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LysM Domain Receptor Kinases Regulating Rhizobial Nod Factor-Induced Infection
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jmbi.2000.3778openalex-snapshot
The structure of a LysM domain from E. coli membrane-bound lytic murein transglycosylase D (MltD) 1 1Edited by P. E. Wight
inferredcites →https://doi.org/10.1007/bf02184279openalex-snapshot
Host genes inPisum sativum L. conferring resistance to EuropeanRhizobium leguminosarum strains
inferredcites →https://doi.org/10.1016/s1360-1385(00)01810-0openalex-snapshot
Perception of lipo-chitooligosaccharidic Nod factors in legumes
inferredcites →https://doi.org/10.1016/s1369-5266(03)00006-2openalex-snapshot
Legume genomes: more than peas in a pod
inferredcites →https://doi.org/10.1023/a:1016085523752openalex-snapshot
Microsynteny between pea and Medicago truncatula in the SYM2 region
inferredcites →https://doi.org/10.1038/344781a0openalex-snapshot
Symbiotic host-specificity of Rhizobium meliloti is determined by a sulphated and acylated glucosamine oligosaccharide signal
inferredcites →https://doi.org/10.1038/nature00842openalex-snapshot
A receptor kinase gene regulating symbiotic nodule development
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01149.xopenalex-snapshot
Evidence for structurally specific negative feedback in the Nod factor signal transduction pathway
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01743.xopenalex-snapshot
The NFP locus of Medicago truncatula controls an early step of Nod factor signal transduction upstream of a rapid calcium flux and root hair deformation
inferredcites →https://doi.org/10.1073/pnas.060034297openalex-snapshot
Specific and heritable genetic interference by double-stranded RNA in Arabidopsis thaliana
inferredcites →https://doi.org/10.1094/mpmi.2000.13.7.754openalex-snapshot
Entry of Rhizobium leguminosarum bv. viciae into Root Hairs Requires Minimal Nod Factor Specificity, but Subsequent Infection Thread Growth Requires nodO or nodE
inferredcites →https://doi.org/10.1094/mpmi.2001.14.6.695openalex-snapshot
Agrobacterium rhizogenes -Transformed Roots of Medicago truncatula for the Study of Nitrogen-Fixing and Endomycorrhizal Symbiotic Associations
inferredcites →https://doi.org/10.1104/pp.115.2.351openalex-snapshot
Sym2 of Pea Is Involved in a Nodulation Factor-Perception Mechanism That Controls the Infection Process in the Epidermis
inferredcites →https://doi.org/10.1104/pp.123.2.439openalex-snapshot
TargetingInducedLocalLesionsIN Genomes (TILLING) for Plant Functional Genomics
inferredcites →https://doi.org/10.1105/tpc.002451openalex-snapshot
RhizobiumNod Factor Perception and Signalling
inferredcites →https://doi.org/10.1105/tpc.10.5.781openalex-snapshot
The Sex-Inducing Pheromone and Wounding Trigger the Same Set of Genes in the Multicellular Green Alga Volvox
inferredcites →https://doi.org/10.1105/tpc.6.10.1357openalex-snapshot
Rhizobium meliloti lipooligosaccharide nodulation factors: different structural requirements for bacterial entry into target root hair cells and induction of plant symbiotic developmental responses.
