Gene regulation during cold stress acclimation in plants.
about
Abscisic Acid and Abiotic Stress Tolerance in Crop PlantsA central role for thiols in plant tolerance to abiotic stressStress-Mediated cis-Element Transcription Factor Interactions Interconnecting Primary and Specialized Metabolism in plantaChinese wild-growing Vitis amurensis ICE1 and ICE2 encode MYC-type bHLH transcription activators that regulate cold tolerance in ArabidopsisA proteome analysis of freezing tolerance in red clover (Trifolium pratense L.)Identification of Differentially Expressed Genes in Chilling-Induced Potato (Solanum tuberosum L.); a Data Analysis Study.Global transcriptome profiles of Camellia sinensis during cold acclimationDeep-sequencing transcriptome analysis of low temperature perception in a desert tree, Populus euphratica.The function of OsbHLH068 is partially redundant with its homolog, AtbHLH112, in the regulation of the salt stress response but has opposite functions to control flowering in Arabidopsis.Transcriptome sequencing and identification of cold tolerance genes in hardy Corylus species (C. heterophylla Fisch) floral budsA transcriptomic analysis of Chrysanthemum nankingense provides insights into the basis of low temperature tolerance.Identification and characterization of cold-responsive microRNAs in tea plant (Camellia sinensis) and their targets using high-throughput sequencing and degradome analysisAdaptation of grapevine flowers to cold involves different mechanisms depending on stress intensity.Chilling acclimation provides immunity to stress by altering regulatory networks and inducing genes with protective functions in cassavaGenome wide transcriptional profile analysis of Vitis amurensis and Vitis vinifera in response to cold stress.Transcriptome analysis in sheepgrass (Leymus chinensis): a dominant perennial grass of the Eurasian Steppe.Ambient temperature enhanced freezing tolerance of Chrysanthemum dichrum CdICE1 Arabidopsis via miR398.MicroRNA319 positively regulates cold tolerance by targeting OsPCF6 and OsTCP21 in rice (Oryza sativa L.).Transcriptional profiling of Petunia seedlings reveals candidate regulators of the cold stress response.Differential protein expression in Phalaenopsis under low temperature.Deep sequencing-based characterization of transcriptome of trifoliate orange (Poncirus trifoliata (L.) Raf.) in response to cold stress.De novo transcriptome profiling of cold-stressed siliques during pod filling stages in Indian mustard (Brassica juncea L.).Temperature expression patterns of genes and their coexpression with LncRNAs revealed by RNA-Seq in non-heading Chinese cabbageChloroplast RNA-Binding Protein RBD1 Promotes Chilling Tolerance through 23S rRNA Processing in ArabidopsisDe Novo Assembly and Transcriptome Analysis of Bulb Onion (Allium cepa L.) during Cold Acclimation Using Contrasting Genotypes.De novo transcriptome sequencing and gene expression profiling of Elymus nutans under cold stress.Identification of Mild Freezing Shock Response Pathways in Barley Based on Transcriptome Profiling.Cross-talk between freezing response and signaling for regulatory transcriptions of MIR475b and its targets by miR475b promoter in Populus suaveolensCold signaling and cold response in plantsTransgenic barley lines prove the involvement of TaCBF14 and TaCBF15 in the cold acclimation process and in frost toleranceCloning and characterization of cold, salt and drought inducible C-repeat binding factor gene from a highly cold adapted ecotype of Lepidium latifolium L.High-Throughput MicroRNA and mRNA Sequencing Reveals That MicroRNAs May Be Involved in Melatonin-Mediated Cold Tolerance in Citrullus lanatus L.Differential Coexpression Analysis Reveals Extensive Rewiring of Arabidopsis Gene Coexpression in Response to Pseudomonas syringae Infection.Molecular and functional characterization of cold-responsive C-repeat binding factors from Brachypodium distachyon.Improved cold tolerance in Elymus nutans by exogenous application of melatonin may involve ABA-dependent and ABA-independent pathwaysRNA-seq Analysis of Cold and Drought Responsive Transcriptomes of Zea mays ssp. mexicana L.Gene Expression, Protein Function and Pathways of Arabidopsis thaliana Responding to Silver Nanoparticles in Comparison to Silver Ions, Cold, Salt, Drought, and Heat.Coping with stresses: roles of calcium- and calcium/calmodulin-regulated gene expression.Physiological and molecular changes in plants grown at low temperatures.Nitric oxide-cold stress signalling cross-talk, evolution of a novel regulatory mechanism.
