The Arabidopsis ETHYLENE RESPONSE FACTOR1 regulates abiotic stress-responsive gene expression by binding to different cis-acting elements in response to different stress signals.
about
Exploring Jasmonates in the Hormonal Network of Drought and Salinity ResponsesThe Role of Ethylene in Plants Under Salinity Stress.Circadian regulation of abiotic stress tolerance in plantsEthylene responsive factors in the orchestration of stress responses in monocotyledonous plantsNetwork Candidate Genes in Breeding for Drought Tolerant CropsStress-Mediated cis-Element Transcription Factor Interactions Interconnecting Primary and Specialized Metabolism in plantaArabidopsis ERF1 Mediates Cross-Talk between Ethylene and Auxin Biosynthesis during Primary Root Elongation by Regulating ASA1 ExpressionGmCYP82A3, a Soybean Cytochrome P450 Family Gene Involved in the Jasmonic Acid and Ethylene Signaling Pathway, Enhances Plant Resistance to Biotic and Abiotic StressesA novel bioinformatics pipeline to discover genes related to arbuscular mycorrhizal symbiosis based on their evolutionary conservation pattern among higher plantsAssessing reference genes for accurate transcript normalization using quantitative real-time PCR in pearl millet [Pennisetum glaucum (L.) R. Br]Bacteria-triggered systemic immunity in barley is associated with WRKY and ETHYLENE RESPONSIVE FACTORs but not with salicylic acid.The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat.Cadmium-induced ethylene production and responses in Arabidopsis thaliana rely on ACS2 and ACS6 gene expression.The AP2/ERF transcription factor SlERF52 functions in flower pedicel abscission in tomato.Abscisic acid regulates root growth under osmotic stress conditions via an interacting hormonal network with cytokinin, ethylene and auxin.Genomic Selection for Drought Tolerance Using Genome-Wide SNPs in MaizeExpression patterns of members of the ethylene signaling-related gene families in response to dehydration stresses in cassava.Variable Level of Dominance of Candidate Genes Controlling Drought Functional Traits in Maize Hybrids.A step-by-step protocol for formaldehyde-assisted isolation of regulatory elements from Arabidopsis thaliana.Identification of candidate genes involved in early iron deficiency chlorosis signaling in soybean (Glycine max) roots and leaves.Genome-wide analysis of the distribution of AP2/ERF transcription factors reveals duplication and CBFs genes elucidate their potential function in Brassica oleracea.Identification of potential transcriptional regulators of actinorhizal symbioses in Casuarina glauca and Alnus glutinosa.The ethylene response factor Pti5 contributes to potato aphid resistance in tomato independent of ethylene signallingIsolation and characterization of six AP2/ERF transcription factor genes in Chrysanthemum nankingense.Isolation and functional characterization of the promoter of a DEAD-box helicase Psp68 using Agrobacterium-mediated transient assay.Functional mechanisms of drought tolerance in subtropical maize (Zea mays L.) identified using genome-wide association mapping.Ethylene Response Factors Are Controlled by Multiple Harvesting Stresses in Hevea brasiliensisSubstantial reprogramming of the Eutrema salsugineum (Thellungiella salsuginea) transcriptome in response to UV and silver nitrate challenge.Cysteine-rich receptor-like kinase CRK5 as a regulator of growth, development, and ultraviolet radiation responses in Arabidopsis thalianaImplications of ethylene biosynthesis and signaling in soybean drought stress tolerance.De novo transcriptome analysis of Medicago falcata reveals novel insights about the mechanisms underlying abiotic stress-responsive pathwayComparative miRNAs analysis of Two contrasting broccoli inbred lines with divergent head-forming capacity under temperature stress.Transcriptome Analysis of Salt Stress Responsiveness in the Seedlings of Dongxiang Wild Rice (Oryza rufipogon Griff.).Identification of Multiple Stress Responsive Genes by Sequencing a Normalized cDNA Library from Sea-Land Cotton (Gossypium barbadense L.).Origination, Expansion, Evolutionary Trajectory, and Expression Bias of AP2/ERF Superfamily in Brassica napus.Differences and commonalities of plant responses to single and combined stresses.Overexpression of Hevea brasiliensis ethylene response factor HbERF-IXc5 enhances growth, tolerance to abiotic stress and affects laticifer differentiation.Whole Plant Temperature Manipulation Affects Flavonoid Metabolism and the Transcriptome of Grapevine Berries.An Ethylene-responsive Factor BpERF11 Negatively Modulates Salt and Osmotic Tolerance in Betula platyphylla.Ethylene positively regulates cold tolerance in grapevine by modulating the expression of ETHYLENE RESPONSE FACTOR 057.
