On the public citation graph

Molecular Physiology of Freeze Tolerance in Vertebrates

https://doi.org/10.1152/physrev.00016.2016

0 signed · 536 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1097-010x(19980201)280:2<197::aid-jez11>3.0.co;2-jopenalex-snapshot

Freeze duration influences postfreeze survival in the frogRana sylvatica

inferredcites →https://doi.org/10.1002/(sici)1097-010x(19990215)283:3<221::aid-jez1>3.0.co;2-qopenalex-snapshot

Freeze tolerance and cryoprotectant mobilization in the gray treefrog (Hyla versicolor)

inferredcites →https://doi.org/10.1002/9780470015902.a0020621.pub2openalex-snapshot

Water Transport Across Cell Membranes

inferredcites →https://doi.org/10.1002/bip.22250openalex-snapshot

Peptide design for antimicrobial and immunomodulatory applications

inferredcites →https://doi.org/10.1002/cphy.c130007openalex-snapshot

Molecular Biology of Freezing Tolerance

inferredcites →https://doi.org/10.1002/jez.1030openalex-snapshot

Freeze tolerance in the gray treefrog: Cryoprotectant mobilization and organ dehydration

inferredcites →https://doi.org/10.1002/jez.1402150311openalex-snapshot

Adaptation of nitrogen metabolism to hyperosmotic environment in Amphibia

inferredcites →https://doi.org/10.1002/jez.1402490203openalex-snapshot

Seasonal variation in freeze tolerance and ice content of the tree frog Hyla versicolor

inferredcites →https://doi.org/10.1002/jez.1402540215openalex-snapshot

Natural freeze tolerance in the terrestrial turtle, Terrapene carolina

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.1885openalex-snapshot

Effect of physiological stress on expression of glucose transporter 2 in liver of the wood frog, Rana sylvatica

inferredcites →https://doi.org/10.1002/jez.1905openalex-snapshot

Hepatocyte responses to in vitro freezing and β‐adrenergic stimulation: Insights into the extreme freeze tolerance of subarctic Rana sylvatica

inferredcites →https://doi.org/10.1002/jez.1930openalex-snapshot

Identification of a novel dehydration responsive gene, drp10, from the African clawed frog, Xenopus laevis

inferredcites →https://doi.org/10.1002/jez.436openalex-snapshot

Metabolic depression induced by urea in organs of the wood frog,Rana sylvatica: effects of season and temperature

inferredcites →https://doi.org/10.1002/jez.460openalex-snapshot

Physiological ecology of overwintering in hatchling turtles

inferredcites →https://doi.org/10.1002/jez.479openalex-snapshot

Urea production capacity in the wood frog (Rana sylvatica) varies with season and experimentally induced hyperuremia

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.572openalex-snapshot

Evidence for urea‐induced hypometabolism in isolated organs of dormant ectotherms

inferredcites →https://doi.org/10.1002/jez.603openalex-snapshot

Physiology of hibernation under the ice by turtles and frogs

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.a.10285openalex-snapshot

Survival and metabolic responses to freezing by the water frog (Rana ridibunda)

inferredcites →https://doi.org/10.1002/jez.a.20042openalex-snapshot

Comparison of the cold hardiness capacities of the oviparous and viviparous forms of Lacerta vivipara

inferredcites →https://doi.org/10.1002/pmic.201300229openalex-snapshot

Proteomic changes in the brain of the western painted turtle ( Chrysemys picta bellii ) during exposure to anoxia

inferredcites →https://doi.org/10.1002/prca.201200101openalex-snapshot

Glycated proteome: From reaction to intervention

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.1999.2194openalex-snapshot

Temperature Regulation of Glucose Metabolism in Red Blood Cells of the Freeze-Tolerant Wood Frog

inferredcites →https://doi.org/10.1006/cryo.2000.2289openalex-snapshot

Ice Nucleation and Antinucleation in Nature

inferredcites →https://doi.org/10.1006/cryo.2001.2338openalex-snapshot

Freeze-Thaw Effects on Metabolic Enzymes in Wood Frog Organs

inferredcites →https://doi.org/10.1007/978-1-4419-6315-4_1openalex-snapshot

Aquaporins: A Family of Highly Regulated Multifunctional Channels

inferredcites →https://doi.org/10.1007/978-3-319-19060-0_11openalex-snapshot

Anhydrobiosis: An Unsolved Problem with Applications in Human Welfare

inferredcites →https://doi.org/10.1007/978-3-642-02421-4openalex-snapshot

Aestivation

inferredcites →https://doi.org/10.1007/978-3-662-05014-9_6openalex-snapshot

The Amphibia

inferredcites →https://doi.org/10.1007/bf00260815openalex-snapshot

Supercooling, ice inoculation and freeze tolerance in the European common lizard, Lacerta vivipara

inferredcites →https://doi.org/10.1007/bf00300945openalex-snapshot

Supercooling and freeze-tolerance in the European wall lizard, Podarcis muralis, with a revisional history of the discovery of freeze-tolerance in vertebrates

inferredcites →https://doi.org/10.1007/bf00301174openalex-snapshot

Freezing tolerance/intolerance and cryoprotectant synthesis in terrestrially overwintering anurans in the Great Plains, USA

inferredcites →https://doi.org/10.1007/bf00688788openalex-snapshot

Biochemical adaption for freezing tolerance in the wood frog,Rana sylvatica

inferredcites →https://doi.org/10.1007/bf00714587openalex-snapshot

Effects of dehydration on organ metabolism in the frogPseudacris crucifer: hyperglycemic responses to dehydration mimic freezing-induced cryoprotectant production

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/s00018-007-7383-5openalex-snapshot

Endoplasmic reticulum stress responses

inferredcites →https://doi.org/10.1007/s00018-011-0720-8openalex-snapshot

Structural diversity and species distribution of host-defense peptides in frog skin secretions

inferredcites →https://doi.org/10.1007/s00360-003-0373-5openalex-snapshot

Adaptations to terrestrial overwintering of hatchling northern map turtles, Graptemys geographica

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/s00360-006-0092-9openalex-snapshot

Physiological responses to freezing in hatchlings of freeze-tolerant and -intolerant turtles

inferredcites →https://doi.org/10.1007/s00360-007-0185-0openalex-snapshot

Oxidative stress and antioxidant capacity of a terrestrially hibernating hatchling turtle

inferredcites →https://doi.org/10.1007/s00360-007-0190-3openalex-snapshot

Osmotic and metabolic responses to dehydration and urea-loading in a dormant, terrestrially hibernating frog

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/s00360-008-0261-0openalex-snapshot

Epigenetic silencers are enriched in dormant desert frog muscle

inferredcites →https://doi.org/10.1007/s00360-008-0304-6openalex-snapshot

Annual variation in glycerol mobilization and effect of freeze rigor on post-thaw locomotion in the freeze-tolerant frog Hyla versicolor

inferredcites →https://doi.org/10.1007/s00360-008-0307-3openalex-snapshot

Survival and metabolism of Rana arvalis during freezing

inferredcites →https://doi.org/10.1007/s00360-009-0414-9openalex-snapshot

Regulation of the heat shock response under anoxia in the turtle, Trachemys scripta elegans

