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Transcriptomic profiling of adaptive responses to ocean acidification

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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/ece3.719openalex-snapshot
Identification of molecular and physiological responses to chronic environmental challenge in an invasive species: the P acific oyster, C rassostrea gigas
inferredcites →https://doi.org/10.1002/pmic.201500198openalex-snapshot
Comparative and quantitative proteomics reveal the adaptive strategies of oyster larvae to ocean acidification
inferredcites →https://doi.org/10.1006/bbrc.1999.1907openalex-snapshot
Purification and Characterization of Perlucin and Perlustrin, Two New Proteins from the Shell of the Mollusc Haliotis laevigata
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/10.1007/978-1-4615-1941-6_72openalex-snapshot
Role of Lectins (C-Reactive Protein) in Defense of Marine Bivalves Against Bacteria
inferredcites →https://doi.org/10.1007/s00227-010-1592-4openalex-snapshot
Populations of the Sydney rock oyster, Saccostrea glomerata, vary in response to ocean acidification
inferredcites →https://doi.org/10.1007/s00227-012-1921-xopenalex-snapshot
Long-term and trans-life-cycle effects of exposure to ocean acidification in the green sea urchin Strongylocentrotus droebachiensis
inferredcites →https://doi.org/10.1007/s00227-012-1930-9openalex-snapshot
Impacts of seawater acidification on mantle gene expression patterns of the Baltic Sea blue mussel: implications for shell formation and energy metabolism
inferredcites →https://doi.org/10.1007/s00227-013-2176-xopenalex-snapshot
Elevated CO2 alters larval proteome and its phosphorylation status in the commercial oyster, Crassostrea hongkongensis
inferredcites →https://doi.org/10.1007/s00227-013-2219-3openalex-snapshot
Impacts of ocean acidification on marine shelled molluscs
inferredcites →https://doi.org/10.1007/s00227-014-2450-6openalex-snapshot
Within- and transgenerational effects of ocean acidification on life history of marine three-spined stickleback (Gasterosteus aculeatus)
inferredcites →https://doi.org/10.1007/s10126-011-9403-6openalex-snapshot
Microarray Analysis Highlights Immune Response of Pacific Oysters as a Determinant of Resistance to Summer Mortality
inferredcites →https://doi.org/10.1007/s10872-004-5763-0openalex-snapshot
Biological Impact of Elevated Ocean CO2 Concentrations: Lessons from Animal Physiology and Earth History
inferredcites →https://doi.org/10.1007/s11103-012-9885-2openalex-snapshot
miRDeepFinder: a miRNA analysis tool for deep sequencing of plant small RNAs
inferredcites →https://doi.org/10.1007/s12192-008-0091-8openalex-snapshot
Transcriptional expression levels of cell stress marker genes in the Pacific oyster Crassostrea gigas exposed to acute thermal stress
inferredcites →https://doi.org/10.1016/bs.ircmb.2015.01.002openalex-snapshot
Comparative Biology of the Pentraxin Protein Family: Evolutionarily Conserved Component of Innate Immune System
inferredcites →https://doi.org/10.1016/j.cbd.2014.12.001openalex-snapshot
Combined metabolome and proteome analysis of the mantle tissue from Pacific oyster Crassostrea gigas exposed to elevated pCO2
inferredcites →https://doi.org/10.1016/j.cbpa.2012.12.025openalex-snapshot
Interactive effects of elevated temperature and CO2 levels on metabolism and oxidative stress in two common marine bivalves (Crassostrea virginica and Mercenaria mercenaria)
inferredcites →https://doi.org/10.1016/j.dci.2011.01.018openalex-snapshot
The C1q domain containing proteins of the Mediterranean mussel Mytilus galloprovincialis: A widespread and diverse family of immune-related molecules
inferredcites →https://doi.org/10.1016/j.fsi.2012.05.032openalex-snapshot
A novel C1qDC protein acting as pattern recognition receptor in scallop Argopecten irradians
inferredcites →https://doi.org/10.1016/j.fsi.2014.02.016openalex-snapshot
Immunomodulation by the interactive effects of cadmium and hypercapnia in marine bivalves Crassostrea virginica and Mercenaria mercenaria
