The DOI matches its Crossref record; 791 of the 791 references it cites were found in a registry or an index.
Recent advances in neuropeptide signaling in Drosophila, from genes to physiology and behavior
Abstract
This review focuses on neuropeptides and peptide hormones, the largest and most diverse class of neuroactive substances, known in Drosophila and other animals to play roles in almost all aspects of daily life, as w;1;ell as in developmental processes. We provide an update on novel neuropeptides and receptors identified in the last decade, and highlight progress in analysis of neuropeptide signaling in Drosophila. Especially exciting is the huge amount of work published on novel functions of neuropeptides and peptide hormones in Drosophila, largely due to the rapid developments of powerful genetic methods, imaging techniques and innovative assays. We critically discuss the roles of peptides in olfaction, taste, foraging, feeding, clock function/sleep, aggression, mating/reproduction, learning and other behaviors, as well as in regulation of development, growth, metabolic and water homeostasis, stress responses, fecundity, and lifespan. We furthermore provide novel information on neuropeptide distribution and organization of peptidergic systems, as well as the phylogenetic relations between Drosophila neuropeptides and those of other phyla, including mammals. As will be shown, neuropeptide signaling is phylogenetically ancient, and not only are the structures of the peptides, precursors and receptors conserved over evolution, but also many functions of neuropeptide signaling in physiology and behavior.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
Brand, A. H., & Perrimon, N. (1993) · Development · doi:10.1242/dev.118.2.401 · Cited by 9,612
The Genome Sequence of Drosophila melanogaster
Adams, M. D., Celniker, S. E., Holt, R. A., Evans, C. A., Gocayne, J. D., Amanatides, P. G., Scherer, S. E., Li, P. W., Hoskins, R. A., Galle, R. F., et al. (2000) · Science · doi:10.1126/science.287.5461.2185 · Cited by 5,929
A C. elegans mutant that lives twice as long as wild type
Kenyon, C., Chang, J., Gensch, E., Rudner, A., & Tabtiang, R. (1993) · Nature · doi:10.1038/366461a0 · Cited by 3,387
Extending Healthy Life Span—From Yeast to Humans
Fontana, L., Partridge, L., & Longo, V. D. (2010) · Science · doi:10.1126/science.1172539 · Cited by 3,023
A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila
Dietzl, G., Chen, D., Schnorrer, F., Su, K.-C., Barinova, Y., Fellner, M., Gasser, B., Kinsey, K., Oppel, S., Scheiblauer, S., et al. (2007) · Nature · doi:10.1038/nature05954 · Cited by 2,644
Lee, T., & Luo, L. (1999) · Neuron · doi:10.1016/s0896-6273(00)80701-1 · Cited by 2,571
Comprehensive Molecular Insect Science
(2026) · Elsevier eBooks · doi:10.1016/c2021-1-02770-5 · Cited by 1,701
Tatar, M., Kopelman, A., Epstein, D., Tu, M.-P., Yin, C.-M., & Garofalo, R. S. (2001) · Science · doi:10.1126/science.1057987 · Cited by 1,628
Pharmacology, physiology, and mechanisms of incretin hormone action.
Campbell, J. E., & Drucker, D. J. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.04.008 · Cited by 1,500
The developmental transcriptome of Drosophila melanogaster
Graveley, B. R., Brooks, A. N., Carlson, J. W., Duff, M. O., Landolin, J. M., Yang, L., Artieri, C. G., van Baren, M. J., Boley, N., Booth, B. W., et al. (2011) · Nature · doi:10.1038/nature09715 · Cited by 1,484
Research works printed but not linked: 509
- Abdel-latief, 2010, Neuropeptide regulators of the juvenile hormone biosynthesis (in vitro) in the beetle, Tenebrio molitor (Coleoptera, Tenebrionidae), Arch. Insect Biochem. Physiol., 74, 135, 10.1002/arch.20359 · doi:10.1002/arch.20359
- Audsley, 2015, G protein coupled receptors as targets for next generation pesticides, Insect. Biochem. Mol., 67, 27, 10.1016/j.ibmb.2015.07.014 · doi:10.1016/j.ibmb.2015.07.014
- Audsley, 2009, Neuropeptides associated with the regulation of feeding in insects, Gen. Comp. Endocrinol., 162, 93, 10.1016/j.ygcen.2008.08.003 · doi:10.1016/j.ygcen.2008.08.003
- Audsley, 2013, Characterisation and tissue distribution of the PISCF allatostatin receptor in the red flour beetle, Tribolium castaneum, Insect. Biochem. Mol. Biol., 43, 65, 10.1016/j.ibmb.2012.09.007 · doi:10.1016/j.ibmb.2012.09.007
- Bendena, 2012, Families of allatoregulator sequences: a 2011 perspective, Can. J. Zool. Rev. Can. Zool., 90, 521, 10.1139/z2012-012 · doi:10.1139/z2012-012
- Berridge, 1967, Fine-structural changes in relation to ion and water transport in the rectal papillae of the blowfly, Calliphora, J. Cell Sci., 2, 89, 10.1242/jcs.2.1.89 · doi:10.1242/jcs.2.1.89
- Boureme, 1987, Production and characterization of antibodies to neuroparsins A and B isolated from the corpora cardiaca of the locust, Gen. Comp. Endocrinol., 67, 169, 10.1016/0016-6480(87)90145-6 · doi:10.1016/0016-6480(87)90145-6
- Brown, 2001, Distribution of ovary ecdysteroidogenic hormone I in the nervous system and gut of mosquitoes, J. Insect Sci., 1, 3, 10.1673/031.001.0301 · doi:10.1673/031.001.0301
- Cabrero, 2013, A biogenic amine and a neuropeptide act identically: tyramine signals through calcium in Drosophila tubule stellate cells, Proc. Biol. Sci., 280
- Chang, 2009, Receptor guanylyl cyclases in Inka cells targeted by eclosion hormone, Proc. Natl. Acad. Sci. U S A, 106, 13371, 10.1073/pnas.0812593106 · doi:10.1073/pnas.0812593106
- Chintapalli, 2012, Functional correlates of positional and gender-specific renal asymmetry in Drosophila, PLoS ONE, 7, e32577, 10.1371/journal.pone.0032577 · DOI
