Publications that involve processing of small organisms, such as insects. For experiments in which isolated tissues were processed, visit the “Other Small Animal Tissue” page.
Crustaceans
Chen, I.-T., Lee, D.-Y., Huang, Y.-T., Kou, G.-H., Wang, H.-C., Chang, G.-D., & Lo, C.-F. (2016). Six Hours after Infection, the Metabolic Changes Induced by WSSV Neutralize the Host’s Oxidative Stress Defenses. Scientific Reports, 6, 27732. https://doi.org/10.1038/srep27732
Collas, M., Becking, T., Delpy, M., Pflieger, M., Bohn, P., Reynolds, J., & Grandjean, F. (2016). Monitoring of white-clawed crayfish ( Austropotamobius pallipes ) population during a crayfish plague outbreak followed by rescue. Knowledge and Management of Aquatic Ecosystems, (417), 1. https://doi.org/10.1051/kmae/2015037
Becking, T., Mrugała, A., Delaunay, C., Svoboda, J., Raimond, M., Viljamaa-Dirks, S., Petrusek, A., Grandjean, F., & Braquart-Varnier, C. (2015). Effect of experimental exposure to differently virulent Aphanomyces astaci strains on the immune response of the noble crayfish Astacus astacus. Journal of Invertebrate Pathology, 132, 115–124. https://doi.org/10.1016/j.jip.2015.08.007
Filipová, L., Petrusek, A., Matasová, K., Delaunay, C., & Grandjean, F. (2013). Prevalence of the Crayfish Plague Pathogen Aphanomyces astaci in Populations of the Signal Crayfish Pacifastacus leniusculus in France: Evaluating the Threat to Native Crayfish. PLoS ONE, 8(7), e70157. https://doi.org/10.1371/journal.pone.0070157
Buck, J. C., Truong, L., & Blaustein, A. R. (2011). Predation by zooplankton on Batrachochytrium dendrobatidis: biological control of the deadly amphibian chytrid fungus? Biodiversity and Conservation, 20(14), 3549–3553. https://doi.org/10.1007/s10531-011-0147-4
Fish
Sarasamma, S., Audira, G., Juniardi, S., Sampurna, B., Lai, Y.-H., Hao, E., Chen, J.-R., & Hsiao, C.-D. (2018). Evaluation of the Effects of Carbon 60 Nanoparticle Exposure to Adult Zebrafish: A Behavioral and Biochemical Approach to Elucidate the Mechanism of Toxicity. International Journal of Molecular Sciences, 19(12), 3853. https://doi.org/10.3390/ijms19123853
McDougall, M. Q., Choi, J., Stevens, J. F., Truong, L., Tanguay, R. L., & Traber, M. G. (2016). Lipidomics and H218O labeling techniques reveal increased remodeling of DHA-containing membrane phospholipids associated with abnormal locomotor responses in α-tocopherol deficient zebrafish (danio rerio) embryos. Redox Biology, 8, 165–174. https://doi.org/10.1016/j.redox.2016.01.004
Metzger, D. C. H., Hemmer-Hansen, J., & Schulte, P. M. (2016). Conserved structure and expression of hsp70 paralogs in teleost fishes. Comparative Biochemistry and Physiology Part D: Genomics and Proteomics, 18, 10–20. https://doi.org/10.1016/j.cbd.2016.01.007
Chatzopoulou, A., Heijmans, J. P. M., Burgerhout, E., Oskam, N., Spaink, H. P., Meijer, A. H., & Schaaf, M. J. M. (2016). Glucocorticoid-induced attenuation of the inflammatory response in zebrafish. Endocrinology, en20152050. https://doi.org/10.1210/en.2015-2050
Techer, D., Milla, S., Fontaine, P., Viot, S., & Thomas, M. (2015). Influence of waterborne gallic and pelargonic acid exposures on biochemical and reproductive parameters in the zebrafish ( Danio rerio ): Influence Of Gallic and Pelargonic Acid Exposure. Environmental Toxicology, n/a-n/a. https://doi.org/10.1002/tox.22228
Gibbons, T. C., Rudman, S. M., & Schulte, P. M. (2015). Responses to simulated winter conditions differ between threespine stickleback ecotypes. Molecular Ecology, n/a-n/a. https://doi.org/10.1111/mec.13507
