scholarly article | Q13442814 |
P2093 | author name string | Yan-Jie Wang | |
Tadao Asami | |||
Kai Shi | |||
Zhixiang Chen | |||
Jing-Quan Yu | |||
Xiao-Jian Xia | |||
Yan-Hong Zhou | |||
Yuan Tao | |||
Wei-Hua Mao | |||
P2860 | cites work | A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 |
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 | ||
Hydrogen peroxide is involved in abscisic acid-induced stomatal closure in Vicia faba | Q28345872 | ||
Reactive oxygen species: metabolism, oxidative stress, and signal transduction | Q29547615 | ||
The LKA gene is a BRASSINOSTEROID INSENSITIVE 1 homolog of pea | Q33195017 | ||
Loss of function of a rice brassinosteroid insensitive1 homolog prevents internode elongation and bending of the lamina joint | Q33334966 | ||
Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants | Q33893345 | ||
Chlorophyll fluorescence--a practical guide | Q33913359 | ||
Promotive effect of brassinosteroids on cell division involves a distinct CycD3-induction pathway in Arabidopsis | Q33928675 | ||
A putative leucine-rich repeat receptor kinase involved in brassinosteroid signal transduction | Q34065165 | ||
The GSK3-like kinase BIN2 phosphorylates and destabilizes BZR1, a positive regulator of the brassinosteroid signaling pathway in Arabidopsis | Q34099624 | ||
BRASSINOSTEROIDS: Essential Regulators of Plant Growth and Development | Q34304462 | ||
Regulation of brassinosteroid signaling by a GSK3/SHAGGY-like kinase | Q34521124 | ||
BRI1/BAK1, a receptor kinase pair mediating brassinosteroid signaling | Q34525831 | ||
BAK1, an Arabidopsis LRR receptor-like protein kinase, interacts with BRI1 and modulates brassinosteroid signaling | Q34525838 | ||
Brassinosteroids and plant steroid hormone signaling. | Q34667514 | ||
Hydrogen peroxide signalling | Q34787005 | ||
The role of abscisic acid in plant-pathogen interactions. | Q36154037 | ||
Functions of the respiratory burst oxidase in biotic interactions, abiotic stress and development | Q36154041 | ||
Signal crosstalk and induced resistance: straddling the line between cost and benefit | Q36217898 | ||
Crosstalk between abiotic and biotic stress responses: a current view from the points of convergence in the stress signaling networks | Q36499476 | ||
Reactive oxygen species as signals that modulate plant stress responses and programmed cell death | Q36623806 | ||
A role of brassinosteroids in early fruit development in cucumber | Q36712201 | ||
Networks of WRKY transcription factors in defense signaling. | Q36888216 | ||
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) function as transcriptional activators in abscisic acid signaling | Q38856598 | ||
Brassinosteroid confers tolerance in Arabidopsis thaliana and Brassica napus to a range of abiotic stresses. | Q39115187 | ||
Brassinosteroid-Mediated Stress Responses | Q39148500 | ||
OXI1 kinase is necessary for oxidative burst-mediated signalling in Arabidopsis | Q42457720 | ||
Brassinosteroids rescue the deficiency of CYP90, a cytochrome P450, controlling cell elongation and de-etiolation in Arabidopsis. | Q42628760 | ||
Nuclear protein phosphatases with Kelch-repeat domains modulate the response to brassinosteroids in Arabidopsis | Q43182368 | ||
BRI1 is a critical component of a plasma-membrane receptor for plant steroids | Q43553702 | ||
Selective interaction of triazole derivatives with DWF4, a cytochrome P450 monooxygenase of the brassinosteroid biosynthetic pathway, correlates with brassinosteroid deficiency in planta | Q43586328 | ||
Development of necrosis and activation of disease resistance in transgenic tobacco plants with severely reduced catalase levels. | Q43733109 | ||
Brassinosteroid-regulated gene expression | Q44062038 | ||
Brassinosteroid functions to protect the translational machinery and heat-shock protein synthesis following thermal stress | Q44083047 | ||
