On the public citation graph
Fungal Sex: The Basidiomycota
0 signed · 320 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.10083openalex-snapshot
Molecular genetics of sexual development in the mushroom Coprinus cinereus
inferredcites →https://doi.org/10.1002/dvg.1020150111openalex-snapshot
Diverse programs of ascus development in pseudohomothallic species of Neurospora, Gelasinospora, and Podospora
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05232.xopenalex-snapshot
A fungal mating type protein that regulates sexual and asexual development contains a POU‐related domain.
inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06425.xopenalex-snapshot
Pheromones trigger filamentous growth in Ustilago maydis.
inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06722.xopenalex-snapshot
A chimeric homeodomain protein causes self‐compatibility and constitutive sexual development in the mushroom Coprinus cinereus.
inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb00211.xopenalex-snapshot
The mating‐type locus B alpha 1 of Schizophyllum commune contains a pheromone receptor gene and putative pheromone genes.
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00508.xopenalex-snapshot
The pheromone response factor coordinates filamentous growth and pathogenicity in Ustilago maydis.
inferredcites →https://doi.org/10.1002/j.1537-2197.1960.tb07167.xopenalex-snapshot
THE CONTROL OF SEX IN FUNGI
inferredcites →https://doi.org/10.1002/jobm.201000013openalex-snapshot
Mating‐type orthologous genes in the primarily homothallic Moniliophthora perniciosa, the causal agent of Witches' Broom Disease in cacao
inferredcites →https://doi.org/10.1007/978-3-319-25844-7_13openalex-snapshot
13 The Mating-Type Genes of the Basidiomycetes
inferredcites →https://doi.org/10.1007/978-3-319-29137-6_3openalex-snapshot
Future Perspectives and Challenges of Fungal Systematics in the Age of Big Data
inferredcites →https://doi.org/10.1007/978-3-642-19974-5_6openalex-snapshot
6 Mating Type in Basidiomycetes: Unipolar, Bipolar, and Tetrapolar Patterns of Sexuality
inferredcites →https://doi.org/10.1007/bf02174341openalex-snapshot
Identification of the pheromone response element inUstilago maydis
inferredcites →https://doi.org/10.1007/bf02318489openalex-snapshot
Mating type of isolates derived from the spermogonial state of Puccinia coronata var. coronata
inferredcites →https://doi.org/10.1007/s00294-005-0012-7openalex-snapshot
Identification and linkage mapping of the genes for the putative homeodomain protein (hox1) and the putative pheromone receptor protein homologue (rcb1) in a bipolar basidiomycete, Pholiota nameko
inferredcites →https://doi.org/10.1016/0006-291x(78)91505-xopenalex-snapshot
Structure of rhodotorucine A, a novel lipopeptide, inducing mating tube formation in Rhodosporidiumtoruloides
inferredcites →https://doi.org/10.1016/0092-8674(90)90744-yopenalex-snapshot
The b alleles of U. maydis, whose combinations program pathogenic development, code for polypeptides containing a homeodomain-related motif
inferredcites →https://doi.org/10.1016/0092-8674(92)90141-xopenalex-snapshot
A two-component regulatory system for self/non-self recognition in Ustilago maydis
inferredcites →https://doi.org/10.1016/0092-8674(92)90182-copenalex-snapshot
The a mating type locus of U. maydis specifies cell signaling components
inferredcites →https://doi.org/10.1016/0092-8674(95)90372-0openalex-snapshot
Multiallelic recognition: Nonself-dependent dimerization of the bE and bW homeodomain proteins in ustilago maydis
inferredcites →https://doi.org/10.1016/0168-6445(96)00003-4openalex-snapshot
Tetrapolar fungal mating types: Sexes by the thousands
inferredcites →https://doi.org/10.1016/0378-1119(91)90356-gopenalex-snapshot
The a mating-type alleles of Ustilago maydis are idiomorphs
inferredcites →https://doi.org/10.1016/b978-0-12-088642-5.50018-1openalex-snapshot
Repeat-Induced Point Mutation and DNA Methylation
inferredcites →https://doi.org/10.1016/b978-0-12-800271-1.00005-6openalex-snapshot
Unisexual Reproduction
inferredcites →https://doi.org/10.1016/j.fbr.2015.06.001openalex-snapshot
Contrasted patterns in mating-type chromosomes in fungi: Hotspots versus coldspots of recombination
inferredcites →https://doi.org/10.1016/j.fbr.2015.10.002openalex-snapshot
Why mushrooms have evolved to be so promiscuous: Insights from evolutionary and ecological patterns
inferredcites →https://doi.org/10.1016/j.fbr.2015.11.001openalex-snapshot
From two to many: Multiple mating types in Basidiomycetes
inferredcites →https://doi.org/10.1016/j.fgb.2003.08.009openalex-snapshot
Crossing the boundary between the Bα and Bβ mating-type loci in Schizophyllum commune
inferredcites →https://doi.org/10.1016/j.fgb.2015.02.009openalex-snapshot
Recognition of seven species in the Cryptococcus gattii/Cryptococcus neoformans species complex
inferredcites →https://doi.org/10.1016/j.fgb.2015.04.008openalex-snapshot
Unisexual reproduction in Huntiella moniliformis
inferredcites →https://doi.org/10.1016/j.gene.2013.11.036openalex-snapshot
The genetic structure of the A mating-type locus of Lentinula edodes
inferredcites →https://doi.org/10.1016/j.mib.2004.10.006openalex-snapshot
Regulation of mating and pathogenic development in Ustilago maydis
inferredcites →https://doi.org/10.1016/j.mycres.2007.03.004openalex-snapshot
A higher-level phylogenetic classification of the Fungi
inferredcites →https://doi.org/10.1016/j.mycres.2008.11.002openalex-snapshot
Genomic structure of the A mating-type locus in a bipolar basidiomycete, Pholiota nameko
inferredcites →https://doi.org/10.1016/j.phytochem.2014.11.019openalex-snapshot
Genome analysis of medicinal Ganoderma spp. with plant-pathogenic and saprotrophic life-styles
inferredcites →https://doi.org/10.1016/j.simyco.2015.10.004openalex-snapshot
Multigene phylogeny and taxonomic revision of yeasts and related fungi in the Ustilaginomycotina
inferredcites →https://doi.org/10.1016/s0007-1536(51)80061-5openalex-snapshot
A survey of heterothallism in the Ustilaginales
inferredcites →https://doi.org/10.1016/s0007-1536(85)80223-0openalex-snapshot
Modified bifactorial incompatibility in Tremella mesenterica
inferredcites →https://doi.org/10.1016/s0076-6879(10)70034-3openalex-snapshot
The Fungal Genome Initiative and Lessons Learned from Genome Sequencing
inferredcites →https://doi.org/10.1016/s0092-8674(00)81091-0openalex-snapshot
