On the public citation graph
Biological effects of tris (1-chloro-2-propyl) phosphate (TCPP) on immunity in mussel Mytilus galloprovincialis
0 signed · 75 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known work and none has been retracted — and get a dated CiteStamped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/jemt.10100openalex-snapshot
Bacteria–hemocyte interactions and phagocytosis in marine bivalves
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/10.1016/0048-9697(96)05275-8openalex-snapshot
The international mussel watch: a global assessment of environmental levels of chemical contaminants
inferredcites →https://doi.org/10.1016/0272-7714(83)90095-1openalex-snapshot
U.S. Mussel Watch: 1977–1978 results on trace metals and radionuclides
inferredcites →https://doi.org/10.1016/j.aquatox.2011.06.014openalex-snapshot
Molecular and biochemical biomarkers in environmental monitoring: A comparison of biotransformation and antioxidant defense systems in multiple tissues
inferredcites →https://doi.org/10.1016/j.bbabio.2006.04.029openalex-snapshot
Mitochondrial ROS-induced ROS release: An update and review
inferredcites →https://doi.org/10.1016/j.chemosphere.2008.09.022openalex-snapshot
Effect of tris-(2-chloroethyl)-phosphate (TCEP) at environmental concentration on the levels of cell cycle regulatory protein expression in primary cultured rabbit renal proximal tubule cells
inferredcites →https://doi.org/10.1016/j.dci.2007.10.010openalex-snapshot
Requirement for shrimp caspase in apoptosis against virus infection
inferredcites →https://doi.org/10.1016/j.dci.2011.08.003openalex-snapshot
Big defensins and mytimacins, new AMP families of the Mediterranean mussel Mytilus galloprovincialis
inferredcites →https://doi.org/10.1016/j.dci.2013.02.006openalex-snapshot
Toll-like receptors and MyD88 adaptors in Mytilus: Complete cds and gene expression levels
inferredcites →https://doi.org/10.1016/j.envpol.2014.12.037openalex-snapshot
Occurrence and spatial distribution of organophosphate ester flame retardants and plasticizers in 40 rivers draining into the Bohai Sea, north China
inferredcites →https://doi.org/10.1016/j.fsi.2014.07.018openalex-snapshot
Comparative study of immune responses in the deep-sea hydrothermal vent mussel Bathymodiolus azoricus and the shallow-water mussel Mytilus galloprovincialis challenged with Vibrio bacteria
inferredcites →https://doi.org/10.1016/j.fsi.2015.02.013openalex-snapshot
An updated molecular basis for mussel immunity
inferredcites →https://doi.org/10.1016/j.fsi.2016.01.025openalex-snapshot
Identification and functional characterization of three TLR signaling pathway genes in Cyclina sinensis
inferredcites →https://doi.org/10.1016/j.fsi.2017.12.038openalex-snapshot
The immune response of Mytilus edulis hemocytes exposed to Vibrio splendidus LGP32 strain: A transcriptomic attempt at identifying molecular actors
inferredcites →https://doi.org/10.1016/j.marpolbul.2017.06.034openalex-snapshot
Occurrence and spatial distribution of organophosphorus flame retardants and plasticizers in the Bohai and Yellow Seas, China
inferredcites →https://doi.org/10.1016/j.scitotenv.2004.04.021openalex-snapshot
Organophosphorus flame retardants and plasticisers in surface waters
inferredcites →https://doi.org/10.1016/j.scitotenv.2007.08.005openalex-snapshot
Determination of selected organophosphate esters in the aquatic environment of Austria
inferredcites →https://doi.org/10.1016/j.scitotenv.2017.09.272openalex-snapshot
Occurrences and distribution characteristics of organophosphate ester flame retardants and plasticizers in the sediments of the Bohai and Yellow Seas, China
inferredcites →https://doi.org/10.1016/j.trac.2008.07.002openalex-snapshot
Organophosphorus flame retardants and plasticizers in water and air I. Occurrence and fate
inferredcites →https://doi.org/10.1016/j.watres.2010.05.024openalex-snapshot
Occurrence and fate of organophosphorus flame retardants and plasticizers in urban and remote surface waters in Germany
inferredcites →https://doi.org/10.1021/es702549gopenalex-snapshot
Occurrence of Organophosphorus Flame Retardant and Plasticizers in Three Volcanic Lakes of Central Italy
inferredcites →https://doi.org/10.1073/pnas.051630598openalex-snapshot
An orchestrated gene expression component of neuronal programmed cell death revealed by cDNA array analysis
inferredcites →https://doi.org/10.1073/pnas.94.5.2056openalex-snapshot
Prostate enlargement in mice due to fetal exposure to low doses of estradiol or diethylstilbestrol and opposite effects at high doses
inferredcites →https://doi.org/10.1111/j.1600-065x.2009.00790.xopenalex-snapshot
Galectins in innate immunity: dual functions of host soluble β‐galactoside‐binding lectins as damage‐associated molecular patterns (DAMPs) and as receptors for pathogen‐associated molecular patterns (PAMPs)
inferredcites →https://doi.org/10.1186/1471-2164-12-69openalex-snapshot
Insights into the innate immunity of the Mediterranean mussel Mytilus galloprovincialis
inferredcites →https://doi.org/10.1289/ehp.1408111openalex-snapshot
