On the public citation graph
Cell-specific pathways recruited for symbiotic nodulation in the Medicago truncatula legume
0 signed · 245 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known work and none has been retracted — and get a dated CiteStamped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/cppb.20078openalex-snapshot
Enhancing Phenotyping and Molecular Analysis of Plant Root System Using Ultrasound Aeroponic Technology
inferredcites →https://doi.org/10.1002/cppb.20120openalex-snapshot
Isolation of Plant Root Nuclei for Single Cell RNA Sequencing
inferredcites →https://doi.org/10.1007/s00344-005-0106-yopenalex-snapshot
RNAi Phenotypes and the Localization of a Protein::GUS Fusion Imply a Role for Medicago truncatula PIN Genes in Nodulation
inferredcites →https://doi.org/10.1007/s11103-017-0630-8openalex-snapshot
A comparative genomic and transcriptomic analysis at the level of isolated root hair cells reveals new conserved root hair regulatory elements
inferredcites →https://doi.org/10.1016/j.cell.2021.04.048openalex-snapshot
Integrated analysis of multimodal single-cell data
inferredcites →https://doi.org/10.1016/j.celrep.2019.04.054openalex-snapshot
High-Throughput Single-Cell Transcriptome Profiling of Plant Cell Types
inferredcites →https://doi.org/10.1016/j.celrep.2019.06.041openalex-snapshot
Molecular Mechanisms Driving Switch Behavior in Xylem Cell Differentiation
inferredcites →https://doi.org/10.1016/j.cub.2014.03.025openalex-snapshot
Programmed Cell Death Controlled by ANAC033/SOMBRERO Determines Root Cap Organ Size in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2019.09.005openalex-snapshot
NODULE INCEPTION Recruits the Lateral Root Developmental Program for Symbiotic Nodule Organogenesis in Medicago truncatula
inferredcites →https://doi.org/10.1016/j.devcel.2019.02.022openalex-snapshot
Spatiotemporal Developmental Trajectories in the Arabidopsis Root Revealed Using High-Throughput Single Cell RNA Sequencing
inferredcites →https://doi.org/10.1016/j.molp.2015.03.010openalex-snapshot
Rhizobium Lipo-chitooligosaccharide Signaling Triggers Accumulation of Cytokinins in Medicago truncatula Roots
inferredcites →https://doi.org/10.1016/j.molp.2019.01.003openalex-snapshot
MapMan4: A Refined Protein Classification and Annotation Framework Applicable to Multi-Omics Data Analysis
inferredcites →https://doi.org/10.1016/j.molp.2019.04.004openalex-snapshot
A Single-Cell RNA Sequencing Profiles the Developmental Landscape of Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.molp.2020.12.014openalex-snapshot
Transcriptional landscape of rice roots at the single-cell resolution
inferredcites →https://doi.org/10.1016/j.molp.2021.01.001openalex-snapshot
Single-nucleus RNA and ATAC sequencing reveals the impact of chromatin accessibility on gene expression in Arabidopsis roots at the single-cell level
inferredcites →https://doi.org/10.1016/j.pbi.2016.10.007openalex-snapshot
Differentiation of conductive cells: a matter of life and death
inferredcites →https://doi.org/10.1016/j.tplants.2017.06.012openalex-snapshot
Cytokinins in Symbiotic Nodulation: When, Where, What For?
inferredcites →https://doi.org/10.1016/j.tplants.2020.11.009openalex-snapshot
Nitrogen Systemic Signaling: From Symbiotic Nodulation to Root Acquisition
inferredcites →https://doi.org/10.1016/j.xplc.2021.100183openalex-snapshot
NLP1 reciprocally regulates nitrate inhibition of nodulation through SUNN-CRA2 signaling in Medicago truncatula
inferredcites →https://doi.org/10.1038/46058openalex-snapshot
A plant regulator controlling development of symbiotic root nodules
inferredcites →https://doi.org/10.1038/nature00842openalex-snapshot
A receptor kinase gene regulating symbiotic nodule development
inferredcites →https://doi.org/10.1038/nature04812openalex-snapshot
Nodulation independent of rhizobia induced by a calcium-activated kinase lacking autoinhibition
inferredcites →https://doi.org/10.1038/ncomms12636openalex-snapshot
DELLA-mediated gibberellin signalling regulates Nod factor signalling and rhizobial infection
inferredcites →https://doi.org/10.1038/nplants.2015.197openalex-snapshot
A symbiotic SNARE protein generated by alternative termination of transcription
inferredcites →https://doi.org/10.1038/s41467-019-10029-yopenalex-snapshot
A protein complex required for polar growth of rhizobial infection threads
inferredcites →https://doi.org/10.1038/s41467-021-22352-4openalex-snapshot
Single-cell transcriptome atlas and chromatin accessibility landscape reveal differentiation trajectories in the rice root
inferredcites →https://doi.org/10.1038/s41467-021-26820-9openalex-snapshot
Nitrate restricts nodule organogenesis through inhibition of cytokinin biosynthesis in Lotus japonicus
inferredcites →https://doi.org/10.1038/s41477-018-0286-7openalex-snapshot
Whole-genome landscape of Medicago truncatula symbiotic genes
inferredcites →https://doi.org/10.1038/s41477-019-0501-1openalex-snapshot
A CLE–SUNN module regulates strigolactone content and fungal colonization in arbuscular mycorrhiza
inferredcites →https://doi.org/10.1038/s41586-020-3016-zopenalex-snapshot
An SHR–SCR module specifies legume cortical cell fate to enable nodulation
inferredcites →https://doi.org/10.1038/s41598-017-09297-9openalex-snapshot
Functional characterisation of brassinosteroid receptor MtBRI1 in Medicago truncatula
inferredcites →https://doi.org/10.1038/s41598-018-20359-4openalex-snapshot
