On the public citation graph
The evolution of the metazoan Toll receptor family and its expression during protostome development
0 signed · 162 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known work and none has been retracted — and get a dated CiteStamped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/10.1006/dbio.1995.1134openalex-snapshot
The Drosophila Toll Gene Functions Zygotically and Is Necessary for Proper Motoneuron and Muscle Development
inferredcites →https://doi.org/10.1006/jipa.2001.5047openalex-snapshot
Chemical Defense in the Egg Masses of Benthic Invertebrates: An Assessment of Antibacterial Activity in 39 Mollusks and 4 Polychaetes
inferredcites →https://doi.org/10.1007/0-387-24180-9_2openalex-snapshot
Toll-Like Receptors: Linking Innate and Adaptive Immunity
inferredcites →https://doi.org/10.1007/s00251-004-0740-8openalex-snapshot
Identification and sequence analysis of chicken Toll-like receptors
inferredcites →https://doi.org/10.1007/s00251-007-0193-yopenalex-snapshot
Phylogenetic and expression analysis of amphibian Xenopus Toll-like receptors
inferredcites →https://doi.org/10.1007/s002510050017openalex-snapshot
Independent evolution of Toll and related genes in insects and mammals
inferredcites →https://doi.org/10.1007/s00427-019-00636-6openalex-snapshot
Embryonic expression of priapulid Wnt genes
inferredcites →https://doi.org/10.1007/s13127-016-0315-1openalex-snapshot
Transcriptome profiling of Symbion pandora (phylum Cycliophora): insights from a differential gene expression analysis
inferredcites →https://doi.org/10.1016/0092-8674(85)90274-0openalex-snapshot
Establishment of dorsal-ventral polarity in the Drosophila embryo: Genetic studies on the role of the Toll gene product
inferredcites →https://doi.org/10.1016/0092-8674(88)90516-8openalex-snapshot
The Toll gene of drosophila, required for dorsal-ventral embryonic polarity, appears to encode a transmembrane protein
inferredcites →https://doi.org/10.1016/j.aqrep.2019.100248openalex-snapshot
Immune and bacterial toxin genes expression in different giant tiger prawn, penaeus monodon post-larvae stages following AHPND-causing strain of vibrio parahaemolyticus challenge
inferredcites →https://doi.org/10.1016/j.cell.2006.02.015openalex-snapshot
Pathogen Recognition and Innate Immunity
inferredcites →https://doi.org/10.1016/j.celrep.2016.06.036openalex-snapshot
Optogenetic Control of Nodal Signaling Reveals a Temporal Pattern of Nodal Signaling Regulating Cell Fate Specification during Gastrulation
inferredcites →https://doi.org/10.1016/j.coi.2008.06.001openalex-snapshot
NOD-like receptors (NLRs): bona fide intracellular microbial sensors
inferredcites →https://doi.org/10.1016/j.cub.2018.11.042openalex-snapshot
A New Spiralian Phylogeny Places the Enigmatic Arrow Worms among Gnathiferans
inferredcites →https://doi.org/10.1016/j.cub.2019.07.012openalex-snapshot
The Taiman Transcriptional Coactivator Engages Toll Signals to Promote Apoptosis and Intertissue Invasion in Drosophila
inferredcites →https://doi.org/10.1016/j.dci.2007.01.005openalex-snapshot
Expression of immune-related genes in the oyster Crassostrea gigas during ontogenesis
inferredcites →https://doi.org/10.1016/j.dci.2007.11.004openalex-snapshot
Toll-like receptor genes (TLRs) from Capitella capitata and Helobdella robusta (Annelida)
inferredcites →https://doi.org/10.1016/j.dci.2008.10.004openalex-snapshot
Uncovering the evolutionary history of innate immunity: The simple metazoan Hydra uses epithelial cells for host defence
inferredcites →https://doi.org/10.1016/j.dci.2010.03.004openalex-snapshot
Phylogenetic and expression analysis of lamprey toll-like receptors
