about
Achieving food security for one million sub-Saharan African poor through push-pull innovation by 2020Oviposition site-selection by Bactrocera dorsalis is mediated through an innate recognition template tuned to γ-octalactoneVariation in plant responsiveness to defense elicitors caused by genotype and environment.Increasing phosphorus supply is not the mechanism by which arbuscular mycorrhiza increase attractiveness of bean (Vicia faba) to aphids.Next-generation systemic acquired resistance.Responses of parasitoids to volatiles induced by Chilo partellus oviposition on teosinte, a wild ancestor of maize.The first crop plant genetically engineered to release an insect pheromone for defence.Insect host location: a volatile situation.cis-Jasmone induces Arabidopsis genes that affect the chemical ecology of multitrophic interactions with aphids and their parasitoidsPlant defence signalling induced by biotic attacks.Exploiting phytochemicals for developing a 'push-pull' crop protection strategy for cereal farmers in Africa.Phytochemicals of Brassicaceae in plant protection and human health--influences of climate, environment and agronomic practice.Metabolic engineering of plant-derived (E)-β-farnesene synthase genes for a novel type of aphid-resistant genetically modified crop plants.Delivering sustainable crop protection systems via the seed: exploiting natural constitutive and inducible defence pathways.Interplay between insects and plants: dynamic and complex interactions that have coevolved over millions of years but act in milliseconds.Molecular characterization of two isoforms of a farnesyl pyrophosphate synthase gene in wheat and their roles in sesquiterpene synthesis and inducible defence against aphid infestation.How rapid is aphid-induced signal transfer between plants via common mycelial networks?Oviposition induced volatile emissions from African smallholder farmers' maize varieties.Effect of temperature and relative humidity on the development and fecundity of Chilo partellus (Swinhoe) (Lepidoptera: Crambidae).Electrophysiological and behavioral responses of sorghum shoot fly, Atherigona soccata, to sorghum volatiles.Emerging roles in plant defense for cis-jasmone-induced cytochrome P450 CYP81D11.Semiochemicals used in host location by the coffee berry borer, Hypothenemus hampei.Development of semiochemical attractants for monitoring bean seed beetle, Bruchus rufimanus.Responses of female orange wheat Blossom midge, Sitodiplosis mosellana, to wheat panicle volatiles.Response of economically important aphids to components of Hemizygia petiolata essential oil.Specific volatile compounds from mango elicit oviposition in gravid Bactrocera dorsalis females.Isolation and identification of host cues from mango, Mangifera indica, that attract gravid female oriental fruit fly, Bactrocera dorsalis.Underground allies: how and why do mycelial networks help plants defend themselves?: What are the fitness, regulatory, and practical implications of defence-related signaling between plants via common mycelial networks?Development of a pheromone trap monitoring system for orange wheat blossom midge, Sitodiplosis mosellana, in the UK.Behavioural responses of the maize weevil, Sitophilus zeamais, to host (stored-grain) and non-host plant volatiles.Responses of herbivore and predatory mites to tomato plants exposed to jasmonic acid seed treatment.Finding the right connection: what makes a successful decision support system?GM as a route for delivery of sustainable crop protectionBehavioural and Electrophysiological Responses of Female Anopheles gambiae Mosquitoes to Volatiles from a Mango Bait
P50
Q26829253-965375DE-6227-4645-9BEB-499DF48D8A0DQ27333085-DBFF70C0-DE17-4F11-A15E-A7B50452E671Q33923688-6F7BBD74-1813-47F7-96C7-366F60C61219Q34149405-A1926C65-FECD-40B3-BD5F-8E5BF87A5706Q34634122-5ACAC3FB-00A7-4B04-9C53-BB88785F34BBQ35594120-739AD869-94CB-4A1B-9F9F-09F84064F902Q35778863-39883744-B7E0-47BB-B6CC-FC1CC162682EQ36159433-EF46250C-83B5-47CE-A479-E55ECC173EA9Q36534440-9DE1ACFA-DC0E-436C-8208-7062592C308BQ36879757-7423101C-A89F-4893-9B28-26EE761F52A7Q37776595-68CB8B25-AA8C-4F9C-B2C9-061732731D97Q37840381-5B36CD71-4B29-4199-89FE-504D0CAE6CF0Q37986245-6A1C3658-DAED-443D-B9FE-72122F7F740FQ38188842-1631747A-8570-4D7A-B77A-F34D2F6A2683Q38255783-6404861A-3974-40D4-9526-ECBF1D63D710Q41491794-236EF20E-9AA5-4F31-9502-D920F0C3D21EQ41933243-71F7FB22-B054-4D4B-8C79-AAC89998FEE3Q42014076-0445CE27-9DB3-4D86-B0FC-BB2F56CEE1E9Q42016834-7BBE411E-EA83-4896-BAF8-F0576437B90DQ42808381-3590CA72-9364-4D63-87A1-CAE5C0D93D8CQ42838511-8BD785B3-0725-4A1D-B5C5-2ED2962FB779Q43284436-641CAEA4-B4BD-4008-A088-B4EDDDC4778AQ45027742-64D0CC39-C014-4579-873B-50D1CB4E65A3Q45123094-714EDF7A-1C85-4E04-B703-F50E0728C1D5Q46628802-16F9EF09-F2B8-4FDE-9B0C-89DE5CE226A6Q51154274-B939D257-5CB3-49BD-B95D-3EED7953D02FQ51351667-2B8FF305-1AEA-4D13-9869-CB180C6B4F6BQ51502924-158E8F4B-6251-4F11-86E4-FFB26D560121Q51778240-7EA9CD70-6FD4-4C68-BC86-13D069138F92Q52698995-F08A90DF-EAE5-414A-A199-B9055D42E296Q52760606-5C36B960-33AD-49F7-8DC9-7FDD03070F42Q55362605-78C791A9-80F4-4138-8CC2-FF5F941D2017Q82128835-FAFF0400-65D3-4095-829E-17905AEEC06CQ91797451-E09B0749-6C13-46D1-8E49-B206BD1E4AE8
P50
description
researcher ORCID ID = 0000-0002-9912-0605
@en
wetenschapper
@nl
name
Toby Bruce
@ast
Toby Bruce
@en
Toby Bruce
@es
Toby Bruce
@nl
type
label
Toby Bruce
@ast
Toby Bruce
@en
Toby Bruce
@es
Toby Bruce
@nl
prefLabel
Toby Bruce
@ast
Toby Bruce
@en
Toby Bruce
@es
Toby Bruce
@nl
P106
P31
P496
0000-0002-9912-0605