scholarly article | Q13442814 |
review article | Q7318358 |
P819 | ADS bibcode | 2007PNAS..104.1745H |
P356 | DOI | 10.1073/PNAS.0610108104 |
P932 | PMC publication ID | 1794293 |
P698 | PubMed publication ID | 17264211 |
P5875 | ResearchGate publication ID | 6540767 |
P50 | author | David Epel | Q5233404 |
P2093 | author name string | Amro Hamdoun | |
David Epel | |||
P2860 | cites work | Oceanography: Anthropogenic carbon and ocean pH | Q24289359 |
Hermaphroditic, demasculinized frogs after exposure to the herbicide atrazine at low ecologically relevant doses | Q24534138 | ||
Evolvability | Q24595167 | ||
Nitromusk and polycyclic musk compounds as long-term inhibitors of cellular xenobiotic defense systems mediated by multidrug transporters | Q24811210 | ||
Atrazine-induced hermaphroditism at 0.1 ppb in American leopard frogs (Rana pipiens): laboratory and field evidence | Q24814352 | ||
A genomic regulatory network for development | Q28204498 | ||
Molecular chaperones in the cytosol: from nascent chain to folded protein | Q28205903 | ||
Hsp90 as a capacitor for morphological evolution | Q28290854 | ||
The Arabidopsis thaliana ABC transporter AtMRP5 controls root development and stomata movement | Q28362216 | ||
Epigenetic transgenerational actions of endocrine disruptors and male fertility | Q29547704 | ||
Large effects from small exposures. III. Endocrine mechanisms mediating effects of bisphenol A at levels of human exposure | Q29615567 | ||
The segment polarity network is a robust developmental module | Q29618600 | ||
DNA methylation in health and disease | Q30659938 | ||
Acclimation capacity underlies susceptibility to climate change | Q30809472 | ||
Dynamic reprogramming of DNA methylation at an epigenetically sensitive allele in mice | Q33239374 | ||
Biochemical, cellular, and pharmacological aspects of the multidrug transporter | Q33636699 | ||
Absence or pharmacological blocking of placental P-glycoprotein profoundly increases fetal drug exposure | Q33902161 | ||
Diapause | Q33904987 | ||
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. | Q34025724 | ||
Ecological developmental biology: developmental biology meets the real world | Q34229778 | ||
Coping with the inevitable: how cells repair a torn surface membrane | Q34237991 | ||
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21. | Q34504363 | ||
Mycosporine-like amino acids and related Gadusols: biosynthesis, acumulation, and UV-protective functions in aquatic organisms | Q34516178 | ||
The dauerlarva, a post-embryonic developmental variant of the nematode Caenorhabditis elegans | Q34520955 | ||
Chemical structure and biological activity of the Caenorhabditis elegans dauer-inducing pheromone. | Q53627069 | ||
Bacterial symbionts colonize the accessory nidamental gland of the squid Loligo opalescens via horizontal transmission | Q53960524 | ||
Differential alteration by thalidomide of the glutathione content of rat vs. rabbit conceptuses in vitro. | Q54067495 | ||
The plasma membrane estrogen receptor: nuclear or unclear? | Q58875403 | ||
The Control of Oxidant Stress at Fertilization | Q67915639 | ||
Widespread distribution of lysozyme g in egg white of birds | Q68356270 | ||
Control of larval development by chemosensory neurons in Caenorhabditis elegans | Q70121859 | ||
Embryos of Artemia franciscana survive four years of continuous anoxia: the case for complete metabolic rate depression | Q73750190 | ||
A Little Shell to Live In: Evidence That the Fertilization Envelope Can Prevent Mechanically Induced Damage of the Developing Sea Urchin Embryo | Q88211309 | ||
Mechanical Resistance to Shear Stress: The Role of Echinoderm Egg Extracellular Layers | Q89510565 | ||
Establishment of developmental precision and proportions in the early Drosophila embryo | Q34521079 | ||
A gradient of bicoid protein in Drosophila embryos | Q34687844 | ||
Chaperoning signaling pathways: molecular chaperones as stress-sensing 'heat shock' proteins. | Q34704564 | ||
