On the public citation graph
Gene Regulation by Mating Depends on Time, Diet, and Tissue Type in Female Aedes Aegypti
0 signed · 70 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/j.1460-2075.1990.tb07489.xopenalex-snapshot
The immune response in Drosophila: pattern of cecropin expression and biological activity.
inferredcites →https://doi.org/10.1002/mrd.22653openalex-snapshot
A mosquito sperm's journey from male ejaculate to egg: Mechanisms, molecules, and methods for exploration
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/978-3-319-17894-3_13openalex-snapshot
Who’s Zooming Who? Seminal Fluids and Cryptic Female Choice in Diptera
inferredcites →https://doi.org/10.1007/s00441-009-0758-1openalex-snapshot
Drosophila α-1,4-glycosyltransferase (α-4GT1) inhibits reaper-mediated apoptosis in the eye
inferredcites →https://doi.org/10.1007/s11356-014-3471-xopenalex-snapshot
Effects of neonicotinoids and fipronil on non-target invertebrates
inferredcites →https://doi.org/10.1016/j.bcp.2021.114653openalex-snapshot
Ligand gated receptor interactions: A key to the power of neuronal networks
inferredcites →https://doi.org/10.1016/j.cois.2019.07.009openalex-snapshot
Modulation of seminal fluid molecules by males and females
inferredcites →https://doi.org/10.1016/j.cois.2020.11.004openalex-snapshot
The role of cytochrome P450-mediated detoxification in insect adaptation to xenobiotics
inferredcites →https://doi.org/10.1016/j.cub.2004.08.028openalex-snapshot
Genes Regulated by Mating, Sperm, or Seminal Proteins in Mated Female Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.cub.2009.01.040openalex-snapshot
The GABAA Receptor RDL Acts in Peptidergic PDF Neurons to Promote Sleep in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2019.11.065openalex-snapshot
A Feedforward Circuit Regulates Action Selection of Pre-mating Courtship Behavior in Female Drosophila
inferredcites →https://doi.org/10.1016/j.ibmb.2007.05.018openalex-snapshot
The Aedes aegypti glutathione transferase family
inferredcites →https://doi.org/10.1016/j.ibmb.2007.10.007openalex-snapshot
Identity and transfer of male reproductive gland proteins of the dengue vector mosquito, Aedes aegypti: Potential tools for control of female feeding and reproduction
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.jinsphys.2018.05.001openalex-snapshot
Male contributions during mating increase female survival in the disease vector mosquito Aedes aegypti
inferredcites →https://doi.org/10.1016/j.pestbp.2020.104666openalex-snapshot
Cytochrome P450-based metabolic insecticide resistance in Anopheles and Aedes mosquito vectors: Muddying the waters
inferredcites →https://doi.org/10.1016/j.pt.2020.02.003openalex-snapshot
Not Just from Blood: Mosquito Nutrient Acquisition from Nectar Sources
inferredcites →https://doi.org/10.1016/s0012-1606(02)00082-9openalex-snapshot
The drosophila angiotensin-converting enzyme homologue Ance is required for spermiogenesis
inferredcites →https://doi.org/10.1016/s0021-9258(17)39657-6openalex-snapshot
The induction of ribosome biosynthesis in a nonmitotic secretory tissue.