Self/Nonself Recognition in Fungi: Old Mysteries and Simple Solutions
inferredcites →https://doi.org/10.1016/s0092-8674(01)00609-2openalex-snapshot
Meiotic Silencing by Unpaired DNA
inferredcites →https://doi.org/10.1016/s0168-9525(00)02104-1openalex-snapshot
It takes two transposons to tango:transposable-element-mediated chromosomal rearrangements
inferredcites →https://doi.org/10.1016/s0953-7562(09)80107-xopenalex-snapshot
Fungal mating type genes — regulators of sexual development
inferredcites →https://doi.org/10.1017/s0016672300000112openalex-snapshot
Heterokaryon formation in Coprinus lagopus
inferredcites →https://doi.org/10.1017/s0016672300002457openalex-snapshot
Genetic studies of thebincompatability locus ofUstilago maydis
inferredcites →https://doi.org/10.1017/s0953756299001161openalex-snapshot
Phylogenetic placements of ustilaginomycetous anamorphs as deduced from nuclear LSU rDNA sequences
inferredcites →https://doi.org/10.1038/126686a0openalex-snapshot
The Biological Significance of Conjugate Nuclei in Coprinus lagopus and other Hymenomycetes*
inferredcites →https://doi.org/10.1038/262583a0openalex-snapshot
Communication through fimbriae during conjugation in a fungus
inferredcites →https://doi.org/10.1038/emboj.2009.68openalex-snapshot
A constitutively active GPCR governs morphogenic transitions in Cryptococcus neoformans
inferredcites →https://doi.org/10.1038/hdy.1994.38openalex-snapshot
The breeding biology of biotypes of the witches' broom pathogen of cocoa, Crinipellis perniciosa
inferredcites →https://doi.org/10.1038/hdy.2009.34openalex-snapshot
Silene as a model system in ecology and evolution
inferredcites →https://doi.org/10.1038/hdy.2013.67openalex-snapshot
Evolution of uni- and bifactorial sexual compatibility systems in fungi
inferredcites →https://doi.org/10.1038/hdy.2014.37openalex-snapshot
Inferring outcrossing in the homothallic fungus Sclerotinia sclerotiorum using linkage disequilibrium decay
inferredcites →https://doi.org/10.1038/hdy.2015.68openalex-snapshot
Variation in mate-recognition pheromones of the fungal genus Microbotryum
inferredcites →https://doi.org/10.1038/hdy.2016.5openalex-snapshot
The cacao pathogen Moniliophthora roreri (Marasmiaceae) possesses biallelic A and B mating loci but reproduces clonally
inferredcites →https://doi.org/10.1038/nature03448openalex-snapshot
Sexual reproduction between partners of the same mating type in Cryptococcus neoformans
inferredcites →https://doi.org/10.1038/nature05248openalex-snapshot
Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis
inferredcites →https://doi.org/10.1038/nature08252openalex-snapshot
Homothallic and heterothallic mating in the opportunistic pathogen Candida albicans
inferredcites →https://doi.org/10.1038/nature12754openalex-snapshot
Mechanism of farnesylated CAAX protein processing by the intramembrane protease Rce1
inferredcites →https://doi.org/10.1038/nbt.1643openalex-snapshot
Genome sequence of the model mushroom Schizophyllum commune
inferredcites →https://doi.org/10.1038/nbt967openalex-snapshot
Genome sequence of the lignocellulose degrading fungus Phanerochaete chrysosporium strain RP78
inferredcites →https://doi.org/10.1038/nrg3366openalex-snapshot
Y-chromosome evolution: emerging insights into processes of Y-chromosome degeneration
inferredcites →https://doi.org/10.1038/sj.hdy.6800554openalex-snapshot
Patterns of within population dispersal and mating of the fungus Microbotryum violaceum parasitising the plant Silene latifolia
inferredcites →https://doi.org/10.1046/j.1365-2540.2000.00748.xopenalex-snapshot
Intratetrad mating, heterozygosity, and the maintenance of deleterious alleles in Microbotryum violaceum (=Ustilago violacea)
inferredcites →https://doi.org/10.1073/pnas.0706756104openalex-snapshot
Dandruff-associated Malassezia genomes reveal convergent and divergent virulence traits shared with plant and human fungal pathogens
inferredcites →https://doi.org/10.1073/pnas.0809575106openalex-snapshot
Genome, transcriptome, and secretome analysis of wood decay fungus Postia placenta supports unique mechanisms of lignocellulose conversion
inferredcites →https://doi.org/10.1073/pnas.1003391107openalex-snapshot
Insights into evolution of multicellular fungi from the assembled chromosomes of the mushroom Coprinopsis cinerea ( Coprinus cinereus )
inferredcites →https://doi.org/10.1073/pnas.1017234108openalex-snapshot
Interspecies pheromone signaling promotes biofilm formation and same-sex mating in Candida albicans
inferredcites →https://doi.org/10.1073/pnas.1019315108openalex-snapshot
Obligate biotrophy features unraveled by the genomic analysis of rust fungi
inferredcites →https://doi.org/10.1073/pnas.46.6.833openalex-snapshot
THE GENETIC STRUCTURE OF THE INCOMPATIBILITY FACTORS OF SCHIZOPHYLLUM COMMUNE: THE A-FACTOR
inferredcites →https://doi.org/10.1073/pnas.86.3.978openalex-snapshot
Isolation of two alleles of the b locus of Ustilago maydis.
inferredcites →https://doi.org/10.1073/pnas.90.2.664openalex-snapshot
Construction of chimeric alleles with altered specificity at the b incompatibility locus of Ustilago maydis.
inferredcites →https://doi.org/10.1073/pnas.91.15.7085openalex-snapshot
Linkage of mating-type loci distinguishes bipolar from tetrapolar mating in basidiomycetous smut fungi.
inferredcites →https://doi.org/10.1073/pnas.96.26.15026openalex-snapshot
The mating-type and pathogenicity locus of the fungus Ustilago hordei spans a 500-kb region
inferredcites →https://doi.org/10.1080/00275514.1999.12061091openalex-snapshot
Pycnial Nectar of Rust Fungi Induces Cap Formation on Pycniospores of Opposite Mating Type
inferredcites →https://doi.org/10.1080/07352689009382294openalex-snapshot
Sex determination and sexual differentiation in filamentous fungi
inferredcites →https://doi.org/10.1080/10635150121079openalex-snapshot
Analysis of Character Correlations Among Wood Decay Mechanisms, Mating Systems, and Substrate Ranges in Homobasidiomycetes
inferredcites →https://doi.org/10.1086/430098openalex-snapshot
Selfing Propensity under Choice Conditions in a Parasitic Fungus, Microbotryum violaceum, and Parameters Influencing Infection Success in Artificial Inoculations
inferredcites →https://doi.org/10.1086/501507openalex-snapshot
Is It What We Know or Who We Know? Choice of Organism and Robustness of Inference in Ecology and Evolutionary Biology
inferredcites →https://doi.org/10.1091/mbc.e04-05-0370openalex-snapshot
