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Major proliferation of transposable elements shaped the genome of the soybean rust pathogen Phakopsora pachyrhizi.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37551-4
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Identification, evolution and functional characterization of two Zn CDF-family transporters of the ectomycorrhizal fungus Suillus luteus.
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- Environmental Microbiology Reports, 2017, v. 9, n. 4, p. 419, doi. 10.1111/1758-2229.12551
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- Article
Tracking a refined eIF4E-binding motif reveals Angel1 as a new partner of eIF4E.
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- Nucleic Acids Research, 2013, v. 41, n. 16, p. 7783, doi. 10.1093/nar/gkt569
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Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists.
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- Nature Genetics, 2015, v. 47, n. 4, p. 410, doi. 10.1038/ng.3223
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Functional Assays and Metagenomic Analyses Reveals Differences between the Microbial Communities Inhabiting the Soil Horizons of a Norway Spruce Plantation.
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- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0055929
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- Article
RNA-Seq of Early-Infected Poplar Leaves by the Rust Pathogen Melampsora larici-populina Uncovers PtSultr3;5, a Fungal-Induced Host Sulfate Transporter.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0044408
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Characterization of Transposable Elements in the Ectomycorrhizal Fungus Laccaria bicolor.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0040197
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The transcriptional landscape of basidiosporogenesis in mature Pisolithus microcarpus basidiocarp.
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-3545-5
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- Article
Speciation Underpinned by Unexpected Molecular Diversity in the Mycorrhizal Fungal Genus Pisolithus.
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- Molecular Biology & Evolution, 2023, v. 40, n. 3, p. 1, doi. 10.1093/molbev/msad045
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Périgord black truffle genome uncovers evolutionary origins and mechanisms of symbiosis.
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- Nature, 2010, v. 464, n. 7291, p. 1033, doi. 10.1038/nature08867
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Fungal ecological strategies reflected in gene transcription ‐ a case study of two litter decomposers.
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- Environmental Microbiology, 2020, v. 22, n. 3, p. 1089, doi. 10.1111/1462-2920.14873
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- Article
At the nexus of three kingdoms: the genome of the mycorrhizal fungus Gigaspora margarita provides insights into plant, endobacterial and fungal interactions.
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- Environmental Microbiology, 2020, v. 22, n. 1, p. 122, doi. 10.1111/1462-2920.14827
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- Article
Multi‐omic analyses of exogenous nutrient bag decomposition by the black morel Morchella importuna reveal sustained carbon acquisition and transferring.
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- Environmental Microbiology, 2019, v. 21, n. 10, p. 3909, doi. 10.1111/1462-2920.14741
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- Article
Ectomycorrhizal ecology is imprinted in the genome of the dominant symbiotic fungus Cenococcum geophilum.
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- Nature Communications, 2016, v. 7, n. 9, p. 12662, doi. 10.1038/ncomms12662
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- Article
Intraspecific comparative genomics of isolates of the Norway spruce pathogen (<italic>Heterobasidion parviporum</italic>) and identification of its potential virulence factors.
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- BMC Genomics, 2018, v. 19, p. 1, doi. 10.1186/s12864-018-4610-4
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Survey and analysis of simple sequence repeats in the Laccaria bicolor genome, with development of microsatellite markers.
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- Current Genetics, 2011, v. 57, n. 2, p. 75, doi. 10.1007/s00294-010-0328-9
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- Article
Fungal communities mediate but do not control leaf litter chemical transformation in a temperate oak forest.
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- Plant & Soil, 2023, v. 489, n. 1/2, p. 573, doi. 10.1007/s11104-023-06040-4
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- Article
Functional genomics gives new insights into the ectomycorrhizal degradation of chitin.
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- New Phytologist, 2023, v. 238, n. 2, p. 845, doi. 10.1111/nph.18773
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Evolutionary transition to the ectomycorrhizal habit in the genomes of a hyperdiverse lineage of mushroom‐forming fungi.
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- New Phytologist, 2022, v. 233, n. 5, p. 2294, doi. 10.1111/nph.17892
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Evolutionary innovations through gain and loss of genes in the ectomycorrhizal Boletales.
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- New Phytologist, 2022, v. 233, n. 3, p. 1383, doi. 10.1111/nph.17858
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Desert truffle genomes reveal their reproductive modes and new insights into plant–fungal interaction and ectendomycorrhizal lifestyle.
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- New Phytologist, 2021, v. 229, n. 5, p. 2917, doi. 10.1111/nph.17044
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Comparative genomics of Rhizophagus irregularis, R. cerebriforme, R. diaphanus and Gigaspora rosea highlights specific genetic features in Glomeromycotina.
