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Intracellular Protective Functions and Therapeutical Potential of Trehalose

https://doi.org/10.3390/molecules29092088

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What this work says

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

inferredcites →https://doi.org/10.1002/jcp.26583openalex-snapshot

Autophagy induction by trehalose: Molecular mechanisms and therapeutic impacts

inferredcites →https://doi.org/10.1002/jps.22458openalex-snapshot

Trehalose: Current Use and Future Applications

inferredcites →https://doi.org/10.1002/pro.3openalex-snapshot

Effect of trehalose on protein structure

inferredcites →https://doi.org/10.1007/s00018-012-1088-0openalex-snapshot

Molecular mechanisms of desiccation tolerance in resurrection plants

inferredcites →https://doi.org/10.1007/s00294-019-01036-zopenalex-snapshot

New insight into the mechanisms protecting bacteria during desiccation

inferredcites →https://doi.org/10.1007/s00360-023-01497-2openalex-snapshot

Steroid hormone-dependent changes in trehalose physiology in the silkworm, Bombyx mori

inferredcites →https://doi.org/10.1007/s12275-019-9218-0openalex-snapshot

Bacterial persistence: Fundamentals and clinical importance

inferredcites →https://doi.org/10.1007/s40199-023-00468-wopenalex-snapshot

A neuroprotective dose of trehalose is harmless to metabolic organs: comprehensive histopathological analysis of liver, pancreas, and kidney

inferredcites →https://doi.org/10.1016/0014-5793(87)81170-5openalex-snapshot

Trehalose accumulates in Saccharomyces cerevisiae during exposure to agents that induce heat shock response

inferredcites →https://doi.org/10.1016/0014-5793(93)80191-vopenalex-snapshot

Trehalose‐6‐phosphate, a new regulator of yeast glycolysis that inhibits hexokinases

inferredcites →https://doi.org/10.1016/j.abb.2009.09.007openalex-snapshot

Role of naturally occurring osmolytes in protein folding and stability

inferredcites →https://doi.org/10.1016/j.abb.2012.04.021openalex-snapshot

Trehalose inhibits fibrillation of A53T mutant alpha-synuclein and disaggregates existing fibrils

inferredcites →https://doi.org/10.1016/j.bbagen.2006.01.010openalex-snapshot

Trehalose protects Saccharomyces cerevisiae from lipid peroxidation during oxidative stress

inferredcites →https://doi.org/10.1016/j.bbagen.2008.05.011openalex-snapshot

The role of trehalose and its transporter in protection against reactive oxygen species

inferredcites →https://doi.org/10.1016/j.bbagen.2016.04.020openalex-snapshot

Yeast trehalases: Two enzymes, one catalytic mission

inferredcites →https://doi.org/10.1016/j.bbrc.2008.06.094openalex-snapshot

Trehalose impairs aggregation of PrPSc molecules and protects prion-infected cells against oxidative damage

inferredcites →https://doi.org/10.1016/j.biotechadv.2021.107842openalex-snapshot

Bacterial protein acetylation and its role in cellular physiology and metabolic regulation

inferredcites →https://doi.org/10.1016/j.carres.2017.08.003openalex-snapshot

The trehalose-specific transporter LpqY-SugABC is required for antimicrobial and anti-biofilm activity of trehalose analogues in Mycobacterium smegmatis

inferredcites →https://doi.org/10.1016/j.cbpa.2006.02.030openalex-snapshot

Oxidative stress and its effects during dehydration

inferredcites →https://doi.org/10.1016/j.cub.2014.03.034openalex-snapshot

ROS Function in Redox Signaling and Oxidative Stress

inferredcites →https://doi.org/10.1016/j.cub.2014.10.005openalex-snapshot

Trehalose Is a Versatile and Long-Lived Chaperone for Desiccation Tolerance

inferredcites →https://doi.org/10.1016/j.dsx.2019.05.023openalex-snapshot

Molecular mechanisms of trehalose in modulating glucose homeostasis in diabetes

inferredcites →https://doi.org/10.1016/j.envexpbot.2007.11.016openalex-snapshot

Trehalose: Protector of antioxidant enzymes or reactive oxygen species scavenger under heat stress?

inferredcites →https://doi.org/10.1016/j.exger.2019.110755openalex-snapshot

Trehalose administration in C57BL/6N old mice affects healthspan improving motor learning and brain anti-oxidant defences in a sex-dependent fashion: a pilot study

inferredcites →https://doi.org/10.1016/j.fgb.2013.11.005openalex-snapshot

Trehalose 6-phosphate phosphatase is required for development, virulence and mycotoxin biosynthesis apart from trehalose biosynthesis in Fusarium graminearum

inferredcites →https://doi.org/10.1016/j.ijbiomac.2017.12.100openalex-snapshot

Roles of osmolytes in protein folding and aggregation in cells and their biotechnological applications

inferredcites →https://doi.org/10.1016/j.ijmm.2008.12.001openalex-snapshot

Role of trehalose-6P phosphatase (TPS2) in stress tolerance and resistance to macrophage killing in Candida albicans

