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Isolation and characterization of novel cDNA clones of acidic chitinases and β-1,3-glucanases from wheat spikes infected by Fusarium graminearum
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4899-6561-5_4openalex-snapshot
Nullisomic-Tetrasomic Combinations in Hexaploid Wheat
inferredcites →https://doi.org/10.1007/978-3-7091-6684-0_10openalex-snapshot
The Primary Structure of Plant Pathogenesis-related Glucanohydrolases and Their Genes
inferredcites →https://doi.org/10.1007/bf00014941openalex-snapshot
Structure and expression of a barley acidic ?-glucanase gene
inferredcites →https://doi.org/10.1007/bf00023999openalex-snapshot
Nucleotide sequence of a rice genomic clone that encodes a class I endochitinase
inferredcites →https://doi.org/10.1007/bf00221889openalex-snapshot
Seven members of the (1→3)-β-glucanase gene family in barley (Hordeum vulgare) are clustered on the long arm of chromosome 3 (3HL)
inferredcites →https://doi.org/10.1007/s001220051062openalex-snapshot
Genomic mapping of defense response genes in wheat
inferredcites →https://doi.org/10.1007/s001220051204openalex-snapshot
A high-density genetic linkage map of Aegilops tauschii, the D-genome progenitor of bread wheat
inferredcites →https://doi.org/10.1016/0888-7543(87)90010-3openalex-snapshot
MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations
inferredcites →https://doi.org/10.1016/s0021-9258(19)50474-4openalex-snapshot
Antifungal proteins from plants. Purification, molecular cloning, and antifungal properties of chitinases from maize seed.
inferredcites →https://doi.org/10.1016/s0021-9258(19)50609-3openalex-snapshot
Identification of an essential tyrosine residue in the catalytic site of a chitinase isolated from Zea mays that is selectively modified during inactivation with 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide.
inferredcites →https://doi.org/10.1093/genetics/154.2.823openalex-snapshot
Saturation Mapping of a Gene-Rich Recombination Hot Spot Region in Wheat
inferredcites →https://doi.org/10.1094/mpmi.2000.13.2.159openalex-snapshot
Fungal Development and Induction of Defense Response Genes During Early Infection of Wheat Spikes by Fusarium graminearum
inferredcites →https://doi.org/10.1111/j.1432-1033.1992.tb17266.xopenalex-snapshot
Purification, characterization and gene structure of (1→3)‐β‐glucanase isoenzyme GIII from barley (Hordeum vulgare)
inferredcites →https://doi.org/10.1111/j.1469-1809.1943.tb02321.xopenalex-snapshot
THE ESTIMATION OF MAP DISTANCES FROM RECOMBINATION VALUES
inferredcites →https://doi.org/10.1111/j.1749-6632.1988.tb40397.xopenalex-snapshot
Antifungal Proteins from Plantsa
inferredcites →https://doi.org/10.1139/g91-058openalex-snapshot
A genetic linkage map of Triticum tauschii (DD) and its relationship to the D genome of bread wheat (AABBDD)
inferredcites →https://doi.org/10.1139/g95-006openalex-snapshot
Molecular-genetic maps for group 1 chromosomes of Triticeae species and their relation to chromosomes in rice and oat
inferredcites →https://doi.org/10.1139/g95-067openalex-snapshot
Molecular mapping of wheat. Homoeologous group 2
inferredcites →https://doi.org/10.1139/g95-068openalex-snapshot
Molecular mapping of wheat. Homoeologous group 3
inferredcites →https://doi.org/10.1139/g96-046openalex-snapshot
Molecular genetic maps of the group 6 chromosomes of hexaploid wheat (Triticum aestivumL. em. Thell.)