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/s00360-012-0672-9openalex-snapshot

Cell cycle arrest associated with anoxia-induced quiescence, anoxic preconditioning, and embryonic diapause in embryos of the annual killifish Austrofundulus limnaeus

inferredcites →https://doi.org/10.1007/s00360-014-0805-4openalex-snapshot

Membrane adaptation in phospholipids and cholesterol in the widely distributed, freeze-tolerant wood frog, Rana sylvatica

inferredcites →https://doi.org/10.1007/s00360-015-0903-yopenalex-snapshot

Rainbow smelt: the unusual case of cryoprotection by sustained glycerol production in an aquatic animal

inferredcites →https://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

inferredcites →https://doi.org/10.1007/s00360-016-0960-xopenalex-snapshot

The role of DNA methylation during anoxia tolerance in a freshwater turtle (Trachemys scripta elegans)

inferredcites →https://doi.org/10.1007/s00360-016-1012-2openalex-snapshot

Enzymatic regulation of seasonal glycogen cycling in the freeze-tolerant wood frog, Rana sylvatica

inferredcites →https://doi.org/10.1007/s003600050078openalex-snapshot

Second messenger and cAMP-dependent protein kinase responses to dehydration and anoxia stresses in frogs

inferredcites →https://doi.org/10.1007/s003600050231openalex-snapshot

Electrophysiological and ultrastructural correlates of cryoinjury in sciatic nerve of the freeze-tolerant wood frog, Rana sylvatica

inferredcites →https://doi.org/10.1007/s003600100228openalex-snapshot

Freezing survival, body ice content and blood composition of the freeze-tolerant European common lizard, Lacerta vivipara

inferredcites →https://doi.org/10.1007/s00442-015-3450-zopenalex-snapshot

Snow cover and late fall movement influence wood frog survival during an unusually cold winter

inferredcites →https://doi.org/10.1007/s11010-010-0479-5openalex-snapshot

Epigenetics in anoxia tolerance: a role for histone deacetylases

inferredcites →https://doi.org/10.1007/s11010-012-1508-3openalex-snapshot

Activation of the unfolded protein response during anoxia exposure in the turtle Trachemys scripta elegans

inferredcites →https://doi.org/10.1007/s11010-014-2226-9openalex-snapshot

Transcript expression of the freeze responsive gene fr10 in Rana sylvatica during freezing, anoxia, dehydration, and development

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/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(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(92)90038-4openalex-snapshot

Biochemical modification of plasma ice nucleating activity in a freeze-tolerant frog

inferredcites →https://doi.org/10.1016/0016-6480(92)90148-dopenalex-snapshot

Hormonal effects on glycogen metabolism in isolated hepatocytes of a freeze-tolerant frog

inferredcites →https://doi.org/10.1016/0300-9629(77)90239-0openalex-snapshot

Temperature adaptation and effects of thermal acclimation in Rana sylvatica and Rana catesbeiana

inferredcites →https://doi.org/10.1016/0300-9629(86)90699-7openalex-snapshot

Freeze tolerance and intolerance as strategies of winter survival in terrestrially-hibernating amphibians

inferredcites →https://doi.org/10.1016/0304-4165(93)90092-mopenalex-snapshot

6-Phosphofructo-2-kinase and control of cryoprotectant synthesis in freeze tolerant frogs

inferredcites →https://doi.org/10.1016/0306-4565(92)90009-5openalex-snapshot

Postfreeze survival and muscle function in the leopard frog (Rana pipiens) and the wood frog (Rana sylvatica)

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.bbagen.2013.06.020openalex-snapshot

Akt signaling and freezing survival in the wood frog, Rana sylvatica

inferredcites →https://doi.org/10.1016/j.bbagen.2013.12.011openalex-snapshot

Cloning, characterization, and expression of glucose transporter 2 in the freeze-tolerant wood frog, Rana sylvatica

inferredcites →https://doi.org/10.1016/j.bbagen.2014.10.003openalex-snapshot

Free-radical first responders: The characterization of CuZnSOD and MnSOD regulation during freezing of the freeze-tolerant North American wood frog, Rana sylvatica

inferredcites →https://doi.org/10.1016/j.bbagen.2015.02.001openalex-snapshot

Turtle anoxia tolerance: Biochemistry and gene regulation

inferredcites →https://doi.org/10.1016/j.bbagen.2015.12.007openalex-snapshot

A hydrogen peroxide safety valve: The reversible phosphorylation of catalase from the freeze-tolerant North American wood frog, Rana sylvatica

inferredcites →https://doi.org/10.1016/j.cbpa.2006.03.019openalex-snapshot

Anoxia tolerance in turtles: Metabolic regulation and gene expression

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.cbpb.2009.01.012openalex-snapshot

Creatine kinase regulation by reversible phosphorylation in frog muscle

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.cbpb.2012.06.001openalex-snapshot

Regulation of liver lactate dehydrogenase by reversible phosphorylation in response to anoxia in a freshwater turtle

inferredcites →https://doi.org/10.1016/j.cbpb.2015.12.004openalex-snapshot

Comparative enzymology—new insights from studies of an “old” enzyme, lactate dehydrogenase

inferredcites →https://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

inferredcites →https://doi.org/10.1016/j.ceb.2015.02.003openalex-snapshot

Acetyl-CoA and the regulation of metabolism: mechanisms and consequences

inferredcites →https://doi.org/10.1016/j.cmet.2011.12.005openalex-snapshot

Acetylation Negatively Regulates Glycogen Phosphorylase by Recruiting Protein Phosphatase 1

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.2004.11.001openalex-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.2005.09.006openalex-snapshot

Oxidative DNA damage and antioxidant defenses in the European common lizard (Lacerta vivipara) in supercooled and frozen states

inferredcites →https://doi.org/10.1016/j.cryobiol.2006.08.001openalex-snapshot

Stress-induced activation of the AMP-activated protein kinase in the freeze-tolerant frog Rana sylvatica

inferredcites →https://doi.org/10.1016/j.cryobiol.2008.10.122openalex-snapshot

A re-evaluation of the role of type IV antifreeze protein

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.2015.08.009openalex-snapshot

Characterization of the SIRT family of NAD+-dependent protein deacetylases in the context of a mammalian model of hibernation, the thirteen-lined ground squirrel

inferredcites →https://doi.org/10.1016/j.febslet.2015.10.026openalex-snapshot

Low‐temperature microRNA expression in the painted turtle, Chrysemys picta during freezing stress

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2015.07.156openalex-snapshot

Preparation for oxidative stress under hypoxia and metabolic depression: Revisiting the proposal two decades later

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.gene.2009.10.005openalex-snapshot

Molecular mechanisms of turtle anoxia tolerance: A role for NF-κB

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.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.jtherbio.2014.07.006openalex-snapshot

