scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1365-313X.2011.04702.X |
P698 | PubMed publication ID | 21749505 |
P2093 | author name string | Kristin Laluk | |
Tesfaye Mengiste | |||
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The chromatin remodeler SPLAYED regulates specific stress signaling pathways | Q28474227 | ||
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SPLAYED, a novel SWI/SNF ATPase homolog, controls reproductive development in Arabidopsis | Q33336840 | ||
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HISTONE MONOUBIQUITINATION1 interacts with a subunit of the mediator complex and regulates defense against necrotrophic fungal pathogens in Arabidopsis. | Q46087947 | ||
Arabidopsis ethylene-response gene ETR1: similarity of product to two-component regulators | Q46366210 | ||
A role for ETR1 in hydrogen peroxide signaling in stomatal guard cells | Q46371043 | ||
Natural variation in responsiveness of Arabidopsis thaliana to methyl jasmonate is developmentally regulated | Q46411773 | ||
The strawberry gene Cyf1 encodes a phytocystatin with antifungal properties. | Q46493482 | ||
A basic helix-loop-helix transcription factor in Arabidopsis, MYC2, acts as a repressor of blue light-mediated photomorphogenic growth | Q46516521 | ||
Wounding of Arabidopsis leaves causes a powerful but transient protection against Botrytis infection. | Q46614834 | ||
Molecular players regulating the jasmonate signalling network | Q46615409 | ||
Jasmonate signaling: toward an integrated view | Q46663061 | ||
Amylopectin induces fumonisin B1 production by Fusarium verticillioides during colonization of maize kernels | Q46944165 | ||
A MADS domain gene involved in the transition to flowering in Arabidopsis | Q47805950 | ||
EIN2, a bifunctional transducer of ethylene and stress responses in Arabidopsis | Q47952990 | ||
The antagonist function of Arabidopsis WRKY53 and ESR/ESP in leaf senescence is modulated by the jasmonic and salicylic acid equilibrium | Q48080793 | ||
Cuticular defects lead to full immunity to a major plant pathogen. | Q51996027 | ||
Arabidopsis RIN4 is a target of the type III virulence effector AvrRpt2 and modulates RPS2-mediated resistance. | Q52549320 | ||
MYC2 differentially modulates diverse jasmonate-dependent functions in Arabidopsis. | Q52681240 | ||
Wound-Induced Proteinase Inhibitor in Plant Leaves: A Possible Defense Mechanism against Insects. | Q52683811 | ||
Pearl millet cysteine protease inhibitor. Evidence for the presence of two distinct sites responsible for anti-fungal and anti-feedent activities. | Q54077450 | ||
A central role of salicylic Acid in plant disease resistance. | Q54191065 | ||
The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea | Q34509686 | ||
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Plant proteases: from phenotypes to molecular mechanisms. | Q34747312 | ||
Host-selective toxins and avirulence determinants: what's in a name? | Q34766430 | ||
Role of antioxidants in paraquat toxicity | Q34904565 | ||
Nuclear events in ethylene signaling: a transcriptional cascade mediated by ETHYLENE-INSENSITIVE3 and ETHYLENE-RESPONSE-FACTOR1 | Q35211520 | ||
Indirect activation of a plant nucleotide binding site-leucine-rich repeat protein by a bacterial protease | Q35623244 | ||
Cysteine proteases in phytopathogenic bacteria: identification of plant targets and activation of innate immunity | Q35825006 | ||
Natural protein proteinase inhibitors and their interaction with proteinases | Q35898939 | ||
The role of abscisic acid in plant-pathogen interactions. | Q36154037 | ||
Crosstalk between abiotic and biotic stress responses: a current view from the points of convergence in the stress signaling networks | Q36499476 | ||
Photoperiodic control of flowering: not only by coincidence | Q36621032 | ||
Differential expression of soybean cysteine proteinase inhibitor genes during development and in response to wounding and methyl jasmonate | Q36834777 | ||
Plant pathogenesis-related (PR) proteins: a focus on PR peptides. | Q37233373 | ||
Antagonism between abscisic acid and ethylene in Arabidopsis acts in parallel with the reciprocal regulation of their metabolism and signaling pathways | Q37276993 | ||
The multifaceted role of ABA in disease resistance. | Q37482860 | ||
Regulation of flowering in Arabidopsis by an FLC homologue | Q38300883 | ||
tA single amino acid difference distinguishes resistant and susceptible alleles of the rice blast resistance gene Pi-ta | Q38306380 | ||
Antagonistic interaction between abscisic acid and jasmonate-ethylene signaling pathways modulates defense gene expression and disease resistance in Arabidopsis | Q38874619 | ||
Expression of the Arabidopsis abi1-1 mutant allele inhibits proteinase inhibitor wound-induction in tomato. | Q38932882 | ||
ABI1 protein phosphatase 2C is a negative regulator of abscisic acid signaling | Q39029633 | ||
Antagonistic regulation of flowering-time gene SOC1 by CONSTANS and FLC via separate promoter motifs. | Q39647895 | ||