Nitric oxide in oocyte maturation, ovulation, fertilization, cleavage and implantation: a little dab'll do ya. | Q35061333 | ||
Developmental Consequences of Trace Mineral Deficiencies in Rodents: Acute and Long-Term Effects | Q35121101 | ||
Expression and function of small heat shock protein genes during Xenopus development | Q35676783 | ||
Under cover: causes, effects and implications of Hsp90-mediated genetic capacitance | Q35731039 | ||
ABCG2 -- a transporter for all seasons | Q35785902 | ||
Estrogen and xenoestrogen actions on endocrine pancreas: from ion channel modulation to activation of nuclear function. | Q35853377 | ||
Living with the past: evolution, development, and patterns of disease | Q35890929 | ||
Long-term effects of culture of preimplantation mouse embryos on behavior. | Q36160389 | ||
Large plasma membrane disruptions are rapidly resealed by Ca2+-dependent vesicle-vesicle fusion events | Q36273962 | ||
Complex causes of amphibian population declines | Q39135577 | ||
Free radical-mediated oxidative DNA damage in the mechanism of thalidomide teratogenicity | Q39225712 | ||
Habitat diversity and adaptation to environmental stress in encysted embryos of the crustacean Artemia | Q39510161 | ||
Transformation of local Ca2+ spikes to global Ca2+ transients: the combinatorial roles of multiple Ca2+ releasing messengers | Q39646750 | ||
Hsp70 and thermal pretreatment mitigate developmental damage caused by mitotic poisons in Drosophila | Q39956857 | ||
Thalidomide does not interact with P-glycoprotein | Q40379063 | ||
Model systems in developmental biology | Q40547926 | ||
Bacterial challenge stimulates innate immune responses in extra-embryonic tissues of tobacco hornworm eggs. | Q42045686 | ||
Zebrafish Hsp70 is required for embryonic lens formation | Q42715572 | ||
Small heat shock protein p26 associates with nuclear lamins and HSP70 in nuclei and nuclear matrix fractions from stressed cells | Q43867886 | ||
Symbiotic marine bacteria chemically defend crustacean embryos from a pathogenic fungus | Q44114864 | ||
A novel hypothesis for thalidomide-induced limb teratogenesis: redox misregulation of the NF-kappaB pathway | Q44720745 | ||
Apical sensory neurones mediate developmental retardation induced by conspecific environmental stimuli in freshwater pulmonate snails | Q44960232 | ||
Fertilization stimulates lipid peroxidation in the sea urchin egg. | Q45043568 | ||
The oxidative burst at fertilization is dependent upon activation of the dual oxidase Udx1. | Q45168498 | ||
Redox changes during fertilization and maturation of marine invertebrate eggs | Q46041811 | ||
Risk and the evolution of cell-cycle durations of embryos | Q46351321 | ||
Multidrug resistance-associated protein MRP-1 regulates dauer diapause by its export activity in Caenorhabditis elegans | Q47068858 | ||
Multixenobiotic Resistance in Urechis caupo Embryos: Protection From Environmental Toxins | Q47670759 | ||
Multidrug resistance mediated by the ATP-binding cassette transporter protein MRP. | Q47732687 | ||
Status of glutathione during oxidant-induced oxidative stress in the preimplantation mouse embryo | Q49078564 | ||
P-glycoprotein regulates chemosensitivity in early developmental stages of the mouse | Q49127108 | ||
The developmental biology of annual fishes. 3. Pre-embryonic and embryonic diapause of variable duration in the eggs of annual fishes | Q50581228 | ||
Activation of multidrug efflux transporter activity at fertilization in sea urchin embryos (Strongylocentrotus purpuratus). | Q50668517 | ||
Poor maternal environment enhances offspring disease resistance in an invertebrate. | Q51830105 | ||
Hsp70 and larval thermotolerance in Drosophila melanogaster: how much is enough and when is more too much? | Q52104948 | ||
The presence of xenobiotic transporters in rat placenta. | Q52110222 | ||
Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution. | Q52111267 | ||
Evidence that a cell-type-specific efflux pump regulates cell differentiation in Dictyostelium. | Q52170014 | ||
