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