PAK Kinases Ste20 and Pak1 Govern Cell Polarity at Different Stages of Mating inCryptococcus neoformans
inferredcites →https://doi.org/10.1093/bioinformatics/btp348openalex-snapshot
trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses
inferredcites →https://doi.org/10.1093/genetics/143.2.789openalex-snapshot
Pseudohomothallism and Evolution of the Mating-Type Chromosome in Neurospora tetrasperma
inferredcites →https://doi.org/10.1093/genetics/143.4.1601openalex-snapshot
The Pheromone Cell Signaling Components of the Ustilago a Mating-Type Loci Determine Intercompatibility Between Species
inferredcites →https://doi.org/10.1093/genetics/144.1.87openalex-snapshot
Multiple Versions of the A Mating Type Locus of Coprinus cinereus are Generated by Three Paralogous Pairs of Multiallelic Homeobox Genes
inferredcites →https://doi.org/10.1093/genetics/144.4.1471openalex-snapshot
Correlation of Genetic and Physical Maps at the A Mating-Type Locus of Coprinus cinereus
inferredcites →https://doi.org/10.1093/genetics/148.3.1081openalex-snapshot
A Large Pheromone and Receptor Gene Complex Determines Multiple B Mating Type Specificities in Coprinus cinereus
inferredcites →https://doi.org/10.1093/genetics/156.3.1025openalex-snapshot
Self-Compatible B Mutants in Coprinus With Altered Pheromone-Receptor Specificities
inferredcites →https://doi.org/10.1093/genetics/160.2.457openalex-snapshot
Dimorphic Mating-Type Chromosomes in the Fungus Microbotryum violaceum
inferredcites →https://doi.org/10.1093/genetics/45.5.641openalex-snapshot
THE STRUCTURE OF THE A MATING TYPE LOCUS IN COPRINUS LAGOPUS
inferredcites →https://doi.org/10.1093/genetics/80.2.311openalex-snapshot
PRIMARY HOMOTHALLISM—RELATION TO HETEROTHALLISM IN THE REGULATION OF SEXUAL MORPHOGENESIS IN SISTOTREMA
inferredcites →https://doi.org/10.1093/molbev/msq235openalex-snapshot
Maintenance of Fungal Pathogen Species That Are Specialized to Different Hosts: Allopatric Divergence and Introgression through Secondary Contact
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/msu300openalex-snapshot
IQ-TREE: A Fast and Effective Stochastic Algorithm for Estimating Maximum-Likelihood Phylogenies
inferredcites →https://doi.org/10.1093/molbev/msu396openalex-snapshot
Degeneration of the Nonrecombining Regions in the Mating-Type Chromosomes of the Anther-Smut Fungi
inferredcites →https://doi.org/10.1093/nar/gkt1183openalex-snapshot
MycoCosm portal: gearing up for 1000 fungal genomes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026187openalex-snapshot
The divergence-homogenization duality in the evolution of the b1 mating type gene of Coprinus cinereus
inferredcites →https://doi.org/10.1099/00221287-121-1-17openalex-snapshot
Dikaryon Formation in Coprinus cinereus: Selection and Identification of B Factor Mutants
inferredcites →https://doi.org/10.1101/gad.6.4.568openalex-snapshot
The combination of dissimilar alleles of the A alpha and A beta gene complexes, whose proteins contain homeo domain motifs, determines sexual development in the mushroom Coprinus cinereus.
inferredcites →https://doi.org/10.1105/tpc.112.097261openalex-snapshot
Genome Comparison of Barley and Maize Smut Fungi Reveals Targeted Loss of RNA Silencing Components and Species-Specific Presence of Transposable Elements
inferredcites →https://doi.org/10.1105/tpc.7.6.773openalex-snapshot
An N-Terminal Dimerization Domain Permits Homeodomain Proteins To Choose Compatible Partners and Initiate Sexual Development in the Mushroom Coprinus cinereus.
inferredcites →https://doi.org/10.1111/evo.12765openalex-snapshot
Breaking linkage between mating compatibility factors: Tetrapolarity in Microbotryum
inferredcites →https://doi.org/10.1111/j.0014-2956.1985.00489.xopenalex-snapshot
Biosynthesis and secretion of tremerogen A-10, a polysioprenyl peptide mating pheromone of Tremella mesenterica
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06345.xopenalex-snapshot
Pheromone‐regulated target genes respond differentially to MAPK phosphorylation of transcription factor Prf1
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06984.xopenalex-snapshot
The Ustilago maydis b mating type locus controls hyphal proliferation and expression of secreted virulence factors in planta
inferredcites →https://doi.org/10.1111/j.1420-9101.2012.02495.xopenalex-snapshot
Sex, outcrossing and mating types: unsolved questions in fungi and beyond
inferredcites →https://doi.org/10.1111/j.1469-185x.1949.tb00582.xopenalex-snapshot
HETEROTHALLISM and SEX IN THE FUNGI
inferredcites →https://doi.org/10.1111/j.1469-185x.2010.00153.xopenalex-snapshot
Having sex, yes, but with whom? Inferences from fungi on the evolution of anisogamy and mating types
inferredcites →https://doi.org/10.1111/j.1469-8137.1949.tb05120.xopenalex-snapshot
MULTIPLE‐ALLELOMORPH HETEROTHALLISM IN THE FUNGI
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01156.xopenalex-snapshot
Ustilago maydis: how its biology relates to pathogenic development
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02525.xopenalex-snapshot
Gene organization of the mating type regions in the ectomycorrhizal fungus Laccaria bicolor reveals distinct evolution between the two mating type loci
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04128.xopenalex-snapshot
Insight into trade‐off between wood decay and parasitism from the genome of a fungal forest pathogen
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00002.xopenalex-snapshot
PHYLOGENETIC EVIDENCE OF HOST-SPECIFIC CRYPTIC SPECIES IN THE ANTHER SMUT FUNGUS
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00144.xopenalex-snapshot
EVOLUTION OF REPRODUCTIVE ISOLATION WITHIN A PARASITIC FUNGAL SPECIES COMPLEX
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01562.xopenalex-snapshot
WHAT USES ARE MATING TYPES? THE “DEVELOPMENTAL SWITCH” MODEL
inferredcites →https://doi.org/10.1111/j.1567-1364.2008.00475.xopenalex-snapshot
Sexual reproduction and dimorphism in the pathogenic basidiomycetes
inferredcites →https://doi.org/10.1111/j.1574-6968.2008.01173.xopenalex-snapshot
Dimorphism in fungal plant pathogens
inferredcites →https://doi.org/10.1111/j.1574-6976.2008.00131.xopenalex-snapshot
Magnificent seven: roles of G protein-coupled receptors in extracellular sensing in fungi
inferredcites →https://doi.org/10.1111/jeb.12196openalex-snapshot
Deleterious effects of recombination and possible nonrecombinatorial advantages of sex in a fungal model
