review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1093/GLYCOB/12.6.79R |
P698 | PubMed publication ID | 12107077 |
P2093 | author name string | Marcelle Holsters | |
Wim D'Haeze | |||
P2860 | cites work | Studying early nodulin gene ENOD40 expression and induction by nodulation factor and cytokinin in transgenic alfalfa | Q24601180 |
Rhizobial Nodulation Factors Stimulate Mycorrhizal Colonization of Nodulating and Nonnodulating Soybeans | Q24671541 | ||
Srchi24, a chitinase homolog lacking an essential glutamic acid residue for hydrolytic activity, is induced during nodule development on Sesbania rostrata | Q28351049 | ||
Solvent-dependent conformational behaviour of lipochitoligosaccharides related to Nod factors | Q30582496 | ||
Methylotrophic Methylobacterium bacteria nodulate and fix nitrogen in symbiosis with legumes | Q30620816 | ||
Nod factor-induced phosphatidic acid and diacylglycerol pyrophosphate formation: a role for phospholipase C and D in root hair deformation. | Q31908638 | ||
Srchi13, a novel early nodulin from Sesbania rostrata, is related to acidic class III chitinases | Q32060552 | ||
Induction of pre-infection thread structures in the leguminous host plant by mitogenic lipo-oligosaccharides of Rhizobium | Q33344538 | ||
Recent advances in the study of nod factor perception and signal transduction | Q33703195 | ||
Molecular basis of symbiotic promiscuity | Q33855261 | ||
Differential expression of eight chitinase genes in Medicago truncatula roots during mycorrhiza formation, nodulation, and pathogen infection | Q33907753 | ||
Genetic analysis of calcium spiking responses in nodulation mutants of Medicago truncatula | Q33925318 | ||
Unusual methyl-branched alpha,beta-unsaturated acyl chain substitutions in the Nod Factors of an arctic rhizobium, Mesorhizobium sp. strain N33 (Oxytropis arctobia). | Q33948040 | ||
Keys to symbiotic harmony | Q33994648 | ||
Perception of lipo-chitooligosaccharidic Nod factors in legumes | Q34133514 | ||
The Medicago Genome Initiative: a model legume database | Q34318534 | ||
Expression of the early nodulin, ENOD40, in soybean roots in response to various lipo-chitin signal molecules | Q34392624 | ||
Synthesis of "Nod"-like chitin oligosaccharides by the Xenopus developmental protein DG42 | Q34448625 | ||
Nodulation of legumes by members of the beta-subclass of Proteobacteria. | Q34515943 | ||
Perception of Rhizobium nodulation factors by tomato cells and inactivation by root chitinases | Q35098965 | ||
Ligand specificity of a high-affinity binding site for lipo-chitooligosaccharidic Nod factors in Medicago cell suspension cultures. | Q35137267 | ||
Rhizobial lipo-oligosaccharides: answers and questions | Q35593020 | ||
Sinorhizobium teranga bv. acaciae ORS1073 and Rhizobium sp. strain ORS1001, two distantly related Acacia-nodulating strains, produce similar Nod factors that are O carbamoylated, N methylated, and mainly sulfated | Q35623070 | ||
nodZ, a unique host-specific nodulation gene, is involved in the fucosylation of the lipooligosaccharide nodulation signal of Bradyrhizobium japonicum | Q36104994 | ||
Three unusual modifications, a D-arabinosyl, an N-methyl, and a carbamoyl group, are present on the Nod factors of Azorhizobium caulinodans strain ORS571 | Q36113574 | ||
An important developmental role for oligosaccharides during early embryogenesis of cyprinid fish | Q36299202 | ||
A nod factor binding lectin with apyrase activity from legume roots | Q36373519 | ||
Wild type Rhizobium etli, a bean symbiont, produces acetyl-fucosylated, N-methylated, and carbamoylated nodulation factors | Q36719716 | ||
Rhizobium meliloti produces a family of sulfated lipooligosaccharides exhibiting different degrees of plant host specificity | Q36763558 | ||
Rhizobium lipo-chitooligosaccharide nodulation factors: signaling molecules mediating recognition and morphogenesis | Q36820158 | ||
Microspectroscopic imaging of nodulation factor-binding sites on living Vicia sativa roots using a novel bioactive fluorescent nodulation factor | Q36857568 | ||
A 2-O-methylfucose moiety is present in the lipo-oligosaccharide nodulation signal of Bradyrhizobium japonicum | Q37209846 | ||
Dissection of nodulation signaling using pea mutants defective for calcium spiking induced by nod factors and chitin oligomers. | Q37297190 | ||
