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Three new species ofNeonectria(Nectriaceae, Hypocreales) with notes on their phylogenetic positions
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/mpev.1996.0376openalex-snapshot
Two Divergent Intragenomic rDNA ITS2 Types within a Monophyletic Lineage of the FungusFusariumAre Nonorthologous
inferredcites →https://doi.org/10.1007/s10267-006-0300-1openalex-snapshot
Neonectria amamiensis and Cylindrocarpon amamiense, a new nectrioid fungus and its sporodochial anamorph on Pinus luchuensis from Japan
inferredcites →https://doi.org/10.1007/s10267-006-0330-8openalex-snapshot
Taxonomic studies of nectrioid fungi in Japan. I: The genus Neonectria
inferredcites →https://doi.org/10.1007/s11557-008-0577-xopenalex-snapshot
Cyanonectria, a new genus for Nectria cyanostoma and its Fusarium anamorph
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/j.femsle.2004.11.003openalex-snapshot
Development of a nested PCR detection procedure forNectria fuckelianadirect from Norway spruce bark extracts
inferredcites →https://doi.org/10.1016/j.mycres.2007.10.004openalex-snapshot
Cylindrocarpon pauciseptatum sp. nov., with notes on Cylindrocarpon species with wide, predominantly 3-septate macroconidia
inferredcites →https://doi.org/10.1016/s0953-7562(10)80001-2openalex-snapshot
Variation in Nectria radicicola and its anamorph, Cylindrocarpon destructans
inferredcites →https://doi.org/10.1017/s0953756200002719openalex-snapshot
Phylogenetic analysis of the phytopathogenic fungus Fusarium solani based on the rDNA-ITS region
inferredcites →https://doi.org/10.1046/j.1469-8137.2001.00038.xopenalex-snapshot
Genetic diversity of fungi closely associated with common reed
inferredcites →https://doi.org/10.1080/15572536.2005.11832955openalex-snapshot
NeonectriaandCylindrocarpon: the Nectria mammoidea group and species lacking microconidia
inferredcites →https://doi.org/10.1080/15572536.2006.11832755openalex-snapshot
Neonectria castaneicolaandNeo. rugulosain Japan
inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025813openalex-snapshot
Can three incongruence tests predict when data should be combined?
inferredcites →https://doi.org/10.1094/phyto.2003.93.12.1533openalex-snapshot
Molecular Differentiation and Detection of Ginseng-Adapted Isolates of the Root Rot Fungus Cylindrocarpon destructans
inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00181.xopenalex-snapshot
TESTING SIGNIFICANCE OF INCONGRUENCE
inferredcites →https://doi.org/10.1128/aem.61.4.1323-1330.1995openalex-snapshot
Development of primer sets designed for use with the PCR to amplify conserved genes from filamentous ascomycetes
inferredcites →https://doi.org/10.1139/b01-002openalex-snapshot
Phylogenetic relationships in Neonectria species having Cylindrocarpon anamorphs inferred from mitochondrial ribosomal DNA sequences
inferredcites →https://doi.org/10.1139/b06-105openalex-snapshot
Phylogenetic relationships of Neonectria/Cylindrocarpon on Fagus in North AmericaMention of trade names or commercial products in this article is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the US Department of Agriculture.
inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot
BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT
inferredcites →https://doi.org/10.2307/3760508openalex-snapshot
Some Didymosporous Species of Nectria with Nonmicroconidial Cylindrocarpon Anamorphs
inferredcites →https://doi.org/10.2307/3762176openalex-snapshot
Neonectria and Cylindrocarpon: The Nectria Mammoidea Group and Species Lacking Microconidia
inferredcites →https://doi.org/10.3114/sim.55.1.227openalex-snapshot
Neonectria liriodendri sp. nov., the main causal agent of black foot disease of grapevines
inferredcites →https://doi.org/10.3852/mycologia.97.5.1058openalex-snapshot
Neonectria castaneicola and Neo. rugulosa in Japan
inferredcites →https://doi.org/10.5962/bhl.title.144788openalex-snapshot
Color standards and color nomenclature /
inferredcites →https://doi.org/10.5962/bhl.title.62375openalex-snapshot
Color standards and color nomenclature,
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.319.2.6zenodo-depositor-declared
Two new species of Neocosmospora from China
inferred← citeshttps://doi.org/10.11646/phytotaxa.491.1.7zenodo-depositor-declared
A new species of Sarcopodium (Hypocreales, Nectriaceae) from China
inferred← citeshttps://doi.org/10.11646/phytotaxa.85.1.3zenodo-depositor-declared
Four new taxa of Ilyonectria and Thelonectria (Nectriaceae) revealed by morphology and combined ITS and β-tubulin sequence data
inferred← citeshttps://doi.org/10.1007/s11427-011-4184-8openalex-snapshot
DNA barcoding of the fungal genus Neonectria and the discovery of two new species
inferred← citeshttps://doi.org/10.1007/s11557-014-0980-4openalex-snapshot
A new holomorphic species of Mariannaea and epitypification of M. samuelsii
inferred← citeshttps://doi.org/10.1007/s11557-016-1201-0openalex-snapshot
A new species of Cosmospora and the first record of sexual state of C. lavitskiae
inferred← citeshttps://doi.org/10.1007/s11557-021-01672-1openalex-snapshot
Our current understanding of the genus Pseudocosmospora (Hypocreales, Nectriaceae) in China
inferred← citeshttps://doi.org/10.1007/s13225-010-0064-yopenalex-snapshot
Practice towards DNA barcoding of the nectriaceous fungi
inferred← citeshttps://doi.org/10.1007/s13225-019-00418-5openalex-snapshot
One stop shop II: taxonomic update with molecular phylogeny for important phytopathogenic genera: 26–50 (2019)
inferred← citeshttps://doi.org/10.1007/s13225-019-00433-6openalex-snapshot
One stop shop III: taxonomic update with molecular phylogeny for important phytopathogenic genera: 51–75 (2019)
inferred← citeshttps://doi.org/10.1007/s13225-023-00521-8openalex-snapshot
Taxonomy, phylogeny and evolution of freshwater Hypocreomycetidae (Sordariomycetes)
inferred← citeshttps://doi.org/10.14601/phytopathol_mediterr-14976openalex-snapshot
Lineages in Nectriaceae : re-evaluating the generic status of Ilyonectria and allied genera
inferred← citeshttps://doi.org/10.3114/sim.2011.68.03openalex-snapshot
Delimitation of Neonectria and Cylindrocarpon (Nectriaceae, Hypocreales, Ascomycota) and related genera with Cylindrocarpon-like anamorphs
inferred← citeshttps://doi.org/10.3390/jof10090632openalex-snapshot
Comparative Genomics of Fungi in Nectriaceae Reveals Their Environmental Adaptation and Conservation Strategies
inferred← citeshttps://doi.org/10.3390/life13071515openalex-snapshot
New Species of Neocosmospora (Ascomycota) from China as Evidenced by Morphological and Molecular Data
inferred← citeshttps://doi.org/10.3897/mycokeys.42.27664openalex-snapshot
Two new species of Geejayessia (Hypocreales) from Asia as evidenced by morphology and multi-gene analyses
inferred← citeshttps://doi.org/10.3897/mycokeys.55.34527openalex-snapshot
The genera Rugonectria and Thelonectria (Hypocreales, Nectriaceae) in China
inferred← citeshttps://doi.org/10.3897/mycokeys.71.55009openalex-snapshot
Ascomycetes from the Qilian Mountains, China – Hypocreales
inferred← citeshttps://doi.org/10.5248/120.67openalex-snapshot
A new species of Nectria on Populus from China
inferred← citeshttps://doi.org/10.5941/myco.2014.42.2.174openalex-snapshot
Genetic Diversity and Pathogenicity of Cylindrocarpon destructans Isolates Obtained from Korean Panax ginseng
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