inferredcites →https://doi.org/10.1016/j.intimp.2021.107598openalex-snapshot

MCP-1: Function, regulation, and involvement in disease

inferredcites →https://doi.org/10.1016/j.lfs.2010.10.020openalex-snapshot

Protein and DNA destabilization by osmolytes: The other side of the coin

inferredcites →https://doi.org/10.1016/j.micres.2023.127335openalex-snapshot

Protein aggregation and glycation in Escherichia coli exposed to desiccation-rehydration stress

inferredcites →https://doi.org/10.1016/j.molstruc.2023.135957openalex-snapshot

Deciphering the structure-property relationship and antioxidant mechanisms of Trehalose – An in-silico approach

inferredcites →https://doi.org/10.1016/j.nbd.2005.02.003openalex-snapshot

Trehalose differentially inhibits aggregation and neurotoxicity of beta-amyloid 40 and 42

inferredcites →https://doi.org/10.1016/j.neuint.2011.01.008openalex-snapshot

The accumulation of neurotoxic proteins, induced by proteasome inhibition, is reverted by trehalose, an enhancer of autophagy, in human neuroblastoma cells

inferredcites →https://doi.org/10.1016/j.nutres.2010.10.009openalex-snapshot

Trehalose prevents adipocyte hypertrophy and mitigates insulin resistance

inferredcites →https://doi.org/10.1016/j.phrs.2016.06.024openalex-snapshot

mTOR-Independent autophagy inducer trehalose rescues against insulin resistance-induced myocardial contractile anomalies: Role of p38 MAPK and Foxo1

inferredcites →https://doi.org/10.1016/s0278-6915(02)00011-xopenalex-snapshot

Trehalose: a review of properties, history of use and human tolerance, and results of multiple safety studies

inferredcites →https://doi.org/10.1016/s0923-2508(02)01321-9openalex-snapshot

Role of trehalose biosynthesis in environmental survival and virulence of Salmonella enterica serovar typhimurium

inferredcites →https://doi.org/10.1021/acs.jmedchem.3c01442openalex-snapshot

Trehalose-Bearing Carriers to Target Impaired Autophagy and Protein Aggregation Diseases

inferredcites →https://doi.org/10.1021/jacsau.2c00309openalex-snapshot

Synthesis and Application of Trehalose Materials

inferredcites →https://doi.org/10.1038/nchembio.915openalex-snapshot

Signaling-mediated bacterial persister formation

inferredcites →https://doi.org/10.1038/ncomms14338openalex-snapshot

mTORC1-independent TFEB activation via Akt inhibition promotes cellular clearance in neurodegenerative storage diseases

inferredcites →https://doi.org/10.1038/nm985openalex-snapshot

Trehalose alleviates polyglutamine-mediated pathology in a mouse model of Huntington disease

inferredcites →https://doi.org/10.1038/s41392-024-01743-1openalex-snapshot

Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases

inferredcites →https://doi.org/10.1038/s41419-018-0749-9openalex-snapshot

Mechanism of neuroprotection by trehalose: controversy surrounding autophagy induction

inferredcites →https://doi.org/10.1038/s41467-019-10975-7openalex-snapshot

Transient drug-tolerance and permanent drug-resistance rely on the trehalose-catalytic shift in Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1038/s41564-023-01420-zopenalex-snapshot

Phytophthora sojae boosts host trehalose accumulation to acquire carbon and initiate infection

inferredcites →https://doi.org/10.1038/s41579-019-0196-3openalex-snapshot

Definitions and guidelines for research on antibiotic persistence

inferredcites →https://doi.org/10.1038/s41579-020-00460-0openalex-snapshot

The gut microbiota–brain axis in behaviour and brain disorders

inferredcites →https://doi.org/10.1038/s42003-022-04015-2openalex-snapshot

Trehalose and tardigrade CAHS proteins work synergistically to promote desiccation tolerance

inferredcites →https://doi.org/10.1038/sj.emboj.7601795openalex-snapshot

Tps1 regulates the pentose phosphate pathway, nitrogen metabolism and fungal virulence

inferredcites →https://doi.org/10.1038/srep01218openalex-snapshot

Microscopic mechanism of protein cryopreservation in an aqueous solution with trehalose

inferredcites →https://doi.org/10.1039/c9cc01300hopenalex-snapshot

Degradation-resistant trehalose analogues block utilization of trehalose by hypervirulent Clostridioides difficile

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03625.xopenalex-snapshot

Three pathways for trehalose metabolism in Corynebacterium glutamicum ATCC13032 and their significance in response to osmotic stress

inferredcites →https://doi.org/10.1073/pnas.142314099openalex-snapshot

Trehalose synthesis is induced upon exposure of Escherichia coli to cold and is essential for viability at low temperatures

inferredcites →https://doi.org/10.1073/pnas.1506415112openalex-snapshot

Increasing intracellular trehalose is sufficient to confer desiccation tolerance to Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1073/pnas.1714178115openalex-snapshot