Doldur-Balli, F., Ozel, M. N., Gulsuner, S., Tekinay, A. B., Ozcelik, T., Konu, O., & Adams, M. M. (2015). Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ). BMC Neuroscience, 16(1). https://doi.org/10.1186/s12868-015-0229-4
Wong, R. Y., & Godwin, J. (2015). Neurotranscriptome profiles of multiple zebrafish strains. Genomics Data, 5, 206–209. https://doi.org/10.1016/j.gdata.2015.06.004
Goodale, B. C., La Du, J., Tilton, S. C., Sullivan, C. M., Bisson, W. H., Waters, K. M., & Tanguay, R. L. (2015). Ligand-specific transcriptional mechanisms underlie aryl hydrocarbon receptor-mediated developmental toxicity of oxygenated PAHs. Toxicological Sciences, kfv139. https://doi.org/10.1093/toxsci/kfv139
Elie, M. R., Choi, J., Nkrumah-Elie, Y. M., Gonnerman, G. D., Stevens, J. F., & Tanguay, R. L. (2015). Metabolomic analysis to define and compare the effects of PAHs and oxygenated PAHs in developing zebrafish. Environmental Research, 140, 502–510. https://doi.org/10.1016/j.envres.2015.05.009
Kollitz, E. M., Zhang, G., Hawkins, M. B., Whitfield, G. K., Reif, D. M., & Kullman, S. W. (2015). Molecular Cloning, Functional Characterization, and Evolutionary Analysis of Vitamin D Receptors Isolated from Basal Vertebrates. PLOS ONE, 10(4), e0122853. https://doi.org/10.1371/journal.pone.0122853
Peterman, E. M., Sullivan, C., Goody, M. F., Rodriguez-Nunez, I., Yoder, J. A., & Kim, C. H. (2015). Neutralization of Mitochondrial Superoxide by Superoxide Dismutase 2 Promotes Bacterial Clearance and Regulates Phagocyte Numbers in Zebrafish. Infection and Immunity, 83(1), 430–440. https://doi.org/10.1128/IAI.02245-14
Lashgari, M., & Lee, H. K. (2014). Determination of perfluorinated carboxylic acids in fish fillet by micro-solid phase extraction, followed by liquid chromatography–triple quadrupole mass spectrometry. Journal of Chromatography A, 1369, 26–32. https://doi.org/10.1016/j.chroma.2014.09.082
Lindenburg, P. W., Ramautar, R., Jayo, R. G., Chen, D. D. Y., & Hankemeier, T. (2014). Capillary electrophoresis-mass spectrometry using a flow-through microvial interface for cationic metabolome analysis: CE and CEC. ELECTROPHORESIS, 35(9), 1308–1314. https://doi.org/10.1002/elps.201300357
van der Plas-Duivesteijn, S. J., Mohammed, Y., Dalebout, H., Meijer, A., Botermans, A., Hoogendijk, J. L., Henneman, A. A., Deelder, A. M., Spaink, H. P., & Palmblad, M. (2014). Identifying Proteins in Zebrafish Embryos Using Spectral Libraries Generated from Dissected Adult Organs and Tissues. Journal of Proteome Research, 13(3), 1537–1544. https://doi.org/10.1021/pr4010585
Tonyushkina, K. N., Shen, M.-C., Ortiz-Toro, T., & Karlstrom, R. O. (2014). Embryonic exposure to excess thyroid hormone causes thyrotrope cell death. Journal of Clinical Investigation, 124(1), 321–327. https://doi.org/10.1172/JCI70038
Goodale, B. C., Tilton, S. C., Corvi, M. M., Wilson, G. R., Janszen, D. B., Anderson, K. A., Waters, K. M., & Tanguay, R. L. (2013). Structurally distinct polycyclic aromatic hydrocarbons induce differential transcriptional responses in developing zebrafish. Toxicology and Applied Pharmacology, 272(3), 656–670. https://doi.org/10.1016/j.taap.2013.04.024
Knecht, A. L., Goodale, B. C., Truong, L., Simonich, M. T., Swanson, A. J., Matzke, M. M., Anderson, K. A., Waters, K. M., & Tanguay, R. L. (2013). Comparative developmental toxicity of environmentally relevant oxygenated PAHs. Toxicology and Applied Pharmacology, 271(2), 266–275. https://doi.org/10.1016/j.taap.2013.05.006