inferredcites →https://doi.org/10.1111/mec.12642openalex-snapshot
Global distribution, diversity hot spots and niche transitions of an astaxanthin‐producing eukaryotic microbe
inferredcites →https://doi.org/10.1126/science.1195330openalex-snapshot
Pathogenicity Determinants in Smut Fungi Revealed by Genome Comparison
inferredcites →https://doi.org/10.1126/science.209.4455.501openalex-snapshot
Multiple Mating-Type Specificities in the Flax Rust Melampsora lini
inferredcites →https://doi.org/10.1128/9781555815837.ch17openalex-snapshot
The Origin of Multiple Mating Types in the Model MushroomsCoprinopsis cinereaandSchizophyllum commune
inferredcites →https://doi.org/10.1128/9781555815837.ch19openalex-snapshot
Analysis of Mating-Type Locus Organization and Synteny in Mushroom Fungi: Beyond Model Species
inferredcites →https://doi.org/10.1128/9781555815837.ch3openalex-snapshot
Mechanisms of Homothallism in Fungi and Transitions between Heterothallism and Homothallism
inferredcites →https://doi.org/10.1128/9781555815837.ch32openalex-snapshot
Why Sex Is Good: On Fungi and Beyond
inferredcites →https://doi.org/10.1128/aem.72.4.2366-2372.2006openalex-snapshot
Evidence for Outcrossing via the Buller Phenomenon in a Substrate Simultaneously Inoculated with Spores and Mycelium of Agaricus bisporus
inferredcites →https://doi.org/10.1128/ec.00025-08openalex-snapshot
Identification of Mating Type Genes in the Bipolar Basidiomycetous Yeast Rhodosporidium toruloides : First Insight into the MAT Locus Structure of the Sporidiobolales
inferredcites →https://doi.org/10.1128/ec.00065-13openalex-snapshot
Molecular and Genetic Evidence for a Tetrapolar Mating System in the Basidiomycetous Yeast Kwoniella mangrovensis and Two Novel Sibling Species
inferredcites →https://doi.org/10.1128/ec.00212-10openalex-snapshot
A Single Mating-Type Locus Composed of Homeodomain Genes Promotes Nuclear Migration and Heterokaryosis in the White-Rot Fungus Phanerochaete chrysosporium
inferredcites →https://doi.org/10.1128/ec.00271-08openalex-snapshot
Transitions in Sexuality: Recapitulation of an Ancestral Tri- and Tetrapolar Mating System in Cryptococcus neoformans
inferredcites →https://doi.org/10.1128/ec.00319-09openalex-snapshot
Basidiomycete Mating Type Genes and Pheromone Signaling
inferredcites →https://doi.org/10.1128/ec.00440-07openalex-snapshot
Mating System of the Anther Smut Fungus Microbotryum violaceum : Selfing under Heterothallism
inferredcites →https://doi.org/10.1128/ec.3.1.180-189.2004openalex-snapshot
An ste20 Homologue in Ustilago maydis Plays a Role in Mating and Pathogenicity
inferredcites →https://doi.org/10.1128/ec.4.3.526-535.2005openalex-snapshot
Sex-Specific Homeodomain Proteins Sxi1α and Sxi2 a Coordinately Regulate Sexual Development in Cryptococcus neoformans
inferredcites →https://doi.org/10.1128/ec.4.8.1317-1327.2005openalex-snapshot
Mating Type Loci of Sporisorium reilianum : Novel Pattern with Three a and Multiple b Specificities
inferredcites →https://doi.org/10.1128/jb.122.2.710-718.1975openalex-snapshot
Morphological change in the early stages of the mating process of Rhodosporidium toruloides
inferredcites →https://doi.org/10.1128/mbio.00572-12openalex-snapshot
Genomic Insights into the Atopic Eczema-Associated Skin Commensal Yeast Malassezia sympodialis
inferredcites →https://doi.org/10.1128/mbio.00918-15openalex-snapshot
Genomics and Transcriptomics Analyses of the Oil-Accumulating Basidiomycete Yeast Trichosporon oleaginosus : Insights into Substrate Utilization and Alternative Evolutionary Trajectories of Fungal Mating Systems
inferredcites →https://doi.org/10.1128/mcb.13.3.1962-1970.1993openalex-snapshot
The α-Mating Type Locus of Cryptococcus neoformans Contains a Peptide Pheromone Gene
inferredcites →https://doi.org/10.1128/mcb.18.1.221openalex-snapshot
Dual Sets of Chimeric Alleles Identify Specificity Sequences for the bE and bW Mating and Pathogenicity Genes of Ustilago maydis
inferredcites →https://doi.org/10.1128/mcb.9.8.3491-3498.1989openalex-snapshot
Multiple Genes Coding for Precursors of Rhodotorucine A, a Farnesyl Peptide Mating Pheromone of the Basidiomycetous Yeast Rhodosporidium toruloides
inferredcites →https://doi.org/10.1128/microbiolspec.funk-0005-2016openalex-snapshot
Fungal Sex: The Ascomycota
inferredcites →https://doi.org/10.1128/mmbr.00005-10openalex-snapshot
The Evolution of Sex: a Perspective from the Fungal Kingdom
inferredcites →https://doi.org/10.1128/mmbr.00010-12openalex-snapshot
Biogenesis of the Saccharomyces cerevisiae Pheromone a -Factor, from Yeast Mating to Human Disease
inferredcites →https://doi.org/10.1128/mmbr.59.3.406-422.1995openalex-snapshot
Fungal lipopeptide mating pheromones: a model system for the study of protein prenylation
inferredcites →https://doi.org/10.1128/mmbr.62.1.55-70.1998openalex-snapshot
Molecular Genetics of Mating Recognition in Basidiomycete Fungi
inferredcites →https://doi.org/10.1128/mmbr.64.2.316-353.2000openalex-snapshot
Life History and Developmental Processes in the BasidiomyceteCoprinus cinereus
inferredcites →https://doi.org/10.1186/1471-2148-11-249openalex-snapshot
Evidence for maintenance of sex determinants but not of sexual stages in red yeasts, a group of early diverged basidiomycetes
inferredcites →https://doi.org/10.1186/1471-2164-15-996openalex-snapshot
Genome sequencing of Sporisorium scitamineum provides insights into the pathogenic mechanisms of sugarcane smut
inferredcites →https://doi.org/10.1186/1471-2180-14-50openalex-snapshot
Molecular characterization of KU70 and KU80 homologues and exploitation of a KU70-deficient mutant for improving gene deletion frequency in Rhodosporidium toruloides
inferredcites →https://doi.org/10.1186/s12864-015-2166-0openalex-snapshot
Genome-wide analysis of Fusarium graminearum field populations reveals hotspots of recombination
inferredcites →https://doi.org/10.1186/s12864-016-3244-7openalex-snapshot
Comparative genomics provides new insights into the diversity, physiology, and sexuality of the only industrially exploited tremellomycete: Phaffia rhodozyma
inferredcites →https://doi.org/10.1242/jcs.104.2.227openalex-snapshot
The origin of multiple mating types in mushrooms
inferredcites →https://doi.org/10.1271/bbb1961.42.1239openalex-snapshot
Isolation of rhodotorucine A, a peptidyl factor inducing the mating tube formation in Rhodospordium toruloides.
