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Transcriptional expression of immune system genes inLitopenaeus vannameiduring ontogenetic development
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/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/s13353-013-0191-8openalex-snapshot
Cloning of Hsp21 gene and its expression in Chinese shrimp Fenneropenaeus chinensis in response to WSSV challenge
inferredcites →https://doi.org/10.1016/j.aquaculture.2012.05.005openalex-snapshot
Ontogenetic changes of innate immune parameters from eggs to early postlarvae of white shrimp Litopenaeus vannamei (Crustacea:Decapoda)
inferredcites →https://doi.org/10.1016/j.aquaculture.2013.10.042openalex-snapshot
Gene expression responses of white shrimp (Litopenaeus vannamei) infected with necrotizing hepatopancreatitis bacterium
inferredcites →https://doi.org/10.1016/j.cbpc.2005.07.005openalex-snapshot
Starvation and diet composition affect mRNA levels of the high density-lipoprotein-β glucan binding protein in the shrimp Litopenaeus vannamei
inferredcites →https://doi.org/10.1016/j.dci.2006.05.007openalex-snapshot
Expression and characterisation of tiger shrimp Penaeus monodon penaeidin (mo-penaeidin) in various tissues, during early embryonic development and moulting stages
inferredcites →https://doi.org/10.1016/j.fsi.2004.08.002openalex-snapshot
Molecular cloning and characterisation of a pattern recognition molecule, lipopolysaccharide- and β-1,3-glucan binding protein (LGBP) from the white shrimp Litopenaeus vannamei
inferredcites →https://doi.org/10.1016/j.fsi.2004.10.005openalex-snapshot
The peroxinectin of white shrimp Litopenaeus vannamei is synthesised in the semi-granular and granular cells, and its transcription is up-regulated with Vibrio alginolyticus infection
inferredcites →https://doi.org/10.1016/j.fsi.2007.03.003openalex-snapshot
Expression of immune-related genes in larval stages of the giant tiger shrimp, Penaeus monodon
inferredcites →https://doi.org/10.1016/j.fsi.2010.10.013openalex-snapshot
Transcriptional regulation of extracellular copper zinc superoxide dismutase from white shrimp Litopenaeus vannamei following Vibrio alginolyticus and WSSV infection
inferredcites →https://doi.org/10.1016/j.fsi.2012.03.020openalex-snapshot
Gene expression and protein levels of thioredoxin in the gills from the whiteleg shrimp (Litopenaeus vannamei) infected with two different viruses: The WSSV or IHHNV
inferredcites →https://doi.org/10.1016/s0044-8486(00)00413-0openalex-snapshot
Shrimp immunity and disease control
inferredcites →https://doi.org/10.1016/s0044-8486(03)00521-0openalex-snapshot
Anti-infectious immune effectors in marine invertebrates: potential tools for disease control in larviculture
inferredcites →https://doi.org/10.1016/s0145-305x(02)00102-7openalex-snapshot
Expression of penaeidin antimicrobial peptides in early larval stages of the shrimp Penaeus vannamei
inferredcites →https://doi.org/10.1016/s0145-305x(03)00121-6openalex-snapshot
Recognition of infectious non-self and activation of immune responses by peptidoglycan recognition protein (PGRP)-family members in Drosophila
inferredcites →https://doi.org/10.1016/s0305-0491(99)00191-1openalex-snapshot
Differential expression of ras in organs and embryos of shrimp Penaeus monodon (Crustacea: Decapoda)
inferredcites →https://doi.org/10.1016/s1050-4648(02)00176-6openalex-snapshot
cDNA cloning of the lysozyme of the white shrimp Penaeus vannamei
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/10.1046/j.1432-1033.2002.02934.xopenalex-snapshot
Expression and distribution of penaeidin antimicrobial peptides are regulated by haemocyte reactions in microbial challenged shrimp
inferredcites →https://doi.org/10.1074/jbc.m114.605568openalex-snapshot