Van Wettere, A. J., Law, J. M., Hinton, D. E., & Kullman, S. W. (2013). Anchoring Hepatic Gene Expression with Development of Fibrosis and Neoplasia in a Toxicant-induced Fish Model of Liver Injury. Toxicologic Pathology, 41(5), 744–760. https://doi.org/10.1177/0192623312464308
Kim, K.-T., Zaikova, T., Hutchison, J. E., & Tanguay, R. L. (2013). Gold Nanoparticles Disrupt Zebrafish Eye Development and Pigmentation. Toxicological Sciences, 133(2), 275–288. https://doi.org/10.1093/toxsci/kft081
Yang, J., & Xu, X. (2012). Actinin2 is required for the lateral alignment of Z discs and ventricular chamber enlargement during zebrafish cardiogenesis. The FASEB Journal, 26(10), 4230–4242. https://doi.org/10.1096/fj.12-207969
Saili, K. S., Corvi, M. M., Weber, D. N., Patel, A. U., Das, S. R., Przybyla, J., Anderson, K. A., & Tanguay, R. L. (2012). Neurodevelopmental low-dose bisphenol A exposure leads to early life-stage hyperactivity and learning deficits in adult zebrafish. Toxicology, 291(1–3), 83–92. https://doi.org/10.1016/j.tox.2011.11.001
Van Wettere, A. J. (2012). Pathogenesis of liver fibrosis and regeneration in the Japanese medaka (Oryzias latipes). North Carolina State University.
Noyes, P. D., Hinton, D. E., & Stapleton, H. M. (2011). Accumulation and Debromination of Decabromodiphenyl Ether (BDE-209) in Juvenile Fathead Minnows (Pimephales promelas) Induces Thyroid Disruption and Liver Alterations. Toxicological Sciences, 122(2), 265–274. https://doi.org/10.1093/toxsci/kfr105
Chen, C.-F., Chu, C.-Y., Chen, T.-H., Lee, S.-J., Shen, C.-N., & Hsiao, C.-D. (2011). Establishment of a Transgenic Zebrafish Line for Superficial Skin Ablation and Functional Validation of Apoptosis Modulators In Vivo. PLoS ONE, 6(5), e20654. https://doi.org/10.1371/journal.pone.0020654
Roberts, S. C., Noyes, P. D., Gallagher, E. P., & Stapleton, H. M. (2011). Species-Specific Differences and Structure−Activity Relationships in the Debromination of PBDE Congeners in Three Fish Species. Environmental Science & Technology, 45(5), 1999–2005. https://doi.org/10.1021/es103934x
Foott, J. S., & Fogarty, R. (2011). Juvenile Stanislaus River Chinook salmon pathogen and physiology assessment: January – May 2011. U.S. Fish & Wildlife Service California – Nevada Fish Health Center, Anderson, CA. http://www.fws.gov/lodi/afrp/documents/STAN11%20REPORT%207-14%20final.pdf
Techer, D., Milla, S., Fontaine, P., Viot, S., & Thomas, M. (2015). Acute toxicity and sublethal effects of gallic and pelargonic acids on the zebrafish Danio rerio. Environmental Science and Pollution Research, 22(7), 5020–5029. https://doi.org/10.1007/s11356-015-4098-2
Saili, K. S., Tilton, S. C., Waters, K. M., & Tanguay, R. L. (2013). Global gene expression analysis reveals pathway differences between teratogenic and non-teratogenic exposure concentrations of bisphenol A and 17β-estradiol in embryonic zebrafish. Reproductive Toxicology, 38, 89–101. https://doi.org/10.1016/j.reprotox.2013.03.009
Tuckey, N. P. L., Forgan, L. G., & Jerrett, A. R. (2012). Fillet colour correlates with biochemical status in Australasian snapper (Pagrus auratus) during storage in refrigerated seawater. Aquaculture, 356–357, 256–263. https://doi.org/10.1016/j.aquaculture.2012.05.008
Insects
Murari, A., & Owusu-Ansah, E. (2021). Analyzing the integrity of oxidative phosphorylation complexes in Drosophila flight muscles. STAR Protocols, 2(4), 101021. https://doi.org/10.1016/j.xpro.2021.101021