Ligand Binding and Activation of PPAR γ by Firemaster® 550: Effects on Adipogenesis and Osteogenesis in Vitro
inferredcites →https://doi.org/10.1371/journal.pone.0017003openalex-snapshot
New Insights into the Apoptotic Process in Mollusks: Characterization of Caspase Genes in Mytilus galloprovincialis
inferredcites →https://doi.org/10.1371/journal.pone.0045148openalex-snapshot
Two Goose-Type Lysozymes in Mytilus galloprovincialis: Possible Function Diversification and Adaptive Evolution
inferredcites →https://doi.org/10.1371/journal.pone.0067469openalex-snapshot
A Novel C-Type Lysozyme from Mytilus galloprovincialis: Insight into Innate Immunity and Molecular Evolution of Invertebrate C-Type Lysozymes
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.4747834openalex-extracted
Tris (1-Chloropropan-2-Yl) Phosphate Enhances the Adverse Effects of Biodegradable Polylactic Acid Microplastics on the Thick-Shelled Mussel Mytilus Coruscus
inferred← citeshttps://doi.org/10.1002/jez.2446openalex-snapshot
Embryotoxicity characterization of the flame retardant tris(1‐chloro‐2‐propyl)phosphate (TCPP) in the invertebrate chordate Ciona intestinalis
inferred← citeshttps://doi.org/10.1007/s10646-023-02702-2openalex-snapshot
Toxicity assessment of microplastics within the Loire River in the clam Corbicula fluminea exposed to environmentally relevant exposure conditions
inferred← citeshttps://doi.org/10.1007/s11030-026-11681-5openalex-snapshot
Integrated network toxicology and bioinformatics approaches explore potential mechanisms linking organophosphate flame retardant exposure to rheumatoid arthritis
inferred← citeshttps://doi.org/10.1007/s11356-020-08721-4openalex-snapshot
Biomarkers of oxidative stress and cell damage in freshwater bivalves Diplodon parodizi exposed to landfill leachate
inferred← citeshttps://doi.org/10.1007/s44169-024-00077-xopenalex-snapshot
A Review on Co-Occurrence of Microplastics and Flame Retardants in Global Aquatic Environment with A Focus on Microfibers: Sources and Impacts on Their Toxic Effects
inferred← citeshttps://doi.org/10.1016/j.buildenv.2021.107888openalex-snapshot
Evaluation of a four-zone indoor exposure model for predicting TCPP concentrations in a low-energy test house
inferred← citeshttps://doi.org/10.1016/j.cej.2025.160094openalex-snapshot
Regulating electron transfer in Fe3O4/BiVO4 Z-scheme heterojunction for synergistic photocatalytic degradation of tri(2,3-dichloropropyl)phosphate
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.05.188openalex-snapshot
Biodegradation of tricresyl phosphate isomers by Brevibacillus brevis: Degradation pathway and metabolic mechanism
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.130347openalex-snapshot
Phytotoxicity of tris-(1-chloro-2-propyl) phosphate in soil and its uptake and accumulation by pakchoi (Brassica chinensis L. cv. SuZhou)
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2023.140122openalex-snapshot
Remediation of soil contaminated with tris-(1-chloro-2-propyl) phosphate using plant and microorganism combined technology: A greenhouse experiment
inferred← citeshttps://doi.org/10.1016/j.cotox.2020.07.002openalex-snapshot
Plastics and plastic additives as inducers of oxidative stress
inferred← citeshttps://doi.org/10.1016/j.cotox.2022.02.009openalex-snapshot
Hormesis dose–response contaminant-induced hormesis in animals
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113796openalex-snapshot
Sub-chronic ecotoxicity of triphenyl phosphate to earthworms (Eisenia fetida) in artificial soil: Oxidative stress and DNA damage
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.114313openalex-snapshot
Parental whole life-cycle exposure to tris (2-chloroethyl) phosphate (TCEP) disrupts embryonic development and thyroid system in zebrafish offspring
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118718openalex-snapshot
Damage and immunosuppression to Mytilus galloprovincialis hemocytes caused by chronic tris(chloropropyl)phosphate exposure
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.124741openalex-snapshot
Tris(1-chloro-2-propyl) phosphate enhances the adverse effects of biodegradable polylactic acid microplastics on the mussel Mytilus coruscus
inferred← citeshttps://doi.org/10.1016/j.envres.2026.125889openalex-snapshot
Biochemical Responses of Mytilus galloprovincialis to Individual and Binary Exposures to PFDoA, Bisphenol A and Tricresyl Phosphate: Exposure and Post-exposure Dynamics
inferred← citeshttps://doi.org/10.1016/j.etap.2021.103699openalex-snapshot
Effects of tris (2-chloroethyl) phosphate (TCEP) on survival, growth, histological changes and gene expressions in juvenile yellow catfish Pelteobagrus fulvidraco
inferred← citeshttps://doi.org/10.1016/j.fsi.2025.110147openalex-snapshot
Exploring the immune resilience of Mediterranean mussels: Recent advances and future directions
inferred← citeshttps://doi.org/10.1016/j.jes.2025.10.042openalex-snapshot
Co-occurrence of organophosphate triesters and diesters in coral polyps, algae, and sediments from Sanya, China: di-OPEs having direct commercial applications?
