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Phylogenic analysis of adhesion related genes Mad1 revealed a positive selection for the evolution of trapping devices of nematode-trapping fungi

https://doi.org/10.1038/srep22609
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-94-007-1933-0_4openalex-snapshot
Fungi as Biological Control Agents of Plant-Parasitic Nematodes
inferredcites →https://doi.org/10.1007/978-94-010-0263-9_20openalex-snapshot
Maximum likelihood methods for detecting adaptive evolution after gene duplication
inferredcites →https://doi.org/10.1007/978-94-017-8730-7openalex-snapshot
Nematode-Trapping Fungi
inferredcites →https://doi.org/10.1007/978-94-017-8730-7_1openalex-snapshot
Nematode-Trapping Fungi
inferredcites →https://doi.org/10.1007/978-94-017-8730-7_3openalex-snapshot
Taxonomy of Nematode-Trapping Fungi from Orbiliaceae, Ascomycota
inferredcites →https://doi.org/10.1007/s00239-004-2597-8openalex-snapshot
A Maximum Likelihood Method for Detecting Functional Divergence at Individual Codon Sites, with Application to Gene Family Evolution
inferredcites →https://doi.org/10.1007/s00253-013-5178-1openalex-snapshot
Proteomic and transcriptional analyses of Arthrobotrys oligospora cell wall related proteins reveal complexity of fungal virulence against nematodes
inferredcites →https://doi.org/10.1007/s004250000451openalex-snapshot
Heterotrimeric G-protein and signal transduction in the nematode-trapping fungus Arthrobotrys dactyloides
inferredcites →https://doi.org/10.1007/s13238-012-2031-8openalex-snapshot
How carnivorous fungi use three-celled constricting rings to trap nematodes
inferredcites →https://doi.org/10.1016/0167-7799(90)90215-jopenalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/0168-9525(90)90186-aopenalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/0304-4017(93)90165-jopenalex-snapshot
Biological control of nematode parasites in cattle with nematode-trapping fungi: a survey of Danish studies
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.fgb.2015.02.012openalex-snapshot
A proposed adhesin AoMad1 helps nematode-trapping fungus Arthrobotrys oligospora recognizing host signals for life-style switching
inferredcites →https://doi.org/10.1016/s0168-9525(02)02722-1openalex-snapshot
The Ka/Ks ratio: diagnosing the form of sequence evolution
inferredcites →https://doi.org/10.1016/s0378-1097(97)00519-3openalex-snapshot
Phylogeny of nematode-trapping fungi based on 18S rDNA sequences
inferredcites →https://doi.org/10.1016/s0378-1135(02)00309-7openalex-snapshot
Characterization of the functional domain of major surface protein 1a involved in adhesion of the rickettsia Anaplasma marginale to host cells
inferredcites →https://doi.org/10.1016/s0960-8524(96)00122-8openalex-snapshot
Biological control of plant parasitic nematodes by fungi: A review
inferredcites →https://doi.org/10.1016/s0966-842x(01)01984-9openalex-snapshot
The ALS gene family of Candida albicans
inferredcites →https://doi.org/10.1023/a:1022642807731openalex-snapshot
Maximum likelihood methods for detecting adaptive evolution after gene duplication
inferredcites →https://doi.org/10.1038/npg.els.0004293openalex-snapshot
Nematophagous Fungi
inferredcites →https://doi.org/10.1073/pnas.0702770104openalex-snapshot
Evolution of nematode-trapping cells of predatory fungi of the Orbiliaceae based on evidence from rRNA-encoding DNA and multiprotein sequences
inferredcites →https://doi.org/10.1073/pnas.1120915109openalex-snapshot
Origin and evolution of carnivorism in the Ascomycota (fungi)
inferredcites →https://doi.org/10.1080/00275514.1994.12026433openalex-snapshot
Orbilia fimicola , a nematophagous discomycete and its Arthrobotrys anamorph
inferredcites →https://doi.org/10.1080/00275514.1995.12026584openalex-snapshot
Two Arthrobotrys anamorphs from Orbilia auricolor
inferredcites →https://doi.org/10.1080/10635150390235520openalex-snapshot
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
inferredcites →https://doi.org/10.1080/10635150590924208openalex-snapshot
Polytomies and Bayesian Phylogenetic Inference
inferredcites →https://doi.org/10.1080/10635150701472164openalex-snapshot
Improvement of Phylogenies after Removing Divergent and Ambiguously Aligned Blocks from Protein Sequence Alignments
inferredcites →https://doi.org/10.1091/mbc.9.1.161openalex-snapshot
The Cell Surface Flocculin Flo11 Is Required for Pseudohyphae Formation and Invasion by Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot
MODELTEST: testing the model of DNA substitution.
