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A receptor kinase gene of the LysM type is involved in legumeperception of rhizobial signals
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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/bf00247546openalex-snapshot
Nodulation and nitrogen fixation mutants of pea, Pisum sativum
inferredcites →https://doi.org/10.1007/bf00261158openalex-snapshot
Alfalfa nodulation in the absence of Rhizobium
inferredcites →https://doi.org/10.1007/s00122-002-0896-2openalex-snapshot
Mapping of the nodulation loci sym9 and sym10 of pea (Pisum sativum L.)
inferredcites →https://doi.org/10.1007/s004380050831openalex-snapshot
Symbiotic mutants deficient in nodule establishment identified after T-DNA transformation of Lotus japonicus
inferredcites →https://doi.org/10.1016/0168-9452(89)90168-4openalex-snapshot
Mutagenesis of pea (Pisum sativum L.) and the isolation of mutants for nodulation and nitrogen fixation
inferredcites →https://doi.org/10.1016/s0092-8674(02)00741-9openalex-snapshot
The Conformational Plasticity of Protein Kinases
inferredcites →https://doi.org/10.1016/s0167-4889(98)00178-5openalex-snapshot
Signal perception and transduction: the role of protein kinases
inferredcites →https://doi.org/10.1016/s1369-5266(00)00181-3openalex-snapshot
Genetics and genomics of root symbiosis
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/10.1038/351670a0openalex-snapshot
Sulphated lipo-oligosaccharide signals of Rhizobium meliloti elicit root nodule organogenesis in alfalfa
inferredcites →https://doi.org/10.1038/354125a0openalex-snapshot
A novel highly unsaturated fatty acid moiety of lipo-oligosaccharide signals determines host specificity of Rhizobium
inferredcites →https://doi.org/10.1038/nature00841openalex-snapshot
A plant receptor-like kinase required for both bacterial and fungal symbiosis
inferredcites →https://doi.org/10.1038/nature01207openalex-snapshot
Shoot control of root development and nodulation is mediated by a receptor-like kinase
inferredcites →https://doi.org/10.1038/nature02039openalex-snapshot
Plant recognition of symbiotic bacteria requires two LysM receptor-like kinases
inferredcites →https://doi.org/10.1074/jbc.m211055200openalex-snapshot
Cell Wall Attachment of a Widely Distributed Peptidoglycan Binding Domain Is Hindered by Cell Wall Constituents
inferredcites →https://doi.org/10.1093/dnares/10.3.115openalex-snapshot
Structural Analysis of a Lotus japonicus Genome. IV. Sequence Features and Mapping of Seventy-three TAC Clones Which Cover the 7.5 Mb Regions of the Genome
inferredcites →https://doi.org/10.1093/dnares/9.2.63openalex-snapshot
Structural Analysis of a Lotus japonicus Genome. II. Sequence Features and Mapping of Sixty-five TAC Clones Which Cover the 6.5-Mb Regions of the Genome
inferredcites →https://doi.org/10.1093/genetics/161.4.1673openalex-snapshot
A Genetic Linkage Map of the Model LegumeLotus japonicusand Strategies for Fast Mapping of New Loci
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111410openalex-snapshot
Non-nodulating Mutants of Pisum Sativum (L.) cv. Sparkle
inferredcites →https://doi.org/10.1094/mpmi.1998.11.7.684openalex-snapshot
Nodule Organogenesis and Symbiotic Mutants of the Model Legume Lotus japonicus
inferredcites →https://doi.org/10.1094/mpmi.1998.11.9.933openalex-snapshot
Mycorrhiza Mutants of Lotus japonicus Define Genetically Independent Steps During Symbiotic Infection
inferredcites →https://doi.org/10.1094/mpmi.2000.13.4.475openalex-snapshot
A Lotus japonicus Nodulation System Based on Heterologous Expression of the Fucosyl Transferase NodZ and the Acetyl Transferase NolL in Rhizobium leguminosarum
inferredcites →https://doi.org/10.1094/mpmi.2001.14.7.848openalex-snapshot
Responses of a Model Legume Lotus japonicus to Lipochitin Oligosaccharide Nodulation Factors Purified from Mesorhizobium loti JRL501
inferredcites →https://doi.org/10.1098/rspb.2001.1782openalex-snapshot
Evolution of the angiosperms: calibrating the family tree
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/10.1105/tpc.8.10.1885openalex-snapshot
Rhizobium Symbiosis: Nod Factors in Perspective
inferredcites →https://doi.org/10.1111/j.1365-2958.1995.tb02372.xopenalex-snapshot