Human males and females body thermoregulation: Perfusion effect analysis

inferredcites →https://doi.org/10.1016/j.jtherbio.2014.09.001openalex-snapshot

The ins and outs of water dynamics in cold tolerant soil invertebrates

inferredcites →https://doi.org/10.1016/j.jtherbio.2016.09.008openalex-snapshot

Exploration of low temperature microRNA function in an anoxia tolerant vertebrate ectotherm, the red eared slider turtle ( Trachemys scripta elegans )

inferredcites →https://doi.org/10.1016/j.mam.2012.07.001openalex-snapshot

The SLC2 (GLUT) family of membrane transporters

inferredcites →https://doi.org/10.1016/j.plantsci.2010.07.011openalex-snapshot

Molecular mechanisms underlying frost tolerance in perennial grasses adapted to cold climates

inferredcites →https://doi.org/10.1016/j.tibs.2010.09.003openalex-snapshot

Regulation of intermediary metabolism by protein acetylation

inferredcites →https://doi.org/10.1016/j.tibs.2014.09.005openalex-snapshot

Ice-binding proteins: a remarkable diversity of structures for stopping and starting ice growth

inferredcites →https://doi.org/10.1016/j.tree.2011.04.006openalex-snapshot

The need for jumpstarting amphibian genome projects

inferredcites →https://doi.org/10.1016/j.ygcen.2006.12.007openalex-snapshot

Arginine vasotocin promotes urea permeability through urea transporter expressed in the toad urinary bladder cells

inferredcites →https://doi.org/10.1016/s0005-2736(99)00147-9openalex-snapshot

Molecular and functional characterization of an amphibian urea transporter

inferredcites →https://doi.org/10.1016/s0014-5793(00)02102-5openalex-snapshot

Induction of synthesis of an antimicrobial peptide in the skin of the freeze‐tolerant frog, Rana sylvatica, in response to environmental stimuli

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/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/s0968-0004(00)89005-2openalex-snapshot

D-type cyclins

inferredcites →https://doi.org/10.1016/s1095-6433(02)00206-4openalex-snapshot

Life in the slow lane: molecular mechanisms of estivation

inferredcites →https://doi.org/10.1016/s1096-4959(01)00477-8openalex-snapshot

Protein phosphatase type-1 from skeletal muscle of the freeze-tolerant wood frog

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/10.1017/cbo9780511675997openalex-snapshot

Low Temperature Biology of Insects

inferredcites →https://doi.org/10.1017/s1464793103006195openalex-snapshot

Metabolic rate depression in animals: transcriptional and translational controls

inferredcites →https://doi.org/10.1017/s1464793106007032openalex-snapshot

The ecology of overwintering among turtles: where turtles overwinter and its consequences

inferredcites →https://doi.org/10.1023/a:1006817806010openalex-snapshot

Antioxidant systems and anoxia tolerance in a freshwater turtle Trachemys scripta elegans

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/10.1038/38644openalex-snapshot

Frogs reabsorb glucose from urinary bladder

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/nm.2378openalex-snapshot

Inhibition of Notch signaling ameliorates insulin resistance in a FoxO1-dependent manner

inferredcites →https://doi.org/10.1038/nrg2843openalex-snapshot

The widespread regulation of microRNA biogenesis, function and decay

inferredcites →https://doi.org/10.1038/srep16413openalex-snapshot

Initial characterization of the large genome of the salamander Ambystoma mexicanum using shotgun and laser capture chromosome sequencing

inferredcites →https://doi.org/10.1042/bj2380345openalex-snapshot

Coypu insulin. Primary structure, conformation and biological properties of a hystricomorph rodent insulin

inferredcites →https://doi.org/10.1042/bst20130003openalex-snapshot

Cross-talk among epigenetic modifications: lessons from histone arginine methylation

inferredcites →https://doi.org/10.1073/pnas.1501764112openalex-snapshot

Whole-genome sequence of the Tibetan frog Nanorana parkeri and the comparative evolution of tetrapod genomes

inferredcites →https://doi.org/10.1073/pnas.85.21.8350openalex-snapshot

Hatchling turtles survive freezing during winter hibernation.

inferredcites →https://doi.org/10.1074/jbc.272.20.12978openalex-snapshot

Alanine Scanning Mutagenesis of Insulin

inferredcites →https://doi.org/10.1086/374282openalex-snapshot

Postfreeze Reduction of Locomotor Endurance in the Freeze‐Tolerant Wood Frog,Rana sylvatica

inferredcites →https://doi.org/10.1086/378141openalex-snapshot

Physiological Ecology of Overwintering in the Hatchling Painted Turtle: Multiple‐Scale Variation in Response to Environmental Stress

inferredcites →https://doi.org/10.1086/420952openalex-snapshot

Accumulation of Lactate by Frozen Painted Turtles (Chrysemys picta) and Its Relationship to Freeze Tolerance

inferredcites →https://doi.org/10.1086/605416openalex-snapshot

Brief Chilling to Subzero Temperature Increases Cold Hardiness in the Hatchling Painted Turtle (Chrysemys picta)

inferredcites →https://doi.org/10.1086/bblv229n1p109openalex-snapshot

Molecular Machinery for Vasotocin-Dependent Transepithelial Water Movement in Amphibians: Aquaporins and Evolution

inferredcites →https://doi.org/10.1093/acprof:oso/9780198570325.001.0001openalex-snapshot

Ecological and Environmental Physiology of Amphibians

inferredcites →https://doi.org/10.1093/nar/gkn522openalex-snapshot

miR-16 family induces cell cycle arrest by regulating multiple cell cycle genes

inferredcites →https://doi.org/10.1093/nar/gku956openalex-snapshot

Xenbase, the Xenopus model organism database; new virtualized system, data types and genomes

inferredcites →https://doi.org/10.1093/protein/2.2.157openalex-snapshot

Soluble, prolonged-acting insulin derivatives. III. Degree of protraction, crystallizability and chemical stability of insulins substituted in positions A21, B13, B23, B27 and B30

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/10.1096/fj.13-230573openalex-snapshot

Expression of freeze‐responsive proteins, Fr10 and Li16, from freeze‐tolerant frogs enhances freezing survival of BmN insect cells

inferredcites →https://doi.org/10.1098/rstb.2002.1081openalex-snapshot

Structure and function of antifreeze proteins

inferredcites →https://doi.org/10.1111/brv.12137openalex-snapshot

Daily torpor and hibernation in birds and mammals

inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03611.xopenalex-snapshot

Postglacial range expansion from northern refugia by the wood frog,Rana sylvatica

inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04580.xopenalex-snapshot

Environmentally induced phenotypes and DNA methylation: how to deal with unpredictable conditions until the next generation and after

inferredcites →https://doi.org/10.1111/j.1432-1033.1996.0083t.xopenalex-snapshot

Anoxia‐Induced Gene Expression in Turtle Heart

inferredcites →https://doi.org/10.1111/j.1469-185x.2008.00035.xopenalex-snapshot

Physiological Ecology of Aquatic Overwintering in Ranid Frogs

inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06068.xopenalex-snapshot

Modulation of stress proteins and apoptotic regulators in the anoxia tolerant turtle brain

inferredcites →https://doi.org/10.1111/j.1558-5646.1978.tb00645.xopenalex-snapshot

