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abiotic stress response

12859 relationships annotated with this phrase. Showing first 500 of 12859.
Source entity Relationship Target entity Species
SA plays important role in plant response to abiotic stresses
heat stress is one of diverse abiotic stress conditions Arabidopsis thaliana
early responses to various abiotic stresses exhibited negative correlations to several ROS indices Arabidopsis thaliana
ultraviolet light stress is one of diverse abiotic stress conditions Arabidopsis thaliana
nonmycorrhizal (NM) plants have higher proline content in leaves Medicago truncatula
drought causes crop losses
warming climate affects rice yields Oryza sativa
genes are mainly involved in plant growth and responses to pathogen and abiotic stress Fragaria vesca
inositol-requiring enzyme 1A ( (ATIRE1-2, AtIRE1A, IRE1-2, IRE1A, AT2G17520) ) is associated with subcellular redistribution of transcription factors from ER membrane by proteolytic cleavage Arabidopsis thaliana
Δ VmRDR1 -21/34 and Δ VmRDR2 -3/33 mutants displays diminished stress resistance to Na+ and K+ Valsa mali
ABA receptors role in abiotic stress is well-documented
signals and regulatory networks involved in abiotic stress perception remain inadequately understood abiotic stress perception
receiver domain of ETHYLENE RECEPTOR 1 (AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) is important for the control of germination under most of the additional stress conditions Arabidopsis thaliana
abscisic acid (ABA) is involved in mediating contrasting roles of ETHYLENE RECEPTOR 1 (AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) and ETHYLENE RECEPTOR 2 (ETR2, AT3G23150) in germination under many stress conditions Arabidopsis thaliana
AM fungi accumulate trehalose in extraradical hyphae Glomus intraradices
exogenous SA treatment could restore abiotic stress sensitivity phenotype of Osaim1 mutant Oryza sativa
salt and submergence treatments led to significant increases in ACC Arabidopsis thaliana
stomatal density (SD) requires compromise in choosing to tackle multiple future environmental stresses Oryza sativa
phytochemical compounds mediate interactions with abiotic environment
salinity and drought induce expression of RePRPs Oryza sativa
chromosomal-level genome assembly for Syntrichia ruralis can provide insights to plant abiotic stress responses Syntrichia ruralis
abiotic stresses applied for 24 h Arabidopsis thaliana
RELATED TO (AP2, AtAP2, FL1, FLO2, AT4G36920) (Rap2.6L, AT5G13330) has been previously characterized as having a role in abiotic stress responses Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) (MORE AXILLARY GROWTH2) has an important role in plant responses to abiotic stress conditions Arabidopsis thaliana
Zfp177 has been analyzed in detail transcript analysis under different abiotic stresses
MACC did not show changes except for increase after 2 h of treatment Arabidopsis thaliana
Solanaceae (ATSUC4, ATSUT4, SUC4, SUT4, AT1G09960) are involved in response to a broad range of environmental stimuli, including drought, salt, and heat stress, and different light conditions
transcriptional regulation of phloem-loading SUTs and vacuolar SUTs shows important role in stress response in source leaves
ETHYLENE RECEPTOR 2 (ETR2, AT3G23150) have contrasting roles in the control of seed germination under NaCl stress Arabidopsis thaliana
stomatal density (SD) contributes to rice abiotic stress resilience Oryza sativa
HIGS-RiMsn2-RNAi lines have increased free proline content Medicago truncatula
ACC and its conjugates quantified in Arabidopsis shoots exposed to abiotic stresses Arabidopsis thaliana
rice RePRP family may participate in regulation of root growth under ABA and abiotic stresses Oryza sativa
significant up-regulation by ABA and abiotic stresses in rice roots implies RePRPs might play important roles in the root response to abiotic stresses Oryza sativa
SWI/SNF-class factors could have important functions in abiotic stress responses
five type III wall peroxidases are coexpressed and up-regulated in roots undergoing abiotic stress Arabidopsis thaliana
abiotic stresses (cold, drought, genotoxic, osmotic, oxidative, salt, wounding) leads to strong up-regulation of transcript levels of SAP family members Arabidopsis thaliana
heat-shock proteins were notably up-regulated in mature (MEX1, RCP1, AT5G17520) leaves
plant microRNA (miRNA) play essential roles in response to abiotic stress
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) is likely to enable abiotic stress responses
RD29A:LUC transgene responds to low temperature Arabidopsis thaliana
PP2A-C2 overexpression alters plant response to drought
osmotic stress is associated with drought
ETHYLENE RECEPTOR 1 (AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) have contrasting roles in the control of seed germination under NaCl stress Arabidopsis thaliana
MAPKs regulate response to drought
rice F-box gene (Os02g44990) is induced by abiotic stress Oryza sativa
drought and salt stress require the same adaptations regarding transport of sugars
transcriptional regulation of SUTs shows important role in stress response in source leaves
MAPKs play key roles in the regulation of plant's response to abiotic stresses
(AtCPK21, CPK21, AT4G04720) wild-type restores stress responsitivity in (AtCPK21, CPK21, AT4G04720) mutant background Arabidopsis thaliana
OsFKBP20-1b plays an essential role in environmental stress responses mediated by pre-mRNA splicing and/or transcriptional regulation Oryza sativa
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) is constitutively expressed in other abiotic stress and different tissues Arabidopsis thaliana