Thangaraj, S. R., McCulloch, G. A., Subbarayalu, M., Subramaniam, C., & Walter, G. H. (2016). Development of microsatellite markers and a preliminary assessment of population structuring in the rice weevil, Sitophilus oryzae (L.). Journal of Stored Products Research, 66, 12–17. https://doi.org/10.1016/j.jspr.2015.12.005
Perkin, L., Elpidina, E. N., & Oppert, B. (2016). Expression patterns of cysteine peptidase genes across the Tribolium castaneum life cycle provide clues to biological function. PeerJ, 4, e1581. https://doi.org/10.7717/peerj.1581
Nguyen, A. D., Gotelli, N. J., & Cahan, S. H. (2016). The evolution of heat shock protein sequences, cis-regulatory elements, and expression profiles in the eusocial Hymenoptera. BMC Evolutionary Biology, 16, 15. https://doi.org/10.1186/s12862-015-0573-0
Stanton-Geddes, J., Nguyen, A., Chick, L., Vincent, J., Vangala, M., Dunn, R. R., Ellison, A. M., Sanders, N. J., Gotelli, N. J., & Cahan, S. H. (2016). Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species. BMC Genomics, 17, 171. https://doi.org/10.1186/s12864-016-2466-z
Chick, L. (2015). Linking physiology and biogeography: Disentangling the constraints on the distributions of ant species [University of Tennessee-Knoxville]. http://trace.tennessee.edu/cgi/viewcontent.cgi?article=4928&context=utk_graddiss
Herter, E. K., Stauch, M., Gallant, M., Wolf, E., Raabe, T., & Gallant, P. (2015). snoRNAs are a novel class of biologically relevant Myc targets. BMC Biology, 13(1). https://doi.org/10.1186/s12915-015-0132-6
Fros, J. J., Miesen, P., Vogels, C. B., Gaibani, P., Sambri, V., Martina, B. E., Koenraadt, C. J., van Rij, R. P., Vlak, J. M., Takken, W., & Pijlman, G. P. (2015). Comparative Usutu and West Nile virus transmission potential by local Culex pipiens mosquitoes in north-western Europe. One Health, 1, 31–36. https://doi.org/10.1016/j.onehlt.2015.08.002
Kwon, D. H., Park, J. H., Ashok, P. A., Lee, U., & Lee, S. H. (2015). Screening of target genes for RNAi in Tetranychus urticae and RNAi toxicity enhancement by chimeric genes. Pesticide Biochemistry and Physiology. https://doi.org/10.1016/j.pestbp.2015.11.005
Fros, J. J., Geertsema, C., Vogels, C. B., Roosjen, P. P., Failloux, A.-B., Vlak, J. M., Koenraadt, C. J., Takken, W., & Pijlman, G. P. (2015). West Nile Virus: High Transmission Rate in North-Western European Mosquitoes Indicates Its Epidemic Potential and Warrants Increased Surveillance. PLOS Neglected Tropical Diseases, 9(7), e0003956. https://doi.org/10.1371/journal.pntd.0003956
Blenkiron, C., Tsai, P., Brown, L. A., Tintinger, V., Askelund, K. J., Windsor, J. A., & Phillips, A. R. (2015). Characterisation of the Small RNAs in the Biomedically Important Green-Bottle Blowfly Lucilia sericata. PLOS ONE, 10(3), e0122203. https://doi.org/10.1371/journal.pone.0122203
Osborne, C. J., Mayo, C. E., Mullens, B. A., McDermott, E. G., Gerry, A. C., Reisen, W. K., & MacLachlan, N. J. (2015). Lack of Evidence for Laboratory and Natural Vertical Transmission of Bluetongue Virus in Culicoides sonorensis (Diptera: Ceratopogonidae). Journal of Medical Entomology, 52(2), 274–277. https://doi.org/10.1093/jme/tju063
Marshall, K. E., & Sinclair, B. J. (2015). The relative importance of number, duration and intensity of cold stress events in determining survival and energetics of an overwintering insect. Functional Ecology, 29(3), 357–366. https://doi.org/10.1111/1365-2435.12328
Luo, S., Ahola, V., Shu, C., Xu, C., & Wang, R. (2015). Heat shock protein 70 gene family in the Glanville fritillary butterfly and their response to thermal stress. Gene, 556(2), 132–141. https://doi.org/10.1016/j.gene.2014.11.043