inferredcites →https://doi.org/10.1016/j.dci.2010.09.011openalex-snapshot
Characterization and immune function of two intracellular sensors, HmTLR1 and HmNLR, in the injured CNS of an invertebrate
inferredcites →https://doi.org/10.1016/j.dci.2012.11.011openalex-snapshot
A novel myeloid differentiation factor 88 homolog, SpMyD88, exhibiting SpToll-binding activity in the mud crab Scylla paramamosain
inferredcites →https://doi.org/10.1016/j.dci.2013.08.009openalex-snapshot
Molecular cloning and expression of TLR in the Eisenia andrei earthworm
inferredcites →https://doi.org/10.1016/j.dci.2014.06.002openalex-snapshot
TIR-domain-containing protein repertoire of nine anthozoan species reveals coral–specific expansions and uncharacterized proteins
inferredcites →https://doi.org/10.1016/j.dci.2015.04.007openalex-snapshot
A member of the Tlr family is involved in dsRNA innate immune response in Paracentrotus lividus sea urchin
inferredcites →https://doi.org/10.1016/j.dci.2017.10.016openalex-snapshot
A conserved Toll-like receptor-to-NF-κB signaling pathway in the endangered coral Orbicella faveolata
inferredcites →https://doi.org/10.1016/j.fsi.2010.07.023openalex-snapshot
Expression of immune-related genes in embryos and larvae of sea cucumber Apostichopus japonicus
inferredcites →https://doi.org/10.1016/j.fsi.2013.04.044openalex-snapshot
Immune responses during the larval stages of Mytilus galloprovincialis: Metamorphosis alters immunocompetence, body shape and behavior
inferredcites →https://doi.org/10.1016/j.fsi.2015.05.018openalex-snapshot
Immune and stress responses in oysters with insights on adaptation
inferredcites →https://doi.org/10.1016/j.fsi.2016.01.025openalex-snapshot
Identification and functional characterization of three TLR signaling pathway genes in Cyclina sinensis
inferredcites →https://doi.org/10.1016/j.fsi.2017.09.060openalex-snapshot
The TLR13-MyD88-NF-κB signalling pathway of Cyclina sinensis plays vital roles in innate immune responses
inferredcites →https://doi.org/10.1016/j.fsi.2018.10.011openalex-snapshot
Responses of Mytilus galloprovincialis to challenge with the emerging marine pathogen Vibrio coralliilyticus
inferredcites →https://doi.org/10.1016/j.fsi.2018.10.062openalex-snapshot
Transcriptome-wide identification, functional characterization, and expression analysis of two novel invertebrate-type Toll-like receptors from disk abalone (Haliotis discus discus)
inferredcites →https://doi.org/10.1016/j.jmb.2013.11.024openalex-snapshot
Toll-Like Receptors in Antiviral Innate Immunity
inferredcites →https://doi.org/10.1016/j.molimm.2003.10.001openalex-snapshot
Toll-like receptor gene family and TIR-domain adapters in Danio rerio
inferredcites →https://doi.org/10.1016/j.molimm.2009.03.022openalex-snapshot
An amphioxus TLR with dynamic embryonic expression pattern responses to pathogens and activates NF-κB pathway via MyD88
inferredcites →https://doi.org/10.1016/j.neuron.2015.02.003openalex-snapshot
Toll Receptors Instruct Axon and Dendrite Targeting and Participate in Synaptic Partner Matching in a Drosophila Olfactory Circuit
inferredcites →https://doi.org/10.1016/j.smim.2009.05.005openalex-snapshot
Modulation of adaptive immunity with Toll-like receptors
inferredcites →https://doi.org/10.1016/j.smim.2014.06.005openalex-snapshot
Innate immune system and tissue regeneration in planarians: An area ripe for exploration
inferredcites →https://doi.org/10.1016/j.vph.2015.02.007openalex-snapshot
The innate immune system, toll-like receptors and dermal wound healing: A review
inferredcites →https://doi.org/10.1016/j.ydbio.2006.08.065openalex-snapshot
The immune gene repertoire encoded in the purple sea urchin genome
inferredcites →https://doi.org/10.1016/j.ydbio.2017.11.015openalex-snapshot