THE EVOLUTIONARY SIGNIFICANCE OF DELAYED EMERGENCE FROM THE NEST BY HATCHLING TURTLES

inferredcites →https://doi.org/10.1111/j.1748-1716.2009.01975.xopenalex-snapshot

AMP‐activated protein kinase – a sensor of glycogen as well as AMP and ATP?

inferredcites →https://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

inferredcites →https://doi.org/10.1113/jphysiol.2002.024729openalex-snapshot

Hibernating without Oxygen: Physiological Adaptations of the Painted Turtle

inferredcites →https://doi.org/10.1126/science.1063127openalex-snapshot

Translating the Histone Code

inferredcites →https://doi.org/10.1126/science.1179689openalex-snapshot

Regulation of Cellular Metabolism by Protein Lysine Acetylation

inferredcites →https://doi.org/10.1126/science.1183670openalex-snapshot

The Genome of the Western Clawed Frog Xenopus tropicalis

inferredcites →https://doi.org/10.1126/science.172.3988.1152openalex-snapshot

Glycoproteins as Biological Antifreeze Agents in Antarctic Fishes

inferredcites →https://doi.org/10.1126/science.7058335openalex-snapshot

Survival of Frogs in Low Temperature

inferredcites →https://doi.org/10.1134/s0012496610020171openalex-snapshot

The Schrenck newt (Salamandrella schrenckii, Amphibia, Caudata, Hynobiidae) is the second amphibian that withstands extremely low temperatures

inferredcites →https://doi.org/10.1134/s0012496612020068openalex-snapshot

Is the western boundary of the Siberian salamander (Salamandrella keyserlingii, Amphibia, Caudata, Hynobiidae) range determined by the specific features of its wintering?

inferredcites →https://doi.org/10.1139/y94-223openalex-snapshot

Alterations in hepatic adrenergic receptor status in Rana sylvatica in response to freezing and thawing: implications to the freeze-induced glycemic response

inferredcites →https://doi.org/10.1139/z03-202openalex-snapshot

Postfreeze locomotion performance in wood frogs (Rana sylvatica) and spring peepers (Pseudacris crucifer)

inferredcites →https://doi.org/10.1139/z04-027openalex-snapshot

Cold-hardiness and dehydration resistance of hatchling Blanding's turtles (Emydoidea blandingii): implications for overwintering in a terrestrial habitat

inferredcites →https://doi.org/10.1139/z2012-011openalex-snapshot

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…

inferredcites →https://doi.org/10.1139/z85-009openalex-snapshot

Adaptations of metabolism for freeze tolerance in the gray tree frog, Hyla versicolor

inferredcites →https://doi.org/10.1139/z86-008openalex-snapshot

Freeze tolerant frogs: cryoprotectants and tissue metabolism during freeze–thaw cycles

inferredcites →https://doi.org/10.1139/z87-315openalex-snapshot

Freeze tolerance and the dynamics of ice formation in wood frogs (Rana sylvatica) from southern Ohio

inferredcites →https://doi.org/10.1139/z92-015openalex-snapshot

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/10.1139/z99-087openalex-snapshot

Terrestrial hibernation in the northern cricket frog,Acris crepitans

inferredcites →https://doi.org/10.1146/annurev.ecolsys.27.1.365openalex-snapshot

NATURAL FREEZING SURVIVAL IN ANIMALS

inferredcites →https://doi.org/10.1146/annurev.ph.54.030192.003155openalex-snapshot

Natural Freeze Tolerance In Ectothermic Vertebrates

inferredcites →https://doi.org/10.1146/annurev.physiol.60.1.55openalex-snapshot

BIOLOGICAL ICE NUCLEATION AND ICE DISTRIBUTION IN COLD-HARDY ECTOTHERMIC ANIMALS

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/10.1146/annurev.physiol.63.1.327openalex-snapshot

Antifreeze and Ice Nucleator Proteins in Terrestrial Arthropods

inferredcites →https://doi.org/10.1146/annurev.physiol.63.1.359openalex-snapshot

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

inferredcites →https://doi.org/10.1152/ajpregu.00378.2001openalex-snapshot

The respiratory metabolism of a lizard (Lacerta vivipara) in supercooled and frozen states

inferredcites →https://doi.org/10.1152/ajpregu.00434.2006openalex-snapshot

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.00711.2004openalex-snapshot

Freezing tolerance of the European water frogs: the good, the bad, and the ugly

inferredcites →https://doi.org/10.1152/ajpregu.1987.253.2.r292openalex-snapshot

Organ-specific metabolism during freezing and thawing in a freeze-tolerant frog

inferredcites →https://doi.org/10.1152/ajpregu.1989.257.5.r1046openalex-snapshot

Freezing-induced changes in the heart rate of wood frogs (Rana sylvatica)

inferredcites →https://doi.org/10.1152/ajpregu.1991.261.1.r134openalex-snapshot

Resumption of physiological functions in the wood frog (Rana sylvatica) after freezing

inferredcites →https://doi.org/10.1152/ajpregu.1992.262.3.r530openalex-snapshot

Natural freezing survival by painted turtles Chrysemys picta marginata and C. picta bellii

inferredcites →https://doi.org/10.1152/ajpregu.1992.263.1.r185openalex-snapshot

Cryomicroscopic analysis of freezing in liver of the freeze-tolerant wood frog

showing the first 200 of 292 · page through all 292

What points at this work

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

inferred← citeshttps://doi.org/10.1080/00222933.2019.1704458zenodo-depositor-declared

Breeding preferences in the treefrogsDryophytes japonicus(Hylidae) in Mongolia

inferred← citeshttps://doi.org/10.1002/1873-3468.14440openalex-snapshot

Epigenetics of the frozen brain: roles for lysine methylation in hypometabolism

inferred← citeshttps://doi.org/10.1002/9780470015902.a0029373openalex-snapshot

Vertebrate Respiration and Circulation in Extreme Conditions

inferred← citeshttps://doi.org/10.1002/adma.202510982openalex-snapshot

Nature‐Inspired Multidisciplinary Strategies for Tissue and Organ Cryopreservation

inferred← citeshttps://doi.org/10.1002/advs.202506968openalex-snapshot

Anti‐Icing Organogel Enables Quasi‐Homogeneous Supercooling Preservation of Mouse Hearts

inferred← citeshttps://doi.org/10.1002/arch.21618openalex-snapshot

Glucose‐6‐phosphate dehydrogenase is posttranslationally regulated in the larvae of the freeze‐tolerant gall fly, Eurosta solidaginis, in response to freezing

inferred← citeshttps://doi.org/10.1002/bies.201800092openalex-snapshot

Solving Donor Organ Shortage with Insights from Freeze Tolerance in Nature

inferred← citeshttps://doi.org/10.1002/bies.201800144openalex-snapshot

Comparative Physiology as an Idea Factory for Preserving and Freezing Organs and Cells for Transplantation

inferred← citeshttps://doi.org/10.1002/biof.1511openalex-snapshot

Mitochondria, metabolic control and microRNA: Advances in understanding amphibian freeze tolerance

inferred← citeshttps://doi.org/10.1002/bit.28832openalex-snapshot

Molecular mechanisms of natural antifreeze phenomena and their application in cryopreservation