P2860
Q26747353-58E6B067-060F-4B7D-96C8-87F171C4668EQ27027679-68EF7427-2AA2-4045-9CE1-C6E1E1A08A32Q28068326-882B0287-D1CD-45C4-A491-56197BCB1890Q28540679-6CB0AC81-AACD-4224-B556-A53F2EEF6223Q28602822-4BCF2785-FA91-4C52-957C-F82A1DAC1019Q30986310-E5767825-47C4-4223-93EB-DEDDEF6271DDQ31121707-592D45DE-8765-4E9C-9086-B45A9CD929AAQ33669150-A6CA202D-E778-40C4-A94E-6C0E43A74904Q33890599-AF1A7587-0AFC-40CB-826C-127A8E8B07BAQ34277379-953B1726-04F2-49FE-B699-2F5D224DF765Q34340151-DC64F95E-ECA8-4200-9BE1-03E49FC13222Q34402101-AF0B7956-CCC8-4687-9F63-975B84D9733CQ34447702-612A8F16-0DB4-400D-A673-00731F51B947Q34539235-6A1FD5E3-9039-4D84-BB93-AA340BFF4DD8Q34629966-67266198-584F-4812-9ABD-00684AD70F68Q34826631-DF200B7F-B372-47B8-8285-C2AD84719933Q35071428-37CAD544-8989-437E-8278-7F2726100ABAQ35131009-F703ED90-1203-4484-B2CA-B8750B73EAD8Q35135435-4C9AF37F-06D8-4BF1-A73C-67E715283E88Q35370119-83383E18-96BE-487D-A1B9-62CEA35ABD98Q35721140-41E6ED51-CE68-49E2-90C3-BEEC5069CD6EQ35844714-C09912AA-903F-48BA-91FD-943F603A8CFDQ35996650-3643EA07-A268-450B-96E3-BD7542BE5B45Q36006521-7A2448C4-FF73-4056-B520-59C02FFF9AD8Q36132730-EAB916B6-2EDF-492E-A866-B1E2C14353B0Q36183138-E70C9D54-8C00-452D-9F13-08D0ADE8BC00Q36554985-B413C875-5D78-4AB1-BCD3-12623565B7AAQ36555569-DEB4A40E-CC1F-47C5-9C39-27563739723EQ36790491-90B4AB3B-7E8E-4AE4-9A24-865E3D2F28B4Q36802507-398A3287-A1A1-4564-B1A7-3F14F55B2A50Q36850015-61FFFDF8-C61E-435C-BA74-566D557682F8Q37172438-60B8FB99-5D96-422D-A3BE-16769B9DCE62Q37323863-22391AC3-605C-48A9-9EB2-1660DF4D75B7Q37501460-932186E6-DA2F-4285-A88A-18420F54826BQ37550138-551B324B-19B4-4DEC-9108-A5C0A63CD110Q37627074-ABBB5A4C-6F25-4FFD-B65B-7BAB9F82F173Q37646361-86FC07C7-EB5B-46FD-B4A5-B35ED047A27AQ37885101-9B91F062-D0D7-4E27-A4CE-07107F858128Q38004808-530B290B-427F-47E7-BB61-169EF4C11CE5Q38098491-BB2F740F-71C5-45CD-926A-56A07635EE5B
P2860
Gene regulation during cold stress acclimation in plants.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh
2010年學術文章
@zh-hant
name
Gene regulation during cold stress acclimation in plants.
@en
type
label
Gene regulation during cold stress acclimation in plants.
@en
prefLabel
Gene regulation during cold stress acclimation in plants.
@en
P2093
P2860
P1476
Gene regulation during cold stress acclimation in plants.
@en
P2093
Jian-Kang Zhu
Ramanjulu Sunkar
Viswanathan Chinnusamy
P2860
P356
10.1007/978-1-60761-702-0_3
P407
P577
2010-01-01T00:00:00Z