MtNRLK1, a CLAVATA1-like leucine-rich repeat receptor-like kinase upregulated during nodulation in Medicago truncatula
inferredcites →https://doi.org/10.1038/s41598-019-42407-3openalex-snapshot
MtGA2ox10 encoding C20-GA2-oxidase regulates rhizobial infection and nodule development in Medicago truncatula
inferredcites →https://doi.org/10.1042/bj1251075openalex-snapshot
Control of leghaemoglobin synthesis in snake beans
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00963.xopenalex-snapshot
The spatial expression patterns of a phosphate transporter (MtPT1) from Medicago truncatula indicate a role in phosphate transport at the root/soil interface
inferredcites →https://doi.org/10.1073/pnas.0710273105openalex-snapshot
The RPG gene of Medicago truncatula controls Rhizobium -directed polar growth during infection
inferredcites →https://doi.org/10.1073/pnas.0910081107openalex-snapshot
Plant flotillins are required for infection by nitrogen-fixing bacteria
inferredcites →https://doi.org/10.1073/pnas.1113992109openalex-snapshot
Legume pectate lyase required for root infection by rhizobia
inferredcites →https://doi.org/10.1073/pnas.1200407109openalex-snapshot
Rhizobium –legume symbiosis shares an exocytotic pathway required for arbuscule formation
inferredcites →https://doi.org/10.1073/pnas.1611763113openalex-snapshot
Increasing seed size and quality by manipulating BIG SEEDS1 in legume species
inferredcites →https://doi.org/10.1093/aob/mcaa022openalex-snapshot
Mutational analysis indicates that abnormalities in rhizobial infection and subsequent plant cell and bacteroid differentiation in pea (Pisum sativum) nodules coincide with abnormal cytokinin responses and localization
inferredcites →https://doi.org/10.1093/bioinformatics/btab209openalex-snapshot
ShinyCell: simple and sharable visualization of single-cell gene expression data
inferredcites →https://doi.org/10.1093/bioinformatics/bty332openalex-snapshot
DEsingle for detecting three types of differential expression in single-cell RNA-seq data
inferredcites →https://doi.org/10.1093/emboj/18.16.4476openalex-snapshot
The mitotic inhibitor ccs52 is required for endoreduplication and ploidy‐dependent cell enlargement in plants
inferredcites →https://doi.org/10.1093/gigascience/giaa151openalex-snapshot
SoupX removes ambient RNA contamination from droplet-based single-cell RNA sequencing data
inferredcites →https://doi.org/10.1093/jxb/10.2.250openalex-snapshot
Some Observations on Root-hair Infection by Nodule Bacteria
inferredcites →https://doi.org/10.1093/jxb/erv295openalex-snapshot
The root cap: a short story of life and death
inferredcites →https://doi.org/10.1093/jxb/erx059openalex-snapshot
Medicago truncatula ABCG10 is a transporter of 4-coumarate and liquiritigenin in the medicarpin biosynthetic pathway
inferredcites →https://doi.org/10.1093/jxb/ery465openalex-snapshot
Unraveling new molecular players involved in the autoregulation of nodulation in Medicago truncatula
inferredcites →https://doi.org/10.1093/pcp/pcz177openalex-snapshot
LeGOO: An Expertized Knowledge Database for the Model Legume Medicago truncatula
inferredcites →https://doi.org/10.1094/mpmi-11-18-0322-ropenalex-snapshot
Digalactosyldiacylglycerol Synthase Gene MtDGD1 Plays an Essential Role in Nodule Development and Nitrogen Fixation
inferredcites →https://doi.org/10.1094/mpmi-12-10-0281openalex-snapshot
A Dual-Targeted Soybean Protein Is Involved in Bradyrhizobium japonicum Infection of Soybean Root Hair and Cortical Cells
inferredcites →https://doi.org/10.1094/mpmi-12-14-0402-ropenalex-snapshot
ARP2/3-Mediated Actin Nucleation Associated With Symbiosome Membrane Is Essential for the Development of Symbiosomes in Infected Cells of Medicago truncatula Root Nodules
inferredcites →https://doi.org/10.1094/mpmi-20-0082openalex-snapshot
Involvement of the Octadecanoid Pathway in Bluegreen Aphid Resistance in Medicago truncatula
inferredcites →https://doi.org/10.1094/mpmi-20-8-0912openalex-snapshot
A Novel Nuclear Protein Interacts With the Symbiotic DMI3 Calcium- and Calmodulin-Dependent Protein Kinase of Medicago truncatula
inferredcites →https://doi.org/10.1094/mpmi-20-9-1138openalex-snapshot
Genomic Organization and Evolutionary Insights on GRP and NCR Genes, Two Large Nodule-Specific Gene Families in Medicago truncatula
inferredcites →https://doi.org/10.1094/mpmi-21-8-1118openalex-snapshot
Evidence for the Involvement in Nodulation of the Two Small Putative Regulatory Peptide-Encoding Genes MtRALFL1 and MtDVL1
inferredcites →https://doi.org/10.1094/mpmi.1998.11.6.504openalex-snapshot
The Medicago truncatula MtAnn1 Gene Encoding an Annexin Is Induced by Nod Factors and During the Symbiotic Interaction with Rhizobium meliloti
inferredcites →https://doi.org/10.1094/mpmi.2003.16.10.903openalex-snapshot
The Medicago truncatula Sucrose Synthase Gene MtSucS1 Is Activated Both in the Infected Region of Root Nodules and in the Cortex of Roots Colonized by Arbuscular Mycorrhizal Fungi
inferredcites →https://doi.org/10.1101/gad.14.4.475openalex-snapshot
A Krüppel-like zinc finger protein is involved in nitrogen-fixing root nodule organogenesis
inferredcites →https://doi.org/10.1101/gad.402806openalex-snapshot
MtHAP2-1 is a key transcriptional regulator of symbiotic nodule development regulated by microRNA169 in Medicago truncatula
inferredcites →https://doi.org/10.1104/pp.105.070326openalex-snapshot
Transcript Analysis of Early Nodulation Events in Medicago truncatula