inferredcites →https://doi.org/10.1371/journal.pbio.1001653openalex-snapshot
Unisexual and Heterosexual Meiotic Reproduction Generate Aneuploidy and Phenotypic Diversity De Novo in the Yeast Cryptococcus neoformans
inferredcites →https://doi.org/10.1371/journal.pgen.0020184openalex-snapshot
Recombination Hotspots Flank the Cryptococcus Mating-Type Locus: Implications for the Evolution of a Fungal Sex Chromosome
inferredcites →https://doi.org/10.1371/journal.pgen.1000961openalex-snapshot
The Mating Type Locus (MAT) and Sexual Reproduction of Cryptococcus heveanensis: Insights into the Evolution of Sex and Sex-Determining Chromosomal Regions in Fungi
inferredcites →https://doi.org/10.1371/journal.pgen.1001052openalex-snapshot
A Deviation from the Bipolar-Tetrapolar Mating Paradigm in an Early Diverged Basidiomycete
inferredcites →https://doi.org/10.1371/journal.pgen.1002436openalex-snapshot
Interspecific Sex in Grass Smuts and the Genetic Diversity of Their Pheromone-Receptor System
inferredcites →https://doi.org/10.1371/journal.pgen.1002528openalex-snapshot
Discovery of a Modified Tetrapolar Sexual Cycle in Cryptococcus amylolentus and the Evolution of MAT in the Cryptococcus Species Complex
inferredcites →https://doi.org/10.1371/journal.pgen.1003587openalex-snapshot
Extensive Intra-Kingdom Horizontal Gene Transfer Converging on a Fungal Fructose Transporter Gene
inferredcites →https://doi.org/10.1371/journal.pgen.1004261openalex-snapshot
Analysis of the Genome and Transcriptome of Cryptococcus neoformans var. grubii Reveals Complex RNA Expression and Microevolution Leading to Virulence Attenuation
inferredcites →https://doi.org/10.1371/journal.pgen.1004849openalex-snapshot
Unisexual Reproduction Drives Meiotic Recombination and Phenotypic and Karyotypic Plasticity in Cryptococcus neoformans
inferredcites →https://doi.org/10.1371/journal.pgen.1005614openalex-snapshot
Genus-Wide Comparative Genomics of Malassezia Delineates Its Phylogeny, Physiology, and Niche Adaptation on Human Skin
inferredcites →https://doi.org/10.1371/journal.pgen.1006110openalex-snapshot
Genetic Dissection of Sexual Reproduction in a Primary Homothallic Basidiomycete
inferredcites →https://doi.org/10.1371/journal.pone.0005524openalex-snapshot
Chromosomal Rearrangements between Serotype A and D Strains in Cryptococcus neoformans
inferredcites →https://doi.org/10.1371/journal.pone.0022249openalex-snapshot
Comparative Genomics of the Mating-Type Loci of the Mushroom Flammulina velutipes Reveals Widespread Synteny and Recent Inversions
inferredcites →https://doi.org/10.1371/journal.pone.0120400openalex-snapshot
Multigene Assessment of the Species Boundaries and Sexual Status of the Basidiomycetous Yeasts Cryptococcus flavescens and C. terrestris (Tremellales)
inferredcites →https://doi.org/10.1371/journal.pone.0129318openalex-snapshot
Complete Genome Sequence of Sporisorium scitamineum and Biotrophic Interaction Transcriptome with Sugarcane
inferredcites →https://doi.org/10.1371/journal.pone.0147107openalex-snapshot
On the Evolutionary History of Uleiella chilensis, a Smut Fungus Parasite of Araucaria araucana in South America: Uleiellales ord. nov. in Ustilaginomycetes
inferredcites →https://doi.org/10.1534/g3.116.032797openalex-snapshot
Comparative Analysis Highlights Variable Genome Content of Wheat Rusts and Divergence of the Mating Loci
inferredcites →https://doi.org/10.1534/genetics.104.029900openalex-snapshot
Shared Forces of Sex Chromosome Evolution in Haploid-Mating and Diploid-Mating OrganismsSequence data from this article have been deposited with the EMBL/GenBank Data Libraries under the accession nos. BZ81929 and BZ782612.
inferredcites →https://doi.org/10.1534/genetics.105.040774openalex-snapshot
The Origin of Multiple B Mating Specificities in Coprinus cinereus
inferredcites →https://doi.org/10.1534/genetics.105.051128openalex-snapshot
Evolution of the Bipolar Mating System of the Mushroom Coprinellus disseminatus From Its Tetrapolar Ancestors Involves Loss of Mating-Type-Specific Pheromone Receptor Function
inferredcites →https://doi.org/10.1534/genetics.108.093708openalex-snapshot
Ancient Trans-specific Polymorphism at Pheromone Receptor Genes in Basidiomycetes
inferredcites →https://doi.org/10.1534/genetics.108.096859openalex-snapshot
Thea2Mating-Type Locus Geneslga2andrga2Direct Uniparental Mitochondrial DNA (mtDNA) Inheritance and Constrain mtDNA Recombination During Sexual Development ofUstilago maydis
inferredcites →https://doi.org/10.1534/genetics.112.146266openalex-snapshot
Extensive Divergence Between Mating-Type Chromosomes of the Anther-Smut Fungus
inferredcites →https://doi.org/10.1534/genetics.114.170472openalex-snapshot
Unisexual Reproduction Reverses Muller’s Ratchet
inferredcites →https://doi.org/10.1534/genetics.115.177709openalex-snapshot
Chaos of Rearrangements in the Mating-Type Chromosomes of the Anther-Smut Fungus Microbotryum lychnidis-dioicae
inferredcites →https://doi.org/10.1534/genetics.115.177717openalex-snapshot
Evolution of Mating Systems in Basidiomycetes and the Genetic Architecture Underlying Mating-Type Determination in the Yeast Leucosporidium scottii
inferredcites →https://doi.org/10.3852/12-253openalex-snapshot
Evolution of fungal sexual reproduction
inferredcites →https://doi.org/10.3852/13-162openalex-snapshot
Polyporales genomes reveal the genetic architecture underlying tetrapolar and bipolar mating systems
inferredcites →https://doi.org/10.3852/mycologia.98.6.896openalex-snapshot
An overview of the higher level classification of Pucciniomycotina based on combined analyses of nuclear large and small subunit rDNA sequences
inferredcites →https://doi.org/10.3852/mycologia.98.6.917openalex-snapshot
A phylogenetic overview of the Agaricomycotina
inferredcites →https://doi.org/10.5598/imafungus.2015.06.01.13openalex-snapshot
Homothallism: an umbrella term for describing diverse sexual behaviours
inferredcites →https://doi.org/10.5962/bhl.title.56861openalex-snapshot
Comparative morphology and biology of the fungi, mycetozoa and bacteria
inferredcites →https://doi.org/10.7554/elife.20522openalex-snapshot
A complete toolset for the study of Ustilago bromivora and Brachypodium sp. as a fungal-temperate grass pathosystem
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.621.1.1zenodo-depositor-declared
Checklist, typification details, and nomenclature status of Basidiomycota, originally described from Sri Lanka
inferred← citeshttps://doi.org/10.2139/ssrn.4457492openalex-extracted
Histone-2b-Egfp And-Mcherry Fusion Proteins Enables Visualization of Nuclear Behavior in the Basidiomycete Schizophyllum Commune Mating Interactions
inferred← citeshttps://doi.org/10.3897/imafungus.17.180524zenodo-depositor-declared
The saprotrophic dimension of Exobasidium (Exobasidiales, Basidiomycota): evidence for greater diversity and ecological flexibility than previously recognized
inferred← citeshttps://doi.org/10.5281/zenodo.5592783zenodo-depositor-declared
Contigs carrying mating orthologous genes in Austropuccinia psidii strains MF-1, Aus3 and PREM
inferred← citeshttps://doi.org/10.1002/1873-3468.13469openalex-snapshot
