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Molecular Biology of Freezing Tolerance
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/047167558x.ch12openalex-snapshot
Oxygen in Biology and Biochemistry: Role of Free Radicals
inferredcites →https://doi.org/10.1002/9781444345988.ch3openalex-snapshot
Oxidative Stress in Estuarine and Intertidal Environments (Temperate and Tropical)
inferredcites →https://doi.org/10.1002/arch.20138openalex-snapshot
Cloning of heat shock protein genes (hsp90 andhsc70) and their expression during larval diapause and cold tolerance acquisition in the rice stem borer,Chilo suppressalis Walker
inferredcites →https://doi.org/10.1002/arch.20418openalex-snapshot
Reversible phosphorylation regulation of NADPH‐linked polyol dehydrogenase in the freeze‐avoiding gall moth, Epiblema scudderiana: role in glycerol metabolism
inferredcites →https://doi.org/10.1002/iub.463openalex-snapshot
The induction of anhydrobiosis in the sleeping chironomid: Current status of our knowledge
inferredcites →https://doi.org/10.1002/jez.1733openalex-snapshot
Seasonal Variation and Response to Osmotic Challenge in Urea Transporter Expression in the Dehydration‐ and Freeze‐Tolerant Wood Frog, Rana sylvatica
inferredcites →https://doi.org/10.1002/jez.460openalex-snapshot
Physiological ecology of overwintering in hatchling turtles
inferredcites →https://doi.org/10.1002/jez.495openalex-snapshot
Phosphoglycerate kinase 1 expression responds to freezing, anoxia, and dehydration stresses in the freeze tolerant wood frog, Rana sylvatica
inferredcites →https://doi.org/10.1002/jez.689openalex-snapshot
Dynamic regulation of aquaglyceroporin expression in erythrocyte cultures from cold‐ and warm‐acclimated cope's gray treefrog, Hyla chrysoscelis
inferredcites →https://doi.org/10.1002/jez.696openalex-snapshot
Regulation of cell cycle components during exposure to anoxia or dehydration stress in the wood frog, Rana sylvatica
inferredcites →https://doi.org/10.1006/cryo.1995.1036openalex-snapshot
Isolation of Ice-Nucleating Active Bacteria from the Freeze-Tolerant Frog, Rana sylvatica
inferredcites →https://doi.org/10.1006/cryo.1996.0019openalex-snapshot
β-Adrenergic, Hormonal, and Nervous Influences on Cryoprotectant Synthesis by Liver of the Freeze-Tolerant Wood FrogRana sylvatica
inferredcites →https://doi.org/10.1006/cryo.2000.2289openalex-snapshot
Ice Nucleation and Antinucleation in Nature
inferredcites →https://doi.org/10.1006/cryo.2001.2353openalex-snapshot
The Trehalose Myth Revisited: Introduction to a Symposium on Stabilization of Cells in the Dry State
inferredcites →https://doi.org/10.1007/978-1-4757-0190-6_2openalex-snapshot
Principles of Insect Low Temperature Tolerance
inferredcites →https://doi.org/10.1007/978-1-4757-0190-6_4openalex-snapshot
Biochemistry of Cryoprotectants
inferredcites →https://doi.org/10.1007/bf00301477openalex-snapshot
Anoxia and freezing exposures stimulate covalent modification of enzymes of carbohydrate metabolism in Littorina littorea
inferredcites →https://doi.org/10.1007/bf00683219openalex-snapshot
Purification and composition of an ice nucleating protein from queens of the hornet,Vespula maculata
inferredcites →https://doi.org/10.1007/bf01955768openalex-snapshot
Nucleating agents in the haemolymph of an intertidal mollusc tolerant to freezing
inferredcites →https://doi.org/10.1007/s00018-002-8410-1openalex-snapshot
Regulation of cyclin-Cdk activity in mammalian cells
inferredcites →https://doi.org/10.1007/s00018-009-8320-6openalex-snapshot
The bugs that came in from the cold: molecular adaptations to low temperatures in insects
inferredcites →https://doi.org/10.1007/s00239-005-0256-3openalex-snapshot
Evolution of Hyperactive, Repetitive Antifreeze Proteins in Beetles
inferredcites →https://doi.org/10.1007/s00300-006-0152-3openalex-snapshot
Ecophysiological strategies of Antarctic intertidal invertebrates faced with freezing stress
inferredcites →https://doi.org/10.1007/s00335-007-9041-5openalex-snapshot
Comparative functional analysis of aquaporins/glyceroporins in mammals and anurans
inferredcites →https://doi.org/10.1007/s00360-003-0378-0openalex-snapshot
The environmental physiology of Antarctic terrestrial nematodes: a review
inferredcites →https://doi.org/10.1007/s00360-005-0478-0openalex-snapshot
Anoxia tolerance and freeze tolerance in hatchling turtles
inferredcites →https://doi.org/10.1007/s00360-007-0233-9openalex-snapshot
Urea loading enhances postfreeze performance of frog skeletal muscle
inferredcites →https://doi.org/10.1007/s00360-008-0286-4openalex-snapshot
How insects survive the cold: molecular mechanisms—a review
inferredcites →https://doi.org/10.1007/s00360-008-0288-2openalex-snapshot
Invertebrate aquaporins: a review
inferredcites →https://doi.org/10.1007/s00360-010-0487-5openalex-snapshot
Regulation of glucose-6-phosphate dehydrogenase by reversible phosphorylation in liver of a freeze tolerant frog
inferredcites →https://doi.org/10.1007/s00360-010-0496-4openalex-snapshot
Glycerol uptake by erythrocytes from warm- and cold-acclimated Cope’s gray treefrogs
inferredcites →https://doi.org/10.1007/s00360-011-0552-8openalex-snapshot
A thermal hysteresis-producing xylomannan glycolipid antifreeze associated with cold tolerance is found in diverse taxa
inferredcites →https://doi.org/10.1007/s00360-011-0561-7openalex-snapshot
Skin ice nucleators and glycerol in the freezing-tolerant frog Litoria ewingii
inferredcites →https://doi.org/10.1007/s003600050140openalex-snapshot
Molecular characterization and sequencing of antifreeze proteins from larvae of the beetle Dendroides canadensis
inferredcites →https://doi.org/10.1007/s00792-011-0423-yopenalex-snapshot
Bacterial gene expression at low temperatures
inferredcites →https://doi.org/10.1007/s12026-010-8199-1openalex-snapshot
The role of iron in the immune response to bacterial infection
inferredcites →https://doi.org/10.1007/s12192-008-0068-7openalex-snapshot
Guidelines for the nomenclature of the human heat shock proteins
inferredcites →https://doi.org/10.1007/s12275-012-2411-zopenalex-snapshot
Identification of chaperones in freeze tolerance in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/0011-2240(86)90051-9openalex-snapshot
Inhibition of recrystallization of ice by insect thermal hysteresis proteins: A possible cryoprotective role
inferredcites →https://doi.org/10.1016/0011-2240(87)90036-8openalex-snapshot
Modes of interaction of cryoprotectants with membrane phospholipids during freezing
inferredcites →https://doi.org/10.1016/0011-2240(90)90032-yopenalex-snapshot
Ice nucleating activity in the blood of the freeze-tolerant frog, Rana sylvatica
inferredcites →https://doi.org/10.1016/0011-2240(91)90058-vopenalex-snapshot
Purification and partial characterization of an ice nucleator protein from the intertidal gastropod, Melampus bidentatus
inferredcites →https://doi.org/10.1016/0011-2240(92)90038-4openalex-snapshot
Biochemical modification of plasma ice nucleating activity in a freeze-tolerant frog
inferredcites →https://doi.org/10.1016/0022-1910(85)90034-4openalex-snapshot
Freeze-tolerance adaptations, including haemolymph protein and lipoprotein nucleators, in the larvae of the cranefly Tipula trivittata
inferredcites →https://doi.org/10.1016/0300-9629(82)90262-6openalex-snapshot
Nucleating agents in cold-hardy insects
inferredcites →https://doi.org/10.1016/0305-0491(91)90341-aopenalex-snapshot
Further characterization of the lipoprotein ice nucleator from freeze tolerant larvae of the cranefly Tipula trivittata
inferredcites →https://doi.org/10.1016/0965-1748(94)90080-9openalex-snapshot
Mitochondrial enzymes during overwintering in two species of cold-hardy gall insects
inferredcites →https://doi.org/10.1016/j.ab.2011.05.015openalex-snapshot
Amplification and sequencing of mature microRNAs in uncharacterized animal models using stem–loop reverse transcription–polymerase chain reaction
inferredcites →https://doi.org/10.1016/j.bbagen.2010.03.015openalex-snapshot
Activation of antioxidant defenses in response to freezing in freeze-tolerant painted turtle hatchlings
inferredcites →https://doi.org/10.1016/j.bbrc.2011.12.070openalex-snapshot
Genome-wide identification of cold-responsive and new microRNAs in Populus tomentosa by high-throughput sequencing
inferredcites →https://doi.org/10.1016/j.cbpa.2009.02.035openalex-snapshot
Molecular and cellular regulation of water homeostasis in anuran amphibians by aquaporins
inferredcites →https://doi.org/10.1016/j.cbpa.2009.10.026openalex-snapshot
Intracellular ice formation in insects: Unresolved after 50years?