inferredcites →https://doi.org/10.1104/pp.106.090985openalex-snapshot
The Lipopolysaccharide of Sinorhizobium meliloti Suppresses Defense-Associated Gene Expression in Cell Cultures of the Host Plant Medicago truncatula
inferredcites →https://doi.org/10.1104/pp.107.100495openalex-snapshot
Medicago LYK3, an Entry Receptor in Rhizobial Nodulation Factor Signaling
inferredcites →https://doi.org/10.1104/pp.108.124867openalex-snapshot
Finding and Comparing Syntenic Regions among Arabidopsis and the Outgroups Papaya, Poplar, and Grape: CoGe with Rosids
inferredcites →https://doi.org/10.1104/pp.109.143024openalex-snapshot
Knockdown ofCELL DIVISION CYCLE16Reveals an Inverse Relationship between Lateral Root and Nodule Numbers and a Link to Auxin inMedicago truncatula
inferredcites →https://doi.org/10.1104/pp.109.143933openalex-snapshot
LIN, a Novel Type of U-Box/WD40 Protein, Controls Early Infection by Rhizobia in Legumes
inferredcites →https://doi.org/10.1104/pp.109.148379openalex-snapshot
Complete Transcriptome of the Soybean Root Hair Cell, a Single-Cell Model, and Its Alteration in Response to Bradyrhizobium japonicum Infection
inferredcites →https://doi.org/10.1104/pp.111.178756openalex-snapshot
The ROOT DETERMINED NODULATION1 Gene Regulates Nodule Number in Roots of Medicago truncatula and Defines a Highly Conserved, Uncharacterized Plant Gene Family
inferredcites →https://doi.org/10.1104/pp.112.196444openalex-snapshot
Functional Assessment of the Medicago truncatula NIP/LATD Protein Demonstrates That It Is a High-Affinity Nitrate Transporter
inferredcites →https://doi.org/10.1104/pp.113.222380openalex-snapshot
A Regulatory Network-Based Approach Dissects Late Maturation Processes Related to the Acquisition of Desiccation Tolerance and Longevity of Medicago truncatula Seeds
inferredcites →https://doi.org/10.1104/pp.113.223966openalex-snapshot
The Nodulation Factor Hydrolase of Medicago truncatula: Characterization of an Enzyme Specifically Cleaving Rhizobial Nodulation Signals
inferredcites →https://doi.org/10.1104/pp.15.00350openalex-snapshot
Deep Sequencing of the Medicago truncatula Root Transcriptome Reveals a Massive and Early Interaction between Nodulation Factor and Ethylene Signals
inferredcites →https://doi.org/10.1104/pp.15.01853openalex-snapshot
A Medicago truncatula Cystathionine-β-Synthase-like Domain-Containing Protein Is Required for Rhizobial Infection and Symbiotic Nitrogen Fixation
inferredcites →https://doi.org/10.1104/pp.16.00113openalex-snapshot
Different Pathways Act Downstream of the CEP Peptide Receptor CRA2 to Regulate Lateral Root and Nodule Development
inferredcites →https://doi.org/10.1104/pp.16.00230openalex-snapshot
The Symbiosis-Related ERN Transcription Factors Act in Concert to Coordinate Rhizobial Host Root Infection
inferredcites →https://doi.org/10.1104/pp.16.00711openalex-snapshot
A Laser Dissection-RNAseq Analysis Highlights the Activation of Cytokinin Pathways by Nod Factors in the Medicago truncatula Root Epidermis
inferredcites →https://doi.org/10.1104/pp.16.01473openalex-snapshot
MtLAX2, a Functional Homologue of the Arabidopsis Auxin Influx Transporter AUX1, Is Required for Nodule Organogenesis
inferredcites →https://doi.org/10.1104/pp.17.00278openalex-snapshot
ROOT DETERMINED NODULATION1 Is Required for M. truncatula CLE12, But Not CLE13, Peptide Signaling through the SUNN Receptor Kinase
inferredcites →https://doi.org/10.1104/pp.17.00919openalex-snapshot
DELLA1-Mediated Gibberellin Signaling Regulates Cytokinin-Dependent Symbiotic Nodulation
inferredcites →https://doi.org/10.1104/pp.17.01096openalex-snapshot
Genome-Wide Identification of Medicago Peptides Involved in Macronutrient Responses and Nodulation
inferredcites →https://doi.org/10.1104/pp.17.01587openalex-snapshot
The MtDMI2-MtPUB2 Negative Feedback Loop Plays a Role in Nodulation Homeostasis
inferredcites →https://doi.org/10.1104/pp.18.01482openalex-snapshot
Single-Cell RNA Sequencing Resolves Molecular Relationships Among Individual Plant Cells
inferredcites →https://doi.org/10.1104/pp.18.01572openalex-snapshot
NIN Acts as a Network Hub Controlling a Growth Module Required for Rhizobial Infection
inferredcites →https://doi.org/10.1104/pp.68.5.1144openalex-snapshot
Transient Susceptibility of Root Cells in Four Common Legumes to Nodulation by Rhizobia
inferredcites →https://doi.org/10.1105/tpc.105.035394openalex-snapshot
RNA Interference Identifies a Calcium-Dependent Protein Kinase Involved inMedicago truncatulaRoot Development
inferredcites →https://doi.org/10.1105/tpc.106.043778openalex-snapshot
The Medicago truncatula CRE1 Cytokinin Receptor Regulates Lateral Root Development and Early Symbiotic Interaction with Sinorhizobium meliloti
inferredcites →https://doi.org/10.1105/tpc.106.048264openalex-snapshot
An ERF Transcription Factor in Medicago truncatula That Is Essential for Nod Factor Signal Transduction
inferredcites →https://doi.org/10.1105/tpc.107.052944openalex-snapshot
AP2-ERF Transcription Factors Mediate Nod Factor–Dependent MtENOD11Activation in Root Hairs via a Novelcis-Regulatory Motif
inferredcites →https://doi.org/10.1105/tpc.108.059857openalex-snapshot
EFD Is an ERF Transcription Factor Involved in the Control of Nodule Number and Differentiation inMedicago truncatula
inferredcites →https://doi.org/10.1105/tpc.108.063255openalex-snapshot
Lotus japonicusCASTOR and POLLUX Are Ion Channels Essential for Perinuclear Calcium Spiking in Legume Root Endosymbiosis
