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1 one precursor genes encoded by a filamentous ascomycete.
2 osporum, the other sequenced ectomycorrhizal ascomycete.
3 genes as observed in homothallic filamentous Ascomycetes.
4 fungal virulence factor in plant pathogenic ascomycetes.
5 imilar to those encoded by other filamentous ascomycetes.
6 er in specificity at het loci in filamentous ascomycetes.
7 the control of sexual differentiation in the ascomycetes.
8 ing Ophiocordyceps species, and not in other ascomycetes.
9 which might act as antifungal drugs against ascomycetes.
10 also provide insight into early evolution of ascomycetes.
11 ntaining and generating the diversity of the ascomycetes.
12 s, some of which are also conserved in other ascomycetes.
13 exin that is conserved across diverse fungal ascomycetes.
14 s large and diverse family of lichen-forming ascomycetes.
15 es and beta2-tubulin genes were lost in most ascomycetes.
16 tion of Nbp2p appears to be conserved across Ascomycetes.
17 ication is required for successful mating in ascomycetes.
18 e, unmutated copy in the genomes of 11 other ascomycetes.
19 ared with those of 13 more distantly related Ascomycetes.
20 .181) versus 1.210 (95% CI, 1.161-1.261) for ascomycetes, 1.112 (95% CI, 1.085-1.14) versus 1.302 (95
21 d that homologs of DES are widespread in the ascomycetes, although in most cases the homologs must pa
22 eptor and pheromone genes from a filamentous ascomycete and a basidiomycete and expressed these in th
23 scovered that Nbp2p orthologues exist in all Ascomycete and Basidiomycete fungal genomes and that all
25 ters used in these vectors function in other ascomycete and basidiomycete fungi, we anticipate that t
26 o significantly inversely correlated with EM Ascomycete and EM short-contact exploration type abundan
28 resses two Galpha subunits, most filamentous ascomycetes and basidiomycetes have three Galpha subunit
29 onophyletic clade of fungi, the Dikarya (the ascomycetes and basidiomycetes), and the ancestral state
31 lls for mating are found only in filamentous ascomycetes and even here, a single individual produces
33 alcineurin-responsive zinc fingers (Crz1) of ascomycetes and to the Pkc1-dependent specificity protei
35 diomycete to be successfully expressed in an ascomycete, and paves the way for the exploitation of a
37 in controlling asexual growth in filamentous Ascomycetes but also confirm that heterothallic and homo
38 ex, long treated as a zone of differentiated ascomycete cells, appears to consistently contain two un
39 ly encountered symbiont on tree roots is the ascomycete Cenococcum geophilum, the only mycorrhizal sp
40 invasive human mycoses caused by the phaeoid ascomycete, Chaetomium perlucidum, and review the Englis
43 aria inaequalis, a widely distributed litter ascomycete, chlorinated the aromatic rings of lignin in
45 entrapped cellobiose dehydrogenase from the ascomycete Corynascus thermophilus (CtCDH) in a photocro
46 of chestnut blight caused by the filamentous ascomycete Cryphonectria parasitica can be achieved with
47 diversification; in the clade of filamentous ascomycetes, dense-core Woronin bodies bud from peroxiso
48 itis are dimorphic, soil-dwelling pathogenic ascomycetes endemic to the southwestern United States.
49 hogen effectors from three branches of life (ascomycete, eubacteria, and oomycete) converge onto the
51 esent classification, be placed in different ascomycete families: the Microcyclus sexual morph in the
52 nary history of spore shapes within a single ascomycete family we measure the relative contributions
53 nd electron microscopy to show that a common Ascomycete filamentous fungus, Stilbella aciculosa, oxid
54 sp. hordei (Bgh), is an obligate biotrophic ascomycete fungal pathogen that can grow and reproduce o
55 ion is not required for successful mating of ascomycete fungi and confirm that, in budding yeast, the
56 d S. japonicus--occupies the basal branch of Ascomycete fungi and is an important model of eukaryote
57 th is a ubiquitous phenomenon in filamentous ascomycete fungi and is termed heterokaryon incompatibil
58 a distinct group that was closely related to ascomycete fungi and that human-derived P. carinii was m
59 oscopic size, the forcibly ejected spores of ascomycete fungi are quickly brought to rest by drag.
