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stress tolerance

17671 relationships annotated with this phrase. Showing first 500 of 17671.
Source entity Relationship Target entity Species
BRAHMA stability promotes boron tolerance Arabidopsis thaliana
Posidonia australis in this study maintained its shoots under 8-week low light exposure Posidonia australis
triploids are at higher risk of mortality in hotter and drier environments Populus tremuloides
gibberellic acid (GA) inhibitor treatment leads to higher tolerance to oxidative stress Hordeum vulgare
overexpression of sunflower HEAT SHOCK TRANSCRIPTION FACTOR A9 (AT-HSFA9, HSFA9, AT5G54070) leads to increase of seed longevity and thermal tolerance of seedlings Nicotiana tabacum
filmy ferns cannot endure high sun exposure and aridity
total tree NSC pools are large and resilient to short-term stress
drought-responsive TF HaDREB2 co-overexpressed with sunflower (AT-HSFA9, HSFA9, AT5G54070) Helianthus annuus
high-yielding rice varieties can withstand multiple abiotic stresses
clonal plants prevail in some but not all stressful conditions
persistence of leaf metabolism of Posidonia australis in Shark Bay may be challenged by occurrence of marine heatwaves Posidonia australis
stoloniferous plants have weaker stress tolerance
diatoms possess unique physiological and metabolic characteristics
homologous genes from Arabidopsis endow the plant with enhanced tolerance when overexpressed Arabidopsis thaliana
dry seed allows desiccation tolerance Arabidopsis thaliana
OXrPPR1 plants have longer roots than wild-type (WT) or OXmiR400 plants under Cd stress Arabidopsis thaliana
gibberellic acid (GA) inhibitor treatment leads to higher tolerance to heat stress Hordeum vulgare
late-embryogenesis abundant (LEA) proteins are involved in abiotic stress tolerance in plants Oryza sativa
ROS maintained at low levels likely causes enhanced Cd tolerance in OXrPPR1 plants Arabidopsis thaliana
annuals have weaker stress tolerance
resting cells enable diatoms to endure prolonged periods of unfavourable conditions
plant species vary in physiological tolerance of a variety of stressors
Haberlea rhodopensis can survive long-term darkness Haberlea rhodopensis
boron supply has beneficial impact on plant resistance to Al stress Pisum sativum
combination of GC-ToF-MS data and pronounced up-regulation of (AtSIP2, RS2, SIP2, AT3G57520) led to hypothesis that in IDL, imported raffinose could play a dual role of delivering reduced carbon and acting as stress tolerance mechanism Arabidopsis thaliana
imported raffinose in individually darkened leaves (IDL) could play a dual role of acting as a stress tolerance mechanism Arabidopsis thaliana
members of the A20/AN1 zinc-finger polypeptides are critically involved in stress tolerance of higher plants
dark septate root endophytes and other putative root-associated ascomycetes are generally well protected against harsh conditions by thick and melanized cell walls
OXrPPR1 transgenic plants has longer root length than wild-type (WT) plants under CuSO4, NaCl and ABA treatments Arabidopsis thaliana
leaf metabolites in Posidonia australis showed resistance to future warming temperature of 1.5°C for 1.5 weeks under ambient light conditions Posidonia australis
abscisic acid (ABA) production may benefit whole plant stress tolerance
belowground growth forms (BGF) relationship to stressful conditions depends on particular BGF
development of resting cells is crucial for ability to withstand harsh environmental conditions Thalassiosira pseudonana
homoeologous exchange correlates with salinity and hyperosmotic (drought-like) stresses
fungal endophytes may improve host resilience to abiotic stress like drought and heat
heat-induced plasticity may help protect flowers against various abiotic stresses
epigeogenous rhizomes occurrence is correlated with disturbance frequency, drought, cold, and shade
epigeogenous rhizomes is most tolerant to stressful conditions
OXmiR400/OXrPPR1 transgenic plants have root length comparable to OXrPPR1 plants Arabidopsis thaliana
increased leaf dry matter content (LDMC) increases stress tolerance by reducing fast growth Conyza canadensis
black fungi have in common ability to withstand hostile environments
root oxygen loss (ROL) barrier significantly reduced toxic effect of hydrogen sulphide
proline accumulation and scavenging of reactive oxygen species (ROS) enhance tolerance to abiotic stress
heterologous expression of OsSAP1 in tobacco conferred cold stress tolerance Nicotiana tabacum
Sorghum bicolor L. has tolerance to drought, waterlogging and salinity Sorghum bicolor L.
