of the
filamentous fungus are constantly inhaled, but cause inf
19 es essential for septin ring assembly in the
filamentous fungus Ashbya gossypii and demonstrate here
20 In the multinucleate
filamentous fungus Ashbya gossypii, the RNA-binding prot
21 ng membrane curvature sensing in vivo in the
filamentous fungus Ashbya, the functionality of these do
22 More than 90% of the cell wall of the
filamentous fungus Aspergillus fumigatus comprises polys
23 In the pathogenic
filamentous fungus Aspergillus fumigatus, this polysacch
24 ing antimicrobial produced by the ubiquitous
filamentous fungus Aspergillus fumigatus.
25 hiodioxopiperazine toxin that is made by the
filamentous fungus Aspergillus fumigatus.
26 The nudF gene of the
filamentous fungus Aspergillus nidulans acts in the cyto
27 In the
filamentous fungus Aspergillus nidulans BrlA triggers th
28 The
filamentous fungus Aspergillus nidulans contains a clust
29 s were added to the cultivation media of the
filamentous fungus Aspergillus nidulans for the study of
30 The NUDF protein of the
filamentous fungus Aspergillus nidulans functions in the
31 Here, we analyzed in the
filamentous fungus Aspergillus nidulans functions of the
32 The
filamentous fungus Aspergillus nidulans grows by polariz
33 The
filamentous fungus Aspergillus nidulans has previously b
34 Recent work with the
filamentous fungus Aspergillus nidulans has provided new
35 ere we present unequivocal evidence that the
filamentous fungus Aspergillus nidulans houses both pero
36 Asexual development (conidiation) in the
filamentous fungus Aspergillus nidulans is governed by o
37 Vegetative growth signaling in the
filamentous fungus Aspergillus nidulans is primarily med
38 The
filamentous fungus Aspergillus nidulans possesses both a
39 Asexual sporulation (conidiation) in the
filamentous fungus Aspergillus nidulans requires the ear
40 In the
filamentous fungus Aspergillus nidulans SPBs and septum-
41 In a search for proteins in the
filamentous fungus Aspergillus nidulans that possess an
42 Engineered strains of the
filamentous fungus Aspergillus nidulans then biosyntheti
43 Here, we used the
filamentous fungus Aspergillus nidulans to examine wheth
44 cterized the transcriptional response of the
filamentous fungus Aspergillus nidulans to the presence
45 Using the
filamentous fungus Aspergillus nidulans we found that hi
46 We previously showed that in the
filamentous fungus Aspergillus nidulans, a GFP-tagged cy
47 In the
filamentous fungus Aspergillus nidulans, a heterotrimeri
48 In the
filamentous fungus Aspergillus nidulans, both cytoplasmi
49 In the
filamentous fungus Aspergillus nidulans, cytokinesis/sep
50 In the
filamentous fungus Aspergillus nidulans, germination of
51 alc gene-expression system, derived from the
filamentous fungus Aspergillus nidulans, has previously
52 In the
filamentous fungus Aspergillus nidulans, inactivation of
53 AbaA) class of transcription factors of the
filamentous fungus Aspergillus nidulans, induces pseudoh
54 nderstanding of signalling mechanisms in the
filamentous fungus Aspergillus nidulans, intensive analy
55 In the
filamentous fungus Aspergillus nidulans, the dynein HC i
56 mycotoxin sterigmatocystin (ST) in the model
filamentous fungus Aspergillus nidulans, the molecular m
57 In the
filamentous fungus Aspergillus nidulans, the multisubuni
58 Herein, we show that in the
filamentous fungus Aspergillus nidulans, the septin AspB
59 ynamic behavior of cytoplasmic dynein in the
filamentous fungus Aspergillus nidulans, we replaced the
60 ing the long, highly polarized hyphae of the
filamentous fungus Aspergillus nidulans, we show that th
61 alysis utilizing an engineered strain of the
filamentous fungus Aspergillus nidulans, which gives acc
62 This screen exploits the
filamentous fungus Aspergillus nidulans, which has many
63 g a homologous protein was isolated from the
filamentous fungus Aspergillus nidulans, whose mycelium
64 er In Mitosis, gene A (NIMA) kinase from the
filamentous fungus Aspergillus nidulans.
