Works matching DE "MEDICAGO truncatula"
Results: 906
Genetic control and molecular responses of Medicago truncatula to cadmium stress.
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- Euphytica, 2023, v. 219, n. 8, p. 1, doi. 10.1007/s10681-023-03200-6
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Identification of transcripts associated with the acquisition of superior freezing tolerance in recurrently-selected populations of alfalfa.
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- Euphytica, 2020, v. 216, n. 2, p. 1, doi. 10.1007/s10681-020-2559-2
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Physiological and metabolomic analysis of a knockout mutant suggests a critical role of MtP5CS3 gene in osmotic stress tolerance of Medicago truncatula.
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- Euphytica, 2013, v. 193, n. 1, p. 101, doi. 10.1007/s10681-013-0957-4
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Molecular characterization and expression analysis of the Na<sup>+</sup>/H<sup>+</sup> exchanger gene family in <italic>Medicago truncatula</italic>.
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- Functional & Integrative Genomics, 2018, v. 18, n. 2, p. 141, doi. 10.1007/s10142-017-0581-9
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The F-box family genes as key elements in response to salt, heavy mental, and drought stresses in Medicago truncatula.
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- Functional & Integrative Genomics, 2015, v. 15, n. 4, p. 495, doi. 10.1007/s10142-015-0438-z
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Genome-wide identification, characterization and expression analysis of HAK genes and decoding their role in responding to potassium deficiency and abiotic stress in Medicago truncatula.
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- PeerJ, 2022, p. 1, doi. 10.7717/peerj.14034
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Genome-wide identification and expression analysis of the VQ gene family in Cicer arietinum and Medicago truncatula.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.8471
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Mapping-by-sequencing using NGS-based 3'-MACE-Seq reveals a new mutant allele of the essential nodulation gene Sym33 (IPD3) in pea (Pisum sativum L.).
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.6662
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The transcriptomic response to a short day to long day shift in leaves of the reference legume Medicago truncatula.
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.6626
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Arbuscular mycorrhizal fungi in soil, roots and rhizosphere of Medicago truncatula: diversity and heterogeneity under semi-arid conditions.
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.6401
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Regulation of somatic embryogenesis induction in Medicago truncatula Gaertn. at the physiological and molecular level.
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- Biotechnologia, 2018, v. 99, n. 3, p. 231
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Correction to: Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula.
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- 2021
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- Correction Notice
Soil origin and plant genotype structure distinct microbiome compartments in the model legume Medicago truncatula.
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- Microbiome, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40168-020-00915-9
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Genome-Wide Identification of Glyoxalase Genes in Medicago truncatula and Their Expression Profiling in Response to Various Developmental and Environmental Stimuli.
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- Frontiers in Plant Science, 2017, p. 1, doi. 10.3389/fpls.2017.00836
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- Article
LeafletAnalyzer, an Automated Software for Quantifying, Comparing and Classifying Blade and Serration Features of Compound Leaves during Development, and among Induced Mutants and Natural Variants in the Legume Medicago truncatula.
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- Frontiers in Plant Science, 2017, p. 1, doi. 10.3389/fpls.2017.00915
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Interface Symbiotic Membrane Formation in Root Nodules of Medicago truncatula: the Role of Synaptotagmins MtSyt1, MtSyt2 and MtSyt3.
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- Frontiers in Plant Science, 2017, v. 8, p. 1, doi. 10.3389/fpls.2017.00201
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Identification and Network-Enabled Characterization of Auxin Response Factor Genes in Medicago truncatula.
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- Frontiers in Plant Science, 2016, v. 7, p. 1, doi. 10.3389/fpls.2016.01857
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MtNF-YA1, A Central Transcriptional Regulator of Symbiotic Nodule Development, Is Also a Determinant of Medicago truncatula Susceptibility toward a Root Pathogen.
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- Frontiers in Plant Science, 2016, v. 7, p. 1, doi. 10.3389/fpls.2016.01837
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NIN Is Involved in the Regulation of Arbuscular Mycorrhizal Symbiosis.
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- Frontiers in Plant Science, 2016, v. 7, p. 1, doi. 10.3389/fpls.2016.01704
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- Article
Quantitative Resistance to Verticillium Wilt in Medicago truncatula Involves Eradication of the Fungus from Roots and Is Associated with Transcriptional Responses Related to Innate Immunity.
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- Frontiers in Plant Science, 2016, p. 1, doi. 10.3389/fpls.2016.01431
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A Snapshot of Functional Genetic Studies in Medicago truncatula.
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- Frontiers in Plant Science, 2016, p. 1, doi. 10.3389/fpls.2016.01175
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Bioinformatics Analysis of MAPKKK Family Genes in Medicago truncatula.
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- Genes, 2016, v. 7, n. 4, p. 13, doi. 10.3390/genes7040013
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Physiological and biochemical characterization of rootlets response to salt stress in two Medicago truncatula Gaertn. ecotypes.
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- Plant Root, 2018, v. 12, p. 1, doi. 10.3117/plantroot.12.1
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- Article
Contribution of Rhizobium–Legume Symbiosis in Salt Stress Tolerance in Medicago truncatula Evaluated through Photosynthesis, Antioxidant Enzymes, and Compatible Solutes Accumulation.
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- Sustainability (2071-1050), 2021, v. 13, n. 6, p. 3369, doi. 10.3390/su13063369
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Morphological and genetic changes induced by excess Zn in roots of Medicago truncatula A17 and a Zn accumulating mutant.
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- BMC Research Notes, 2012, v. 5, n. 1, p. 1, doi. 10.1186/1756-0500-5-657
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Biogenesis of protein bodies during vicilin accumulation in Medicago truncatula immature seeds.