inferredcites →https://doi.org/10.1016/j.cbpa.2010.04.007openalex-snapshot
Expression and immunolocalization of aquaporins HC-1, -2, and -3 in Cope's gray treefrog, Hyla chrysoscelis
inferredcites →https://doi.org/10.1016/j.cbpa.2012.11.002openalex-snapshot
Urea is not a universal cryoprotectant among hibernating anurans: Evidence from the freeze-tolerant boreal chorus frog (Pseudacris maculata)
inferredcites →https://doi.org/10.1016/j.cbpa.2013.03.009openalex-snapshot
Metabolic mechanisms for anoxia tolerance and freezing survival in the intertidal gastropod, Littorina littorea
inferredcites →https://doi.org/10.1016/j.cbpb.2011.05.003openalex-snapshot
Regulation of hexokinase by reversible phosphorylation in skeletal muscle of a freeze-tolerant frog
inferredcites →https://doi.org/10.1016/j.cell.2009.01.002openalex-snapshot
MicroRNAs: Target Recognition and Regulatory Functions
inferredcites →https://doi.org/10.1016/j.cell.2012.04.005openalex-snapshot
Roles for MicroRNAs in Conferring Robustness to Biological Processes
inferredcites →https://doi.org/10.1016/j.cryobiol.2003.10.008openalex-snapshot
Strategies for exploration of freeze responsive gene expression: advances in vertebrate freeze tolerance
inferredcites →https://doi.org/10.1016/j.cryobiol.2004.01.004openalex-snapshot
Inorganic ions in cold-hardiness
inferredcites →https://doi.org/10.1016/j.cryobiol.2004.11.001openalex-snapshot
Up-regulation of acidic ribosomal phosphoprotein P0 in response to freezing or anoxia in the freeze tolerant wood frog, Rana sylvatica
inferredcites →https://doi.org/10.1016/j.cryobiol.2005.09.005openalex-snapshot
Reptile freeze tolerance: Metabolism and gene expression
inferredcites →https://doi.org/10.1016/j.cryobiol.2009.01.001openalex-snapshot
Freeze tolerance evolution among anurans: Frequency and timing of appearance
inferredcites →https://doi.org/10.1016/j.cryobiol.2009.08.009openalex-snapshot
MicroRNA regulation below zero: Differential expression of miRNA-21 and miRNA-16 during freezing in wood frogs
inferredcites →https://doi.org/10.1016/j.cryobiol.2010.10.158openalex-snapshot
Ice restructuring inhibition activities in antifreeze proteins with distinct differences in thermal hysteresis
inferredcites →https://doi.org/10.1016/j.cryobiol.2012.01.008openalex-snapshot
Environmental stress responsive expression of the gene li16 in Rana sylvatica, the freeze tolerant wood frog
inferredcites →https://doi.org/10.1016/j.cryobiol.2012.06.005openalex-snapshot
Differential expression of microRNA species in a freeze tolerant insect, Eurosta solidaginis
inferredcites →https://doi.org/10.1016/j.drudis.2007.04.002openalex-snapshot
Prediction of microRNA targets
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.07.001openalex-snapshot
Transferrin inhibits stress-induced apoptosis in a beetle
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2011.05.005openalex-snapshot
Distinct role of Hsp70 in Drosophila hemocytes during severe hypoxia
inferredcites →https://doi.org/10.1016/j.gene.2007.10.021openalex-snapshot
Increasing genomic information in bivalves through new EST collections in four species: Development of new genetic markers for environmental studies and genome evolution
inferredcites →https://doi.org/10.1016/j.gene.2008.07.023openalex-snapshot
Cold acclimation-induced up-regulation of the ribosomal protein L7 gene in the freeze tolerant wood frog, Rana sylvatica
inferredcites →https://doi.org/10.1016/j.gpb.2012.09.002openalex-snapshot
MicroRNA Regulation in Extreme Environments: Differential Expression of MicroRNAs in the Intertidal Snail Littorina Littorea During Extended Periods of Freezing and Anoxia
inferredcites →https://doi.org/10.1016/j.ibmb.2007.07.004openalex-snapshot
Proteomic profiling of a parasitic wasp exposed to constant and fluctuating cold exposure
inferredcites →https://doi.org/10.1016/j.ibmb.2007.07.007openalex-snapshot
Upregulation of a desaturase is associated with the enhancement of cold hardiness in the onion maggot, Delia antiqua
inferredcites →https://doi.org/10.1016/j.ibmb.2007.12.003openalex-snapshot
Mitochondria of cold hardy insects: Responses to cold and hypoxia assessed at enzymatic, mRNA and DNA levels
inferredcites →https://doi.org/10.1016/j.ibmb.2008.05.006openalex-snapshot
High resistance to oxidative damage in the Antarctic midge Belgica antarctica, and developmentally linked expression of genes encoding superoxide dismutase, catalase and heat shock proteins
inferredcites →https://doi.org/10.1016/j.ibmb.2009.09.001openalex-snapshot
Glycerol kinase activity and glycerol kinase-3 gene are up-regulated by acclimation to 5 °C in diapause eggs of the silkworm, Bombyx mori
inferredcites →https://doi.org/10.1016/j.ibmb.2009.10.004openalex-snapshot
Cell cycle arrest as a hallmark of insect diapause: Changes in gene transcription during diapause induction in the drosophilid fly, Chymomyza costata
inferredcites →https://doi.org/10.1016/j.ibmb.2009.12.006openalex-snapshot
The trehalose transporter 1 gene sequence is conserved in insects and encodes proteins with different kinetic properties involved in trehalose import into peripheral tissues
inferredcites →https://doi.org/10.1016/j.ibmb.2011.02.007openalex-snapshot
Cloning of cDNAs encoding sorbitol dehydrogenase-2a and b, enzymatic characterization, and up-regulated expression of the genes in Bombyx mori diapause eggs exposed to 5 °C
inferredcites →https://doi.org/10.1016/j.jembe.2010.08.022openalex-snapshot
Seasonal freezing adaptations of the mid-intertidal gastropod Nucella lima from southeast Alaska
inferredcites →https://doi.org/10.1016/j.jinsphys.2003.12.003openalex-snapshot
Antifreeze proteins in Alaskan insects and spiders
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.08.002openalex-snapshot
Role of HSF activation for resistance to heat, cold and high-temperature knock-down
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.11.001openalex-snapshot
Role of membrane transport of water and glycerol in the freeze tolerance of the rice stem borer, Chilo suppressalis Walker (Lepidoptera: Pyralidae)
inferredcites →https://doi.org/10.1016/j.jinsphys.2006.08.008openalex-snapshot
Diapause-specific gene expression in the northern house mosquito, Culex pipiens L., identified by suppressive subtractive hybridization
inferredcites →https://doi.org/10.1016/j.jinsphys.2007.04.005openalex-snapshot
Effects of diapause and cold-acclimation on the avoidance of freezing injury in fat body tissue of the rice stem borer, Chilo suppressalis Walker
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.04.001openalex-snapshot
Suppression of Na+K+-ATPase activity by reversible phosphorylation over the winter in a freeze-tolerant insect
inferredcites →https://doi.org/10.1016/j.jinsphys.2009.01.010openalex-snapshot
Selection for cold resistance alters gene transcript levels in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2009.12.003openalex-snapshot
Changes in abundance of aquaporin-like proteins occurs concomitantly with seasonal acquisition of freeze tolerance in the goldenrod gall fly, Eurosta solidaginis
inferredcites →https://doi.org/10.1016/j.jinsphys.2009.12.007openalex-snapshot
Isolation of diapause-regulated genes from the flesh fly, Sarcophaga crassipalpis by suppressive subtractive hybridization
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.03.023openalex-snapshot
Expression of heat shock protein 70a mRNA in Bombyx mori diapause eggs
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.08.008openalex-snapshot
Survival rate and expression of Heat-shock protein 70 and Frost genes after temperature stress in Drosophila melanogaster lines that are selected for recovery time from temperature coma
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.02.006openalex-snapshot
Function and immuno-localization of aquaporins in the Antarctic midge Belgica antarctica
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.02.016openalex-snapshot
Chaperone proteins and winter survival by a freeze tolerant insect
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.03.001openalex-snapshot
Cryoprotective dehydration is widespread in Arctic springtails
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.03.004openalex-snapshot
Cold tolerance of New Zealand alpine insects
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.03.023openalex-snapshot
Functional characterization of an aquaporin in the Antarctic midge Belgica antarctica
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.03.025openalex-snapshot
Do ice nucleating lipoproteins protect frozen insects against toxic chemical agents?