Metabolic shift from glycogen to trehalose promotes lifespan and healthspan in Caenorhabditis elegans

inferredcites →https://doi.org/10.1074/jbc.m101487200openalex-snapshot

Trehalose Accumulation during Cellular Stress Protects Cells and Cellular Proteins from Damage by Oxygen Radicals

inferredcites →https://doi.org/10.1074/jbc.m103081200openalex-snapshot

Chemical Chaperones Regulate Molecular Chaperones in Vitro and in Cells under Combined Salt and Heat Stresses

inferredcites →https://doi.org/10.1074/jbc.m115.653899openalex-snapshot

Yeast Tolerance to Various Stresses Relies on the Trehalose-6P Synthase (Tps1) Protein, Not on Trehalose

inferredcites →https://doi.org/10.1074/jbc.m414232200openalex-snapshot

The OtsAB Pathway Is Essential for Trehalose Biosynthesis in Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1074/jbc.ra120.012809openalex-snapshot

Mycobacterium tuberculosis (Mtb) lipid mediated lysosomal rewiring in infected macrophages modulates intracellular Mtb trafficking and survival

inferredcites →https://doi.org/10.1080/15548627.2018.1535292openalex-snapshot

Trehalose induces autophagy via lysosomal-mediated TFEB activation in models of motoneuron degeneration

inferredcites →https://doi.org/10.1080/15548627.2021.1896906openalex-snapshot

Trehalose causes low-grade lysosomal stress to activate TFEB and the autophagy-lysosome biogenesis response

inferredcites →https://doi.org/10.1080/21505594.2016.1195529openalex-snapshot

Trehalose pathway as an antifungal target

inferredcites →https://doi.org/10.1080/21505594.2016.1199316openalex-snapshot

Trehalase plays a role in macrophage colonization and virulence ofBurkholderia pseudomalleiin insect and mammalian hosts

inferredcites →https://doi.org/10.1091/mbc.e17-04-0257openalex-snapshot

Desiccation tolerance: an unusual window into stress biology

inferredcites →https://doi.org/10.1093/emboj/cdg018openalex-snapshot

Trehalose synthesis and metabolism are required at different stages of plant infection by Magnaporthe grisea

inferredcites →https://doi.org/10.1093/g3journal/jkac196openalex-snapshot

Characterizing phenotypic diversity of trehalose biosynthesis mutants in multiple wild strains of Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1093/glycob/cwg047openalex-snapshot

New insights on trehalose: a multifunctional molecule

inferredcites →https://doi.org/10.1093/jxb/erv095openalex-snapshot

The dual nature of trehalose in citrus canker disease: a virulence factor for Xanthomonas citri subsp. citri and a trigger for plant defence responses

inferredcites →https://doi.org/10.1094/mpmi-08-19-0218-ropenalex-snapshot

Trehalose Synthesis Contributes to Osmotic Stress Tolerance and Virulence of the Bacterial Wilt Pathogen Ralstonia solanacearum

inferredcites →https://doi.org/10.1094/mpmi-10-20-0298-ropenalex-snapshot

Ralstonia solanacearum Depends on Catabolism of Myo-Inositol, Sucrose, and Trehalose for Virulence in an Infection Stage–Dependent Manner

inferredcites →https://doi.org/10.1097/j.jcrs.0000000000000652openalex-snapshot

Dry eye and inflammation of the ocular surface after cataract surgery: effectiveness of a tear film substitute based on trehalose/hyaluronic acid vs hyaluronic acid to resolve signs and symptoms

inferredcites →https://doi.org/10.1099/00221287-146-1-199openalex-snapshot

Three pathways for trehalose biosynthesis in mycobacteria

inferredcites →https://doi.org/10.1099/mic.0.000012openalex-snapshot

Lack of intracellular trehalose affects formation of Escherichia coli persister cells

inferredcites →https://doi.org/10.1099/mic.0.29044-0openalex-snapshot

Trehalose metabolism is important for heat stress tolerance and spore germination of Botrytis cinerea

inferredcites →https://doi.org/10.1101/2019.12.27.889063openalex-snapshot

Trehalose Stabilizing Protein in a Water Replacement Scenario: Insights from Molecular Dynamics Simulation

inferredcites →https://doi.org/10.1111/1462-2920.12567openalex-snapshot

Toxin YafQ increases persister cell formation by reducing indole signalling

inferredcites →https://doi.org/10.1111/1541-4337.13048openalex-snapshot

Trehalose and its applications in the food industry

inferredcites →https://doi.org/10.1111/1751-7915.12029openalex-snapshot

Trends in bacterial trehalose metabolism and significant nodes of metabolic pathway in the direction of trehalose accumulation

inferredcites →https://doi.org/10.1111/j.1365-2958.1993.tb01564.xopenalex-snapshot

Trehalose metabolism in Escherichia coli: stress protection and stress regulation of gene expression

inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07254.xopenalex-snapshot

Trehalose 6‐phosphate phosphatase is required for cell wall integrity and fungal virulence but not trehalose biosynthesis in the human fungal pathogen Aspergillus fumigatus

inferredcites →https://doi.org/10.1111/j.1432-1033.1994.tb19928.xopenalex-snapshot