60 ve the signature of horizontal transfer from ascomycete fungi associated with wood decay and from pro
62 dly permeabilizes the plasma membrane of the ascomycete fungi Fusarium graminearum and Neurospora cra
66 s spp. examined, in several other classes of ascomycete fungi, and in animals but not in basidiomycet
67 l glycine-leucine motif in SREBP homologs of ascomycete fungi, including the opportunistic human path
68 llus flavus, like approximately one-third of ascomycete fungi, is thought to be cosmopolitan and clon
69 ant defensin, MtDef4, inhibits growth of the ascomycete fungi, Neurospora crassa and Fusarium gramine
74 ic interactions with natural variants of the ascomycete fungus Blumeria graminis f. sp. hordei (Bgh),
75 ic interactions with natural variants of the ascomycete fungus Blumeria graminis f.sp. hordei (Bgh),
79 hain mutations using a genetic screen of the ascomycete fungus Neurospora crassa, in which dynein is
80 ng patterns of nuclear movement in the model ascomycete fungus Neurospora crassa, we show that geneti
83 roach in a study of Coccidioides immitis, an ascomycete fungus responsible for a recent epidemic of c
84 letotrichum higginsianum is a hemibiotrophic ascomycete fungus that is adapted to Arabidopsis (Arabid
85 genome alignment of five individuals of the ascomycete fungus Zymoseptoria pseudotritici, a close re
86 ur study of the mating system of the haploid ascomycete fungus, Cryphonectria parasitica, resulted in
87 New cosmid vectors were constructed for the ascomycete fungus, Magnaporthe grisea and the basidiomyc
88 he isolation of a common mosquito-associated ascomycete fungus, Penicillium chrysogenum, from the mid
89 ic alpha-pheromone from the plant pathogenic ascomycete Fusarium oxysporum revealed the presence of a
90 ied a comparative genomic approach across 14 Ascomycete genomes, mapping phenotypes and genotypes ont
93 known to form meiotic (sexual) stages in the ascomycete genus Ajellomyces (Onygenaceae, Onygenales),
96 s of other basidiomycete natural products in ascomycete heterologous hosts, and open up new possibili
97 y system, typical of other self-incompatible Ascomycetes, in which mating is only successful between
99 mainly in the coding regions in filamentous ascomycetes, involving adenosine deamination mechanisms
100 olution of the biologically diverse forms of ascomycetes is not well understood, largely because the
101 (phylum Ascomycota) but not early diverging ascomycetes, like Saccharomyces cerevisiae (Saccharomyco
102 e last common ancestor of basidiomycetes and ascomycetes likely possessed two paralogs of alpha-tubul
103 ese substrates with orthologs throughout the ascomycete lineage revealed that the position of most ph
104 Peroxidases of unknown function from the ascomycete Magnaporthe grisea were found to be the close
106 of H3K9me2/3 heterochromatin, the origin of ascomycete mating-type switching, and panascomycete synt
109 Deletion of the homolog in the filamentous ascomycete Neurospora crassa affects the circadian clock
110 gi--or fungi in general other than the model ascomycete Neurospora crassa--has been neglected, leavin
113 quality genomic data sets of the filamentous ascomycete Neurospora tetrasperma, a fungus that lacks r
114 type has been reported in several species of Ascomycetes, no peptide has been reported to function as
115 e family provides a compelling example in an ascomycete of chromatin-based silencing of natural subte
116 We report the identification of a novel Ascomycete PAMP, RcCDI1, recognized by Solanaceae but no
117 tion network of virulence effectors from the ascomycete pathogen Golovinomyces orontii and Arabidopsi
118 ation pattern and symptom development by the ascomycete pathogen Plectosphaerella cucumerina (P. cucu
120 Sclerotinia sclerotiorum is a filamentous ascomycete phytopathogen able to infect an extremely wid
123 ndo-beta-1,4-mannanases from the coprophilic ascomycete Podospora anserina contribute to the enzymati
124 Neurospora crassa and related heterothallic ascomycetes produce eight homokaryotic self-sterile asco
127 studies have begun to reveal how filamentous ascomycete species exploit carbon sources in different h
132 e slow-growing environmental rock-inhabiting ascomycete synthesizing a constitutive DHN-melanin, Cryo
135 t infects the fungus Rosellinia necatrix, an ascomycete that is pathogenic to a wide range of plants.
136 plete loss of annexin sequences from another ascomycete, the budding yeast Saccharomyces cerevisiae.
137 any common lichens are composed of the known ascomycete, the photosynthesizing partner, and, unexpect
140 f MAT genes from a wide array of filamentous ascomycetes, thereby providing MAT-based technology for
141 transceptor activity likely occur in related ascomycetes used for industrial cellulase production.
142 graphic history of worldwide invasion of the ascomycete Verticillium dahliae, a soil-borne pathogen,
143 le the relative percent of tips colonized by Ascomycetes was positively correlated with soil pH.
145 ilable for alpha pheromones from filamentous ascomycetes, which are significantly shorter and share a
146 ungi are less tractable genetically than the ascomycetes, which predominantly produce lower-potential
147 zae giving production of pleuromutilin in an ascomycete, with a significant increase (2106%) in produ
148 viously uncharacterized proteins specific to Ascomycetes, with SAD-4 having a range that spans severa
151 hich is known to be involved in autophagy in ascomycete yeast, was defective in the formation of auto
155 such as the early diverging lineages and the ascomycete yeasts, but was otherwise slightly inferior t
156 red through a series of experiments in three ascomycete yeasts: the bakers' yeast Saccharomyces cerev
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