A safer, urea-based in situ hybridization method improves detection of gene expression in diverse animal species
inferredcites →https://doi.org/10.1016/s0014-5793(96)01506-2openalex-snapshot
The cloning and characterization of human MyD88: a member of an IL‐1 receptor related family1
inferredcites →https://doi.org/10.1016/s0065-2776(01)78001-7openalex-snapshot
Toll-like Receptors and Innate Immunity
inferredcites →https://doi.org/10.1016/s0092-8674(00)80172-5openalex-snapshot
The Dorsoventral Regulatory Gene Cassette spätzle/Toll/cactus Controls the Potent Antifungal Response in Drosophila Adults
inferredcites →https://doi.org/10.1016/s0092-8674(01)00489-5openalex-snapshot
The LRR Proteins Capricious and Tartan Mediate Cell Interactions during DV Boundary Formation in the Drosophila Wing
inferredcites →https://doi.org/10.1016/s0145-305x(03)00030-2openalex-snapshot
The gene encoding the sea urchin complement protein, SpC3, is expressed in embryos and can be upregulated by bacteria
inferredcites →https://doi.org/10.1016/s0959-440x(01)00266-4openalex-snapshot
The leucine-rich repeat as a protein recognition motif
inferredcites →https://doi.org/10.1016/s0960-9822(01)00241-xopenalex-snapshot
A reverse genetic analysis of components of the Toll signaling pathway in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/s0962-8924(01)02004-9openalex-snapshot
Toll receptors in innate immunity
inferredcites →https://doi.org/10.1016/s0965-1748(02)00053-xopenalex-snapshot
Characterization of four Toll related genes during development and immune responses in Anopheles gambiae
inferredcites →https://doi.org/10.1016/s1097-2765(00)80136-7openalex-snapshot
MyD88 Is an Adaptor Protein in the hToll/IL-1 Receptor Family Signaling Pathways
inferredcites →https://doi.org/10.1016/s1471-4906(03)00242-4openalex-snapshot
Leucine-rich repeats and pathogen recognition in Toll-like receptors
inferredcites →https://doi.org/10.1038/311223a0openalex-snapshot
Information for the dorsal–ventral pattern of the Drosophila embryo is stored as maternal mRNA
inferredcites →https://doi.org/10.1038/35021228openalex-snapshot
Toll-like receptors in the induction of the innate immune response
inferredcites →https://doi.org/10.1038/35100529openalex-snapshot
Toll-like receptors and innate immunity
inferredcites →https://doi.org/10.1038/41131openalex-snapshot
A human homologue of the Drosophila Toll protein signals activation of adaptive immunity
inferredcites →https://doi.org/10.1038/nature11413openalex-snapshot
The oyster genome reveals stress adaptation and complexity of shell formation
inferredcites →https://doi.org/10.1038/nature11696openalex-snapshot
Insights into bilaterian evolution from three spiralian genomes
inferredcites →https://doi.org/10.1038/nature12031openalex-snapshot
The genomes of four tapeworm species reveal adaptations to parasitism
inferredcites →https://doi.org/10.1038/nature12326openalex-snapshot
Genomic evidence for ameiotic evolution in the bdelloid rotifer Adineta vaga
inferredcites →https://doi.org/10.1038/nature13400openalex-snapshot
The ctenophore genome and the evolutionary origins of neural systems
inferredcites →https://doi.org/10.1038/nature14668openalex-snapshot
The octopus genome and the evolution of cephalopod neural and morphological novelties
inferredcites →https://doi.org/10.1038/nature16520openalex-snapshot
Xenacoelomorpha is the sister group to Nephrozoa
inferredcites →https://doi.org/10.1038/nature16994openalex-snapshot
The mid-developmental transition and the evolution of animal body plans
inferredcites →https://doi.org/10.1038/nbt.3519openalex-snapshot
Near-optimal probabilistic RNA-seq quantification
inferredcites →https://doi.org/10.1038/ncb1629openalex-snapshot