Regulation of transcript levels of the Arabidopsis cytochrome p450 genes involved in brassinosteroid biosynthesis | Q44134008 | ||
Microarray analysis of brassinosteroid-regulated genes in Arabidopsis | Q44213656 | ||
Cloning the tomato curl3 gene highlights the putative dual role of the leucine-rich repeat receptor kinase tBRI1/SR160 in plant steroid hormone and peptide hormone signaling. | Q44240482 | ||
Brassinosteroid functions in a broad range of disease resistance in tobacco and rice | Q44331884 | ||
Signaling of systemic acquired resistance in tobacco depends on ethylene perception | Q44496735 | ||
A role for brassinosteroids in the regulation of photosynthesis in Cucumis sativus. | Q44859184 | ||
Binding of brassinosteroids to the extracellular domain of plant receptor kinase BRI1. | Q45224133 | ||
A R2R3 type MYB transcription factor is involved in the cold regulation of CBF genes and in acquired freezing tolerance. | Q46032386 | ||
Molecular players regulating the jasmonate signalling network | Q46615409 | ||
Do brassinosteroids mediate the water stress response? | Q46747483 | ||
Initiation of runaway cell death in an Arabidopsis mutant by extracellular superoxide | Q48059911 | ||
A role for brassinosteroids in light-dependent development of Arabidopsis | Q48064776 | ||
Evidence for Chilling-Induced Oxidative Stress in Maize Seedlings and a Regulatory Role for Hydrogen Peroxide | Q50115937 | ||
The role of reactive oxygen species in hormonal responses. | Q53595551 | ||
Activation of Host Defense Mechanisms by Elevated Production of H2O2 in Transgenic Plants. | Q53959275 | ||
The presence of glutathione and glutathione reductase in chloroplasts: A proposed role in ascorbic acid metabolism | Q56806641 | ||
Downstream nuclear events in brassinosteroid signalling | Q59066292 | ||
BES1 Accumulates in the Nucleus in Response to Brassinosteroids to Regulate Gene Expression and Promote Stem Elongation | Q59303786 | ||
Parallel Changes in H2O2and Catalase during Thermotolerance Induced by Salicylic Acid or Heat Acclimation in Mustard Seedlings | Q61831912 | ||
The BRI1-Associated Kinase 1, BAK1, Has a Brassinolide-Independent Role in Plant Cell-Death Control | Q63255876 | ||
Localization of hydrogen peroxide accumulation during the hypersensitive reaction of lettuce cells to Pseudomonas syringae pv phaseolicola | Q73135101 | ||
Characterization of brassinazole, a triazole-type brassinosteroid biosynthesis inhibitor | Q73778185 | ||
Brassinosteroid-induced exaggerated growth in hydroponically grown Arabidopsis plants | Q73798346 | ||
Systemic signaling and acclimation in response to excess excitation energy in Arabidopsis | Q77358046 | ||
Treatment with 24-epibrassinolide, a brassinosteroid, increases the basic thermotolerance of Brassica napus and tomato seedlings | Q78019970 | ||
Brassinosteroid signaling: a paradigm for steroid hormone signaling from the cell surface | Q79397311 | ||
BAK1 and BKK1 regulate brassinosteroid-dependent growth and brassinosteroid-independent cell-death pathways | Q80546429 | ||
Emerging MAP kinase pathways in plant stress signalling | Q81845056 | ||
Involvement of hydrogen peroxide in the regulation of senescence in pear | Q83250713 | ||
Lipid peroxidation associated with accelerated aging of soybean axes | Q83254065 | ||
Commentary to: "Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds" by Hodges et al., Planta (1999) 207:604-611 | Q87956597 | ||
Comparative biochemistry of the oxidative burst produced by rose and french bean cells reveals two distinct mechanisms | Q95432329 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | brassinosteroid | Q421976 |
reactive oxygen species | Q424361 | ||
P1104 | number of pages | 14 | |
P304 | page(s) | 801-814 | |
P577 | publication date | 2009-04-22 | |
P1433 | published in | Plant Physiology | Q3906288 |
P1476 | title | Reactive oxygen species are involved in brassinosteroid-induced stress tolerance in cucumber | |
P478 | volume | 150 |