65 uclear migration through the mycelium of the
filamentous fungus Aspergillus nidulans.
66 anization of multicellular structures in the
filamentous fungus Aspergillus nidulans.
67 xin (sterigmatocystin; ST) production by the
filamentous fungus Aspergillus nidulans.
68 gion for myosin I function in vivo using the
filamentous fungus Aspergillus nidulans.
69 a high-affinity purine transporter from the
filamentous fungus Aspergillus nidulans.
70 nein-mediated early endosome movement in the
filamentous fungus Aspergillus nidulans.
71 limiting factor for hyphal tip growth in the
filamentous fungus Aspergillus nidulans.
72 development and secondary metabolism in the
filamentous fungus Aspergillus nidulans.
73 dy we examined the effect of farnesol in the
filamentous fungus Aspergillus nidulans.
74 culum (ER)-associated stress response in the
filamentous fungus Aspergillus niger.
75 carbohydrate active enzymes (CAZymes) of the
filamentous fungus Aspergillus niger.
76 thway for protocatechuate utilization in the
filamentous fungus Aspergillus niger.
77 as initially applied to a cell lysate of the
filamentous fungus Aspergillus niger.
78 asured eight-locus fitness landscape for the
filamentous fungus Aspergillus niger.
79 The level of aflatoxin accumulation in the
filamentous fungus Aspergillus parasiticus is modulated
80 ess response and secondary metabolism in the
filamentous fungus Aspergillus parasiticus.
81 The
filamentous fungus Aspergillus terreus produces acetylar
82 ducing polyketide synthase (HR-PKS) from the
filamentous fungus Aspergillus terreus.
83 is produced by fermentation of sugars by the
filamentous fungus Aspergillus terreus.
84 have been heterologously expressed in both a
filamentous fungus (
Aspergillus nidulans) and in a methy
85 rt the characterization of SUN proteins in a
filamentous fungus,
Aspergillus fumigatus.
86 In the
filamentous fungus,
Aspergillus nidulans, multiple round
87 A new study shows that the
filamentous fungus,
Aspergillus nidulans, which has a cl
88 fication and cloning of the telomeres of the
filamentous fungus,
Aspergillus nidulans.
89 ly described as red mold, is a red-pigmented
filamentous fungus attracting a great interest for the p
90 fungus-like organism Pythium ultimum and the
filamentous fungus Botrytis cinerea was inhibited.
91 that secretion of extracellular protein by a
filamentous fungus can be significantly increased by mut
92 Race 1 isolates of the
filamentous fungus Cochliobolus carbonum are exceptional
93 Strains of the
filamentous fungus Cochliobolus carbonum that produce th
94 lase (HDAC) gene HOS2, was isolated from the
filamentous fungus Cochliobolus carbonum, a pathogen of
95 The ribosome structure from this
filamentous fungus contains clearly resolved ribosomal p
96 d in rat and dog liver microsomes and in the
filamentous fungus Cunninghamella elegans.
97 Here we use the genetically modified
filamentous fungus expression system Thermothelomyces he
98 ein kinase (FsMAPK) from the phytopathogenic
filamentous fungus F. solani f. sp. pisi T8 strain.
99 t fungus (Cryphonectria parasitica), a model
filamentous fungus for studying virus-host interactions.
100 Aspergillus flavus is a
filamentous fungus found in nature and characterized by
101 A genetic map of the
filamentous fungus Fusarium graminearum (teleomorph: Gib
102 The ubiquitous
filamentous fungus Fusarium graminearum causes the impor
103 We sequenced and annotated the genome of the
filamentous fungus Fusarium graminearum, a major pathoge
104 cotoxins produced in wheat infected with the
filamentous fungus Fusarium graminearum.
105 In the present work, for the first time, the
filamentous fungus Fusarium sp. was utilized for devisin
106 oxidative phosphorylation in the pathogenic
filamentous fungus,
Gaeumannomyces graminis var. tritici
107 ed a novel alcohol oxidase (Hv-p68) from the
filamentous fungus Helminthosporium (Cochliobolus) victo
108 xins produced by Fusarium verticillioides, a
filamentous fungus infecting corn and contaminating food
109 The
filamentous fungus Magnaporthe grisea can cause disease
110 To cause rice blast disease, the
filamentous fungus Magnaporthe oryzae secretes a battery
111 cultivated rice world-wide, is caused by the
filamentous fungus Magnaporthe oryzae.