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.04.005openalex-snapshot
Effect of freezing and dehydration on ion and cryoprotectant distribution and hemolymph volume in the goldenrod gall fly, Eurosta solidaginis
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.04.021openalex-snapshot
A cross-species compendium of proteins/gene products related to cold stress identified by bioinformatic approaches
inferredcites →https://doi.org/10.1016/j.jprot.2011.10.034openalex-snapshot
Investigating the deep supercooling ability of an Alaskan beetle, Cucujus clavipes puniceus, via high throughput proteomics
inferredcites →https://doi.org/10.1016/j.tplants.2004.06.007openalex-snapshot
Antifreeze proteins in overwintering plants: a tale of two activities
inferredcites →https://doi.org/10.1016/s0022-0981(01)00283-0openalex-snapshot
Isolation and identification of an ice-nucleating bacterium from the gills of the intertidal bivalve mollusc Geukensia demissa
inferredcites →https://doi.org/10.1016/s0022-0981(97)00132-9openalex-snapshot
Antioxidant defenses and lipid peroxidation during anoxia stress and aerobic recovery in the marine gastropod Littorina littorea
inferredcites →https://doi.org/10.1016/s0022-1910(97)00143-1openalex-snapshot
Accumulation of Hsp70 mRNA under environmental stresses in diapausing and nondiapausing adults of Drosophila triauraria
inferredcites →https://doi.org/10.1016/s0065-2423(10)52003-1openalex-snapshot
Metabolic rate depression
inferredcites →https://doi.org/10.1016/s0167-4781(02)00603-6openalex-snapshot
Freeze-induced expression of a novel gene, fr47, in the liver of the freeze-tolerant wood frog, Rana sylvatica
inferredcites →https://doi.org/10.1016/s0167-4781(97)00057-2openalex-snapshot
Differential regulation of the mitochondrial ADP/ATP translocase gene in wood frogs under freezing stress
inferredcites →https://doi.org/10.1016/s0300-9629(96)00270-8openalex-snapshot
Organic Solutes in Freezing Tolerance
inferredcites →https://doi.org/10.1016/s0300-9629(97)00237-5openalex-snapshot
Glycolytic controls in estivation and anoxia: A comparison of metabolic arrest in land and marine molluscs
inferredcites →https://doi.org/10.1016/s0378-1119(97)00332-6openalex-snapshot
Upregulation of a novel gene by freezing exposure in the freeze-tolerant wood frog (Rana sylvatica)
inferredcites →https://doi.org/10.1016/s0959-437x(98)80042-7openalex-snapshot
Evolution of the diverse antifreeze proteins
inferredcites →https://doi.org/10.1016/s0965-1748(97)00037-4openalex-snapshot
Reversible phosphorylation of fructose 1,6-bisphosphatase mediates enzyme role in glycerol metabolism in the freeze-avoiding gall moth Epiblema scudderiana
inferredcites →https://doi.org/10.1016/s0967-0653(97)84807-7openalex-snapshot
10.1016/s0967-0653(97)84807-7
inferredcites →https://doi.org/10.1016/s1146-609x(03)00045-6openalex-snapshot
Cold hardiness in molluscs
inferredcites →https://doi.org/10.1016/s1532-0456(02)00080-7openalex-snapshot
Animal response to drastic changes in oxygen availability and physiological oxidative stress
inferredcites →https://doi.org/10.1016/s1672-0229(11)60022-3openalex-snapshot
Plant Small RNAs: Biogenesis, Mode of Action and Their Roles in Abiotic Stresses
inferredcites →https://doi.org/10.1017/cbo9780511675997openalex-snapshot
Low Temperature Biology of Insects
inferredcites →https://doi.org/10.1017/cbo9780511675997.007openalex-snapshot
Oxygen: Stress and adaptation in cold-hardy insects
inferredcites →https://doi.org/10.1017/s1464793102006024openalex-snapshot
Climatic variability and the evolution of insect freeze tolerance
inferredcites →https://doi.org/10.1017/s1464793103006195openalex-snapshot
Metabolic rate depression in animals: transcriptional and translational controls
inferredcites →https://doi.org/10.1021/pr200518yopenalex-snapshot
Elucidating the Biochemical Overwintering Adaptations of Larval Cucujus clavipes puniceus, a Nonmodel Organism, via High Throughput Proteomics
inferredcites →https://doi.org/10.1023/b:jobb.0000031974.35812.c9openalex-snapshot
Upregulation of the Mitochondrial Phosphate Carrier During Freezing in the Wood Frog Rana sylvatica: Potential Roles of Transporters in Freeze Tolerance
inferredcites →https://doi.org/10.1038/41908openalex-snapshot
Hyperactive antifreeze protein from beetles
inferredcites →https://doi.org/10.1038/nature08684openalex-snapshot
Transcriptional role of cyclin D1 in development revealed by a genetic–proteomic screen
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/nbt0997-887openalex-snapshot
The antifreeze potential of the spruce budworm thermal hysteresis protein
inferredcites →https://doi.org/10.1038/nm.2378openalex-snapshot
Inhibition of Notch signaling ameliorates insulin resistance in a FoxO1-dependent manner
inferredcites →https://doi.org/10.1038/nrg2521openalex-snapshot
Long non-coding RNAs: insights into functions
inferredcites →https://doi.org/10.1038/nrn3234openalex-snapshot
Emerging roles of non-coding RNAs in brain evolution, development, plasticity and disease
inferredcites →https://doi.org/10.1038/sj.emboj.7601138openalex-snapshot
Molecular chaperones of the Hsp110 family act as nucleotide exchange factors of Hsp70s
inferredcites →https://doi.org/10.1042/bj20021469openalex-snapshot
Protein kinase CK2: structure, regulation and role in cellular decisions of life and death
inferredcites →https://doi.org/10.1042/bst0301082openalex-snapshot
The role of desaturases in cold-induced lipid restructuring
inferredcites →https://doi.org/10.1046/j.1365-2583.2003.00413.xopenalex-snapshot
Variations in mitochondrial DNA and gene transcription in freezing‐tolerant larvae of Eurosta solidaginis (Diptera: Tephritidae) and Gynaephora groenlandica (Lepidoptera: Lymantriidae)
inferredcites →https://doi.org/10.1046/j.1523-1755.2002.00285.xopenalex-snapshot
Sorbitol transport in rat renal inner medullary interstitial cells
inferredcites →https://doi.org/10.1073/pnas.0606840103openalex-snapshot
Continuous up-regulation of heat shock proteins in larvae, but not adults, of a polar insect
inferredcites →https://doi.org/10.1073/pnas.0702538104openalex-snapshot
Trehalose transporter 1, a facilitated and high-capacity trehalose transporter, allows exogenous trehalose uptake into cells
inferredcites →https://doi.org/10.1073/pnas.0703538104openalex-snapshot
Up-regulation of heat shock proteins is essential for cold survival during insect diapause
inferredcites →https://doi.org/10.1073/pnas.1007075107openalex-snapshot
Mechanisms of suspended animation are revealed by transcript profiling of diapause in the flesh fly
inferredcites →https://doi.org/10.1073/pnas.1214911110openalex-snapshot
Long-range protein–water dynamics in hyperactive insect antifreeze proteins
inferredcites →https://doi.org/10.1074/jbc.m110.150623openalex-snapshot
Identification of Anhydrobiosis-related Genes from an Expressed Sequence Tag Database in the Cryptobiotic Midge Polypedilum vanderplanki (Diptera; Chironomidae)
inferredcites →https://doi.org/10.1080/07315724.2007.10719667openalex-snapshot
Mechanisms and Significance of Cell Volume Regulation
inferredcites →https://doi.org/10.1086/341021openalex-snapshot
To Freeze or Not to Freeze? An Evolutionary Perspective on the Cold‐Hardiness Strategies of Overwintering Ectotherms
inferredcites →https://doi.org/10.1086/653489openalex-snapshot
In Cold‐Hardy Insects, Seasonal, Temperature, and Reversible Phosphorylation Controls Regulate Sarco/Endoplasmic Reticulum Ca2+‐ATPase (SERCA)
inferredcites →https://doi.org/10.1086/physzool.69.5.30164247openalex-snapshot