- Christie, 2008, Identification of putative crustacean neuropeptides using in silico analyses of publicly accessible expressed sequence tags, Gen. Comp. Endocrinol., 156, 246, 10.1016/j.ygcen.2008.01.018 · doi:10.1016/j.ygcen.2008.01.018
- Chung, 2017, Drosophila neuropeptide F signaling independently regulates feeding and sleep–wake behavior, Cell Rep., 19, 2441, 10.1016/j.celrep.2017.05.085 · doi:10.1016/j.celrep.2017.05.085
- Claeys, 2003, cDNA cloning and transcript distribution of two novel members of the neuroparsin family in the desert locust, Schistocerca gregaria, Insect. Mol. Biol., 12, 473, 10.1046/j.1365-2583.2003.00431.x · doi:10.1046/j.1365-2583.2003.00431.x
- Coast, 2007, The endocrine control of salt balance in insects, Gen. Comp. Endocrinol., 152, 332, 10.1016/j.ygcen.2007.02.018 · doi:10.1016/j.ygcen.2007.02.018
- Coast, 2009, Neuroendocrine control of ionic homeostasis in blood-sucking insects, J. Exp. Biol., 212, 378, 10.1242/jeb.024109 · doi:10.1242/jeb.024109
- Coast, 2011, Toward a consensus nomenclature for insect neuropeptides and peptide hormones, Peptides, 32, 620, 10.1016/j.peptides.2010.11.006 · doi:10.1016/j.peptides.2010.11.006
- Corl, 2005, Insulin signaling in the nervous system regulates ethanol intoxication in Drosophila melanogaster, Nat. Neurosci., 8, 18, 10.1038/nn1363 · doi:10.1038/nn1363
- Davis, 1992, Vasopressin-immunoreactive neurons and neurohemal systems in cockroaches and mantids, J. Comp. Neurol., 320, 381, 10.1002/cne.903200309 · doi:10.1002/cne.903200309
- Dewey, 2004, Identification of the gene encoding bursicon, an insect neuropeptide responsible for cuticle sclerotization and wing spreading, Curr. Biol., 14, 1208, 10.1016/j.cub.2004.06.051 · doi:10.1016/j.cub.2004.06.051
- Dow, 2006, The Malpighian tubule: rapid insights from post-genomic biology, J. Insect. Physiol., 52, 365, 10.1016/j.jinsphys.2005.10.007 · doi:10.1016/j.jinsphys.2005.10.007
- Downer, 2007, Insect satiety: sulfakinin localization and the effect of drosulfakinin on protein and carbohydrate ingestion in the blow fly, Phormia regina (Diptera: Calliphoridae), J. Insect. Physiol., 53, 106, 10.1016/j.jinsphys.2006.10.013 · doi:10.1016/j.jinsphys.2006.10.013
- Drummond-Barbosa, 2004, Alpha-endosulfine, a potential regulator of insulin secretion, is required for adult tissue growth control in Drosophila, Dev. Biol., 266, 310, 10.1016/j.ydbio.2003.10.028 · doi:10.1016/j.ydbio.2003.10.028
- Duve, 1999, Regulation of lepidopteran foregut movement by allatostatins and allatotropin from the frontal ganglion, J. Comp. Neurol., 413, 405, 10.1002/(SICI)1096-9861(19991025)413:3<405::AID-CNE4>3.0.CO;2-R · doi:10.1002/(sici)1096-9861(19991025)413:3<405::aid-cne4>3.0.co;2-r
- Duve, 2000, Triple co-localisation of two types of allatostatin and an allatotropin in the frontal ganglion of the lepidopteran Lacanobia oleracea (Noctuidae): innervation and action on the foregut, Cell Tissue Res., 300, 153, 10.1007/s004410050056 · doi:10.1007/s004410050056
- Fujii, 2010, Ventral lateral and DN1 clock neurons mediate distinct properties of male sex drive rhythm in Drosophila, Proc. Natl. Acad. Sci. U S A, 107, 10590, 10.1073/pnas.0912457107 · doi:10.1073/pnas.0912457107
- Furuya, 2000, Cockroach diuretic hormones: characterization of a calcitonin-like peptide in insects, Proc. Natl. Acad. Sci. U S A, 97, 6469, 10.1073/pnas.97.12.6469 · doi:10.1073/pnas.97.12.6469
- Geary, 2005, Neuropeptide G-protein-coupled receptors, their cognate ligands and behavior in Caenorhabditis elegans, Trends Pharmacol. Sci., 26, 56, 10.1016/j.tips.2004.12.006 · doi:10.1016/j.tips.2004.12.006
- Girardie, 1989, Amino acid sequence of locust neuroparsins, FEBS Lett., 245, 4, 10.1016/0014-5793(89)80179-6 · doi:10.1016/0014-5793(89)80179-6
- Girardie, 1998, Isolation, sequence determination, physical and physiological characterization of the neuroparsins and ovary maturing parsins of Schistocerca gregaria, Insect Biochem. Mol. Biol., 28, 641, 10.1016/S0965-1748(98)00053-8 · doi:10.1016/s0965-1748(98)00053-8
- Hyun, 2011, Physiological effects of manipulating the level of insulin-degrading enzyme in insulin-producing cells of Drosophila, Fly (Austin), 5, 53, 10.4161/fly.5.1.14080 · doi:10.4161/fly.5.1.14080
- Janssen, 2001, cDNA cloning and transcript distribution of two different neuroparsin precursors in the desert locust, Schistocerca gregaria, Insect. Mol. Biol., 10, 183, 10.1046/j.1365-2583.2001.00257.x · doi:10.1046/j.1365-2583.2001.00257.x
- Johard, 2003, Diuretic action of the peptide locustatachykinin I: cellular localisation and effects on fluid secretion in Malpighian tubules of locusts, Peptides, 24, 1571, 10.1016/j.peptides.2003.08.012 · doi:10.1016/j.peptides.2003.08.012
- Kaneko, 2014, Short neuropeptide F (sNPF) is a stage-specific suppressor for juvenile hormone biosynthesis by corpora allata, and a critical factor for the initiation of insect metamorphosis, Dev. Biol., 393, 312, 10.1016/j.ydbio.2014.07.014 · doi:10.1016/j.ydbio.2014.07.014
- Kataoka, 1989, Isolation and identification of a diuretic hormone from the tobacco hornworm, manduca-sexta, Proc. Natl. Acad. Sci. U S A, 86, 2976, 10.1073/pnas.86.8.2976 · doi:10.1073/pnas.86.8.2976
- Kim, 2006, Central peptidergic ensembles associated with organization of an innate behavior, Proc. Natl. Acad. Sci. U S A, 103, 14211, 10.1073/pnas.0603459103 · doi:10.1073/pnas.0603459103
- Koziol, 2018, Precursors of neuropeptides and peptide hormones in the genomes of tardigrades, Gen. Comp. Endocrinol., 267, 116, 10.1016/j.ygcen.2018.06.012 · doi:10.1016/j.ygcen.2018.06.012
- Kubli, 2012, Sexual behavior: how Sex Peptide flips the postmating switch of female flies, Curr. Biol., 22, R520, 10.1016/j.cub.2012.04.058 · doi:10.1016/j.cub.2012.04.058