Heisig, M., Abraham, N. M., Liu, L., Neelakanta, G., Mattessich, S., Sultana, H., Shang, Z., Ansari, J. M., Killiam, C., Walker, W., Cooley, L., Flavell, R. A., Agaisse, H., & Fikrig, E. (2014). Antivirulence Properties of an Antifreeze Protein. Cell Reports, 9(2), 417–424. https://doi.org/10.1016/j.celrep.2014.09.034
Mayo, C. E., Mullens, B. A., Reisen, W. K., Osborne, C. J., Gibbs, E. P. J., Gardner, I. A., & MacLachlan, N. J. (2014). Seasonal and Interseasonal Dynamics of Bluetongue Virus Infection of Dairy Cattle and Culicoides sonorensis Midges in Northern California – Implications for Virus Overwintering in Temperate Zones. PLoS ONE, 9(9), e106975. https://doi.org/10.1371/journal.pone.0106975
Li, M. W. M., Wang, J., Zhao, Y. O., & Fikrig, E. (2014). Innexin AGAP001476 Is Critical for Mediating Anti-Plasmodium Responses in Anopheles Mosquitoes. Journal of Biological Chemistry, 289(36), 24885–24897. https://doi.org/10.1074/jbc.M114.554519
Kang, S., Shields, A. R., Jupatanakul, N., & Dimopoulos, G. (2014). Suppressing Dengue-2 Infection by Chemical Inhibition of Aedes aegypti Host Factors. PLoS Neglected Tropical Diseases, 8(8), e3084. https://doi.org/10.1371/journal.pntd.0003084
Kim, Y. H., Kwon, D. H., Ahn, H. M., Koh, Y. H., & Lee, S. H. (2014). Induction of soluble AChE expression via alternative splicing by chemical stress in Drosophila melanogaster. Insect Biochemistry and Molecular Biology, 48, 75–82. https://doi.org/10.1016/j.ibmb.2014.03.001
Jupatanakul, N., Sim, S., & Dimopoulos, G. (2014). Aedes aegypti ML and Niemann-Pick type C family members are agonists of dengue virus infection. Developmental & Comparative Immunology, 43(1), 1–9. https://doi.org/10.1016/j.dci.2013.10.002
Hu, Y., Sopko, R., Foos, M., Kelley, C., Flockhart, I., Ammeux, N., Wang, X., Perkins, L., Perrimon, N., & Mohr, S. E. (2013). FlyPrimerBank: An Online Database for Drosophila melanogaster Gene Expression Analysis and Knockdown Evaluation of RNAi Reagents. G3: Genes|Genomes|Genetics, 3(9), 1607–1616. https://doi.org/10.1534/g3.113.007021
Kasumovic, M. M., & Seebacher, F. (2013). The active metabolic rate predicts a male spider’s proximity to females and expected fitness. Biology Letters, 9(2), 20121164–20121164. https://doi.org/10.1098/rsbl.2012.1164
Marshall, K. E. (2013). The sub-lethal effects of repeated cold exposure in insects. University of Western Ontario.
Koles, K., Nunnari, J., Korkut, C., Barria, R., Brewer, C., Li, Y., Leszyk, J., Zhang, B., & Budnik, V. (2012). Mechanism of Evenness Interrupted (Evi)-Exosome Release at Synaptic Boutons. Journal of Biological Chemistry, 287(20), 16820–16834. https://doi.org/10.1074/jbc.M112.342667
MacMillan, H. A., Williams, C. M., Staples, J. F., & Sinclair, B. J. (2012). Metabolism and energy supply below the critical thermal minimum of a chill-susceptible insect. Journal of Experimental Biology, 215(8), 1366–1372. https://doi.org/10.1242/jeb.066381
Bazinet, A. L., Marshall, K. E., MacMillan, H. A., Williams, C. M., & Sinclair, B. J. (2010). Rapid changes in desiccation resistance in Drosophila melanogaster are facilitated by changes in cuticular permeability. Journal of Insect Physiology, 56(12), 2006–2012. https://doi.org/10.1016/j.jinsphys.2010.09.002
Bourgeois, L., Sheppard, W. S., Sylvester, H. A., & Rinderer, T. E. (2010). Genetic Stock Identification of Russian Honey Bees. Journal of Economic Entomology, 103(3), 917–924. https://doi.org/10.1603/EC09335