LOC_Os05g10670 was part of 1,432 up-regulated genes in meta-analysis of abiotic stresses Oryza sativa
osmotic stress is associated with high soil salinity
gas chromatography (GC)-mass spectrometry (MS) and liquid chromatography (LC)-mass spectrometry (MS) facilitated assessment of altered regulatory responses to various abiotic stresses
COLD RESPONSIVE BINDING FACTOR (CBF4, DREB1D, AT5G51990) has been previously characterized as having a role in abiotic stress responses Arabidopsis thaliana
DEGs in abiotic stresses are predominantly down-regulated
rice responds to abiotic stresses through complexity of signaling pathways Oryza sativa
abiotic stress-related treatments show associations with (RLK, AT5G67280) subfamilies Arabidopsis thaliana
drought and salt stress have the same effect on SUT expression in all species
MAPKs regulate response to salinity
defects in VLCFA synthesis should lead to phenotypic disruptions in normal response to abiotic stresses
phloem-loading SUTs are up-regulated in Arabidopsis and soybean in response to drought and salt stress Arabidopsis thaliana; Glycine max
DNA/RNA methylation is epigenetic mechanism for coping with abiotic stress
noncoding RNA-mediated gene expression adjustment is epigenetic mechanism for coping with abiotic stress
HOS10 R2R3 MYB transcription factor regulates cold, dehydration and salt stress
osmotic stress is associated with cold
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutants is involved in regulating abiotic stress responses at both seedling and adult stages Arabidopsis thaliana
identification of metabolomic behaviors under abiotic stresses such as UV irradiation, cold, and drought may help understand differences in responses to abiotic stresses Arabidopsis thaliana
(ATSUC1, SUC1, AT1G71880) expression was found to consistently respond to abiotic stress Arabidopsis thaliana
down-regulation of PtaSUT4 in response to drought and salt stress coincides with reduced sucrose export from the leaf Populus trichocarpa
histone acetylation/deacetylation has important role in abiotic stress responses
(ATSUC4, ATSUT4, SUC4, SUT4, AT1G09960) was down-regulated in response to drought and salt stress in all four tested monocot species
MYB30-INTERACTING E3 LIGASE1 modulates degradation of MdMYB1 Malus domestica
INDETERMINATE SPIKELET1 (IDS1) may directly associate with GCC-box-containing motifs in promoter regions Oryza sativa
ABFs respond selectively to various abiotic stresses
heat stress may occur simultaneously with or independently of drought
OsFKBP20-1b plays important roles in response to intracellular and extracellular stimuli Oryza sativa
high-salinity treatment induces MAIF1 mRNA accumulation Oryza sativa
(AtCPK21, CPK21, AT4G04720) mutant plants show increased stress responses with respect to marker gene expression Arabidopsis thaliana
osmotic stress increases intracellular levels of abscisic acid (ABA) Physcomitrella patens
abscisic acid (ABA) is associated with abiotic stress Arabidopsis thaliana
water availability imbalance is one of abiotic stress
cell-type specific isolation of protoplasts and nuclei enables insight into how cells and tissues respond transcriptionally to abiotic stress
salt stress induces widespread occurrence of alternative polyadenylation (APA) Sorghum
dehydration-responsive element binding protein (DREB) family plays central role in vegetative abiotic stress responses
(ATWRKY11, WRKY11, AT4G31550) and (ATWRKY17, WRKY17, AT2G24570) expression is enhanced upon abiotic stresses Arabidopsis thaliana
(PER3, RCI3, RCI3A, AT1G05260) is up-regulated under high salt stress
WRKY gene family can be involved in abiotic resistance
OsiSAP8 is induced by heat stress Oryza sativa
OsFKBP20-1b is involved in abiotic stress response Oryza sativa
GO terms associated with other abiotic stresses, especially heat stress were also enriched in upregulated genes of the triple mutant
osmotic stress induces expression of five of the six genes (the exception was SRO1f) Zea mays
phosphatidylinositol 4,5-bisphosphate regulates during abiotic responses
one-week-old seedlings of loss-of-function and gain-of-function mutants of OsFKBP20-1b treated with ABA, NaCl, and methyl viologen (MV) showed significantly different phenotypes compared with wild-type (WT) Oryza sativa
nsLTPs are involved in defence against drought
rapidly expressed genes following mechanical stress include (CID1, ERD15, LSR1, AT2G41430)
AtEML is responsive to abiotic stress Arabidopsis thaliana
OsFKBP20-1b overexpression plants strikingly upregulates expression of stress-responsive genes Oryza sativa
Arabidopsis DREB proteins are divided into six subgroups designated A1–A6 Arabidopsis thaliana
OsRLCK gene family showed association with cold tolerance QTL Oryza sativa
hrf1 overexpression enhanced drought tolerance Oryza sativa
SnRK2s function in abiotic stress signalling in plants
(PER3, RCI3, RCI3A, AT1G05260) is up-regulated under cold stress
salinity stress regulates TAP genes Physcomitrella patens; Arabidopsis thaliana
expression level of OsFKBP20-1b was markedly increased in seedlings under salt, mannitol, heat, cold, hydrogen peroxide (H2O2), and abscisic acid (ABA) treatments Oryza sativa
OsFKBP20-1b functions under abiotic stress conditions Oryza sativa
overexpression of ZmDREB2A enhanced vegetative abiotic stress tolerance Arabidopsis thaliana
(AtCPK21, CPK21, AT4G04720) and (ATCPK23, CPK23, GCA2, AT4G04740) appear to fulfill role as negative regulators in the plant abiotic stress response Arabidopsis thaliana
OsFKBP20-1b affected pre-mRNA splicing of abiotic stress-responsive genes Oryza sativa L.