- Lee, 2017, Central peptidergic modulation of peripheral olfactory responses, BMC Biol., 15, 10.1186/s12915-017-0374-6 · doi:10.1186/s12915-017-0374-6
- Lenaerts, 2017, The ecdysis triggering hormone system is essential for successful moulting of a major hemimetabolous pest insect, Schistocerca gregaria, Sci. Rep., 7, 46502, 10.1038/srep46502 · doi:10.1038/srep46502
- Lismont, 2015, Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria, Front. Neurosci., 9, 10.3389/fnins.2015.00084 · doi:10.3389/fnins.2015.00084
- Loveall, 2010, The essential role of bursicon during Drosophila development, BMC Dev. Biol., 10, 92, 10.1186/1471-213X-10-92 · doi:10.1186/1471-213x-10-92
- Lwalaba, 2010, Control of the release of digestive enzymes in the larvae of the fall armyworm, Spodoptera frugiperda, Arch. Insect. Biochem. Physiol., 73, 14, 10.1002/arch.20332 · doi:10.1002/arch.20332
- MacMillan, 2018, Anti-diuretic activity of a CAPA neuropeptide can compromise Drosophila chill tolerance, J. Exp. Biol., 221
- Masood, 2014, Molecular characterization and possible biological roles of allatotropin in Rhodnius prolixus, Peptides, 53, 159, 10.1016/j.peptides.2013.10.017 · doi:10.1016/j.peptides.2013.10.017
- Matsui, 2013, The pars intercerebralis affects digestive activities of the American cockroach, Periplaneta Americana, via crustacean cardioactive peptide and allatostatin-A, J. Insect Physiol., 59, 33, 10.1016/j.jinsphys.2012.06.010 · doi:10.1016/j.jinsphys.2012.06.010
- Meiselman, 2018, Stress-induced reproductive arrest in Drosophila occurs through ETH deficiency-mediated suppression of oogenesis and ovulation, BMC Biol., 16, 18, 10.1186/s12915-018-0484-9 · doi:10.1186/s12915-018-0484-9
- Nagai, 2014, Identification and characterization of receptors for ion transport peptide (ITP) and ITP-like (ITPL) in the silkworm Bombyx mori, J. Biol. Chem., 289, 32166, 10.1074/jbc.M114.590646 · doi:10.1074/jbc.m114.590646
- Nagai-Okatani, 2016, Tachykinin-related peptides share a G protein-coupled receptor with ion transport peptide-like in the silkworm Bombyx mori, PLoS ONE, 11, e0156501, 10.1371/journal.pone.0156501 · doi:10.1371/journal.pone.0156501
- Nagata, 2012, Identification of cDNAs encoding allatotropin and allatotropin-like peptides from the silkworm, Bombyx mori, Peptides, 34, 98, 10.1016/j.peptides.2012.01.002 · doi:10.1016/j.peptides.2012.01.002
- Nässel, 1991, Insect tachykinin-like peptide: distribution of leucokinin immunoreactive neurons in the cockroach and blowfly brains, Neurosci. Lett., 130, 225, 10.1016/0304-3940(91)90402-F · doi:10.1016/0304-3940(91)90402-f
- Nässel, 2014, Cholecystokinin-Like Peptide (DSK) in Drosophila, Not Only for Satiety Signaling, Front. Endocrinol. (Lausanne), 5, 219, 10.3389/fendo.2014.00219 · doi:10.3389/fendo.2014.00219
- Nässel, 1994, Neuropeptides in neurosecretory and efferent neural systems of insect thoracic and abdominal ganglia, Zool. Sci., 11, 15
- Nässel, 2000, Baratin, a nonamidated neurostimulating neuropeptide, isolated from cockroach brain: Distribution and actions in the cockroach and locust nervous systems, J. Comp. Neurol., 422, 267, 10.1002/(SICI)1096-9861(20000626)422:2<267::AID-CNE8>3.0.CO;2-J · doi:10.1002/(sici)1096-9861(20000626)422:2<267::aid-cne8>3.0.co;2-j
- O’Donnell, 2003, Inorganic and organic anion transport by insect renal epithelia, Biochim. Biophys. Acta, 1618, 194, 10.1016/j.bbamem.2003.07.003 · doi:10.1016/j.bbamem.2003.07.003
- On, 2015, Functional Pairing of Class B1 Ligand-GPCR in Cephalochordate Provides Evidence of the Origin of PTH and PACAP/Glucagon Receptor Family, Mol. Biol. Evol., 32, 2048, 10.1093/molbev/msv087 · doi:10.1093/molbev/msv087
- Ons, 2016, Neuropeptides in the regulation of Rhodnius prolixus physiology, J. Insect. Physiol.
- Orchard, 2009, Diuretic and antidiuretic hormones in the blood-gorging bug Rhodnius prolixus, Ann. N. Y. Acad. Sci., 1163, 501, 10.1111/j.1749-6632.2008.03634.x · doi:10.1111/j.1749-6632.2008.03634.x
- Overend, 2012, The receptor guanylate cyclase Gyc76C and a peptide ligand, NPLP1-VQQ, modulate the innate immune IMD pathway in response to salt stress, Peptides, 34, 209, 10.1016/j.peptides.2011.08.019 · doi:10.1016/j.peptides.2011.08.019
- Paluzzi, 2008, Isolation, cloning, and expression mapping of a gene encoding an antidiuretic hormone and other CAPA-related peptides in the disease vector, Rhodnius prolixus, Endocrinology, 149, 4638, 10.1210/en.2008-0353 · doi:10.1210/en.2008-0353
- Persson, 1999, Neuropeptides in insect sensory neurones: tachykinin-, FMRFamide- and allatotropin-related peptides in terminals of locust thoracic sensory afferents, Brain Res., 816, 131, 10.1016/S0006-8993(98)01139-1 · doi:10.1016/s0006-8993(98)01139-1
- Predel, 2007, Social behavior and the evolution of neuropeptide genes: lessons from the honeybee genome, Bioessays, 29, 416, 10.1002/bies.20571 · doi:10.1002/bies.20571
- Rachinsky, 2006, Allatotropin-like peptide in Heliothis virescens: Tissue localization and quantification, Arch. Insect. Biochem. Physiol., 62, 11, 10.1002/arch.20117 · doi:10.1002/arch.20117
- Redeker, 2017, Identification and distribution of products from novel tryptopyrokinin genes in the locust, Locusta migratoria, Biochem. Biophys. Res. Commun., 486, 70, 10.1016/j.bbrc.2017.02.135 · doi:10.1016/j.bbrc.2017.02.135
- Robertson, 2012, The neural and peptidergic control of gut contraction in Locusta migratoria: the effect of an FGLa/AST, J. Exp. Biol., 215, 3394
- Robertson, 2014, Allatostatin A-like immunoreactivity in the nervous system and gut of the larval midge Chironomus riparius: modulation of hindgut motility, rectal K+ transport and implications for exposure to salinity, J. Exp. Biol., 217, 3815