inferredcites →https://doi.org/10.1016/s0965-1748(03)00105-xopenalex-snapshot
Angiotensin I-converting enzyme (ACE) activity of the tomato moth, Lacanobia oleracea: changes in levels of activity during development and after copulation suggest roles during metamorphosis and reproduction
inferredcites →https://doi.org/10.1038/344330a0openalex-snapshot
Female sticklebacks use male coloration in mate choice and hence avoid parasitized males
inferredcites →https://doi.org/10.1038/nn.3581openalex-snapshot
Female contact modulates male aggression via a sexually dimorphic GABAergic circuit in Drosophila
inferredcites →https://doi.org/10.1038/nn2005openalex-snapshot
Specific requirement of NMDA receptors for long-term memory consolidation in Drosophila ellipsoid body
inferredcites →https://doi.org/10.1038/nprot.2006.83openalex-snapshot
The single-step method of RNA isolation by acid guanidinium thiocyanate–phenol–chloroform extraction: twenty-something years on
inferredcites →https://doi.org/10.1038/s41467-021-25146-wopenalex-snapshot
The sugar-responsive enteroendocrine neuropeptide F regulates lipid metabolism through glucagon-like and insulin-like hormones in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/s41467-022-28592-2openalex-snapshot
The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response
inferredcites →https://doi.org/10.1038/s41586-019-1675-4openalex-snapshot
A glucose-sensing neuron pair regulates insulin and glucagon in Drosophila
inferredcites →https://doi.org/10.1073/pnas.0604046103openalex-snapshot
Mating-responsive genes in reproductive tissues of female Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.0809723105openalex-snapshot
Molecular and cellular components of the mating machinery in Anopheles gambiae females
inferredcites →https://doi.org/10.1073/pnas.2105075118openalex-snapshot
Suppression of female fertility in Aedes aegypti with a CRISPR-targeted male-sterile mutation
inferredcites →https://doi.org/10.1073/pnas.92.9.4056openalex-snapshot
Expression cloning of dSR-CI, a class C macrophage-specific scavenger receptor from Drosophila melanogaster.
inferredcites →https://doi.org/10.1091/mbc.e11-09-0745openalex-snapshot
A secreted MMP is required for reepithelialization during wound healing
inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-snapshot
STAR: ultrafast universal RNA-seq aligner
inferredcites →https://doi.org/10.1093/jhered/esp013openalex-snapshot
Battle and Ballet: Molecular Interactions between the Sexes in Drosophila
inferredcites →https://doi.org/10.1093/jme/tjaa005openalex-snapshot
Sugar Feeding Patterns for Aedes aegypti and Culex quinquefasciatus (Diptera: Culicidae) Mosquitoes in South Texas
inferredcites →https://doi.org/10.1093/molbev/msaa264openalex-snapshot
Differences in Postmating Transcriptional Responses between Conspecific and Heterospecific Matings in Drosophila
inferredcites →https://doi.org/10.1093/nar/gkab971openalex-snapshot
FlyAtlas 2 in 2022: enhancements to the Drosophila melanogaster expression atlas
inferredcites →https://doi.org/10.1093/nar/gkx976openalex-snapshot
FlyAtlas 2: a new version of the Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
inferredcites →https://doi.org/10.1098/rsbl.2007.0192openalex-snapshot
Twin intromittent organs of Drosophila for traumatic insemination
inferredcites →https://doi.org/10.1098/rspb.2008.1559openalex-snapshot
Sex-specific variation in the emphasis, inducibility and timing of the post-mating immune response in Drosophila melanogaster
inferredcites →https://doi.org/10.1098/rstb.2012.0429openalex-snapshot
Role of cytochrome P450s in insecticide resistance: impact on the control of mosquito-borne diseases and use of insecticides on Earth
inferredcites →https://doi.org/10.1101/cshperspect.a017533openalex-snapshot
Sexual Conflict and Seminal Fluid Proteins: A Dynamic Landscape of Sexual Interactions
inferredcites →https://doi.org/10.1101/pdb.prot5439openalex-snapshot
Purification of RNA Using TRIzol (TRI Reagent)
inferredcites →https://doi.org/10.1111/imb.12719openalex-snapshot
Post‐mating gene expression of Mexican fruit fly females: disentangling the effects of the male accessory glands