OsFKBP20-1a and OsFKBP20-1b share abiotic stress response Oryza sativa
NBS-LRR gene family can be involved in abiotic resistance
regulatory hubs control effects of stress on crop yield
(AtCPK21, CPK21, AT4G04720) loss-of-function seedlings are more tolerant to hyperosmotic stress Arabidopsis thaliana
k/o and k/d seedlings showed higher sensitivity to environmental conditions Oryza sativa
OsFKBP20-1a responds weakly to abiotic stresses Oryza sativa
nsLTPs are involved in defence against cold
poly(ADP-ribose) polymerases (PARPs) are required for abiotic stress response
downregulation of anthocyanin accumulation leads to sensitivity to several abiotic stress-inducing agents Zea mays; Arabidopsis thaliana
variation between accessions includes timing and nature of responses to abiotic stress
Os.49736.1.S1_x_at is related to a transcript encoding C3HC4-type RING finger protein Oryza sativa
abiotic stress induces OsFKBP20-1b localization to cytoplasmic foci and nuclear speckles Oryza sativa
plant IMMs function as positive regulators of abiotic stress response
global response of Sorghum to abiotic stresses involves the re-direction of transcriptional and translational output into non-productive pathways Sorghum
methylation of histone H3 lysine residues 4 and 27 is key element in regulation of genes involved in abiotic stress responses
response to abiotic stimuli seems to be highly active throughout the year Picea abies
abiotic stress responses include changes in proteins
Computational solutions enable characterization of novel gene functions
new knowledge from spatial transcriptomics will shed light on complex plant mechanisms ranging from development to responses to external abiotic and biotic factors
(ECT8, AT1G79270) is involved in abiotic stress regulation Arabidopsis thaliana
AtEML interacts with AtGCN5 Arabidopsis thaliana
(MIR165, MIR165B, AT4G00885) /166-mediated regulatory module plays critical roles in response to abiotic stress
nsLTPs are involved in defence against heat
karrikin (KAR) signalling exhibits crosstalk with abiotic stress signalling
(MIR319C, AT2G40805) was originally reported to be responsive to cold stress Arabidopsis thaliana
iron chlorosis affects fruit trees
semiaquatic conditions expose rice to abiotic stresses Oryza sativa
OsFKBP20-1b is responsive to other abiotic stresses Oryza sativa
(ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) is directly regulated by SCR but not SHORTROOT (EAL1, SGR7, SHR, AT4G37650)
ROS act as signalling molecules for defence against abiotic stress
RADICAL-INDUCED CELL DEATH 1 (ATP8, AtRCD1, CEO, CEO1, RCD1, RIMB1, AT1G32230) is involved in abiotic stress through interaction with SALT OVERLY SENSITIVE 1 (ATNHX7, ATSOS1, SOS1, AT2G01980) Arabidopsis thaliana
maize (SRO1, AT2G35510) genes play important roles in plant responses to abiotic stress Zea mays
SNAP25 participates in abiotic stress responses
ASKα phosphorylates (G6PD6, AT5G40760) at Thr-467
repression of anthocyanin over-accumulation occurs under abiotic stress Zea mays
ion toxicity is one of abiotic stress
mPing confers its own responsiveness to other genes when inserting in their proximity other genes Oryza sativa
novel gene functions coordinate responses to abiotic stress conditions
cytokinin has a role in response to abiotic stress
Computational solutions enable modeling protein-mediated stress responses
silicon (Si) increases resistance to metal toxicity
nitric oxide (NO) is a key molecule triggering signalling cascades in response to abiotic stresses
ZmSRO1e is most stress responsive of all SRO genes in maize Zea mays
correlation-based network analysis has utility for abiotic stress transcriptional networks
in silico approaches have facilitated development of multi-scale models of responses to other abiotic stress conditions
DNA methylation and small RNA play role in plant response to abiotic stress Oryza sativa
salt stress induces BdFAR4 levels Brachypodium distachyon
auxin acts as key mediator in plant response to abiotic stress
OX plants show curled and wilted leaves more severely than WT plants Zea mays
OsClo5 is involved in stress responses at the seedling stage Oryza sativa
abiotic stress responses include changes in non-coding RNAs
(DSK2, DSK2b, AT2G17200) lesions lead to enhanced sensitivity to osmotic and drought stress
plant response to abiotic stresses is complex
ABA application induces (ATNCED3, NCED3, SIS7, STO1, AT3G14440) expression Arabidopsis thaliana
hypersensitivity of (SCR, SGR1, AT3G54220) mutant to abscisic acid (ABA) suggests that SCARECROW (SCR, SGR1, AT3G54220) may play a role in the response to abiotic stress Arabidopsis thaliana
(ATSNAP33, ATSNAP33B, SNAP33, SNP33, AT5G61210) participates in abiotic stress responses
defense responses to abiotic factors require regulatory changes to activation of multiple genes and pathways
TE families enriched near genes up-regulated by abiotic stress were found enriched near genes up-regulated by abiotic stress (heat, cold, salt stress or UV)
exogenous ABA treatment induces BdFAR4 transcript levels Brachypodium distachyon
TE families enriched near genes down-regulated by abiotic stress were found enriched near genes down-regulated by abiotic stress
priming leads to sustained up-regulation of adaptive responses
Aluminium (Al) toxicity limits common bean production Phaseolus vulgaris
Ran influences abiotic stress response
OsRAN2 overexpression results in hypersensitivity to salinity stress Oryza sativa; Arabidopsis thaliana
WRKY genes regulate plant responses to salinity Arabidopsis thaliana
soluble sugars derived from starch breakdown accumulate in plants to increase stress tolerance
hypersensitivity of the ZmSRO1e transgenic plants to abiotic stress is attributable to decrease in the accumulation of anthocyanins Arabidopsis thaliana
abiotic stress inhibits (AtSPL9, SPL9, AT2G42200) Arabidopsis thaliana
abiotic responses are upregulated by AtCYS-1-OE and (ATCDK8, CDK8, CDKE1, CDKE;1, HEN3, AT5G63610) mutants Arabidopsis thaliana
10 SnRK2 members in maize were induced by one or more abiotic stresses Zea mays
OsRAN2 is speculated to be involved in NaCl stress signalling Oryza sativa