inferredcites →https://doi.org/10.1093/bioinformatics/17.9.847openalex-snapshot
InterProScan – an integration platform for the signature-recognition methods in InterPro
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/genetics/148.3.929openalex-snapshot
Likelihood Models for Detecting Positively Selected Amino Acid Sites and Applications to the HIV-1 Envelope Gene
inferredcites →https://doi.org/10.1093/molbev/msi097openalex-snapshot
Bayes Empirical Bayes Inference of Amino Acid Sites Under Positive Selection
inferredcites →https://doi.org/10.1093/molbev/msi237openalex-snapshot
Evaluation of an Improved Branch-Site Likelihood Method for Detecting Positive Selection at the Molecular Level
inferredcites →https://doi.org/10.1093/molbev/msm088openalex-snapshot
PAML 4: Phylogenetic Analysis by Maximum Likelihood
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025957openalex-snapshot
Likelihood ratio tests for detecting positive selection and application to primate lysozyme evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026334openalex-snapshot
Selection of Conserved Blocks from Multiple Alignments for Their Use in Phylogenetic Analysis
inferredcites →https://doi.org/10.1093/sysbio/42.2.193openalex-snapshot
Is There Something Wrong with the Bootstrap on Phylogenies? A Reply to Hillis and Bull
inferredcites →https://doi.org/10.1099/00221287-137-6-1231openalex-snapshot
Surface polymers of the nematode-trapping fungus Arthrobotrys oligospora
inferredcites →https://doi.org/10.1111/j.1574-6968.1998.tb12817.xopenalex-snapshot
Phylogeny of nematode-trapping fungi based on 18S rDNA sequences
inferredcites →https://doi.org/10.1128/ec.00120-06openalex-snapshot
Threonine-Rich Repeats Increase Fibronectin Binding in the Candidaalbicans Adhesin Als5p
inferredcites →https://doi.org/10.1128/ec.00409-06openalex-snapshot
The MAD1 Adhesin of Metarhizium anisopliae Links Adhesion with Blastospore Production and Virulence to Insects, and the MAD2 Adhesin Enables Attachment to Plants
inferredcites →https://doi.org/10.1128/jb.110.3.1163-1170.1972openalex-snapshot
Ultrastructure of Nematode-Trapping Fungi
inferredcites →https://doi.org/10.1146/annurev-phyto-080614-120336openalex-snapshot
Molecular Mechanisms of Nematode-Nematophagous Microbe Interactions: Basis for Biological Control of Plant-Parasitic Nematodes
inferredcites →https://doi.org/10.1186/1471-2164-15-114openalex-snapshot
Drechslerella stenobrocha genome illustrates the mechanism of constricting rings and the origin of nematode predation in fungi
inferredcites →https://doi.org/10.1371/journal.pgen.1003909openalex-snapshot
Genomic Mechanisms Accounting for the Adaptation to Parasitism in Nematode-Trapping Fungi
inferredcites →https://doi.org/10.1371/journal.ppat.1002179openalex-snapshot
Genomic and Proteomic Analyses of the Fungus Arthrobotrys oligospora Provide Insights into Nematode-Trap Formation
inferredcites →https://doi.org/10.1371/journal.ppat.1003027openalex-snapshot
Morphogenesis in Fungal Pathogenicity: Shape, Size, and Surface
inferredcites →https://doi.org/10.3852/mycologia.97.5.1034openalex-snapshot
Phylogenetics and evolution of nematode-trapping fungi (Orbiliales) estimated from nuclear and protein coding genes
inferredcites →https://doi.org/10.4135/9781412961288.n455openalex-snapshot
Teoria Statistica Delle Classi e Calcolo Delle Probabilità

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.568.3.2zenodo-depositor-declared
Two new nematode-trapping fungi (Arthrobotrys, Orbiliaceae) from Yunnan, China
inferred← citeshttps://doi.org/10.11646/phytotaxa.591.4.3zenodo-depositor-declared
Morphological and multigene phylogenetic analyses reveal two new nematode-trapping fungi (Arthrobotrys, Orbiliaceae) from Yunnan, China
inferred← citeshttps://doi.org/10.1016/j.actatropica.2025.107751openalex-snapshot
Entomopathogenic fungi: Natural biocontrol of insects, challenges under climate change, advancements and future prospects in Modern Agriculture
inferred← citeshttps://doi.org/10.1093/molbev/msaf249openalex-snapshot
Genomic Insights Into Convergent Evolution: Adaptation to Rocky Habitats in Rock-Inhabiting Fungi
inferred← citeshttps://doi.org/10.1111/1751-7915.70412openalex-snapshot
WC1 / WC2 –Sre1 Transcriptional Cascade Controls Predation and Chlamydospore Formation in the Nematode‐Trapping Fungus Arthrobotrys flagrans
inferred← citeshttps://doi.org/10.1515/hsz-2020-0199openalex-snapshot
Diversity of GPI-anchored fungal adhesins
inferred← citeshttps://doi.org/10.17957/ijab/15.1786openalex-snapshot
Molecular Characteristics and Adhesion Activity of a Novel Protein ADP1 of Arthrobotrys oligospora to Nematodes
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3077296/v1openalex-snapshot
The AL-ao379 gene plays a role in promoting the invasion stage of Bursaphelenchus xylophilus trapped by Arthrobotrys cladodes
inferred← citeshttps://doi.org/10.3390/jof4020059openalex-snapshot
What We Do Not Know about Fungal Cell Adhesion Molecules
inferred← citeshttps://doi.org/10.3390/jof8070671openalex-snapshot
New Arthrobotrys Nematode-Trapping Species (Orbiliaceae) from Terrestrial Soils and Freshwater Sediments in China
inferred← citeshttps://doi.org/10.3390/jof9040451openalex-snapshot
Arthrobotrys blastospora sp. nov. (Orbiliomycetes): A Living Fossil Displaying Morphological Traits of Mesozoic Carnivorous Fungi
inferred← citeshttps://doi.org/10.3390/jof9121125openalex-snapshot
Isolation, Identification, and Evaluation of the Predatory Activity of Chinese Arthrobotrys Species towards Economically Important Plant-Parasitic Nematodes
inferred← citeshttps://doi.org/10.3390/jof9121183openalex-snapshot
Analysis of Nuclear Dynamics in Nematode-Trapping Fungi Based on Fluorescent Protein Labeling
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