The role of trehalose synthesis for the acquisition of thermotolerance in yeast

inferredcites →https://doi.org/10.1111/j.1432-1033.1994.tb19929.xopenalex-snapshot

The role of trehalose synthesis for the acquisition of thermotolerance in yeast

inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02171.xopenalex-snapshot

Identification of the trehalose biosynthetic loci of Pseudomonas syringae and their contribution to fitness in the phyllosphere

inferredcites →https://doi.org/10.1111/j.1469-0691.2007.01663.xopenalex-snapshot

Role of trehalose in resistance to macrophage killing: study with a tps1/tps1 trehalose-deficient mutant of Candida albicans

inferredcites →https://doi.org/10.1111/j.1474-9726.2010.00582.xopenalex-snapshot

Trehalose extends longevity in the nematode Caenorhabditis elegans

inferredcites →https://doi.org/10.1111/j.1567-1364.2006.00066.xopenalex-snapshot

Intracellular trehalose is neither necessary nor sufficient for desiccation tolerance in yeast

inferredcites →https://doi.org/10.1111/j.1574-6976.2002.tb00598.xopenalex-snapshot

Bacterial osmoadaptation: the role of osmolytes in bacterial stress and virulence

inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00736.xopenalex-snapshot

Trehalose Biosynthesis in Response to Abiotic Stresses

inferredcites →https://doi.org/10.1111/mmi.14322openalex-snapshot

Trehalose protects Escherichia coli against carbon stress manifested by protein acetylation and aggregation

inferredcites →https://doi.org/10.1126/scisignal.aac5472openalex-snapshot

Trehalose inhibits solute carrier 2A (SLC2A) proteins to induce autophagy and prevent hepatic steatosis

inferredcites →https://doi.org/10.1128/aem.00412-07openalex-snapshot

Trehalose Biosynthesis in Rhizobium leguminosarum bv. trifolii and Its Role in Desiccation Tolerance

inferredcites →https://doi.org/10.1128/aem.00757-11openalex-snapshot

Increased Thermal and Osmotic Stress Resistance in Listeria monocytogenes 568 Grown in the Presence of Trehalose Due to Inactivation of the Phosphotrehalase-Encoding Gene treA

inferredcites →https://doi.org/10.1128/iai.00241-18openalex-snapshot

The Periplasmic Trehalase Affects Type 1 Fimbria Production and Virulence of Extraintestinal Pathogenic Escherichia coli Strain MT78

inferredcites →https://doi.org/10.1128/iai.00624-06openalex-snapshot

Characterization and Regulation of the Trehalose Synthesis Pathway and Its Importance in the Pathogenicity of Cryptococcus neoformans

inferredcites →https://doi.org/10.1128/iai.00813-09openalex-snapshot

Role of Trehalose Biosynthesis in Aspergillus fumigatus Development, Stress Response, and Virulence

inferredcites →https://doi.org/10.1128/jb.173.24.7918-7924.1991openalex-snapshot

Trehalose synthesis genes are controlled by the putative sigma factor encoded by rpoS and are involved in stationary-phase thermotolerance in Escherichia coli

inferredcites →https://doi.org/10.1128/jb.178.21.6250-6257.1996openalex-snapshot

Characterization of a cytoplasmic trehalase of Escherichia coli

inferredcites →https://doi.org/10.1128/jb.183.11.3365-3371.2001openalex-snapshot

Role of Trehalose in Growth at High Temperature of Salmonella enterica Serovar Typhimurium

inferredcites →https://doi.org/10.1128/jvi.00237-20openalex-snapshot

Trehalose Inhibits Human Immunodeficiency Virus Type 1 Infection in Primary Human Macrophages and CD4 + T Lymphocytes through Two Distinct Mechanisms

inferredcites →https://doi.org/10.1128/jvi.02651-15openalex-snapshot

Trehalose, an mTOR-Independent Inducer of Autophagy, Inhibits Human Cytomegalovirus Infection in Multiple Cell Types

inferredcites →https://doi.org/10.1128/mbio.00390-21openalex-snapshot

Bradyrhizobium diazoefficiens Requires Chemical Chaperones To Cope with Osmotic Stress during Soybean Infection

inferredcites →https://doi.org/10.1128/mbio.00676-19openalex-snapshot

Indole Reverses Intrinsic Antibiotic Resistance by Activating a Novel Dual-Function Importer

inferredcites →https://doi.org/10.1128/mbio.02065-14openalex-snapshot

A Ralstonia solanacearum Type III Effector Directs the Production of the Plant Signal Metabolite Trehalose-6-Phosphate

inferredcites →https://doi.org/10.1128/microbiolspec.mgm2-0002-2013openalex-snapshot