inferredcites →https://doi.org/10.1016/j.jembe.2010.02.007openalex-snapshot
Long-term effects of nutrient and CO2 enrichment on the temperate coral Astrangia poculata (Ellis and Solander, 1786)
inferredcites →https://doi.org/10.1016/j.margen.2010.08.005openalex-snapshot
Transcriptomic response of the Pacific oyster Crassostrea gigas to hypoxia
inferredcites →https://doi.org/10.1016/j.marpolbul.2012.07.043openalex-snapshot
Analysis of Pacific oyster larval proteome and its response to high-CO2
inferredcites →https://doi.org/10.1021/es501581jopenalex-snapshot
Multigenerational Exposure to Ocean Acidification during Food Limitation Reveals Consequences for Copepod Scope for Growth and Vital Rates
inferredcites →https://doi.org/10.1021/pr500940sopenalex-snapshot
Proteomic Basis of Stress Responses in the Gills of the Pacific OysterCrassostrea gigas
inferredcites →https://doi.org/10.1038/nature11413openalex-snapshot
The oyster genome reveals stress adaptation and complexity of shell formation
inferredcites →https://doi.org/10.1038/nclimate1323openalex-snapshot
Rapid transgenerational acclimation of a tropical reef fish to climate change
inferredcites →https://doi.org/10.1038/nclimate1599openalex-snapshot
Parental environment mediates impacts of increased carbon dioxide on a coral reef fish
inferredcites →https://doi.org/10.1038/nclimate2400openalex-snapshot
Effects of elevated CO2 on fish behaviour undiminished by transgenerational acclimation
inferredcites →https://doi.org/10.1038/nclimate2724openalex-snapshot
Molecular processes of transgenerational acclimation to a warming ocean
inferredcites →https://doi.org/10.1038/nclimate3087openalex-snapshot
Molecular signatures of transgenerational response to ocean acidification in a species of reef fish
inferredcites →https://doi.org/10.1038/ncomms5426openalex-snapshot
Family-wide analysis of poly(ADP-ribose) polymerase activity
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1046/j.1432-1327.2000.01602.xopenalex-snapshot
The amino‐acid sequence of the abalone (Haliotis laevigata) nacre protein perlucin
inferredcites →https://doi.org/10.1073/pnas.1422301112openalex-snapshot
Building coral reef resilience through assisted evolution
inferredcites →https://doi.org/10.1080/10409230701648502openalex-snapshot
Mutation as a Stress Response and the Regulation of Evolvability
inferredcites →https://doi.org/10.1093/bioinformatics/btp616openalex-snapshot
edgeR : a Bioconductor package for differential expression analysis of digital gene expression data
inferredcites →https://doi.org/10.1093/bioinformatics/btu170openalex-snapshot
Trimmomatic: a flexible trimmer for Illumina sequence data
inferredcites →https://doi.org/10.1093/molbev/msu107openalex-snapshot
Lineage-Specific Transcriptional Profiles of Symbiodinium spp. Unaltered by Heat Stress in a Coral Host
inferredcites →https://doi.org/10.1093/nar/gks596openalex-snapshot
Primer3—new capabilities and interfaces
inferredcites →https://doi.org/10.1098/rsbl.2016.0798openalex-snapshot
Adult exposure to ocean acidification is maladaptive for larvae of the Sydney rock oyster Saccostrea glomerata in the presence of multiple stressors
inferredcites →https://doi.org/10.1098/rspb.2013.2179openalex-snapshot
Parental effects improve escape performance of juvenile reef fish in a high-CO2world
inferredcites →https://doi.org/10.1111/are.12012openalex-snapshot
Evaluation of the progeny of the fourth-generation Sydney rock oyster Saccostrea glomerata (Gould, 1850) breeding lines for resistance to QX disease (Marteilia sydneyi) and winter mortality (Bonamia roughleyi)
inferredcites →https://doi.org/10.1111/gcb.12109openalex-snapshot
Food availability outweighs ocean acidification effects in juvenile M ytilus edulis : laboratory and field experiments
inferredcites →https://doi.org/10.1111/gcb.13249openalex-snapshot
Quantitative analysis of oyster larval proteome provides new insights into the effects of multiple climate change stressors
inferredcites →https://doi.org/10.1111/j.1365-2486.2011.02520.xopenalex-snapshot
Adult exposure influences offspring response to ocean acidification in oysters