The T-loop extension of the tomato protein kinase AvrPto-dependent Pto-interacting protein 3 (Adi3) directs nuclear localization for suppression of plant cell death. | Q40813679 | ||
Conserved MYC transcription factors play a key role in jasmonate signaling both in tomato and Arabidopsis | Q41023009 | ||
The Arabidopsis abscisic acid response gene ABI5 encodes a basic leucine zipper transcription factor | Q41729659 | ||
Tomato protein kinase 1b mediates signaling of plant responses to necrotrophic fungi and insect herbivory. | Q42028742 | ||
Kunitz trypsin inhibitor: an antagonist of cell death triggered by phytopathogens and fumonisin b1 in Arabidopsis | Q42029474 | ||
The membrane-anchored BOTRYTIS-INDUCED KINASE1 plays distinct roles in Arabidopsis resistance to necrotrophic and biotrophic pathogens | Q42487716 | ||
Receptor-like cytoplasmic kinases integrate signaling from multiple plant immune receptors and are targeted by a Pseudomonas syringae effector | Q43088542 | ||
Constitutive expression of ETHYLENE-RESPONSE-FACTOR1 in Arabidopsis confers resistance to several necrotrophic fungi. | Q44024586 | ||
Regulation and role of the Arabidopsis abscisic acid-insensitive 5 gene in abscisic acid, sugar, and stress response | Q44102599 | ||
Arabidopsis local resistance to Botrytis cinerea involves salicylic acid and camalexin and requires EDS4 and PAD2, but not SID2, EDS5 or PAD4. | Q44505294 | ||
The BOTRYTIS SUSCEPTIBLE1 gene encodes an R2R3MYB transcription factor protein that is required for biotic and abiotic stress responses in Arabidopsis | Q44615209 | ||
The tomato homolog of CORONATINE-INSENSITIVE1 is required for the maternal control of seed maturation, jasmonate-signaled defense responses, and glandular trichome development | Q44701468 | ||
Detection of protease inhibitors by a reverse zymography method, performed in a tris(hydroxymethyl)aminomethane-Tricine buffer system | Q44702990 | ||
Purification and characterization of serine proteases that exhibit caspase-like activity and are associated with programmed cell death in Avena sativa | Q44799823 | ||
JASMONATE-INSENSITIVE1 encodes a MYC transcription factor essential to discriminate between different jasmonate-regulated defense responses in Arabidopsis. | Q44945509 | ||
Oxalate production by Sclerotinia sclerotiorum deregulates guard cells during infection | Q45122055 | ||
P433 | issue | 3 | |
P921 | main subject | insect | Q1390 |
herbivory | Q45874067 | ||
necrotrophy | Q123924226 | ||
P304 | page(s) | 480-494 | |
P577 | publication date | 2011-08-22 | |
P1433 | published in | The Plant Journal | Q15766987 |
P1476 | title | The Arabidopsis extracellular UNUSUAL SERINE PROTEASE INHIBITOR functions in resistance to necrotrophic fungi and insect herbivory | |
P478 | volume | 68 |
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Q46580744 | Abiotic induction affects the costs and benefits of inducible herbivore defenses in Datura wrightii. |
Q35876968 | Acetylation of cell wall is required for structural integrity of the leaf surface and exerts a global impact on plant stress responses. |
Q34072673 | Alkamides activate jasmonic acid biosynthesis and signaling pathways and confer resistance to Botrytis cinerea in Arabidopsis thaliana. |
Q37214965 | An Ethylene-Protected Achilles' Heel of Etiolated Seedlings for Arthropod Deterrence |
Q44529902 | CYCLIN-DEPENDENT KINASE8 differentially regulates plant immunity to fungal pathogens through kinase-dependent and -independent functions in Arabidopsis |
Q36651642 | Friends or foes? Emerging insights from fungal interactions with plants. |
Q50035276 | GTL1 and DF1 regulate root hair growth through transcriptional repression of ROOT HAIR DEFECTIVE 6-LIKE 4 in Arabidopsis |
Q40108709 | HISTONE DEACETYLASE 6 Represses Pathogen Defense Responses in Arabidopsis thaliana. |
Q57428255 | Higher expression of induced defenses in teosintes (Zeaspp.) is correlated with greater resistance to fall armyworm,Spodoptera frugiperda |
Q42005934 | Inducible expression of a fusion gene encoding two proteinase inhibitors leads to insect and pathogen resistance in transgenic rice |
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Q40531982 | Knock-down of transcript abundance of a family of Kunitz proteinase inhibitor genes in white clover (Trifolium repens) reveals a redundancy and diversity of gene function. |
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Q64083623 | Plant Serine Protease Inhibitors: Biotechnology Application in Agriculture and Molecular Farming |
Q37686035 | Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3. |
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Q36606123 | Simultaneous induction of jasmonic acid and disease-responsive genes signifies tolerance of American elm to Dutch elm disease |
Q26797307 | The battle in the apoplast: further insights into the roles of proteases and their inhibitors in plant-pathogen interactions |
Q30363504 | The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa |
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