112 been cloned and partially sequenced from the
filamentous fungus,
Metarhizium anisopliae.
113 ukotrienes but it is also accumulated by the
filamentous fungus Mortierella alpina.
114 Isolated organisms included
filamentous fungus (
n = 301 [91%]), Acanthamoeba (n = 10
115 The PDA1 gene of the
filamentous fungus Nectria haematococca MPVI (anamorph:
116 H3K27 methylation-mediated silencing in the
filamentous fungus Neurospora crassa and identified a br
117 We identified and analyzed H3K27me3 in the
filamentous fungus Neurospora crassa and in other Neuros
118 We use the
filamentous fungus Neurospora crassa as a model to study
119 report the crystal structure of LAD from the
filamentous fungus Neurospora crassa at 2.6 A resolution
120 omponent histidine kinases in the eukaryotic
filamentous fungus Neurospora crassa based on screening
121 p of phenotypically identical mutants of the
filamentous fungus Neurospora crassa encode proteins tha
122 The
filamentous fungus Neurospora crassa has been shown to b
123 The eukaryotic
filamentous fungus Neurospora crassa has proven to be a
124 sion yeast Schizosaccharomyces pombe and the
filamentous fungus Neurospora crassa have served as impo
125 The
filamentous fungus Neurospora crassa is a model laborato
126 The model
filamentous fungus Neurospora crassa is capable of utili
127 The model
filamentous fungus Neurospora crassa is capable of utili
128 sly demonstrated that heterochromatin in the
filamentous fungus Neurospora crassa is marked by cytosi
129 The
filamentous fungus Neurospora crassa played a central ro
130 We previously reported that the
filamentous fungus Neurospora crassa possesses a Galpha
131 ling PCD in germinated asexual spores in the
filamentous fungus Neurospora crassa rcd-1 alleles are h
132 omparative systems analysis of how the model
filamentous fungus Neurospora crassa responds to the thr
133 The completion of the genome sequence of the
filamentous fungus Neurospora crassa reveals a gene numb
134 We therefore used the model
filamentous fungus Neurospora crassa to search for uncha
135 The
filamentous fungus Neurospora crassa undergoes a well-de
136 e-scale comparison of sequence data from the
filamentous fungus Neurospora crassa with the complete g
137 thesis, we studied cell communication in the
filamentous fungus Neurospora crassa, a simple and exper
138 We examined three TPP riboswitches in the
filamentous fungus Neurospora crassa, and found that one
139 In the
filamentous fungus Neurospora crassa, cell fusion occurs
140 In the
filamentous fungus Neurospora crassa, genetically identi
141 In the
filamentous fungus Neurospora crassa, HET-C regulates a
142 In the
filamentous fungus Neurospora crassa, however, the mecha
143 In the
filamentous fungus Neurospora crassa, the IME2 homolog (
144 In the
filamentous fungus Neurospora crassa, the proteins Frequ
145 During meiosis in the
filamentous fungus Neurospora crassa, unpaired genes are
146 Using the
filamentous fungus Neurospora crassa, we performed a gen
147 en isolated, including the sre gene from the
filamentous fungus Neurospora crassa.
148 e shown that it is little metabolized in the
filamentous fungus Neurospora crassa.
149 the G protein alpha subunit, gna-3, from the
filamentous fungus Neurospora crassa.
150 of an opsin gene, nop-1, from the eukaryotic
filamentous fungus Neurospora crassa.
151 molog of the histidine kinase Nik-1 from the
filamentous fungus Neurospora crassa.
152 that encode G protein alpha subunits in the
filamentous fungus Neurospora crassa.
153 dentified a G alpha i homologue gna-1 in the
filamentous fungus Neurospora crassa.
154 r cytoplasmic dynein/dynactin mutants in the
filamentous fungus Neurospora crassa.
155 r oscillator, in a mathematical model of the
filamentous fungus Neurospora crassa.
156 lencing of H3K27-methylated chromatin in the
filamentous fungus Neurospora crassa.
157 ngency of start codon selection in the model
filamentous fungus Neurospora crassa.
158 is essential for normal hyphal growth in the
filamentous fungus Neurospora crassa.