Protein‐facilitated transport of hydrophobic molecules across the yeast plasma membrane
inferred← citeshttps://doi.org/10.1007/978-3-030-41870-0_3openalex-snapshot
G-protein-coupled Receptors in Fungi
inferred← citeshttps://doi.org/10.1007/978-3-030-57246-4_7openalex-snapshot
Genome Evolution of Asexual Organisms and the Paradox of Sex in Eukaryotes
inferred← citeshttps://doi.org/10.1007/s00203-025-04605-8openalex-snapshot
Rhodotorula and Phaffia: pigment producing basidiomycetous yeasts for application in aquaculture practices
inferred← citeshttps://doi.org/10.1007/s00253-024-13220-4openalex-snapshot
Airlift bioreactor–based strategies for prolonged semi-continuous cultivation of edible Agaricomycetes
inferred← citeshttps://doi.org/10.1007/s00253-025-13579-yopenalex-snapshot
Burst agitation rate promotes sustained semicontinuous cultivation of filamentous fungi in stirred tank reactors
inferred← citeshttps://doi.org/10.1007/s00253-026-13839-5openalex-snapshot
Relief of bHD1 autoinhibition and modular coupling support MAT-A pathway activation in Flammulina filiformis
inferred← citeshttps://doi.org/10.1007/s11157-026-09785-3openalex-snapshot
Key denitrification microbial communities and their contributions to nitrous oxide emissions from paddy soil
inferred← citeshttps://doi.org/10.1007/s11427-023-2309-1openalex-snapshot
Atmospheric humidity regulates same-sex mating in Candida albicans through the trehalose and osmotic signaling pathways
inferred← citeshttps://doi.org/10.1007/s11557-023-01918-0openalex-snapshot
Resources and tools for studying convergent evolution in different lineages of smut fungi
inferred← citeshttps://doi.org/10.1007/s11557-026-02151-1openalex-snapshot
Genome-wide comparative analysis of structural features in fungal GATA transcription factors: insights from 796 fungal species
inferred← citeshttps://doi.org/10.1007/s42832-025-0364-5openalex-snapshot
Livestock-induced changes in soil properties and microbial dominance determine soil microbial diversity in a conifer forest
inferred← citeshttps://doi.org/10.1016/b978-0-12-818619-0.00003-4openalex-snapshot
Cryptococcus neoformans: life cycle, morphogenesis, and virulence
inferred← citeshttps://doi.org/10.1016/b978-0-12-818619-0.00034-4openalex-snapshot
Classification of medically important fungi
inferred← citeshttps://doi.org/10.1016/b978-0-12-819990-9.00048-2openalex-snapshot
Fossil Ascomycota and Basidiomycota, With Notes on Fossil Lichens and Nematophytes
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116603openalex-snapshot
Inhibition of respiration prompts commitment to unisexual reproduction in Cryptococcus deneoformans
inferred← citeshttps://doi.org/10.1016/j.cub.2023.08.039openalex-snapshot
Extending the reach of homology by using successive computational filters to find yeast pheromone genes
inferred← citeshttps://doi.org/10.1016/j.cub.2025.04.003openalex-snapshot
Patterns and mechanisms of fungal genome plasticity
inferred← citeshttps://doi.org/10.1016/j.fgb.2019.02.007openalex-snapshot
The smut fungus Ustilago esculenta has a bipolar mating system with three idiomorphs larger than 500 kb
inferred← citeshttps://doi.org/10.1016/j.fgb.2025.103990openalex-snapshot
Analysis of the genetic diversity of the soybean rust pathogen Phakopsora pachyrhizi reveals two major evolutionary lineages
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c07771openalex-snapshot
Identification, Validation, and Evidence of Frequent Exchange of HD Alleles in Puccinia striiformis Reveal High Genetic Diversity of Chinese Stripe Rust Population
inferred← citeshttps://doi.org/10.1038/s41467-022-35549-yopenalex-snapshot
Regulatory basis for reproductive flexibility in a meningitis-causing fungal pathogen
inferred← citeshttps://doi.org/10.1038/s41467-023-42317-zopenalex-snapshot
Invasive Californian death caps develop mushrooms unisexually and bisexually
inferred← citeshttps://doi.org/10.1038/s41467-025-60222-5openalex-snapshot
Repeated loss of function at HD mating-type genes and of recombination in anther-smut fungi
inferred← citeshttps://doi.org/10.1038/s41598-019-51477-2openalex-snapshot
Bioimaging structural signatures of the oomycete pathogen Sclerospora graminicola in pearl millet using different microscopic techniques
inferred← citeshttps://doi.org/10.1038/s42003-021-01724-yopenalex-snapshot
Evolutionary and genomic comparisons of hybrid uninucleate and nonhybrid Rhizoctonia fungi
inferred← citeshttps://doi.org/10.1039/9781837672097openalex-snapshot
Phytochemistry and Nutritional Composition of Significant Wild Medicinal and Edible Mushrooms
inferred← citeshttps://doi.org/10.1039/bk9781837672097-00001openalex-snapshot
An Overview on Mushrooms
inferred← citeshttps://doi.org/10.1053/j.jepm.2022.05.002openalex-snapshot
Comparison of ear canal microbiome in rabbits with and without otitis externa using next generation DNA sequencing
inferred← citeshttps://doi.org/10.1073/pnas.1701658114openalex-snapshot
Evolutionary strata on young mating-type chromosomes despite the lack of sexual antagonism
inferred← citeshttps://doi.org/10.1073/pnas.2219120120openalex-snapshot
On the evolution of variation in sexual reproduction through the prism of eukaryotic microbes
inferred← citeshttps://doi.org/10.1073/pnas.2305094120openalex-snapshot
Frequent transitions in mating-type locus chromosomal organization in Malassezia and early steps in sexual reproduction
inferred← citeshttps://doi.org/10.1080/21501203.2022.2103194openalex-snapshot
Fungal taxonomy: current status and research agendas for the interdisciplinary and globalisation era
inferred← citeshttps://doi.org/10.1093/evolut/qpad076openalex-snapshot
Self-compatibility in yeast is selected for reproductive assurance not population-level compatibility
inferred← citeshttps://doi.org/10.1093/g3journal/jkaa012openalex-snapshot
The master regulator MAT1-1-1 of fungal mating binds to its targets via a conserved motif in the human pathogen Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1093/g3journal/jkab398openalex-snapshot
Draft genome sequences of strains CBS6241 and CBS6242 of the basidiomycetous yeastFilobasidium floriforme
inferred← citeshttps://doi.org/10.1093/g3journal/jkab448openalex-snapshot
Comparative transcriptome analysis of genes and metabolic pathways involved in sporulation in Ganoderma lingzhi
inferred← citeshttps://doi.org/10.1093/g3journal/jkaf069openalex-snapshot
A haplotype-resolved chromosomal reference genome for the porcini mushroom Boletus edulis
inferred← citeshttps://doi.org/10.1093/g3journal/jkaf255openalex-snapshot
Host adaptation and genome evolution of the broad host range fungal rust pathogen, Austropuccinia psidii
inferred← citeshttps://doi.org/10.1093/gbe/evaa028openalex-snapshot
Differential Gene Expression between Fungal Mating Types Is Associated with Sequence Degeneration
inferred← citeshttps://doi.org/10.1093/genetics/iyad069openalex-snapshot
Genomic determination of breeding systems and trans-specific evolution of HD MAT genes in suilloid fungi
inferred← citeshttps://doi.org/10.1093/icb/icad037openalex-snapshot
Sex Without Sexes: Can the Cost of Finding a Mate Explain Diversity in Fungal Mating Systems?