inferredcites →https://doi.org/10.1105/tpc.108.064410openalex-snapshot
Medicago N2-Fixing Symbiosomes Acquire the Endocytic Identity Marker Rab7 but Delay the Acquisition of Vacuolar Identity
inferredcites →https://doi.org/10.1105/tpc.110.075861openalex-snapshot
TheMedicago truncatulaE3 Ubiquitin Ligase PUB1 Interacts with the LYK3 Symbiotic Receptor and Negatively Regulates Infection and Nodulation
inferredcites →https://doi.org/10.1105/tpc.111.089771openalex-snapshot
Strigolactone Biosynthesis in Medicago truncatula and Rice Requires the Symbiotic GRAS-Type Transcription Factors NSP1 and NSP2
inferredcites →https://doi.org/10.1105/tpc.112.098475openalex-snapshot
The Recent Evolution of a Symbiotic Ion Channel in the Legume Family Altered Ion Conductance and Improved Functionality in Calcium Signaling
inferredcites →https://doi.org/10.1105/tpc.113.114017openalex-snapshot
The C2H2 Transcription Factor REGULATOR OF SYMBIOSOME DIFFERENTIATION Represses Transcription of the Secretory Pathway Gene VAMP721a and Promotes Symbiosome Development in Medicago truncatula
inferredcites →https://doi.org/10.1105/tpc.114.133496openalex-snapshot
The Root Hair “Infectome” of Medicago truncatula Uncovers Changes in Cell Cycle Genes and Reveals a Requirement for Auxin Signaling in Rhizobial Infection
inferredcites →https://doi.org/10.1105/tpc.15.00440openalex-snapshot
The Plant Peptidome: An Expanding Repertoire of Structural Features and Biological Functions
inferredcites →https://doi.org/10.1105/tpc.17.00420openalex-snapshot
Role of the Nod Factor Hydrolase MtNFH1 in Regulating Nod Factor Levels during Rhizobial Infection and in Mature Nodules of Medicago truncatula
inferredcites →https://doi.org/10.1105/tpc.18.00785openalex-snapshot
Dynamics of Gene Expression in Single Root Cells of Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.19.00279openalex-snapshot
Celebrating 20 Years of Genetic Discoveries in Legume Nodulation and Symbiotic Nitrogen Fixation
inferredcites →https://doi.org/10.1105/tpc.19.00494openalex-snapshot
Gene Expression in Nitrogen-Fixing Symbiotic Nodule Cells in Medicago truncatula and Other Nodulating Plants
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02016.xopenalex-snapshot
mapman : a user‐driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02245.xopenalex-snapshot
The Arabidopsis COW1 gene encodes a phosphatidylinositol transfer protein essential for root hair tip growth
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03326.xopenalex-snapshot
How to usefully compare homologous plant genes and chromosomes as DNA sequences
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03531.xopenalex-snapshot
The Medicago truncatula ortholog of Arabidopsis EIN2, sickle , is a negative regulator of symbiotic and pathogenic microbial associations
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04414.xopenalex-snapshot
Identification of legume RopGEF gene families and characterization of a Medicago truncatula RopGEF mediating polar growth of root hairs
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04415.xopenalex-snapshot
Vapyrin, a gene essential for intracellular progression of arbuscular mycorrhizal symbiosis, is also essential for infection by rhizobia in the nodule symbiosis of Medicago truncatula
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04447.xopenalex-snapshot
MtCRE1‐dependent cytokinin signaling integrates bacterial and plant cues to coordinate symbiotic nodule organogenesis in Medicago truncatula
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04810.xopenalex-snapshot
Arbuscule‐containing and non‐colonized cortical cells of mycorrhizal roots undergo extensive and specific reprogramming during arbuscular mycorrhizal development
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04859.xopenalex-snapshot
Dual involvement of a Medicago truncatula NAC transcription factor in root abiotic stress response and symbiotic nodule senescence
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03509.xopenalex-snapshot
A Medicago truncatula NADPH oxidase is involved in symbiotic nodule functioning
inferredcites →https://doi.org/10.1111/nph.12091openalex-snapshot
Medicago truncatula DNF 2 is a PI ‐ PLC ‐ XD ‐containing protein required for bacteroid persistence and prevention of nodule early senescence and defense‐like reactions
inferredcites →https://doi.org/10.1111/nph.12120openalex-snapshot
Hydrogen peroxide‐regulated genes in the Medicago truncatula–Sinorhizobium meliloti symbiosis
inferredcites →https://doi.org/10.1111/nph.14146openalex-snapshot
KNAT 3/4/5‐like class 2 KNOX transcription factors are involved in Medicago truncatula symbiotic nodule organ development
inferredcites →https://doi.org/10.1111/nph.14503openalex-snapshot
Resolution of deep eudicot phylogeny and their temporal diversification using nuclear genes from transcriptomic and genomic datasets
inferredcites →https://doi.org/10.1111/nph.16462openalex-snapshot
Medicago truncatula Phytoglobin 1.1 controls symbiotic nodulation and nitrogen fixation via the regulation of nitric oxide concentration
inferredcites →https://doi.org/10.1111/pce.13035openalex-snapshot
Medicago truncatula Zinc‐Iron Permease6 provides zinc to rhizobia‐infected nodule cells
inferredcites →https://doi.org/10.1111/ppl.12533openalex-snapshot
MtMAPKK4 is an essential gene for growth and reproduction of Medicago truncatula