Genetics of Mycobacterial Trehalose Metabolism

inferredcites →https://doi.org/10.1128/mmbr.00020-15openalex-snapshot

Acylation of Biomolecules in Prokaryotes: a Widespread Strategy for the Control of Biological Function and Metabolic Stress

inferredcites →https://doi.org/10.1128/mmbr.00053-16openalex-snapshot

Central Role of the Trehalose Biosynthesis Pathway in the Pathogenesis of Human Fungal Infections: Opportunities and Challenges for Therapeutic Development

inferredcites →https://doi.org/10.1128/mmbr.66.2.300-372.2002openalex-snapshot

Osmotic Stress Signaling and Osmoadaptation in Yeasts

inferredcites →https://doi.org/10.1128/spectrum.03510-22openalex-snapshot

Trehalose Biosynthesis Gene otsA Protects against Stress in the Initial Infection Stage of Burkholderia -Bean Bug Symbiosis

inferredcites →https://doi.org/10.1146/annurev-arplant-071219-105542openalex-snapshot

Desiccation Tolerance: Avoiding Cellular Damage During Drying and Rehydration

inferredcites →https://doi.org/10.1146/annurev-micro-020518-115650openalex-snapshot

Bacterial Persisters and Infection: Past, Present, and Progressing

inferredcites →https://doi.org/10.1146/annurev.micro.112408.134306openalex-snapshot

Persister Cells

inferredcites →https://doi.org/10.1172/jci.insight.120794openalex-snapshot

Hepatocyte ALOXE3 is induced during adaptive fasting and enhances insulin sensitivity by activating hepatic PPARγ

inferredcites →https://doi.org/10.1186/s12934-016-0590-8openalex-snapshot

The effect of protein acetylation on the formation and processing of inclusion bodies and endogenous protein aggregates in Escherichia coli cells

inferredcites →https://doi.org/10.1186/s12935-022-02652-5openalex-snapshot

The autophagy inducer trehalose stimulates macropinocytosis in NF1-deficient glioblastoma cells

inferredcites →https://doi.org/10.1371/journal.pone.0023500openalex-snapshot

Isolation of Genes Involved in Biofilm Formation of a Klebsiella pneumoniae Strain Causing Pyogenic Liver Abscess

inferredcites →https://doi.org/10.1371/journal.pone.0054737openalex-snapshot

The Formation of Persister Cells in Stationary-Phase Cultures of Escherichia Coli Is Associated with the Aggregation of Endogenous Proteins

inferredcites →https://doi.org/10.1371/journal.pone.0099113openalex-snapshot

In Candida parapsilosis the ATC1 Gene Encodes for an Acid Trehalase Involved in Trehalose Hydrolysis, Stress Resistance and Virulence

inferredcites →https://doi.org/10.1371/journal.ppat.1003217openalex-snapshot

Trehalose Biosynthesis Promotes Pseudomonas aeruginosa Pathogenicity in Plants

inferredcites →https://doi.org/10.1529/biophysj.107.125542openalex-snapshot

The Mycobacterium tuberculosis Virulence Factor Trehalose Dimycolate Imparts Desiccation Resistance to Model Mycobacterial Membranes

inferredcites →https://doi.org/10.2174/0929867324666170426142826openalex-snapshot

Divergent Roles of IRS (Insulin Receptor Substrate) 1 and 2 in Liver and Skeletal Muscle

inferredcites →https://doi.org/10.2436/20.1501.01.197openalex-snapshot

Analysis of validamycin as a potential antifungal compound against Candida albicans.

inferredcites →https://doi.org/10.3177/jnsv.59.393openalex-snapshot

Trehalose Prevents Adipocyte Hypertrophy and Mitigates Insulin Resistance in Mice with Established Obesity

inferredcites →https://doi.org/10.3389/fcimb.2021.670935openalex-snapshot

Trehalose-Induced Remodelling of the Human Microbiota Affects Clostridioides difficile Infection Outcome in an In Vitro Colonic Model: A Pilot Study

inferredcites →https://doi.org/10.3389/fmolb.2021.669664openalex-snapshot

Protein Aggregation as a Bacterial Strategy to Survive Antibiotic Treatment

inferredcites →https://doi.org/10.3389/fpls.2016.01593openalex-snapshot

Exogenous Trehalose Treatment Enhances the Activities of Defense-Related Enzymes and Triggers Resistance against Downy Mildew Disease of Pearl Millet

inferredcites →https://doi.org/10.3390/biom10050809openalex-snapshot

Trehalose for Ocular Surface Health

inferredcites →https://doi.org/10.3390/cells10071837openalex-snapshot

Cryopreservation of Human Adipose Tissues and Adipose-Derived Stem Cells with DMSO and/or Trehalose: A Systematic Review

inferredcites →https://doi.org/10.3390/ijms25010294openalex-snapshot

VdPT1 Encoding a Neutral Trehalase of Verticillium dahliae Is Required for Growth and Virulence of the Pathogen

inferredcites →https://doi.org/10.3390/jcm12237301openalex-snapshot

Trehalose and Dry Eye Disease: A Comprehensive Systematic Review of Randomized Controlled Trials