redundant or partially redundant protein kinase such as CALCIUM-DEPENDENT PROTEIN KINASE 23 (ATCPK23, CPK23, GCA2, AT4G04740) compensate for CALCIUM-DEPENDENT PROTEIN KINASE 21 (AtCPK21, CPK21, AT4G04720) function Arabidopsis thaliana
abscisic acid (ABA) is involved in abiotic stress signaling
abscisic acid (ABA) enhances plant adaptability to salinity stress
stress-inducible poly(A) sites suggests existence of numerous unidentified genes whose expression is strongly regulated by abiotic stresses Sorghum
abiotic stress genes from PARP, NBS-LRR, thioredoxin, and heat shock protein (HSP)70 families were identified by QTL mapping and GWAS
RLCK family is associated with abiotic stress Oryza sativa
DREB factors regulate expression of stress-inducible genes under drought stress
TaSnRK2.7 was characterized for expression pattern under diverse environmental stresses Triticum aestivum
ZmSRO1e is involved in abiotic stress responses Zea mays
ROS homeostasis balances relationship between plant growth and abiotic stress tolerance Zea mays; Arabidopsis thaliana
Pro synthesis or turnover modulates decrease in shoot/root ratio
PARPs in plants are involved in resistance to abiotic stress
NaCl treatment induces (ATPLC, ATPLC1, PLC1, AT5G58670) expression Arabidopsis thaliana
ectopic expression of hrf1 improved plant tolerance to drought
miR393 was originally reported to be responsive to dehydration stress Arabidopsis thaliana
OsRAN2 expression is reduced under salinity stress Oryza sativa
(MIR168, MIR168B, AT5G45307) is responsive to high salinity stress Arabidopsis thaliana
Cysteine-rich receptor-like kinases (CRKs) play important roles in response to abiotic stimuli
beta-aminobutyric acid (BABA) increases drought tolerance Arabidopsis thaliana
improved drought tolerance in plants resulting from exogenous application of Harpin is consistent with hrf1 enhanced drought tolerance when overexpressed in rice Oryza sativa
ERF subfamily members bind DRE/CRT elements
SlCDF3 and SlCDF5 maximum increase observed for 24h after heat treatment Solanum lycopersicum
SlCDFs responding to abiotic stresses show different timing and spatial expression patterns in roots and shoots Solanum lycopersicum
plant miRNAs play an important role in response to cold stress
plant miRNAs play an important role in response to drought stress
some drought-responsive lincRNAs were also responsive to water stress Populus trichocarpa
significant increase in (DREB2, DREB2A, AT5G05410) transcripts might have resulted in increased expression levels of downstream drought stress- and cold-responsive genes Arabidopsis thaliana
(MIR402, AT1G77235) was originally reported to be responsive to ABA treatment Arabidopsis thaliana
stress response-related genes most were involved in abiotic stress response Phyllostachys praecox
beta-aminobutyric acid (BABA) increases salt tolerance Arabidopsis thaliana
(ATMYB44, ATMYBR1, MYB44, MYBR1, AT5G67300) overexpression enhanced salt tolerance Arabidopsis thaliana
nucleo-cytoplasmic trafficking through Ran-dependent karyopherin proteins might provide alternative regulatory way in response to abiotic stress
exogenous ABA can induce (ATPLC, ATPLC1, PLC1, AT5G58670) expression Arabidopsis thaliana
OsRAN2 is speculated to regulate expression of (ATPLC, ATPLC1, PLC1, AT5G58670) Oryza sativa; Arabidopsis thaliana
(ATMYB2, MYB2, AT2G47190) expression is induced in transgenic Arabidopsis seedlings Arabidopsis thaliana
OsRAN2 overexpression results in hypersensitivity to osmotic stresses Oryza sativa; Arabidopsis thaliana
miR389a.1 was originally reported to be responsive to dehydration stress Arabidopsis thaliana
dehydration-responsive element binding (DREB) transcription factor family plays a central role in regulating expression of stress-inducible genes under abiotic stresses
arginine decarboxylase (ADC) is main enzyme involved in response to abiotic stresses
OsAGP20 expression level is up-regulated by cold stress Oryza sativa
NaCl stress causes greater expression level of (ATNCED3, NCED3, SIS7, STO1, AT3G14440) Arabidopsis thaliana
GsCBRLK might serve as master regulator in plant abiotic stress response Glycine soja
plants have evolved series of mechanisms in response to abiotic stresses
abiotic stress responses include changes in signaling components
(MIR402, AT1G77235) was originally reported to be responsive to dehydration stress Arabidopsis thaliana
miR389a.1 was originally reported to be responsive to cold stress Arabidopsis thaliana
(EMA1, GIR1, SAD2, URM9, AT2G31660) mutation causes hypersensitivity to ABA Arabidopsis thaliana
ABA plays critical role in response to various stress responses
DGAT transgenics demonstrate potential utility when grown under drought conditions Brassica napus
miR169 has been previously reported to be responsive to cold stress Arabidopsis thaliana
DREB factors regulate expression of stress-inducible genes under high salt stress
toxic ROS is generated mainly in chloroplasts and mitochondria
TaSnRK2.4 overexpression resulted in enhanced tolerance to abiotic stresses Arabidopsis thaliana
cytosolic/nuclear (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) overexpression specifically conferred tolerance to salt stress Arabidopsis thaliana
(ATNCED3, NCED3, SIS7, STO1, AT3G14440) expression is induced in transgenic Arabidopsis seedlings Arabidopsis thaliana
increased ROS-scavenging activity in NJH12 is partially attributed to increased drought tolerance of NJH12 plants Oryza sativa
strigolactone (SL) signalling exhibits crosstalk with abiotic stress signalling
tasiRNAs have not been found to be responsive to abiotic stresses
OsAGP1, OsAGP15, and OsELA3 may be stress-inducible genes Oryza sativa
miR396 is responsive to cold stress Arabidopsis thaliana
seed oil content in canola is drastically reduced by severe summer weather conditions (high temperature and/or drought) during flowering Brassica napus
nsLTPs are involved in defence against salt
ZmSRO1e reveals differences under abiotic stress when compared with (ATP8, AtRCD1, CEO, CEO1, RCD1, RIMB1, AT1G32230) and OsSRO1c Zea mays; Arabidopsis thaliana; Oryza sativa
abiotic stress conditions dynamically alters polar localization and/or activity of PINs
anoxia/hypoxia conditions induce Arabidopsis rboh genes Arabidopsis thaliana