less below-ground respiratory demand in Halophila uninervis may allow it to acclimate more than larger seagrasses under light deprivation Halophila uninervis
Hordeum vulgare seedlings with largest endogenous GA concentrations are most susceptible to abiotic stresses Hordeum vulgare
anthocyanins may contribute to tolerance to environmental stresses
AM fungi enhance drought tolerance
improving root systems of crop plants may achieve secured plant productivity under nonoptimal conditions
(ALN, ATALN, AT4G04955) mutants that accumulate high levels of allantoin exhibit higher tolerance to drought and osmotic stress Arabidopsis thaliana
sequencing of the genome of a desiccation-tolerant moss and a second drought-tolerant moss, when used in conjunction with existing P. patens tools would undoubtedly serve to clarify mechanisms of stress tolerance in poikilohydric plants Tortula; Ceratodon; Physcomitrella patens
heterologous expression of OsSAP1 in tobacco conferred salt stress tolerance Nicotiana tabacum
transcription factors (TFs) function to enhance plants' tolerance via processes such as vegetative growth attenuation, osmoprotectant accumulation, and transpiration reduction
Piriformospora indica enhances resistance to biotic stresses Piriformospora indica
(ALN, ATALN, AT4G04955) mutants that accumulate high levels of allantoin compared with wild-type and (ATXDH1, XDH1, AT4G34890) plants Arabidopsis thaliana
genetic variation provides basis for tolerance to unfavorable osmotic and other environmental conditions
abscisic acid (ABA) promotes desiccation tolerance
transgenic wheat with moderate mannitol accumulation shows increased biomass and plant height compared to wild-type wheat under stressed conditions Triticum aestivum
HvDhn4s: TaNAC69-1 transgenic plants (D4:NAC69-L3) produce significantly more shoot biomass than Bobwhite Triticum aestivum
pre-treatment of adult plants with antimycin A significantly improved flooding survival in adult plants Arabidopsis thaliana
stress-tolerant progeny maintained healthy vegetative growth under high salinity stress Arabidopsis thaliana
double mutant cells are able to grow under excess illumination Chlamydomonas reinhardtii
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) plants are more tolerant to carbon starvation conditions Arabidopsis thaliana
heterologous expression of OsSAP1 in tobacco conferred dehydration stress tolerance Nicotiana tabacum
LOC_Os05g10670 was recently reported to confer improved tolerance to high-salt and drought stresses Oryza sativa
endopolyploidy plays role in abiotic stress response
sequencing of the genome of a desiccation-tolerant moss would serve to clarify mechanisms of stress tolerance in poikilohydric plants Tortula
cell proliferation and growth coordination through activation and repression of gibberellin (GA) signaling via DELLA stabilization is necessary to establish stress tolerance in the whole plant and in specific organs Oryza sativa
angiosperm perennials might better tolerate long-term darkness
crops exhibit sensitivity to harsh climates and soil conditions
up-regulation of phytochrome genes may serve to mitigate detrimental effects of darkness Haberlea rhodopensis
exogenous gibberellic acid (GA) application reverses salt stress-induced inhibition of germination
molecular chaperones function to enhance plants' tolerance via processes such as vegetative growth attenuation, osmoprotectant accumulation, and transpiration reduction
HvDhn4s: TaNAC69-1 transgenic plants (D4:NAC69-L3) produce significantly more shoot biomass under mild salt stress and water limitation Triticum aestivum
genes related to ROS homeostasis, mitochondrial functioning and cell wall remodelling potentially improve survival under stress conditions Arabidopsis thaliana
Al resistance was not significantly different between WT and rah1 single mutant WT and (RAH1, AT5G27920) Arabidopsis thaliana
Halodule uninervis did not appear to be impacted by high temperatures and low light Halodule uninervis
role of natural or synthetic 'anti-ER stress' chaperones ( (BIP3, HSP70-13, AT1G09080) or TUDCA, respectively) is demonstrated in tolerance of Arabidopsis to high light stress Arabidopsis thaliana
2-week-old plants display better flooding tolerance than 3-week-old plants Arabidopsis thaliana
corn hpPARP-transgenic plants show significant difference in yield under drought Zea mays
DH maize cell cultures displays tolerance to lethal concentrations of DCB Zea mays
ABA pre-treatment reduced submergence survival at both ages Arabidopsis thaliana
SALT TOLERANCE (BBX24, STO, AT1G06040) is stress-tolerance-related gene
DH maize cell cultures has I90 values very dissimilar to H12 maize cell cultures Zea mays
variegated phenotype observed in the (ATMSH1, CHM, CHM1, MSH1, AT3G24320) mutant has been reported to enhance plant survival under natural conditions of environmental stress, such as photooxidative light conditions
best hpPARP-transgenic lines show yield increase of 20–40% under drought Brassica napus; Zea mays
dehydration-like stress jeopardizes plant fitness and survival
(RAE1, AT5G01720) mutant showed higher Al resistance than WT Arabidopsis thaliana
glyoxalase I has been shown to confer tolerance to abiotic stresses such as salt Nicotiana tabacum
alkenal reductase overexpression are usually more tolerant to stress conditions
shoot length of OE lines were longer than those of WT under abiotic stress conditions Oryza sativa
DH maize cell cultures has I50 values comparable to NH maize cell cultures Zea mays
DH maize cell cultures incubated with DCB displays behavior similar to maize cultures never cultured in presence of DCB Zea mays
stress-related genes were applied in genetic engineering of drought-tolerant crops
programmed cell death (PCD) promotes plant survival
pre-treatment of juvenile plants with antimycin A did not improve flooding survival Arabidopsis thaliana
cuticle serves as shield against osmotic stress
engineered plants have manifested improved stress-resistance phenotypes
1 µg ml–1 Tunicamycin (Tm)-treated plants exhibit clear tolerant phenotype to high light stress Arabidopsis thaliana
C4 photosynthesis provides greater resilience to abiotic stresses
better climate tolerance could be achieved in current and re- or de novo domesticated crops
Strobilanthes cusia is capable of extreme environmental adaptation Strobilanthes cusia
Ex-TAQed plants 10 of 10 944 were insensitive to high salinity stress during seed germination Arabidopsis thaliana