Homologs of the Xenopus developmental gene DG42 are present in zebrafish and mouse and are involved in the synthesis of Nod-like chitin oligosaccharides during early embryogenesis | Q37597054 | ||
Sugar-binding activity of pea (Pisum sativum) lectin is essential for heterologous infection of transgenic white clover hairy roots by Rhizobium leguminosarum biovar viciae | Q38289767 | ||
Characterization of a binding site for chemically synthesized lipo-oligosaccharidic NodRm factors in particulate fractions prepared from roots | Q38299357 | ||
Heterologous rhizobial lipochitin oligosaccharides and chitin oligomers induce cortical cell divisions in red clover roots, transformed with the pea lectin gene | Q38314679 | ||
Nod factor requirements for efficient stem and root nodulation of the tropical legume Sesbania rostrata. | Q38959295 | ||
Broad-host-range Rhizobium species strain NGR234 secretes a family of carbamoylated, and fucosylated, nodulation signals that are O-acetylated or sulphated | Q39368865 | ||
Bradyrhizobium sp. Strains that nodulate the leguminous tree Acacia albida produce fucosylated and partially sulfated nod factors | Q39488453 | ||
Plant chitinases | Q40860512 | ||
A Nod factor-binding lectin is a member of a distinct class of apyrases that may be unique to the legumes | Q41695598 | ||
Nod factors modulate the concentration of cytosolic free calcium differently in growing and non-growing root hairs of Medicago sativa L. | Q42475888 | ||
Rhizobium sp. BR816 produces a complex mixture of known and novel lipochitooligosaccharide molecules. | Q42648739 | ||
Nod factors of Rhizobium are a key to the legume door | Q43549417 | ||
Responses of a model legume Lotus japonicus to lipochitin oligosaccharide nodulation factors purified from Mesorhizobium loti JRL501. | Q43661714 | ||
Rhizobium meliloti lipooligosaccharide nodulation factors: different structural requirements for bacterial entry into target root hair cells and induction of plant symbiotic developmental responses | Q44868690 | ||
Lotus corniculatus nodulation specificity is changed by the presence of a soybean lectin gene | Q46019805 | ||
Sugar-binding activity of pea lectin enhances heterologous infection of transgenic alfalfa plants by Rhizobium leguminosarum biovar viciae | Q46086869 | ||
Calcium spiking in plant root hairs responding to Rhizobium nodulation signals | Q46129099 | ||
Localization of a Nod factor-binding protein in legume roots and factors influencing its distribution and expression | Q46566943 | ||
Differential expression of two soybean apyrases, one of which is an early nodulin | Q47820422 | ||
Novel branched nod factor structure results from alpha-(1-->3) fucosyl transferase activity: the major lipo-chitin oligosaccharides from Mesorhizobium loti strain NZP2213 bear an alpha-(1-->3) fucosyl substituent on a nonterminal backbone residue. | Q47943063 | ||
The early nodulin gene MtN6 is a novel marker for events preceding infection of Medicago truncatula roots by Sinorhizobium meliloti | Q47958732 | ||
Comparison of characteristics of the nodX genes from various Rhizobium leguminosarum strains | Q47983143 | ||
The Medicago truncatula MtAnn1 gene encoding an annexin is induced by Nod factors and during the symbiotic interaction with Rhizobium meliloti | Q48013264 | ||
Transient induction of a peroxidase gene in Medicago truncatula precedes infection by Rhizobium meliloti | Q48076514 | ||
A third highly conserved group 1 Lea gene from Arabidopsis thaliana L. | Q48078577 | ||
Rhizobium meliloti elicits transient expression of the early nodulin gene ENOD12 in the differentiating root epidermis of transgenic alfalfa. | Q48154298 | ||
The ENOD12 gene product is involved in the infection process during the pea-Rhizobium interaction | Q48277001 | ||
Nod factors of Azorhizobium caulinodans strain ORS571 can be glycosylated with an arabinosyl group, a fucosyl group, or both. | Q49173563 | ||
Four genes of Medicago truncatula controlling components of a nod factor transduction pathway. | Q52164977 | ||
Rhizobium nod factor signaling. Evidence for a g protein-mediated transduction mechanism | Q52187227 | ||
Rhizobium meliloti Nod factors elicit cell-specific transcription of the ENOD12 gene in transgenic alfalfa. | Q52215499 | ||