inferred← citeshttps://doi.org/10.1093/icb/icag138openalex-snapshot
The Rewiring of Who Mates with Whom: Evolutionary Transitions of Mating Systems, Mating Classes and Their Genetic Architecture
inferred← citeshttps://doi.org/10.1093/molbev/msac060openalex-snapshot
Tempo of Degeneration Across Independently Evolved Nonrecombining Regions
inferred← citeshttps://doi.org/10.1093/molbev/msz252openalex-snapshot
Higher Gene Flow in Sex-Related Chromosomes than in Autosomes during Fungal Divergence
inferred← citeshttps://doi.org/10.1094/mpmi-08-25-0111-ropenalex-snapshot
Haplotype-Resolved Genomes of Diverse Oat Crown Rust Isolates Reveal Global Dispersion of Long-Lived Clonal Haplotypes with Limited Recombination
inferred← citeshttps://doi.org/10.1094/mpmi-10-24-0122-fiopenalex-snapshot
Beyond Asexual: Genomics-Driven Progress in Unveiling Sexual Reproduction in Cereal Rust Fungi
inferred← citeshttps://doi.org/10.1094/pdis-04-24-0873-reopenalex-snapshot
Genetic Diversity of Moniliophthora roreri from Cacao Trees Growing in the Soconusco Area, Chiapas, Mexico
inferred← citeshttps://doi.org/10.1094/pdis-10-24-2111-sropenalex-snapshot
Eight Novel Diagnostic Markers Differentiate Lineages of the Highly Invasive Myrtle Rust Pathogen Austropuccinia psidii
inferred← citeshttps://doi.org/10.1101/2023.01.09.523226openalex-snapshot
Comparative genomics of smut fungi suggest the ability of meiosis and mating in asexual species of the genus Pseudozyma (Ustilaginales)
inferred← citeshttps://doi.org/10.1101/2024.02.19.580897openalex-snapshot
Mating-compatibility genes employed as diagnostic markers to identify novel incursions of the myrtle rust pathogen Austropuccinia psidii
inferred← citeshttps://doi.org/10.1101/2024.03.27.583983openalex-snapshot
A high-resolution haplotype pangenome uncovers somatic hybridization, recombination and intercontinental migration in oat crown rust
inferred← citeshttps://doi.org/10.1101/2024.10.03.616435openalex-snapshot
The genetic diversity of the soybean rust pathogen Phakopsora pachyrhizi has been driven by two major evolutionary lineages
inferred← citeshttps://doi.org/10.1101/2025.05.06.652357openalex-snapshot
Development, validation, and evidence of frequent exchange of mating type HD alleles of Puccinia striiformis f. sp. tritici provide an insight into highly genetic diversity
inferred← citeshttps://doi.org/10.1101/2025.09.01.673225openalex-snapshot
Mating-Type Imputation (MTI) provides an efficient tool for the mating-type inference of tetrapolar fungi
inferred← citeshttps://doi.org/10.1101/777102openalex-snapshot
Mating-type specific ribosomal proteins control aspects of sexual reproduction in Cryptococcus neoformans
inferred← citeshttps://doi.org/10.1101/gr.242578.118openalex-snapshot
Convergent recombination cessation between mating-type genes and centromeres in selfing anther-smut fungi
inferred← citeshttps://doi.org/10.1101/gr.262188.120openalex-snapshot
Corrigendum: Convergent recombination cessation between mating-type genes and centromeres in selfing anther-smut fungi
inferred← citeshttps://doi.org/10.1111/ele.14275openalex-snapshot
Temperature affects the timing and duration of fungal fruiting patterns across major terrestrial biomes
inferred← citeshttps://doi.org/10.1111/jeb.13991openalex-snapshot
Onset and stepwise extensions of recombination suppression are common in mating‐type chromosomes of Microbotryum anther‐smut fungi
inferred← citeshttps://doi.org/10.1111/mpp.70082openalex-snapshot
Genomics Research on the Road of Studying Biology and Virulence of Cereal Rust Fungi
inferred← citeshttps://doi.org/10.1111/nph.17039openalex-snapshot
Recombination suppression and evolutionary strata around mating‐type loci in fungi: documenting patterns and understanding evolutionary and mechanistic causes
inferred← citeshttps://doi.org/10.1111/nph.70395openalex-snapshot
Genetic variation among progeny shapes symbiosis in a basidiomycete with poplar
inferred← citeshttps://doi.org/10.1111/nph.71381openalex-snapshot
Global population structures and demographic history of Suillus luteus , a pine co‐introduced ectomycorrhizal fungus associated with exotic forestry and invasion
inferred← citeshttps://doi.org/10.1128/mbio.00059-26openalex-snapshot
Dissecting the homeodomain MAT locus and engineering novel tripolar and bipolar mating systems in Cryptococcus amylolentus
inferred← citeshttps://doi.org/10.1128/mbio.00764-19openalex-snapshot
Genetic and Genomic Analyses Reveal Boundaries between Species Closely Related to Cryptococcus Pathogens
inferred← citeshttps://doi.org/10.1128/mbio.03130-20openalex-snapshot
Multiple Pathways to Homothallism in Closely Related Yeast Lineages in the Basidiomycota
inferred← citeshttps://doi.org/10.1128/mmbr.00009-21openalex-snapshot
Pneumocystis Mating-Type Locus and Sexual Cycle during Infection
inferred← citeshttps://doi.org/10.1128/mmbr.00019-21openalex-snapshot
Evolutionary Morphogenesis of Sexual Fruiting Bodies in Basidiomycota: Toward a New Evo-Devo Synthesis
inferred← citeshttps://doi.org/10.1128/mmbr.00104-22openalex-snapshot
The Role of Chromatin and Transcriptional Control in the Formation of Sexual Fruiting Bodies in Fungi
inferred← citeshttps://doi.org/10.1128/mmbr.00165-21openalex-snapshot
Chemotropism and Cell-Cell Fusion in Fungi
inferred← citeshttps://doi.org/10.1146/annurev-genet-120116-024755openalex-snapshot
The Evolution of Sexual Reproduction and the Mating-Type Locus: Links to Pathogenesis of Cryptococcus Human Pathogenic Fungi
inferred← citeshttps://doi.org/10.1146/annurev-micro-060321-045510openalex-snapshot
Quorum Sensing in Fungal Species
inferred← citeshttps://doi.org/10.1146/annurev-phyto-082718-095947openalex-snapshot
Understanding Adaptation, Coevolution, Host Specialization, and Mating System in Castrating Anther-Smut Fungi by Combining Population and Comparative Genomics
inferred← citeshttps://doi.org/10.11606/d.97.2023.tde-19072023-125611openalex-snapshot
Aumento de escala na produção de lacase por Trametes versicolor utilizando biorreator de baixo cisalhamento
inferred← citeshttps://doi.org/10.1186/s12864-023-09210-xopenalex-snapshot
A genetic linkage map and improved genome assembly of the termite symbiont Termitomyces cryptogamus
inferred← citeshttps://doi.org/10.1186/s12864-023-09387-1openalex-snapshot
Comparative genomics of smut fungi suggest the ability of meiosis and mating in asexual species of the genus Pseudozyma (Ustilaginales)
inferred← citeshttps://doi.org/10.1186/s12864-025-11905-2openalex-snapshot
Proteome study of dikaryotic and monokaryotic mycelia reveals the transfer between biological processes contributing to dikaryon growth advantage of the medicinal fungus Ganoderma lucidum
inferred← citeshttps://doi.org/10.1186/s12915-023-01717-9openalex-snapshot
Uncovering the history of recombination and population structure in western Canadian stripe rust populations through mating type alleles
inferred← citeshttps://doi.org/10.12688/f1000research.134814.1openalex-snapshot
Amanita thiersii and Amanita foetens are closely related but genetically and geographically distinct species, leaving the origins of A. thiersii and its range expansion enigmatic
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002682openalex-snapshot
Comparative genomics of the closely related fungal genera Cryptococcus and Kwoniella reveals karyotype dynamics and suggests evolutionary mechanisms of pathogenesis
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003417openalex-snapshot
The complex evolution and genomic dynamics of mating-type loci in Cryptococcus and Kwoniella
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007377openalex-snapshot
A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008365openalex-snapshot
Convergent evolution of linked mating-type loci in basidiomycete fungi