- Robertson, 2014, K(+) absorption by locust gut and inhibition of ileal K(+) and water transport by FGLamide allatostatins, J. Exp. Biol., 217, 3377
- Roller, 2010, Ecdysis triggering hormone signaling in arthropods, Peptides, 31, 429, 10.1016/j.peptides.2009.11.022 · doi:10.1016/j.peptides.2009.11.022
- Rudwall, 2000, Allatotropin-like neuropeptide in the cockroach abdominal nervous system: myotropic actions, sexually dimorphic distribution and colocalization with serotonin, J. Comp. Neurol., 428, 159, 10.1002/1096-9861(20001204)428:1<159::AID-CNE11>3.0.CO;2-Y · doi:10.1002/1096-9861(20001204)428:1<159::aid-cne11>3.0.co;2-y
- Sajadi, 2018, Anti-diuretic action of a CAPA neuropeptide against a subset of diuretic hormones in the disease vector Aedes aegypti, J. Exp. Biol., 221
- Sakai, 2004, Characterization of crustacean cardioactive peptide as a novel insect midgut factor: isolation, localization, and stimulation of alpha-amylase activity and gut contraction, Endocrinology, 145, 5671, 10.1210/en.2004-0722 · doi:10.1210/en.2004-0722
- Santos, 2006, Morphology and metamorphosis of the peptidergic Va neurons and the median nerve system of the fruit fly, Drosophila melanogaster, Cell Tissue Res., 326, 187, 10.1007/s00441-006-0211-7 · doi:10.1007/s00441-006-0211-7
- Saunders, 1990, The circadian basis of ovarian diapause regulation in Drosophila melanogaster: is the period gene causally involved in photoperiodic time measurement?, J. Biol. Rhythms, 5, 315, 10.1177/074873049000500404 · doi:10.1177/074873049000500404
- Shafer, 2014, Pigment-dispersing factor signaling and circadian rhythms in insect locomotor activity, Curr. Opin. Insect. Sci., 1, 73, 10.1016/j.cois.2014.05.002 · doi:10.1016/j.cois.2014.05.002
- Sturm, 2016, Agatoxin-like peptides in the neuroendocrine system of the honey bee and other insects, J. Proteomics, 132, 77, 10.1016/j.jprot.2015.11.021 · doi:10.1016/j.jprot.2015.11.021
- Sugahara, 2015, Knockdown of the corazonin gene reveals its critical role in the control of gregarious characteristics in the desert locust, J. Insect. Physiol., 79, 80, 10.1016/j.jinsphys.2015.06.009 · doi:10.1016/j.jinsphys.2015.06.009
- Suh, 2015, Nutrient sensor in the brain directs the action of brain-gut axis in Drosophila, Chem. Sens., 40, 607
- Sundarrajan, 2016, Nesfatin-1-Like Peptide Encoded in Nucleobindin-1 in Goldfish is a Novel Anorexigen Modulated by Sex Steroids, Macronutrients and Daily Rhythm, Sci. Rep., 6, 28377, 10.1038/srep28377 · doi:10.1038/srep28377
- Taussig, 1984, A Cdna Clone Encoding Neuropeptides Isolated from Aplysia Neuron L11, Proc. Natl. Acad. Sci. U S A, 81, 4988, 10.1073/pnas.81.15.4988 · doi:10.1073/pnas.81.15.4988
- Terhzaz, 2012, Mechanism and function of Drosophila capa GPCR: a desiccation stress-responsive receptor with functional homology to human neuromedin U receptor, PLOS ONE, 7, 10.1371/journal.pone.0029897 · doi:10.1371/journal.pone.0029897
- Terhzaz, 2014, The D. melanogaster capa-1 neuropeptide activates renal NF-kB signaling, Peptides, 53, 218, 10.1016/j.peptides.2013.08.004 · doi:10.1016/j.peptides.2013.08.004
- Terhzaz, 2015, Insect capa neuropeptides impact desiccation and cold tolerance, Proc. Natl. Acad. Sci. U S A, 112, 2882, 10.1073/pnas.1501518112 · doi:10.1073/pnas.1501518112
- Thompson, 1991, The vasopressin-like immunoreactive (VPLI) neurons of the locust, Locusta migratoria. I. Anatomy, J. Comp. Physiol. A, 168, 605, 10.1007/BF00215083 · doi:10.1007/bf00215083
- Uchiyama, 2018, Elevenin regulates the body color through a G protein-coupled receptor NlA42 in the brown planthopper Nilaparvata lugens, Gen. Comp. Endocr., 258, 33, 10.1016/j.ygcen.2017.07.017 · doi:10.1016/j.ygcen.2017.07.017
- Utz, 2008, Mas-allatotropin in the developing antennal lobe of the sphinx moth Manduca sexta: distribution, time course, developmental regulation, and colocalization with other neuropeptides, Dev. Neurobiol., 68, 123, 10.1002/dneu.20579 · doi:10.1002/dneu.20579
- Veenstra, 2016, Allatostatins C, double C and triple C, the result of a local gene triplication in an ancestral arthropod, Gen. Comp. Endocr., 230, 153, 10.1016/j.ygcen.2016.04.013 · doi:10.1016/j.ygcen.2016.04.013
- Veenstra, 2014, More Drosophila enteroendocrine peptides: Orcokinin B and the CCHamides 1 and 2, Cell Tissue Res., 357, 607, 10.1007/s00441-014-1880-2 · doi:10.1007/s00441-014-1880-2
- Veenstra, 2012, In silico cloning of genes encoding neuropeptides, neurohormones and their putative G-protein coupled receptors in a spider mite, Insect. Biochem. Mol., 42, 277, 10.1016/j.ibmb.2011.12.009 · doi:10.1016/j.ibmb.2011.12.009
- Verlinden, 2015, The pleiotropic allatoregulatory neuropeptides and their receptors: A mini-review, J. Insect. Physiol., 80, 2, 10.1016/j.jinsphys.2015.04.004 · doi:10.1016/j.jinsphys.2015.04.004
- Wei, 2000, Sulfakinins reduce food intake in the desert locust, Schistocerca gregaria, J. Insect. Physiol., 46, 1259, 10.1016/S0022-1910(00)00046-9 · doi:10.1016/s0022-1910(00)00046-9
- Wulff, 2017, Orcokinin neuropeptides regulate ecdysis in the hemimetabolous insect Rhodnius prolixus, Insect. Biochem. Mol. Biol., 81, 91, 10.1016/j.ibmb.2017.01.003 · doi:10.1016/j.ibmb.2017.01.003
- Yanez-Guerra, 2018, Discovery and functional characterisation of a luqin-type neuropeptide signalling system in a deuterostome, Sci. Rep., 8, 7220, 10.1038/s41598-018-25606-2 · doi:10.1038/s41598-018-25606-2
- Yu, 2013, Characterization of sulfakinin and sulfakinin receptor and their roles in food intake in the red flour beetle Tribolium castaneum, Gen. Comp. Endocr., 188, 196, 10.1016/j.ygcen.2013.03.006 · doi:10.1016/j.ygcen.2013.03.006
