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Angiotensin-converting enzymes modulate aphid–plant interactions
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781118382806openalex-snapshot
Phloem: Molecular Cell Biology, Systemic Communication, Biotic Interactions
inferredcites →https://doi.org/10.1002/arch.20023openalex-snapshot
The angiotensin converting enzyme inhibitor captopril reduces oviposition and ecdysteroid levels in Lepidoptera
inferredcites →https://doi.org/10.1002/pmic.200800692openalex-snapshot
The secreted salivary proteome of the pea aphid Acyrthosiphon pisum characterised by mass spectrometry
inferredcites →https://doi.org/10.1007/bf00195720openalex-snapshot
Autoradiographic and biochemical evidence for the systemic translocation of systemin in tomato plants
inferredcites →https://doi.org/10.1016/0925-4773(95)00349-5openalex-snapshot
Race: a drosophila homologue of the angiotensin converting enzyme
inferredcites →https://doi.org/10.1016/b978-0-12-374144-8.00089-8openalex-snapshot
Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.bpc.2014.03.006openalex-snapshot
Characterization of an aphid-specific, cysteine-rich protein enriched in salivary glands
inferredcites →https://doi.org/10.1016/j.cub.2010.04.039openalex-snapshot
The Leucokinin Pathway and Its Neurons Regulate Meal Size in Drosophila
inferredcites →https://doi.org/10.1016/j.ibmb.2004.03.007openalex-snapshot
Zinc-metalloproteases in insects: ACE and ECE
inferredcites →https://doi.org/10.1016/j.ibmb.2007.10.004openalex-snapshot
Angiotensin-converting enzyme in Spodoptera littoralis: Molecular characterization, expression and activity profile during development
inferredcites →https://doi.org/10.1016/j.pbi.2011.05.003openalex-snapshot
Effector proteins that modulate plant–insect interactions
inferredcites →https://doi.org/10.1016/j.peptides.2006.08.029openalex-snapshot
Angiotensin-converting enzyme as a target for the development of novel insect growth regulators
inferredcites →https://doi.org/10.1016/s0006-8993(97)01398-xopenalex-snapshot
Immunocytochemical distribution of angiotensin I-converting enzyme-like immunoreactivity in the brain and testis of insects
inferredcites →https://doi.org/10.1016/s0022-1910(03)00110-0openalex-snapshot
Molecular evidence for the expression of angiotensin converting enzyme in hemocytes of Locusta migratoria: stimulation by bacterial lipopolysaccharide challenge
inferredcites →https://doi.org/10.1016/s0022-1910(03)00163-xopenalex-snapshot
Antibacterial and proteolytic activity in venom from the endoparasitic wasp Pimpla hypochondriaca (Hymenoptera: Ichneumonidae)
inferredcites →https://doi.org/10.1016/s0041-0101(01)00230-6openalex-snapshot
Identification of bradykinins in solitary wasp venoms
inferredcites →https://doi.org/10.1016/s0167-0115(03)00165-4openalex-snapshot
Allatostatin gene expression in brain and midgut, and activity of synthetic allatostatins on feeding-related processes in the cockroach Blattella germanica
inferredcites →https://doi.org/10.1016/s0196-9781(02)00144-4openalex-snapshot
Isolation and characterization of an angiotensin converting enzyme substrate from vitellogenic ovaries of Neobellieria bullata
inferredcites →https://doi.org/10.1016/s0196-9781(96)00232-xopenalex-snapshot
Hydrolysis of Insect Neuropeptides by an Angiotensin-Converting Enzyme From the Housefly, Musca domestica
inferredcites →https://doi.org/10.1016/s0301-0082(02)00057-6openalex-snapshot
Neuropeptides in the nervous system of Drosophila and other insects: multiple roles as neuromodulators and neurohormones
inferredcites →https://doi.org/10.1016/s0965-1748(00)00112-0openalex-snapshot
Isolation and expression of the ecdysteroid-inducible angiotensin-converting enzyme-related gene in wing discs of Bombyx mori
inferredcites →https://doi.org/10.1016/s0965-1748(97)00020-9openalex-snapshot
Expression of angiotensin-converting enzyme-related carboxydipeptidases in the larvae of four species of fly
inferredcites →https://doi.org/10.1016/s1096-4959(03)00019-8openalex-snapshot
ACE inhibitors reduce fecundity in the mosquito, Anopheles stephensi
inferredcites →https://doi.org/10.1016/s1360-1385(99)01463-6openalex-snapshot
Macromolecular trafficking in the phloem
inferredcites →https://doi.org/10.1017/s0007485300005526openalex-snapshot
Plant penetration by feeding aphids (Hemiptera, Aphidoidea): a review
inferredcites →https://doi.org/10.1021/bi00439a001openalex-snapshot
Angiotensin-converting enzyme: new concepts concerning its biological role
inferredcites →https://doi.org/10.1021/pr100881qopenalex-snapshot
Predicted Effector Molecules in the Salivary Secretome of the Pea Aphid ( Acyrthosiphon pisum ): A Dual Transcriptomic/Proteomic Approach
