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Neuropeptidomics of the Carpenter Ant Camponotus floridanus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.20571openalex-snapshot
Social behavior and the evolution of neuropeptide genes: lessons from the honeybee genome
inferredcites →https://doi.org/10.1002/cne.22405openalex-snapshot
Multiple neuropeptides in the Drosophila antennal lobe suggest complex modulatory circuits
inferredcites →https://doi.org/10.1002/cne.22745openalex-snapshot
Toward a single‐cell‐based analysis of neuropeptide expression in Periplaneta americana antennal lobe neurons
inferredcites →https://doi.org/10.1002/cne.23399openalex-snapshot
Neuropeptidome of Tribolium castaneum antennal lobes and mushroom bodies
inferredcites →https://doi.org/10.1002/cne.23434openalex-snapshot
Neuropeptides in the antennal lobe of the yellow fever mosquito, Aedes aegypti
inferredcites →https://doi.org/10.1002/dneu.20785openalex-snapshot
Visual experience and age affect synaptic organization in the mushroom bodies of the desert ant Cataglyphis fortis
inferredcites →https://doi.org/10.1002/dneu.20982openalex-snapshot
Visual experience affects both behavioral and neuronal aspects in the individual life history of the desert ant Cataglyphis fortis
inferredcites →https://doi.org/10.1002/dneu.22195openalex-snapshot
Light exposure leads to reorganization of microglomeruli in the mushroom bodies and influences juvenile hormone levels in the honeybee
inferredcites →https://doi.org/10.1006/jmbi.1997.0951openalex-snapshot
Prediction of complete gene structures in human genomic DNA
inferredcites →https://doi.org/10.1007/978-1-60761-535-4_10openalex-snapshot
Direct Peptide Profiling of Brain Tissue by MALDI-TOF Mass Spectrometry
inferredcites →https://doi.org/10.1007/bf02223405openalex-snapshot
Observations sur la structure du système nerveux céphalique (cerveau, masse sous-œsophagienne et complexe rétro-cérébral) de la fourmiAphænogaster senilis (Mayr, 1853) (Hymenoptera myrmicinæ)
inferredcites →https://doi.org/10.1007/s00018-006-6187-3openalex-snapshot
Biology of the CAPA peptides in insects
inferredcites →https://doi.org/10.1007/s00040-013-0314-6openalex-snapshot
Systemic gene knockdown in Camponotus floridanus workers by feeding of dsRNA
inferredcites →https://doi.org/10.1007/s00441-008-0721-6openalex-snapshot
PBAN/pyrokinin peptides in the central nervous system of the fire ant, Solenopsis invicta
inferredcites →https://doi.org/10.1016/0020-7322(80)90020-3openalex-snapshot
Ultrastructure des organes retrocerebraux de Lasius niger l. (Hymenoptera : Formicidae)
inferredcites →https://doi.org/10.1016/c2010-0-66490-xopenalex-snapshot
Handbook of Biologically Active Peptides
inferredcites →https://doi.org/10.1016/j.cub.2014.01.018openalex-snapshot
The Genome of the Clonal Raider Ant Cerapachys biroi
inferredcites →https://doi.org/10.1016/j.euprot.2014.02.007openalex-snapshot
Peptidomics and processing of regulatory peptides in the fruit fly Drosophila
inferredcites →https://doi.org/10.1016/j.febslet.2014.04.028openalex-snapshot
Identification of a novel insect neuropeptide, CNMa and its receptor
inferredcites →https://doi.org/10.1016/j.ibmb.2009.06.001openalex-snapshot
Peptidomic survey of the locust neuroendocrine system
inferredcites →https://doi.org/10.1016/j.jinsphys.2012.06.005openalex-snapshot
Phenotypic impacts of PBAN RNA interference in an ant, Solenopsis invicta, and a moth, Helicoverpa zea
inferredcites →https://doi.org/10.1016/j.neuron.2005.08.004openalex-snapshot
Social Circuits: Peptidergic Regulation of Mammalian Social Behavior
inferredcites →https://doi.org/10.1016/j.neuron.2013.12.017openalex-snapshot
A Systematic Nomenclature for the Insect Brain
inferredcites →https://doi.org/10.1016/j.npep.2013.10.008openalex-snapshot
The social brain: Neurobiological basis of affiliative behaviours and psychological well-being
inferredcites →https://doi.org/10.1016/j.peptides.2012.02.019openalex-snapshot
Allatotropin, leucokinin and AKH in honey bees and other Hymenoptera
inferredcites →https://doi.org/10.1016/j.pneurobio.2010.04.010openalex-snapshot
Drosophila neuropeptides in regulation of physiology and behavior
inferredcites →https://doi.org/10.1016/s0022-1910(02)00205-6openalex-snapshot
Juvenile hormone and circadian locomotor activity in the honey bee Apis mellifera
inferredcites →https://doi.org/10.1016/s0168-9525(00)02024-2openalex-snapshot
EMBOSS: The European Molecular Biology Open Software Suite
inferredcites →https://doi.org/10.1016/s0925-4773(02)00175-2openalex-snapshot
The Drosophila hugin gene codes for myostimulatory and ecdysis-modifying neuropeptides