All SlCDF genes regulated by salt and drought Solanum lycopersicum
35S::SlCDF3 plants showed increased levels of glutamine Arabidopsis thaliana
cortical microtubules are important components of signalling hub central to processing of abiotic stress
stress-induced expression of (ATWRKY48, WRKY48, AT5G49520) suggests that WRKY48 may play a role in plant responses to abiotic stresses Arabidopsis thaliana
(ATERF-7, ATERF7, ERF7, AT3G20310) and (ATHD1, ATHDA19, HD1, HDA1, HDA19, HDAC19, RPD3A, AT4G38130) regulate abiotic stress response genes Arabidopsis thaliana
ABA application induces (ATMYB2, MYB2, AT2G47190) expression Arabidopsis thaliana
AtMYB is induced by ABA treatment Arabidopsis thaliana
ROS control abiotic stress responses
low-concentration Reactive oxygen species (ROS) is essential for plant responses to abiotic stresses
(MIR402, AT1G77235) was originally reported to be responsive to NaCl stress Arabidopsis thaliana
WRKY genes regulate plant responses to oxidative stress Arabidopsis thaliana
Harpin proteins enhance drought tolerance
ABA is extensively involved in responses to abiotic stresses such as drought and low temperature, as well as osmotic stress
bZIP-type transcription factors play significant roles in regulation of Cor (LEA, AT2G21490) gene expression Triticum aestivum
translational regulation regulates abiotic responses
perception of small molecules mediates responses to abiotic cues
RLCKs falling within the range of QTLs are identified as RLCKs associated with abiotic stress-related QTLs Oryza sativa
OsELA3 is responsive to drought and salt stresses Oryza sativa
nucleo-cytoplasmic partitioning of regulatory proteins is involved in abiotic stress responses
DREB (dehydration-responsive element binding)-type transcription factors regulate expression of stress-inducible genes
salicylic acid (SA) is believed to play a role in plant responses to osmotic stress
WCBF2 and WDREB2 trans-activate wheat Cor (LEA, AT2G21490) genes Triticum aestivum
TaOBF1 transcript level decreased in roots after exposure to cold, drought, or ABA Triticum aestivum
(ATDSI-1VOC, DSI-1VOC, AT1G07645) mRNA transcripts are expressed in A. thaliana seed, but are not activated in seedlings in response to abiotic stress abiotic stress response Arabidopsis thaliana
cytosolic/nuclear (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) overexpression specifically conferred tolerance to cadmium (Cd) stress Arabidopsis thaliana
seven cloned fragments were highly homologous to cDNA sequences responding to abiotic stresses (drought, cold, ABA, ZnSO4, UV exposure, and γ-ray irradiation) Oryza sativa
nitrogen stress induces Arabidopsis rboh genes Arabidopsis thaliana
compatible solutes are classified as protective compounds in stress response
wPR4e promoter contains abiotic stress-responsive elements Triticum aestivum
leaf bronzing under different abiotic stresses could be due to similar physiological mechanisms under common genetic control Oryza sativa
sunflower HAHB4 confers drought tolerance Helianthus annuus
overexpression of (ABX45, AS11, ATDGAT, AtDGAT1, DGAT1, RDS1, TAG1, AT2G19450) reduces decrease in oil content caused by severe summer weather Brassica napus
miR389a.1 was originally reported to be responsive to NaCl stress Arabidopsis thaliana
abiotic stress response includes temperature response Phyllostachys praecox
annexin genes in Arabidopsis thaliana include annexins associated with abiotic stress responses Arabidopsis thaliana
(LTP, LTP7, AT2G15050) genes ( (AtLtpI-5, cdf3, LP2, LTP2, AT2G38530) (LTP3, AT5G59320) (AtLtpI-11, LTP4, AT5G59310) (AtLtpI-6, LTP6, AT3G08770) ) may be involved in abiotic stress responses Arabidopsis thaliana
WRKY genes regulate plant responses to heat Arabidopsis thaliana
increase in P2-G6PDH protein content following ABA supply strongly supports involvement of this isoform in the response to abiotic stress in plants Hordeum vulgare
two wheat varieties with different levels of stress tolerance are discussed for WLIP19-mediated Cor (LEA, AT2G21490) expression and abiotic stress tolerance development Triticum aestivum
CBF/DREB subfamily genes recognize dehydration responsive or cold-repeat element (DRE/CRT) with core motif A/GCCGAC
autophagy plays important role in maintaining proper balance of cellular proteome during abiotic stresses
overexpression of SlCDF1 and SlCDF3 in Arabidopsis promotes expression of (ERD10, LTI29, LTI45, AT1G20450) Arabidopsis thaliana
lincRNA3241 is down-regulated by cold stress Populus trichocarpa
Brassicaceae family species including Hirschfeldia, Capsella, Thlaspi, and Lepidium have been tested for performance under abiotic stresses Hirschfeldia; Capsella; Thlaspi; Lepidium
JERF1 participates in abiotic stress responses Solanum lycopersicum
SlCDFs regulate expression of genes involved in abiotic stress responses Solanum lycopersicum
many genes involved in abiotic stress response show higher expression levels in rd29A-CcCDR-transgenic plants Arabidopsis thaliana
Arabidopsis plants overexpressing SlCDF1 differentially activated expression of (COR78, LTI140, LTI78, RD29A, AT5G52310) Arabidopsis thaliana
GmERF3 gene expression is induced by salt treatment Glycine max
MYB gene is up-regulated in CcCDR-transgenic plants Arabidopsis thaliana
MAPKKK gene is up-regulated in CcCDR-transgenic plants Arabidopsis thaliana
RLCKs are differentially expressed during abiotic stress Oryza sativa
drought stress limits common bean production Phaseolus vulgaris
OsRAN2 overexpression results in hypersensitivity to exogenous ABA Oryza sativa; Arabidopsis thaliana
OsRLCK genes differentially expressed during abiotic stress Oryza sativa
(ATNCED3, NCED3, SIS7, STO1, AT3G14440) expression is induced by ABA application Arabidopsis thaliana
ERFVIIs enhance abiotic stress responses
jasmonyl-ACC (JA-ACC) could be linked to abiotic stress responses
ethylene regulates more than 50% of genes in abiotic stress gene core
rice seedlings grown on medium with high concentrations of NaCl or polyethylene glycol show elevated RePRP transcripts Oryza sativa
traits of OsEPF1oe plants together appeared to positively impact on drought avoidance and increased salinity tolerance Oryza sativa
BBX proteins play multifaceted roles in diverse abiotic stresses