Marshall, K. E., & Sinclair, B. J. (2010). Repeated stress exposure results in a survival-reproduction trade-off in Drosophila melanogaster. Proceedings of the Royal Society B: Biological Sciences, 277(1683), 963–969. https://doi.org/10.1098/rspb.2009.1807
Bourgeois, A. L., & Rinderer, T. E. (2009). Genetic Characterization of Russian Honey Bee Stock Selected for Improved Resistance to Varroa destructor. Journal of Economic Entomology, 102(3), 1233–1238. https://doi.org/10.1603/029.102.0349
Kwon, D. H., Park, J. H., & Lee, S. H. (2013). Screening of lethal genes for feeding RNAi by leaf disc-mediated systematic delivery of dsRNA in Tetranychus urticae. Pesticide Biochemistry and Physiology, 105(1), 69–75. https://doi.org/10.1016/j.pestbp.2012.12.001
Bourgeois, A. L., Rinderer, T. E., Beaman, L. D., & Danka, R. G. (2010). Genetic detection and quantification of Nosema apis and N. ceranae in the honey bee. Journal of Invertebrate Pathology, 103(1), 53–58. https://doi.org/10.1016/j.jip.2009.10.009
Bourgeois, A. L., Rinderer, T. E., Sylvester, H. A., Holloway, B., & Oldroyd, B. P. (2012). Patterns of Apis mellifera infestation by Nosema ceranae support the parasite hypothesis for the evolution of extreme polyandry in eusocial insects. Apidologie, 43(5), 539–548. https://doi.org/10.1007/s13592-012-0121-5
Choi, J. B., Heo, W. I., Shin, T. Y., Bae, S. M., Kim, W. J., Kim, J. I., Kwon, M., Choi, J. Y., Je, Y. H., Jin, B. R., & Woo, S. D. (2013). Complete genomic sequences and comparative analysis of Mamestra brassicae nucleopolyhedrovirus isolated in Korea. Virus Genes, 47(1), 133–151. https://doi.org/10.1007/s11262-013-0922-2
Marshall, K. E., & Sinclair, B. J. (2012). Threshold temperatures mediate the impact of reduced snow cover on overwintering freeze-tolerant caterpillars. Naturwissenschaften, 99(1), 33–41. https://doi.org/10.1007/s00114-011-0866-0
Nematodes
Romero-Afrima, L., Zelmanovich, V., Abergel, Z., Zuckerman, B., Shaked, M., Abergel, R., Livshits, L., Smith, Y., & Gross, E. (2020). Ferritin is regulated by a neuro-intestinal axis in the nematode Caenorhabditis elegans. Redox Biology, 28, 101359. https://doi.org/10.1016/j.redox.2019.101359
Gooyit, M., Tricoche, N., Lustigman, S., & Janda, K. D. (2014). Dual Protonophore–Chitinase Inhibitors Dramatically Affect O. volvulus Molting. Journal of Medicinal Chemistry, 57(13), 5792–5799. https://doi.org/10.1021/jm5006435
Kang, J. S., Moon, Y. S., & Lee, S. H. (2012). Inhibition properties of three acetylcholinesterases of the pinewood nematode Bursaphelenchus xylophilus by organophosphates and carbamates. Pesticide Biochemistry and Physiology, 104(2), 157–162. https://doi.org/10.1016/j.pestbp.2012.06.002
Chen, A. L., Lum, K. M., Lara-Gonzalez, P., Ogasawara, D., Cognetta, A. B., To, A., Parsons, W. H., Simon, G. M., Desai, A., Petrascheck, M., Bar-Peled, L., & Cravatt, B. F. (2019). Pharmacological convergence reveals a lipid pathway that regulates C. elegans lifespan. Nature Chemical Biology, 15(5), 453–462. https://doi.org/10.1038/s41589-019-0243-4
Kang, J. S., Koh, Y. H., Moon, Y. S., & Lee, S. H. (2012). Molecular properties of a venom allergen-like protein suggest a parasitic function in the pinewood nematode Bursaphelenchus xylophilus. International Journal for Parasitology, 42(1), 63–70. https://doi.org/10.1016/j.ijpara.2011.10.006
Kang, J. S., Moon, Y.-S., Lee, S. H., & Park, I.-K. (2013). Inhibition of acetylcholinesterase and glutathione S-transferase of the pinewood nematode (Bursaphelenchus xylophilus) by aliphatic compounds. Pesticide Biochemistry and Physiology, 105(3), 184–188. https://doi.org/10.1016/j.pestbp.2013.02.001