- Yu, 2016, Ion transport peptide (ITP) regulates wing expansion and cuticle melanism in the brown planthopper, Nilaparvata lugens, Insect. Mol. Biol., 25, 778, 10.1111/imb.12262 · doi:10.1111/imb.12262
- Zandawala, 2012, Cloning of the cDNA, localization, and physiological effects of FGLamide-related allatostatins in the blood-gorging bug, Rhodnius prolixus, Insect. Biochem. Mol. Biol., 42, 10, 10.1016/j.ibmb.2011.10.002 · doi:10.1016/j.ibmb.2011.10.002
- Zandawala, 2015, Structure-activity relationships of two Rhodnius prolixus calcitonin-like diuretic hormone analogs, Peptides, 68, 211, 10.1016/j.peptides.2014.03.019 · doi:10.1016/j.peptides.2014.03.019
- Zhang, 2009, Deletion of Drosophila insulin-like peptides causes growth defects and metabolic abnormalities, Proc. Natl. Acad. Sci. U S A, 106, 19617, 10.1073/pnas.0905083106 · doi:10.1073/pnas.0905083106
- Abdel-latief, 2010, Neuropeptide regulators of the juvenile hormone biosynthesis (in vitro) in the beetle, Tenebrio molitor (Coleoptera, Tenebrionidae), Arch. Insect. Biochem. Physiol., 74, 135, 10.1002/arch.20359 · doi:10.1002/arch.20359
- Adachi, 1989, cDNA structure and expression of bombyxin, an insulin-like brain secretory peptide of the silkmoth Bombyx mori, J. Biol. Chem., 264, 7681, 10.1016/S0021-9258(18)83288-4 · doi:10.1016/s0021-9258(18)83288-4
- Al-Anzi, 2010, The leucokinin pathway and its neurons regulate meal size in Drosophila, Curr. Biol., 20, 969, 10.1016/j.cub.2010.04.039 · DOI · Paper page
- Alfa, 2016, Using Drosophila to discover mechanisms underlying type 2 diabetes, Dis. Model. Mech., 9, 365, 10.1242/dmm.023887 · DOI
- Alfa, 2015, Suppression of insulin production and secretion by a decretin hormone, Cell metabolism, 21, 323, 10.1016/j.cmet.2015.01.006 · DOI · Paper page
- An, 2012, Insect Neuropeptide Bursicon Homodimers Induce Innate Immune and Stress Genes during Molting by Activating the NF-kappa B Transcription Factor Relish, Plos One, 7
- Anderson, 1988, Identification of the neuropeptide transmitter proctolin in Drosophila larvae: characterization of muscle fiber-specific neuromuscular endings, J. Neurosci., 8, 242, 10.1523/JNEUROSCI.08-01-00242.1988 · DOI
- Antonova, 2012, Insulin-like peptides: Structure, Signaling, and Function, Insect Endocrinology, 63, 10.1016/B978-0-12-384749-2.10002-0 · DOI
- Arakane, 2008, Functional analysis of four neuropeptides, EH, ETH, CCAP and bursicon, and their receptors in adult ecdysis behavior of the red flour beetle, Tribolium castaneum, Mech. Dev., 125, 984, 10.1016/j.mod.2008.09.002 · DOI · Paper page
- Asahina, 2014, Tachykinin-Expressing Neurons Control Male-Specific Aggressive Arousal in Drosophila, Cell, 156, 221, 10.1016/j.cell.2013.11.045 · DOI · Paper page
- Audsley, 2013, Characterisation and tissue distribution of the PISCF allatostatin receptor in the red flour beetle, Tribolium castaneum, Insect. Biochem. Mol. Biol., 43, 65, 10.1016/j.ibmb.2012.09.007 · doi:10.1016/j.ibmb.2012.09.007
- Bachtel, 2018, Allatostatin C modulates nociception and immunity in Drosophila, Sci. Rep., 8, 7501, 10.1038/s41598-018-25855-1 · DOI
- Bader, 2007, Comparative neuroanatomy and genomics of hugin and pheromone biosynthesis activating neuropeptide (PBAN), Fly (Austin), 1, 228, 10.4161/fly.4749 · doi:10.4161/fly.4749
- Badisco, 2008, Purification and characterization of an insulin-related peptide in the desert locust, Schistocerca gregaria: immunolocalization, cDNA cloning, transcript profiling and interaction with neuroparsin, J. Mol. Endocrinol., 40, 137, 10.1677/JME-07-0161 · DOI
- Baggerman, 2005, Peptidomic analysis of the larval Drosophila melanogaster central nervous system by two-dimensional capillary liquid chromatography quadrupole time-of-flight mass spectrometry, J. Mass Spectrom., 40, 250, 10.1002/jms.744 · DOI · Paper page
- Baggerman, 2002, Peptidomics of the larval Drosophila melanogaster central nervous system, J. Biol. Chem., 277, 40368, 10.1074/jbc.M206257200 · DOI · Paper page
- Bai, 2018, A Conserved Circadian Function for the Neurofibromatosis 1 Gene, Cell Rep., 22, 3416, 10.1016/j.celrep.2018.03.014 · DOI
- Barnstedt, 2016, Memory-Relevant Mushroom Body Output Synapses Are Cholinergic, Neuron, 89, 1237, 10.1016/j.neuron.2016.02.015 · DOI · Paper page
- Bauknecht, 2015, Large-Scale Combinatorial Deorphanization of Platynereis Neuropeptide GPCRs, Cell Rep., 12, 684, 10.1016/j.celrep.2015.06.052 · DOI
- Baumann, 1990, Structure-function studies on neurohormone D: activity of naturally-occurring hormone analogues, J. Comp. Physiol. B, 160, 423, 10.1007/BF01075674 · doi:10.1007/bf01075674
- Begum, 2009, Functions of ion transport peptide and ion transport peptide-like in the red flour beetle Tribolium castaneum, Insect. Biochem. Mol. Biol., 39, 717, 10.1016/j.ibmb.2009.08.005 · doi:10.1016/j.ibmb.2009.08.005
- Bendena, 2012, Select Neuropeptides and their G-Protein Coupled Receptors in Caenorhabditis Elegans and Drosophila Melanogaster, Front. Endocrinol. (Lausanne), 3, 93, 10.3389/fendo.2012.00093 · DOI
- Bendena, 1997, Molecular characterization of the inhibitory myotropic peptide leucomyosuppressin, Peptides, 18, 157, 10.1016/S0196-9781(96)00237-9 · doi:10.1016/s0196-9781(96)00237-9
- Bendena, 2011, 2012. Families of allatoregulator sequences: a perspective, Canadian Journal of Zoology-Revue Canadienne De Zoologie, 90, 521, 10.1139/z2012-012 · doi:10.1139/z2012-012
- Benguettat, 2018, The DH31/CGRP enteroendocrine peptide triggers intestinal contractions favoring the elimination of opportunistic bacteria, PLoS Pathog., 14, e1007279, 10.1371/journal.ppat.1007279 · DOI