inferred← citeshttps://doi.org/10.1002/cbf.3362openalex-snapshot

Effects of anoxic exposure on the nuclear factor of activated T cell (NFAT) transcription factors in the stress‐tolerant wood frog

inferred← citeshttps://doi.org/10.1002/cbf.3710openalex-snapshot

One‐step purification and regulation of fructose 1,6‐bisphosphatase from the liver of the freeze‐tolerant wood frog, Rana sylvatica

inferred← citeshttps://doi.org/10.1002/cbf.3783openalex-snapshot

MicroRNA transcriptomics in liver of the freeze‐tolerant gray tree frog (Dryophytes versicolor) indicates suppression of energy‐expensive pathways

inferred← citeshttps://doi.org/10.1002/ece3.2985openalex-snapshot

Genomic and phenotypic signatures of climate adaptation in anAnolislizard

inferred← citeshttps://doi.org/10.1002/ece3.70042openalex-snapshot

Physiological responses to a changing winter climate in an early spring‐breeding amphibian

inferred← citeshttps://doi.org/10.1002/ece3.74131openalex-snapshot

Climate‐Driven Spatiotemporal Dynamics of Potential Distribution for Nanorana quadranus in China

inferred← citeshttps://doi.org/10.1002/iub.1910openalex-snapshot

The Living Dead: Mitochondria and Metabolic Arrest

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

inferred← citeshttps://doi.org/10.1002/jez.b.23013openalex-snapshot

Molecular mechanism of Chinese alligator ( Alligator sinensis ) adapting to hibernation

inferred← citeshttps://doi.org/10.1002/ps.7941openalex-snapshot

Sequential expression of small heat shock proteins contributing to the cold response of Haemaphysalis longicornis ( Acari: Ixodidae )

inferred← citeshttps://doi.org/10.1007/978-1-0716-1170-8_16openalex-snapshot

Role of MicroRNAs in Extreme Animal Survival Strategies

inferred← citeshttps://doi.org/10.1007/978-3-030-41929-5_8openalex-snapshot

Antifreeze Proteins in Other Species

inferred← citeshttps://doi.org/10.1007/978-3-030-41948-6_7openalex-snapshot

Inhibition of Recrystallization

inferred← citeshttps://doi.org/10.1007/978-3-031-13771-6_7openalex-snapshot

Epigenetics and the Extreme Stress Response

inferred← citeshttps://doi.org/10.1007/978-3-032-00074-3_11openalex-snapshot

Physiological Ecology of Andean Amphibians Associated with Freezing Temperatures

inferred← citeshttps://doi.org/10.1007/978-3-319-76768-0openalex-snapshot

Advances in Comparative Immunology

inferred← citeshttps://doi.org/10.1007/978-3-662-61595-9_10openalex-snapshot

Wärmehaushalt: Adaptation und Regulation

inferred← citeshttps://doi.org/10.1007/s00018-018-2821-0openalex-snapshot

Micromanaging freeze tolerance: the biogenesis and regulation of neuroprotective microRNAs in frozen brains

inferred← citeshttps://doi.org/10.1007/s00214-023-02986-xopenalex-snapshot

Structure and dynamics of a glucose-based cryoprotectant mixture: a computer simulation study

inferred← citeshttps://doi.org/10.1007/s00360-018-1153-6openalex-snapshot

The cryoprotectant system of Cope’s gray treefrog, Dryophytes chrysoscelis: responses to cold acclimation, freezing, and thawing

inferred← citeshttps://doi.org/10.1007/s00360-018-1159-0openalex-snapshot

Urea and plasma ice-nucleating proteins promoted the modest freeze tolerance in Pleske’s high altitude frog Nanorana pleskei

inferred← citeshttps://doi.org/10.1007/s00360-018-1182-1openalex-snapshot

Nitric oxide metabolites in hypoxia, freezing, and hibernation of the wood frog, Rana sylvatica

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/s00360-022-01444-7openalex-snapshot

MicroRNA biogenesis proteins follow tissue-dependent expression during freezing in Dryophytes versicolor

inferred← citeshttps://doi.org/10.1007/s00360-023-01500-wopenalex-snapshot

Biochemical response of two earthworm taxa exposed to freezing

inferred← citeshttps://doi.org/10.1007/s10340-021-01461-5openalex-snapshot

Rapid evolution of Ophraella communa cold tolerance in new low-temperature environments

inferred← citeshttps://doi.org/10.1007/s10695-025-01516-9openalex-snapshot

Melatonin receptor–mediated signaling pathways drive time-dependent physiological recovery from freezing in Perccottus glenii

inferred← citeshttps://doi.org/10.1007/s11010-018-3468-8openalex-snapshot

Purification of carbamoyl phosphate synthetase 1 (CPS1) from wood frog (Rana sylvatica) liver and its regulation in response to ice-nucleation and subsequent whole-body freezing

inferred← citeshttps://doi.org/10.1007/s11010-020-03820-9openalex-snapshot

MondoA:MLX complex regulates glucose-dependent gene expression and links to circadian rhythm in liver and brain of the freeze-tolerant wood frog, Rana sylvatica

inferred← citeshttps://doi.org/10.1007/s11427-025-3008-4openalex-snapshot

Understanding animal temperature sensation: from molecular thermosensors to physiological impacts

inferred← citeshttps://doi.org/10.1007/s12192-018-0926-xopenalex-snapshot

Stress-induced antioxidant defense and protein chaperone response in the freeze-tolerant wood frog Rana sylvatica

inferred← citeshttps://doi.org/10.1007/s12192-022-01275-zopenalex-snapshot

Regulation of the unfolded protein response during dehydration stress in African clawed frogs, Xenopus laevis

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/10.1016/b978-0-12-817366-4.00016-xopenalex-snapshot

1954: Oxygen without red blood cells, life without freezing—The polar fish experiment

inferred← citeshttps://doi.org/10.1016/b978-0-12-817366-4.00048-1openalex-snapshot

1936–1961: Cryoprotectants in comparative physiology—Convergent strategies for life below zero

inferred← citeshttps://doi.org/10.1016/b978-0-12-823344-3.00011-xopenalex-snapshot

A Primer on Cryobiology and Cryoprotectants for Ovarian Tissue Freezing

inferred← citeshttps://doi.org/10.1016/b978-0-443-21964-1.00010-0openalex-snapshot

Dormancy

inferred← citeshttps://doi.org/10.1016/j.abb.2017.10.010openalex-snapshot

Regulation of glutamate dehydrogenase (GDH) in response to whole body freezing in wood frog liver linked to differential acetylation and ADP-ribosylation

inferred← citeshttps://doi.org/10.1016/j.actbio.2023.11.035openalex-snapshot

Advances in single ice crystal shaping materials: From nature to synthesis and applications in cryopreservation

inferred← citeshttps://doi.org/10.1016/j.aqrep.2025.103265openalex-snapshot

Effects of acute cold and heat shocks on the protein profile of crayfish hemolymph: Implications for crustacean adaptation to thermal stress

inferred← citeshttps://doi.org/10.1016/j.bcab.2025.103807openalex-snapshot

Enhancing drought tolerance in rice (Oryza sativa L.): Advancements in transgenic varieties and stress-responsive Gene pathways

inferred← citeshttps://doi.org/10.1016/j.biochi.2023.01.001openalex-snapshot

Cardiac microRNA expression profile in response to estivation

inferred← citeshttps://doi.org/10.1016/j.biochi.2023.03.008openalex-snapshot

Role of NADP+-dependent isocitrate dehydrogenase from muscle tissue of Rana sylvatica in ROS defense during freeze-tolerance

inferred← citeshttps://doi.org/10.1016/j.carbpol.2025.124138openalex-snapshot

Water-polysaccharide interactions and their properties in freezing conditions

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.cbd.2025.101487openalex-snapshot