Fatty Acid Content and Enzymes of Fatty Acid Metabolism in Overwintering Cold-Hardy Gall Insects
inferredcites →https://doi.org/10.1093/ae/57.2.110openalex-snapshot
i5k: The 5,000 Insect Genome Project
inferredcites →https://doi.org/10.1093/dnares/11.1.27openalex-snapshot
The Genome Sequence of Silkworm, Bombyx mori
inferredcites →https://doi.org/10.1093/jmcb/mjq045openalex-snapshot
The emerging roles of microRNAs in the molecular responses of metabolic rate depression
inferredcites →https://doi.org/10.1096/fj.02-0017fjeopenalex-snapshot
Identification and characterization of a novel freezing‐inducible gene, li16, in the wood frog Rana sylvatica
inferredcites →https://doi.org/10.1098/rstb.2002.1074openalex-snapshot
Insects and low temperatures: from molecular biology to distributions and abundance
inferredcites →https://doi.org/10.1098/rstb.2002.1081openalex-snapshot
Structure and function of antifreeze proteins
inferredcites →https://doi.org/10.1098/rstb.2006.1946openalex-snapshot
Molecular ecophysiology of Antarctic notothenioid fishes
inferredcites →https://doi.org/10.1111/j.1365-2583.2005.00589.xopenalex-snapshot
Cold hardening and transcriptional change in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00739.xopenalex-snapshot
Gene transcription during exposure to, and recovery from, cold and desiccation stress in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2583.2008.00827.xopenalex-snapshot
Rapid cold hardening elicits changes in brain protein profiles of the flesh fly, Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1111/j.1365-2583.2009.00871.xopenalex-snapshot
Aquaporin and aquaglyceroporin in silkworms, differently expressed in the hindgut and midgut of Bombyx mori
inferredcites →https://doi.org/10.1111/j.1365-2583.2010.01062.xopenalex-snapshot
Proteomics of cryoprotective dehydration in Megaphorura arctica Tullberg 1876 (Onychiuridae: Collembola)
inferredcites →https://doi.org/10.1111/j.1420-9101.2007.01326.xopenalex-snapshot
Gene expression profile analysis of Drosophila melanogaster selected for resistance to environmental stressors
inferredcites →https://doi.org/10.1111/j.1420-9101.2010.02071.xopenalex-snapshot
An EST‐based genome scan using 454 sequencing in the marine snailLittorina saxatilis
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A Draft Sequence for the Genome of the Domesticated Silkworm ( Bombyx mori )
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Defense Strategies Against Hypoxia and Hypothermia
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Insect cold hardiness: metabolic, gene, and protein adaptation 1 This review is part of a virtual symposium on recent advances in understanding a variety of complex regulatory processes in insect physiology and endocrinology, including development, metabolism, cold hardiness, food intake and…
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Freezing survival of the garter snake Thamnophis sirtalis parietalis
inferredcites →https://doi.org/10.1139/z95-001openalex-snapshot
Seasonal changes in plasma membrane glucose transporters enhance cryoprotectant distribution in the freeze-tolerant wood frog
inferredcites →https://doi.org/10.11416/kontyushigen1930.68.93openalex-snapshot
Induction of cryoprotectants and lower supercooling points in the eggs of the silkworm Bombyx mori, by a synthetic diapause hormone
inferredcites →https://doi.org/10.1146/annurev.en.06.010161.000415openalex-snapshot
Principles of Insect Cold-Hardiness
inferredcites →https://doi.org/10.1146/annurev.ento.43.1.85openalex-snapshot
Life On the Edge: Insect Ecology in Arctic Environments
inferredcites →https://doi.org/10.1146/annurev.nutr.25.050304.092514openalex-snapshot
ANNUAL LIPID CYCLES IN HIBERNATORS: Integration of Physiology and Behavior
inferredcites →https://doi.org/10.1146/annurev.ph.45.030183.001445openalex-snapshot
Freezing Resistance in Intertidal Invertebrates
inferredcites →https://doi.org/10.1146/annurev.ph.54.030192.003155openalex-snapshot
Natural Freeze Tolerance In Ectothermic Vertebrates
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Mammalian Facilitative Glucose Transporter Family: Structure And Molecular Regulation
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HEAT-SHOCK PROTEINS, MOLECULAR CHAPERONES, AND THE STRESS RESPONSE: Evolutionary and Ecological Physiology
inferredcites →https://doi.org/10.1146/annurev.physiol.63.1.327openalex-snapshot
Antifreeze and Ice Nucleator Proteins in Terrestrial Arthropods
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Antifreeze Proteins of Teleost Fishes
inferredcites →https://doi.org/10.1146/annurev.physiol.67.040403.103635openalex-snapshot
MOLECULAR AND EVOLUTIONARY BASIS OF THE CELLULAR STRESS RESPONSE
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Excretion and conservation of glycerol, and expression of aquaporins and glyceroporins, during cold acclimation in Cope's gray tree frogHyla chrysoscelis
inferredcites →https://doi.org/10.1152/ajpregu.00905.2006openalex-snapshot
Gene cloning and expression of an aquaporin (AQP-h3BL) in the basolateral membrane of water-permeable epithelial cells in osmoregulatory organs of the tree frog
inferredcites →https://doi.org/10.1152/ajpregu.1993.265.5.r1036openalex-snapshot
Adaptations of plasma membrane glucose transport facilitate cryoprotectant distribution in freeze-tolerant frogs
inferredcites →https://doi.org/10.1152/ajpregu.1993.265.6.r1324openalex-snapshot
Dehydration tolerance in wood frogs: a new perspective on development of amphibian freeze tolerance
inferredcites →https://doi.org/10.1152/ajpregu.1996.271.3.r545openalex-snapshot
Oxidative damage and antioxidants in Rana sylvatica, the freeze-tolerant wood frog
inferredcites →https://doi.org/10.1152/ajpregu.1997.272.5.r1480openalex-snapshot
Freezing-induced genes in wood frog (Rana sylvatica): fibrinogen upregulation by freezing and dehydration
inferredcites →https://doi.org/10.1152/ajpregu.1999.277.6.r1612openalex-snapshot
Role of metallothionein against oxidative stress in the musselMytilus galloprovincialis
inferredcites →https://doi.org/10.1152/japplphysiol.01029.2002openalex-snapshot
Invited Review: Effect of oxygen deprivation on cell cycle activity: a profile of delay and arrest
inferredcites →https://doi.org/10.1152/physiolgenomics.00042.2012openalex-snapshot
Combined transcriptomic and metabolomic approach uncovers molecular mechanisms of cold tolerance in a temperate flesh fly
inferredcites →https://doi.org/10.1152/physrev.1985.65.4.799openalex-snapshot
Physiology of cold tolerance in insects
inferredcites →https://doi.org/10.1152/physrev.1988.68.1.27openalex-snapshot
Freeze tolerance in animals
inferredcites →https://doi.org/10.1186/1471-2164-10-234openalex-snapshot
Gene discovery using massively parallel pyrosequencing to develop ESTs for the flesh fly Sarcophaga crassipalpis
inferredcites →https://doi.org/10.1186/1471-2164-10-328openalex-snapshot
Surviving the cold: molecular analyses of insect cryoprotective dehydration in the Arctic springtail Megaphorura arctica (Tullberg)
inferredcites →https://doi.org/10.1186/1471-2164-10-633openalex-snapshot
Sympatric ecological speciation meets pyrosequencing: sampling the transcriptome of the apple maggot Rhagoletis pomonella
inferredcites →https://doi.org/10.1186/1471-2164-10-69openalex-snapshot
Desiccation survival in an Antarctic nematode: molecular analysis using expressed sequenced tags
inferredcites →https://doi.org/10.1186/1471-2164-10-72openalex-snapshot
MytiBase: a knowledgebase of mussel (M. galloprovincialis) transcribed sequences
inferredcites →https://doi.org/10.1186/1471-2164-11-694openalex-snapshot