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- New Phytologist, 2019, v. 222, n. 3, p. 1584, doi. 10.1111/nph.15687
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The Hydrophobin-Like OmSSP1 May Be an Effector in the Ericoid Mycorrhizal Symbiosis.
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- Frontiers in Plant Science, 2018, p. 1, doi. 10.3389/fpls.2018.00546
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- Article
Secretome Analysis from the Ectomycorrhizal Ascomycete Cenococcum geophilum.
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- Frontiers in Microbiology, 2018, p. 1, doi. 10.3389/fmicb.2018.00141
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- Article
The SlZRT1 Gene Encodes a Plasma Membrane-Located ZIP (Zrt-, Irt-Like Protein) Transporter in the Ectomycorrhizal Fungus Suillus luteus.
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- Frontiers in Microbiology, 2017, p. 1, doi. 10.3389/fmicb.2017.02320
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Isolation of Intact and Functional Melanosomes from the Retinal Pigment Epithelium.
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- PLoS ONE, 2016, v. 11, n. 8, p. 1, doi. 10.1371/journal.pone.0160352
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- Article
The Ectomycorrhizal Fungus Laccaria bicolor Stimulates Lateral Root Formation in Poplar and Arabidopsis through Auxin Transport and Signaling.
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- Plant Physiology, 2009, v. 151, n. 4, p. 1991, doi. 10.1104/pp.109.147231
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- Article
Comparative transcriptomics of Gymnosporangium spp. teliospores reveals a conserved genetic program at this specific stage of the rust fungal life cycle.
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- BMC Genomics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12864-019-6099-x
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Phylogenomics and Comparative Genomics Highlight Specific Genetic Features in Ganoderma Species.
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- Journal of Fungi, 2022, v. 8, n. 3, p. 311, doi. 10.3390/jof8030311
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- Article
High intraspecific genome diversity in the model arbuscular mycorrhizal symbiont Rhizophagus irregularis.
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- New Phytologist, 2018, v. 220, n. 4, p. 1161, doi. 10.1111/nph.14989
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Comparative genomics and transcriptomics depict ericoid mycorrhizal fungi as versatile saprotrophs and plant mutualists.
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- New Phytologist, 2018, v. 217, n. 3, p. 1213, doi. 10.1111/nph.14974
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- Article
Comparative genomics, proteomics and transcriptomics give new insight into the exoproteome of the basidiomycete Hebeloma cylindrosporum and its involvement in ectomycorrhizal symbiosis.
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- New Phytologist, 2015, v. 208, n. 4, p. 1169, doi. 10.1111/nph.13546
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Genome-wide search and functional identification of transcription factors in the mycorrhizal fungus Tuber melanosporum.
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- New Phytologist, 2011, v. 189, n. 3, p. 736, doi. 10.1111/j.1469-8137.2010.03525.x
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Comparative Analysis of Secretomes from Ectomycorrhizal Fungi with an Emphasis on Small-Secreted Proteins.
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- Frontiers in Microbiology, 2015, v. 6, p. 1, doi. 10.3389/fmicb.2015.01278
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A survey of genome-wide single nucleotide polymorphisms through genome resequencing in the Périgord black truffle ( Tuber melanosporum Vittad.).
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- Molecular Ecology Resources, 2015, v. 15, n. 5, p. 1243, doi. 10.1111/1755-0998.12391
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- Article
Patterns of genomic variation in the poplar rust fungus Melampsora larici-populina identify pathogenesis-related factors.
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- Frontiers in Plant Science, 2014, v. 5, p. 1, doi. 10.3389/fpls.2014.00450
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Overview of the functional virulent genome of the coffee leaf rust pathogen Hemileia vastatrix with an emphasis on early stages of infection.
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- Frontiers in Plant Science, 2014, v. 5, p. 1, doi. 10.3389/fpls.2014.00088
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- Article
Modulation of Plant and Fungal Gene Expression Upon Cd Exposure and Symbiosis in Ericoid Mycorrhizal Vaccinium myrtillus.
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- Frontiers in Microbiology, 2020, p. 1, doi. 10.3389/fmicb.2020.00341
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- Article
The mineral weathering ability of Collimonas pratensis PMB3(1) involves a Malleobactin‐mediated iron acquisition system.
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- Environmental Microbiology, 2022, v. 24, n. 2, p. 784, doi. 10.1111/1462-2920.15508
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- Article
Gene family expansions and transcriptome signatures uncover fungal adaptations to wood decay.
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- Environmental Microbiology, 2021, v. 23, n. 10, p. 5716, doi. 10.1111/1462-2920.15423
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Large-scale genome sequencing of mycorrhizal fungi provides insights into the early evolution of symbiotic traits.
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- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18795-w
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- Article