inferredcites →https://doi.org/10.1111/tpj.12482openalex-snapshot
Correlation of mRNA and protein abundance in the developing maize leaf
inferredcites →https://doi.org/10.1111/tpj.12520openalex-snapshot
Lotus japonicus SUNERGOS 1 encodes a predicted subunit A of a DNA topoisomerase VI that is required for nodule differentiation and accommodation of rhizobial infection
inferredcites →https://doi.org/10.1111/tpj.13471openalex-snapshot
Diverse functions of multidrug and toxin extrusion ( MATE ) transporters in citric acid efflux and metal homeostasis in Medicago truncatula
inferredcites →https://doi.org/10.1111/tpj.14234openalex-snapshot
Mt ABCG 20 is an ABA exporter influencing root morphology and seed germination of Medicago truncatula
inferredcites →https://doi.org/10.1126/science.1090022openalex-snapshot
A Gene Expression Map of the Arabidopsis Root
inferredcites →https://doi.org/10.1126/science.1092986openalex-snapshot
Medicago truncatula DMI1 Required for Bacterial and Fungal Symbioses in Legumes
inferredcites →https://doi.org/10.1126/science.1110951openalex-snapshot
Nodulation Signaling in Legumes Requires NSP2, a Member of the GRAS Family of Transcriptional Regulators
inferredcites →https://doi.org/10.1126/science.1111025openalex-snapshot
NSP1 of the GRAS Protein Family Is Essential for Rhizobial Nod Factor-Induced Transcription
inferredcites →https://doi.org/10.1126/science.1132514openalex-snapshot
A Cytokinin Perception Mutant Colonized by Rhizobium in the Absence of Nodule Organogenesis
inferredcites →https://doi.org/10.1126/science.1184057openalex-snapshot
Plant Peptides Govern Terminal Differentiation of Bacteria in Symbiosis
inferredcites →https://doi.org/10.1126/science.1184096openalex-snapshot
A Nodule-Specific Protein Secretory Pathway Required for Nitrogen-Fixing Symbiosis
inferredcites →https://doi.org/10.1126/science.aae0109openalex-snapshot
Nuclear-localized cyclic nucleotide–gated channels mediate symbiotic calcium oscillations
inferredcites →https://doi.org/10.1126/science.aax2153openalex-snapshot
A shared gene drives lateral root development and root nodule symbiosis pathways in Lotus
inferredcites →https://doi.org/10.1186/s12859-019-2599-6openalex-snapshot
Comparative analysis of differential gene expression analysis tools for single-cell RNA sequencing data
inferredcites →https://doi.org/10.1186/s12864-019-5724-zopenalex-snapshot
Diversification of cytokinin phosphotransfer signaling genes in Medicago truncatula and other legume genomes
inferredcites →https://doi.org/10.1186/s12870-019-2194-zopenalex-snapshot
The Medicago truncatula nodule identity gene MtNOOT1 is required for coordinated apical-basal development of the root
inferredcites →https://doi.org/10.1242/dev.089631openalex-snapshot
TRICOTencodes an AMP1-related carboxypeptidase that regulates root nodule development and shoot apical meristem maintenance inLotus japonicus
inferredcites →https://doi.org/10.1242/dev.110775openalex-snapshot
Fate map of Medicago truncatula root nodules
inferredcites →https://doi.org/10.1242/dev.124.9.1781openalex-snapshot
Ethylene provides positional information on cortical cell division but is not involved in Nod factor-induced root hair tip growth in Rhizobium-legume interaction
inferredcites →https://doi.org/10.1371/journal.pgen.1004891openalex-snapshot
Local and Systemic Regulation of Plant Root System Architecture and Symbiotic Nodulation by a Receptor-Like Kinase
inferredcites →https://doi.org/10.2139/ssrn.4089544openalex-snapshot
MtPT5 phosphate transporter is involved in leaf growth and phosphate accumulation of Medicago truncatula
inferredcites →https://doi.org/10.3389/fpls.2015.00073openalex-snapshot
Genome-wide identification and expression analysis of auxin response factor gene family in Medicago truncatula
inferredcites →https://doi.org/10.3389/fpls.2016.00794openalex-snapshot
Nod Factor Effects on Root Hair-Specific Transcriptome of Medicago truncatula: Focus on Plasma Membrane Transport Systems and Reactive Oxygen Species Networks
inferredcites →https://doi.org/10.3389/fpls.2016.01240openalex-snapshot
How Auxin and Cytokinin Phytohormones Modulate Root Microbe Interactions
inferredcites →https://doi.org/10.3389/fpls.2017.00201openalex-snapshot
Interface Symbiotic Membrane Formation in Root Nodules of Medicago truncatula: the Role of Synaptotagmins MtSyt1, MtSyt2 and MtSyt3
inferredcites →https://doi.org/10.3389/fpls.2018.00304openalex-snapshot
Identification and Expression Analysis of Medicago truncatula Isopentenyl Transferase Genes (IPTs) Involved in Local and Systemic Control of Nodulation
inferredcites →https://doi.org/10.3389/fpls.2018.00923openalex-snapshot
Evolutionary History of Plant LysM Receptor Proteins Related to Root Endosymbiosis
inferredcites →https://doi.org/10.3390/agriculture8110179openalex-snapshot
Phylogeny and Expression of NADPH Oxidases during Symbiotic Nodule Formation
inferredcites →https://doi.org/10.3390/ijms17050680openalex-snapshot
Legume NADPH Oxidases Have Crucial Roles at Different Stages of Nodulation
inferredcites →https://doi.org/10.4161/psb.5.11.13358openalex-snapshot
Computational identification of root hair-specific genes in Arabidopsis
inferredcites →https://doi.org/10.4161/psb.7.1.18491openalex-snapshot
TheM. truncatula SUNNgene is expressed in vascular tissue, similarly toRDN1, consistent with the role of these nodulation regulation genes in long distance signaling