inferredcites →https://doi.org/10.1042/bj20020567openalex-snapshot
Ance, a Drosophila angiotensin-converting enzyme homologue, is expressed in imaginal cells during metamorphosis and is regulated by the steroid, 20-hydroxyecdysone
inferredcites →https://doi.org/10.1042/bj3180125openalex-snapshot
Drosophila melanogaster angiotensin I-converting enzyme expressed in Pichia pastoris resembles the C domain of the mammalian homologue and does not require glycosylation for secretion and enzymic activity
inferredcites →https://doi.org/10.1073/pnas.0703535104openalex-snapshot
Molecular sabotage of plant defense by aphid saliva
inferredcites →https://doi.org/10.1073/pnas.0708958105openalex-snapshot
A protein from the salivary glands of the pea aphid, Acyrthosiphon pisum , is essential in feeding on a host plant
inferredcites →https://doi.org/10.1073/pnas.1200778109openalex-snapshot
Allatostatin-A neurons inhibit feeding behavior in adult Drosophila
inferredcites →https://doi.org/10.1074/jbc.270.23.13613openalex-snapshot
Cloning and Expression of an Evolutionary Conserved Single-domain Angiotensin Converting Enzyme from Drosophila melanogaster
inferredcites →https://doi.org/10.1093/aesa/64.2.353openalex-snapshot
Continuous Rearing of the Pea Aphid, Acyrthosiphon pisum,1 on a Holidic Diet2
inferredcites →https://doi.org/10.1093/mp/ssr008openalex-snapshot
Systemin/Jasmonate-Mediated Systemic Defense Signaling in Tomato
inferredcites →https://doi.org/10.1094/mpmi-07-12-0172-fiopenalex-snapshot
Aphid Protein Effectors Promote Aphid Colonization in a Plant Species-Specific Manner
inferredcites →https://doi.org/10.1096/fj.14-266023openalex-snapshot
Armet is an effector protein mediating aphid‐plant interactions
inferredcites →https://doi.org/10.1097/00004872-199509003-00002openalex-snapshot
Recent advances in knowledge of the structure and function of the angiotensin I converting enzyme
inferredcites →https://doi.org/10.1111/j.1365-2583.2008.00790.xopenalex-snapshot
Identification of aphid salivary proteins: a proteomic investigation of Myzus persicae
inferredcites →https://doi.org/10.1111/j.1744-7917.2011.01415.xopenalex-snapshot
Impact of potato psyllid (Hemiptera: Triozidae) feeding on free amino acid composition in potato
inferredcites →https://doi.org/10.1111/j.1749-6632.1998.tb10777.xopenalex-snapshot
Toward a Role for Angiotensin‐Converting Enzyme in Insects
inferredcites →https://doi.org/10.1111/j.1749-6632.1999.tb07904.xopenalex-snapshot
Insect Angiotensin‐converting Enzyme: A Processing Enzyme with Broad Substrate Specificity and a Role in Reproduction
inferredcites →https://doi.org/10.1371/journal.pgen.1001216openalex-snapshot
A Functional Genomics Approach Identifies Candidate Effectors from the Aphid Species Myzus persicae (Green Peach Aphid)
inferredcites →https://doi.org/10.1371/journal.pone.0039303openalex-snapshot
Transcriptomic Analysis of the Salivary Glands of an Invasive Whitefly
inferredcites →https://doi.org/10.1673/031.006.3801openalex-snapshot
RNAi Knockdown of a Salivary Transcript Leading to Lethality in the Pea Aphid, Acyrthosiphon pisum
inferredcites →https://doi.org/10.4049/jimmunol.153.11.5158openalex-snapshot
A protective "concealed" antigen from Boophilus microplus. Purification, localization, and possible function.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.113008zenodo-depositor-declared
Characterized constituents of insect herbivore oral secretions and their influence on the regulation of plant defenses
inferred← citeshttps://doi.org/10.1002/arch.21602openalex-snapshot
Characterization of multicopper oxidase genes in the green rice leafhopper, Nephotettix cincticeps (Hemiptera: Cicadellidae), with focus on salivary gland‐specific genes
inferred← citeshttps://doi.org/10.1002/fes3.247openalex-snapshot
RNAi technology for management of banana bunchy top disease
inferred← citeshttps://doi.org/10.1002/ps.4258openalex-snapshot
RNAi‐mediated plant protection against aphids
inferred← citeshttps://doi.org/10.1002/ps.7966openalex-snapshot
Sast1 ‐mediated manifold effects inhibit Plutella xylostella fertility
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Double-Strand RNA (dsRNA) Delivery Methods in Insects: Diaphorina citri
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Antixenosis and Antibiosis Mechanisms of Resistance to Turnip Aphid, Lipaphis erysimi (Kaltenbach) in Brassica: Conventional and Biotechnological Approaches
inferred← citeshttps://doi.org/10.1007/978-3-319-90650-8_4openalex-snapshot
RNAi for Resistance Against Biotic Stresses in Crop Plants
inferred← citeshttps://doi.org/10.1007/s11829-020-09769-2openalex-snapshot