- Beshel, 2017, A Leptin Analog Locally Produced in the Brain Acts via a Conserved Neural Circuit to Modulate Obesity-Linked Behaviors in Drosophila, Cell Metab., 25, 208, 10.1016/j.cmet.2016.12.013 · DOI
- Beshel, 2013, Graded encoding of food odor value in the Drosophila brain, J. Neurosci., 33, 15693, 10.1523/JNEUROSCI.2605-13.2013 · DOI
- Bharucha, 2008, A glucagon-like endocrine pathway in Drosophila modulates both lipid and carbohydrate homeostasis, J. Exp. Biol., 211, 3103, 10.1242/jeb.016451 · DOI · Paper page
- Birgul, 1999, Reverse physiology in Drosophila: identification of a novel allatostatin-like neuropeptide and its cognate receptor structurally related to the mammalian somatostatin/galanin/opioid receptor family, EMBO J., 18, 5892, 10.1093/emboj/18.21.5892 · DOI · Paper page
- Birse, 2006, Widely distributed Drosophila G-protein-coupled receptor (CG7887) is activated by endogenous tachykinin-related peptides, J. NEUROBIOL., 66, 33, 10.1002/neu.20189 · DOI
- Birse, 2011, Regulation of insulin-producing cells in the adult Drosophila brain via the tachykinin peptide receptor DTKR, J. Exp. Biol., 214, 4201, 10.1242/jeb.062091 · DOI
- Brogiolo, 2001, An evolutionarily conserved function of the Drosophila insulin receptor and insulin-like peptides in growth control, Curr. Biol., 11, 213, 10.1016/S0960-9822(01)00068-9 · DOI · Paper page
- Broughton, 2005, Longer lifespan, altered metabolism, and stress resistance in Drosophila from ablation of cells making insulin-like ligands, Proc. Natl. Acad. Sci. U. S. A., 102, 3105, 10.1073/pnas.0405775102 · DOI · Paper page
- Brown, 1999, Identification of a Drosophila brain-gut peptide related to the neuropeptide Y family, Peptides, 20, 1035, 10.1016/S0196-9781(99)00097-2 · DOI · Paper page
- Cabrero, 2002, The Dh gene of Drosophila melanogaster encodes a diuretic peptide that acts through cyclic AMP, J. Exp. Biol., 205, 3799, 10.1242/jeb.205.24.3799 · DOI · Paper page
- Caers, 2012, More than two decades of research on insect neuropeptide GPCRs: an overview, Front. Endocrinol. (Lausanne), 3, 151, 10.3389/fendo.2012.00151 · DOI · Paper page
- Cannell, 2016, The Corticotropin-releasing factor-like diuretic hormone 44 (DH) and kinin neuropeptides modulate desiccation and starvation tolerance in Drosophila melanogaster, Peptides, 80, 96, 10.1016/j.peptides.2016.02.004 · DOI
- Cantera, 1992, Segmental peptidergic innervation of abdominal targets in larval and adult dipteran insects revealed with an antiserum against leucokinin I, Cell Tissue Res., 269, 459, 10.1007/BF00353901 · DOI
- Cantera, 1994, Postembryonic development of corazonin-containing neurons and neurosecretory cells in the blowfly, Phormia terraenovae, J. Comp. Neurol., 350, 559, 10.1002/cne.903500405 · DOI
- Cao, 2001, Localization of an insulin-like peptide in brains of two flies, Cell Tissue Res., 304, 317, 10.1007/s004410100367 · DOI · Paper page
- Carlsson, 2010, Multiple neuropeptides in the Drosophila antennal lobe suggest complex modulatory circuits, J. Comp. Neurol., 518, 3359, 10.1002/cne.22405 · DOI · Paper page
- Cavanaugh, 2014, Identification of a circadian output circuit for rest:activity rhythms in Drosophila, Cell, 157, 689, 10.1016/j.cell.2014.02.024 · DOI · Paper page
- Cavey, 2016, Circadian rhythms in neuronal activity propagate through output circuits, Nat. Neurosci., 19, 587, 10.1038/nn.4263 · DOI
- Cazzamali, 2003, Molecular identification of a Drosophila G protein-coupled receptor specific for crustacean cardioactive peptide, Biochem. Biophys. Res. Commun., 303, 146, 10.1016/S0006-291X(03)00302-4 · doi:10.1016/s0006-291x(03)00302-4
- Chang, 2009, Receptor guanylyl cyclases in Inka cells targeted by eclosion hormone, Proc. Natl. Acad. Sci. U. S. A., 106, 13371, 10.1073/pnas.0812593106 · doi:10.1073/pnas.0812593106
- Chapman, 2003, The sex peptide of Drosophila melanogaster: female post-mating responses analyzed by using RNA interference, Proc. Natl. Acad. Sci. U. S. A., 100, 9923, 10.1073/pnas.1631635100 · DOI · Paper page
- Chell, 2010, Nutrition-responsive glia control exit of neural stem cells from quiescence, Cell, 143, 1161, 10.1016/j.cell.2010.12.007 · DOI · Paper page
- Chen, 2016, Allatostatin A Signalling in Drosophila Regulates Feeding and Sleep and Is Modulated by PDF, PLoS Genet., 12, e1006346, 10.1371/journal.pgen.1006346 · DOI
- Chen, 2006, The short neuropeptide F-like receptor from the red imported fire ant, Solenopsis invicta Buren (Hymenoptera: Formicidae), Arch. Insect Biochem. Physiol., 61, 195, 10.1002/arch.20103 · doi:10.1002/arch.20103
- Chen, 1988, A male accessory gland peptide that regulates reproductive behavior of female D. melanogaster, Cell, 54, 291, 10.1016/0092-8674(88)90192-4 · DOI · Paper page
- Chen, 2013, Regulation of sleep by the short neuropeptide F (sNPF) in Drosophila melanogaster, Insect. Biochem. Molec., 43, 809, 10.1016/j.ibmb.2013.06.003 · DOI
- Chen, 1994, A comparative study of leucokinin-immunoreactive neurons in insects, Cell Tissue Res., 276, 69, 10.1007/BF00354786 · doi:10.1007/bf00354786
- Chintapalli, 2012, Functional correlates of positional and gender-specific renal asymmetry in Drosophila, PLoS One, 7, e32577, 10.1371/journal.pone.0032577 · DOI
- Chintapalli, 2007, Using FlyAtlas to identify better Drosophila melanogaster models of human disease, Nat. Genet., 39, 715, 10.1038/ng2049 · DOI · Paper page
- Choi, 2001, Pyrokinin/PBAN-like peptides in the central nervous system of Drosophila melanogaster, Cell Tissue Res., 306, 459, 10.1007/s00441-001-0467-x · doi:10.1007/s00441-001-0467-x
- Chung, 2017, Drosophila Neuropeptide F Signaling Independently Regulates Feeding and Sleep-Wake Behavior, Cell Rep., 19, 2441, 10.1016/j.celrep.2017.05.085 · doi:10.1016/j.celrep.2017.05.085