inferredcites →https://doi.org/10.3390/jof8040371openalex-snapshot

Lack of Functional Trehalase Activity in Candida parapsilosis Increases Susceptibility to Itraconazole

inferredcites →https://doi.org/10.3390/molecules13081773openalex-snapshot

Trehalose and Trehalose-based Polymers for Environmentally Benign, Biocompatible and Bioactive Materials

inferredcites →https://doi.org/10.3390/nu15061393openalex-snapshot

Dietary Trehalose as a Bioactive Nutrient

inferredcites →https://doi.org/10.3390/pathogens12030379openalex-snapshot

The Devastating Rice Blast Airborne Pathogen Magnaporthe oryzae—A Review on Genes Studied with Mutant Analysis

inferredcites →https://doi.org/10.3390/plants8120568openalex-snapshot

Trehalose Protects Maize Plants from Salt Stress and Phosphorus Deficiency

inferredcites →https://doi.org/10.4014/jmb.1906.06041openalex-snapshot

Trehalose Protects the Probiotic Yeast Saccharomyces boulardii against Oxidative Stress-Induced Cell Death

inferredcites →https://doi.org/10.4103/1673-5374.308085openalex-snapshot

Therapeutic potential of trehalose in neurodegenerative diseases: the knowns and unknowns

inferredcites →https://doi.org/10.4103/1673-5374.360164openalex-snapshot

Profiling neuroprotective potential of trehalose in animal models of neurodegenerative diseases: a systematic review

What points at this work

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

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Drought stress responses revealed by genomic and transcriptomic analyses of two macrofungi (Inonotus hispidus and Inocutis levis) from Populus euphratica

inferred← citeshttps://doi.org/10.1002/jsfa.71150openalex-snapshot

Genomic insights into high‐sugar tolerance and probiotic properties of Pediococcus pentosaceus MP13 , a potential probiotic isolated from traditional fermented rose jam

inferred← citeshttps://doi.org/10.1002/nap2.70116openalex-snapshot

Surface‐Engineered Dual‐Emission of Carbon Dots for Ratiometric Detection of Hydroxyl Radicals

inferred← citeshttps://doi.org/10.1007/978-981-92-0038-2_9openalex-snapshot

Caenorhabditis elegans as a Model Organism for Proteinopathies

inferred← citeshttps://doi.org/10.1007/s00217-025-05026-zopenalex-snapshot

Oxidative quality parameters of royal jelly under different storage conditions: insights into protein oxidation (AOPPs), lipid peroxidation (MDA), and Maillard reaction (HMF)

inferred← citeshttps://doi.org/10.1007/s00248-026-02782-7openalex-snapshot

Anhydrobiosis as a Model of Aging and Longevity: The Role of Autophagy and Metabolism in Yeast Cells

inferred← citeshttps://doi.org/10.1007/s00253-024-13391-0openalex-snapshot

Maize drought protection by Azospirillum argentinense Az19 requires bacterial trehalose accumulation

inferred← citeshttps://doi.org/10.1007/s00253-025-13539-6openalex-snapshot

The phenomenon of anhydrobiosis—structural and functional changes in yeast cells

inferred← citeshttps://doi.org/10.1007/s00284-026-04750-3openalex-snapshot

Seasonal Variation in the Mutagenic and Oxidative Properties of Gut Microbiota in Active and Hibernating Common Noctules (Nyctalus noctula)

inferred← citeshttps://doi.org/10.1007/s11259-025-10832-7openalex-snapshot

Trehalose prevents glyphosate-induced kidney damage in roosters via inhibiting apoptosis

inferred← citeshttps://doi.org/10.1007/s11274-026-04890-5openalex-snapshot

Unraveling the halotolerant degradative machinery of Candida tropicalis JH: a novel biocatalyst for sustainable treatment of hypersaline azo dye effluents

inferred← citeshttps://doi.org/10.1007/s12355-026-01752-0openalex-snapshot

Vinasse Improves Biomass Quality and Aluminum Tolerance in Saccharomyces cerevisiae PE-2

inferred← citeshttps://doi.org/10.1016/bs.apcsb.2024.09.012openalex-snapshot

Role of protein aggregates in bacteria

inferred← citeshttps://doi.org/10.1016/j.bbrep.2025.102284openalex-snapshot

Hypoxia response in glioblastoma cells: effect of trehalose on macropinocytosis, autophagy and cell survival

inferred← citeshttps://doi.org/10.1016/j.biortech.2025.133580openalex-snapshot

Engineering a cyclic enzymatic cascade for efficient trehalose biosynthesis from maltodextrin substrates

inferred← citeshttps://doi.org/10.1016/j.fbio.2025.107958openalex-snapshot

Encapsulation of ethanol-metabolizing Lacticaseibacillus casei DACN609 in a sodium alginate-trehalose-lentinan matrix improves gastrointestinal tolerance and storage stability

inferred← citeshttps://doi.org/10.1016/j.fm.2026.105153openalex-snapshot

Physiological and transcriptomic insights deciphering cAMP-induced oxidative stress tolerance of antagonistic yeast Sporidiobolus pararoseus Y16