inferredcites →https://doi.org/10.5511/plantbiotechnology.17.0216aopenalex-snapshot
Expression of rice 45S rRNA promotes cell proliferation, leading to enhancement of growth in transgenic tobacco
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4480360openalex-extracted
Synergism of Vesicle Trafficking and Cytoskeleton During Regulation of Plant Growth and Development: A Mechanistic Outlook
inferred← citeshttps://doi.org/10.1007/s00344-024-11487-5openalex-snapshot
The Role of the BELL1-2 Transcription Factor in the Development of Legume-rhizobial Symbiosis
inferred← citeshttps://doi.org/10.1007/s11104-025-07689-9openalex-snapshot
An isoflavone from Medicago truncatula, methylnissolin, induces expression of Sinorhizobium meliloti nodulation genes
inferred← citeshttps://doi.org/10.1007/s11240-026-03527-7openalex-snapshot
Single-cell omics in plants: technological advances and biological insights
inferred← citeshttps://doi.org/10.1007/s11816-025-00967-zopenalex-snapshot
Recent progress in single-cell transcriptomic studies in plants
inferred← citeshttps://doi.org/10.1007/s42994-024-00190-4openalex-snapshot
Applying conventional and cell-type-specific CRISPR/Cas9 genome editing in legume plants
inferred← citeshttps://doi.org/10.1007/s42994-025-00196-6openalex-snapshot
PhytoCluster: a generative deep learning model for clustering plant single-cell RNA-seq data
inferred← citeshttps://doi.org/10.1007/s44372-025-00337-7openalex-snapshot
Exploring recent advances, limitations, and future prospects of OMICS-based technologies in plant-pathogen interaction studies: a systematic review
inferred← citeshttps://doi.org/10.1007/s44372-026-00512-4openalex-snapshot
Decoding plant complexity through spatially resolved multi-omics approaches
inferred← citeshttps://doi.org/10.1016/b978-0-443-23736-2.00001-0openalex-snapshot
An overview of single-cell high-throughput technology in plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-23736-2.00006-xopenalex-snapshot
Single-cell technology for disease-resistant plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-23736-2.00013-7openalex-snapshot
Single-cell omics to dissect molecular features in plant root development
inferred← citeshttps://doi.org/10.1016/b978-0-443-23736-2.00015-0openalex-snapshot
Annotation of single-cell clusters using marker genes within and across species
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113747openalex-snapshot
The single-cell transcriptome program of nodule development cellular lineages in Medicago truncatula
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115240openalex-snapshot
A single-cell and spatial wheat root atlas with cross-species annotations delineates conserved tissue-specific marker genes and regulators
inferred← citeshttps://doi.org/10.1016/j.chom.2023.08.019openalex-snapshot
Cell-type-specific responses to fungal infection in plants revealed by single-cell transcriptomics
inferred← citeshttps://doi.org/10.1016/j.cropd.2023.100041openalex-snapshot
Recent progresses in plant single-cell transcriptomics
inferred← citeshttps://doi.org/10.1016/j.cub.2026.05.019openalex-snapshot
Nodule development in Medicago truncatula is promoted by EPIDERMAL PATTERNING FACTOR-LIKE peptides
inferred← citeshttps://doi.org/10.1016/j.cub.2026.05.057openalex-snapshot
Decoding stage-specific symbiotic programs in the Rhizophagus irregularis-tomato interaction using single-nucleus transcriptomics
inferred← citeshttps://doi.org/10.1016/j.cub.2026.07.065openalex-snapshot
Co-option of a conserved lateral-root development program by symbiotic signals
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.02.006openalex-snapshot
snRNA-seq analysis of the moss Physcomitrium patens identifies a conserved cytokinin-ESR module promoting pluripotent stem cell identity
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e21976openalex-snapshot
RETRACTED: Synergism of vesicle trafficking and cytoskeleton during regulation of plant growth and development: A mechanistic outlook
inferred← citeshttps://doi.org/10.1016/j.molp.2022.12.023openalex-snapshot
Dissecting symbiosis cell by cell
inferred← citeshttps://doi.org/10.1016/j.molp.2024.08.003openalex-snapshot
Single-cell RNA sequencing facilitates the elucidation of the complete biosynthesis of the antidepressant hyperforin in St. John’s wort
inferred← citeshttps://doi.org/10.1016/j.molp.2024.12.015openalex-snapshot
Medicago2035: Genomes, functional genomics, and molecular breeding
inferred← citeshttps://doi.org/10.1016/j.molp.2025.02.003openalex-snapshot
A large-scale integrated transcriptomic atlas for soybean organ development
inferred← citeshttps://doi.org/10.1016/j.molp.2025.12.026openalex-snapshot
PlantscRNAdb 4.0: Improved marker identification and annotation under a cell-type uniformity for plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102378openalex-snapshot
Analysis of meristems and plant regeneration at single-cell resolution
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102444openalex-snapshot
Resolving plant development in space and time with single-cell genomics
inferred← citeshttps://doi.org/10.1016/j.pbi.2024.102597openalex-snapshot
Cellular insights into legume root infection by rhizobia
inferred← citeshttps://doi.org/10.1016/j.pbi.2025.102755openalex-snapshot
From roots to nodules: regulation of organogenesis in nitrogen-fixing symbiosis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112964openalex-snapshot
Probing cellular landscapes in plants via single-cell transcriptomics