inferredcites →https://doi.org/10.1111/j.1365-2818.2003.01263.xopenalex-snapshot
The nacre protein perlucin nucleates growth of calcium carbonate crystals
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05018.xopenalex-snapshot
The transcriptomic responses of the eastern oyster, Crassostrea virginica , to environmental conditions
inferredcites →https://doi.org/10.1111/j.1742-4658.2005.04960.xopenalex-snapshot
Response of the Pacific oyster Crassostrea gigas to hypoxia exposure under experimental conditions
inferredcites →https://doi.org/10.1111/j.1742-4658.2007.06156.xopenalex-snapshot
Identification of differentially expressed genes of the Pacific oysterCrassostrea gigasexposed to prolonged thermal stress
inferredcites →https://doi.org/10.1111/mec.13047openalex-snapshot
RNA ‐seq reveals regional differences in transcriptome response to heat stress in the marine snail C hlorostoma funebralis
inferredcites →https://doi.org/10.1111/mec.13111openalex-snapshot
Differential proteomic responses of selectively bred and wild‐type Sydney rock oyster populations exposed to elevated CO 2
inferredcites →https://doi.org/10.1111/mec.13808openalex-snapshot
Rapid transcriptional acclimation following transgenerational exposure of oysters to ocean acidification
inferredcites →https://doi.org/10.1126/science.1157130openalex-snapshot
Marine Calcifiers in a High-CO 2 Ocean
inferredcites →https://doi.org/10.1146/annurev-physiol-021909-135900openalex-snapshot
Living in the Now: Physiological Mechanisms to Tolerate a Rapidly Changing Environment
inferredcites →https://doi.org/10.1146/annurev.physiol.61.1.243openalex-snapshot
HEAT-SHOCK PROTEINS, MOLECULAR CHAPERONES, AND THE STRESS RESPONSE: Evolutionary and Ecological Physiology
inferredcites →https://doi.org/10.1186/1471-2164-15-951openalex-snapshot
Shotgun proteomics reveals physiological response to ocean acidification in Crassostrea gigas
inferredcites →https://doi.org/10.1186/s12864-017-3818-zopenalex-snapshot
Contrasting impacts of ocean acidification and warming on the molecular responses of CO2-resilient oysters
inferredcites →https://doi.org/10.1186/s13059-014-0410-6openalex-snapshot
Corset: enabling differential gene expression analysis for de novoassembled transcriptomes
inferredcites →https://doi.org/10.1186/s40665-016-0019-yopenalex-snapshot
Molecular analysis of the Sydney rock oyster (Saccostrea glomerata) CO2 stress response
inferredcites →https://doi.org/10.1242/jcs.01604openalex-snapshot
Distinct functions of condensin I and II in mitotic chromosome assembly
inferredcites →https://doi.org/10.1242/jeb.055475openalex-snapshot
Proteomic response to elevated PCO2 level in eastern oysters, Crassostrea virginica: evidence for oxidative stress
inferredcites →https://doi.org/10.1242/jeb.123018openalex-snapshot
Preconditioning in the reef-building coralPocillopora damicornisand the potential for trans-generational acclimatization in coral larvae under future climate change conditions
inferredcites →https://doi.org/10.1242/jeb.126748openalex-snapshot
Interactive effects of seawater acidification and elevated temperature on biomineralization and amino acid metabolism in the musselMytilus edulis
inferredcites →https://doi.org/10.1371/journal.pone.0005661openalex-snapshot
Shellfish Face Uncertain Future in High CO2 World: Influence of Acidification on Oyster Larvae Calcification and Growth in Estuaries
inferredcites →https://doi.org/10.1371/journal.pone.0022881openalex-snapshot
Quantifying Rates of Evolutionary Adaptation in Response to Ocean Acidification
inferredcites →https://doi.org/10.1371/journal.pone.0081821openalex-snapshot
RNA-seq Profiles of Immune Related Genes in the Staghorn Coral Acropora cervicornis Infected with White Band Disease
inferredcites →https://doi.org/10.1371/journal.pone.0105097openalex-snapshot
Transcriptome of American Oysters, Crassostrea virginica, in Response to Bacterial Challenge: Insights into Potential Mechanisms of Disease Resistance
inferredcites →https://doi.org/10.1371/journal.pone.0118839openalex-snapshot