inferredcites →https://doi.org/10.1016/s0959-4388(00)00146-xopenalex-snapshot
Neuropeptides and the evolution of social behavior
inferredcites →https://doi.org/10.1021/pr100570jopenalex-snapshot
Genomics and Peptidomics of Neuropeptides and Protein Hormones Present in the Parasitic Wasp Nasonia vitripennis
inferredcites →https://doi.org/10.1021/pr101116gopenalex-snapshot
Peptidomics and Peptide Hormone Processing in theDrosophilaMidgut
inferredcites →https://doi.org/10.1021/pr500224bopenalex-snapshot
MALDI Imaging Analysis of Neuropeptides in the Africanized Honeybee (Apis mellifera) Brain: Effect of Ontogeny
inferredcites →https://doi.org/10.1038/nmeth.1701openalex-snapshot
SignalP 4.0: discriminating signal peptides from transmembrane regions
inferredcites →https://doi.org/10.1038/nprot.2007.261openalex-snapshot
Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips
inferredcites →https://doi.org/10.1093/nar/gkh379openalex-snapshot
AUGUSTUS: a web server for gene finding in eukaryotes
inferredcites →https://doi.org/10.1093/nar/gkl161openalex-snapshot
NeuroPred: a tool to predict cleavage sites in neuropeptide precursors and provide the masses of the resulting peptides
inferredcites →https://doi.org/10.1093/nar/gkq1145openalex-snapshot
Hymenoptera Genome Database: integrated community resources for insect species of the order Hymenoptera
inferredcites →https://doi.org/10.1101/gr.121392.111openalex-snapshot
The genome of the leaf-cutting ant Acromyrmex echinatior suggests key adaptations to advanced social life and fungus farming
inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06361.xopenalex-snapshot
Conservation of the function counts: homologous neurons express sequence‐related neuropeptides that originate from different genes
inferredcites →https://doi.org/10.1126/science.1124128openalex-snapshot
From the Genome to the Proteome: Uncovering Peptides in the Apis Brain
inferredcites →https://doi.org/10.1126/science.1192428openalex-snapshot
Genomic Comparison of the Ants Camponotus floridanus and Harpegnathos saltator
inferredcites →https://doi.org/10.1159/000092309openalex-snapshot
Environment- and Age-Dependent Plasticity of Synaptic Complexes in the Mushroom Bodies of Honeybee Queens
inferredcites →https://doi.org/10.1159/000356091openalex-snapshot
Biogenic Amines and Collective Organization in a Superorganism: Neuromodulation of Social Behavior in Ants
inferredcites →https://doi.org/10.1186/gb-2013-14-7-212openalex-snapshot
Ant genomics sheds light on the molecular regulation of social organization
inferredcites →https://doi.org/10.1242/jeb.00261openalex-snapshot
Conservation of ecdysis-triggering hormone signalling in insects
inferredcites →https://doi.org/10.1242/jeb.061499openalex-snapshot
IRS and TOR nutrient-signaling pathways act via juvenile hormone to influence honey bee caste fate
inferredcites →https://doi.org/10.1242/jeb.199.9.2011openalex-snapshot
Age-Dependent and Task-Related Morphological Changes in the Brain and The Mushroom Bodies of The Ant Camponotus Floridanus
inferredcites →https://doi.org/10.1371/journal.pone.0050400openalex-snapshot
Ant Trail Pheromone Biosynthesis Is Triggered by a Neuropeptide Hormone
inferredcites →https://doi.org/10.1371/journal.pone.0094274openalex-snapshot
Identification and Expression of Capa Gene in the Fire Ant, Solenopsis invicta
inferredcites →https://doi.org/10.4161/fly.4749openalex-snapshot
Comparative Neuroanatomy and Genomics ofhuginand Pheromone Biosynthesis Activating Neuropeptide (PBAN)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.25849/myrmecol.news_029:001openalex-extracted
Neuroplasticity in desert ants (Hymenoptera: Formicidae) – importance for the ontogeny of navigation
inferred← citeshttps://doi.org/10.1002/arch.21625openalex-snapshot
Genome‐wide characterization and transcriptomic analyses of neuropeptides and their receptors in an endoparasitoid wasp, Pteromalus puparum
inferred← citeshttps://doi.org/10.1002/cne.24109openalex-snapshot
Neuropeptides in the desert ant Cataglyphis fortis: Mass spectrometric analysis, localization, and age‐related changes
inferred← citeshttps://doi.org/10.1002/cne.24310openalex-snapshot
Distribution of tachykinin‐related peptides in the brain of the tobacco budworm Heliothis virescens
inferred← citeshttps://doi.org/10.1007/s00441-020-03329-zopenalex-snapshot
Plasticity and modulation of olfactory circuits in insects
inferred← citeshttps://doi.org/10.1016/bs.aiip.2015.07.001openalex-snapshot
The PRXamide Neuropeptide Signalling System
inferred← citeshttps://doi.org/10.1016/j.cbd.2021.100882openalex-snapshot