inferred← citeshttps://doi.org/10.1016/j.fochx.2025.102969openalex-snapshot

Metabolomic and bioactivity analysis of plum pulp fermented with Lactiplantibacillus, Lacticaseibacillus, and Bifidobacterium strains

inferred← citeshttps://doi.org/10.1016/j.foodchem.2026.149930openalex-snapshot

Comparative effect of gum arabic and psyllium husk on alginate hydrogels for Lactiplantibacillus plantarum encapsulation

inferred← citeshttps://doi.org/10.1016/j.foodchem.2026.150408openalex-snapshot

Multidimensional strategies for human milk extracellular vesicle preservation: a systematic evaluation based on liquid, solid and semi-solid states

inferred← citeshttps://doi.org/10.1016/j.foohum.2025.100534openalex-snapshot

Additives for sustainable fruit packaging: A systematic review

inferred← citeshttps://doi.org/10.1016/j.jip.2026.108675openalex-snapshot

Overexpression of transcription factor genes VvbHLH and VvCBF from Volvariella volvacea (bull.) singer enhances environmental stress tolerance and insecticidal toxicity of Beauveria bassiana

inferred← citeshttps://doi.org/10.1016/j.micres.2025.128138openalex-snapshot

Functional analysis of the CRP and TreR-treBC regulon in trehalose utilization of Vibrio parahaemolyticus

inferred← citeshttps://doi.org/10.1016/j.molliq.2025.128781openalex-snapshot

Improving the stability and catalytic efficiency of urate oxidase with natural deep eutectic solvents: Integrated in vitro and in silico approaches

inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111651openalex-snapshot

Multi-omics profiling unravels the synergistic roles of defence priming and metabolic remodeling in wheat waterlogging tolerance

inferred← citeshttps://doi.org/10.1016/j.postharvbio.2026.114734openalex-snapshot

Quercetin inhibits Alternaria alternata in postharvest jujube via disrupting membrane integrity, energy metabolism and stress adaptation

inferred← citeshttps://doi.org/10.1016/j.postharvbio.2026.114775openalex-snapshot

Trehalose biosynthesis mediated by PeTPS2 alleviates postharvest senescence of Pleurotus eryngii by maintaining cell wall structural homeostasis

inferred← citeshttps://doi.org/10.1016/j.sbi.2026.103254openalex-snapshot

Chemical chaperones at the interface of proteostasis and metabolostasis

inferred← citeshttps://doi.org/10.1016/j.syapm.2026.126730openalex-snapshot

Gelidimonas denitrificans gen. nov., sp. nov., and Gelidimonas diazotrophica sp. nov. psychrophilic bacteria involved in the nitrogen cycle in tundra soils of South Spitsbergen

inferred← citeshttps://doi.org/10.1021/acs.jafc.4c08669openalex-snapshot

Trehalose Ameliorates Nonalcoholic Fatty Liver Disease by Regulating IRE1α–TFEB Signaling Pathway

inferred← citeshttps://doi.org/10.1021/acsbiomaterials.5c01435openalex-snapshot

Structural Control for Tunable Hyperthermia-Induced Cellular Responses Using 3D-Printed Platforms

inferred← citeshttps://doi.org/10.1038/s41598-024-80440-zopenalex-snapshot

Deep eutectic solvent enhances antibacterial activity of a modular lytic enzyme against Acinetobacter baumannii

inferred← citeshttps://doi.org/10.1039/d6fo00946hopenalex-snapshot

Ameliorative effect of docosahexaenoic acid-acylated astaxanthin ester on diabetic nephropathy: association with the trehalose/HSP90AA1 and colon–kidney axis

inferred← citeshttps://doi.org/10.1051/bioconf/202519401057openalex-snapshot

Response of moderately halophilic bacterium Salinicola socius strain SMB35 T cells to oxidative stress induced by the action of hydrogen peroxide

inferred← citeshttps://doi.org/10.1093/jee/toaf235openalex-snapshot

Trehalose promotes the response of CYP genes in Tribolium castaneum (Coleoptera: Tenebrionidae) to high-CO2 stress

inferred← citeshttps://doi.org/10.1093/sumbio/qvag013openalex-snapshot

Insights into trehalose synthase function in the rhizobium Paraburkholderia phymatum STM815T under abiotic stresses and during symbiosis

inferred← citeshttps://doi.org/10.1101/2025.07.14.664280openalex-snapshot

Survival strategies of the entomopathogenic nematode encapsulated by nanoparticle-stabilized emulsions at rapid desiccation

inferred← citeshttps://doi.org/10.1115/1.4068905openalex-snapshot

Trehalose and Neurodegeneration: A Review of Its Role in Autophagy, Protein Aggregation, and Neuroprotection

inferred← citeshttps://doi.org/10.1126/sciadv.adv8896openalex-snapshot

A trehalase-derived MAMP triggers LecRK-V–mediated immune responses in Arabidopsis