(AtSTOP1, STOP1, AT1G34370) is required for both Al resistance and proton tolerance Arabidopsis thaliana
(RAE1, AT5G01720) mutation could increase proton tolerance Arabidopsis thaliana
RADICAL-INDUCED CELL DEATH 1 (ATP8, AtRCD1, CEO, CEO1, RCD1, RIMB1, AT1G32230) is stress-tolerance-related gene
T-DNA-mediated inactivation of (anac017, NAC017, RAO2, AT1G34190) significantly reduced survival under submergence conditions Arabidopsis thaliana
VOCs mediate tolerance to abiotic stresses including elevated temperature
ER–PCD network-inhibiting (ATBI-1, ATBI1, BI-1, BI1, AT5G47120) ultimately raises plant tolerance to oxidative stress
cuticle serves as shield against salt stress
(anac017, NAC017, RAO2, AT1G34190) knockout provides evidence for the involvement of ANAC017 in flooding tolerance Arabidopsis thaliana
genetic engineering (GE) introduces drought tolerance
higher H + uptake ability in als5 mutant under low-pH stress was abolished by exposure to Al Arabidopsis thaliana
overexpression of TaABC1 conferred tolerance to drought Arabidopsis thaliana
UWO and perhaps other extremophiles can survive multistress environments Chlamydomonas raudensis
(AtCEST, CEST, Y3IP1, AT5G44650) is involved in stress tolerance Arabidopsis thaliana
MAIF1 overexpression reduces inhibition of abiotic stressors
Overexpression of spinach monooxygenases increased tolerance to salt, temperature and drought stress Oryza sativa; Nicotiana tabacum
deoxybrassinolide is known to have protective effects on membrane stability Zea mays
cuticle serves as shield against drought
low Tunicamycin (Tm) concentration enhanced phototolerance Arabidopsis thaliana
Arabidopsis with reduced PARP activity following transformation with PARP hairpin (hpPARP) construct are more resistant to heat Arabidopsis thaliana
H12 maize cell cultures has I90 values approximately 10 times higher than DH maize cell cultures Zea mays
Arabidopsis with reduced PARP activity following transformation with PARP hairpin (hpPARP) construct are more resistant to high light Arabidopsis thaliana
DH maize cell cultures has I10 values very dissimilar to H12 maize cell cultures Zea mays
large-effect QTLs confer tolerance to submergence
cellulose deficient mutant plants are typically more sensitive to abiotic stress
cell wall plays prominent role in abiotic stress tolerance
liquid-liquid phase separation (LLPS) influences stress tolerance
DNA methylation changes are linked to improved stress tolerance
mucilage production is low in overexpressors compared to WT Coccomyxa subellipsoidea
abiotic stress tolerance has implications for plant community dynamics
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) plants develop visibly better ability to regreen and produce new leaves after carbon starvation Arabidopsis thaliana
flavonoids protect plants from various abiotic stresses
sugar transport and accumulation in flowers is crucial factor determining resilience of tolerant genotypes to combined heat and drought stress
highly hydroxylated sphingolipids provide protection against environmental stresses
WT colonies during starvation secrete mucilage Coccomyxa subellipsoidea
new plant varieties have to be stress resilient
ancient genomes offer practical resources to improve resilience
late embryogenesis abundant proteins are directly involved in stress tolerance
aluminium resistance is related to lower Al accumulation in the root tip Phaseolus vulgaris
canola with reduced PARP activity following transformation with PARP hairpin (hpPARP) construct are more resistant to heat Brassica napus
DH maize cell cultures has I50 values very dissimilar to H12 maize cell cultures Zea mays
population genetic studies have identified striking degree of variability in tolerance to abiotic factors Hordeum vulgare
endophytes support host through abiotic stress alleviation
soil isolate collection from arsenic-contaminated rhizosphere was analyzed for arsenic resistance
plants endure abiotic and biotic stresses under fluctuating environmental challenges
this type of study allows plant resistance to a multistress situation
overexpression of (ATCBF1, CBF1, DREB1B, AT4G25490) conferred stress tolerance
UWO could maintain growth if lake temperatures increased and salinity decreased simultaneously Chlamydomonas raudensis
(ATMTP11, MTP11, AT2G39450) functions in Mn tolerance Arabidopsis
overexpression of polyamine-synthesizing enzymes allows generation of plants with increased stress tolerance
flooding conditions in the present study exposed tolerance differences between the provenances
abiotic stress tolerance has implications for agricultural productivity
canola with reduced PARP activity following transformation with PARP hairpin (hpPARP) construct are more resistant to drought Brassica napus
tolerance enhancement by genetic engineering to increase glycine betaine (GB) biosynthesis is more successful in salt and chilling stresses
anthocyanins contribute to plant tolerance to abiotic stress
PG mutant lines support notion that plastoglobules are important mediators of plant stress tolerance capacity
climate-resilient cultivars have enhanced resistance/tolerance to anticipated biotic and abiotic stresses
increasing longevity makes increasingly important constitutive tolerance of environmental stress
rice (Oryza sativa) shows highest tolerance to Al toxicity Oryza sativa
genetic polymorphisms are associated with environmental stress responses
CcCIPK-interacting proteins may reveal mechanism underlying improved stress tolerance in pigeon pea
excessive activation of anaerobic metabolism could be detrimental to surviving the stress
H12 maize cell cultures has I10 values approximately 10 times higher than DH maize cell cultures Zea mays
floral pigments are line of defense against desiccation
mRNA-binding proteins are directly involved in stress tolerance
(DORN1, LecRK-I.9, P2K1, AT5G60300) mutants rescued from fumonisin B1 toxicity Arabidopsis thaliana
mucilage secretion is adaptive mechanism against unfavorable conditions Coccomyxa subellipsoidea
increase in H2O2 and ABA levels resulting in improved stress tolerance to heat Solanum lycopersicum
wild-type plants are less sensitive to abiotic stress
chaperones are directly involved in stress tolerance
acid soils that permit deep rooting require drought resistance
overexpression of adenine isopentenyl transferase (ipt) gene improves heat tolerance in perennial grass species
als5 mutant shows tolerance to low pH Arabidopsis thaliana