Toll-like receptors modulate adult hippocampal neurogenesis
inferredcites →https://doi.org/10.1038/ncomms10507openalex-snapshot
Genomic insights into the Ixodes scapularis tick vector of Lyme disease
inferredcites →https://doi.org/10.1038/ncomms11388openalex-snapshot
Arabidopsis PROTEASOME REGULATOR1 is required for auxin-mediated suppression of proteasome activity and regulates auxin signalling
inferredcites →https://doi.org/10.1038/ncomms12808openalex-snapshot
Extremotolerant tardigrade genome and improved radiotolerance of human cultured cells by tardigrade-unique protein
inferredcites →https://doi.org/10.1038/ncomms15451openalex-snapshot
Whole genome analysis of a schistosomiasis-transmitting freshwater snail
inferredcites →https://doi.org/10.1038/ncomms6945openalex-snapshot
Quorum sensing triggers the stochastic escape of individual cells from Pseudomonas putida biofilms
inferredcites →https://doi.org/10.1038/ncomms9301openalex-snapshot
The Lingula genome provides insights into brachiopod evolution and the origin of phosphate biomineralization
inferredcites →https://doi.org/10.1038/ng.2585openalex-snapshot
Genomics of Loa loa, a Wolbachia-free filarial parasite of humans
inferredcites →https://doi.org/10.1038/ni.1863openalex-snapshot
The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors
inferredcites →https://doi.org/10.1038/ni922openalex-snapshot
The Drosophila immune system detects bacteria through specific peptidoglycan recognition
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.216openalex-snapshot
The genome of Onchocerca volvulus, agent of river blindness
inferredcites →https://doi.org/10.1038/nrg2303openalex-snapshot
Toll-like receptors — taking an evolutionary approach
inferredcites →https://doi.org/10.1038/s41559-017-0389-yopenalex-snapshot
Nemertean and phoronid genomes reveal lophotrochozoan evolution and the origin of bilaterian heads
inferredcites →https://doi.org/10.1038/s41559-019-0833-2openalex-snapshot
The genome of the jellyfish Clytia hemisphaerica and the evolution of the cnidarian life-cycle
inferredcites →https://doi.org/10.1038/srep06534openalex-snapshot
Transcriptome analysis elucidates key developmental components of bryozoan lophophore development
inferredcites →https://doi.org/10.1038/srep08693openalex-snapshot
Massive expansion and functional divergence of innate immune genes in a protostome
inferredcites →https://doi.org/10.1038/srep32387openalex-snapshot
Expression of segment polarity genes in brachiopods supports a non-segmental ancestral role of engrailed for bilaterians
inferredcites →https://doi.org/10.1073/pnas.0502272102openalex-snapshot
The evolution of vertebrate Toll-like receptors
inferredcites →https://doi.org/10.1073/pnas.0610108104openalex-snapshot
Embryo stability and vulnerability in an always changing world
inferredcites →https://doi.org/10.1073/pnas.1213110109openalex-snapshot
MyD88-deficient Hydra reveal an ancient function of TLR signaling in sensing bacterial colonizers
inferredcites →https://doi.org/10.1073/pnas.1516718112openalex-snapshot
Genome and transcriptome of the regeneration-competent flatworm, Macrostomum lignano
inferredcites →https://doi.org/10.1073/pnas.1614501114openalex-snapshot
Clustered brachiopod Hox genes are not expressed collinearly and are associated with lophotrochozoan novelties
inferredcites →https://doi.org/10.1073/pnas.1617722114openalex-snapshot
Toll-like receptor pathway evolution in deuterostomes
inferredcites →https://doi.org/10.1073/pnas.1711530114openalex-snapshot
Sea anemone model has a single Toll-like receptor that can function in pathogen detection, NF-κB signal transduction, and development