inferredcites →https://doi.org/10.1111/j.1365-2958.1993.tb01961.xopenalex-snapshot
Resistance to nodulation of cv. Afghanistan peas is overcome by nodX, which mediates an O‐acetylation of the Rhizobium leguminosarum lipo‐oligosaccharide nodulation factor
inferredcites →https://doi.org/10.1128/jb.180.19.5183-5191.1998openalex-snapshot
Succinoglycan Is Required for Initiation and Elongation of Infection Threads during Nodulation of Alfalfa by Rhizobium meliloti
inferredcites →https://doi.org/10.1128/jb.184.24.7042-7046.2002openalex-snapshot
Analysis of Infection Thread Development Using Gfp- and DsRed-Expressing Sinorhizobium meliloti
inferredcites →https://doi.org/10.1242/dev.128.9.1507openalex-snapshot
The HCL gene of Medicago truncatula controls Rhizobium-induced root hair curling
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.5091071openalex-extracted
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inferred← citeshttps://doi.org/10.1002/0470869143.kc027openalex-snapshot
Genetics and Genomics of Nodulation and Symbiotic Nitrogen Fixation
inferred← citeshttps://doi.org/10.1002/1873-3468.12191openalex-snapshot
LYR 3, a high‐affinity LCO ‐binding protein of Medicago truncatula , interacts with LYK 3, a key symbiotic receptor
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inferred← citeshttps://doi.org/10.1002/9780470959404.ch16openalex-snapshot
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The Path of Rhizobia: From a Free‐living Soil Bacterium to Root Nodulation
inferred← citeshttps://doi.org/10.1002/9780470960707.ch20openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118297674.ch45openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119409144.ch38openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119409144.ch57openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119409144.ch58openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119409144.ch66openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119409144.ch71openalex-snapshot
Features of Sinorhizobium meliloti exopolysaccharide succinoglycan required for successful invasion of Medicago truncatula nodules
inferred← citeshttps://doi.org/10.1002/9781119409144.ch72openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/1-4020-3570-5_39openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/7089_2008_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/7089_2008_6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4020-3548-7_6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-43275-5_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-540-74543-3_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-540-79405-9_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-540-79405-9_6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-13145-5_5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-23044-8_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-23044-8_6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-23047-9_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-27515-9_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-32463-5_14openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-39317-4_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-662-49880-4_27openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-90-481-9479-7_5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-13-5767-1_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-99-8220-2_6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00018-011-0651-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-010-1493-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00239-004-0221-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00344-022-10830-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00344-025-11833-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-004-1397-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-006-0268-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-018-2944-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-021-03789-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-023-04090-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00709-013-0589-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10059-012-0131-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10265-019-01122-wopenalex-snapshot
ERN1 and CYCLOPS coordinately activate NIN signaling to promote infection thread formation in Lotus japonicus
inferred← citeshttps://doi.org/10.1007/s10535-009-0085-0openalex-snapshot
A mutation affecting symbiosis in the pea line Risnod27 changes the ion selectivity filter of the DMI1 homolog
inferred← citeshttps://doi.org/10.1007/s10719-015-9609-3openalex-snapshot
Lipo-chitooligosaccharidic nodulation factors and their perception by plant receptors
inferred← citeshttps://doi.org/10.1007/s11032-012-9780-1openalex-snapshot
Identifying quantitative trait loci for symbiotic nitrogen fixation capacity and related traits in common bean
inferred← citeshttps://doi.org/10.1007/s11032-013-9985-yopenalex-snapshot
Fine mapping of the Rj4 locus, a gene controlling nodulation specificity in soybean
inferred← citeshttps://doi.org/10.1007/s11103-005-8102-yopenalex-snapshot
The Medicago truncatula SUNN Gene Encodes a CLV1-like Leucine-rich Repeat Receptor Kinase that Regulates Nodule Number and Root Length