enhancement of osmotic potential (OP) leads to avoidance of damage to cell membranes
4% oxygen treatment results in increased tolerance to anoxia
overexpression of P5CS conferred stress tolerance
ER–PCD network-inhibiting (ATBI-1, ATBI1, BI-1, BI1, AT5G47120) ultimately raises plant tolerance to intense light
Epigenome engineering could be utilized to develop crops with enhanced resistance to abiotic stresses
overexpression of tomato ASR1 or lily ASR1 enhances tolerance to drought and salt stresses Nicotiana tabacum; Arabidopsis thaliana
DH maize cell cultures has I10 values comparable to NH maize cell cultures Zea mays
molecular and biochemical changes ameliorate exposure to particular stress
(anac017, NAC017, RAO2, AT1G34190) contributes positively to plant responses to submergence also at later vegetative stages Arabidopsis thaliana
Brassica juncea glyoxalase I overexpression line showed significant increase in tolerance compared to wild-type when treated with methylglyoxal and sodium chloride Nicotiana tabacum
down-regulation of AO activity during storage probably contributes to improved fruit tolerance to stressful conditions imposed by detachment from plant Pisum sativum
(AtVIP1, SUE3, VIP1, AT1G43700) mutant displayed enhanced tolerance to heavy metal stress Arabidopsis thaliana
Sullu is previously shown to be drought-tolerant
abscisic acid (ABA) signalling up-regulates genes with roles in stress tolerance
(AtVIP1, SUE3, VIP1, AT1G43700) and (SUE4, AT3G55880) mutants displayed enhanced tolerance to oxidative stress (paraquat) Arabidopsis thaliana
additional mortality on exposure to acute stress after the conditioning appears to be little little additional mortality Oryza sativa
constitutive expression of rice OsTOP6A or OsTOP6B confers abiotic stress tolerance to transgenic Arabidopsis plants Arabidopsis thaliana
plants have intricate defence mechanisms
versatility of hormonal regulation allows avoidance of detrimental effects of stress
transgenic plants overexpressing (STZ, ZAT10, AT1G27730) were found to be more tolerant to drought, salinity, osmotic stress, heat stress, and high-light stress Arabidopsis thaliana
root hair length had a strong relationship with Al 3+ tolerance of root hairs
CsubMADS1 transcription factor probably governs stress tolerance in C-169 during lag phase Coccomyxa subellipsoidea
engineering plants with enhanced stress tolerance avoids commonly associated growth penalties
survival of the conditioned plants was better than that of plants that had not been conditioned Oryza sativa
drought stress may reduce ozone (O3) injury in crop plants and forest species
alr104 mutant shows tolerance to combined low-pH/Al treatment Arabidopsis thaliana
Arabidopsis and wheat might employ similar mechanisms to combat combined low-pH/Al stress Arabidopsis thaliana; Triticum aestivum
these compounds are drought-responsive and putatively related to tolerance
anti-freeze proteins are directly involved in stress tolerance
survival of plants conditioned with 100 mM NaCl stress was significantly better on subsequent exposure to toxic 200 mM NaCl compared with unconditioned plants Oryza sativa
altered protein expression may indicate potential role in alleviating a later-occurring drought stress episode Triticum aestivum
secondary metabolites serve as chemical defence strategy
tobacco and Arabidopsis plants with suppressed expression of apoplastic AO gene were more tolerant to salt stress Nicotiana tabacum; Arabidopsis thaliana
sensitivity to drought determined magnitude of ozone (O₃) tolerance in wheat species under combination of drought and ozone (O₃) exposure Triticum aestivum
alr104 mutant was tolerant to low pH Arabidopsis thaliana
morphological, physiological, and biochemical responses decrease stress exposure damage
heterogonous over-expression of GsCBRLK in Arabidopsis resulted in enhanced plant tolerance to salt and ABA stress Arabidopsis thaliana
cross-tolerance between drought and ozone (O3) stress in winter wheat species is little known about whether any cross-tolerance exists
fine-tuned interaction of hormones and ROS with signaling components allow plant to survive different abiotic stress conditions
abscisic acid (ABA) confers tolerance to environmental stresses
exogenous application of cytokinins (CKs) mitigates root electrolyte leakage
Low-pH tolerance (als5 mutant) was associated with higher H + uptake under low-pH stress Arabidopsis thaliana
Arabidopsis thaliana accession Ler-1 tolerated Sr2+ concentrations up to 1 mM Arabidopsis thaliana
free amino acid accumulation appears to be of major importance in protection of plants
increased root viability contributes to tolerance of creeping bentgrass to water stress Agrostis stolonifera
rice FOX line R07303 contained (AtCEST, CEST, Y3IP1, AT5G44650) Oryza sativa
chloroplastic SODs overexpression improves stress tolerance
habitat-adapted fungal endophytes are required for plant survival in native habitats
efficient recovery from NH4+ toxicity in rice under moderate K+ conditions may offer focal point for bioengineering of ammonium tolerance into sensitive crop genotypes Oryza sativa
over-expressed poplar peroxisomal ascorbate peroxidase (APX) gene in tobacco could enhance plants' stress tolerance tobacco
TaABC1 overexpression confers increased tolerance to cold stress Arabidopsis thaliana
CEST-overexpressing transgenic Arabidopsis retained more chlorophyll than wild-type Arabidopsis thaliana
delay of Al uptake by cytosol improves plant resistance to Al
RIL46 was also tolerant to ozone Oryza sativa
alleviative effect of Si on Mn toxicity was described for common bean Phaseolus vulgaris
mechanisms that underlie plant tolerance to acidic and Al stresses appear to be different Arabidopsis thaliana
increasing endogenous SODs enhances stress tolerance
lower levels of reactive electrophile species (RES) may contribute to survival during severe stress
sugar beet is relatively robust when grown under hot, dry, or saline conditions
heterologous expression of (ASH2R, TRAUCO, TRO, AT1G51450) in Bre2p Δ yeast partially restores growth in formamide
high-dormancy seeds are more tolerant to high temperatures imposed at imbibition Lolium rigidum Gaud
TaABC1-overexpressing transgenic Arabidopsis had increased tolerance to abiotic stresses Arabidopsis thaliana
slight osmotic response may allow increased tolerance via adaption for subsequent stress
poor root functioning is key limitation for waterlogging tolerance in dryland crops Triticum aestivum L.; Hordeum vulgare L.; Zea mays L.