A garter snake transcriptome: pyrosequencing, de novo assembly, and sex-specific differences
inferredcites →https://doi.org/10.1186/1471-2164-13-481openalex-snapshot
Genome wide identification of chilling responsive microRNAs in Prunus persica
inferredcites →https://doi.org/10.1186/1471-2164-8-475openalex-snapshot
Surviving extreme polar winters by desiccation: clues from Arctic springtail (Onychiurus arcticus) EST libraries
inferredcites →https://doi.org/10.1186/1472-6785-10-3openalex-snapshot
Changes in gene expression linked with adult reproductive diapause in a northern malt fly species: a candidate gene microarray study
inferredcites →https://doi.org/10.1201/9780203647073.ch7openalex-snapshot
Physiology, Biochemistry, and Molecular Biology of Vertebrate Freeze Tolerance
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Endogenous and exogenous ice-nucleating agents constrain supercooling in the hatchling painted turtle
showing the first 200 of 232 · page through all 232
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Winter survival strategies of cave-adapted amphipods in the Ice Caves of Sam’s Point area of Minnewaska State Park Preserve, NY, USA
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Winter Temperature Affects Fatty Acid Composition and Gene Expression, but Not Fat Content and Survival in a Northern Population of a Range‐Expanding Spider
inferred← citeshttps://doi.org/10.1002/jez.1885openalex-snapshot
Effect of physiological stress on expression of glucose transporter 2 in liver of the wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.1002/jez.2262openalex-snapshot
Postfreeze viability of erythrocytes from Dryophytes chrysoscelis
inferred← citeshttps://doi.org/10.1002/jez.2306openalex-snapshot
In defense of proteins: Chaperones respond to freezing, anoxia, or dehydration stress in tissues of freeze tolerant wood frogs
inferred← citeshttps://doi.org/10.1002/jez.2681openalex-snapshot
mRNA m6A methylation in wood frog brain is maintained during freezing and anoxia
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Mechanically Robust Shape‐Memory Organohydrogels Based on Silk Fibroin with Organogel Microinclusions of Various Sizes
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inferred← citeshttps://doi.org/10.1007/978-3-030-41929-5_4openalex-snapshot
Ice Formation in Living Organisms
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Phsiological Ecology of Tarantulas: Thermoregulation, Metabolism, and Performance Traits
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Diversity and Geography of Torpor and Heterothermy
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Pro-oxidant Challenges and Antioxidant Adaptation of Pleuragramma antarctica in Platelet Ice
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The cold tolerance of the terrestrial slug, Ambigolimax valentianus
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Membrane adaptation in phospholipids and cholesterol in the widely distributed, freeze-tolerant wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.1007/s00360-015-0903-yopenalex-snapshot
Rainbow smelt: the unusual case of cryoprotection by sustained glycerol production in an aquatic animal
inferred← citeshttps://doi.org/10.1007/s00360-015-0951-3openalex-snapshot
MicroRNA regulation in heart and skeletal muscle over the freeze–thaw cycle in the freeze tolerant wood frog
inferred← citeshttps://doi.org/10.1007/s00360-018-1189-7openalex-snapshot
Overwintering adaptations and extreme freeze tolerance in a subarctic population of the wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.1007/s00360-020-01275-4openalex-snapshot
Metabolic characteristics of overwintering by the high-altitude dwelling Xizang plateau frog, Nanorana parkeri
inferred← citeshttps://doi.org/10.1007/s00360-020-01314-0openalex-snapshot
Freeze tolerance and the underlying metabolite responses in the Xizang plateau frog, Nanorana parkeri
inferred← citeshttps://doi.org/10.1007/s00360-021-01420-7openalex-snapshot
Seasonal variations in the intermediate metabolism in South American tree-frog Boana pulchella
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Proteostasis in ice: the role of heat shock proteins and ubiquitin in the freeze tolerance of the intertidal mussel, Mytilus trossulus
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Acclimation of Antarctic Chlamydomonas to the sea-ice environment: a transcriptomic analysis
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Rapid evolution of Ophraella communa cold tolerance in new low-temperature environments
inferred← citeshttps://doi.org/10.1007/s10493-025-01074-yopenalex-snapshot
Physiological reprogramming during cold acclimation in the predatory mite Neoseiulus bicaudus
inferred← citeshttps://doi.org/10.1007/s10561-019-09797-0openalex-snapshot
Influence of cryopreservation on structure and function of mammalian spermatozoa: an overview
inferred← citeshttps://doi.org/10.1007/s11010-021-04214-1openalex-snapshot
Epigenetic regulation by DNA methyltransferases during torpor in the thirteen-lined ground squirrel Ictidomys tridecemlineatus
inferred← citeshttps://doi.org/10.1007/s12192-014-0518-3openalex-snapshot
Group 1 LEA proteins contribute to the desiccation and freeze tolerance of Artemia franciscana embryos during diapause
inferred← citeshttps://doi.org/10.1007/s12192-022-01307-8openalex-snapshot
Role of unfolded protein response and ER-associated degradation under freezing, anoxia, and dehydration stresses in the freeze-tolerant wood frogs
inferred← citeshttps://doi.org/10.1007/s12192-022-01312-xopenalex-snapshot
Chaperone proteins: universal roles in surviving environmental stress
inferred← citeshttps://doi.org/10.1007/s13258-021-01069-0openalex-snapshot
Transcriptional reprogramming caused by cold acclimation in Meloidogyne incognita eggs
inferred← citeshttps://doi.org/10.1007/s40883-019-00131-4openalex-snapshot
Liver Cryopreservation for Regenerative Medicine Applications
inferred← citeshttps://doi.org/10.1016/j.apsoil.2023.105110openalex-snapshot
An Antarctic worm and its soil ecosystem: A review of an emerging research program in ecological genomics
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2021.736747openalex-snapshot
MicroRNA roles and their potential use as selection tool to cold tolerance of domesticated teleostean species: A systematic review
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.04.007openalex-snapshot
Potential role for microRNA in regulating hypoxia-induced metabolic suppression in jumbo squids
inferred← citeshttps://doi.org/10.1016/j.cbd.2013.10.001openalex-snapshot
CryomiRs: Towards the identification of a cold-associated family of microRNAs
inferred← citeshttps://doi.org/10.1016/j.cbd.2023.101147openalex-snapshot
Hepatic transcriptome and gut microbiome provide insights into freeze tolerance in the high-altitude frog, Nanorana parkeri
inferred← citeshttps://doi.org/10.1016/j.cbpa.2016.01.023openalex-snapshot
How widespread is preparation for oxidative stress in the animal kingdom?
inferred← citeshttps://doi.org/10.1016/j.cbpa.2021.110957openalex-snapshot
Cold tolerance of laboratory-reared Asian longhorned beetles
inferred← citeshttps://doi.org/10.1016/j.cbpa.2024.111775openalex-snapshot
Influence of temperature changes on oxidative stress and antioxidant defense system in the bay scallop, Argopecten irradians
inferred← citeshttps://doi.org/10.1016/j.cbpb.2015.04.004openalex-snapshot
Expression of stress-related genes in diapause of European corn borer (Ostrinia nubilalis Hbn.)
