scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1029025194 |
P356 | DOI | 10.1186/1746-4811-7-34 |
P932 | PMC publication ID | 3207920 |
P698 | PubMed publication ID | 22014154 |
P5875 | ResearchGate publication ID | 51734078 |
P50 | author | Ian T. Baldwin | Q1655646 |
P2093 | author name string | Sang-Gyu Kim | |
Variluska Fragoso | |||
Hannah Goddard | |||
P2860 | cites work | Nicotine's defensive function in nature | Q21090242 |
Silencing the hydroxyproline-rich glycopeptide systemin precursor in two accessions of Nicotiana attenuata alters flower morphology and rates of self-pollination | Q24649721 | ||
Opportunistic out-crossing in Nicotiana attenuata (Solanaceae), a predominantly self-fertilizing native tobacco | Q24795094 | ||
Grafting the way to the systemic silencing signal in plants | Q24798803 | ||
Manipulation of endogenous trypsin proteinase inhibitor production in Nicotiana attenuata demonstrates their function as antiherbivore defenses | Q28246099 | ||
The hydroxyproline-rich glycopeptide systemin precursor NapreproHypSys does not play a central role in Nicotiana attenuata's anti-herbivore defense responses | Q28250726 | ||
FD, a bZIP protein mediating signals from the floral pathway integrator FT at the shoot apex | Q28267220 | ||
Insects betray themselves in nature to predators by rapid isomerization of green leaf volatiles | Q28291876 | ||
Defensive function of herbivore-induced plant volatile emissions in nature. | Q42054565 | ||
R2R3-NaMYB8 regulates the accumulation of phenylpropanoid-polyamine conjugates, which are essential for local and systemic defense against insect herbivores in Nicotiana attenuata. | Q43188246 | ||
Nicotiana attenuata SIPK, WIPK, NPR1, and fatty acid-amino acid conjugates participate in the induction of jasmonic acid biosynthesis by affecting early enzymatic steps in the pathway | Q43246237 | ||
Virus-induced gene silencing of jasmonate-induced direct defences, nicotine and trypsin proteinase-inhibitors in Nicotiana attenuata | Q44659704 | ||
Antisense LOX expression increases herbivore performance by decreasing defense responses and inhibiting growth-related transcriptional reorganization in Nicotiana attenuata | Q44693284 | ||
Revealing complexity and specificity in the activation of lipase-mediated oxylipin biosynthesis: a specific role of the Nicotiana attenuata GLA1 lipase in the activation of jasmonic acid biosynthesis in leaves and roots | Q48058382 | ||
EOBII controls flower opening by functioning as a general transcriptomic switch. | Q48059050 | ||
Retracted: Small RNA duplexes function as mobile silencing signals between plant cells. | Q50555663 | ||
Efficient screening of transgenic plant lines for ecological research. | Q51172770 | ||
Ectopic expression of AtJMT in Nicotiana attenuata: creating a metabolic sink has tissue-specific consequences for the jasmonate metabolic network and silences downstream gene expression. | Q51593244 | ||
C12 derivatives of the hydroperoxide lyase pathway are produced by product recycling through lipoxygenase-2 in Nicotiana attenuata leaves. | Q51597660 | ||
Independently silencing two JAR family members impairs levels of trypsin proteinase inhibitors but not nicotine. | Q51713943 | ||
Isolation and characterization of the threonine deaminase promoter in Nicotiana attenuata. | Q51720488 | ||
Micrografting techniques for testing long-distance signalling in Arabidopsis. | Q53955699 | ||
Small Silencing RNAs in Plants Are Mobile and Direct Epigenetic Modification in Recipient Cells | Q56926901 | ||
Allocation of nitrogen to an inducible defense and seed production in Nicotiana attenuata | Q57259852 | ||
Highly Branched Phenotype of the Petunia dad1-1 Mutant Is Reversed by Grafting | Q74776395 | ||
Branching Mutant rms-2 in Pisum sativum (Grafting Studies and Endogenous Indole-3-Acetic Acid Levels) | Q74789533 | ||
??? | Q28362494 | ||