inferredcites →https://doi.org/10.1073/pnas.180130797openalex-snapshot
Toll-related receptors and the control of antimicrobial peptide expression in Drosophila
inferredcites →https://doi.org/10.1073/pnas.231471798openalex-snapshot
Drosophila MyD88 is an adapter in the Toll signaling pathway
inferredcites →https://doi.org/10.1073/pnas.94.26.14614openalex-snapshot
Drosophila host defense: Differential induction of antimicrobial peptide genes after infection by various classes of microorganisms
inferredcites →https://doi.org/10.1073/pnas.95.1.334openalex-snapshot
Large-scale temporal gene expression mapping of central nervous system development
inferredcites →https://doi.org/10.1073/pnas.95.11.5857openalex-snapshot
SMART, a simple modular architecture research tool: Identification of signaling domains
inferredcites →https://doi.org/10.1073/pnas.95.2.588openalex-snapshot
A family of human receptors structurally related to Drosophila Toll
inferredcites →https://doi.org/10.1074/jbc.m109.032433openalex-snapshot
Toll-like Receptors of the Ascidian Ciona intestinalis
inferredcites →https://doi.org/10.1074/jbc.ra118.006804openalex-snapshot
Toll family members bind multiple Spätzle proteins and activate antimicrobial peptide gene expression in Drosophila
inferredcites →https://doi.org/10.1083/jcb.200804010openalex-snapshot
Toll-like receptor 4 restricts retinal progenitor cell proliferation
inferredcites →https://doi.org/10.1083/jcb.201712113openalex-snapshot
Endosomal TLR3, TLR7, and TLR8 control neuronal morphology through different transcriptional programs
inferredcites →https://doi.org/10.1086/bblv227n2p201openalex-snapshot
Repurposed Transcriptomic Data Facilitate Discovery of Innate Immunity Toll-Like Receptor (TLR) Genes Across Lophotrochozoa
inferredcites →https://doi.org/10.1093/bioinformatics/btp348openalex-snapshot
trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses
inferredcites →https://doi.org/10.1093/bioinformatics/btu170openalex-snapshot
Trimmomatic: a flexible trimmer for Illumina sequence data
inferredcites →https://doi.org/10.1093/gbe/evz266openalex-snapshot
Evolutionary History of the Toll-Like Receptor Gene Family across Vertebrates
inferredcites →https://doi.org/10.1093/icb/icz116openalex-snapshot
Still Enigmatic: Innate Immunity in the Ctenophore Mnemiopsis leidyi
inferredcites →https://doi.org/10.1093/molbev/msl208openalex-snapshot
Toll-Like Receptors Are Part of the Innate Immune Defense System of Sponges (Demospongiae: Porifera)
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/msu143openalex-snapshot
Platyzoan Paraphyly Based on Phylogenomic Data Supports a Noncoelomate Ancestry of Spiralia
inferredcites →https://doi.org/10.1093/molbev/msu235openalex-snapshot
Phylogenomic Interrogation of Arachnida Reveals Systemic Conflicts in Phylogenetic Signal
inferredcites →https://doi.org/10.1093/molbev/msu300openalex-snapshot
IQ-TREE: A Fast and Effective Stochastic Algorithm for Estimating Maximum-Likelihood Phylogenies
inferredcites →https://doi.org/10.1093/molbev/msv093openalex-snapshot
Comparative Genomics Reveals the Origins and Diversity of Arthropod Immune Systems
inferredcites →https://doi.org/10.1093/molbev/msy050openalex-snapshot
Evolutionary Origins of Toll-like Receptor Signaling
inferredcites →https://doi.org/10.1093/nar/25.17.3389openalex-snapshot
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
inferredcites →https://doi.org/10.1093/nar/gku949openalex-snapshot
SMART: recent updates, new developments and status in 2015
inferredcites →https://doi.org/10.1101/gad.5.5.797openalex-snapshot
Dominant and recessive mutations define functional domains of Toll, a transmembrane protein required for dorsal-ventral polarity in the Drosophila embryo.