Structural identification of the iipo‐chitin oligosaccharide nodulation signals of Rhizobium loti
inferredcites →https://doi.org/10.1111/j.1365-313x.1992.00487.xopenalex-snapshot
Lotus japonicus , an autogamous, diploid legume species for classical and molecular genetics
inferredcites →https://doi.org/10.1111/j.1432-1033.1991.tb16147.xopenalex-snapshot
Kluyveromyces lactis toxin has an essential chitinase activity
inferredcites →https://doi.org/10.1385/0-89603-321-x:49openalex-snapshot
Agrobacterium rhizogenes as a Vector for Transforming Higher Plants: Application in Lotus corniculatus Transformation
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/s00425-023-04251-8openalex-snapshot
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Long-Distance Control of Nodulation: Molecules and Models
inferred← citeshttps://doi.org/10.1007/s10059-012-0131-1openalex-snapshot
Plant Hormonal Regulation of Nitrogen-Fixing Nodule Organogenesis
inferred← citeshttps://doi.org/10.1007/s10265-015-0719-6openalex-snapshot
Sequence and expression analysis of putative Arachis hypogaea (peanut) Nod factor perception proteins
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/s10265-019-01126-6openalex-snapshot
An anthocyanin marker for direct visualization of plant transformation and its use to study nitrogen-fixing nodule development
inferred← citeshttps://doi.org/10.1007/s10327-007-0030-zopenalex-snapshot
A novel pathosystem to study the interactions between Lotus japonicus and Fusarium solani
inferred← citeshttps://doi.org/10.1007/s10457-019-00382-8openalex-snapshot
Regulation of nodule number by GmNORK is dependent on expression of GmNIC in soybean
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/s10725-009-9420-xopenalex-snapshot
Synthesis of four oligosaccharides derived from Paris polyphylla var. yunnanensis and their tobacco (Nicotiana tabacum L.) growth-regulatory activity
inferred← citeshttps://doi.org/10.1007/s10725-013-9814-7openalex-snapshot
A novel GRAS protein gene MtSymSCL1 plays a role in regulating nodule number in Medicago truncatula
inferred← citeshttps://doi.org/10.1007/s10725-018-0392-6openalex-snapshot
LjCOCH interplays with LjAPP1 to maintain the nodule development in Lotus japonicus
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/s11103-008-9397-2openalex-snapshot
Transposition of a 600 thousand-year-old LTR retrotransposon in the model legume Lotus japonicus
inferred← citeshttps://doi.org/10.1007/s11103-009-9585-8openalex-snapshot
Salicylic acid differentially affects suspension cell cultures of Lotus japonicus and one of its non-symbiotic mutants
inferred← citeshttps://doi.org/10.1007/s11103-013-0042-3openalex-snapshot
Splice variants of the SIP1 transcripts play a role in nodule organogenesis in Lotus japonicus
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/s11103-022-01307-3openalex-snapshot
Nod factor perception: an integrative view of molecular communication during legume symbiosis
inferred← citeshttps://doi.org/10.1007/s11104-005-0871-1openalex-snapshot
Root-based N2-fixing symbioses: Legumes, actinorhizal plants, Parasponia sp. and cycads
inferred← citeshttps://doi.org/10.1007/s11104-005-5881-5openalex-snapshot
Root-based N2-fixing Symbioses: Legumes, Actinorhizal Plants, Parasponia sp. and Cycads
inferred← citeshttps://doi.org/10.1007/s11104-025-07349-yopenalex-snapshot
Lotus japonicus CIP73 functions as a transcriptional repressor to inhibit Nodule Inception gene expression in nodule 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/s11105-016-0978-yopenalex-snapshot
Phosphoproteomic Analysis in Phaseolus vulgaris Roots Treated with Rhizobium etli Nodulation Factors
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/s11427-018-9444-9openalex-snapshot
An MAP kinase interacts with LHK1 and regulates nodule organogenesis in Lotus japonicus
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/s11434-007-0417-4openalex-snapshot
Identification of two novel nodule-specific genes from Astragalus sinicus L. by suppressive subtractive hybridization
inferred← citeshttps://doi.org/10.1007/s12010-011-9351-7openalex-snapshot
Elicitor-Induced Cellular and Molecular Events Are Responsible for Productivity Enhancement in Hairy Root Cultures: An Insight Study
