Works matching DE "NEMATODE-destroying fungi"
Results: 275
Independence Effects of Heat and Ash on Forest Soil Nematode-Trapping Fungi Communities.
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- Fire (2571-6255), 2023, v. 6, n. 1, p. 27, doi. 10.3390/fire6010027
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捕食线虫真菌少孢节丛孢 Arthrobotrys oligospora 线粒体基因组的异质性.
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- Mycosystema, 2022, v. 41, n. 4, p. 529, doi. 10.13346/j.mycosystema.210285
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少孢节丛孢中CRISPR/Cas9基因编辑系统的建立及6-甲基水杨酸合酶新活性位点的发现.
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- Mycosystema, 2021, v. 40, n. 9, p. 2282, doi. 10.13346/j.mycosystema.210169
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The Velvet Proteins VosA and VelB Play Different Roles in Conidiation, Trap Formation, and Pathogenicity in the Nematode-Trapping Fungus Arthrobotrys oligospora.
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- Frontiers in Microbiology, 2019, p. 1, doi. 10.3389/fmicb.2019.01917
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Methylglyoxal Has Different Impacts on the Fungistatic Roles of Ammonia and Benzaldehyde, and Lactoylglutathione Lyase Is Necessary for the Resistance of Arthrobotrys oligospora to Soil Fungistasis.
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- Frontiers in Cellular & Infection Microbiology, 2021, v. 11, p. N.PAG, doi. 10.3389/fcimb.2021.640823
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Fungal biocontrol reduces the populations of the lesion nematode, Pratylenchus brachyurus, in soybean and corn.
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- Nematology, 2021, v. 23, n. 6, p. 619, doi. 10.1163/15685411-bja10064
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Nematophagous Pleurotus Species Consume Some Nematode Species but Are Themselves Consumed by Others.
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- Forests (19994907), 2019, v. 10, n. 5, p. 404, doi. 10.3390/f10050404
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Autophagy is required for trap formation in the nematode-trapping fungus Arthrobotrys oligospora.
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- Environmental Microbiology Reports, 2013, v. 5, n. 4, p. 511, doi. 10.1111/1758-2229.12054
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Divergence and dispersal of the nematode-trapping fungus Arthrobotrys oligospora from China.
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- Environmental Microbiology Reports, 2011, v. 3, n. 6, p. 763, doi. 10.1111/j.1758-2229.2011.00297.x
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Proteolytic activity of the nematophagous fungus Arthrobotrys sinensis on Angiostrongylus vasorum larvae.
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- BMC Research Notes, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1756-0500-7-811
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Mycelial mass production of fungi Duddingtonia flagrans and Monacrosporium thaumasium under different culture conditions.
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- BMC Research Notes, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1756-0500-6-340
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Phanerochaete chrysosporium strain B-22, a nematophagous fungus parasitizing Meloidogyne incognita.
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- PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0216688
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Insecticidal activity of Conidia of Paecilomyces lilacinus (Thom) Samson against Malaria and Filaria Vectors.
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- EurAsian Journal of Biosciences, 2020, v. 14, n. 2, p. 5695
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ROOT-KNOT NEMATODES FROM ASPARAGUS AND ASSOCIATED BIOLOGICAL ANTAGONISTS IN PERU.
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- Nematropica, 2012, v. 42, n. 1, p. 57
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Biological and proteomic analysis of a new isolate of the nematophagous fungus lecanicillium sp.
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- BMC Microbiology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12866-023-02855-4
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Intercellular communication is required for trap formation in the nematode-trapping fungus Duddingtonia flagrans.
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- PLoS Genetics, 2019, v. 15, n. 3, p. 1, doi. 10.1371/journal.pgen.1008029
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Succession of soil nematode-trapping fungi following fire disturbance in forest.
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- Journal of Forest Research, 2020, v. 25, n. 6, p. 433, doi. 10.1080/13416979.2020.1793465
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Determination of cyclic adenosine phosphate and protein content in dormant chlamydospore and nondormant chlamydospore of Arthrobotrys flagrans.