MicroRNA-mediated regulation in anoxic Lithobates sylvaticus liver

inferred← citeshttps://doi.org/10.1016/j.cbpa.2019.110623openalex-snapshot

Advances and applications of environmental stress adaptation research

inferred← citeshttps://doi.org/10.1016/j.cbpa.2020.110653openalex-snapshot

Differential protein phosphorylation is responsible for hypoxia-induced regulation of the Akt/mTOR pathway in naked mole rats

inferred← citeshttps://doi.org/10.1016/j.cbpa.2024.111626openalex-snapshot

REVIEW: Evidence supporting the ‘preparation for oxidative stress’ (POS) strategy in animals in their natural environment

inferred← citeshttps://doi.org/10.1016/j.cbpa.2025.111824openalex-snapshot

Melatonin modulates autophagy, mitochondria and antioxidant in the liver and brain of Perccottus glenni during recovery from freezing

inferred← citeshttps://doi.org/10.1016/j.cbpa.2026.111974openalex-snapshot

Life without air: Metabolic responses of the tree frog Boana pulchella under anoxic conditions

inferred← citeshttps://doi.org/10.1016/j.cbpb.2020.110436openalex-snapshot

Regulation of antioxidant systems in response to anoxia and reoxygenation in 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.cbpb.2024.111005openalex-snapshot

DNA hypomethylation in wood frog liver under anoxia and dehydration stresses

inferred← citeshttps://doi.org/10.1016/j.cellsig.2022.110305openalex-snapshot

A “notch” in the cellular communication network in response to anoxia by wood frog (Rana sylvatica)

inferred← citeshttps://doi.org/10.1016/j.cellsig.2022.110408openalex-snapshot

RAGE management: ETS1- EGR1 mediated transcriptional networks regulate angiogenic factors in wood frogs

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.2018.02.012openalex-snapshot

Digital Gene Expression Profiling reveals transcriptional responses to acute cold stress in Chinese soft-shelled turtle Pelodiscus sinensis juveniles

inferred← citeshttps://doi.org/10.1016/j.cryobiol.2019.01.006openalex-snapshot

Metabolic reorganization in winter: Regulation of pyruvate dehydrogenase (PDH) during long-term freezing and anoxia

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.cryobiol.2021.01.015openalex-snapshot

Antioxidant defense response during hibernation and arousal in Chinese soft-shelled turtle Pelodiscus sinensis juveniles

inferred← citeshttps://doi.org/10.1016/j.cryobiol.2022.08.003openalex-snapshot

Status of the Janus Kinase-Signal Transducer and Activator of Transcription (JAK-STAT) pathway in liver and skin of the freeze tolerant wood frog

inferred← citeshttps://doi.org/10.1016/j.cryobiol.2022.11.242openalex-snapshot

Hypoxia inducible factor-1α responds to freezing, anoxia and dehydration stresses in a freeze-tolerant frog

inferred← citeshttps://doi.org/10.1016/j.cryobiol.2022.12.018openalex-snapshot

Role of FOXO transcription factors in the tolerance of whole-body freezing in the wood frog, Rana sylvatica

inferred← citeshttps://doi.org/10.1016/j.cryobiol.2025.105545openalex-snapshot

Physiological and molecular responses of Rana kukunoris to underwater hibernation in ice covered water: Balancing cold adaption and osmotic homeostasis

inferred← citeshttps://doi.org/10.1016/j.cryobiol.2026.105595openalex-snapshot

Can a tropical lizard (Xenosaurus platyceps) survive freezing temperatures?

inferred← citeshttps://doi.org/10.1016/j.fmre.2025.12.035openalex-snapshot

Bio-inspired DMSO-free ice controlling strategy for the cryopreservation of oocytes

inferred← citeshttps://doi.org/10.1016/j.gene.2020.145039openalex-snapshot

RAGE against the stress: Mitochondrial suppression in hypometabolic hearts

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.gene.2023.147184openalex-snapshot

TXNIP shuttling - a key molecular link in regulating inflammation and mitochondrial dysfunction in freeze tolerant wood frogs

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.ijbiomac.2020.03.040openalex-snapshot

The properties, biotechnologies, and applications of antifreeze proteins

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.2025.139847openalex-snapshot

Tough, highly conductive and frost-resistant chitosan based hydrogel for flexible sensor

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.153960openalex-snapshot

On the differential impact of point mutations of antifreeze protein type III on ice recrystallization inhibition and thermal hysteresis activities

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.jspr.2021.101853openalex-snapshot

Trehalose and proline failed to enhance cold tolerance of the cowpea weevil, Callosobruchus maculatus (F.) (Col.: Bruchidae)

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.2019.07.030openalex-snapshot

Characterization of ice recrystallization inhibition activity in the novel freeze-responsive protein Fr10 from freeze-tolerant wood frogs, Rana sylvatica

inferred← citeshttps://doi.org/10.1016/j.jtherbio.2019.08.002openalex-snapshot

Analysis of global and gene-specific acetylation of histones in the liver of American bullfrog (Rana catesbeiana) tadpoles acclimated to low temperature

inferred← citeshttps://doi.org/10.1016/j.jtherbio.2021.103132openalex-snapshot

Antioxidant and non-specific immune defenses in partially freeze-tolerant Xizang plateau frogs, Nanorana parkeri

inferred← citeshttps://doi.org/10.1016/j.jtherbio.2022.103274openalex-snapshot

DNA damage and repair responses to freezing and anoxia stresses in wood frogs, Rana sylvatica

inferred← citeshttps://doi.org/10.1016/j.jtherbio.2023.103652openalex-snapshot

Bat-derived cells use glucose as a cryoprotectant

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.jtherbio.2024.103854openalex-snapshot

Urea and glucose modulation during freezing exposure in three temperate frogs reveals specific targets in relation to climate

inferred← citeshttps://doi.org/10.1016/j.jtherbio.2024.103865openalex-snapshot

Dynamics of epigenetic regulation in Dryophytes versicolor skeletal muscle: Lysine methylation and acetylation involvement in metabolic rate depression

inferred← citeshttps://doi.org/10.1016/j.jtherbio.2026.104548openalex-snapshot

Effect of exposure to extreme temperatures on fertility of males of the eurythermic lizard Barisia imbricata

inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120937openalex-snapshot

Characterization of eutectic mixtures of sugars and sugar-alcohols for cryopreservation

inferred← citeshttps://doi.org/10.1016/j.nephro.2020.05.001openalex-snapshot

Ischémie reperfusion en transplantation rénale

inferred← citeshttps://doi.org/10.1016/j.pocean.2020.102466openalex-snapshot

Seasonal strategies in the world’s oceans

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/10.1016/j.toxicon.2025.108234openalex-snapshot