The bicoid protein determines position in the Drosophila embryo in a concentration-dependent manner | Q52461853 | ||
Robustness, flexibility, and the role of lateral inhibition in the neurogenic network. | Q52596238 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 6 | |
P304 | page(s) | 1745-1750 | |
P577 | publication date | 2007-01-30 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Embryo stability and vulnerability in an always changing world | |
P478 | volume | 104 |
Q51962707 | A genetic component of resistance to fungal infection in frog embryos. |
Q30876028 | A review and meta-analysis of the effects of multiple abiotic stressors on marine embryos and larvae |
Q28603461 | A scenario for the evolution of selective egg coloration: the roles of enemy-free space, camouflage, thermoregulation and pigment limitation |
Q50708328 | ATP-binding cassette transporters protect sea urchin gametes and embryonic cells against the harmful effects of ultraviolet light. |
Q34775084 | Abcb4 acts as multixenobiotic transporter and active barrier against chemical uptake in zebrafish (Danio rerio) embryos |
Q27325354 | Adaptive capacity of the habitat modifying sea urchin Centrostephanus rodgersii to ocean warming and ocean acidification: performance of early embryos |
Q35834503 | Adaptive divergence of the moor frog (Rana arvalis) along an acidification gradient |
Q51189016 | Amino-modified polystyrene nanoparticles affect signalling pathways of the sea urchin (Paracentrotus lividus) embryos. |
Q28705526 | Animals in a bacterial world, a new imperative for the life sciences |
Q46948002 | Antarctic emerald rockcod have the capacity to compensate for warming when uncoupled from CO2 -acidification |
Q30432956 | Anthropogenic noise playback impairs embryonic development and increases mortality in a marine invertebrate |
Q39406107 | Assessing physiological tipping point of sea urchin larvae exposed to a broad range of pH. |
Q27694216 | Autophagy as a defense strategy against stress: focus on Paracentrotus lividus sea urchin embryos exposed to cadmium |
Q27317135 | C. elegans are protected from lethal hypoxia by an embryonic diapause |
Q92530122 | Cadmium stress effects indicating marine pollution in different species of sea urchin employed as environmental bioindicators |
Q46452129 | Can multi-generational exposure to ocean warming and acidification lead to the adaptation of life history and physiology in a marine metazoan? |
Q43290199 | Characterization of functional activity of ABCB1 and ABCC1 proteins in eggs and embryonic cells of the sea urchin Echinometra lucunter. |
Q30430075 | Chronic playback of boat noise does not impact hatching success or post-hatching larval growth and survival in a cichlid fish. |
Q41193771 | Ciona intestinalis as a marine model system to study some key developmental genes targeted by the diatom-derived aldehyde decadienal |
Q30601222 | Climate change reduces offspring fitness in littoral spawners: a study integrating organismic response and long-term time-series |
Q64117156 | Cofilin-Mediated Actin Stress Response Is Maladaptive in Heat-Stressed Embryos |
Q48100669 | Computational Model of Secondary Palate Fusion and Disruption. |
Q57736256 | Contributions of genetic and environmental variance in early development of the Antarctic sea urchin Sterechinus neumayeri in response to increased ocean temperature and acidification |
Q37200589 | Cost, effectiveness and environmental relevance of multidrug transporters in sea urchin embryos |
Q30696294 | Developing Xenopus embryos recover by compacting and expelling single wall carbon nanotubes. |
Q36218115 | Development of Embryonic Market Squid, Doryteuthis opalescens, under Chronic Exposure to Low Environmental pH and [O2]. |
Q46149303 | Developmental effects of two different copper oxide nanomaterials in sea urchin (Lytechinus pictus) embryos |
Q51892144 | Differences in susceptibility to Saprolegnia infections among embryonic stages of two anuran species. |