Suppression of Shrimp Melanization during White Spot Syndrome Virus Infection
inferredcites →https://doi.org/10.1080/09712119.2010.9707170openalex-snapshot
Effect of Dose and Feeding Frequency of Glucan as Immunostimulant to ChineseFenneropenaeus chinensisfrom Zoea to Postlarvae
inferredcites →https://doi.org/10.1100/2012/193403openalex-snapshot
Erratum to “Fusion Pore Diameter Regulation by Cations Modulating Local Membrane Anisotropy”
inferredcites →https://doi.org/10.1100/2012/389623openalex-snapshot
World Aquaculture: Environmental Impacts and Troubleshooting Alternatives
inferredcites →https://doi.org/10.1111/j.0105-2896.2004.00115.xopenalex-snapshot
Insights into the anti‐microbial defense of marine invertebrates: the penaeid shrimps and the oyster Crassostrea gigas
inferredcites →https://doi.org/10.1111/j.0105-2896.2004.00116.xopenalex-snapshot
The prophenoloxidase‐activating system in invertebrates
inferredcites →https://doi.org/10.1111/j.1432-1033.1993.tb17798.xopenalex-snapshot
Characterization of a clotting protein, isolated from plasma of the freshwater crayfish Pacifastacus leniusculus
inferredcites →https://doi.org/10.1146/annurev.immunol.20.083001.084359openalex-snapshot
Innate Immune Recognition
inferredcites →https://doi.org/10.1379/csc-47r.1openalex-snapshot
Cloning and molecular characterization of heat shock cognate 70 from tiger shrimp (Penaeus monodon)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4779250openalex-extracted
Growth, Survival, and Immune Response of Penaeus Monodon Post-Larvae Co-Cultured with Quorum Quenching Marine Benthic Filamentous Cyanobacteria Leptolyngbya Sp. Macc32 Oq550416
inferred← citeshttps://doi.org/10.1007/s10499-020-00532-1openalex-snapshot
Gut microbiota shifts in the giant tiger shrimp, Penaeus monodon, during the postlarvae, juvenile, and adult stages
inferred← citeshttps://doi.org/10.1016/j.aggene.2018.05.002openalex-snapshot
Ontogenetic and expression of different genes involved in the Toll pathway of black tiger shrimp (Penaeus monodon) following immersion challenge with Vibrio harveyi and white spot syndrome virus (WSSV)
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2023.107280openalex-snapshot
A novel technique for mass induction of propagation in small fish species: Hormone immersion
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2017.05.030openalex-snapshot
Ontogenesis of metabolic gene expression in whiteleg shrimp (Litopenaeus vannamei): New molecular tools for programming in the future
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2023.740266openalex-snapshot
Terminalia catappa L. leaf extract interferes with biofilm formation of Vibrio parahaemolyticus and enhances immune response of Penaeus vannamei against acute hepatopancreatic necrosis disease (AHPND)
inferred← citeshttps://doi.org/10.1016/j.dci.2019.103577openalex-snapshot
Induction of innate immune response in whiteleg shrimp (Litopenaeus vannamei) embryos
inferred← citeshttps://doi.org/10.1016/j.jip.2020.107527openalex-snapshot
Vibrio and major commercially important vibriosis diseases in decapod crustaceans
inferred← citeshttps://doi.org/10.1080/09712119.2022.2050736openalex-snapshot
Identification, characterization and infection dynamics of Vibrio strains in phyllosoma of Thenus unimaculatus
inferred← citeshttps://doi.org/10.3389/fmars.2026.1745901openalex-snapshot
Litsea citrata essential oil provides insights into the modulation of heat stress–associated transcriptomic responses in Artemia franciscana
inferred← citeshttps://doi.org/10.7717/peerj.7475openalex-snapshot
Antibacterial immune functions of subadults and adults in a semelparous spider
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