inferredcites →https://doi.org/10.1104/pp.18.00185openalex-snapshot
Out of Water: The Origin and Early Diversification of Plant R-Genes
inferredcites →https://doi.org/10.1109/gce.2010.5676129openalex-snapshot
Creating the CIPRES Science Gateway for inference of large phylogenetic trees
inferredcites →https://doi.org/10.1111/1755-0998.13157openalex-snapshot
Chromosome‐level analysis of the Crassostrea hongkongensis genome reveals extensive duplication of immune‐related genes in bivalves
inferredcites →https://doi.org/10.1111/j.0105-2896.2004.0131.xopenalex-snapshot
A Toll‐like receptor in horseshoe crabs
inferredcites →https://doi.org/10.1111/j.1525-142x.2010.00436.xopenalex-snapshot
The genome of the sponge Amphimedon queenslandica provides new perspectives into the origin of Toll‐like and interleukin 1 receptor pathways
inferredcites →https://doi.org/10.1126/science.1085536openalex-snapshot
Toll-Like Receptor Signaling Pathways
inferredcites →https://doi.org/10.1126/science.1194167openalex-snapshot
Plasticity of Animal Genome Architecture Unmasked by Rapid Evolution of a Pelagic Tunicate
inferredcites →https://doi.org/10.1126/science.1197761openalex-snapshot
The Ecoresponsive Genome of Daphnia pulex
inferredcites →https://doi.org/10.1126/science.1258236openalex-snapshot
An ancient defense system eliminates unfit cells from developing tissues during cell competition
inferredcites →https://doi.org/10.1126/stke.4012007pe46openalex-snapshot
The Functions of Plant TIR Domains
inferredcites →https://doi.org/10.1128/mcb.25.10.4200-4210.2005openalex-snapshot
Expression, Regulation, and Requirement of the Toll Transmembrane Protein during Dorsal Vessel Formation in Drosophila melanogaster
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154111openalex-snapshot
Role of Leucine-Rich Repeat Proteins in the Development and Function of Neural Circuits
inferredcites →https://doi.org/10.1146/annurev-ecolsys-120213-091627openalex-snapshot
Animal Phylogeny and Its Evolutionary Implications
inferredcites →https://doi.org/10.1146/annurev.biochem.76.060305.151318openalex-snapshot
Structure and Function of Toll Receptors and Their Ligands
inferredcites →https://doi.org/10.1177/1753425912465661openalex-snapshot
LRRfinder2.0: A webserver for the prediction of leucine-rich repeats
inferredcites →https://doi.org/10.1186/1471-2105-12-323openalex-snapshot
RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome
inferredcites →https://doi.org/10.1186/1471-2164-8-320openalex-snapshot
The extracellular Leucine-Rich Repeat superfamily; a comparative survey and analysis of evolutionary relationships and expression patterns
inferredcites →https://doi.org/10.1186/gb-2010-11-3-r25openalex-snapshot
A scaling normalization method for differential expression analysis of RNA-seq data
inferredcites →https://doi.org/10.1186/s12864-016-2493-9openalex-snapshot
Clam focal and systemic immune responses to QPX infection revealed by RNA-seq technology
inferredcites →https://doi.org/10.1186/s12864-018-5377-3openalex-snapshot
Innate immunity in the simplest animals – placozoans
inferredcites →https://doi.org/10.1186/s12864-019-5556-xopenalex-snapshot
Linear models enable powerful differential activity analysis in massively parallel reporter assays
inferredcites →https://doi.org/10.1186/s12915-014-0111-3openalex-snapshot
Dynamic response of RNA editing to temperature in Drosophila
inferredcites →https://doi.org/10.1186/s12915-015-0202-9openalex-snapshot
Horizontal gene transfer in bdelloid rotifers is ancient, ongoing and more frequent in species from desiccating habitats