fractions containing high DP fructans (DP >7) do not protect liposomes from drying
exudation of OAs by plant roots to the rhizosphere is effective strategy to cope with cation toxicity and Pi deficiency
most effective EBR concentration is approximately 200nM in AC and pTRV plants
foliar application of secondary messengers increased tolerance to salt stress
instructive chromatin regulators activity can be modulated to allow enhanced primary stress tolerance
(MSRA4, PMSR4, AT4G25130) expression confers protection against oxidative stress Arabidopsis thaliana
detoxification of Al in the apoplast through root exudates plays important role in Al resistance
sustaining cell cycle progression is integral part of the stress tolerance mechanism in plant roots
interaction of stress and sugar signalling is essential for plants to tolerate stress
stress tolerance genes include heat shock factors Zea mays
lack of acclimation in SAG relative to UWO resulted in sharp transition point between salt concentrations that enable or limit growth Chlamydomonas raudensis
basal thermotolerance is the inherent ability to survive temperatures above optimal growth temperatures
fungal endophytes confer habitat-specific stress tolerance
good barrier function 1 week after returning the plants to control medium may be expected to be reflected in enhanced survival Oryza sativa
ABA-deficient not mutant exhibits reduced tolerance to photo-oxidative stress
virus-induced gene silencing of (ATMPK1, MPK1, AT1G10210) /2 compromises acclimation-induced cross-tolerance Solanum lycopersicum
functional stay-green is valuable trait for improving crop stress tolerance
(ATHAL3, ATHAL3A, HAL3, HAL3A, AT3G18030) overexpression showed improved growth Arabidopsis thaliana; Oryza sativa
activation of antioxidant enzyme machinery by polyamines (PAs) reduces oxidative stress-induced membrane injury and electrolyte leak
some species of associative and endophytic diazotrophic bacteria are reported to increase plant tolerance against biotic and abiotic stresses
potato is less tolerant to copper stress
amino acids (mostly proline and glycine betaine) may act as protective compounds durum wheat
transgenic Arabidopsis lines with different expression levels of ABP9 show consistent phenotypes in stress performance Arabidopsis thaliana
GmERF057 expression in transgenic tobacco plants conferred enhanced tolerance to salt and pathogen stress Nicotiana tabacum
ammonium (NH4+) tolerance in rice depends upon potassium (K+) supply Oryza sativa
high ascorbate content plants and their fruit would not only be more nutritious but may also be more resistant to abiotic stresses such as high light, ozone, salt, and drought
high Al resistance in wheat was attributed to Triticum aestivum Al-activated malate transporter (TaALMT1) Triticum aestivum
silicon (Si) alleviates aluminium toxicity
efficient water use contributes to tolerance of creeping bentgrass to water stress Agrostis stolonifera
spermidine may have dual functions in plant stress tolerance
exogenous application of ABA has been reported to increase tolerance and crop yield
flowering ensures production of flowers even when plants are growing under adverse conditions
rice varieties with tolerance to various abiotic stress factors include tolerance to salinity, mineral deficiencies or toxicities, and flooding rice
glyoxalase I overexpression in tobacco showed higher tolerance to salt and methylglyoxal Nicotiana tabacum
membrane integrity and stability is major component of environmental stress tolerance
Arabidopsis (ATPRXIIF, PRXIIF, AT3G06050) is implicated in tolerance to salt stress Arabidopsis thaliana
EBR treatment is ineffective at restoring stress tolerance at ABA-deficient not mutant at 24h after application
changes in chromatin organization may endow plants with ability to survive combinations of stresses
fructans are believed to confer drought tolerance Lolium perenne
heat-responsive proteins is critical for understanding molecular mechanisms of stress tolerance
sorbitol is thought to be important in stress tolerance
screening for high g s may be the most effective way of selecting genotypes that will grow fast in saline soil durum wheat
genome of H. chilense seems to confer a certain degree of tolerance to drought and salt Hordeum chilense
diurnal leaf curling is example of plant architectural elements that correlate with improved tolerance to stress Sorghum bicolor
positive correlation of increased levels of glutathione and SA has been related to abiotic stress tolerance in several Brassicaceae species Brassicaceae
constitutive high growth rather than high physiological tolerance (i.e. small phenotypic plasticity), confers adaptation to salinity durum wheat
(ATMPK1, MPK1, AT1G10210) and (ATMPK2, MPK2, AT1G59580) are necessary components for acclimation-induced stress tolerance Solanum lycopersicum
cytokinin effects on plant resistance to stress plant resistance to stress
Salicornia europaea can survive under high salinity and N-deficient habitat conditions Salicornia europaea
GmERF089 transgenic plants had enhanced tolerance to salt and drought stresses
potassium (K+) homeostasis in rice shows more effective recovery from ammonium (NH4+) toxicity Oryza sativa; Hordeum vulgare
overexpression of ERF genes enhances resistance to biotic and abiotic stresses
genotypic evaluation during the first part of the crop cycle (perhaps even at the seedling stage) may be a valid option to select for salt tolerance in durum wheat durum wheat
silencing of (ATMPK1, MPK1, AT1G10210) /2 compromised PA-induced chilling tolerance Solanum lycopersicum
cold-acclimation-induced cold tolerance is associated with increased H2O2 accumulation
fungal endophytes confer habitat-specific stress tolerance to monocots
differences in ROS stress level formed in the leaves rather than the activity of ROS scavenging enzymes accounted for tolerance Oryza sativa
K+ acquisition and homeostasis in rice is resistant to ammonium (NH4+) nutrition Oryza sativa
transgenic overexpression of UDP-glucose-4-epimerase conferred tolerance to salt, drought, and freezing stress in Arabidopsis thaliana Arabidopsis thaliana
magnesium-dependent mechanisms govern alleviation of aluminium toxicity
morphological, physiological, and biochemical responses facilitate repair of damaged systems
overexpression of TaABC1 increased stress tolerance levels in transgenic Arabidopsis Arabidopsis thaliana
mutualistic fungi confer tolerance to disease
Aechmea 'Maya' is not particularly tolerant of severe light limitation in the short term Aechmea 'Maya'
improved root functioning should aid tolerance of soil toxins in anaerobic soils
heat tolerance has molecular basis in molecular mechanisms
ectopic expression of XhDsi-1 VOC in yeast did not confer tolerance to methylglyoxal in yeast glyoxalase I mutant Saccharomyces cerevisiae