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010097openalex-snapshot
Large-scale fungal strain sequencing unravels the molecular diversity in mating loci maintained by long-term balancing selection
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010347openalex-snapshot
Stepwise recombination suppression around the mating-type locus in an ascomycete fungus with self-fertile spores
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011207openalex-snapshot
Genome biology and evolution of mating-type loci in four cereal rust fungi
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011493openalex-snapshot
A high-resolution haplotype collection uncovers somatic hybridization, recombination and intercontinental movement in oat crown rust
inferred← citeshttps://doi.org/10.1534/genetics.119.302740openalex-snapshot
Mating-Type-Specific Ribosomal Proteins Control Aspects of Sexual Reproduction in Cryptococcus neoformans
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8904859/v1openalex-snapshot
Assessment of characteristic orthologs in Ascomycota and Basidiomycota and their implications for fungal taxonomy
inferred← citeshttps://doi.org/10.2139/ssrn.5252493openalex-snapshot
Comprehensive Genome-Wide Analyses and Functional Validation of C22 Desaturases and C24 Methyltransferases for the Regulatory Dynamics between Steroidal Saponins and Brassinosteroids in Three Asparagus L. Species
inferred← citeshttps://doi.org/10.21577/1984-6835.20200082openalex-snapshot
Chemical Composition and Biological Potential of Mycelium Extract from Basidiomicete Tyromyces pulcherrimus (Rodway) G. Cunn. Cultivated in Liquid Medium
inferred← citeshttps://doi.org/10.3389/fcimb.2023.1325418openalex-snapshot
First genome assembly and annotation of Sanghuangporus weigelae uncovers its medicinal functions, metabolic pathways, and evolution
inferred← citeshttps://doi.org/10.3389/fmicb.2019.02019openalex-snapshot
Population Genomics of an Obligately Halophilic Basidiomycete Wallemia ichthyophaga
inferred← citeshttps://doi.org/10.3389/fmicb.2026.1669303openalex-snapshot
Chromosome-scale genome assembly of Naematelia sinensis (Jin Er mushroom) offers new insights into the distinct mating-type genomes feature and genome evolution
inferred← citeshttps://doi.org/10.3390/ijms27010509openalex-snapshot
Hybrid Genome Assembly and Annotation of the Basidiomycete Fungus Candolleomyces candolleanus Strain CMU-8613 Using a Cost-Effective Iterative Pipeline
inferred← citeshttps://doi.org/10.3390/jof11040277openalex-snapshot
Evidence for the Existence of Mating Subtypes Within the Schizophyllum commune: Mating Behavior and Genetic Divergence
inferred← citeshttps://doi.org/10.3390/jof11080551openalex-snapshot
High Carbon Dioxide Concentration Inhibits Pileus Growth of Flammulina velutipes by Downregulating Cyclin Gene Expression
inferred← citeshttps://doi.org/10.3390/jof12040287openalex-snapshot
Mating-Type Imputation (MTI) Provides an Efficient Tool for the Mating-Type Inference of Tetrapolar Fungi
inferred← citeshttps://doi.org/10.3390/jof4030088openalex-snapshot
Cryptococcal Traits Mediating Adherence to Biotic and Abiotic Surfaces
inferred← citeshttps://doi.org/10.3390/jof7050399openalex-snapshot
What Role Might Non-Mating Receptors Play in Schizophyllum commune?
inferred← citeshttps://doi.org/10.3390/jof7100787openalex-snapshot
The First Whole Genome Sequencing of Sanghuangporus sanghuang Provides Insights into Its Medicinal Application and Evolution
inferred← citeshttps://doi.org/10.3390/jof8020167openalex-snapshot
Haplotype-Resolved Genome Analyses Reveal Genetically Distinct Nuclei within a Commercial Cultivar of Lentinula edodes
inferred← citeshttps://doi.org/10.3390/jof9111043openalex-snapshot
Nuclear-Localized Fluorescent Proteins Enable Visualization of Nuclear Behavior in the Basidiomycete Schizophyllum commune Early Mating Interactions
inferred← citeshttps://doi.org/10.3390/life10060089openalex-snapshot
Mass Spectrometry: A Rosetta Stone to Learn How Fungi Interact and Talk
inferred← citeshttps://doi.org/10.3390/microorganisms8111651openalex-snapshot
The Untapped Australasian Diversity of Astaxanthin-Producing Yeasts with Biotechnological Potential—Phaffia australis sp. nov. and Phaffia tasmanica sp. nov.
inferred← citeshttps://doi.org/10.3897/bdj.11.e101950openalex-snapshot
First insights into diversity and potential metabolic pathways of bacterial and fungal communities in the rhizosphere of Argemone mexicana L. (Papaveraceae) from the water-level-fluctuation zone of Wudongde Reservoir of the upper Yangtze river, China
inferred← citeshttps://doi.org/10.4103/ijmy.ijmy_167_18openalex-snapshot
Antimicrobial properties of basidiomycota macrofungi to Mycobacterium abscessus isolated from patients with cystic fibrosis
inferred← citeshttps://doi.org/10.47371/mycosci.2020.11.008openalex-snapshot
Identification, characterization and expression of A-mating type genes in monokaryons and dikaryons of the edible mushroom Mycoleptodonoides aitchisonii (Bunaharitake)
inferred← citeshttps://doi.org/10.5194/bg-22-8047-2025openalex-snapshot
Transporter gene family evolution in ectomycorrhizal fungi in relation to mineral weathering capabilities
inferred← citeshttps://doi.org/10.54612/a.39o6ovnn6mopenalex-snapshot
Insights into genomics and gene expression of oleaginous yeasts of the genus Rhodoturula
inferred← citeshttps://doi.org/10.6084/m9.figshare.26632006openalex-snapshot
Additional file 1 of Uncovering the history of recombination and population structure in western Canadian stripe rust populations through mating type alleles
inferred← citeshttps://doi.org/10.6084/m9.figshare.26632009openalex-snapshot
Additional file 2 of Uncovering the history of recombination and population structure in western Canadian stripe rust populations through mating type alleles
inferred← citeshttps://doi.org/10.6084/m9.figshare.26632012openalex-snapshot
Additional file 3 of Uncovering the history of recombination and population structure in western Canadian stripe rust populations through mating type alleles
inferred← citeshttps://doi.org/10.6084/m9.figshare.26632015openalex-snapshot
Additional file 4 of Uncovering the history of recombination and population structure in western Canadian stripe rust populations through mating type alleles
inferred← citeshttps://doi.org/10.6084/m9.figshare.26632018openalex-snapshot
Additional file 5 of Uncovering the history of recombination and population structure in western Canadian stripe rust populations through mating type alleles
inferred← citeshttps://doi.org/10.70675/7668b44az0a0ez46d3z8ee7zb60c6c38f267openalex-snapshot
The evolution of non-recombining regions of mating-type chromosomes and transposable element dynamics in fungi
inferred← citeshttps://doi.org/10.70675/9bc6c219z0f18z4e80z83a4z42db089a597eopenalex-snapshot
Modélisation de la fermentation en milieu solide
inferred← citeshttps://doi.org/10.70675/d444c892zebb3z4f09zb27czb6ca28a76bc0openalex-snapshot
Evolution of non-recombining region in mating-type chromosome from the fungal genus Microbotryum
inferred← citeshttps://doi.org/10.7554/elife.79114openalex-snapshot
Obligate sexual reproduction of a homothallic fungus closely related to the Cryptococcus pathogenic species complex
inferred← citeshttps://doi.org/10.7717/peerj.14988openalex-snapshot
Community differentiation of rhizosphere microorganisms and their responses to environmental factors at different development stages of medicinal plant Glehnia littoralis
inferred← citeshttps://doi.org/10.7717/peerj.6292openalex-snapshot
A second HD mating type sublocus of Flammulina velutipes is at least di-allelic and active: new primers for identification of HD-a and HD-b subloci
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.