inferred← citeshttps://doi.org/10.1007/s11103-019-00857-3openalex-snapshot
Quantitative phosphoproteomic analyses provide evidence for extensive phosphorylation of regulatory proteins in the rhizobia–legume 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/s11105-019-01188-9openalex-snapshot
Expression of the Legume-Specific Nod Factor Receptor Proteins Alters Developmental and Immune Responses in Rice
inferred← citeshttps://doi.org/10.1007/s11248-026-00490-zopenalex-snapshot
CRISPR/Cas9-mediated knockout of PsLykX gene of pea (Pisum sativum L.) leads to loss of symbiotic nodules
inferred← citeshttps://doi.org/10.1007/s11427-016-0115-2openalex-snapshot
Plant pattern-recognition receptors controlling innate immunity
inferred← citeshttps://doi.org/10.1007/s11427-019-1608-7openalex-snapshot
Rhizobial infection triggers systemic transport of endogenous RNAs between shoots and roots in soybean
inferred← citeshttps://doi.org/10.1007/s11427-025-2978-xopenalex-snapshot
MtLICK1/2: gatekeepers of symbiosis and immunity in Medicago truncatula
inferred← citeshttps://doi.org/10.1007/s11434-006-2093-1openalex-snapshot
Identification of genes induced during Medicago sativa nodule development by using the cDNA-AFLP technique
inferred← citeshttps://doi.org/10.1007/s12223-024-01220-wopenalex-snapshot
Macronutrients-availing microbiomes: biodiversity, mechanisms, and biotechnological applications for agricultural sustainability
inferred← citeshttps://doi.org/10.1007/s12298-017-0471-6openalex-snapshot
Genome scanning for identification and mapping of receptor-like kinase (RLK) gene superfamily in Solanum tuberosum
inferred← citeshttps://doi.org/10.1007/s13199-009-0009-yopenalex-snapshot
Piriformospora indica, a cultivable root endophyte with multiple biotechnological applications
inferred← citeshttps://doi.org/10.1007/s13213-010-0117-1openalex-snapshot
Soil beneficial bacteria and their role in plant growth promotion: a review
inferred← citeshttps://doi.org/10.1007/s42994-024-00193-1openalex-snapshot
Enacting partner specificity in legume–rhizobia symbioses
inferred← citeshttps://doi.org/10.1007/s42994-025-00208-5openalex-snapshot
Harnessing omics to decode the mechanisms of symbiotic nitrogen fixation
inferred← citeshttps://doi.org/10.1016/b978-0-08-047514-1.50018-4openalex-snapshot
BIOLOGICAL N INPUTS
inferred← citeshttps://doi.org/10.1016/b978-0-12-384986-1.00011-9openalex-snapshot
Nitrogen fixation enables plants to use the nitrogen of the air for growth
inferred← citeshttps://doi.org/10.1016/b978-0-12-415955-6.00015-3openalex-snapshot
Biological N Inputs
inferred← citeshttps://doi.org/10.1016/b978-0-12-815355-0.00003-5openalex-snapshot
Nod factor signaling in legume-Rhizobium symbiosis: Specificity and molecular genetics of nod factor signaling
inferred← citeshttps://doi.org/10.1016/b978-0-240-52118-3.00010-7openalex-snapshot
Modifications of Glycans and Glycoconjugates
inferred← citeshttps://doi.org/10.1016/b978-0-323-85193-0.00013-9openalex-snapshot
Rhizobium: Eco-friendly microbes for global food security
inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00002-8openalex-snapshot
Structural and functional analysis of lysin motif receptor-like kinases in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00005-3openalex-snapshot
An overview of receptor-like kinases in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-90613-5.00020-0openalex-snapshot
Plant transcription factors and nodule development
inferred← citeshttps://doi.org/10.1016/b978-0-323-91734-6.00019-3openalex-snapshot
Molecular genetics of arbuscular mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00022-1openalex-snapshot
Regulation of receptors and receptor-like kinases in nitrogen fixation by plants
inferred← citeshttps://doi.org/10.1016/b978-0-444-63987-5.00006-2openalex-snapshot
Innate Immunity Engaged or Disengaged in Plant-Microbe Interactions ☆
inferred← citeshttps://doi.org/10.1016/b978-012088391-2/50012-2openalex-snapshot
Nitrogen fixation enables the nitrogen in the air to be used for plant growth
inferred← citeshttps://doi.org/10.1016/bs.abr.2016.11.003openalex-snapshot
Commonalities in Symbiotic Plant-Microbe Signalling
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.09.007openalex-snapshot
Rhizobia infection, a journey to the inside of plant cells
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.09.009openalex-snapshot
Nodule diversity, evolution, organogenesis and identity
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.10.002openalex-snapshot
Nod factor signaling in symbiotic nodulation
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2015.01.004openalex-snapshot
Leguminous Plants: Inventors of Root Nodules to Accommodate Symbiotic Bacteria
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2017.03.010openalex-snapshot
Use of CRISPR/Cas9 for Symbiotic Nitrogen Fixation Research in Legumes
inferred← citeshttps://doi.org/10.1016/j.abiote.2026.100042openalex-snapshot
Coordination of PTI and ETI in legume–rhizobium mutualism
inferred← citeshttps://doi.org/10.1016/j.apsoil.2014.08.010openalex-snapshot
Signal molecules and cell-surface components involved in early stages of the legume–rhizobium interactions
inferred← citeshttps://doi.org/10.1016/j.bbagen.2005.04.004openalex-snapshot
Evidence for lectin activity of a plant receptor-like protein kinase by application of neoglycoproteins and bioinformatic algorithms