Aphid saliva: a powerful recipe for modulating host resistance towards aphid clonal propagation
inferred← citeshttps://doi.org/10.1007/s41348-024-01002-zopenalex-snapshot
Unraveling insect feeding patterns and their ecological impacts on plant defense mechanisms
inferred← citeshttps://doi.org/10.1007/s44154-026-00336-yopenalex-snapshot
Molecular and transcriptional regulation of plant defense responses to aphid infestation
inferred← citeshttps://doi.org/10.1016/j.cois.2018.01.003openalex-snapshot
Mechanisms of aphid adaptation to host plant resistance
inferred← citeshttps://doi.org/10.1016/j.gene.2017.01.017openalex-snapshot
The angiotensin-converting enzyme (ACE) gene family of Bombyx mori
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e29201openalex-snapshot
Roles of herbivorous insects salivary proteins
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Identification of salivary proteins of the cowpea aphid Aphis craccivora by transcriptome and LC-MS/MS analyses
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2017.09.007openalex-snapshot
The angiotensin converting enzyme (ACE) inhibitor, captopril disrupts the motility activation of sperm from the silkworm, Bombyx mori
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105645openalex-snapshot
Fusion dsRNA in targeting salivary protein genes enhance the RNAi-based aphid control
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.04.027openalex-snapshot
Plant defense against aphids, the pest extraordinaire
inferred← citeshttps://doi.org/10.1016/j.pmpp.2015.04.006openalex-snapshot
High expression of a unique aphid protein in the salivary glands of Acyrthosiphon pisum
inferred← citeshttps://doi.org/10.1016/j.pmpp.2019.101442openalex-snapshot
Brassica-aphid interaction: Challenges and prospects of genetic engineering for integrated aphid management
inferred← citeshttps://doi.org/10.1016/j.virol.2019.05.007openalex-snapshot
Immune function of an angiotensin-converting enzyme against Rice stripe virus infection in a vector insect
inferred← citeshttps://doi.org/10.1016/j.ygcen.2016.06.024openalex-snapshot
A quantitative peptidomics approach to unravel immunological functions of angiotensin converting enzyme in Locusta migratoria
inferred← citeshttps://doi.org/10.1038/s41598-017-16092-zopenalex-snapshot
Transcriptome analysis of the salivary glands of the grain aphid, Sitobion avenae
inferred← citeshttps://doi.org/10.1038/s41598-020-62856-5openalex-snapshot
Gene silencing of Diaphorina citri candidate effectors promotes changes in feeding behaviors
inferred← citeshttps://doi.org/10.1038/srep19344openalex-snapshot
Performances of survival, feeding behavior and gene expression in aphids reveal their different fitness to host alteration
inferred← citeshttps://doi.org/10.1042/cs20200899openalex-snapshot
ACE2 and ACE: structure-based insights into mechanism, regulation and receptor recognition by SARS-CoV
inferred← citeshttps://doi.org/10.1093/gbe/evy097openalex-snapshot
Fast Evolution and Lineage-Specific Gene Family Expansions of Aphid Salivary Effectors Driven by Interactions with Host-Plants
inferred← citeshttps://doi.org/10.1093/jisesa/ieaf053openalex-snapshot
Identification of candidate host-manipulating effector genes in Aphis gossypii (Hemiptera: Aphididae) using a combination of transcriptome, genome, and differential gene expression data
inferred← citeshttps://doi.org/10.1093/plcell/koac058openalex-snapshot
Effector-mediated plant–virus–vector interactions
inferred← citeshttps://doi.org/10.1101/2021.08.12.456154openalex-snapshot
Mechanisms of Coupling between Angiotensin Converting Enzyme 2 and Nicotinic Acetylcholine Receptors
inferred← citeshttps://doi.org/10.1111/ens.12436openalex-snapshot
Multi‐approach comparative study of the two most prevalent genotypes of pea aphid Acyrthosiphon pisum (Hemiptera: Aphididae) in Chile
inferred← citeshttps://doi.org/10.1111/jipb.12438openalex-snapshot
Hemipteran and dipteran pests: Effectors and plant host immune regulators
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Aphid effector Me10 interacts with tomato TFT 7, a 14‐3‐3 isoform involved in aphid resistance
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Next Generation Sequencing Identifies Five Major Classes of Potentially Therapeutic Enzymes Secreted by Lucilia sericata Medical Maggots
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Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
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Whole-body transcriptome mining for candidate effectors from Diuraphis noxia
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The green rice leafhopper, Nephotettix cincticeps (Hemiptera: Cicadellidae), salivary protein NcSP75 is a key effector for successful phloem ingestion