Molecular and biochemical evolution of maize terpene synthase 10, an enzyme of indirect defense | Q30319049 | ||
Pectin methylesterase NaPME1 contributes to the emission of methanol during insect herbivory and to the elicitation of defence responses in Nicotiana attenuata | Q30489065 | ||
Host-plant-mediated effects of Nadefensin on herbivore and pathogen resistance in Nicotiana attenuata | Q33379282 | ||
The two alpha-dox genes of Nicotiana attenuata: overlapping but distinct functions in development and stress responses | Q33654715 | ||
Graft-transmitted siRNA signal from the root induces visual manifestation of endogenous post-transcriptional gene silencing in the scion | Q33828686 | ||
Distinct roles for jasmonate synthesis and action in the systemic wound response of tomato | Q34029515 | ||
New insights into plant responses to the attack from insect herbivores | Q34127348 | ||
Exchange of genetic material between cells in plant tissue grafts | Q34607134 | ||
A reagent for the single-step simultaneous isolation of RNA, DNA and proteins from cell and tissue samples | Q34721532 | ||
Field experiments with transformed plants reveal the sense of floral scents | Q34816501 | ||
SNF1-related kinases allow plants to tolerate herbivory by allocating carbon to roots | Q35036542 | ||
Systemic signaling in the wound response | Q36154065 | ||
Constitutive and inducible trypsin proteinase inhibitor production incurs large fitness costs in Nicotiana attenuata | Q36160480 | ||
The underestimated role of roots in defense against leaf attackers | Q37593281 | ||
Silencing RNA-directed RNA polymerase 2 increases the susceptibility of Nicotiana attenuata to UV in the field and in the glasshouse | Q39336222 | ||
RNA-directed RNA polymerase3 from Nicotiana attenuata is required for competitive growth in natural environments | Q39336229 | ||
RNA-directed RNA polymerase 1 (RdR1) mediates the resistance of Nicotiana attenuata to herbivore attack in nature | Q39336237 | ||
Co(i)-ordinating defenses: NaCOI1 mediates herbivore- induced resistance in Nicotiana attenuata and reveals the role of herbivore movement in avoiding defenses | Q39340915 | ||
PR-13/Thionin but not PR-1 mediates bacterial resistance in Nicotiana attenuata in nature, and neither influences herbivore resistance | Q39387355 | ||
Induced plant defenses in the natural environment: Nicotiana attenuata WRKY3 and WRKY6 coordinate responses to herbivory. | Q39469671 | ||
NaRALF, a peptide signal essential for the regulation of root hair tip apoplastic pH in Nicotiana attenuata, is required for root hair development and plant growth in native soils | Q39604948 | ||
Nicotiana attenuata LECTIN RECEPTOR KINASE1 suppresses the insect-mediated inhibition of induced defense responses during Manduca sexta herbivory | Q42015877 | ||
Silencing NOA1 elevates herbivory-induced jasmonic acid accumulation and compromises most of the carbon-based defense metabolites in Nicotiana attenuata(F). | Q42017720 | ||
Oxylipin channelling in Nicotiana attenuata: lipoxygenase 2 supplies substrates for green leaf volatile production | Q42020576 | ||
Jasmonic acid and ethylene modulate local responses to wounding and simulated herbivory in Nicotiana attenuata leaves. | Q42021410 | ||
Changing pollinators as a means of escaping herbivores | Q42022250 | ||
Jasmonate and ppHsystemin regulate key Malonylation steps in the biosynthesis of 17-Hydroxygeranyllinalool Diterpene Glycosides, an abundant and effective direct defense against herbivores in Nicotiana attenuata | Q42022299 | ||
Silencing two herbivory-activated MAP kinases, SIPK and WIPK, does not increase Nicotiana attenuata's susceptibility to herbivores in the glasshouse and in nature | Q42026980 | ||
Independently silencing two photosynthetic proteins in Nicotiana attenuata has different effects on herbivore resistance | Q42028177 | ||