inferred← citeshttps://doi.org/10.1016/j.cbpb.2015.12.004openalex-snapshot
Comparative enzymology—new insights from studies of an “old” enzyme, lactate dehydrogenase
inferred← citeshttps://doi.org/10.1016/j.cbpb.2016.07.003openalex-snapshot
Regulation of SMAD transcription factors during freezing in the freeze tolerant wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.1016/j.cbpb.2021.110573openalex-snapshot
Freezing stress adaptations: Critical elements to activate Nrf2 related antioxidant defense in liver and skeletal muscle of the freeze tolerant wood frogs
inferred← citeshttps://doi.org/10.1016/j.cbpb.2022.110747openalex-snapshot
Lessons from nature: Leveraging the freeze-tolerant wood frog as a model to improve organ cryopreservation and biobanking
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.09.034openalex-snapshot
Antivirulence Properties of an Antifreeze Protein
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2017.01.003openalex-snapshot
Molecular snapshot of an intracellular freezing event in an Antarctic nematode
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2017.04.004openalex-snapshot
Cryoprotectants: A review of the actions and applications of cryoprotective solutes that modulate cell recovery from ultra-low temperatures
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2017.04.013openalex-snapshot
Cryopreservation of boar sperm induces differential microRNAs expression
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2017.06.002openalex-snapshot
Regulation of pyruvate kinase in skeletal muscle of the freeze tolerant wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2017.06.005openalex-snapshot
Cryopreservation of Luciola praeusta Kiesenwetter (Coleoptera: Lampyridae) embryos by vitrification
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2017.09.003openalex-snapshot
TonEBP/NFAT5 regulates downstream osmoregulatory proteins during freeze-thaw stress in the wood frog
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2020.10.012openalex-snapshot
Regulation of NF-κB, FHC and SOD2 in response to oxidative stress in the freeze tolerant wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2020.11.019openalex-snapshot
Response of Anatolian mountain frogs (Rana macrocnemis and Rana holtzi) to freezing, anoxia, and dehydration: Glucose as a cryoprotectant
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.103958openalex-snapshot
Expression analysis of aquaporin genes in Saussurea involucrata rosette leaves and functional analysis of upregulated SiPIP1;5A under low-temperature stress
inferred← citeshttps://doi.org/10.1016/j.foodchem.2023.137808openalex-snapshot
Natural deep eutectic solvent: A promising eco-friendly food bio-inspired antifreezing
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145671openalex-snapshot
Coordinated expression of Jumonji and AHCY under OCT transcription factor control to regulate gene methylation in wood frogs during anoxia
inferred← citeshttps://doi.org/10.1016/j.genrep.2018.10.010openalex-snapshot
Transcriptome sequencing, de novo assembly and annotation of the freeze tolerant earthworm, Dendrobaena octaedra
inferred← citeshttps://doi.org/10.1016/j.giant.2020.100014openalex-snapshot
Anti-Freezing multiphase gel materials: Bioinspired design strategies and applications
inferred← citeshttps://doi.org/10.1016/j.ibmb.2021.103638openalex-snapshot
The draft genome of the Asian corn borer yields insights into ecological adaptation of a devastating maize pest
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.124718openalex-snapshot
Hepatic citrate synthase suppression in the freeze-tolerant wood frog (Rana sylvatica)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.136861openalex-snapshot
Functional and evolutionary analysis of key enzymes triacylglycerol lipase, glycogen hydrolases in the glycerol and glucose biosynthesis pathway and cellular chaperones for freeze-tolerance of the Rice stem borer, Chilo suppressalis
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101202openalex-snapshot
A Unique Energy-Saving Strategy during Hibernation Revealed by Multi-Omics Analysis in the Chinese Alligator
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106128openalex-snapshot
Microhabitat-specific diurnal metabolomic responses of the intertidal limpet Cellana toreuma to winter low temperature
inferred← citeshttps://doi.org/10.1016/j.jbior.2022.100944openalex-snapshot
Freeze-induced suppression of pyruvate kinase in liver of the wood frog (Rana sylvatica)
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2016.03.009openalex-snapshot
All or nothing: Survival, reproduction and oxidative balance in Spotted Wing Drosophila (Drosophila suzukii) in response to cold
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2019.103971openalex-snapshot
Suppression of glycogen synthase expression reduces glycogen and lipid storage during mosquito overwintering diapause
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2021.104298openalex-snapshot
Epigenetic underpinnings of freeze avoidance in the goldenrod gall moth, Epiblema scudderiana
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2025.104809openalex-snapshot
Tissue- and temperature-dependent expression, enzyme activity, and RNAi knockdown of Catalase in a freeze-tolerant insect
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2014.07.007openalex-snapshot
Linking energetics and overwintering in temperate insects
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2015.11.003openalex-snapshot
An invitation to measure insect cold tolerance: Methods, approaches, and workflow
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2016.06.001openalex-snapshot
Dietary alpha-ketoglutarate increases cold tolerance in Drosophila melanogaster and enhances protein pool and antioxidant defense in sex-specific manner
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2017.03.012openalex-snapshot
Low temperature tolerance, cold hardening and acclimation in tadpoles of the neotropical túngara frog ( Engystomops pustulosus )
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2017.04.007openalex-snapshot
Freeze-responsive regulation of MEF2 proteins and downstream gene networks in muscles of the wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2018.03.018openalex-snapshot
Cold tolerance mechanisms of two arthropods from the Andean Range of Central Chile: Agathemera crassa (Insecta: Agathemeridae) and Euathlus condorito (Arachnida: Theraphosidae)
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2023.103705openalex-snapshot
Metabolic changes in the subtropical frog Boana pulchella during experimental cooling and recovery conditions
inferred← citeshttps://doi.org/10.1016/j.marenvres.2017.04.007openalex-snapshot
Nrf2 and regulation of the antioxidant system in the Antarctic silverfish, Pleuragramma antarctica: Adaptation to environmental changes of pro-oxidant pressure
inferred← citeshttps://doi.org/10.1016/j.pmpp.2024.102391openalex-snapshot
Deciphering anhydrobiosis and plant parasitism of the wheat seed gall nematode, Anguina tritici through transcriptomic analysis
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.03.006openalex-snapshot
Expression of glycogenic genes in the oviduct of Chinese brown frog (Rana dybowskii) during pre-brumation
inferred← citeshttps://doi.org/10.1016/j.tibtech.2021.06.004openalex-snapshot
Bioinspired materials and technology for advanced cryopreservation
inferred← citeshttps://doi.org/10.1021/acs.jced.4c00330openalex-snapshot
Density and Isobaric Thermal Expansion of the Liquid-Phase Binary Glycerol + Dimethyl Sulfoxide Mixture at Temperatures from 278.15 to 333.15 K and Ambient Pressure
inferred← citeshttps://doi.org/10.1021/acsabm.3c00017openalex-snapshot
Silk Fibroin-Based Shape-Memory Organohydrogels with Semicrystalline Microinclusions
inferred← citeshttps://doi.org/10.1021/acsami.4c12648openalex-snapshot
Silk Fibroin-Based Multiple-Shape-Memory Organohydrogels
inferred← citeshttps://doi.org/10.1021/acsapm.2c00741openalex-snapshot
Silk Fibroin Cryogel Building Adaptive Organohydrogels with Switching Mechanics and Viscoelasticity
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.7b00201openalex-snapshot
Predehydration and Ice Seeding in the Presence of Trehalose Enable Cell Cryopreservation
inferred← citeshttps://doi.org/10.1021/jp4126705openalex-snapshot
Dissecting the Effects of Concentrated Carbohydrate Solutions on Protein Diffusion, Hydration, and Internal Dynamics
inferred← citeshttps://doi.org/10.1038/hdy.2015.6openalex-snapshot
How consistent are the transcriptome changes associated with cold acclimation in two species of the Drosophila virilis group?