this study provides useful information for strategies aimed at improving abiotic stress tolerance Oryza sativa
LebZIP2 participates in abiotic stress responses Solanum lycopersicum
overexpression of SlCDF1 and SlCDF3 in Arabidopsis promotes expression of (COR78, LTI140, LTI78, RD29A, AT5G52310) Arabidopsis thaliana
35S::SlCDF3 plants showed increased levels of proline Arabidopsis thaliana
CcCDR protein shows ~70% homology with cold-induced Src1 protein Cajanus cajan; Glycine max
nuclear-localized (ATCDSP32, CDSP32, TRXL1, AT1G76080) led to salt tolerance Arabidopsis thaliana
laccase copper proteins are associated with lignin synthesis; metal nutrition; response to abiotic stresses Arabidopsis thaliana
Populus euphratica is characterized by wide temperature range, salinity, aridity, and drought stress Populus euphratica
salicylic acid (SA) is believed to play a role in plant responses to salt stress
cold stress is one of diverse abiotic stress conditions Arabidopsis thaliana
non-nuclear-localized XBAT35.2 regulates responses to abiotic stresses Arabidopsis thaliana
Oryza sativa gamma rays-induced RING finger protein1 (OsGIRP1) is one of RING finger proteins Oryza sativa
high salinity has adverse effects on plant growth
mutant plants with knockout mutation in both (CKA4, cpCK2, pCK2, AT2G23070) and (CKA3, AT2G23080) shows similar results to (CKA4, cpCK2, pCK2, AT2G23070) mutant phenotype Arabidopsis thaliana
TaWRKY2 and TaWRKY19 regulate abiotic stress tolerance in transgenic Arabidopsis plants Arabidopsis thaliana
TERF1 participates in abiotic stress responses Solanum lycopersicum
C2H2-type zinc finger proteins (ZFPs) are involved in responses of plants to various abiotic stresses Arabidopsis thaliana
PROAtCAPE2 gene in shoots decreased upon saline and drought stresses Arabidopsis thaliana
MiDi19-4B has important regulatory roles in tolerance to multiple abiotic stresses Arabidopsis thaliana
OsEPF1oe plants showed enhanced resilience to multiple abiotic stresses Oryza sativa
rapid increase in ACC observed after 1 h of treatment Arabidopsis thaliana
SlCDF2 and SlCDF4 transcript levels particularly increased after 24h Solanum lycopersicum
well-characterized receptor-like cytoplasmic kinase (RLCK) genes indicate implication in disease resistance, abiotic stress response, and hormone signalling
PROAtCAPE6 gene in roots suppressed by salt, osmotic, and drought stresses Arabidopsis thaliana
35S::SlCDF3 plants showed increased levels of sucrose Arabidopsis thaliana
OsPYL/RCAR5-OE transgenic rice exhibits abiotic stress-tolerance phenotype Oryza sativa
autophagy affects stress tolerance
transcripts of the other seven PROAtCAPEs regulated by more than two abiotic stresses Arabidopsis thaliana
ABA is associated with plant response to abiotic stresses
Cor (cold-responsive) (LEA, AT2G21490) (late embryogenesis-abundant) gene family gene products function in stress tolerance
plant miRNAs play an important role in response to oxidative stresses induced by heavy metals, salinity, and nutrient deficiency
Arabidopsis plants lacking (DAL1, SP1, AT1G63900) are hypersensitive to oxidative stress Arabidopsis thaliana
aluminum treatment results in rapid reduction in DNA methylation Nicotiana tabacum
OsPYL (PYL11, RCAR5, AT5G45860) is not induced by abiotic stresses Oryza sativa
increased ROS production has been reported in response to flooding stress
increased ROS production has been reported in response to heavy metal stress
(ATWRKY33, WRKY33, AT2G38470) plays critical roles in plant responses to a spectrum of abiotic stresses Arabidopsis thaliana
abscisic acid (ABA) mediates drought stress response
exogenous pyruvate treatment enhances expression of (ADC2, ATADC2, SPE2, AT4G34710) Arabidopsis thaliana
DREB (dehydration-responsive element binding) protein family comprises transcription factors
drought stress reduces TaCHP transcript abundance Triticum aestivum
drought (D) stress is an abiotic stress affecting rice plant Oryza sativa
transgenic plants expressing the GUS reporter gene under the control of a native OsACA6 promoter were used to study transcriptional activation of OsACA6 during abiotic stresses Oryza sativa
StPPI1 transcript levels slightly increase with drought stress Solanum tuberosum L.
13 genes related to abiotic stress identified Zea mays
CBF/DREB family members function in abscisic acid (ABA)-independent stress signalling pathways
hydrogen peroxide (H2O2) seems to play the central role as initiator of the response pathways
all SlCDFs responded to different abiotic stresses like salt, drought, and extreme temperatures Solanum lycopersicum
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) plays key role in plant responses to abiotic stress Arabidopsis thaliana
HSF family may be involved in wheat responses to drought and salt stress Triticum aestivum
Arabidopsis plants overexpressing SlCDF1 differentially activated expression of (AtCOR15A, COR15, COR15A, AT2G42540) Arabidopsis thaliana
PP2A-C2 overexpression alters plant response to sugar stress
mutations in several of these genes affect germination in response to ABA and NaCl Arabidopsis thaliana
OsPYL (PYL11, RCAR5, AT5G45860) is repressed under ABA treatment Oryza sativa
cytokinin functions in stress responses
abscisic acid (ABA) plays critical roles in plant response to drought
(ATSUC9, SUC9, AT5G06170) does not show changes in response to abiotic stress Arabidopsis thaliana
phloem-loading SUTs do not show any significant change in Solanaceae potato and tomato in response to drought and salt stress Solanum tuberosum; Solanum lycopersicum
different abiotic stresses often affect similar genes
physiological/phenotypic characterization of abiotic stress responses is considered to be essential prerequisite for understanding genetic and genomics-type studies
(AIM1, AT4G29010) participates in abiotic stress responses Solanum lycopersicum
some genes in cluster 1 respond to additional stresses
(LOS1, AT1G56070) likely plays role in responding to abiotic stresses such as dehydration Arabidopsis thaliana
desiccation tolerance (DT) and dormancy module is associated with abiotic stress response genes Medicago truncatula
WRKY transcription factors (TFs) play critical roles in drought stress response