Meta-Analysis of Studies Using Suppression Subtractive Hybridization and Microarrays to Investigate the Effects of Environmental Stress on Gene Transcription in Oysters
inferredcites →https://doi.org/10.1371/journal.pone.0132276openalex-snapshot
Persistence of Positive Carryover Effects in the Oyster, Saccostrea glomerata, following Transgenerational Exposure to Ocean Acidification
inferredcites →https://doi.org/10.2174/0929866511320050014openalex-snapshot
The Expression and Induction of Heat Shock Proteins in Molluscs
inferredcites →https://doi.org/10.3354/aei00058openalex-snapshot
Assessing the risk of climate change to aquaculture: a case study from south-east Australia
inferredcites →https://doi.org/10.3354/meps07802openalex-snapshot
Effects of CO2-driven ocean acidification on the early developmental stages of invertebrates
inferredcites →https://doi.org/10.3354/meps08430openalex-snapshot
Reduced salinity, but not estuarine acidification, is a cause of immune-suppression in the Sydney rock oyster Saccostrea glomerata
inferredcites →https://doi.org/10.3354/meps08841openalex-snapshot
Elevated level of carbon dioxide affects metabolism and shell formation in oysters Crassostrea virginica (Gmelin)
inferredcites →https://doi.org/10.3354/meps12109openalex-snapshot
Lack of genetic introgression between wild and selectively bred Sydney rock oysters Saccostrea glomerata
inferredcites →https://doi.org/10.3390/biology2020651openalex-snapshot
Predicting the Response of Molluscs to the Impact of Ocean Acidification
inferredcites →https://doi.org/10.3390/md8082318openalex-snapshot
Impact of Ocean Acidification on Energy Metabolism of Oyster, Crassostrea gigas—Changes in Metabolic Pathways and Thermal Response
inferredcites →https://doi.org/10.48550/arxiv.1203.4802openalex-snapshot
A Reference-Free Algorithm for Computational Normalization of Shotgun Sequencing Data

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4665415openalex-extracted
inferred← citeshttps://doi.org/10.1002/ece3.70953openalex-snapshot
Transcriptome‐To‐Phenome Response of Larval Eastern Oysters Under Multiple Drivers of Aragonite Undersaturation
inferred← citeshttps://doi.org/10.1002/smll.202107407openalex-snapshot
Is Ocean Acidification Really a Threat to Marine Calcifiers? A Systematic Review and Meta‐Analysis of 980+ Studies Spanning Two Decades
inferred← citeshttps://doi.org/10.1007/13836_2019_70openalex-snapshot
Marine Population Genomics: Challenges and Opportunities
inferred← citeshttps://doi.org/10.1007/978-3-319-95954-2_19openalex-snapshot
Natura Fecit Saltum: Punctuationalism Pervades the Natural Sciences
inferred← citeshttps://doi.org/10.1007/s00343-025-4353-4openalex-snapshot
Parental exposure to ocean acidification impacts the larval development and transcriptome of the Pacific oyster Crassostrea gigas
inferred← citeshttps://doi.org/10.1007/s10126-022-10183-3openalex-snapshot
Molecular Features Associated with Resilience to Ocean Acidification in the Northern Quahog, Mercenaria mercenaria
inferred← citeshttps://doi.org/10.1007/s10126-023-10255-yopenalex-snapshot
Combination of RNAseq and RADseq to Identify Physiological and Adaptive Responses to Acidification in the Eastern Oyster (Crassostrea virginica)
inferred← citeshttps://doi.org/10.1007/s10592-021-01343-4openalex-snapshot
Genetic structure and effective population size of Sydney rock oysters in eastern Australia
inferred← citeshttps://doi.org/10.1016/b978-0-12-822330-7.00005-8openalex-snapshot
Potential mechanisms underpinning the impacts of ocean acidification on marine animals
inferred← citeshttps://doi.org/10.1016/b978-0-443-15938-1.00003-9openalex-snapshot
Effects of ocean acidification on the growth and development of marine mollusks
inferred← citeshttps://doi.org/10.1016/b978-0-443-15938-1.00008-8openalex-snapshot
Limitations and outlook of research in ecophysiology and ocean acidification in marine mollusks
inferred← citeshttps://doi.org/10.1016/b978-0-443-33606-5.00006-0openalex-snapshot
Multiomic resources and MolluscDB database
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2022.739153openalex-snapshot