159 atic cell fusion in a wild population of the
filamentous fungus Neurospora crassa.
160 al changes during asexual sporulation in the
filamentous fungus Neurospora crassa.
161 n QDE-2 and a new class of small RNAs in the
filamentous fungus Neurospora crassa.
162 ion of proteins and protein complexes in the
filamentous fungus Neurospora crassa.
163 RRG-1, a response regulator protein from the
filamentous fungus Neurospora crassa.
164 entral components of the RNAi pathway in the
filamentous fungus Neurospora crassa.
165 In the
filamentous fungus Neurospora, FRQ, FRH, WC-1, and WC-2
166 Here, we show that in the
filamentous fungus Neurospora, the Argonaute homolog QDE
167 the model yeast Saccharomyces and the model
filamentous fungus Neurospora, we examine intrinsic rest
168 at there is a strong codon usage bias in the
filamentous fungus Neurospora.
169 irst publicly available complete genome of a
filamentous fungus (
Neurospora crassa) was released.
170 mino acid (aa) identity to P5CR from another
filamentous fungus,
Neurospora crassa (Nc).
171 A model
filamentous fungus,
Neurospora crassa, is a multinucleat
172 Using the model
filamentous fungus,
Neurospora crassa, our microfluidic
173 isiae and Schizosaccharomyces pombe, and one
filamentous fungus,
Neurospora crassa-three species that
174 nal profiling of conidial germination in the
filamentous fungus,
Neurospora crassa.
175 Penicillium chrysogenum is a
filamentous fungus of major medical and historical impor
176 r study provides the first evidence that the
filamentous fungus P. graminis has evolved to produce fu
177 The
filamentous fungus Penicillium brevicompactum produces t
178 btained from derived deletion strains of the
filamentous fungus Penicillium chrysogenum were used to
179 n esterase was isolated from cultures of the
filamentous fungus Penicillium funiculosum grown on suga
180 of the genus Cochliobolus but absent in the
filamentous fungus,
Penicillium chrysogenum, as well as
181 structure of ligand-free APS kinase from the
filamentous fungus,
Penicillium chrysogenum.
182 structure of ligand-free APS kinase from the
filamentous fungus,
Penicillium chrysogenum.
183 ed by the het-Q allorecognition genes in the
filamentous fungus Podospora anserina We show that the c
184 In the
filamentous fungus Podospora anserina, a well establishe
185 r peroxisome biogenesis and caryogamy in the
filamentous fungus Podospora anserina.
186 Aspergillus fumigatus, a
filamentous fungus producing bluish-green conidia, is an
187 ene disruption at an efficiency >90% in this
filamentous fungus,
promises to be applicable to other e
188 which shares homology with a lipase from the
filamentous fungus Rhizomucor miehei.
189 Here we implant bacteria into the
filamentous fungus Rhizopus microsporus to follow the fa
190 lved in the erection of aerial hyphae in the
filamentous fungus Schizophyllum commune was also capabl
191 us family, as essential for karyogamy in the
filamentous fungus Sordaria macrospora, thus uncovering
192 microscopy to show that a common Ascomycete
filamentous fungus,
Stilbella aciculosa, oxidizes Mn(II)
193 reovirus from Cryphonectria parasitica, the
filamentous fungus that causes chestnut blight disease.
194 Fusarium proliferatum is a toxigenic
filamentous fungus that produces the harmful mycotoxins
195 A. flavus is a toxic
filamentous fungus that significantly impacts the agricu
196 Here, we use Neurospora crassa as a model
filamentous fungus to interrogate the requirements for t
197 Here, we describe that in the
filamentous fungus Trichoderma atroviride, injury result
198 Replicate populations of the
filamentous fungus Trichoderma citrinoviride underwent 8
199 The
filamentous fungus Trichoderma reesei produces and secre
200 etter than Rad51, we used the Pezizomycotina
filamentous fungus Trichoderma reesei to address if and
201 folding of an endoglucanase (EGIII) from the
filamentous fungus Trichoderma reesei was investigated b
202 We have previously shown that the beneficial
filamentous fungus Trichoderma virens secretes the highl
203 ndida lusitaniae, Mycobacterium avium, and a
filamentous fungus,
Trichophyton fischeri.
204 Neurospora crassa is a heterothallic
filamentous fungus with two mating types, mat a and mat