inferredcites →https://doi.org/10.1146/annurev.bi.59.070190.004301openalex-snapshot
DEFENSE-RELATED PROTEINS IN HIGHER PLANTS
inferredcites →https://doi.org/10.1201/9781420049299.ch1openalex-snapshot
Occurrence and Properties of Plant Pathogenesis-Related Proteins
inferredcites →https://doi.org/10.1201/9781420049299.ch4openalex-snapshot
Plant Chitinases (PR-3, PR-4, PR-8, PR-11)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Elevated Atmospheric Co2 and Silicon Antagonistically Regulate Anti-Herbivore Phytohormone and Defence Gene Expression Levels in Wheat
inferred← citeshttps://doi.org/10.1002/pmic.200401317openalex-snapshot
Differential proteomic analysis of proteins in wheat spikes induced by Fusarium graminearum
inferred← citeshttps://doi.org/10.1002/pmic.200600052openalex-snapshot
Identification of differentially regulated proteins in response to a compatible interaction between the pathogen Fusarium graminearum and its host, Triticum aestivum
inferred← citeshttps://doi.org/10.1002/pmic.200700115openalex-snapshot
Differential expression of proteins in response to the interaction between the pathogen Fusarium graminearum and its host, Hordeum vulgare
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Benzothiadiazole-induced gene expression in wheat spikes does not provide resistance to Fusarium head blight
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The Fusarium Head Blight Pathosystem
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Control of Fungal Diseases in Agricultural Crops by Chitinase and Glucanase Transgenes
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Stress Tolerance in Plants: A Proteomics Approach
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inferred← citeshttps://doi.org/10.1007/s00122-008-0935-8openalex-snapshot
Differential gene expression of related wheat lines with contrasting levels of head blight resistance after Fusarium graminearum inoculation
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Expression of Lignin Biosynthetic Genes in Wheat during Development and upon Infection by Fungal Pathogens
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inferred← citeshttps://doi.org/10.1007/s11240-015-0913-1openalex-snapshot
Resistance to Fusarium oxysporum f. sp. gladioli in transgenic Gladiolus plants expressing either a bacterial chloroperoxidase or fungal chitinase genes
inferred← citeshttps://doi.org/10.1007/s11248-006-0016-1openalex-snapshot
Expression of the lipid transfer protein Ace-AMP1 in transgenic wheat enhances antifungal activity and defense responses
inferred← citeshttps://doi.org/10.1007/s42360-019-00186-xopenalex-snapshot
Current status of resistant source to Fusarium head blight disease of wheat: a review
inferred← citeshttps://doi.org/10.1007/s42976-026-00820-1openalex-snapshot
Integrated genome-wide analysis of wheat disease resistance proteins provides insights into Fusarium head blight defense mechanism
inferred← citeshttps://doi.org/10.1016/j.cj.2017.09.006openalex-snapshot
A journey to understand wheat Fusarium head blight resistance in the Chinese wheat landrace Wangshuibai
inferred← citeshttps://doi.org/10.1016/j.dci.2004.04.002openalex-snapshot
A putative double role of a chitinase in a cnidarian: pattern formation and immunity
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Elevated atmospheric CO2 and silicon antagonistically regulate anti-herbivore phytohormone and defence gene expression levels in wheat
inferred← citeshttps://doi.org/10.1016/j.genrep.2020.100693openalex-snapshot
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Biolistic-mediated oil palm transformation with alfalfa glucanase (AGLU1) and rice chitinase (RCH10) genes for increasing oil palm resistance towards Ganoderma boninense
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Ultrastructural changes and location of β-1,3-glucanase in resistant and susceptible cotton callus cells in response to treatment with toxin of Verticillium dahliae and salicylic acid
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Treatment of Amaranthus cruentus with chemical and biological inducers of resistance has contrasting effects on fitness and protection against compatible Gram positive and Gram negative bacterial pathogens
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A novel β-1,3-glucanase Gns6 from rice possesses antifungal activity against Magnaporthe oryzae
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Identification of genes induced by Fusarium graminearum inoculation in the resistant durum wheat line Langdon(Dic-3A)10 and the susceptible parental line Langdon
inferred← citeshttps://doi.org/10.1016/j.pep.2007.06.013openalex-snapshot
Heterologous expression of new antifungal chitinase from wheat
inferred← citeshttps://doi.org/10.1016/j.pestbp.2006.02.008openalex-snapshot
Molecular biology and biotechnology for reduction of Fusarium mycotoxin contamination
inferred← citeshttps://doi.org/10.1016/j.phytol.2015.12.011openalex-snapshot
Induced resistance during the interaction pathogen x plant and the use of resistance inducers
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.02.017openalex-snapshot
Genome-wide identification and expression analysis of chitinase gene family in Brassica rapa reveals its role in clubroot resistance