Novel tryptophyllin peptides from Physalaemus centralis inhibit oxidative stress-induced endothelial dysfunction in rat aorta preparation

inferred← citeshttps://doi.org/10.1016/s1762-0945(18)76912-xopenalex-snapshot

10.1016/s1762-0945(18)76912-x

inferred← citeshttps://doi.org/10.1021/acs.cgd.3c01345openalex-snapshot

Inhibition of Crystal Nucleation and Growth: A Review

inferred← citeshttps://doi.org/10.1021/acs.langmuir.5c00569openalex-snapshot

Mechanism Unraveling of Scalable Antifreeze Oligopeptides for Enhanced Cryopreservation

inferred← citeshttps://doi.org/10.1021/jacs.2c00203openalex-snapshot

Bioinspired Ice-Binding Materials for Tissue and Organ Cryopreservation

inferred← citeshttps://doi.org/10.1038/s41409-021-01368-wopenalex-snapshot

A bioinspired and chemically defined alternative to dimethyl sulfoxide for the cryopreservation of human hematopoietic stem cells

inferred← citeshttps://doi.org/10.1038/s41536-018-0062-3openalex-snapshot

Skeletal muscle stem cells in comfort and stress

inferred← citeshttps://doi.org/10.1038/s41598-018-31974-6openalex-snapshot

The Siberian wood frog survives for months underwater without oxygen

inferred← citeshttps://doi.org/10.1038/s41598-022-22166-4openalex-snapshot

Real time monitoring of cold Ca2+ dependent transcription and its modulation by NCX inhibitors

inferred← citeshttps://doi.org/10.1038/s41598-024-65417-2openalex-snapshot

Proteomic analysis of Rana sylvatica reveals differentially expressed proteins in liver in response to anoxia, dehydration or freezing stress

inferred← citeshttps://doi.org/10.1038/s41598-024-79594-7openalex-snapshot

Insights into tail-belting by wild mice encourages fresh perspectives on physiological mechanisms that safeguard mammal tissues from freezing

inferred← citeshttps://doi.org/10.1038/s41598-024-82713-zopenalex-snapshot

Evaluation of overwintering risk of tropical and subtropical insect pests in temperate regions

inferred← citeshttps://doi.org/10.1038/s41598-025-24105-5openalex-snapshot

Amphibian supercooling capacity is not limited to sub-zero thermal environments

inferred← citeshttps://doi.org/10.1038/s42003-024-05818-1openalex-snapshot

Establishment and characterization of turtle liver organoids provides a potential model to decode their unique adaptations

inferred← citeshttps://doi.org/10.1039/d3tb00131hopenalex-snapshot

Investigation into antifreeze performances of natural amino acids for novel CPA development

inferred← citeshttps://doi.org/10.1039/d4cs00718bopenalex-snapshot

Antifreezing hydrogels: from mechanisms and strategies to applications

inferred← citeshttps://doi.org/10.1073/pnas.2117503120openalex-snapshot

Evolutionary isolation of ryanodine receptor isoform 1 for muscle-based thermogenesis in mammals

inferred← citeshttps://doi.org/10.1080/15230430.2025.2572150openalex-snapshot

Living in ice: Examining the effects of temperature on thermal and metabolic physiology of glacier ice worms ( Mesenchytraeus solifugus )

inferred← citeshttps://doi.org/10.1086/706463openalex-snapshot

Carb-Loading: Freeze-Induced Activation of the Glucose-Responsive ChREBP Transcriptional Network in Wood Frogs

inferred← citeshttps://doi.org/10.1086/718764openalex-snapshot

Physiological Ecology of Winter Hibernation by the High-Altitude Frog Nanorana parkeri

inferred← citeshttps://doi.org/10.1093/icb/icaf052openalex-snapshot

Similar Biomolecular Constraints Drive Convergent Adaptation to Extreme Cold and High Pressure

inferred← citeshttps://doi.org/10.1093/iob/obaf008openalex-snapshot

Winter Is Coming: Integrative Analysis of Cold Acclimation in a Freeze Tolerant Frog

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/10.1097/prs.0000000000005541openalex-snapshot

Cryopreservation and Transplantation of Vascularized Composite Transplants: Unique Challenges and Opportunities

inferred← citeshttps://doi.org/10.1097/tp.0000000000005494openalex-snapshot

Cryopreservation Strategies to Improve Access to Organ Transplantation

inferred← citeshttps://doi.org/10.1098/rsbl.2020.0873openalex-snapshot

Effects of hypoxia on the thermal physiology of a high-elevation lizard: implications for upslope-shifting species

inferred← citeshttps://doi.org/10.1098/rspb.2024.1336openalex-snapshot

Longer days, larger grays: carryover effects of photoperiod and temperature in gray treefrogs, Hyla versicolor

inferred← citeshttps://doi.org/10.1098/rstb.2022.0011openalex-snapshot

Assessing the role of family level variation and heat shock gene expression in the thermal stress response of the mosquito Aedes aegypti

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/10.1101/2022.12.08.519683openalex-snapshot

Mathematical modeling of ion homeostasis & cell volume stabilization: impact of ion transporters, impermeant molecules, & Donnan effect

inferred← citeshttps://doi.org/10.1109/sensors59705.2025.11330459openalex-snapshot

Nature-Inspired Tough and Freezing-Resistant Organohydrogel via 3D Printing for Flexible Sensors

inferred← citeshttps://doi.org/10.1111/1365-2656.70125openalex-snapshot

Freeze‐tolerant frogs accumulate cryoprotectants using photoperiod: A potential ecological trap

inferred← citeshttps://doi.org/10.1111/1749-4877.12994openalex-snapshot

Effects of Climate Warming on Overwintering of Qinghai Toad‐Headed Lizards at Two Contrasting Elevations

inferred← citeshttps://doi.org/10.1111/1749-4877.70141openalex-snapshot

Adaptations That Track Environmental Temperature Cues in Hibernation: Insights From Time‐Series Transcriptomic Profiles in a Hibernating Freshwater Turtle

inferred← citeshttps://doi.org/10.1111/brv.12588openalex-snapshot

Insect responses to heat: physiological mechanisms, evolution and ecological implications in a warming world

inferred← citeshttps://doi.org/10.1111/btp.12875openalex-snapshot

Thermal adaptations to extreme freeze–thaw cycles in the high tropical Andes

inferred← citeshttps://doi.org/10.1111/dgd.12814openalex-snapshot

Involvement of glucose in freeze tolerance in the Japanese tree frog Hyla japonica

inferred← citeshttps://doi.org/10.1111/febs.14683openalex-snapshot

Bringing nature back: using hibernation to reboot organ preservation

inferred← citeshttps://doi.org/10.1111/gcb.16956openalex-snapshot

Winter is coming: Interactions of multiple stressors in winter and implications for the natural world