Transgenerational transfer of the microbiome is altered by ocean acidification in oyster larvae
inferred← citeshttps://doi.org/10.1016/j.aquatox.2019.105331openalex-snapshot
Antioxidant responses to seawater acidification in an invasive fouling mussel are alleviated by transgenerational acclimation
inferred← citeshttps://doi.org/10.1016/j.cbd.2020.100716openalex-snapshot
Expected ocean warming conditions significantly alter the transcriptome of developing postlarval American lobsters (Homarus americanus): Implications for energetic trade-offs
inferred← citeshttps://doi.org/10.1016/j.ecss.2020.106620openalex-snapshot
A review of transgenerational effects of ocean acidification on marine bivalves and their implications for sclerochronology
inferred← citeshttps://doi.org/10.1016/j.isci.2025.113187openalex-snapshot
Epigenetic insights into physiological resilience: Multigenerational readouts of CO2-induced seawater acidification effects on fish embryos
inferred← citeshttps://doi.org/10.1016/j.jes.2025.06.033openalex-snapshot
Developmental and transgenerational effects of climate change on inorganic mercury toxicity in a marine copepod
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2019.05.071openalex-snapshot
Immunotoxicity of four nanoparticles to a marine bivalve species, Tegillarca granosa
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133819openalex-snapshot
Exposure to virgin and marine incubated microparticles of biodegradable and conventional polymers modulates the hepatopancreas transcriptome of Mytilus galloprovincialis
inferred← citeshttps://doi.org/10.1016/j.marenvres.2019.104872openalex-snapshot
Experimental acidification increases susceptibility of Mercenaria mercenaria to infection by Vibrio species
inferred← citeshttps://doi.org/10.1016/j.marenvres.2020.104883openalex-snapshot
Molecular adaptation of molluscan biomineralisation to high-CO2 oceans – The known and the unknown
inferred← citeshttps://doi.org/10.1016/j.marenvres.2020.105091openalex-snapshot
Season specific influence of projected ocean changes on the response to cadmium of stress-related genes in Mytilus galloprovincialis
inferred← citeshttps://doi.org/10.1016/j.marenvres.2021.105430openalex-snapshot
Molecular mechanisms underlying responses of the Antarctic coral Malacobelemnon daytoni to ocean acidification
inferred← citeshttps://doi.org/10.1016/j.marenvres.2024.106561openalex-snapshot
Transcriptomic insights into cessation of clam embryonic development following transgenerational exposure to ocean acidity extreme
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2020.111006openalex-snapshot
Transgenerational acclimation to changes in ocean acidification in marine invertebrates
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.119130openalex-snapshot
Effect of experimental seawater acidification on the prooxidant-antioxidant system of the Pacific oyster Magallana gigas (Thunberg, 1793) under normoxic and hypoxic conditions
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2026.119667openalex-snapshot
Differential mercury tolerance in a planktonic copepod under different climate scenarios: A multigeneration perspective
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2026.119981openalex-snapshot
Short-term plasticity and long-term transcriptomic rewiring under natural ocean acidification in an ecosystem-relevant sea urchin
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.04.005openalex-snapshot
Living in future ocean acidification, physiological adaptive responses of the immune system of sea urchins resident at a CO2 vent system
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.06.466openalex-snapshot
Assessing the impact of elevated pCO2 within and across generations in a highly invasive fouling mussel (Musculista senhousia)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.136420openalex-snapshot
Transgenerational biochemical effects of seawater acidification on the Manila clam (Ruditapes philippinarum)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.138001openalex-snapshot
Diel-cycling seawater acidification and hypoxia impair the physiological and growth performance of marine mussels