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Characterization of a tissue-specific and developmentally regulated β-1,3-glucanase gene family in Prunus persica
inferred← citeshttps://doi.org/10.1016/j.plaphy.2006.10.022openalex-snapshot
Cloning and characterization of six highly similar endo-1,3-β-glucanase genes in hexaploid wheat
inferred← citeshttps://doi.org/10.1016/j.plaphy.2008.05.007openalex-snapshot
Characterization of a new antifungal lipid transfer protein from wheat
inferred← citeshttps://doi.org/10.1016/j.plaphy.2012.06.015openalex-snapshot
Molecular characterization of stress resistance-related chitinase genes of Brassica rapa
inferred← citeshttps://doi.org/10.1016/j.pmpp.2005.12.007openalex-snapshot
Methyl jasmonate induced gene expression in wheat delays symptom development by the crown rot pathogen Fusarium pseudograminearum
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Rearrangement of cell wall polymers in flax infected with a pathogenic strain of Fusarium culmorum
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Selenium improves wheat resistance against Fusarium pseudograminearum through antioxidant defense and cell wall reinforcement
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Polyphenol oxidase genes as integral part of the evolutionary history of domesticated tetraploid wheat
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Expression Comparisons of Pathogenesis-Related (PR) Genes in Wheat in Response to Infection/Infestation by Fusarium, Yellow dwarf virus (YDV) Aphid-Transmitted and Hessian Fly
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Systemic acquired resistance, NPR1, and pathogenesis-related genes in wheat and barley
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Pathogenesis-related protein genes involved in race-specific all-stage resistance and non-race specific high-temperature adult-plant resistance to Puccinia striiformis f. sp. tritici in wheat
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Identification of proteins associated with Fusarium crown rot resistance in wheat using label-free quantification analysis
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inferred← citeshttps://doi.org/10.1021/jf010007fopenalex-snapshot
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MAMP and DAMP signaling contributes resistance to Fusarium graminearum in Arabidopsis
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Greenhouse and field testing of transgenic wheat plants stably expressing genes for thaumatin-like protein, chitinase and glucanase against Fusarium graminearum
inferred← citeshttps://doi.org/10.1093/jxb/ern103openalex-snapshot
Transgenic wheat expressing a barley class II chitinase gene has enhanced resistance against Fusarium graminearum
inferred← citeshttps://doi.org/10.1093/plphys/kiab383openalex-snapshot
Transcription factor BZR2 activates chitinase Cht20.2 transcription to confer resistance to wheat stripe rust
inferred← citeshttps://doi.org/10.1094/mpmi-19-0407openalex-snapshot
Transcriptome Analysis of the Barley-Fusarium graminearumInteraction
inferred← citeshttps://doi.org/10.1094/mpmi-19-0512openalex-snapshot
Fusarium Phytotoxin Trichothecenes Have an Elicitor-Like Activity in Arabidopsis thaliana, but the Activity Differed Significantly Among Their Molecular Species
inferred← citeshttps://doi.org/10.1094/mpmi-20-11-1364openalex-snapshot
Transcriptome Analysis of Trichothecene-Induced Gene Expression in Barley
inferred← citeshttps://doi.org/10.1094/mpmi.2002.15.5.445openalex-snapshot
Functional and Comparative Bioinformatic Analysis of Expressed Genes from Wheat Spikes Infected with Fusarium graminearum
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Apoplastic Extracts from a Transgenic Wheat Line Exhibiting Lesion-Mimic Phenotype Have Multiple Pathogenesis-Related Proteins That Are Antifungal
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inferred← citeshttps://doi.org/10.1111/j.1439-0434.2012.01960.xopenalex-snapshot
Isolation and Characterization of Chitinase from Tomato Infected by Fusarium oxysporum f. sp. lycopersici
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inferred← citeshttps://doi.org/10.1111/nph.13959openalex-snapshot
SnTox1, a Parastagonospora nodorum necrotrophic effector, is a dual‐function protein that facilitates infection while protecting from wheat‐produced chitinases
inferred← citeshttps://doi.org/10.1111/nph.14577openalex-snapshot
Puccinia striiformis f. sp. tritici mi croRNA ‐like RNA 1 ( Pst ‐milR1), an important pathogenicity factor of Pst , impairs wheat resistance to Pst by suppressing the wheat pathogenesis‐related 2 gene
inferred← citeshttps://doi.org/10.1139/g04-097openalex-snapshot
Induction of wheat defense and stress-related genes in response toFusarium graminearum
inferred← citeshttps://doi.org/10.1139/g04-098openalex-snapshot
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inferred← citeshttps://doi.org/10.1139/g07-085openalex-snapshot
Expression analysis of defense-related genes in wheat in response to infection byFusarium graminearumContribution from Purdue University Agricultural Research Programs as journal article No. 2007-18090.