WRKY transcription factors (TFs) play critical roles in nutrient stress response
(ARA-6, ARA6, AtARA6, ATRAB5C, ATRABF1, RABF1, AT3G54840) is involved in salt stress Arabidopsis thaliana
overlap of plant responses to osmotic stresses such as drought and salinity shown in genomics studies
increased ROS production has been reported in response to cold stress
SlCDF4 and SlCDF5 showed induction after 24h of salt treatment Solanum lycopersicum
MYB transcription factors (TFs) are pivotal regulators of responses to biotic and abiotic stresses Arabidopsis thaliana
Cu-containing nanoparticles (Cu NPs) affects plant resistance to abiotic stress factors
putrescine is involved in plant response to abiotic stress
(HSP21, AT4G27670) functions under abiotic stress conditions Arabidopsis thaliana
Arabidopsis (ATCBF3, CBF3, DREB1A, AT4G25480) overexpression generates drought tolerant rice plants Oryza sativa
salinity stress raises expression level of (ATCBF3, CBF3, DREB1A, AT4G25480) Arabidopsis thaliana
MdSAT1 has abiotic stress functions in abiotic stress response
TaSnRK2.7 dynamic expression under PEG, salt, and cold stress Triticum aestivum
(AtbZIP, bZIP, AT1G68880) transcription factors are involved in modulation of drought
NaCl treatment results in rapid reduction in DNA methylation Nicotiana tabacum
constitutive expression of OsPYL/ (PYL11, RCAR5, AT5G45860) induces expression of stress-responsive genes Oryza sativa
(AtbZIP, bZIP, AT1G68880) transcription factor gene is up-regulated in CcCDR-transgenic plants Arabidopsis thaliana
(LEA, AT2G21490) gene is up-regulated in CcCDR-transgenic plants Arabidopsis thaliana
rapidly expressed genes following mechanical stress include (STZ, ZAT10, AT1G27730)
Arabidopsis plants overexpressing (ATCPK23, CPK23, GCA2, AT4G04740) show enhanced sensitivity toward abiotic salt stress and drought conditions Arabidopsis thaliana
OsFKBP20-1b-mediated RNA processing contributes to stress adaptation Oryza sativa
submergence treatment showing most notable rise in MACC levels compared with control Arabidopsis thaliana
DEGs overlapping with environmentally linked DMRs mainly related to plant growth, response to pathogens and abiotic stresses Fragaria vesca
early responses to various abiotic stresses clustered together independent of later responses Arabidopsis thaliana
O-acetylated rhamnogalacturonan-I (RG-I) plays a role in abiotic stress responses Arabidopsis thaliana
significant increase in ACC enhanced throughout 3 h time course Arabidopsis thaliana
(ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) (ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA1E, HSFA1E, AT3G02990) exhibits subfunctionalization in diverse abiotic stress responses Arabidopsis thaliana
(AtCYS2, CYS2, AT2G31980) /His2 zinc finger proteins play important roles in responses to abiotic stresses
ethylene well-known involvement in abiotic stress responses
severe drought stress (30% FWC) increases free proline content in leaves Medicago truncatula
stomatal size (SS) requires compromise in choosing to tackle multiple future environmental stresses Oryza sativa
drought stress is one of diverse abiotic stress conditions Arabidopsis thaliana
cytokinins are important regulators of plant response to abiotic stresses
high temperature causes crop losses
root elongation inhibited by 0.5 µm abscisic acid (ABA) or 150 mm NaCl or polyethylene glycol treatment Oryza sativa
differentially expressed genes in BiP-overexpressing leaves show overrepresentation of abiotic stress-responsive genes (13%) Glycine max
major cluster of 288 genes are generally only weakly induced by cold, drought, oxidative, UV-B, genotoxic, wound, or heat stress
mature trichomes contain genes involved in abiotic stress response Arabidopsis thaliana
flooding causes crop losses
seed and fruit set is vulnerable to abiotic stress
(AtCPK21, CPK21, AT4G04720) mutant plants show increased stress responses with respect to metabolite accumulation Arabidopsis thaliana
specific mutant allele of (ATCPK23, CPK23, GCA2, AT4G04740) show enhanced tolerance Arabidopsis thaliana
stomatal size (SS) contributes to rice abiotic stress resilience Oryza sativa
Arabidopsis wild-type (WT) and various ACC-biosynthesis mutants were analyzed under abiotic stress Arabidopsis thaliana
ACC concentrations exhibited slight yet nonsignificant increase under osmotic and wounding stresses Arabidopsis thaliana
MADS-box transcription factors (MADS-box TFs) may affect abiotic stress tolerance through phosphorylation or dephosphorylation
Plant Raf-like MAPKKKs phosphorylate SNF1-related protein kinase 2s
MYB transcription factors are related to abiotic stress responses
free proline content is plant abiotic stress marker
Salinity and dehydration treatment significantly reduces root growth Oryza sativa
jasmonates is related to abiotic stresses
ATLs participate in abiotic stress responses Arabidopsis thaliana
short-term wounding treatment performed to investigate rapid ACC response Arabidopsis thaliana
Salinity and dehydration treatment has similar effects to abscisic acid (ABA) treatment Oryza sativa
numbers of lateral roots increased by 0.5 µm abscisic acid (ABA) or 150 mm NaCl or polyethylene glycol treatment Oryza sativa
salt stress is one of diverse abiotic stress conditions Arabidopsis thaliana
ROS transcriptome signature of abiotic stresses showed limited correlation to a few indices Arabidopsis thaliana
GIGANTEA (GI) modulates abiotic stress pathway
salinity stress induces H2O2 accumulation Arabidopsis thaliana
action of (NAA10, AT5G13780) in abiotic stress response is dependent on OsHYPK function Oryza sativa
mannitol is accumulated in response to abiotic stresses
MYB transcription factors (TFs) are regulated by abscisic acid (ABA) Arabidopsis thaliana
TaCHP overexpression line in JN17 cultivar improves performance in salinity stress tolerance Triticum aestivum
stress-inducible over-expression of (ATCBF3, CBF3, DREB1A, AT4G25480) may have the potential to enhance abiotic stress tolerance Avena sativa
OsiSAP8 is induced by salinity stress Oryza sativa
transgenic Arabidopsis lines expressing (ATCDPK3, ATCPK6, CPK6, AT2G17290) under control of double CaMV 35S promoter show increased tolerance to drought and salt stress Arabidopsis thaliana