Q28384059 | Distribution of single wall carbon nanotubes in the Xenopus laevis embryo after microinjection |
Q41108651 | Ecologically relevant levels of multiple, common marine stressors suggest antagonistic effects |
Q37126379 | Effect of embryonic fibroblast cell co-culture on development of mouse embryos following exposure to visible light |
Q42713930 | Effects of cadmium exposure on sea urchin development assessed by SSH and RT-qPCR: metallothionein genes and their differential induction |
Q38604113 | Effects of chronic crude oil exposure on early developmental stages of the Northern krill (Meganyctiphanes norvegica). |
Q35971720 | Effects of light on development of mammalian zygotes |
Q31135661 | Effects of ocean acidification increase embryonic sensitivity to thermal extremes in Atlantic cod, Gadus morhua |
Q34222062 | Effects of seawater acidification on cell cycle control mechanisms in Strongylocentrotus purpuratus embryos |
Q39827228 | Effects of seawater acidification on early development of the intertidal sea urchin Paracentrotus lividus (Lamarck 1816) |
Q35178607 | Efflux transporters: newly appreciated roles in protection against pollutants |
Q46389750 | Embryo arrest and reactivation: potential candidates controlling embryonic diapause in the tammar wallaby and mink†. |
Q31120695 | Embryogenesis and early skeletogenesis in the antarctic bullhead notothen, Notothenia coriiceps. |
Q51921720 | Embryonic development and skeletogenic gene expression affected by X-rays in the Mediterranean sea urchin Paracentrotus lividus. |
Q30740632 | Embryonic response to long-term exposure of the marine crustacean Nephrops norvegicus to ocean acidification and elevated temperature |
Q43770844 | Energy-limited tolerance to stress as a conceptual framework to integrate the effects of multiple stressors |
Q33609122 | Environmental sensing and response genes in cnidaria: the chemical defensome in the sea anemone Nematostella vectensis. |
Q98394667 | Environmentally-induced parental or developmental conditioning influences coral offspring ecological performance |
Q35485756 | Experimental ocean acidification alters the allocation of metabolic energy |
Q42175832 | Expression of hsp70, hsp90 and hsf1 in the reef coral Acropora digitifera under prospective acidified conditions over the next several decades |
Q52691969 | Fenoxycarb exposure disrupted the reproductive success of the amphipod Gammarus fossarum with limited effects on the lipid profile. |
Q31065440 | From pole to pole: the potential for the Arctic seastar Asterias amurensis to invade a warming Southern Ocean |
Q51962944 | Genetic variation in pathogen-induced early hatching of toad embryos. |
Q38202875 | Heavy metals and metalloids as autophagy inducing agents: focus on cadmium and arsenic |
Q55691762 | Hypoxia tolerance of common sole juveniles depends on dietary regime and temperature at the larval stage: evidence for environmental conditioning. |
Q50929273 | Identification of ABC transporter genes in gonad tissue of two Mediterranean sea urchin species: black, Arbacia lixula L., and rocky, Paracentrotus lividus L. |
Q33529402 | Impact of near-future ocean acidification on echinoderms |
Q35243036 | Impact of nutrition and salinity changes on biological performances of green and white sturgeon |
Q34241439 | In an early branching metazoan, bacterial colonization of the embryo is controlled by maternal antimicrobial peptides |
Q30882734 | Increased temperature, but not acidification, enhances fertilization and development in a tropical urchin: potential for adaptation to a tropicalized eastern Australia. |
Q28477549 | Influences of DMP on the fertilization process and subsequent embryogenesis of abalone (Haliotis diversicolor supertexta) by gametes exposure |
Q44976731 | Involvement of l(-)-rhamnose in sea urchin gastrulation. Part II: α-l-Rhamnosidase |
Q35054297 | Large birth size does not reduce negative latent effects of harsh environments across life stages in two coral species |
Q39118484 | Larvae of the coral eating crown-of-thorns starfish, Acanthaster planci in a warmer-high CO2 ocean |