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- Journal of Basic Microbiology, 2024, v. 64, n. 7, p. 1, doi. 10.1002/jobm.202400008
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Chlamydospore dormancy and predatory activity of nematophagous fungus Duddingtonia flagrans.
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- Journal of Basic Microbiology, 2024, v. 64, n. 3, p. 1, doi. 10.1002/jobm.202300365
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A putative F‐box‐domain‐encoding gene AOL_s00076g207 regulates the development and pathogenicity of Arthrobotrys oligospora.
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- Journal of Basic Microbiology, 2022, v. 62, n. 1, p. 74, doi. 10.1002/jobm.202100388
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In vitro evaluation of physicochemical variables on the nematophagous fungus Duddingtonia flagrans.
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- Journal of Basic Microbiology, 2021, v. 61, n. 6, p. 547, doi. 10.1002/jobm.202100039
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Morphological variability, molecular phylogeny, and biological characteristics of the nematophagous fungus Duddingtonia flagrans.
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- Journal of Basic Microbiology, 2019, v. 59, n. 6, p. 645, doi. 10.1002/jobm.201800610
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In vitro and in vivo studies of the native isolates of nematophagous fungi from China against the larvae of trichostrongylides.
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- Journal of Basic Microbiology, 2017, v. 57, n. 3, p. 265, doi. 10.1002/jobm.201600620
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Screening of different sample types associated with sheep and cattle for the presence of nematophagous fungi in China.
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- Journal of Basic Microbiology, 2016, v. 56, n. 3, p. 214, doi. 10.1002/jobm.201500281
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Insight into the transcriptome of Arthrobotrys conoides using high throughput sequencing.
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- Journal of Basic Microbiology, 2015, v. 55, n. 12, p. 1394, doi. 10.1002/jobm.201500237
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Isolation, identification, and characterization of the nematophagous fungus Monacrosporium salinum from China.
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- Journal of Basic Microbiology, 2015, v. 55, n. 8, p. 992, doi. 10.1002/jobm.201400909
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In vitro evaluation of nematophagous activity of fungal isolates.
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- Journal of Basic Microbiology, 2014, v. 54, n. 1, p. 1, doi. 10.1002/jobm.201200431
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Characterization of an Extracellular Serine Protease Gene from the Nematophagous Fungus Lecanicillium psalliotae.
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- Biotechnology Letters, 2005, v. 27, n. 17, p. 1329, doi. 10.1007/s10529-005-0482-1
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Isolation and Characterization of a Serine Protease from the Nematophagous Fungus, Lecanicillium psalliotae, Displaying Nematicidal Activity.
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- Biotechnology Letters, 2005, v. 27, n. 15, p. 1123, doi. 10.1007/s10529-005-8461-0
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The living strategy of nematophagous fungi.
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- Mycoscience (Springer Nature), 2009, v. 50, n. 1, p. 20, doi. 10.47371/mycosci.myc50020
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Ion Beam Mutagenesis in Arthrobotrys oligospora Enhances Nematode-Trapping Ability.
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- Current Microbiology, 2013, v. 66, n. 6, p. 594, doi. 10.1007/s00284-013-0322-9
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Variabilities of Two Drechslerella dactyloides Isolates in Korea and High Predacity Against Bursaphelenchus xylophilus.
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- Current Microbiology, 2011, v. 62, n. 2, p. 472, doi. 10.1007/s00284-010-9731-1
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Variability in Indian Isolates of Arthrobotrys dactyloides Drechsler: A Nematode-Trapping Fungus.
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- Current Microbiology, 2006, v. 52, n. 4, p. 293, doi. 10.1007/s00284-005-0274-9
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DNA methylation plays important roles in lifestyle transition of Arthrobotrys oligospora.
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- IET Systems Biology (Wiley-Blackwell), 2024, v. 18, n. 3, p. 92, doi. 10.1049/syb2.12094
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The essential role of arginine biosynthetic genes in lunate conidia formation, conidiation, mycelial growth, and virulence of nematophagous fungus, Esteya vermicolaCBS115803.