Resistance to nodulation of cv. Afghanistan peas is overcome by nodX, which mediates an O-acetylation of the Rhizobium leguminosarum lipo-oligosaccharide nodulation factor. | Q54230563 | ||
Lipochito-oligosaccharides re-initiate root hair tip growth in Vicia sativa with high calcium and spectrin-like antigen at the tip | Q57463584 | ||
Oscillation, activation, expression | Q59053716 | ||
A novel highly unsaturated fatty acid moiety of lipo-oligosaccharide signals determines host specificity of Rhizobium | Q59060597 | ||
Symbiotic host-specificity of Rhizobium meliloti is determined by a sulphated and acylated glucosamine oligosaccharide signal | Q59086169 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 79R-105R | |
P577 | publication date | 2002-06-01 | |
P1433 | published in | Glycobiology | Q5572596 |
P1476 | title | Nod factor structures, responses, and perception during initiation of nodule development | |
P478 | volume | 12 |
Q46835256 | 3-hydroxy-3-methylglutaryl coenzyme a reductase 1 interacts with NORK and is crucial for nodulation in Medicago truncatula. |
Q36113073 | A Proteomic Approach to Lipo-Chitooligosaccharide and Thuricin 17 Effects on Soybean GerminationUnstressed and Salt Stress |
Q39734920 | A Rhizobium leguminosarum AcpXL mutant produces lipopolysaccharide lacking 27-hydroxyoctacosanoic acid. |
Q57630125 | A Unique Bicyclic Monosaccharide from the Bradyrhizobium Lipopolysaccharide and Its Role in the Molecular Interaction with Plants |
Q58494536 | A Unique Bicyclic Monosaccharide from the Bradyrhizobium Lipopolysaccharide and Its Role in the Molecular Interaction with Plants |
Q38918829 | A comparative study of phase States of the peribacteroid membrane from yellow lupin and broad bean nodules |
Q79799027 | A nonsymbiotic root hair tip growth phenotype in NORK-mutated legumes: implications for nodulation factor-induced signaling and formation of a multifaceted root hair pocket for bacteria |
Q48081789 | A novel ankyrin-repeat membrane protein, IGN1, is required for persistence of nitrogen-fixing symbiosis in root nodules of Lotus japonicus |
Q30363736 | A structural and biochemical model of processive chitin synthesis |
Q64281128 | A subcompatible rhizobium strain reveals infection duality in Lotus |
Q38969951 | A symbiotic plant peroxidase involved in bacterial invasion of the tropical legume Sesbania rostrata. |
Q84598494 | A ubiquitin ligase of symbiosis receptor kinase involved in nodule organogenesis |
Q48077708 | AP2-ERF transcription factors mediate Nod factor dependent Mt ENOD11 activation in root hairs via a novel cis-regulatory motif. |
Q43011040 | Activation of a mitogen-activated protein kinase pathway in Arabidopsis by chitin |
Q46418156 | Arabidopsis E3 ubiquitin ligase PLANT U-BOX13 (PUB13) regulates chitin receptor LYSIN MOTIF RECEPTOR KINASE5 (LYK5) protein abundance |
Q38841605 | Bacterial Molecular Signals in the Sinorhizobium fredii-Soybean Symbiosis |
Q38936714 | Biological roles of glycans |
Q38931523 | Calcium spiking patterns and the role of the calcium/calmodulin-dependent kinase CCaMK in lateral root base nodulation of Sesbania rostrata. |
Q34163644 | Changes in soybean global gene expression after application of lipo-chitooligosaccharide from Bradyrhizobium japonicum under sub-optimal temperature |
Q48145529 | Changes in the Common Bean Transcriptome in Response to Secreted and Surface Signal Molecules of Rhizobium etli. |
Q38356492 | Characterization of the lipid linkage region and chain length of the cellubiuronic acid capsule of Streptococcus pneumoniae |
Q37773167 | Chitooligosaccharide sensing and downstream signaling: contrasted outcomes in pathogenic and beneficial plant-microbe interactions. |
Q49211760 | Co-inoculation of a Pea Core-Collection with Diverse Rhizobial Strains Shows Competitiveness for Nodulation and Efficiency of Nitrogen Fixation Are Distinct traits in the Interaction. |
Q41005158 | Combined genetic and transcriptomic analysis reveals three major signalling pathways activated by Myc-LCOs in Medicago truncatula |
Q37301783 | Comparative genome-wide transcriptional profiling of Azorhizobium caulinodans ORS571 grown under free-living and symbiotic conditions |
Q37508139 | Comparative genomics of aeschynomene symbionts: insights into the ecological lifestyle of nod-independent photosynthetic bradyrhizobia. |