inferred← citeshttps://doi.org/10.1038/s41587-019-0223-yopenalex-snapshot
Supercooling extends preservation time of human livers
inferred← citeshttps://doi.org/10.1038/s41596-020-0319-3openalex-snapshot
Subzero non-frozen preservation of human livers in the supercooled state
inferred← citeshttps://doi.org/10.1038/srep13965openalex-snapshot
Parallel molecular routes to cold adaptation in eight genera of New Zealand stick insects
inferred← citeshttps://doi.org/10.1039/c4ra07313dopenalex-snapshot
Nutrients responses of Pleurotus ostreatus to slow frozen storage in the short term
inferred← citeshttps://doi.org/10.1080/07391102.2020.1796793openalex-snapshot
Characteristics, dynamics and mechanisms of actions of some major stress-induced biomacromolecules; addressing Artemia as an excellent biological model
inferred← citeshttps://doi.org/10.1093/ee/nvx153openalex-snapshot
Rapid Cold-Hardening of a Subtropical Species, Maruca vitrata (Lepidoptera: Crambidae), Accompanies Hypertrehalosemia by Upregulating Trehalose-6-Phosphate Synthase
inferred← citeshttps://doi.org/10.1093/gbe/evz104openalex-snapshot
The Parallel Molecular Adaptations to the Antarctic Cold Environment in Two Psychrophilic Green Algae
inferred← citeshttps://doi.org/10.1093/molbev/msad040openalex-snapshot
Multi-omics Investigation of Freeze Tolerance in the Amur Sleeper, an Aquatic Ectothermic Vertebrate
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.001.0001openalex-snapshot
Respiratory Biology of Animals
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0002openalex-snapshot
A very brief history of respiratory biology
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0003openalex-snapshot
A primer on respiratory physiology
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0004openalex-snapshot
Structure, function, and evolution of respiratory proteins
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0005openalex-snapshot
Coping with extremes
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0006openalex-snapshot
Respiratory faculties of aquatic invertebrates
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0007openalex-snapshot
Respiratory faculties of amphibious and terrestrial invertebrates
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0008openalex-snapshot
Control of breathing in invertebrates
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0009openalex-snapshot
The evolution of water-breathing respiratory faculties in invertebrates
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0010openalex-snapshot
The evolution of air-breathing respiratory faculties in invertebrates
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0011openalex-snapshot
Respiratory faculties of aquatic craniotes
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0012openalex-snapshot
Respiratory faculties of amphibious and terrestrial craniotes
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0013openalex-snapshot
Control of breathing in craniotes
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0014openalex-snapshot
The evolution of water-breathing respiratory faculties in craniotes
inferred← citeshttps://doi.org/10.1093/oso/9780199238460.003.0015openalex-snapshot
The evolution of air-breathing respiratory faculties in craniotes
inferred← citeshttps://doi.org/10.1097/mot.0000000000000534openalex-snapshot
Cryopreservation by vitrification
inferred← citeshttps://doi.org/10.1098/rspb.2022.0308openalex-snapshot
Insect cross-tolerance to freezing and drought stress: role of metabolic rearrangement
inferred← citeshttps://doi.org/10.1101/2021.08.30.458284openalex-snapshot
Molecular evidence of intertidal habitats selecting for repeated ice-binding protein evolution in invertebrates
inferred← citeshttps://doi.org/10.1101/2022.05.10.491133openalex-snapshot
Multiple omic investigations of freeze tolerance adaptation in the aquatic ectothermic vertebrate, the Amur sleeper
inferred← citeshttps://doi.org/10.1101/2024.12.28.630119openalex-snapshot
Winter temperature effects in a cold-adapted northern population of a range-expanding spider: survival, energy stores, and differential gene expression
inferred← citeshttps://doi.org/10.1101/2025.02.22.639691openalex-snapshot
Meltome Atlas of Arabidopsis thaliana Proteome: A Melting Temperature-Based Identification of Heat & Cold Resistant Proteins
inferred← citeshttps://doi.org/10.1101/449330openalex-snapshot
Transcriptional dynamics following freezing stress reveal selection for mechanisms of freeze tolerance at the poleward range margin in the cold water intertidal barnacle Semibalanus balanoides
inferred← citeshttps://doi.org/10.1103/physreve.104.045102openalex-snapshot
Theory of freezing point depression in charged porous media
inferred← citeshttps://doi.org/10.1104/pp.15.00942openalex-snapshot
Genetic Architecture of Natural Variation in Thermal Responses of Arabidopsis
inferred← citeshttps://doi.org/10.1111/1365-2435.13718openalex-snapshot
A unifying, eco‐physiological framework for animal dormancy
inferred← citeshttps://doi.org/10.1111/1365-2656.70078openalex-snapshot
Multi‐dimensional tolerance to low temperature for high‐latitude invasion success by the rapidly expanding golden mussel
inferred← citeshttps://doi.org/10.1111/1744-7917.12320openalex-snapshot
Transcriptomic and proteomic analyses on the supercooling ability and mining of antifreeze proteins of the Chinese white wax scale insect
inferred← citeshttps://doi.org/10.1111/1748-5967.12561openalex-snapshot
Suppression of glycerol biosynthesis‐related genes decreases the effect of rapid cold hardening in Helicoverpa assulta
inferred← citeshttps://doi.org/10.1111/1755-0998.13078openalex-snapshot
A chromosome‐level genome assembly reveals the genetic basis of cold tolerance in a notorious rice insect pest, Chilo suppressalis
inferred← citeshttps://doi.org/10.1111/brv.12137openalex-snapshot
Daily torpor and hibernation in birds and mammals
inferred← citeshttps://doi.org/10.1111/brv.12425openalex-snapshot
Mechanisms underlying insect freeze tolerance
inferred← citeshttps://doi.org/10.1111/jph.12897openalex-snapshot
Pre‐cold acclimation promotes cryoprotectant accumulation and enhances freezing tolerance of Meloidogyne incognita
inferred← citeshttps://doi.org/10.1111/jzo.12255openalex-snapshot
Seasonal variation and freezing response of glucose transporter 2 in liver of the wood frog: implications for geographic variation in freeze tolerance
inferred← citeshttps://doi.org/10.1111/mec.16748openalex-snapshot
Selective effects of a short transient environmental fluctuation on a natural population
inferred← citeshttps://doi.org/10.1111/rda.12728openalex-snapshot
Membrane Stress During Thawing Elicits Redistribution of Aquaporin 7 But Not of Aquaporin 9 in Boar Spermatozoa
inferred← citeshttps://doi.org/10.1139/bcb-2021-0519openalex-snapshot
Mitochondrial DNA methyltransferases and their regulation under freezing and dehydration stresses in the freeze-tolerant wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.1152/physrev.00016.2016openalex-snapshot
Molecular Physiology of Freeze Tolerance in Vertebrates
inferred← citeshttps://doi.org/10.11606/t.41.2018.tde-16042018-131823openalex-snapshot
Processos fisiológicos envolvidos na aquisição, perda e recolocação da zooxantela ligados ao branqueamento de cnidários
inferred← citeshttps://doi.org/10.1186/1471-2164-16-s13-s8openalex-snapshot
A comparison of the transcriptome of Drosophila melanogaster in response to entomopathogenic fungus, ionizing radiation, starvation and cold shock
inferred← citeshttps://doi.org/10.1186/s12864-024-10248-8openalex-snapshot
Comparative transcriptomic analysis delineates adaptation strategies of Rana kukunoris toward cold stress on the Qinghai-Tibet Plateau
inferred← citeshttps://doi.org/10.1186/s12864-025-12136-1openalex-snapshot
Identification of key genes associated with overwintering in Histia rhodope larva using gene co-expression network analysis
inferred← citeshttps://doi.org/10.1186/s12983-018-0252-2openalex-snapshot
Functional characterization of the Hyles euphorbiae hawkmoth transcriptome reveals strong expression of phorbol ester detoxification and seasonal cold hardiness genes
inferred← citeshttps://doi.org/10.1186/s12983-021-00428-7openalex-snapshot
Metabolic responses of plasma to extreme environments in overwintering Tibetan frogs Nanorana parkeri: a metabolome integrated analysis
inferred← citeshttps://doi.org/10.1186/s40659-025-00621-6openalex-snapshot
Metabolism dynamics in tropical cockroach during a cold-induced recovery period
inferred← citeshttps://doi.org/10.1242/bio.023341openalex-snapshot
Investigating trehalose synthesis genes after cold acclimation in the Antarctic nematodePanagrolaimussp. DAW1
inferred← citeshttps://doi.org/10.1242/bio.058524openalex-snapshot
Morphological mechanism allowing a parasitic leech, Ozobranchus jantseanus (Rhynchobdellida: Ozobranchidae), to survive in ultra-low temperatures
inferred← citeshttps://doi.org/10.1242/jeb.116905openalex-snapshot
Animal ice-binding (antifreeze) proteins and glycolipids: an overview with emphasis on physiological function
inferred← citeshttps://doi.org/10.1242/jeb.160176openalex-snapshot
CRISPR-induced null alleles show that Frost protects Drosophila melanogaster reproduction after cold exposure
inferred← citeshttps://doi.org/10.1242/jeb.233478openalex-snapshot
Drivers of plasticity in freeze tolerance in the intertidal mussel, Mytilus trossulus
inferred← citeshttps://doi.org/10.1242/jeb.243409openalex-snapshot
Molecular evidence of intertidal habitats selecting for repeated ice-binding protein evolution in invertebrates
inferred← citeshttps://doi.org/10.1242/jeb.247043openalex-snapshot
Ice in the intertidal: patterns and processes of freeze tolerance in intertidal invertebrates
inferred← citeshttps://doi.org/10.1242/jeb.247259openalex-snapshot
Gluconeogenesis in frogs during cooling and dehydration exposure: new insights into tissue plasticity of the gluconeogenic pathway dependent on abiotic factors
inferred← citeshttps://doi.org/10.1242/jeb.249947openalex-snapshot
Freeze-tolerant crickets fortify their actin cytoskeleton in fat body tissue
inferred← citeshttps://doi.org/10.1371/journal.pone.0116562openalex-snapshot
Frostbite Protection in Mice Expressing an Antifreeze Glycoprotein
inferred← citeshttps://doi.org/10.1371/journal.pone.0173100openalex-snapshot
The physiological role of fat body and muscle tissues in response to cold stress in the tropical cockroach Gromphadorhina coquereliana
inferred← citeshttps://doi.org/10.14716/ijtech.v13i8.6129openalex-snapshot
Can Cryoprotectant’s modification in Spermatozoa Cryopreservation be an Alternative to Improve Embryo Quality? A Review
inferred← citeshttps://doi.org/10.1515/biolog-2017-0042openalex-snapshot
Dietary alpha-ketoglutarate partially prevents age-related decline in locomotor activity and cold tolerance in Drosophila melanogaster
inferred← citeshttps://doi.org/10.15407/ubj94.01.086openalex-snapshot
Protein content in the parental diet affects cold tolerance and antioxidant system state in the offspring Drosophila
inferred← citeshttps://doi.org/10.1893/bios-d-17-00007openalex-snapshot
Antifreeze proteins: effective adaptations of organisms for low temperature survival
inferred← citeshttps://doi.org/10.22215/etd/2016-11495openalex-snapshot
Regulation of pyruvate kinase in hypometabolic states
inferred← citeshttps://doi.org/10.22215/etd/2016-11689openalex-snapshot
Involvement of Reversible Protein Methylation in 13-Lined Ground Squirrel Hibernation.