inferredcites →https://doi.org/10.1111/j.1432-1033.1995.694_2.xopenalex-snapshot
Metchnikowin, a Novel Immune‐Inducible Proline‐Rich Peptide from Drosophila with Antibacterial and Antifungal Properties
inferredcites →https://doi.org/10.1128/mbio.02531-21openalex-snapshot
Pleiotropic Odorant-Binding Proteins Promote Aedes aegypti Reproduction and Flavivirus Transmission
inferredcites →https://doi.org/10.1146/annurev-ento-120709-144823openalex-snapshot
Insect Seminal Fluid Proteins: Identification and Function
inferredcites →https://doi.org/10.1177/0960327119836230openalex-snapshot
Abnormal methylation of spermatozoa induced by benzo(a)pyrene in rats
inferredcites →https://doi.org/10.1186/1471-213x-8-114openalex-snapshot
Tissue remodeling: a mating-induced differentiation program for the Drosophilaoviduct
inferredcites →https://doi.org/10.1186/gb-2010-11-2-r14openalex-snapshot
Gene ontology analysis for RNA-seq: accounting for selection bias
inferredcites →https://doi.org/10.1186/s12864-015-2239-0openalex-snapshot
The neurotranscriptome of the Aedes aegypti mosquito
inferredcites →https://doi.org/10.1186/s12864-020-6543-yopenalex-snapshot
Transcriptional profiling and physiological roles of Aedes aegypti spermathecal-related genes
inferredcites →https://doi.org/10.1186/s12915-022-01465-2openalex-snapshot
Female factors modulate Sex Peptide’s association with sperm in Drosophila melanogaster
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1248/bpb.35.838openalex-snapshot
Recent Studies on Insect Hormone Metabolic Pathways Mediated by Cytochrome P450 Enzymes
inferredcites →https://doi.org/10.1371/journal.pbio.2005004openalex-snapshot
Midgut-derived neuropeptide F controls germline stem cell proliferation in a mating-dependent manner
inferredcites →https://doi.org/10.1371/journal.pgen.1002779openalex-snapshot
Gustatory Perception and Fat Body Energy Metabolism Are Jointly Affected by Vitellogenin and Juvenile Hormone in Honey Bees
inferredcites →https://doi.org/10.1371/journal.pntd.0002486openalex-snapshot
Functional and Genetic Characterization of Neuropeptide Y-Like Receptors in Aedes aegypti
inferredcites →https://doi.org/10.1371/journal.pntd.0004451openalex-snapshot
Mating-Induced Transcriptome Changes in the Reproductive Tract of Female Aedes aegypti
inferredcites →https://doi.org/10.1371/journal.pntd.0006933openalex-snapshot
CYP-mediated permethrin resistance in Aedes aegypti and evidence for trans-regulation
inferredcites →https://doi.org/10.1371/journal.pntd.0009815openalex-snapshot
The impact of mating and sugar feeding on blood-feeding physiology and behavior in the arbovirus vector mosquito Aedes aegypti
inferredcites →https://doi.org/10.1371/journal.pone.0188243openalex-snapshot
Feeding-induced changes in allatostatin-A and short neuropeptide F in the antennal lobes affect odor-mediated host seeking in the yellow fever mosquito, Aedes aegypti
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads
inferredcites →https://doi.org/10.1534/genetics.113.160945openalex-snapshot
Neprilysins: An Evolutionarily Conserved Family of Metalloproteases That Play Important Roles in Reproduction in Drosophila
inferredcites →https://doi.org/10.1653/024.095.0204openalex-snapshot
Mating Status and Body Size inAedes albopictus(Diptera: Culicidae) Affect Host Finding and Deet Repellency
inferredcites →https://doi.org/10.2147/ijn.s254480openalex-snapshot
Low-Dose Exposure of Silica Nanoparticles Induces Neurotoxicity via Neuroactive Ligand–Receptor Interaction Signaling Pathway in Zebrafish Embryos
inferredcites →https://doi.org/10.3390/biom11040509openalex-snapshot
The 40-Year Mystery of Insect Odorant-Binding Proteins
inferredcites →https://doi.org/10.7554/elife.13238openalex-snapshot
Gap junction networks in mushroom bodies participate in visual learning and memory in Drosophila
inferredcites →https://doi.org/10.7554/elife.86409openalex-snapshot
The seminal odorant binding protein Obp56g is required for mating plug formation and male fertility in Drosophila melanogaster
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.