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- Pest Management Science, 2024, v. 80, n. 2, p. 786, doi. 10.1002/ps.7809
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The combination of two Bacillus strains suppresses Meloidogyne incognita and fungal pathogens, but does not enhance plant growth.
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- Pest Management Science, 2022, v. 78, n. 2, p. 722, doi. 10.1002/ps.6685
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In vivo infection of Bursaphelenchus xylophilus by the fungus Esteya vermicola.
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- Pest Management Science, 2020, v. 76, n. 8, p. 2854, doi. 10.1002/ps.5839
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食线虫真菌防治植物寄生线虫研究进展.
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- Journal of Henan Agricultural Sciences, 2021, v. 50, n. 1, p. 1, doi. 10.15933/j.cnki.1004-3268.2021.01.001
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New species of Hohenbuehelia, with comments on the Hohenbuehelia atrocoerulea - Nematoctonus robustus species complex.
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- Persoonia, 2018, v. 41, n. 1, p. 202, doi. 10.3767/persoonia.2018.41.10
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Arabidopsis thaliana root colonization by the nematophagous fungus Pochonia chlamydosporia is modulated by jasmonate signaling and leads to accelerated flowering and improved yield.
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- New Phytologist, 2017, v. 213, n. 1, p. 351, doi. 10.1111/nph.14106
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Third Generation Genome Sequencing Reveals That Endobacteria in Nematophagous Fungi Esteya vermicola Contain Multiple Genes Encoding for Nematicidal Proteins.
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- Frontiers in Microbiology, 2022, p. 1, doi. 10.3389/fmicb.2022.842684
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AoBck1 and AoMkk1 Are Necessary to Maintain Cell Wall Integrity, Vegetative Growth, Conidiation, Stress Resistance, and Pathogenicity in the Nematode-Trapping Fungus Arthrobotrys oligospora.
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- Frontiers in Microbiology, 2021, v. 12, p. 1, doi. 10.3389/fmicb.2021.649582
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Soil microcosms and the population biology of...
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- Ecology, 1996, v. 77, n. 3, p. 690, doi. 10.2307/2265493
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Two novel hyphomycetes associated with ferns from China.
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- MycoKeys, 2025, n. 113, p. 101, doi. 10.3897/mycokeys.113.137678
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The cAMP-PKA pathway regulates prey sensing and trap morphogenesis in the nematode-trapping fungus Arthrobotrys oligospora.
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- G3: Genes | Genomes | Genetics, 2022, v. 12, n. 10, p. 1, doi. 10.1093/g3journal/jkac217
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Forward genetic screens identified mutants with defects in trap morphogenesis in the nematode-trapping fungus Arthrobotrys oligospora.
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- G3: Genes | Genomes | Genetics, 2021, v. 11, n. 2, p. 1, doi. 10.1093/g3journal/jkaa022
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- Article
GREEN MANURE AND Pochonia chlamydosporia FOR Meloidogyne javanica CONTROL IN SOYBEAN.
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- Revista Caatinga, 2022, v. 35, n. 3, p. 625, doi. 10.1590/1983-21252022v35n313rc
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Nematode-trapping fungus Arthrobotrys oligospora recruited rhizosphere microorganisms to cooperate in controlling root-knot nematodes in tomato.
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- Journal of Applied Microbiology, 2024, v. 135, n. 9, p. 1, doi. 10.1093/jambio/lxae218
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Phospholipase C (AoPLC2) regulates mycelial development, trap morphogenesis, and pathogenicity of the nematode‐trapping fungus Arthrobotrys oligospora.
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- Journal of Applied Microbiology, 2022, v. 132, n. 3, p. 2144, doi. 10.1111/jam.15370
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Scale-Up of Duddingtonia flagrans Chlamydospores Production from Laboratory to Pilot-Scale Using a Solid-State Fermentation System.
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- Applied Biochemistry & Biotechnology, 2020, v. 192, n. 3, p. 1044, doi. 10.1007/s12010-020-03370-2
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