inferred← citeshttps://doi.org/10.1371/journal.pone.0208538openalex-snapshot
Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection
inferred← citeshttps://doi.org/10.24072/pcjournal.208openalex-snapshot
Transcriptome responses of the aphid vector Myzus persicae are shaped by identities of the host plant and the virus
inferred← citeshttps://doi.org/10.31488/jjm.1000105openalex-snapshot
Angiotensin converting enzyme, a negative moderator of the innate immune response in both mammals and insects
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Transient Expression of Whitefly Effectors in Nicotiana benthamiana Leaves Activates Systemic Immunity Against the Leaf Pathogen Pseudomonas syringae and Soil-Borne Pathogen Ralstonia solanacearum
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Screening Candidate Effectors of the Bean Bug Riptortus pedestris by Proteomic and Transcriptomic Analyses
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An update on angiotensin-converting enzyme 2 structure/functions, polymorphism, and duplicitous nature in the pathophysiology of coronavirus disease 2019: Implications for vascular and coagulation disease associated with severe acute respiratory syndrome coronavirus infection
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Control of aging by the renin–angiotensin system: a review of C. elegans, Drosophila, and mammals
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Induced Systemic Resistance by a Plant Growth-Promoting Rhizobacterium Impacts Development and Feeding Behavior of Aphids
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Faculty Opinions recommendation of The green rice leafhopper, Nephotettix cincticeps (Hemiptera: Cicadellidae), salivary protein NcSP75 is a key effector for successful phloem ingestion.
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Additional file 1 of Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
inferred← citeshttps://doi.org/10.6084/m9.figshare.11986530openalex-snapshot
Additional file 2 of Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
inferred← citeshttps://doi.org/10.6084/m9.figshare.11986542openalex-snapshot
Additional file 3 of Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
inferred← citeshttps://doi.org/10.6084/m9.figshare.11986551openalex-snapshot
Additional file 4 of Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
inferred← citeshttps://doi.org/10.6084/m9.figshare.11986560openalex-snapshot
Additional file 5 of Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
inferred← citeshttps://doi.org/10.6084/m9.figshare.11986563openalex-snapshot
Additional file 6 of Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
inferred← citeshttps://doi.org/10.6084/m9.figshare.11986572openalex-snapshot
Additional file 7 of Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
inferred← citeshttps://doi.org/10.6084/m9.figshare.12872354openalex-snapshot
Additional file of Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267786openalex-snapshot
Additional file 2 of Whole-body transcriptome mining for candidate effectors from Diuraphis noxia
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267792openalex-snapshot
Additional file 4 of Whole-body transcriptome mining for candidate effectors from Diuraphis noxia
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267798openalex-snapshot
Additional file 6 of Whole-body transcriptome mining for candidate effectors from Diuraphis noxia
inferred← citeshttps://doi.org/10.70675/656bf0cazce09z4b9fz9ba7za7508fad74c5openalex-snapshot
Voies d’adaptation d’Aphis gossypii, puceron du melon, aux Cucurbitacées ainsi qu’au gène NLR Vat du melon
inferred← citeshttps://doi.org/10.70675/87262b3fzfe8dz4308z9c2az5c135c65f857openalex-snapshot
Analyse fonctionnelle du récepteur de l'éphrine de Myzus persicae et mise en évidence de son rôle dans la transmissino du virus de la jaunisse du navet
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Un nouveau type de mort cellulaire impliqué dans l’élimination des bactériocytes chez les pucerons : Mécanismes moléculaires et régulations physiologiques
inferred← citeshttps://doi.org/10.70675/b69f314bzd963z4b9dz8025z6d68eb600d32openalex-snapshot
Diversité, caractéristiques évolutives et rôles des effecteurs salivaires du puceron du pois dans l’interaction avec ses plantes hôtes
inferred← citeshttps://doi.org/10.70675/d72a5aa1z8c9az4980z8e91zae0687d39479openalex-snapshot
Caractérisation du rôle de l’acrostyle, un organe localisé à la pointe des stylets de puceron, dans la transmission des virus et dans les interactions plante-insecte
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