Transgenic approaches with genes coding FTs to produce fructans with different DPs, such as PpFT1 and wft1 would probably reveal relationship between the DP of fructans and their physiological roles
RIL432 coped better with nitrate starvation Arabidopsis thaliana
osmotins and osmotin-like proteins are commonly associated with tolerance to osmotic stress
transient system for local and continuous delivery of indole-3-acetic acid (IAA) is used for enhancing stress tolerance in higher plants
rice coleoptiles exposed to combination of anoxia and pH 3.5 demonstrated tolerance to anoxia even during acid load imposed by exposure to pH 3.5 Oryza sativa
catechol is associated with aluminum tolerance
shoot growth and yield of tomato (Solanum lycopersicum) with enhanced abscisic acid (ABA) production were less inhibited by drought and salt stress Solanum lycopersicum
MADS-box transcription factors (MADS-box TFs) regulate proline accumulation
barley is more tolerant to salinity than durum wheat Hordeum vulgare; durum wheat
NAC genes play significant roles in plant tolerance to various environmental stresses
arginase1/2 mutants exhibited increased stress tolerance Arabidopsis thaliana
ABA-deficient not mutant exhibits reduced tolerance to heat stress
chromosome engineering methodologies have enabled transfer of genes controlling abiotic stress tolerance
modulation of instructive chromatin regulators should avoid causing growth or yield trade-offs
genotypic ranking suggests that genetic variability for salinity tolerance in durum wheat is maintained through entire crop cycle durum wheat
transgenic plants showed better survival rate Oryza sativa
fruits have systems in place that help them tolerate dehydration
ApY2SK2 transgenic Arabidopsis thaliana shows enhanced stress tolerance under drought stress Arabidopsis thaliana
Funneliformis mosseae inoculation and selenite application at booting stage significantly enhances saline-alkali tolerance of rice Oryza sativa
stigmasterol helps enhance plant resistance against heat stress Oryza sativa
Arabidopsis lines overexpressing RcFeSOD8 exhibited improved germination under heat stress Arabidopsis thaliana
cell membrane stability has positive association with physiological and biochemical parameters
ethylene affects responses to abiotic stresses
why1why3polIb-1 plants grown for 3 weeks at normal light, then transferred to high-light conditions for 1 week were considerably less affected by high-light treatment Arabidopsis thaliana
copy number variation is well-documented means to increase biotic and abiotic stress tolerance
SlMPK2 is involved in plant tolerance to abiotic stresses Solanum lycopersicum
metabolic homeostasis may confer adaptive and protective functions under abiotic stresses
early life stages of populations from distribution limits of Scots pine have capacity to tolerate and persist under increased temperatures and altered water availability as projected by climate change scenarios Pinus sylvestris
silencing of (ATMPK1, MPK1, AT1G10210) compromised PA-induced chilling tolerance Solanum lycopersicum
ZAT12-overexpressing Arabidopsis plants showed higher tolerance to cold, oxidative, osmotic, and high-light stresses Arabidopsis thaliana
stress tolerance mechanism of nitrate retention is similar to mechanism proposed for (AtNPF7.2, NPF7.2, NRT1.8, AT4G21680) nitrate reallocation Arabidopsis thaliana
newer maize hybrids may have increased tolerance to low soil nitrogen (N)
isoprene emitters are better protected against oxidative stress
temperate japonica subpopulation shows highest relative Al tolerance among five rice subpopulations Oryza sativa
foliar application of secondary messengers increased tolerance to extreme temperature
LeCDJ1 elevated expression may be attributed to enhanced protection of plants against damaging effects of environmental stresses Solanum lycopersicum
Chenopodium rubrum is tolerant to relatively high salt and nitrate concentrations Chenopodium rubrum
closely related species show substantial variations in NH4+ tolerance
Melatonin (MLT) might be beneficial for organisms facing environmentally induced oxidative stress
isoprene achieves protective effect against thermal and oxidative stresses
drought- and salt-inducible TaHsf members may have similar role Triticum aestivum
(ATCESA8, CESA8, IRX1, LEW2, AT4G18780) Arabidopsis gene causes enhanced drought and osmotic stress tolerance when mutant Arabidopsis thaliana
C4 grasses perform better under hot, dry conditions
glutathione peroxidase functionality in GSTs has been demonstrated to be important in tolerance of transgenic tobacco to chilling Nicotiana tabacum
flavodoxin expression in transgenic plants results in increased tolerance to multiple stresses
transgenic plants expressing CcCDR could successfully complete reproductive cycle under drought, salt, and cold stress conditions Arabidopsis thaliana
EBR treatment at 200nM concentration increases Fv/Fm by approximately 20% photo-oxidative stress tolerance
SUPPRESSOR OF (PPI1, AT4G27500) LOCUS1 (DAL1, SP1, AT1G63900) overexpression may be effective strategy in generating crops better able to cope with abiotic stresses Arabidopsis thaliana
Yeasts expressing (ABCG29, AtABCG29, ATPDR1, PDR1, AT3G16340) exhibited increased tolerance to p-coumaryl alcohol
(ATFKBP65, FKBP65, ROF2, AT5G48570) mutant shows similar phenotype to wild-type in presence of sorbic acid Arabidopsis thaliana
mannitol is important to increase tolerance to salt and osmotic stress
wild relative species of Solanaceae show wide tolerance levels to abiotic stresses
SlCDF1 and SlCDF3 were investigated for roles in abiotic stress tolerance Solanum lycopersicum
knockout (AtZAT12, RHL41, ZAT12, AT5G59820) Arabidopsis seedlings suffered increased sensitivity to cold, oxidative, osmotic, and high-light stresses Arabidopsis thaliana
precipitation strongly influences plant survival
35S::miR156 expression increased stress tolerance Arabidopsis thaliana
anthocyanin could protect plants from damage plants
Piriformospora indica improves barley under Al stress Hordeum vulgare
RcFeSOD8 enhances tolerance to drought stress Ricinus communis; Arabidopsis thaliana
exogenous hydrogen sulfide (H 2 S) fumigation alleviates toxic symptoms associated with Cr 6+ stress Arabidopsis thaliana
overexpression of (ATCBF3, CBF3, DREB1A, AT4G25480) conferred stress tolerance
K+ acquisition and homeostasis in rice is only partially resistant to ammonium (NH4+) nutrition Oryza sativa
crops should be enabled to grow in drier and more infertile soils
tobacco and sugar beet plants expressing bacterial levansucrase exhibit increased drought and freezing tolerance
(ART1, HUA2, AT5G23150) (Al-tolerance transcription factor 1) is involved in Al tolerance Oryza sativa
EBR treatment at 30nM concentration increases Fv/Fm only marginally photo-oxidative stress tolerance