Q38931526 | Comparative transcriptome analysis reveals common and specific tags for root hair and crack-entry invasion in Sesbania rostrata. |
Q52370764 | Compatibility between Legumes and Rhizobia for the Establishment of a Successful Nitrogen-Fixing Symbiosis. |
Q34075407 | Contribution of NFP LysM domains to the recognition of Nod factors during the Medicago truncatula/Sinorhizobium meliloti symbiosis |
Q26823296 | Does plant immunity play a critical role during initiation of the legume-rhizobium symbiosis? |
Q36978239 | Early interactions between legumes and rhizobia: disclosing complexity in a molecular dialogue |
Q40863412 | Effect of lipo-chitooligosaccharide on early growth of C4 grass seedlings |
Q37929516 | Evolutionary origin of rhizobium Nod factor signaling |
Q90631760 | Experimental Evolution of Legume Symbionts: What Have We Learnt? |
Q40221621 | From chitin to bioactive chitooligosaccharides and conjugates: access to lipochitooligosaccharides and the TMG-chitotriomycin. |
Q42685347 | Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza. |
Q43765035 | Galega orientalis is more diverse than Galega officinalis in Caucasus--whole-genome AFLP analysis and phylogenetics of symbiosis-related genes. |
Q36010336 | Genetic Diversity and Symbiotic Phenotype of Hairy Vetch Rhizobia in Japan. |
Q55100994 | Genetic and Molecular Mechanisms Underlying Symbiotic Specificity in Legume-Rhizobium Interactions. |
Q42001064 | Genetic and metabolic divergence within a Rhizobium leguminosarum bv. trifolii population recovered from clover nodules. |
Q35191881 | Genome sequencing of two Neorhizobium galegae strains reveals a noeT gene responsible for the unusual acetylation of the nodulation factors. |
Q38417146 | Green leaf volatiles: biosynthesis, biological functions and their applications in biotechnology |
Q42292824 | High yield production of Rhizobium NodB chitin deacetylase and its use for in vitro synthesis of lipo-chitinoligosaccharide precursors. |
Q90617332 | Homocitrate Synthase Genes of Two Wide-Host-Range Bradyrhizobium Strains are Differently Required for Symbiosis Depending on Host Plants |
Q33346588 | Initiation of a legume nodule with an indeterminate meristem involves proliferating host cells that harbour infection threads |
Q52054670 | Invasion of Lotus japonicus root hairless 1 by Mesorhizobium loti involves the nodulation factor-dependent induction of root hairs. |
Q34764528 | Lipo-chitin oligosaccharides, plant symbiosis signalling molecules that modulate mammalian angiogenesis in vitro |
Q38297290 | Lipo-chitooligosaccharidic nodulation factors and their perception by plant receptors. |
Q38276753 | Lipochitooligosaccharide recognition: an ancient story |
Q33851172 | Lipopolysaccharides as a communication signal for progression of legume endosymbiosis |
Q36013398 | LysM domains mediate lipochitin-oligosaccharide recognition and Nfr genes extend the symbiotic host range. |
Q34646548 | MALDI mass spectrometry-assisted molecular imaging of metabolites during nitrogen fixation in the Medicago truncatula-Sinorhizobium meliloti symbiosis |
Q36277865 | Maize growth promotion by inoculation with Azospirillum brasilense and metabolites of Rhizobium tropici enriched on lipo-chitooligosaccharides (LCOs). |
Q27684487 | Molecular basis for bacterial peptidoglycan recognition by LysM domains |
Q37317014 | Molecular determinants of a symbiotic chronic infection. |
Q33849625 | NMR and molecular modeling reveal key structural features of synthetic nodulation factors |
Q37912247 | Never too many? How legumes control nodule numbers. |
Q28821042 | New insights into Nod factor biosynthesis: Analyses of chitooligomers and lipo-chitooligomers of Rhizobium sp. IRBG74 mutants |
Q38715176 | Nice to meet you: genetic, epigenetic and metabolic controls of plant perception of beneficial associative and endophytic diazotrophic bacteria in non-leguminous plants |
Q33359338 | Nod factor receptors form heteromeric complexes and are essential for intracellular infection in medicago nodules |
Q33243022 | O-Acetylation of the terminal N-acetylglucosamine of the lipooligosaccharide inner core in Neisseria meningitidis. Influence on inner core structure and assembly. |
Q50611348 | Pretreatment of clover seeds with nod factors improves growth and nodulation of Trifolium pratense. |
Q38301504 | Production and chitinase-binding ability of lipo-chitopentaose nodulation factor |
