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1. Assessing species composition and insecticide resistance of Anopheles gambiae complex members in three coastal health districts of Côte d'Ivoire.

2. Influence of Pesticide Application Method, Timing, and Rate on Contamination of Nectar with Systemic and Nonsystemic Pesticides.

3. Comparative study on biochemical responses to imidacloprid and clothianidin in cockroaches (Blattella germanica).

4. Proteome of Clothianidin Exposed Honey Bees Reveals a Possible Mechanism Behind Impairment of Sucrose Responsiveness.

5. Potentiation of entomopathogenic fungi with low doses of insecticides for managing Himalayan white grubs.

6. Neonicotinoid pesticides: evidence of developmental neurotoxicity from regulatory rodent studies.

7. Neonicotinoids Impact All Aspects of Bird Life: A Meta‐Analysis.

8. Toxicity of cockroach gel baits to the oothecal parasitoid Aprostocetus hagenowii (Hymenoptera: Eulophidae) and implications for cockroach integrated pest management.

9. Cocktail effects of clothianidin and imidacloprid in zebrafish embryonic development, with high and low concentrations of mixtures.

10. Indoor residual spraying of experimental huts in Cameroon highlights the potential of Fludora® Fusion to control wild pyrethroid-resistant malaria vectors

11. Barley yellow dwarf virus in winter barley: Control in light of resistance issues and loss of neonicotinoid insecticides.

12. Effect of the insecticide clothianidin on the photosynthetic electron transport chain in pea.

13. Low‐Level Dietary Clothianidin Exposure Preferentially Causes Prepupal Mortality of Monarch Butterflies (Danaus plexippus).

14. Potential acetylcholine-based communication in honeybee haemocytes and its modulation by a neonicotinoid insecticide.

15. Quantitative Analysis of Some Insecticide Residues Using Quechers Methodology on Pepper (Capsicum annuum) Fruits Under Greenhouse Conditions.

16. Functional Validation of Endogenous Redox Partner Cytochrome P450 Reductase Reveals the Key P450s CYP6P9a /- b as Broad Substrate Metabolizers Conferring Cross-Resistance to Different Insecticide Classes in Anopheles funestus.

17. Potential exposure of honey bees to neonicotinoid seed treatments in US rice.

18. Characterization of Neonicotinoid Metabolites by Cytochrome P450-Mediated Metabolism in Poultry.

19. Indoor residual spraying of experimental huts in Cameroon highlights the potential of Fludora® Fusion to control wild pyrethroid-resistant malaria vectors.

20. Microbial-assisted remediation approach for neonicotinoids from polluted environment.

21. Development and Validation of a High-Performance Liquid Chromatography Diode Array Detector Method to Measure Seven Neonicotinoids in Wheat.

22. A single dose of clothianidin exposure induces varying sex-specific behavioral changes in adulthood depending on the developmental stage of its administration.

23. Evaluating the Efficacy of Active Ingredients Used in Roach Baits against Small Hive Beetle (Aethina tumida) and Their Safety to Honey Bees (Apis mellifera).

24. Decreases in the number of microglia and neural circuit dysfunction elicited by developmental exposure to neonicotinoid pesticides in mice.

25. Effects of Clothianidin on Biochemical Parameters of Adult Zebrafish.

26. Residue determination of thiamethoxam and its metabolite clothianidin in okra using the modified QuEChERS method with d-SPE clean-up coupled with LC-MS/MS

27. Honeybee gut bacterial strain improved survival and gut microbiota homeostasis in Apis mellifera exposed in vivo to clothianidin

28. Can neonicotinoid and pyrrole insecticides manage malaria vector resistance in high pyrethroid resistance areas in Côte d'Ivoire?

29. Synthesis and Characterization of Composite WO 3 Fibers/g-C 3 N 4 Photocatalysts for the Removal of the Insecticide Clothianidin in Aquatic Media.

30. Estimation of thiamethoxam and its metabolites in wheat using QuEChERS methodology combined with LC-MS/MS.

31. 设施芹菜噻虫嗪和高效氯氟氰菊酯连续施用后 消散、积累与风险评估.

32. Occurrence and inhalation health risk of neonicotinoid pesticides in outdoor air particulate matters from 2019 to 2021 in China.

33. Can neonicotinoid and pyrrole insecticides manage malaria vector resistance in high pyrethroid resistance areas in Côte d'Ivoire?

34. Behavior of Thiamethoxam and Clothianidin in Young Oilseed Rape Plants before Flowering, Monitored by QuEChERS/LC–MS/MS Protocol.

35. Did the prolonged residual efficacy of clothianidin products lead to a greater reduction in vector populations and subsequent malaria transmission compared to the shorter residual efficacy of pirimiphos-methyl?

36. Fluorescence Quenching Detection of Clothianidin in Fruit and Vegetable Samples Using MAPbBr3 Perovskite Quantum Dots.

37. Removal of neonicotinoids present in secondary effluents by ferrate(VI)-based oxidation processes.

38. Transcriptome analyses in juvenile yellow perch (Perca flavescens) exposed in vivo to clothianidin and chlorantraniliprole: Possible sampling bias.

39. Toxic and Environmental Effects of Neonicotinoid Based Insecticides.

40. Application of General Unified Threshold Models to Predict Time-Varying Survival of Mayfly Nymphs Exposed to Three Neonicotinoids.

41. Laboratory evaluation of the contact irritancy of a clothianidin solo formulation vs. clothianidin-deltamethrin mixture formulations for indoor residual spraying against pyrethroid-resistant Anopheles gambiae sensu lato.

42. A smartphone sensing platform for the sensitive and selective detection of clothianidin based on MIP-functionalized lanthanide MOF.

43. Potential acetylcholine-based communication in honeybee haemocytes and its modulation by a neonicotinoid insecticide

44. Clothianidin-resistant Anopheles gambiae adult mosquitoes from Yaoundé, Cameroon, display reduced susceptibility to SumiShield® 50WG, a neonicotinoid formulation for indoor residual spraying

45. Baseline susceptibility of Anopheles gambiae to clothianidin in northern Ghana

48. Behavioral responses and life history traits of Taiwanese and Indonesian populations of Aedes aegypti surviving deltamethrin–clothianidin treatment.

50. Neonicotinoid contamination in conservation areas affects bees more sharply than beetles.

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