inferred← citeshttps://doi.org/10.1128/aac.01349-24openalex-snapshot

The stress-protectant molecule trehalose mediates fluconazole tolerance in Candida glabrata

inferred← citeshttps://doi.org/10.1134/s0026893325700724openalex-snapshot

GLUT8- and AMPK-Dependent Autophagy Signaling in the Mechanism of the Neuroprotective Action of Trehalose

inferred← citeshttps://doi.org/10.1136/egastro-2024-100129openalex-snapshot

Essential roles of the unfolded protein response in intestinal physiology

inferred← citeshttps://doi.org/10.1186/s12864-025-12059-xopenalex-snapshot

Trehalose accumulation contributes to enhanced cold stress tolerance in Telenomus remus, a dominant egg parasitoid of Spodoptera frugiperda

inferred← citeshttps://doi.org/10.1186/s12866-026-04865-4openalex-snapshot

Beyond antibiotics: a new anti-virulence strategy combating ESBL-producing Klebsiella pneumoniae by targeting periplasmic trehalase

inferred← citeshttps://doi.org/10.1186/s12870-024-05514-6openalex-snapshot

Insights into trehalose mediated physiological and biochemical mechanisms in Zea mays L. under chromium stress

inferred← citeshttps://doi.org/10.1186/s40643-026-01102-8openalex-snapshot

Improvement of biosurfactant production by Rhodococcus ruber IEGM 231 grown on waste cooking oil, their emulsifying activity and antioxidant potential

inferred← citeshttps://doi.org/10.1186/s43043-025-00224-xopenalex-snapshot

Comparison of a commercial trehalose-based and laboratory-prepared sucrose-based vitrification solution for human blastocyst cryopreservation: effects on embryological and clinical outcomes

inferred← citeshttps://doi.org/10.12944/crnfsj.14.2.19openalex-snapshot

Insights Into the Cold Stress-Driven Metabolome of Edible Mushrooms from Arid Highlands of the Indian Trans-Himalayas

inferred← citeshttps://doi.org/10.2147/opth.s551503openalex-snapshot

Management of Dry Eye Disease with Artificial Tears Containing Hyaluronic Acid and Trehalose: A Narrative Review

inferred← citeshttps://doi.org/10.21518/ms2024-354openalex-snapshot

Combination of trehalose and botulinum toxin type A in REVITOX skin treatment protocols

inferred← citeshttps://doi.org/10.21518/ms2025-364openalex-snapshot

Combination treatment of melasma with intense pulsed light and biorevitalization injections of trehalose and hyaluronic acid

inferred← citeshttps://doi.org/10.3389/fmicb.2026.1764301openalex-snapshot

Mechanisms of viability loss in dehydrated Metarhizium anisopliae blastospores

inferred← citeshttps://doi.org/10.3389/fvets.2026.1805930openalex-snapshot

Dehydration-based preservation of cat cumulus–oocyte complexes is not improved by membrane-permeable trehalose

inferred← citeshttps://doi.org/10.3390/agronomy15071668openalex-snapshot

An Evaluation of Inoculant Additives on Cell Viability and Their Effects on the Growth and Physiology of Glycine max L.

inferred← citeshttps://doi.org/10.3390/cosmetics13040196openalex-snapshot

Trehalose in an Emulsion-Based Carrier: Effects on Skin Hydration and Transepidermal Water Loss

inferred← citeshttps://doi.org/10.3390/fermentation12040199openalex-snapshot

Exogenous Carbohydrate Effects on Thermoadaptation and Thermostress in Ogataea parapolymorpha Under Different Carbon Sources

inferred← citeshttps://doi.org/10.3390/foods15193453openalex-snapshot

Polyphenol Bioconversion and Volatile Aroma Production by Meyerozyma sp. C3 Isolated from Kombucha in the Theaflavin–Sucrose Fermentation Model

inferred← citeshttps://doi.org/10.3390/healthcare13060619openalex-snapshot

Effects of Trehalose on Halitosis: A Randomized Cross-Over Clinical Trial

inferred← citeshttps://doi.org/10.3390/ijms251910659openalex-snapshot

Trehalose Attenuates In Vitro Neurotoxicity of 6-Hydroxydopamine by Reducing Oxidative Stress and Activation of MAPK/AMPK Signaling Pathways

inferred← citeshttps://doi.org/10.3390/microbiolres17070126openalex-snapshot

Metabolic Stimulants as Functional Enhancers of Sustainable Microbial Omega-3 Fatty Acid Production

inferred← citeshttps://doi.org/10.3390/microorganisms12061232openalex-snapshot

The Enigma of NTH2 Gene in Yeasts

inferred← citeshttps://doi.org/10.3390/microorganisms13122778openalex-snapshot

Bacterial Adaptation to Stress Induced by Glyoxal/Methylglyoxal and Advanced Glycation End Products

inferred← citeshttps://doi.org/10.3390/molecules31193383openalex-snapshot

Preclinical Anxiolytic- and Antidepressant-like Effects of α,α-Trehalose, a Bioactive Compound Identified in Psilocybe cubensis

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