Transgenic tobacco plants with reduced capability to detoxify reactive oxygen intermediates are hyperresponsive to pathogen infection
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Strategies to increase vitamin C in plants: from plant defense perspective to food biofortificationHydrogen peroxide acts as a second messenger for the induction of defense genes in tomato plants in response to wounding, systemin, and methyl jasmonateOverexpression of the wheat aquaporin gene, TaAQP7, enhances drought tolerance in transgenic tobaccoPlant Tolerance: A Unique Approach to Control Hemipteran PestsSuperoxide production by plant homologues of the gp91(phox) NADPH oxidase. Modulation of activity by calcium and by tobacco mosaic virus infectionEnzymes that scavenge reactive oxygen species are down-regulated prior to gibberellic acid-induced programmed cell death in barley aleuroneA candidate RxLR effector from Plasmopara viticola can elicit immune responses in Nicotiana benthamiana.Small RNA sequencing reveals a role for sugarcane miRNAs and their targets in response to Sporisorium scitamineum infectionComparative transcriptional profiling-based identification of raphanusanin-inducible genes.Identification and characterization of genes associated with tapping panel dryness from Hevea brasiliensis latex using suppression subtractive hybridization.Secret lifestyles of Neurospora crassa.A custom microarray analysis of gene expression during programmed cell death in Arabidopsis thaliana.Active oxygen species as mediators of plant immunity: three case studies.A global view of transcriptome dynamics during Sporisorium scitamineum challenge in sugarcane by RNA-Seq.Are diverse signalling pathways integrated in the regulation of arabidopsis antioxidant defence gene expression in response to excess excitation energy?ROS signaling in the hypersensitive response: when, where and what for?Catalase-deficient tobacco plants: tools for in planta studies on the role of hydrogen peroxide.Arabidopsis nonhost resistance gene PSS1 confers immunity against an oomycete and a fungal pathogen but not a bacterial pathogen that cause diseases in soybeanReactive oxygen species in plant cell death.Essential role of the small GTPase Rac in disease resistance of riceHydrogen peroxide and nitric oxide as signalling molecules in plants.Transcriptional profile of sweet orange in response to chitosan and salicylic acidPeroxisome biogenesis and function.The rice thylakoid membrane-bound ascorbate peroxidase OsAPX8 functions in tolerance to bacterial blight.Metabolic engineering of plant L-ascorbic acid biosynthesis: recent trends and applications.TaTypA, a Ribosome-Binding GTPase Protein, Positively Regulates Wheat Resistance to the Stripe Rust Fungus.Overexpression of the soybean GmERF3 gene, an AP2/ERF type transcription factor for increased tolerances to salt, drought, and diseases in transgenic tobaccoClass III peroxidases in plant defence reactions.Application of proteomics to investigate stress-induced proteins for improvement in crop protection.A Microsomal Proteomics View of H₂O₂- and ABA-Dependent Responses.Nucleoredoxin guards against oxidative stress by protecting antioxidant enzymes.Functional analysis of oxidative burst in sugarcane smut-resistant and -susceptible genotypes.Attenuation of Drought Stress in Brassica Seedlings with Exogenous Application of Ca2+ and H₂O₂.An Arabidopsis glutathione peroxidase functions as both a redox transducer and a scavenger in abscisic acid and drought stress responses.Enhanced tolerance to environmental stress in transgenic plants expressing the transcriptional coactivator multiprotein bridging factor 1c.The Intracellular Immune Receptor Sw-5b Confers Broad-spectrum Resistance to Tospoviruses through Recognition of a Conserved 21-amino-acid Viral Effector Epitope.Molecular cloning and characterization of two manganese superoxide dismutases from Miscanthus × giganteus.Changes in the antioxidant systems as part of the signaling pathway responsible for the programmed cell death activated by nitric oxide and reactive oxygen species in tobacco Bright-Yellow 2 cells.Upregulation of jasmonate biosynthesis and jasmonate-responsive genes in rice leaves in response to a bacterial pathogen mimic.Capsicum annuum tobacco mosaic virus-induced clone 1 expression perturbation alters the plant's response to ethylene and interferes with the redox homeostasis.