inferredcites →https://doi.org/10.1186/s13227-018-0114-1openalex-snapshot
Hox gene expression in postmetamorphic juveniles of the brachiopod Terebratalia transversa
inferredcites →https://doi.org/10.1186/s13227-019-0115-8openalex-snapshot
Spatial and temporal patterns of gene expression during neurogenesis in the sea urchin Lytechinus variegatus
inferredcites →https://doi.org/10.1189/jlb.0403160openalex-snapshot
Biology of Toll receptors: lessons from insects and mammals
inferredcites →https://doi.org/10.1242/dev.120.4.885openalex-snapshot
The Drosophila 18 wheeler is required for morphogenesis and has striking similarities to Toll
inferredcites →https://doi.org/10.1242/dev.151423openalex-snapshot
Mechanisms of erythrocyte development and regeneration: implications for regenerative medicine and beyond
inferredcites →https://doi.org/10.1242/dev.156018openalex-snapshot
Toll and Toll-like receptor signalling in development
inferredcites →https://doi.org/10.1371/journal.pbio.2002266openalex-snapshot
Comparative genomics of the tardigrades Hypsibius dujardini and Ramazzottius varieornatus
inferredcites →https://doi.org/10.1371/journal.pone.0037767openalex-snapshot
Expression of Toll-Like Receptors in the Developing Brain
inferredcites →https://doi.org/10.1371/journal.pone.0076464openalex-snapshot
Characteristic and Functional Analysis of Toll-like Receptors (TLRs) in the lophotrocozoan, Crassostrea gigas, Reveals Ancient Origin of TLR-Mediated Innate Immunity
inferredcites →https://doi.org/10.1534/g3.119.400734openalex-snapshot
The Unique Antimicrobial Recognition and Signaling Pathways in Tardigrades with a Comparison Across Ecdysozoa
inferredcites →https://doi.org/10.3389/fimmu.2018.01523openalex-snapshot
Toll-Like Receptors, Associated Biological Roles, and Signaling Networks in Non-Mammals
inferredcites →https://doi.org/10.3389/fimmu.2018.02525openalex-snapshot
Characterization of the TLR Family in Branchiostoma lanceolatum and Discovery of a Novel TLR22-Like Involved in dsRNA Recognition in Amphioxus
inferredcites →https://doi.org/10.3389/fimmu.2018.02638openalex-snapshot
Role of Mechanotransduction and Tension in T Cell Function
inferredcites →https://doi.org/10.3389/fimmu.2019.00858openalex-snapshot
The Advances in Molecular and New Point-of-Care (POC) Diagnosis of Schistosomiasis Pre- and Post-praziquantel Use: In the Pursuit of More Reliable Approaches for Low Endemic and Non-endemic Areas
inferredcites →https://doi.org/10.3389/fimmu.2019.01277openalex-snapshot
Developmental and Immune Role of a Novel Multiple Cysteine Cluster TLR From Eisenia andrei Earthworms
inferredcites →https://doi.org/10.3389/fnins.2014.00272openalex-snapshot
Toll-like receptors as developmental tools that regulate neurogenesis during development: an update
inferredcites →https://doi.org/10.3389/fnins.2014.00405openalex-snapshot
A systematic framework for functional connectivity measures
inferredcites →https://doi.org/10.4049/jimmunol.1002302openalex-snapshot
The Drosophila Toll Signaling Pathway
inferredcites →https://doi.org/10.4049/jimmunol.178.1.397openalex-snapshot
Lamprey TLRs with Properties Distinct from Those of the Variable Lymphocyte Receptors
inferredcites →https://doi.org/10.7554/elife.05503openalex-snapshot
Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2022.04.26.489627openalex-snapshot
The Toll and Imd pathway, the complement system and lectins during immune response of the nemertean Lineus ruber
inferred← citeshttps://doi.org/10.5772/intechopen.1004203openalex-snapshot
Introductory Chapter: Evolution of Toll-Like Receptors
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.