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/s13199-016-0382-2openalex-snapshot
Arbuscular mycorrhiza development in pea (Pisum sativum L.) mutants impaired in five early nodulation genes including putative orthologs of NSP1 and NSP2
inferred← citeshttps://doi.org/10.1007/s13199-017-0501-8openalex-snapshot
Plant-symbiont interactions: the functional role of expansins
inferred← citeshttps://doi.org/10.1007/s13199-024-01022-1openalex-snapshot
Molecular interplay of symbiotic and defensive responses in the non-model legume Arachis hypogaea
inferred← citeshttps://doi.org/10.1007/s13258-014-0209-6openalex-snapshot
Soybean mitogen-activated protein kinase GMK2 is activated with GMK1 in Bradyrhizobium-Soybean interactions
inferred← citeshttps://doi.org/10.1007/s13562-022-00821-1openalex-snapshot
Applications and challenges of harnessing genome editing in oilseed crops
inferred← citeshttps://doi.org/10.1007/s42994-023-00129-1openalex-snapshot
Innovations in functional genomics and molecular breeding of pea: exploring advances and opportunities
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/10.1007/s42994-025-00222-7openalex-snapshot
Nodule-specific AhPUGN1.1 positively regulates nodulation in peanuts
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/b978-0-12-818469-1.00014-6openalex-snapshot
Knock, knock-let the bacteria in: enzymatic potential of plant associated bacteria
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/b978-0-323-90594-7.00002-8openalex-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/b978-0-323-90594-7.00020-xopenalex-snapshot
Phosphorylation-dependent regulation of receptor-like kinases during root nodule symbiosis (RNS)
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/bs.abr.2015.09.007openalex-snapshot
The Implications of Polyploidy for the Evolution of Signalling in Rhizobial Nodulation Symbiosis
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.2019.10.002openalex-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.agrcom.2024.100031openalex-snapshot
Is it possible to engineer nitrogen fixing nodule symbiosis?
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.2005.01.003openalex-snapshot
Elicitor signal transduction leading to production of plant secondary metabolites
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.cj.2023.03.016openalex-snapshot
GmNLP7a inhibits soybean nodulation by interacting with GmNIN1a
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.copbio.2013.08.006openalex-snapshot
Biotechnological solutions to the nitrogen problem
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.cub.2003.11.047openalex-snapshot
Rhizobium Symbiosis: Insight into Nod Factor Receptors
inferred← citeshttps://doi.org/10.1016/j.cub.2013.12.053openalex-snapshot
Cleavage of the SYMBIOSIS RECEPTOR-LIKE KINASE Ectodomain Promotes Complex Formation with Nod Factor Receptor 5
inferred← citeshttps://doi.org/10.1016/j.cub.2019.11.038openalex-snapshot
LCO Receptors Involved in Arbuscular Mycorrhiza Are Functional for Rhizobia Perception in Legumes
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.2022.08.069openalex-snapshot
Arbuscular mycorrhizal fungi induce lateral root development in angiosperms via a conserved set of MAMP receptors
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.2023.07.068openalex-snapshot
LysM-mediated signaling in Marchantia polymorpha highlights the conservation of pattern-triggered immunity in land 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.cub.2025.07.032openalex-snapshot
The sucrose transporter GmSWEET3c drives soybean nodulation by regulating root sucrose allocation
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.gene.2006.05.016openalex-snapshot
Genome-wide comparative analyses of domain organisation of repertoires of protein kinases of Arabidopsis thaliana and Oryza sativa
inferred← citeshttps://doi.org/10.1016/j.gene.2007.07.009openalex-snapshot
Multiple receptor-like kinase cDNAs from liverwort Marchantia polymorpha and two charophycean green algae, Closterium ehrenbergii and Nitella axillaris: Extensive gene duplications and gene shufflings in the early evolution of streptophytes
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