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2023.108263openalex-snapshot
Cytoskeleton as a roadmap navigating rhizobia to establish symbiotic root nodulation in legumes
inferred← citeshttps://doi.org/10.1016/j.cell.2024.12.024openalex-snapshot
A pair of LysM receptors mediates symbiosis and immunity discrimination in Marchantia
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.chom.2025.06.009openalex-snapshot
Networks of the symbiosis-immunity continuum in plants
inferred← citeshttps://doi.org/10.1016/j.chom.2026.01.001openalex-snapshot
Evolution of root nodule symbiosis via paleopolyploidy and modular pathway rewiring
inferred← citeshttps://doi.org/10.1016/j.cj.2026.06.015openalex-snapshot
Reprogramming, not silencing: How plant immunity is gated during legume nodulation
inferred← citeshttps://doi.org/10.1016/j.crmicr.2024.100333openalex-snapshot
Plant-microbe interactions: PGPM as microbial inoculants/biofertilizers for sustaining crop productivity and soil fertility
inferred← citeshttps://doi.org/10.1016/j.csbj.2025.06.029openalex-snapshot
Predicting receptor-ligand pairing preferences in plant-microbe interfaces via molecular dynamics and machine learning
inferred← citeshttps://doi.org/10.1016/j.cub.2003.11.047openalex-snapshot
Rhizobium Symbiosis: Insight into Nod Factor Receptors
inferred← citeshttps://doi.org/10.1016/j.cub.2009.01.054openalex-snapshot
AvrPtoB Targets the LysM Receptor Kinase CERK1 to Promote Bacterial Virulence on Plants
inferred← citeshttps://doi.org/10.1016/j.cub.2020.08.011openalex-snapshot
Developmental Modulation of Root Cell Wall Architecture Confers Resistance to an Oomycete Pathogen
inferred← citeshttps://doi.org/10.1016/j.cub.2021.06.011openalex-snapshot
Nod factor receptor complex phosphorylates GmGEF2 to stimulate ROP signaling during nodulation
inferred← citeshttps://doi.org/10.1016/j.cub.2023.04.053openalex-snapshot
Diversity and regulation of symbiotic nitrogen fixation in plants
inferred← citeshttps://doi.org/10.1016/j.cub.2024.03.015openalex-snapshot
A receptor required for chitin perception facilitates arbuscular mycorrhizal associations and distinguishes root symbiosis from immunity
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.114248openalex-snapshot
Transcriptomic and physiological analyses unravel the effect and mechanism of halosulfuron-methyl on the symbiosis between rhizobium and soybean
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104999openalex-snapshot
Genome-wide identification, expression, and characterization of CaLysM-RLKs in chickpea root nodule symbiosis
inferred← citeshttps://doi.org/10.1016/j.fcr.2009.03.014openalex-snapshot
Model legumes contribute to faba bean breeding
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.11.005openalex-snapshot
Antifungal activities of LysM-domain multimers and their fusion chitinases
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.133436openalex-snapshot
The role of GmHSP23.9 in regulating soybean nodulation under elevated CO2 condition
inferred← citeshttps://doi.org/10.1016/j.ijmm.2019.04.004openalex-snapshot
Interplay of plant glycan hydrolases and LysM proteins in plant—Bacteria interactions
inferred← citeshttps://doi.org/10.1016/j.isci.2020.100825openalex-snapshot
The NMN Module Conducts Nodule Number Orchestra
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110207openalex-snapshot
Comparative genomic and transcriptomic analyses provide new insight into symbiotic host specificity
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.09.008openalex-snapshot
Genetic innovations underlying the evolution of root nodule symbiosis in Leguminosae
inferred← citeshttps://doi.org/10.1016/j.jplph.2006.12.005openalex-snapshot
Nodulation deficiency caused by fast neutron mutagenesis of the model legume Lotus japonicus
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153543openalex-snapshot
Role of hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase 1 in nodule development of soybean
inferred← citeshttps://doi.org/10.1016/j.jprot.2010.07.004openalex-snapshot
Medicago truncatula proteomics
inferred← citeshttps://doi.org/10.1016/j.micinf.2011.07.010openalex-snapshot
The role of chitin detection in plant–pathogen interactions
inferred← citeshttps://doi.org/10.1016/j.micres.2023.127451openalex-snapshot
RNA-Seq analysis of mung bean (Vigna radiata L.) roots shows differential gene expression and predicts regulatory pathways responding to taxonomically different rhizobia
inferred← citeshttps://doi.org/10.1016/j.molp.2015.03.010openalex-snapshot
Rhizobium Lipo-chitooligosaccharide Signaling Triggers Accumulation of Cytokinins in Medicago truncatula Roots
inferred← citeshttps://doi.org/10.1016/j.molp.2019.10.015openalex-snapshot
A LysM Receptor Heteromer Mediates Perception of Arbuscular Mycorrhizal Symbiotic Signal in Rice
inferred← citeshttps://doi.org/10.1016/j.molp.2021.02.006openalex-snapshot
Nuclear phylotranscriptomics and phylogenomics support numerous polyploidization events and hypotheses for the evolution of rhizobial nitrogen-fixing symbiosis in Fabaceae
inferred← citeshttps://doi.org/10.1016/j.molp.2023.12.005openalex-snapshot
Immunobiodiversity: Conserved and specific immunity across land plants and beyond
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