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.152265openalex-snapshot
Assessment of the juvenile vulnerability of symbiont-bearing giant clams to ocean acidification
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.154736openalex-snapshot
Intraspecific hybridization as a mitigation strategy of ocean acidification in marine bivalve noble scallop Chlamys nobilis
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.166577openalex-snapshot
Molecular responses to ocean acidification in an Antarctic bivalve and an ascidian
inferred← citeshttps://doi.org/10.1038/s41598-020-80282-5openalex-snapshot
Comparative transcriptomic analysis for identification of candidate sex-related genes and pathways in Crimson seabream (Parargyrops edita)
inferred← citeshttps://doi.org/10.1038/s41598-025-12130-3openalex-snapshot
Changes in host gene expression patterns underpin responses of the coral Stylophora pistillata to nutrient stress
inferred← citeshttps://doi.org/10.1093/icesjms/fsab071openalex-snapshot
Adult exposure to ocean acidification and warming leads to limited beneficial responses for oyster larvae
inferred← citeshttps://doi.org/10.1098/rsos.240329openalex-snapshot
Neuromolecular mechanisms related to reflex behaviour in Aplysia are affected by ocean acidification
inferred← citeshttps://doi.org/10.1101/2022.03.07.483338openalex-snapshot
Differential DNA methylation in Pacific oyster reproductive tissue in response to ocean acidification
inferred← citeshttps://doi.org/10.1101/2023.09.08.556443openalex-snapshot
Population-specific effects of ocean acidification in the Olympia oyster
inferred← citeshttps://doi.org/10.1101/2023.11.14.567130openalex-snapshot
Ocean acidification alters the transcriptomic response in the nervous system of Aplysia californica during reflex behaviour
inferred← citeshttps://doi.org/10.1111/are.13663openalex-snapshot
The capacity of oysters to regulate energy metabolism‐related processes may be key to their resilience against ocean acidification
inferred← citeshttps://doi.org/10.1111/gcb.14818openalex-snapshot
Selectively bred oysters can alter their biomineralization pathways, promoting resilience to environmental acidification
inferred← citeshttps://doi.org/10.1111/mec.16644openalex-snapshot
Acclimatory gene expression of primed clams enhances robustness to elevated pCO2
inferred← citeshttps://doi.org/10.1111/mec.16751openalex-snapshot
Epigenetic‐associated phenotypic plasticity of the ocean acidification‐acclimated edible oyster in the mariculture environment
inferred← citeshttps://doi.org/10.1186/s12864-022-08399-7openalex-snapshot
The transcriptomic responses of blunt snout bream (Megalobrama amblycephala) to acute hypoxia stress alone, and in combination with bortezomib
inferred← citeshttps://doi.org/10.1186/s12864-022-08781-5openalex-snapshot
Differential DNA methylation in Pacific oyster reproductive tissue in response to ocean acidification
inferred← citeshttps://doi.org/10.1186/s12983-020-0350-9openalex-snapshot
Ocean acidification promotes broad transcriptomic responses in marine metazoans: a literature survey
inferred← citeshttps://doi.org/10.1242/jeb.239269openalex-snapshot
Transgenerational plasticity responses of oysters to ocean acidification differ with habitat
inferred← citeshttps://doi.org/10.1371/journal.pone.0206417openalex-snapshot
Comparative De Novo transcriptome analysis of the Australian black-lip and Sydney rock oysters reveals expansion of repetitive elements in Saccostrea genomes
inferred← citeshttps://doi.org/10.17760/d20439247openalex-snapshot
DNA methylation as an intra- and transgenerational mediator of phenotypic response
inferred← citeshttps://doi.org/10.2139/ssrn.7445848openalex-snapshot
Differential gene expression reveals molecular mechanisms for physiological resilience to ocean acidification stress in native and introduced oyster species
inferred← citeshttps://doi.org/10.31390/gradschool_theses.4353openalex-snapshot
The Impact of CO2-related Ocean Acidification on the Molecular Regulation of Shell Development in the Eastern Oyster (Crassostrea virginica).