inferred← citeshttps://doi.org/10.22215/etd/2016-11700openalex-snapshot
Regulation of the Nuclear Factor of Activated T Cell (NFAT) Family of Transcription Factors in the Freeze Tolerant Wood Frog, Rana sylvatica
inferred← citeshttps://doi.org/10.22215/etd/2017-11819openalex-snapshot
Epigenetic Underpinnings of Freeze Tolerance in the Goldenrod Gall Fly Eurosta Solidaginis and the Goldenrod Gall Moth Epiblema Scudderiana
inferred← citeshttps://doi.org/10.22215/etd/2017-12054openalex-snapshot
Micromanaging Freeze Tolerance: The Biogenesis and Regulation of microRNAs in Frozen Frogs
inferred← citeshttps://doi.org/10.22215/etd/2017-12120openalex-snapshot
Control of selective mRNA translation over the torpor-arousal cycle of thirteen-lined ground squirrels
inferred← citeshttps://doi.org/10.22215/etd/2020-14149openalex-snapshot
Enzymatic Regulation in the Liver of the Freeze-Tolerant Wood Frog in Metabolically Depressed States
inferred← citeshttps://doi.org/10.22215/etd/2020-14320openalex-snapshot
Frozen but alive: Molecular responses to autophagy, angiogenesis and energy metabolism in the stress-tolerant wood frog, Rana sylvatica
inferred← citeshttps://doi.org/10.22215/etd/2021-14760openalex-snapshot
A Winter's Tale: MicroRNA Biogenesis and Regulation in the Freeze-Tolerant Grey Tree Frog, Hyla Versicolor
inferred← citeshttps://doi.org/10.22215/etd/2021-14810openalex-snapshot
Methyl Epigenetic Mechanisms in the Freeze-Tolerance Response of Rana Sylvatica Nervous Tissue
inferred← citeshttps://doi.org/10.22215/etd/2022-15199openalex-snapshot
Role of Glucose-induced Transcription Factor Signalling and Mitochondrial Epigenetics in Stress Tolerant Wood Frog, Rana sylvatica
inferred← citeshttps://doi.org/10.22215/etd/2022-15335openalex-snapshot
Complex Yet Coordinated: Regulation of Transcriptional Factors and Cell Signaling Pathways to Endure Anoxia in Rana sylvatica
inferred← citeshttps://doi.org/10.22215/etd/2023-15834openalex-snapshot
Enzymatic Regulation of Hepatic Carbohydrate Metabolism in Freeze-tolerant Wood Frogs, Rana sylvatica
inferred← citeshttps://doi.org/10.22215/etd/2024-16064openalex-snapshot
Unmasking the Epigenetic Landscape of Freeze Tolerance in the Grey Tree Frog
inferred← citeshttps://doi.org/10.24272/j.issn.2095-8137.2023.171openalex-snapshot
Surviving winter on the Qinghai-Xizang Plateau: Extensive reversible protein phosphorylation plays a dominant role in regulating hypometabolism in hibernating Nanorana parkeri
inferred← citeshttps://doi.org/10.3109/19401736.2015.1033697openalex-snapshot
The complete mitochondrial genome of Lithobates sylvaticus (Anura: Ranidae)
inferred← citeshttps://doi.org/10.31594/commagene.1176451openalex-snapshot
Hayvanlarda Soğuğa Dayanıklılık: Çift Yaşarların Kriyobiyolojisi
inferred← citeshttps://doi.org/10.3384/diss.diva-131862openalex-snapshot
Sperm Membrane Channels, Receptors and Kinematics : Using boar spermatozoa for drug toxicity screening
inferred← citeshttps://doi.org/10.3389/fmars.2023.1158649openalex-snapshot
Surviving the cold: a review of the effects of cold spells on bivalves and mitigation measures
inferred← citeshttps://doi.org/10.3389/fphar.2023.1098976openalex-snapshot
Adenosine and P1 receptors: Key targets in the regulation of sleep, torpor, and hibernation
inferred← citeshttps://doi.org/10.3389/fphys.2024.1358190openalex-snapshot
Extracellular freezing induces a permeability transition in the inner membrane of muscle mitochondria of freeze-sensitive but not freeze-tolerant Chymomyza costata larvae
inferred← citeshttps://doi.org/10.3390/ani12101286openalex-snapshot
Metabolomic Analysis Reveals That the Moor Frog Rana arvalis Uses Both Glucose and Glycerol as Cryoprotectants
inferred← citeshttps://doi.org/10.3390/ani13040724openalex-snapshot
Variations of Supercooling Capacity in Intertidal Gastropods
inferred← citeshttps://doi.org/10.3390/antiox10040543openalex-snapshot
Mitochondria and the Frozen Frog
inferred← citeshttps://doi.org/10.3390/cells10123374openalex-snapshot
MicroRNA Cues from Nature: A Roadmap to Decipher and Combat Challenges in Human Health and Disease?
inferred← citeshttps://doi.org/10.3390/ijms25063100openalex-snapshot
Prolonged Heat Stress during Winter Diapause Alters the Expression of Stress-Response Genes in Ostrinia nubilalis (Hbn.)
inferred← citeshttps://doi.org/10.3390/insects10120426openalex-snapshot
Seasonal Assessment of Supercooling Points for Two Introduced and One Native Laricobius spp. (Coleoptera: Derodontidae), Predators of Adelgidae
inferred← citeshttps://doi.org/10.3390/insects12060549openalex-snapshot
Climate Mismatch between Introduced Biological Control Agents and Their Invasive Host Plants: Improving Biological Control of Tropical Weeds in Temperate Regions
inferred← citeshttps://doi.org/10.3390/insects14010089openalex-snapshot
Insect Freeze-Tolerance Downunder: The Microbial Connection
inferred← citeshttps://doi.org/10.3390/life11121422openalex-snapshot
Activation of the Hippo Pathway in Rana sylvatica: Yapping Stops in Response to Anoxia
inferred← citeshttps://doi.org/10.3390/life15020319openalex-snapshot
Transcriptomic Profiling Reveals Key Genes Underlying Cold Stress Responses in Camphora
inferred← citeshttps://doi.org/10.3390/metabo12020163openalex-snapshot
Cryoprotective Metabolites Are Sourced from Both External Diet and Internal Macromolecular Reserves during Metabolic Reprogramming for Freeze Tolerance in Drosophilid Fly, Chymomyza costata
inferred← citeshttps://doi.org/10.3390/metabo12080756openalex-snapshot
Deterioration in the Quality of Recalcitrant Quercus robur Seeds during Six Months of Storage at Subzero Temperatures: Ineffective Activation of Prosurvival Mechanisms and Evidence of Freezing Stress from an Untargeted Metabolomic Study
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