- Clark, 2006, Proctolin-like immunoreactivity in the central and peripheral nervous systems of the locust, Locusta migratoria, Peptides, 27, 549, 10.1016/j.peptides.2005.06.027 · doi:10.1016/j.peptides.2005.06.027
- Clark, 2006, Proctolin: A possible releasing factor in the corpus cardiacum/corpus allatum of the locust, Peptides, 27, 559, 10.1016/j.peptides.2005.06.028 · doi:10.1016/j.peptides.2005.06.028
- Coast, 1990, The diuretic activity of a series of cephalomyotropic neuropeptides, the achetakinins, on isolated Malpighian tubules of the house cricket Acheta domesticus, J. Insect Physiol., 36, 481, 10.1016/0022-1910(90)90098-Z · DOI
- Coast, 2001, The Drosophila melanogaster homologue of an insect calcitonin-like diuretic peptide stimulates V-ATPase activity in fruit fly Malpighian tubules, J. Exp. Biol., 204, 1795, 10.1242/jeb.204.10.1795 · DOI · Paper page
- Cognigni, 2011, Enteric neurons and systemic signals couple nutritional and reproductive status with intestinal homeostasis, Cell Metab., 13, 92, 10.1016/j.cmet.2010.12.010 · DOI · Paper page
- Collin, 2011, Identification of the Drosophila and Tribolium receptors for the recently discovered insect RYamide neuropeptides, Biochem. Biophys. Res. Commun., 412, 578, 10.1016/j.bbrc.2011.07.131 · doi:10.1016/j.bbrc.2011.07.131
- Colombani, 2015, Drosophila Lgr3 Couples Organ Growth with Maturation and Ensures Developmental Stability, Current biology, 25, 2723, 10.1016/j.cub.2015.09.020 · DOI · Paper page
- Colombani, 2012, Secreted peptide Dilp8 coordinates Drosophila tissue growth with developmental timing, Science, 336, 582, 10.1126/science.1216689 · DOI · Paper page
- Conzelmann, 2013, The neuropeptide complement of the marine annelid Platynereis dumerilii, BMC Genomics, 14, 906, 10.1186/1471-2164-14-906 · DOI · Paper page
- Copenhaver, 1986, Identification of the cerebral neurosecretory cells that contain eclosion hormone in the moth Manduca sexta, J Neurosci, 6, 1738, 10.1523/JNEUROSCI.06-06-01738.1986 · doi:10.1523/jneurosci.06-06-01738.1986
- da Silva, 2006, The association of crustacean cardioactive peptide with the spermatheca of the African migratory locust, Locusta migratoria, Journal of Insect Physiology, 52, 399, 10.1016/j.jinsphys.2006.01.006 · doi:10.1016/j.jinsphys.2006.01.006
- da Silva, 2011, Effects of crustacean cardioactive peptide on the hearts of two Orthopteran insects, and the demonstration of a Frank-Starling-like effect, Gen. Comp. Endocr., 171, 218, 10.1016/j.ygcen.2011.01.015 · doi:10.1016/j.ygcen.2011.01.015
- Dai, 2008, Identification, developmental expression, and functions of bursicon in the tobacco hawkmoth, Manduca sexta, J. Comp. Neurol., 506, 759, 10.1002/cne.21575 · doi:10.1002/cne.21575
- Dai, 2007, Strategic expression of ion transport peptide gene products in central and peripheral neurons of insects, J. Comp. Neurol., 500, 353, 10.1002/cne.21192 · doi:10.1002/cne.21192
- Davies, 1995, CAP2b, a cardioacceleratory peptide, is present in Drosophila and stimulates tubule fluid secretion via cGMP, Am. J. Physiol., 269, R1321
- Dewey, 2004, Identification of the gene encoding bursicon, an insect neuropeptide responsible for cuticle sclerotization and wing spreading, Curr. Biol., 14, 1208, 10.1016/j.cub.2004.06.051 · doi:10.1016/j.cub.2004.06.051
- Diao, 2016, The Splice Isoforms of the Drosophila Ecdysis Triggering Hormone Receptor Have Developmentally Distinct Roles, Genetics, 202, 175, 10.1534/genetics.115.182121 · DOI
- Dickerson, 2012, Structure-activity and immunochemical data provide evidence of developmental- and tissue-specific myosuppressin signaling, Peptides, 36, 272, 10.1016/j.peptides.2012.05.002 · doi:10.1016/j.peptides.2012.05.002
- Dierick, 2007, Serotonin and neuropeptide F have opposite modulatory effects on fly aggression, Nat. Genet., 39, 678, 10.1038/ng2029 · DOI · Paper page
- Digan, 1992, Characterization of the precursor for Manduca sexta diuretic hormone Mas-DH, Proc. Natl. Acad. Sci. U. S. A., 89, 11074, 10.1073/pnas.89.22.11074 · doi:10.1073/pnas.89.22.11074
- Dircksen, 2008, Ion transport peptide splice forms in central and peripheral neurons throughout postembryogenesis of Drosophila melanogaster, J. Comp. Neurol., 509, 23, 10.1002/cne.21715 · DOI
- Donini, 2002, Evidence for crustacean cardioactive peptide-like innervation of the gut in Locusta migratoria, Peptides, 23, 1915, 10.1016/S0196-9781(02)00174-2 · doi:10.1016/s0196-9781(02)00174-2
- Donlea, 2017, Neuronal substrates of sleep homeostasis; lessons from flies, rats and mice, Curr. Opin. Neurobiol., 44, 228, 10.1016/j.conb.2017.05.003 · DOI · Paper page
- Down, 2010, Effects of Manduca sexta allatostatin and an analog on the pea aphid Acyrthosiphon pisum (Hemiptera: Aphididae) and degradation by enzymes from the aphid gut, Peptides, 31, 489, 10.1016/j.peptides.2009.06.017 · doi:10.1016/j.peptides.2009.06.017
- Drexler, 2007, Molecular characterization and cell-specific expression of an ion transport peptide in the tobacco hornworm, Manduca sexta, Cell Tissue Res., 329, 391, 10.1007/s00441-007-0391-9 · doi:10.1007/s00441-007-0391-9
- Dulcis, 2001, Neuronal control of heart reversal in the hawkmoth Manduca sexta, J. Comp. Physiol., 187, 837, 10.1007/s00359-001-0254-x · doi:10.1007/s00359-001-0254-x
- Dulcis, 2005, Role of the neuropeptide CCAP in Drosophila cardiac function, J. Neurobiol., 64, 259, 10.1002/neu.20136 · doi:10.1002/neu.20136
- Dus, 2015, Nutrient Sensor in the Brain Directs the Action of the Brain-Gut Axis in Drosophila, Neuron, 87, 139, 10.1016/j.neuron.2015.05.032 · DOI · Paper page