inferred← citeshttps://doi.org/10.3389/fimmu.2022.859975openalex-snapshot
Synergistic Interaction of Low Salinity Stress With Vibrio Infection Causes Mass Mortalities in the Oyster by Inducing Host Microflora Imbalance and Immune Dysregulation
inferred← citeshttps://doi.org/10.3389/fmars.2020.566419openalex-snapshot
Ocean Acidification Induces Subtle Shifts in Gene Expression and DNA Methylation in Mantle Tissue of the Eastern Oyster (Crassostrea virginica)
inferred← citeshttps://doi.org/10.3389/fmars.2020.603825openalex-snapshot
Ca2+/Calmodulin-NOS/NO-TNFs Pathway Hallmarks the Inflammation Response of Oyster During Aerial Exposure
inferred← citeshttps://doi.org/10.3389/fmars.2021.782583openalex-snapshot
Ocean Acidification Triggers Cell Signaling, Suppress Immune and Calcification in the Pacific Oyster Larvae
inferred← citeshttps://doi.org/10.3389/fmars.2023.1156831openalex-snapshot
Secretory and transcriptomic responses of mantle cells to low pH in the Pacific oyster (Crassostrea gigas)
inferred← citeshttps://doi.org/10.3389/fphys.2018.00619openalex-snapshot
Ocean Acidification Affects the Cytoskeleton, Lysozymes, and Nitric Oxide of Hemocytes: A Possible Explanation for the Hampered Phagocytosis in Blood Clams, Tegillarca granosa
inferred← citeshttps://doi.org/10.3389/fphys.2018.01967openalex-snapshot
Impact of Ocean Acidification on the Energy Metabolism and Antioxidant Responses of the Yesso Scallop (Patinopecten yessoensis)
inferred← citeshttps://doi.org/10.3390/genes13091529openalex-snapshot
A Transcriptomic Analysis of Phenotypic Plasticity in Crassostrea virginica Larvae under Experimental Acidification
inferred← citeshttps://doi.org/10.3390/ijms22126295openalex-snapshot
Separating the Wheat from the Chaff: The Use of Upstream Regulator Analysis to Identify True Differential Expression of Single Genes within Transcriptomic Datasets
inferred← citeshttps://doi.org/10.3390/ijms26157118openalex-snapshot
Comparative Transcriptomic Analysis for Identification of Environmental-Responsive Genes in Seven Species of Threadfin Breams (Nemipterus)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20438475openalex-snapshot
Additional file 3 of Differential DNA methylation in Pacific oyster reproductive tissue in response to ocean acidification
inferred← citeshttps://doi.org/10.64898/2026.05.22.727234openalex-snapshot
Global adaptation to climate change in the twilight zone revealed by shared signals of selection in mesopelagic lanternfishes
inferred← citeshttps://doi.org/10.70675/9b4a2bc6z3ea3z47a6z8a5dz245dba86d397openalex-snapshot
Effect of hypoxia and acidification on the physiology of the Peruvian scallop Argopecten purpuratus (L.)
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