inferred← citeshttps://doi.org/10.1139/g09-018openalex-snapshot
QTL-specific microarray gene expression analysis of wheat resistance to Fusarium head blight in Sumai-3 and two susceptible NILs
inferred← citeshttps://doi.org/10.1146/annurev.phyto.42.040803.140340openalex-snapshot
MANAGEMENT AND RESISTANCE IN WHEAT AND BARLEY TO FUSARIUM HEAD BLIGHT
inferred← citeshttps://doi.org/10.11606/d.11.2020.tde-01102020-130757openalex-snapshot
Potencial de isolados de >i /i< spp. no controle alternativo da ferrugem-asiática da soja
inferred← citeshttps://doi.org/10.1186/1471-2164-12-161openalex-snapshot
Gene discovery in EST sequences from the wheat leaf rust fungus Puccinia triticina sexual spores, asexual spores and haustoria, compared to other rust and corn smut fungi
inferred← citeshttps://doi.org/10.1186/1471-2164-14-197openalex-snapshot
Transcriptome-based discovery of pathways and genes related to resistance against Fusariumhead blight in wheat landrace Wangshuibai
inferred← citeshttps://doi.org/10.1186/s12864-015-2193-xopenalex-snapshot
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Weighted gene co-expression network analysis unveils gene networks associated with the Fusarium head blight resistance in tetraploid wheat
inferred← citeshttps://doi.org/10.1186/s12864-022-08433-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12870-016-0762-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s41938-022-00614-7openalex-snapshot
Penicillium simplicissimum and Trichoderma asperellum counteract the challenge of Puccinia striiformis f. sp. tritici in wheat plants
inferred← citeshttps://doi.org/10.1186/s42269-019-0139-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s43141-021-00240-0openalex-snapshot
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Expression in Cereal Plants of Genes That InactivateFusariumMycotoxins
inferred← citeshttps://doi.org/10.1371/journal.pone.0019008openalex-snapshot
Resistance to Hemi-Biotrophic F. graminearum Infection Is Associated with Coordinated and Ordered Expression of Diverse Defense Signaling Pathways
inferred← citeshttps://doi.org/10.1371/journal.pone.0069542openalex-snapshot
The Fusarium Mycotoxin Deoxynivalenol Can Inhibit Plant Apoptosis-Like Programmed Cell Death
inferred← citeshttps://doi.org/10.1371/journal.pone.0113309openalex-snapshot
Transcriptome and Allele Specificity Associated with a 3BL Locus for Fusarium Crown Rot Resistance in Bread Wheat
inferred← citeshttps://doi.org/10.1371/journal.pone.0224413openalex-snapshot
Transcriptional analysis of wheat seedlings inoculated with Fusarium culmorum under continual exposure to disease defence inductors
inferred← citeshttps://doi.org/10.1371/journal.pone.0309944openalex-snapshot
Expression patterns of candidate genes for the Lr46/Yr29 “slow rust” locus in common wheat (Triticum aestivum L.) and associated miRNAs inform of the gene conferring the Puccinia triticina resistance trait
inferred← citeshttps://doi.org/10.1515/agri-2017-0002openalex-snapshot
Chitinase Activities in Wheat and Its Relative Species
inferred← citeshttps://doi.org/10.1515/nbec-2016-0013openalex-snapshot
Beta-1,3-Glucanase Activities in Wheat and Relative Species
inferred← citeshttps://doi.org/10.1534/genetics.104.034819openalex-snapshot
Group 3 Chromosome Bin Maps of Wheat and Their Relationship to Rice Chromosome 1
inferred← citeshttps://doi.org/10.15407/frg2019.06.508openalex-snapshot
Isoenzyme composition and some properties of b-1,3-glucanase of wheat seedlings
inferred← citeshttps://doi.org/10.1556/aphyt.46.2011.1.5openalex-snapshot
Induction of a wheat β-1,3-glucanase gene during the defense response toBipolaris sorokiniana
inferred← citeshttps://doi.org/10.1590/0001-3765202620250792openalex-snapshot
Enzyme activity of peroxidase and β-1,3-glucanase in Passiflora spp. seedlings inoculated by Fusarium spp
inferred← citeshttps://doi.org/10.17221/63/2009-cjgpbopenalex-snapshot
Cereal resistance to Fusarium head blight and possibilities of its improvement through breeding
inferred← citeshttps://doi.org/10.17660/actahortic.2016.1145.23openalex-snapshot
Transgenic approaches to enhance disease resistance in carrot plants to fungal pathogens
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2132821/v1openalex-snapshot
Saffron-Fusarium oxysporum R1 dual transcriptomics unravels, defense mechanism of saffron and robust pathogenicity of Fusarium oxysporum R1