Silencing jasmonate signalling and jasmonate-mediated defences reveals different survival strategies between two Nicotiana attenuata accessions | Q42028409 | ||
Comparisons of LIPOXYGENASE3- and JASMONATE-RESISTANT4/6-silenced plants reveal that jasmonic acid and jasmonic acid-amino acid conjugates play different roles in herbivore resistance of Nicotiana attenuata | Q42031148 | ||
Increased SA in NPR1-silenced plants antagonizes JA and JA-dependent direct and indirect defenses in herbivore-attacked Nicotiana attenuata in nature | Q42032035 | ||
Tuning the herbivore-induced ethylene burst: the role of transcript accumulation and ethylene perception in Nicotiana attenuata | Q42033029 | ||
Resistance management in a native plant: nicotine prevents herbivores from compensating for plant protease inhibitors | Q42033363 | ||
Herbivory rapidly activates MAPK signaling in attacked and unattacked leaf regions but not between leaves of Nicotiana attenuata | Q42033897 | ||
Silencing threonine deaminase and JAR4 in Nicotiana attenuata impairs jasmonic acid-isoleucine-mediated defenses against Manduca sexta | Q42035573 | ||
Evolution of proteinase inhibitor defenses in North American allopolyploid species of Nicotiana | Q42038121 | ||
Silencing of a germin-like gene in Nicotiana attenuata improves performance of native herbivores | Q42038467 | ||
Role of beta-oxidation in jasmonate biosynthesis and systemic wound signaling in tomato | Q42042053 | ||
Silencing of hydroperoxide lyase and allene oxide synthase reveals substrate and defense signaling crosstalk in Nicotiana attenuata | Q42043729 | ||
P921 | main subject | Nicotiana attenuata | Q311142 |
P304 | page(s) | 34 | |
P577 | publication date | 2011-10-20 | |
P1433 | published in | Plant Methods | Q15762916 |
P1476 | title | A simple and efficient micrografting method for stably transformed Nicotiana attenuata plants to examine shoot-root signaling | |
P478 | volume | 7 |
Q26748448 | Beyond the Canon: Within-Plant and Population-Level Heterogeneity in Jasmonate Signaling Engaged by Plant-Insect Interactions |
Q89711411 | Determining the scale at which variation in a single gene changes population yields |
Q34310018 | Ectopic terpene synthase expression enhances sesquiterpene emission in Nicotiana attenuata without altering defense or development of transgenic plants or neighbors |
Q39365311 | Emerging role of roots in plant responses to above ground insect herbivory |
Q46441174 | Functional specialization of Nicotiana attenuata phytochromes in leaf development and flowering time |
Q36099580 | Graft-union development: a delicate process that involves cell-cell communication between scion and stock for local auxin accumulation |
Q42012016 | HSPRO controls early Nicotiana attenuata seedling growth during interaction with the fungus Piriformospora indica |
Q46449479 | Herbivore perception decreases photosynthetic carbon assimilation and reduces stomatal conductance by engaging 12-oxo-phytodienoic acid, mitogen-activated protein kinase 4 and cytokinin perception. |
Q21128798 | Herbivory-induced volatiles function as defenses increasing fitness of the native plant Nicotiana attenuata in nature |
Q51338242 | Insect herbivory elicits genome-wide alternative splicing responses in Nicotiana attenuata. |
Q47809252 | JA but not JA-Ile is the cell-nonautonomous signal activating JA mediated systemic defenses to herbivory in Nicotiana attenuata |
Q34892905 | Leaf-herbivore attack reduces carbon reserves and regrowth from the roots via jasmonate and auxin signaling. |
Q92825722 | Molecular Responses during Plant Grafting and Its Regulation by Auxins, Cytokinins, and Gibberellins |
Q39043044 | Plant grafting: how genetic exchange promotes vascular reconnection |
Q37502912 | Root jasmonic acid synthesis and perception regulate folivore-induced shoot metabolites and increase Nicotiana attenuata resistance |
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