Q34958373 | Quorum sensing in nitrogen-fixing rhizobia |
Q36161677 | Reactive oxygen species and ethylene play a positive role in lateral root base nodulation of a semiaquatic legume |
Q52838163 | Rhizobial Nod factors are required for cortical cell division in the nodule morphogenetic programme of the Aeschynomeneae legume Arachis. |
Q39500894 | Rhizobial factors required for stem nodule maturation and maintenance in Sesbania rostrata-Azorhizobium caulinodans ORS571 symbiosis |
Q33281586 | Rhizobium etli CE3 bacteroid lipopolysaccharides are structurally similar but not identical to those produced by cultured CE3 bacteria |
Q41984527 | Role of nodD gene product and flavonoid interactions in induction of nodulation genes in Mesorhizobium ciceri |
Q46199019 | Search for nodulation-related CLE genes in the genome of Glycine max. |
Q52820104 | Segregation of nod-containing and nod-deficient bradyrhizobia as endosymbionts of Arachis hypogaea and as endophytes of Oryza sativa in intercropped fields of Bengal Basin, India. |
Q58034636 | Signaling Interactions During Nodule Development |
Q38175424 | Signaling events during initiation of arbuscular mycorrhizal symbiosis |
Q28761537 | Signals and Responses: Choreographing the Complex Interaction between Legumes and alpha- and beta-Rhizobia |
Q41897365 | Soybean Lectin Enhances Biofilm Formation by Bradyrhizobium japonicum in the Absence of Plants |
Q44073146 | Splice variants of the SIP1 transcripts play a role in nodule organogenesis in Lotus japonicus. |
Q33900614 | SrSymRK, a plant receptor essential for symbiosome formation |
Q42687439 | Studies on lipid A isolated from Phyllobacterium trifolii PETP02T lipopolysaccharide |
Q24657872 | SymRK defines a common genetic basis for plant root endosymbioses with arbuscular mycorrhiza fungi, rhizobia, and Frankiabacteria |
Q46876216 | Symbiont shift towards Rhizobium nodulation in a group of phylogenetically related Phaseolus species |
Q38206827 | Symbiosomes: temporary moonlighting organelles |
Q40709100 | Symbiotic activity of pea (Pisum sativum) after application of Nod factors under field conditions |
Q50948320 | Synthesis of Bradyrhizose Oligosaccharides Relevant to the Bradyrhizobium O-Antigen. |
Q57630116 | Synthesis of bradyrhizose, a unique inositol-fused monosaccharide relevant to a Nod-factor independent nitrogen fixation |
Q30017388 | The Absence of the N-acyl-homoserine-lactone Autoinducer Synthase Genes traI and ngrI Increases the Copy Number of the Symbiotic Plasmid in Sinorhizobium fredii NGR234 |
Q38317326 | The DMI1 and DMI2 early symbiotic genes of medicago truncatula are required for a high-affinity nodulation factor-binding site associated to a particulate fraction of roots |
Q36597948 | The biology of the Gaucher cell: the cradle of human chitinases. |
Q46795450 | The genistein stimulon of Bradyrhizobium japonicum. |
Q21093358 | The genome of the versatile nitrogen fixer Azorhizobium caulinodans ORS571 |
Q24600421 | The nodulation of alfalfa by the acid-tolerant Rhizobium sp. strain LPU83 does not require sulfated forms of lipochitooligosaccharide nodulation signals |
Q38225515 | The plant RWP-RK transcription factors: key regulators of nitrogen responses and of gametophyte development |
Q38328075 | The relative orientation of the lipid and carbohydrate moieties of lipochitooligosaccharides related to nodulation factors depends on lipid chain saturation |
Q42126934 | The rkp-1 cluster is required for secretion of Kdo homopolymeric capsular polysaccharide in Sinorhizobium meliloti strain Rm1021. |
Q46723393 | The symbiotic ion channel homolog DMI1 is localized in the nuclear membrane of Medicago truncatula roots. |
Q48364954 | Transcriptomic Studies of the Effect of nod Gene-Inducing Molecules in Rhizobia: Different Weapons, One Purpose. |
Q37473314 | Unprecedented glycosidase activity at a lectin carbohydrate-binding site exemplified by the cyanobacterial lectin MVL. |
Q33741202 | Uracil DNA glycosylase (UDG) activities in Bradyrhizobium diazoefficiens: characterization of a new class of UDG with broad substrate specificity |
Q64067154 | Use of Plasmid pVMG to Make Transcriptional ß-Glucuronidase Reporter Gene Fusions in the Genome for Monitoring the Expression of Rhizobial Genes In Vivo |
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