maintaining redox homeostasis is prerequisite for development of tolerance against biotic stresses
C4 photosynthesis trait enables efficient growth under water- and nitrogen-limited conditions at high temperatures
Arabidopsis plants overexpressing SlCDF1 and SlCDF3 genes showed improved tolerance compared with wild type (WT) Arabidopsis thaliana
next generation must be preserved against abiotic stresses Triticale
induction of (AtNPF7.2, NPF7.2, NRT1.8, AT4G21680) contributes essentially to Cd 2+ stress tolerance Arabidopsis thaliana
models in different crop systems should increase resilience to environmental stresses
endopolyploidy is linked with higher stress tolerance in plants
Spartina densiflora has physiological and morphological versatility Spartina densiflora
drought priming may alleviate severe drought stress event Triticum aestivum
overexpression of some HsfA genes, such as (ATHSFA2, HSFA2, AT2G26150) and HaHsfA9 can result in thermotolerance and salt and dehydration stress tolerance Arabidopsis thaliana; Helianthus annuus
AOX (alternative oxidase) has a role in maintaining growth and promoting plant survival under adverse conditions
PMTV infection protects plants from drought stress Nicotiana benthamiana
quiescent state enables plant endurance of various environments
petals must resist unfavorable environmental conditions
cost / benefit balance of individual stress tolerance mechanisms is essential for understanding stress tolerance mechanisms Thellungiella; Arabidopsis thaliana; crops
OsACA6 transgenic plants showed greater resistance than wild-type plants Nicotiana tabacum
overexpression of the Arabidopsis ortholog of this gene confers drought and salt tolerance Arabidopsis thaliana
miR156 induction assigns energy to tolerance process plants
ZjDREB1.4 is potentially useful for producing transgenic plants tolerant to high temperature and/or cold stresses with few negative effects Arabidopsis thaliana
growing plants must withstand mechanical disturbances from intense rainfall, wind, or arboreal animals
most plants cannot survive 50 µg mL⁻¹ arsenic
(ATCIPK23, CIPK23, LKS1, PKS17, SnRK3.23, AT1G30270) overexpression significantly enhanced tolerance to low K+ Arabidopsis thaliana
auxin maximum re-establishment and CSCD death mechanism improves root's ability to withstand environmental stresses Arabidopsis thaliana
Serendipita indica enhances host resilience against biotic and abiotic stresses
(ATFKBP65, FKBP65, ROF2, AT5G48570) overexpression line shows less inhibition of growth by acetic acid Arabidopsis thaliana
EBR treatment restores heat and photo-oxidative stress tolerance in ABA-deficient not mutant
upregulated activities of photosynthesis may indicate potential role in alleviating a later-occurring drought stress episode Triticum aestivum
crop plants with enhanced stress tolerance would be beneficial for delaying onset of premature senescence
reduced water availability due to high salt level implies strong correlation between drought and salt stress tolerance
(STZ, ZAT10, AT1G27730) overexpressors and loss-of-function mutants display enhanced tolerance to drought and salinity stresses Arabidopsis thaliana
genetic background of cultivars influences ability to thrive in suboptimal environments
hypothesis predicts that translocon at the outer envelope membrane of chloroplasts mutant with reduced capacity to import photosynthesis-related proteins would show abiotic stress tolerance Arabidopsis thaliana
(ATFKBP62, FKBP62, ROF1, AT3G25230) (ATFKBP65, FKBP65, ROF2, AT5G48570) double mutant germinates less well than wild-type in presence of sorbic acid Arabidopsis thaliana
SUPPRESSOR OF (PPI1, AT4G27500) LOCUS1 (DAL1, SP1, AT1G63900) overexpression significantly promotes stress tolerance Arabidopsis thaliana
(AtSTOP1, STOP1, AT1G34370) (C2H2-type zinc finger transcription factor) is associated with tolerance to low pH Arabidopsis thaliana
EPSs may provide protection from desiccation
flavonoids enhance biotic stress tolerance
tolerance to stress is very important for plant survival
miR156 participates in stress tolerance processes by regulating (DFR, M318, TT3, AT5G42800) Arabidopsis thaliana
ALCOHOL DEHYDROGENASE 1 (ADH, ADH1, ATADH, ATADH1, AT1G77120) confers enhanced resistance to abiotic stress Arabidopsis thaliana
Hemoglobins (Hbs) are one of many different strategies that plants have evolved to overcome stress conditions and survive
β-cyclocitral triggers defense and detoxification mechanisms Arabidopsis thaliana
plants adapted to extreme environments have capacity to cope with adverse environmental cues
seedlings of common ash from different provenances were tested for differences in their physiological response and overall resistance to waterlogging
increased number of periderm layers is trait of agronomical importance in breeding programs targeting stress tolerance Arabidopsis thaliana
Tan et al. (2017) performed association analysis of salinity and drought tolerance Brassica napus
disruption of (PKS1, AT2G02950) impedes zygospore fitness Chlamydomonas reinhardtii
Casuarina equisetifolia (C. equisetifolia) exhibits resistance to typhoon Casuarina equisetifolia
DELLAs promote plant survival Arabidopsis thaliana
(ATFKBP62, FKBP62, ROF1, AT3G25230) (ATFKBP65, FKBP65, ROF2, AT5G48570) double mutant shows greater inhibition of growth by acetic acid Arabidopsis thaliana
ABA treatment restores heat and photo-oxidative stress tolerance in BR-deficient dim mutant
ABA treatment alleviates Fv/Fm reduction in both pTRV and pTRV-RBOH1 plants
overexpression of the C2H2-type ZFP genes ZFP252, ZFP245, and ZFP179 increased the tolerance of rice seedlings to drought, salinity, cold, and oxidative stress Oryza sativa
carbon availability has been shown to affect survival to submergence in Arabidopsis Arabidopsis thaliana
(ATFKBP65, FKBP65, ROF2, AT5G48570) mutant shows similar inhibition of growth by acetic acid to wild-type Arabidopsis thaliana
breeding for crop species that form more specialized types of late adventitious roots (LAR) could be interesting strategy to promote crop multi-stress resilience
DELLA protein accumulation confers tolerance to stress Arabidopsis thaliana
Haberlea rhodopensis remained green and viable throughout dark treatment Haberlea rhodopensis
Haberlea rhodopensis can withstand 30 days of complete darkness Haberlea rhodopensis
plants with higher cellular ploidy are more tolerant to UV-B stress Arabidopsis thaliana
Arabidopsis thaliana is not a stress-tolerant species Arabidopsis thaliana
extremophile models is a new under-utilized component of plant stress biology
H12 maize cell cultures has I50 values approximately 10 times higher than DH maize cell cultures Zea mays
capacity to manipulate auxin signaling pathways under high ammonium and acidic stresses confers tolerance to high ammonium and acidic stresses Oryza sativa