inferred← citeshttps://doi.org/10.1016/j.tplants.2024.06.008openalex-snapshot
Unraveling plant–microbe symbioses using single-cell and spatial transcriptomics
inferred← citeshttps://doi.org/10.1016/j.tplants.2026.01.008openalex-snapshot
Toward a multiomics framework for understanding symbiotic nitrogen fixation
inferred← citeshttps://doi.org/10.1016/j.tplants.2026.03.003openalex-snapshot
Mapping plant cell-type-specific responses to environmental stresses
inferred← citeshttps://doi.org/10.1016/j.xgen.2026.101246openalex-snapshot
Toward telomere-to-telomere genomics in Fabaceae: Unlocking comparative and functional insights into symbiotic nitrogen fixation
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100631openalex-snapshot
scPlant: A versatile framework for single-cell transcriptomic data analysis in plants
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.100984openalex-snapshot
Single-cell transcriptome atlases of soybean root and mature nodule reveal new regulatory programs that control the nodulation process
inferred← citeshttps://doi.org/10.1038/s41467-023-42911-1openalex-snapshot
Single-cell analysis identifies genes facilitating rhizobium infection in Lotus japonicus
inferred← citeshttps://doi.org/10.1038/s41467-024-55755-0openalex-snapshot
Orthologous marker groups reveal broad cell identity conservation across plant single-cell transcriptomes
inferred← citeshttps://doi.org/10.1038/s41477-023-01524-8openalex-snapshot
Single-nucleus transcriptomes reveal spatiotemporal symbiotic perception and early response in Medicago
inferred← citeshttps://doi.org/10.1038/s41477-024-01666-3openalex-snapshot
Spatial co-transcriptomics reveals discrete stages of the arbuscular mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1038/s41477-025-02114-6openalex-snapshot
A mobile DELLA controls Medicago truncatula root cortex patterning to host arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1038/s41477-026-02388-4openalex-snapshot
Decoding the landscape of cell-type-specific co-expressed transcription factors in soybean
inferred← citeshttps://doi.org/10.1038/s42003-023-05156-8openalex-snapshot
Understanding plant pathogen interactions using spatial and single-cell technologies
inferred← citeshttps://doi.org/10.1038/s44318-026-00800-5openalex-snapshot
Benchmarking plant single cell RNA-sequencing sample processing strategies
inferred← citeshttps://doi.org/10.1038/s44383-025-00015-3openalex-snapshot
Inferring hypoxia-responsive regulators of cell fate in plant meristems through single-cell transcriptomics
inferred← citeshttps://doi.org/10.1073/pnas.2518288123openalex-snapshot
Nitrate-induced NLP1 SUMOylation regulates nitrate signaling and root nodulation
inferred← citeshttps://doi.org/10.1093/jxb/erae017openalex-snapshot
Unraveling the rhizobial infection thread
inferred← citeshttps://doi.org/10.1093/jxb/erae107openalex-snapshot
Single-cell transcriptomics reveals heterogeneity in plant responses to the environment: a focus on biotic and abiotic interactions
inferred← citeshttps://doi.org/10.1093/jxb/erae454openalex-snapshot
Investigating biological nitrogen fixation via single-cell transcriptomics
inferred← citeshttps://doi.org/10.1093/jxb/eraf069openalex-snapshot
Ethylene biosynthesis in legumes: gene identification and expression during early symbiotic stages
inferred← citeshttps://doi.org/10.1093/jxb/eraf175openalex-snapshot
The role of reactive oxygen, nitrogen, and sulfur species in the integration of (a)biotic stress signals in legumes
inferred← citeshttps://doi.org/10.1093/jxb/erag314openalex-snapshot
Through the looking glass: a single-cell view of plant–microbe interactions
inferred← citeshttps://doi.org/10.1093/jxb/erag367openalex-snapshot
mRNA translational control during root legume symbioses
inferred← citeshttps://doi.org/10.1093/nar/gkad706openalex-snapshot
scPlantDB: a comprehensive database for exploring cell types and markers of plant cell atlases
inferred← citeshttps://doi.org/10.1093/pcp/pcag065openalex-snapshot
The PXY receptor regulating root stele development promotes root growth and symbiotic nodulation in Medicago truncatula
inferred← citeshttps://doi.org/10.1093/plcell/koae003openalex-snapshot
Best practices for the execution, analysis, and data storage of plant single-cell/nucleus transcriptomics
inferred← citeshttps://doi.org/10.1093/plcell/koae201openalex-snapshot
Gibberellin dynamics governing nodulation revealed using GIBBERELLIN PERCEPTION SENSOR 2 in Medicago truncatula lateral organs
inferred← citeshttps://doi.org/10.1094/mpmi-03-23-0029-ropenalex-snapshot
Laser Capture Microdissection Transcriptome Reveals Spatiotemporal Tissue Gene Expression Patterns of Medicago truncatula Roots Responding to Rhizobia
inferred← citeshttps://doi.org/10.1101/2022.12.23.521739openalex-snapshot
Single-cell analysis maps distinct cellular responses to rhizobia and identifies the novel infection regulator SYMRKL1 in Lotus japonicus
inferred← citeshttps://doi.org/10.1101/2023.06.13.544787openalex-snapshot
The Single-Cell Transcriptome Program of Nodule Development Cellular Lineages in Medicago truncatula
inferred← citeshttps://doi.org/10.1101/2023.07.01.547324openalex-snapshot
Peripheral vascular strand development in nodules is controlled by a bHLH/HLH heterodimer
inferred← citeshttps://doi.org/10.1101/2023.09.09.556959openalex-snapshot
Cellular gibberellin dynamics govern indeterminate nodule development, morphology and function