P2860
Q26773101-EC46E162-AB17-43BE-8330-346D96FCB43FQ26774103-1F6B8837-4BCB-4390-A8D3-067A0BA5ADC9Q26784438-D9252EE6-F21A-42E0-838A-48D3ADD4D71BQ26784443-A58E2999-01FC-4A28-A581-3DB2ACBF88EEQ26801780-16A55464-FB3B-49C4-9685-A5BED50E2BEEQ28068326-2B196CA3-6087-4B57-A0DD-4DF0C9444A19Q28552215-9174B0AD-3D3F-44A0-90D1-8AD18D858C1AQ28553879-DA9B7DE2-477B-4A8E-97AB-89B8A79C6D8AQ28649408-07AE8295-A363-48E3-81D8-ACB0117C05E3Q28656289-5E27C1B7-425D-414D-9163-32421F8DB106Q30317010-CF8387EB-BFD8-43D2-BF2E-EEAE2A136155Q30391565-210DED44-BC94-44A3-8372-45B4613DB31CQ30425657-B5403462-9F3D-45F5-BD12-E1963DED5541Q33358284-270EAF28-82A7-4B71-9193-8BB0CAD90711Q33362607-88FCEAC1-EA24-40E9-B197-1D667992D0ADQ33588719-95B38BA6-5F3D-4611-A270-2AC7D44C3B3CQ33719065-A40937F6-7D0D-4C1E-AFCE-D1803ED0E585Q33780645-E76FEE55-7F37-4729-A377-7D082B91B754Q34039464-AF11B2EA-5D6B-4FB3-BFA3-08BB34F569DCQ34169138-35D44CBA-F56A-4127-91AE-DAEFF33DF205Q34500532-758069FA-ACB0-46C6-B8F8-81A0367D38A3Q34686583-72D50582-EC15-4FD2-804F-FB6262AEB715Q34859590-71848710-BFD9-4923-9E30-18F23D7897EFQ35016712-2B497CC2-9139-4C09-BFAB-AB5182F5D405Q35160680-887506F1-2993-459F-9496-46B235357F53Q35200856-45A4310F-6D39-49A0-A9E0-EE304BAE01E2Q35533030-91E11C31-4179-4A7E-B54E-8CCBDD7CACF9Q35660547-057D78F2-C4BB-4726-A460-C74DAF820E2BQ35666829-FF6E61B7-4DCF-4875-BB9F-D13E35FEAC18Q35763540-FB8B2577-8195-465C-8416-233BCC4B3A5EQ35813351-CEFEA898-6BCB-4C55-80CE-359DF044A488Q35857509-7E291974-9B71-479A-9758-FBA53671ECC3Q35890530-A0F80F46-698F-4747-BA9A-1D3CFD673CECQ35975079-088536A4-FE6A-4D87-88CB-2305482CE1E5Q36115583-D13FFAAE-B03D-4F1D-8F04-B86D31B50356Q36332665-6099E024-5EC3-4AE9-858E-47496D1FB579Q36408710-11E66F56-7D53-4CE6-A105-0A84D285D2BDQ36410859-0628F38A-DAE0-4D95-9AE1-4EA14875D731Q36691225-7A6B1F15-C4DF-4B02-85EC-465BD02DAD48Q36760617-AE1D986D-D10D-465A-BC4E-58232949F7E1
P2860
The Arabidopsis ETHYLENE RESPONSE FACTOR1 regulates abiotic stress-responsive gene expression by binding to different cis-acting elements in response to different stress signals.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh
2013年學術文章
@zh-hant
name
The Arabidopsis ETHYLENE RESPO ...... e to different stress signals.
@en
type
label
The Arabidopsis ETHYLENE RESPO ...... e to different stress signals.
@en
prefLabel
The Arabidopsis ETHYLENE RESPO ...... e to different stress signals.
@en
P2093
P2860
P356
P1433
P1476
The Arabidopsis ETHYLENE RESPO ...... se to different stress signals
@en
P2093
Mei-Chun Cheng
Po-Ming Liao
Wei-Wen Kuo
P2860
P304
P356
10.1104/PP.113.221911
P407
P577
2013-05-29T00:00:00Z