abscisic acid (ABA) is involved in response to salinity
localization of OsFKBP20-1b changes in response to abiotic stress Nicotiana benthamiana
exogenous SA treatment could not restore abiotic stress sensitivity phenotype of Oswrky45 mutant Oryza sativa
up- or down-regulated genes show altered expression levels in response to various stress stressors Arabidopsis thaliana
(ATVOZ1, VOZ1, AT1G28520) and (ATVOZ2, VOZ2, AT2G42400) (VOZs) function as negative regulator of abiotic stress-responsive pathway Arabidopsis thaliana
IbZFP1 gene has potential to be used to enhance tolerance to abiotic stresses in plants
(ATMYB121, MYB121, AT3G30210) mutant displays compromised tolerance to salt stress Arabidopsis thaliana
IbZFP1 confers salt and drought tolerance Arabidopsis thaliana
(AtZAT12, RHL41, ZAT12, AT5G59820) promoter-luciferase fusion demonstrates (AtZAT12, RHL41, ZAT12, AT5G59820) expression activation at transcriptional level during abiotic stresses Arabidopsis thaliana
FaBG3 -RNAi-treated fruit with reduced ABA levels are more sensitive to dehydration stress Fragaria × ananassa
stress-inducible over-expression of (ATCBF3, CBF3, DREB1A, AT4G25480) may have the potential to enhance abiotic stress tolerance in oat Avena sativa
WRKY transcription factors (TFs) play critical roles in oxidative stress response
post-transcriptional regulation includes miRNA- and siRNA-mediated RNA turnover
(AtcPT5, AtHEPS, cPT5, HEPS, AT5G58780) and its product might function in response to abiotic stresses Arabidopsis thaliana
transcription factor activation is important plant response to abiotic stress
Arabidopsis (TIP41, AT4G34270) showed transient upregulation following long-term NaCl, ABA or PEG treatment Arabidopsis thaliana
potentially toxic-free fatty acids released from membrane remodeling are channeled to LD
zinc finger ( (AtZAT6, C2H2, CZF2, ZAT6, AT5G04340) type) protein gene is up-regulated in CcCDR-transgenic plants Arabidopsis thaliana
abscisic acid (ABA) mediates cold temperature stress response
SlPPI1 mRNA levels are increased by cold stress Solanum lycopersicum
β-hydroxy-pyruvic acid indicates crucial role of pyruvate during abiotic stress Arabidopsis thaliana
(ATMYB121, MYB121, AT3G30210) mutant displays compromised tolerance to polyethylene glycol (PEG)-mediated osmotic stress Arabidopsis thaliana
TaMCU3-A gene is involved in drought stress response Triticum aestivum
ZmbZIP76 upregulates expression of abiotic stress-responsive genes Zea mays
StPPI1 is induced by salt stress Solanum tuberosum L.
signal exchange between plant roots and PGPR modulates plant abiotic stress responses
GRAS domain proteins are involved in abiotic stresses Echinochloa
DC1 (ECT12) plays a role in abiotic stress responses Arabidopsis thaliana
SlPPI1 mRNA levels are increased by drought stress Solanum lycopersicum
(bHLH, AT5G51780) proteins function in plant responses to abiotic stresses
OsSRO1c is most stress responsive of all SRO genes in rice Oryza sativa
SlPPI1 mRNA levels are unaffected by salt stress Solanum lycopersicum
(SUT1, AT5G63020) was up-regulated in response to drought and salt stress in all four tested monocot species
genes responding to abiotic stress are highly expressed in gl3–sst (SIM, AT5G04470) trichomes Arabidopsis thaliana
(ERF113, RAP2.6, AT1G43160) is one of 16 most responsive genes towards diverse abiotic stresses (MSTR genes) Arabidopsis thaliana
phytochemical compounds function in protection against abiotic stressors
SA plays important role in plant response to salt, drought, and cold stresses
NAC DOMAIN-CONTAINING PROTEIN102 (ANAC102, NAC102, AT5G63790) has been previously characterized as having a role in abiotic stress responses Arabidopsis thaliana
ETHYLENE RECEPTOR 2 (ETR2, AT3G23150) have contrasting roles in response to abscisic acid (ABA) Arabidopsis thaliana
RD29A:LUC transgene responds to 300 mM NaCl Arabidopsis thaliana
anthocyanins participate in defence response to abiotic stress
(SUT1, AT5G63020) and (ATSUC4, ATSUT4, SUC4, SUT4, AT1G09960) expression pattern in response to drought and salt stress did not depend on severity of the applied stress
HIPPs act in regulating the transcriptional response to abiotic stress Arabidopsis thaliana
ids1-1 seedlings had expression levels of abiotic stress-responsive genes significantly increased in abiotic stress-responsive genes Oryza sativa
meta-analysis of abiotic stresses identified differentially expressed genes (DEGs)
up-regulated genes in msi1-cs plants usually respond to fewer abiotic stresses
transcript profiling data for abiotic stress response obtained from AtGenExpress dataset Arabidopsis thaliana
Grain number, plant height, and heading date7 (Ghd7) is involved in the regulation of abiotic stress response Oryza sativa
(ATSUC4, ATSUT4, SUC4, SUT4, AT1G09960) is up-regulated under all three types of stress Arabidopsis thaliana
(ERD14, AT1G76180) likely plays role in responding to abiotic stresses such as dehydration Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) likely plays role in responding to abiotic stresses such as dehydration Arabidopsis thaliana
Stress-associated proteins (SAP) play crucial role in response to abiotic stresses Arabidopsis thaliana
VIGS-RiMsn2-RNAi lines have higher free proline content in leaves Nicotiana benthamiana
ethylene is related to abiotic stresses
ROSMETER platform was applied to identify ROS signatures profiles in transcriptomes of plants exposed to abiotic stresses Arabidopsis thaliana
(ATSUC9, SUC9, AT5G06170) has been linked to abiotic stress resistance Arabidopsis thaliana
ETHYLENE RECEPTOR 2 (ETR2, AT3G23150) have contrasting roles under conditions that inhibit germination Arabidopsis thaliana
(ERD10, LTI29, LTI45, AT1G20450) likely plays role in responding to abiotic stresses such as dehydration Arabidopsis thaliana
(RD19, RD19A, AT4G39090) likely plays role in responding to abiotic stresses such as dehydration Arabidopsis thaliana
INDOLE-3-ACETIC ACID-LEUCINE RESISTANT3 (bHLH105, ILR3, AT5G54680) has been previously characterized as having a role in abiotic stress responses Arabidopsis thaliana
MdSAT1 transcription is particularly induced by drought stress Malus domestica