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- BMC Research Notes, 2012, v. 5, n. 1, p. 409, doi. 10.1186/1756-0500-5-409
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Correlative evidence for co-regulation of phosphorus and carbon exchanges with symbiotic fungus in the arbuscular mycorrhizal Medicago truncatula.
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- PLoS ONE, 2019, v. 14, n. 11, p. 1, doi. 10.1371/journal.pone.0224938
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Sugar transporters in Fabaceae, featuring SUT MST and SWEET families of the model plant Medicago truncatula and the agricultural crop Pisum sativum.
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- PLoS ONE, 2019, v. 14, n. 9, p. 1, doi. 10.1371/journal.pone.0223173
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First report of Neovaginatispora fuckelii causing stem blight on Rosa chinensis in China.
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- Journal of Plant Pathology, 2021, v. 103, n. 4, p. 1351, doi. 10.1007/s42161-021-00919-w
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Three members of Medicago truncatula ST family are ubiquitous during development and modulated by nutritional status (MtST1) and dehydration (MtST2 and MtST3).
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- BMC Plant Biology, 2017, v. 17, p. 1, doi. 10.1186/s12870-017-1061-z
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Genome-wide analysis identifies gain and loss/change of function within the small multigenic insecticidal Albumin 1 family of Medicago truncatula.
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- BMC Plant Biology, 2016, v. 16, p. 1, doi. 10.1186/s12870-016-0745-0
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Direct purification of detergent-insoluble membranes from Medicago truncatula root microsomes: Comparison between floatation and sedimentation.
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- BMC Plant Biology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/s12870-014-0255-x
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Diverse functional evolution of type II pyridoxal 5'-phosphate decarboxylases: Detection of two novel acetaldehyde synthases that uses hydrophobic amino acids as substrates.
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- BMC Plant Biology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/s12870-014-0247-x
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Strategies for optimizing BioNano and Dovetail explored through a second reference quality assembly for the legume model, Medicago truncatula.
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-3971-4
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High toxicity and specificity of the saponin 3-GlcA- 28-AraRhaxyl-medicagenate, from Medicago truncatula seeds, for Sitophilus oryzae.
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- BMC Chemical Biology, 2012, v. 12, n. 1, p. 3, doi. 10.1186/1472-6769-12-3
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- Article
ITIS, a bioinformatics tool for accurate identification of transposon insertion sites using next-generation sequencing data.
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- BMC Bioinformatics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12859-015-0507-2
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- Article
Salt and Cadmium Stress Tolerance in Four Genotypes of Medicago sativa L.
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- Avances en Investigación Agropecuaria, 2022, v. 26, p. 62, doi. 10.53897/RevAIA.22.26.05
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Genome-wide identification and characterization of filamentation temperature-sensitive H (FtsH) genes and expression analysis in response to multiple stresses in Medicago truncatula.
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- Molecular Biology Reports, 2023, v. 50, n. 12, p. 10097, doi. 10.1007/s11033-023-08851-1
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Identification and characterization of stress responsive homeodomain leucine zipper transcription factors in Medicago truncatula.
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- Molecular Biology Reports, 2022, v. 49, n. 5, p. 3569, doi. 10.1007/s11033-022-07197-4
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ChIP-Seq Analysis Protocol for Identification of PsIPD3 and PsNIN Transcription Factors Binding Sites in Pisum sativum genome.
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- Russian Journal of Plant Physiology, 2023, v. 70, n. 9, p. 1, doi. 10.1134/S1021443723603403
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- Article
Analysis of Glycine max and Galega orientalis Nodules Revealed Specific Features of Symbiotic Interface Organization in Determinate and Indeterminate Nodules.
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- Russian Journal of Plant Physiology, 2023, v. 70, n. 8, p. 1, doi. 10.1134/S1021443723602495
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STENOFOLIA gene and regulation of somatic embryogenesis in Medicago truncatula.
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- Russian Journal of Plant Physiology, 2016, v. 63, n. 6, p. 811, doi. 10.1134/S1021443716060133
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- Article
Role of arbuscular mycorrhizal mediated inter-plant signaling in Medicago truncatula resistance to fungal pathogens Botrytis cinerea and Fusarium sporotrichoides.
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- Environmental & Experimental Biology, 2024, v. 22, n. 1, p. 57
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Investigation of arbuscular mycorrhiza-mediated systemic and inter-plant defence responses in Medicago trucatula.
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- Environmental & Experimental Biology, 2024, v. 22, n. 1, p. 55
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- Article
Medicago truncatula -- model for studyng intra-plant and inter-plant signals during arbuscular mycorrhizal colonisation.
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- Environmental & Experimental Biology, 2023, v. 21, n. 1, p. 37
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Genome-wide analysis of polygalacturonase gene family in Medicago truncatula.
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- Chinese Journal of Bioinformatics, 2020, v. 18, n. 1, p. 31, doi. 10.12113/201907005
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Rhizobial nitrogen fixation efficiency shapes endosphere bacterial communities and Medicago truncatula host growth.
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- Microbiome, 2023, v. 11, n. 1, p. 1, doi. 10.1186/s40168-023-01592-0
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Biodiversity within Medicago truncatula genotypes toward response to iron deficiency: Investigation of main tolerance mechanisms.
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- Plant Species Biology, 2019, v. 34, n. 3, p. 95, doi. 10.1111/1442-1984.12245
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- Article
Legumes display common and host-specific responses to the rhizobial cellulase CelC2 during primary symbiotic infection.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50337-3
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- Article
Biosynthesis of DDMP saponins in soybean is regulated by a distinct UDP‐glycosyltransferase.
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- New Phytologist, 2019, v. 222, n. 1, p. 261, doi. 10.1111/nph.15588
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- Article