P2860
Q21129209-269D6C54-B9AF-4317-A887-89B72B1852A6Q24515240-6C11D4B4-F946-4910-A301-C6EAE903E2E7Q27324700-8B146374-FA41-4375-9AC0-C62F894F3C98Q28072333-B8020D28-5EF8-4E5D-BB41-2A42DA228ACEQ28344252-DDD4ED6E-D4EE-4E9D-9A03-26ECAF5CEB88Q28365098-2D930A98-4DA8-4420-9E57-1B0BEAF6A6FEQ33564403-0B64FF14-2162-433E-BC65-063A22E62BC7Q33602105-9AF2B03A-E0A0-4505-8EB2-DB5183B06597Q33606231-3E1FE2D3-CA96-4B50-B5E1-CDC3332E5C54Q33629378-37C8D01A-A2D2-42B0-B0B1-712CC5BD61A3Q33687069-B7400CA5-780A-4FD0-9B39-ED79635559AFQ33959313-45AC520A-47F7-4C3D-91C8-3CAFE19515E0Q34059325-CE07793F-C5AE-46DC-9BE1-649E75FB4A32Q34110656-4F377101-EABE-4F85-A2F8-E4119B2B9E66Q34112071-A2CBB5D2-CE18-4CF6-8DE1-322A4DC4B2D6Q34219392-570DBB37-B670-47C2-B1E6-C3E5E7650B1CQ34238904-C32D6BDD-CDCE-46A0-A1CB-FC3AE264557AQ34303064-DCF1DDB4-921B-47C4-A531-B5D91C7E6E58Q34535881-DC8959A4-A04E-4734-A308-6947179BA826Q34627419-7E4348F1-6C25-40A1-8DB0-C2667A99E065Q34629051-07B7ED12-6F3C-40F1-A9B3-F978B1BC5124Q35607899-8E8BF36F-D93F-42AE-B381-E1F9D5E4F897Q35625778-33895934-EDB5-4149-934B-26D0AC09339DQ36906456-CED7D0AC-CD62-4CFC-B1A3-080C3103AD66Q36937984-4EFC36E0-F842-4B17-8CB2-A1B2A16C3C14Q37022990-9C0301E0-0637-4C4E-9E84-3693A146DEBCQ37330875-1C34AE57-78CD-40E0-832D-5AC6CFF66302Q37346636-8B10F971-2549-4F73-A449-05A41193910BQ37834447-CB0D4F06-3CD2-44BB-ABB4-B5439874541CQ38371944-F4828BD6-D2D2-4004-BF28-DD5B1661AC95Q38671453-38839E52-8E2F-456F-A0BD-1A137E101B97Q39076198-7402A811-B98F-4EEA-9056-558CC8B313C8Q39132030-94E03754-2CED-45C8-A9B4-B66DFF2722D3Q39249324-68F7575E-D754-461B-8A37-E95CDB270EF5Q39500869-BEBFCE24-EDE1-4911-B609-895633C800FCQ40080815-EAC8BF1D-880C-4C12-8A00-2D7B924A4D30Q40580220-0A711B88-C25B-43A6-AB6D-2C6729884CFEQ40697999-46419808-0E3C-4379-A375-180154D0F0CAQ41600962-A6AEAE0D-FDCE-4E44-B8F5-87AE8CE076E2Q42031142-F4F6E250-17D6-4961-84F1-424ADC59BBDE
P2860
Transgenic tobacco plants with reduced capability to detoxify reactive oxygen intermediates are hyperresponsive to pathogen infection
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Transgenic tobacco plants with ...... sponsive to pathogen infection
@ast
Transgenic tobacco plants with ...... sponsive to pathogen infection
@en
type
label
Transgenic tobacco plants with ...... sponsive to pathogen infection
@ast
Transgenic tobacco plants with ...... sponsive to pathogen infection
@en
prefLabel
Transgenic tobacco plants with ...... sponsive to pathogen infection
@ast
Transgenic tobacco plants with ...... sponsive to pathogen infection
@en
P2093
P2860
P356
P1476
Transgenic tobacco plants with ...... sponsive to pathogen infection
@en
P2093
Willekens H
van Camp W
P2860
P304
14165-14170
P356
10.1073/PNAS.96.24.14165
P407
P577
1999-11-01T00:00:00Z