inferred← citeshttps://doi.org/10.1111/jen.12939openalex-snapshot

Functional analysis of small heat shock proteins providing evidence of temperature tolerance in Hyphantria cunea

inferred← citeshttps://doi.org/10.1111/jzo.13029openalex-snapshot

Macrophysiology for decision‐making

inferred← citeshttps://doi.org/10.1111/mec.15867openalex-snapshot

Molecular mechanisms of local adaptation for salt‐tolerance in a treefrog

inferred← citeshttps://doi.org/10.1134/s0022093020030047openalex-snapshot

Secondary Metabolites and Aspartic Acid in the Brain of the Frog Rana temporaria as Low-Temperature Adaptogens

inferred← citeshttps://doi.org/10.1134/s1062359025700475openalex-snapshot

Overwintering Strategy of the Oriental Fire-Bellied Toad, Bombina orientalis f. sylvatica (Amphibia, Anura)

inferred← citeshttps://doi.org/10.1139/bcb-2017-0117openalex-snapshot

Regulation of the insulin–Akt signaling pathway and glycolysis during dehydration stress in the African clawed frog Xenopus laevis

inferred← citeshttps://doi.org/10.1139/bcb-2019-0091openalex-snapshot

DNA methylation and regulation of DNA methyltransferases in a freeze-tolerant vertebrate

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/10.1139/bcb-2022-0164openalex-snapshot

The regulation of m6A-related proteins during whole-body freezing of the freeze-tolerant wood frog

inferred← citeshttps://doi.org/10.1139/cjz-2022-0100openalex-snapshot

Five months under ice: biologging reveals behaviour patterns of overwintering freshwater turtles

inferred← citeshttps://doi.org/10.1139/cjz-2026-0041openalex-snapshot

Determinants of the northern range limits of amphibians and reptiles in Canada

inferred← citeshttps://doi.org/10.1152/advan.00094.2025openalex-snapshot

Compatibility of eugenol anesthesia with classroom physiology experiments on nerve and muscle of frogs

inferred← citeshttps://doi.org/10.1152/ajpregu.00211.2022openalex-snapshot

Repeated freeze-thaw cycles in freeze-tolerant treefrogs: novel interindividual variation of integrative biochemical, cellular, and organismal responses

inferred← citeshttps://doi.org/10.1186/s12864-020-6602-4openalex-snapshot

Hepatic transcriptome of the freeze-tolerant Cope’s gray treefrog, Dryophytes chrysoscelis: responses to cold acclimation and freezing

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/s12864-026-12535-yopenalex-snapshot

The transcriptomics and differential gene expression of freezing and thawing in a freeze-tolerant vertebrate

inferred← citeshttps://doi.org/10.1186/s12915-025-02262-3openalex-snapshot

Co-opted and canonical glycerol channels play a major role during anhydrobiosis of an extremophile crustacean

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/s12983-021-00448-3openalex-snapshot

Mitochondria as a target and central hub of energy division during cold stress in insects

inferred← citeshttps://doi.org/10.1186/s40850-022-00128-7openalex-snapshot

Mitochondrial gene expression in different organs of Hoplobatrachus rugulosus from China and Thailand under low-temperature stress

inferred← citeshttps://doi.org/10.1242/bio.062072openalex-snapshot

Osmoregulation in the estuarine diamond-backed terrapin across a broad range of naturally occurring salinities

inferred← citeshttps://doi.org/10.1242/jcs.231688openalex-snapshot

Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation

inferred← citeshttps://doi.org/10.1242/jeb.186379openalex-snapshot

Effects of both cold and heat stresses on the liver of giant spiny frog Quasipaa spinosa: stress response and histological changes

inferred← citeshttps://doi.org/10.1242/jeb.204594openalex-snapshot

The OxymiR response to oxygen limitation: a comparative microRNA perspective

inferred← citeshttps://doi.org/10.1242/jeb.246456openalex-snapshot

Mortality caused by extracellular freezing is associated with fragmentation of nuclear DNA in larval haemocytes of two drosophilid flies

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/10.1371/journal.pone.0229689openalex-snapshot

Population dynamics and biological feasibility of sustainable harvesting as a conservation strategy for tropical and temperate freshwater turtles

inferred← citeshttps://doi.org/10.15407/animbiol19.02.115openalex-snapshot

Indices of fatty acids spectrum of lipids in the blood serum of rats under conditions of artificial hypobiosis

inferred← citeshttps://doi.org/10.1643/h2021083openalex-snapshot

Complementary Occupancy of Semi-permanent Wetlands by Tiger Salamander (Ambystoma tigrinum) Larvae and Fishes as Indicated by Zooplankton Size and Color: How Respiratory Physiology Explains Community Ecology

inferred← citeshttps://doi.org/10.18699/vjgb-22-07openalex-snapshot

De novo assembly and analysis of the transcriptome of the Siberian wood frog Rana amurensis

inferred← citeshttps://doi.org/10.21203/rs.3.rs-490874/v1openalex-snapshot

Rapid Adaptive Evolution of Ophraella Communa in New Low Temperature Environment

inferred← citeshttps://doi.org/10.21303/2504-5695.2018.00657openalex-snapshot

INDICATORS OF THE ELEMENT RANGE OF RAT’S BLOOD IN TERM ARTIFICIAL HYPOBYOSIS

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/2017-12056openalex-snapshot

Regulation of glutamate dehydrogenase and lactate dehydrogenase in the freeze tolerant wood frog, Rana sylvatica

inferred← citeshttps://doi.org/10.22215/etd/2017-12164openalex-snapshot

Regulation of urea cycle related enzymes in response to freezing in the wood frog, Rana sylvatica

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/2022-15293openalex-snapshot

The overwintering behaviour and physiology of Northern map turtles (Graptemys geographica) in Ontario

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/2022-15440openalex-snapshot

Histone Arginine Methylation in the Freeze-tolerant Wood Frog, 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/10.2460/javma.253.12.1536openalex-snapshot

Reevaluating the use of hypothermia for anesthetizing and euthanizing amphibians and reptiles

inferred← citeshttps://doi.org/10.25148/etd.fidc006988openalex-snapshot

Survival at the Summits: Amphibian Responses to Thermal Extremes, Disease, and Rapid Climate Change in the High Tropical Andes

inferred← citeshttps://doi.org/10.31594/commagene.1176451openalex-snapshot

Hayvanlarda Soğuğa Dayanıklılık: Çift Yaşarların Kriyobiyolojisi

inferred← citeshttps://doi.org/10.31857/s0044513424110058openalex-snapshot

Overwintering strategy of the oriental fire-bellied toad, Bombina Orientalis f. Sylvatica (Amphibia, Anura)

inferred← citeshttps://doi.org/10.31988/scitrends.26890openalex-snapshot

Organ Cryopreservation: Nature’s Protocol For Freezing Organs

inferred← citeshttps://doi.org/10.3389/fevo.2019.00055openalex-snapshot

Interspecific Variation in Seasonal Migration and Brumation Behavior in Two Closely Related Species of Treefrogs

showing the first 200 of 244 · page through all 244

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.