- Duve, 1992, Isolation, structure, and activity of -Phe-Met-Arg-Phe-NH2 neuropeptides (designated calliFMRFamides) from the blowfly Calliphora vomitoria, Proc. Natl. Acad. Sci. U. S. A., 89, 2326, 10.1073/pnas.89.6.2326 · doi:10.1073/pnas.89.6.2326
- Duve, 1994, Localisation of sulfakinin neuronal pathways in the blowfly Calliphora vomitoria, Cell Tissue Res., 275, 177, 10.1007/BF00305385 · doi:10.1007/bf00305385
- East, 1997, Distribution of sulfakinin-like peptides in the central and sympathetic nervous system of the American cockroach, Periplaneta americana (L.) and the field cricket, Teleogryllus commodus (Walker), Tissue Cell, 29, 347, 10.1016/S0040-8166(97)80010-9 · doi:10.1016/s0040-8166(97)80010-9
- Egerod, 2003, Molecular cloning and functional expression of the first two specific insect myosuppressin receptors, Proc. Natl. Acad. Sci. U. S. A., 100, 9808, 10.1073/pnas.1632197100 · doi:10.1073/pnas.1632197100
- Egerod, 2003, Molecular identification of the first insect proctolin receptor, Biochem. Biophys. Res. Commun., 306, 437, 10.1016/S0006-291X(03)00997-5 · doi:10.1016/s0006-291x(03)00997-5
- Erion, 2016, Neural clocks and Neuropeptide F/Y regulate circadian gene expression in a peripheral metabolic tissue, Elife, 5, e13552, 10.7554/eLife.13552 · DOI
- Ewer, 2005, Behavioral actions of neuropeptides in invertebrates: insights from Drosophila, Horm. Behav., 48, 418, 10.1016/j.yhbeh.2005.05.018 · DOI
- Farhan, 2013, The CCHamide 1 receptor modulates sensory perception and olfactory behavior in starved Drosophila, Sci. Rep., 3, 10.1038/srep02765 · DOI
- Fernandez, 1995, The Drosophila insulin receptor homolog: a gene essential for embryonic development encodes two receptor isoforms with different signaling potential, EMBO J., 14, 3373, 10.1002/j.1460-2075.1995.tb07343.x · DOI · Paper page
- Fraenkel, 1962, Hormonal and nervous control of tanning in the fly, Science, 138, 27, 10.1126/science.138.3536.27 · doi:10.1126/science.138.3536.27
- Fraenkel, 1966, Properties of bursicon: an insect protein hormone that controls cuticular tanning, Science, 151, 91, 10.1126/science.151.3706.91 · doi:10.1126/science.151.3706.91
- Frenkel, 2017, Organization of Circadian Behavior Relies on Glycinergic Transmission, Cell Rep., 19, 72, 10.1016/j.celrep.2017.03.034 · DOI
- Fujiwara, 2018, The CCHamide1 Neuropeptide Expressed in the Anterior Dorsal Neuron 1 Conveys a Circadian Signal to the Ventral Lateral Neurons in Drosophila melanogaster, Front. Physiol., 9, 1276, 10.3389/fphys.2018.01276 · DOI
- Furuya, 2000, Cockroach diuretic hormones: characterization of a calcitonin-like peptide in insects, Proc. Natl. Acad. Sci. U. S. A., 97, 6469, 10.1073/pnas.97.12.6469 · doi:10.1073/pnas.97.12.6469
- Gäde, 2009, Peptides of the Adipokinetic Hormone/Red Pigment-Concentrating Hormone Family A New Take on Biodiversity, Trends Comp. Endocrinol. Neurobiol., 1163, 125
- Gäde, 1997, Hormonal regulation in insects: facts, gaps, and future directions, Physiol. Rev., 77, 963, 10.1152/physrev.1997.77.4.963 · DOI · Paper page
- Galikova, 2015, Energy Homeostasis Control in Drosophila Adipokinetic Hormone Mutants, Genetics, 201, 665, 10.1534/genetics.115.178897 · DOI · Paper page
- Galikova, 2018, The thirsty fly: Ion transport peptide (ITP) is a novel endocrine regulator of water homeostasis in Drosophila, PLoS Genet., 14, e1007618, 10.1371/journal.pgen.1007618 · DOI
- Galikova, 2017, The obesity-related Adipokinetic hormone controls feeding and expression of neuropeptide regulators of Drosophila metabolism, Eur. J. Lipid Sci. Tech., 119
200 of 509 shown
Cited by
A single-cell transcriptomic atlas of the adult Drosophila ventral nerve cord
Allen, A. M., Neville, M. C., Birtles, S., Croset, V., Treiber, C. D., Waddell, S., & Goodwin, S. F. (2020) · eLife · doi:10.7554/elife.54074 · Cited by 177
Network statistics of the whole-brain connectome of Drosophila
Lin, A., Yang, R., Dorkenwald, S., Matsliah, A., Sterling, A. R., Schlegel, P., Yu, S.-C., McKellar, C. E., Costa, M., Eichler, K., et al. (2024) · Nature · doi:10.1038/s41586-024-07968-y · Cited by 147
Network Statistics of the Whole-Brain Connectome of Drosophila
Lin, A., Yang, R., Dorkenwald, S., Matsliah, A., Sterling, A. R., Schlegel, P., Yu, S.-C., McKellar, C. E., Costa, M., Eichler, K., et al. (2023) · doi:10.1101/2023.07.29.551086 · Cited by 147
Neuropeptide repertoire and 3D anatomy of the ctenophore nervous system
Sachkova, M. Y., Nordmann, E.-L., Soto-Àngel, J. J., Meeda, Y., Górski, B., Naumann, B., Dondorp, D., Chatzigeorgiou, M., Kittelmann, M., & Burkhardt, P. (2021) · Current Biology · doi:10.1016/j.cub.2021.09.005 · Cited by 95
A Drosophila computational brain model reveals sensorimotor processing
Shiu, P. K., Sterne, G. R., Spiller, N., Franconville, R., Sandoval, A., Zhou, J., Simha, N., Kang, C. H., Yu, S., Kim, J. S., et al. (2024) · Nature · doi:10.1038/s41586-024-07763-9 · Cited by 97
Metadata
- Authors
- Nässel, D. R., & Zandawala, M.
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2019-08
- Volume
- 179
- Pages
- 101607
- ISSN
- 0301-0082 (ISSN-L)
- OpenAlex
- W2922873188
- Cited by
- 355
- References
- 791
- FWCI
- 16.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- Funders
- Swedish Research Council
- European Commission Horizon (634361)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Recent advances in neuropeptide signaling in Drosophila, from genes to physiology and behavior. https://app.cochat.ai/papers/10.1016/j.pneurobio.2019.02.003
- The paper
- Nässel, D. R., & Zandawala, M. (2019). Recent advances in neuropeptide signaling in Drosophila, from genes to physiology and behavior. Progress in Neurobiology. https://doi.org/10.1016/j.pneurobio.2019.02.003
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.