Q37290372 | Loss of genetic diversity as a consequence of selection in response to high pCO2. |
Q33694705 | Maternal antioxidant provisioning mitigates pollutant-induced oxidative damage in embryos of the temperate sea urchin Evechinus chloroticus |
Q61442984 | Molecular mechanisms underpinning transgenerational plasticity in the green sea urchin Psammechinus miliaris |
Q46020799 | Multistressor impacts of warming and acidification of the ocean on marine invertebrates' life histories. |
Q30489833 | Natural variation in embryo mechanics: gastrulation in Xenopus laevis is highly robust to variation in tissue stiffness |
Q31119890 | Ocean acidification has little effect on developmental thermal windows of echinoderms from Antarctica to the tropics |
Q35990294 | Of light and mouse embryos: less is more |
Q57736243 | Paternal identity influences response of Acanthaster planci embryos to ocean acidification and warming |
Q35082103 | Physiological tolerances across latitudes: thermal sensitivity of larval marine snails (Nucella spp.). |
Q33496776 | Pre- and postnatal nutritional histories influence reproductive maturation and ovarian function in the rat. |
Q47197410 | Pre-hatching exposure to water mold reduces size at metamorphosis in the moor frog |
Q42711150 | Quantification and in situ localisation of abcb1 and abcc9genes in toxicant-exposed sea urchin embryos. |
Q57596327 | Rapid adaptive responses to climate change in corals |
Q46304317 | Redox stress and signaling during vertebrate embryonic development: Regulation and responses. |
Q53822189 | Robustness of larval development of intertidal sea urchin species to simulated ocean warming and acidification. |
Q51923356 | Sea urchin embryos as an in vivo model for the assessment of manganese toxicity: developmental and stress response effects. |
Q36191621 | Sphingolipids, Transcription Factors, and Conserved Toolkit Genes: Developmental Plasticity in the Ant Cardiocondyla obscurior |
Q35562252 | Stress response gene activation protects sea urchin embryos exposed to X-rays |
Q92932138 | Systemic signalling and local effectors in developmental stability, body symmetry, and size |
Q64097627 | TORC1 modulation in adipose tissue is required for organismal adaptation to hypoxia in Drosophila |
Q28534944 | The maternal-to-zygotic transition targets actin to promote robustness during morphogenesis |
Q37172494 | The sea urchin Lytechinus variegatus lives close to the upper thermal limit for early development in a tropical lagoon. |
Q37414587 | Thermal tolerance of Strongylocentrotus purpuratus early life history stages: mortality, stress-induced gene expression and biogeographic patterns |
Q57736336 | Thermal tolerance of early development in tropical and temperate sea urchins: inferences for the tropicalization of eastern Australia |
Q45953031 | Thermal windows and metabolic performance curves in a developing Antarctic fish. |
Q28389670 | Titanium dioxide nanoparticles stimulate sea urchin immune cell phagocytic activity involving TLR/p38 MAPK-mediated signalling pathway |
Q34333605 | Toxic effects of Hoechst staining and UV irradiation on preimplantation development of parthenogenetically activated mouse oocytes |
Q91733932 | Transcriptomic analysis of differentially expressed genes in the oviduct of Rhacophorus omeimontis provides insights into foam nest construction |
Q58122212 | Transgenerational Effects of CO-Driven Ocean Acidification on Adult Mussels Modulate Physiological Response to Multiple Stressors in Larvae |
Q52564893 | Transgenerational deleterious effects of ocean acidification on the reproductive success of a keystone crustacean (Gammarus locusta). |
Q41199725 | Transgenerational exposure of North Atlantic bivalves to ocean acidification renders offspring more vulnerable to low pH and additional stressors |
Q50865747 | Use of Gammarus fossarum (Amphipoda) embryo for toxicity testing: A case study with cadmium. |
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