inferred← citeshttps://doi.org/10.2135/cropsci2005.07.0206tpgopenalex-snapshot
Expression Analysis and Physical Mapping of a cDNA Library of Fusarium Head Blight Infected Wheat Spikes
inferred← citeshttps://doi.org/10.2135/cropsci2008.02.0097openalex-snapshot
Jasmonate and Ethylene Signaling Pathway May Mediate Fusarium Head Blight Resistance in Wheat
inferred← citeshttps://doi.org/10.32615/bp.2021.010openalex-snapshot
The effect of Fusarium culmorum inoculation and deoxynivalenol application on proteome response in wheat cultivars Sumai 3 and SW Kadrilj
inferred← citeshttps://doi.org/10.3389/fpls.2019.01006openalex-snapshot
An Improved Phenotyping Protocol for Panama Disease in Banana
inferred← citeshttps://doi.org/10.3389/fpls.2024.1352105openalex-snapshot
Endophytic non-pathogenic Fusarium oxysporum reorganizes the cell wall in flax seedlings
inferred← citeshttps://doi.org/10.3390/agronomy16020208openalex-snapshot
Transcriptome-Wide Profiling of RNA M6A Modifications in Soybean Reveals Shared and Specific Mechanisms of Resistance to Viral and Bacterial Infections
inferred← citeshttps://doi.org/10.3390/ijms21218358openalex-snapshot
Transcriptomic Analysis Reveals Candidate Genes Responsive to Sclerotinia scleroterum and Cloning of the Ss-Inducible Chitinase Genes in Morus laevigata
inferred← citeshttps://doi.org/10.3390/ijms241512391openalex-snapshot
RNA-Based Control of Fungal Pathogens in Plants
inferred← citeshttps://doi.org/10.3390/jof8020149openalex-snapshot
Monitoring of Host Suitability and Defense-Related Genes in Wheat to Bipolaris sorokiniana
inferred← citeshttps://doi.org/10.3390/microorganisms7120589openalex-snapshot
DNA Methylation Profile of β-1,3-Glucanase and Chitinase Genes in Flax Shows Specificity Towards Fusarium Oxysporum Strains Differing in Pathogenicity
inferred← citeshttps://doi.org/10.3390/pathogens14040398openalex-snapshot
Trans-Kingdom sRNA Silencing in Sclerotinia sclerotiorum for Crop Fungal Disease Management
inferred← citeshttps://doi.org/10.3390/toxins6020679openalex-snapshot
Light Influences How the Fungal Toxin Deoxynivalenol Affects Plant Cell Death and Defense Responses
inferred← citeshttps://doi.org/10.3724/sp.j.1006.2009.00786openalex-snapshot
Cloning and Characterization of a Novel Wheat Glycoside Hydrolase Gene TaGlc2 Induced by Powdery Mildew Pathogen (Erysiphe graminis) Infection
inferred← citeshttps://doi.org/10.4238/2014.march.17.17openalex-snapshot
Characterization of the β-1,3-glucanase gene in peanut (Arachis hypogaea L.) by cloning and genetic transformation
inferred← citeshttps://doi.org/10.5772/27965openalex-snapshot
Olive – Colletotrichum acutatum: An Example of Fruit-Fungal Interaction
inferred← citeshttps://doi.org/10.5958/j.2229-4473.26.2s.141openalex-snapshot
Pathogenesis Related Defence Functions of Plant Chitinases and β-1,3-Glucanases
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408054openalex-snapshot
Additional file 10 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408060openalex-snapshot
Additional file 12 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408069openalex-snapshot
Additional file 15 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408072openalex-snapshot
Additional file 16 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408084openalex-snapshot
Additional file 1 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408087openalex-snapshot
Additional file 20 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408090openalex-snapshot
Additional file 21 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408093openalex-snapshot
Additional file 22 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408099openalex-snapshot
Additional file 3 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.6084/m9.figshare.19408117openalex-snapshot
Additional file 9 of Genomic sequencing of Thinopyrum elongatum chromosome arm 7EL, carrying fusarium head blight resistance, and characterization of its impact on the transcriptome of the introgressed line CS-7EL
inferred← citeshttps://doi.org/10.70675/3b1288f3zbf49z42eczbc32z1fb57ff8b2f4openalex-snapshot
Induction de résistances chez le blé (Triticum aestivum L.) lors d’une interaction compatible avec Blumeria graminis (DC. E.O Speer) : mécanismes mis en jeu après applications de tréhalose et d’heptanoyl d’acide licylique, dérivé fonctionnalisé de l’acide salicylique
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