inferred← citeshttps://doi.org/10.1101/2024.04.01.587592openalex-snapshot
Identification of cell-type-specific response to silicon treatment in soybean leaves through single nucleus RNA-sequencing
inferred← citeshttps://doi.org/10.1101/2024.07.31.606100openalex-snapshot
snRNA-seq analysis of the moss Physcomitrium patens reveals a conserved cytokinin-ESR module promoting pluripotent stem cell identity
inferred← citeshttps://doi.org/10.1111/jipb.13495openalex-snapshot
A high‐resolution transcriptomic atlas depicting nitrogen fixation and nodule development in soybean
inferred← citeshttps://doi.org/10.1111/nph.18759openalex-snapshot
NODULE INCEPTION activates gibberellin biosynthesis genes during rhizobial infection
inferred← citeshttps://doi.org/10.1111/nph.18948openalex-snapshot
NODULE INCEPTION: a direct regulator of gibberellin biosynthesis during symbiotic nodulation
inferred← citeshttps://doi.org/10.1111/nph.19153openalex-snapshot
Exploring the identity of individual plant cells in space and time
inferred← citeshttps://doi.org/10.1111/nph.19766openalex-snapshot
A lateral organ boundaries domain transcription factor acts downstream of the auxin response factor 2 to control nodulation and root architecture in Medicago truncatula
inferred← citeshttps://doi.org/10.1111/nph.20139openalex-snapshot
Genetic and transcriptomic analysis of the Bradyrhizobium T3SS ‐triggered nodulation in the legume Aeschynomene evenia
inferred← citeshttps://doi.org/10.1111/nph.70581openalex-snapshot
Coordination of cortex modifications in time, space, and under stress
inferred← citeshttps://doi.org/10.1111/nph.71323openalex-snapshot
Organized peripheral vascular strand development in nodules is controlled by a bHLH / HLH heterodimer
inferred← citeshttps://doi.org/10.1111/nph.71452openalex-snapshot
A recently evolved Nodulin recruited by NIN for root hair rhizobial infection in Medicago truncatula
inferred← citeshttps://doi.org/10.1111/pce.70912openalex-snapshot
Vesicle Trafficking Orchestrates Root Nodule Symbiosis
inferred← citeshttps://doi.org/10.1111/tpj.70309openalex-snapshot
Cell‐type‐specific response to silicon treatment in soybean leaves revealed by single‐nucleus RNA sequencing and targeted gene editing
inferred← citeshttps://doi.org/10.1126/sciadv.adz6873openalex-snapshot
Hooked hairs: A cellular key adaptation aiding seedling survival in nutrient-limited and drought conditions
inferred← citeshttps://doi.org/10.1186/s12870-024-05479-6openalex-snapshot
The Defective in Autoregulation (DAR) gene of Medicago truncatula encodes a protein involved in regulating nodulation and arbuscular mycorrhiza
inferred← citeshttps://doi.org/10.1186/s13059-026-04024-yopenalex-snapshot
Advances in single-cell and spatial omics for studying symbiotic nitrogen fixation: comparative cellular and evolutionary perspectives
inferred← citeshttps://doi.org/10.1186/s13062-024-00501-1openalex-snapshot
Breaking barriers: improving time and space resolution of arbuscular mycorrhizal symbiosis with single-cell sequencing approaches
inferred← citeshttps://doi.org/10.1186/s42483-025-00398-2openalex-snapshot
Spatial transcriptomics reveals the spatiotemporal response of garden asparagus stem cells to Phomopsis asparagi infection
inferred← citeshttps://doi.org/10.1186/s43897-023-00067-yopenalex-snapshot
Application of single-cell multi-omics approaches in horticulture research
inferred← citeshttps://doi.org/10.20900/cbgg20260015openalex-snapshot
Genetics Has Enabled the Improvement of Breeding Strategies: Single-Cell Analysis, Epigenetics, cis-Regulation and Gene Editing to Exploit Genetic Variants Underlying Phenotypes
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3218858/v1openalex-snapshot
Characterization of root hair curling and nodule development in soybean-rhizobia symbioses
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4618673/v1openalex-snapshot
Cell-type-specific response to silicon treatment in soybean leaves revealed by single nucleus RNA-sequencing and targeted gene-editing
inferred← citeshttps://doi.org/10.3390/cells13181561openalex-snapshot
Single-Cell Transcriptomics Applied in Plants
inferred← citeshttps://doi.org/10.3390/microorganisms14020380openalex-snapshot
Integrating Single-Cell and Spatial Multi-Omics to Decode Plant–Microbe Interactions at Cellular Resolution
inferred← citeshttps://doi.org/10.3390/plants14233615openalex-snapshot
Single-Cell Omics in Legumes: Research Trends and Applications
inferred← citeshttps://doi.org/10.3390/s24175726openalex-snapshot
Characterization of Root Hair Curling and Nodule Development in Soybean–Rhizobia Symbiosis
inferred← citeshttps://doi.org/10.34133/bdr.0029openalex-snapshot
Advances in the Application of Single-Cell Transcriptomics in Plant Systems and Synthetic Biology
inferred← citeshttps://doi.org/10.64898/2026.01.22.701092openalex-snapshot
Decoding stage-specific symbiotic programs in the Rhizophagus irregularis –tomato interaction using single-nucleus transcriptomics
inferred← citeshttps://doi.org/10.64898/2026.06.23.733685openalex-snapshot
4D spatial transcriptomics reveals nodule identity emerges through stacked parallel developmental programs
inferred← citeshttps://doi.org/10.64898/2026.09.29.755433openalex-snapshot
Single-Cell Omics to Uncover Cell-Type-Specific Gene Regulatory Networks Driving Mucilage Production in Specialized Roots
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.