ABA pre-treatment reduced submergence survival Arabidopsis thaliana
strains tolerant of environmental stress (hypersensitive to ABA or tolerant of high salinity) screened for among Ex-TAQ-diversified tetraploid plants Arabidopsis thaliana
STTM400 transgenic plants are more Cd-tolerant relative to wild-type (WT) seedlings Arabidopsis thaliana
100 μM CdSO4 treatment increases root growth by 50% in STTM400 plants relative to WT plants Arabidopsis thaliana
plant life in Atacama Desert highlands is confronted with drought
sunflower (AT-HSFA9, HSFA9, AT5G54070) overexpressed conjointly with drought-responsive TF HaDREB2 positive effects on seed longevity were observed beyond those observed with overexpression of HaHSFA9 alone Nicotiana tabacum
(DPA, AT5G02470) lncRNAs are derived from quantitative trait loci (QTLs) significantly associated with stress tolerance Oryza sativa
leaf metabolism of Posidonia australis in Shark Bay might be able to persist under future global warming if light conditions are sufficient Posidonia australis
OsACA6 has function in imparting salinity/drought stress tolerance Oryza sativa
(DAA1, AT1G64110) knockout mutants are impaired in germination and root growth in response to ABA, NaCl and mannitol Arabidopsis thaliana
(ATMYB12, MYB12, PFG1, AT2G47460) and (ATMYB75, AtPAP1, MYB75, PAP1, PAP1-D, SIAA1, AT1G56650) double overexpressors show enhanced tolerance to drought stress Arabidopsis thaliana
proline is necessary for imparting tolerance toward abiotic stress Arabidopsis thaliana
sustainable ameliorative strategies promote radiocesium tolerance
calcium (Ca 2+) significantly rescued inhibition of root growth caused by Cr 6+ stress in wild type seedlings Arabidopsis thaliana
(PPR1, AT1G06580) mutant shows approximately 30% decrease in root growth relative to wild-type (WT) plants under Cd stress Arabidopsis thaliana
leaf metabolome of Halophila uninervis may not be affected by marine heatwaves occurring under future global warming at higher latitudes Halophila uninervis
biophysical alteration of cytosol and chloroplasts enables endurance of unfavourable conditions of deeper ocean Thalassiosira pseudonana
communities where rhizomes are overrepresented are good at dealing with hypoxia
(ACD11, AT2G34690) (accelerated cell death 11) overexpression improves salt and drought tolerance Arabidopsis thaliana
(AR2, ATR2, AT4G30210) emergence delay promotes higher desiccation tolerance
plant life in Atacama Desert highlands is confronted with daily negative temperatures
plants have evolved complex response systems to cope with environmental stresses
hypogeogenous rhizomes have weaker stress tolerance
belowground growth forms have capacity for survival of anoxia
more conservative risk-averse strategy would allow them to circumvent hostile growing periods such as early onset freeze or unexpected harsh conditions
miR156 overexpression did not improve tolerance to submergence Arabidopsis thaliana
clavicipitaceous fungal endophytes of grasses enhance host physiological tolerances to environmental stresses
irrigated rice cultivation protects against drought and heat stress
genetic manipulation of stomatal physiology or stomatal development can improve abiotic stress resilience
larger individuals can buffer risks
symbioses with AMF can support the maintenance of larger floral display during periods of drought or nutrient stress
persistent seagrasses such as Posidonia are generally characterized by high physiological resistance to environmental disturbances Posidonia australis
sufficient light levels can generally mitigate heat-induced damage in temperate seagrasses Posidonia australis
Posidonia spp. have been classified as species of persistence Posidonia australis
Pteris vittata can thrive in soils containing up to 1,500 µg mL⁻¹ arsenic Pteris vittata
(PPR1, AT1G06580) plays crucial role in enhancing plant stress tolerance Arabidopsis thaliana
larger trees may have greater tolerance for hydraulic and carbon risk Populus tremuloides
OXrPPR1 transgenic plants increase root growth by nearly 60% relative to wild-type (WT) plants under Cd stress Arabidopsis thaliana
plant life in Atacama Desert highlands is confronted with high solar radiation
diverse CRISPR tools used to target specific genes
Pearl millet (Pennisetum glaucum) is well suited to growth under harsh conditions, including low soil fertility, high soil pH, high soil Al 3+ saturation, low soil moisture, high temperature, and high salinity Pennisetum glaucum
priming protects shoot apical meristem (SAM) from growth-terminating damage Arabidopsis thaliana
Ca2+ ATPase pumps have role in stress tolerance
Ca2+ ATPases lead to stress tolerance
over-expression of transcription factors confers abiotic stress tolerance of crops
flavonoid overaccumulation is key to enhanced tolerance to oxidative and drought stress Arabidopsis thaliana
tobacco MAPKK (Nicotiana protein kinase 1 (NPK1)) overexpression led to enhanced tolerance to salt stress Nicotiana tabacum
canola with reduced PARP activity following transformation with PARP hairpin (hpPARP) construct are more resistant to high light Brassica napus
impairment of mitochondrial activity can be linked to superior tolerance to submergence in juvenile plants Arabidopsis thaliana
increased Al-resistance phenotype in the double mutant could be recovered to (RAE1, AT5G01720) level Arabidopsis thaliana
35S::miR156 plants exhibited improved salt and drought tolerance Arabidopsis thaliana
ApSK3 transgenic Arabidopsis thaliana shows enhanced stress tolerance under osmotic stress Arabidopsis thaliana
defense and detoxification mechanisms enhances plant tolerance to abiotic stresses Arabidopsis thaliana
miR156-SPLs-DFR pathway functions as core regulatory module mediating coordinated development and abiotic stress tolerance processes Arabidopsis thaliana
ApSK3 transgenic Arabidopsis thaliana shows enhanced stress tolerance under drought stress Arabidopsis thaliana
selenite alleviates abiotic stresses
Populus cathayana exhibits sexually differential mechanisms to Zn resistance Populus cathayana
(ATFKBP62, FKBP62, ROF1, AT3G25230) positively modulates thermotolerance Arabidopsis thaliana
(ATFKBP65, FKBP65, ROF2, AT5G48570) overexpression line shows improved tolerance to propionic acid Arabidopsis thaliana
melatonin-loaded silica nanoparticles (MLT@SiNPs) holds potential for alleviating other abiotic stresses in crops
sextuple mutant ( (GED1, PRT6, AT5G02310) erfVII) was analyzed for role of Cys-Arg/N-end-rule-pathway-mediated stabilization of ERFVIIs on stress tolerance Arabidopsis thaliana
cell membrane stability has been used for evaluating tolerance to desiccation stress
OsACA6 over-expressing plants confirmed abilities to tolerate changing environment Nicotiana tabacum