inferred← citeshttps://doi.org/10.1016/j.jes.2026.105640openalex-snapshot
Organophosphate flame retardants and immunotoxicity: An integrated bibliometric and systematic review of epidemiological and mechanistic evidence
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.122909openalex-snapshot
Microplastics aggravate the adverse effects of BDE-47 on physiological and defense performance in mussels
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.127782openalex-snapshot
Amino-functionalized MIL-88B as heterogeneous photo-Fenton catalysts for enhancing tris-(2-chloroisopropyl) phosphate (TCPP) degradation: Dual excitation pathways accelerate the conversion of FeIII to FeII under visible light irradiation
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2024.116682openalex-snapshot
Nano titanium dioxide alleviates the toxic effects of tris (2-chloropropyl) phosphate on the digestive gland and hemolymph of thick-shell mussel Mytilus coruscus
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.117628openalex-snapshot
Ecotoxicological responses of marine fish to the organophosphate flame-retardant tris (2-chloroisopropyl) phosphate (TCPP) dietary exposure: Juvenile gilthead seabream (Sparus aurata) as a case study
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.118466openalex-snapshot
The combined effects of aging polylactic acid microplastics and TCPP on the byssus genes of the mussel Mytilus coruscus
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.143694openalex-snapshot
Tris (1-chloro-2-propyl) phosphate exposure to zebrafish causes neurodevelopmental toxicity and abnormal locomotor behavior
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.153295openalex-snapshot
Hormetic dose responses induced by organic flame retardants in aquatic animals: Occurrence and quantification
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.153899openalex-snapshot
Hormesis and insects: Effects and interactions in agroecosystems
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.158176openalex-snapshot
nTiO2 alleviates the toxic effects of TCPP on mussels by adjusting respiratory metabolism and gut microbiota
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.158808openalex-snapshot
Organophosphate ester exposure among Chinese waste incinerator workers: Urinary levels, risk assessment and associations with oxidative stress
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.164415openalex-snapshot
Polybrominated diphenyl ether-47 and food shortage impair the byssal attachment and health of marine mussels
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.177256openalex-snapshot
Toxicity of organophosphate flame retardant in marine rotifers: Evidence from the population, individual, biochemical and molecular levels
inferred← citeshttps://doi.org/10.1021/acs.est.9b01585openalex-snapshot
The Amazon River: A Major Source of Organic Plastic Additives to the Tropical North Atlantic?
inferred← citeshttps://doi.org/10.1021/envhealth.5c00035openalex-snapshot
Aging Enhances the Ecotoxicological Effects of Biobased Microplastic Poly(Lactic Acid) and Its Adsorbed Tris(1-chloro-2-propyl)phosphate on Mussels
inferred← citeshttps://doi.org/10.1038/s43017-022-00277-wopenalex-snapshot
Organophosphate ester pollution in the oceans
inferred← citeshttps://doi.org/10.1080/10643389.2024.2406587openalex-snapshot
A comprehensive and quantitative comparison of organophosphate esters: Characteristics, applications, environmental occurrence, toxicity, and health risks
inferred← citeshttps://doi.org/10.1097/md.0000000000051024openalex-snapshot
Revealing the toxicological effects and mechanisms of tris(1-chloro-2-propyl) phosphate exposure on osteoarthritis based on network toxicology, machine learning, and molecular docking
inferred← citeshttps://doi.org/10.1186/s12302-023-00805-5openalex-snapshot
Non-target screening of surface water samples to identify exposome-related pollutants: a case study from Luxembourg
inferred← citeshttps://doi.org/10.3389/fmars.2021.658361openalex-snapshot
Dose-Dependent Effects of Di-(2-Ethylhexyl) Phthalate (DEHP) in Mussel Mytilus galloprovincialis
inferred← citeshttps://doi.org/10.3390/toxics10120736openalex-snapshot
Genotoxic and Toxic Effects of The Flame Retardant Tris(Chloropropyl) Phosphate (TCPP) in Human Lymphocytes, Microalgae and Bacteria
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636832openalex-snapshot
Additional file 1 of Non-target screening of surface water samples to identify exposome-related pollutants: a case study from Luxembourg
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636835openalex-snapshot
Additional file 2 of Non-target screening of surface water samples to identify exposome-related pollutants: a case study from Luxembourg
inferred← citeshttps://doi.org/10.70675/345f2a37z6143z4e1dz8df6z02e0ed8ec34aopenalex-snapshot
Environmental occurrence and fluxes of organic contaminants of emerging concern in the coastal NW Mediterranean sea and the Rhône river
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.