Coordinated transcriptomics and peptidomics of central nervous system identify neuropeptides and their G protein-coupled receptors in the oriental fruit moth Grapholita molesta
inferred← citeshttps://doi.org/10.1016/j.cell.2017.07.014openalex-snapshot
The Neuropeptide Corazonin Controls Social Behavior and Caste Identity in Ants
inferred← citeshttps://doi.org/10.1016/j.cois.2023.101119openalex-snapshot
Neuropeptide regulations on behavioral plasticity in social insects
inferred← citeshttps://doi.org/10.1016/j.ibmb.2025.104347openalex-snapshot
Neuropeptide profiling of Bombus terrestris (Hymenoptera, Apidae) and comparative analysis across hymenopteran species
inferred← citeshttps://doi.org/10.1016/j.ygcen.2018.12.008openalex-snapshot
GPCR annotation, G proteins, and transcriptomics of fire ant (Solenopsis invicta) queen and worker brain: An improved view of signaling in an invasive superorganism
inferred← citeshttps://doi.org/10.1021/acs.analchem.8b04304openalex-snapshot
Enhanced Coverage of Insect Neuropeptides in Tissue Sections by an Optimized Mass-Spectrometry-Imaging Protocol
inferred← citeshttps://doi.org/10.1021/acs.jproteome.2c00363openalex-snapshot
NeuroPpred-SVM: A New Model for Predicting Neuropeptides Based on Embeddings of BERT
inferred← citeshttps://doi.org/10.1021/acs.jproteome.7b00779openalex-snapshot
Mating-Induced Differential Peptidomics of Neuropeptides and Protein Hormones in Agrotis ipsilon Moths
inferred← citeshttps://doi.org/10.1038/ncomms14225openalex-snapshot
Ethological principles predict the neuropeptides co-opted to influence parenting
inferred← citeshttps://doi.org/10.1038/s41586-026-10747-6openalex-snapshot
Ancient feeding-related neuropeptides regulate alloparenting in ants
inferred← citeshttps://doi.org/10.1111/1744-7917.13264openalex-snapshot
Genomics, transcriptomics, and peptidomics of the greater wax moth Galleria mellonella neuropeptides and their expression in response to lead stress
inferred← citeshttps://doi.org/10.1111/jnc.15346openalex-snapshot
Transcriptomic, peptidomic, and mass spectrometry imaging analysis of the brain in the ant Cataglyphis nodus
inferred← citeshttps://doi.org/10.1242/jeb.151167openalex-snapshot
New techniques, applications and perspectives in neuropeptide research
inferred← citeshttps://doi.org/10.1371/journal.pone.0193561openalex-snapshot
In silico prediction of neuropeptides in Hymenoptera parasitoid wasps
inferred← citeshttps://doi.org/10.3389/fendo.2020.00640openalex-snapshot
Identification and Characterization of Neuropeptides and Their G Protein-Coupled Receptors (GPCRs) in the Cowpea Aphid Aphis craccivora
inferred← citeshttps://doi.org/10.3389/fphys.2019.00767openalex-snapshot
Novel Lom-dh Genes Play Potential Role in Promoting Egg Diapause of Locusta migratoria L.
inferred← citeshttps://doi.org/10.3389/fphys.2020.575655openalex-snapshot
Identification of Neuropeptides and Their Receptors in the Ectoparasitoid, Habrobracon hebetor
inferred← citeshttps://doi.org/10.3390/insects14040386openalex-snapshot
The Role of Biogenic Amines in Social Insects: With a Special Focus on Ants
inferred← citeshttps://doi.org/10.7287/peerj.7144v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Coleoptera genome and transcriptome sequences reveal numerous differences in neuropeptide signaling between species (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7144v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Coleoptera genome and transcriptome sequences reveal numerous differences in neuropeptide signaling between species (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7144v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Coleoptera genome and transcriptome sequences reveal numerous differences in neuropeptide signaling between species (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7144v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Coleoptera genome and transcriptome sequences reveal numerous differences in neuropeptide signaling between species (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.7144v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Coleoptera genome and transcriptome sequences reveal numerous differences in neuropeptide signaling between species (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.7144v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Coleoptera genome and transcriptome sequences reveal numerous differences in neuropeptide signaling between species (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.7144openalex-snapshot
Coleoptera genome and transcriptome sequences reveal numerous differences in neuropeptide signaling between species
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