Identified peptidergic neurons in the Drosophila brain regulate insulin-producing cells, stress responses and metabolism by coexpressed short neuropeptide F and corazonin

Extending Healthy Life Span—From Yeast to Humans

Fontana, L., Partridge, L., & Longo, V. D. (2010) · Science · doi:10.1126/science.1172539 · Cited by 3,023 · see citing works

Using FlyAtlas to identify better Drosophila melanogaster models of human disease

Chintapalli, V. R., Wang, J., & Dow, J. A. T. (2007) · Nature Genetics · doi:10.1038/ng2049 · Cited by 1,479 · see citing works

CRF and CRF receptors: role in stress responsivity and other behaviors

Bale, T. L., & Vale, W. W. (2004) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.44.101802.121410 · Cited by 1,270 · see citing works

An evolutionarily conserved function of the Drosophila insulin receptor and insulin-like peptides in growth control

Brogiolo, W., Stocker, H., Ikeya, T., Rintelen, F., Fernandez, R., & Hafen, E. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00068-9 · Cited by 1,255 · see citing works

Ablation of Insulin-Producing Neurons in Flies: Growth and Diabetic Phenotypes

Rulifson, E. J., Kim, S. K., & Nusse, R. (2002) · Science · doi:10.1126/science.1070058 · Cited by 1,064 · see citing works

Tools for neuroanatomy and neurogenetics in Drosophila

Pfeiffer, B. D., Jenett, A., Hammonds, A. S., Ngo, T.-T. B., Misra, S., Murphy, C., Scully, A. L., Carlson, J. W., Wan, K. H., Laverty, T., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803697105 · Cited by 974 · see citing works

Longer lifespan, altered metabolism, and stress resistance in <i>Drosophila</i> from ablation of cells making insulin-like ligands

Broughton, S. J., Piper, M. D. W., Ikeya, T., Bass, T. M., Jacobson, J., Driege, Y., Martinez, P., Hafen, E., Withers, D. J., Leevers, S. J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405775102 · Cited by 822 · see citing works

A nutrient sensor mechanism controls Drosophila growth

Colombani, J., Raisin, S., Pantalacci, S., Radimerski, T., Montagne, J., & Léopold, P. (2003) · Cell · doi:10.1016/s0092-8674(03)00713-x · Cited by 809 · see citing works

Nutrient-Dependent Expression of Insulin-like Peptides from Neuroendocrine Cells in the CNS Contributes to Growth Regulation in Drosophila

Ikeya, T., Galic, M., Belawat, P., Nairz, K., & Hafen, E. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01043-6 · Cited by 765 · see citing works

Molecular Evolution and Functional Characterization of Drosophila Insulin-Like Peptides

Grönke, S., Clarke, D.-F., Broughton, S. J., Andrews, T. D., & Partridge, L. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000857 · Cited by 651 · see citing works

Hemolymph Sugar Homeostasis and Starvation-Induced Hyperactivity Affected by Genetic Manipulations of the Adipokinetic Hormone-Encoding Gene in Drosophila melanogaster

Lee, G., & Park, J. H. (2004) · Genetics · doi:10.1534/genetics.167.1.311 · Cited by 621 · see citing works

Remote Control of Insulin Secretion by Fat Cells in Drosophila

Géminard, C., Rulifson, E. J., & Léopold, P. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.08.002 · Cited by 585 · see citing works

Neuropeptides and Neuropeptide Receptors in the Drosophila melanogaster GenomePreprint

Hewes, R. S., & Taghert, P. H. (2001) · Genome Research · doi:10.1101/gr.169901 · Cited by 541 · see citing works

Secreted Peptide Dilp8 Coordinates Drosophila Tissue Growth with Developmental Timing

Colombani, J., Andersen, D. S., & Léopold, P. (2012) · Science · doi:10.1126/science.1216689 · Cited by 525 · see citing works

Imaginal Discs Secrete Insulin-Like Peptide 8 to Mediate Plasticity of Growth and Maturation

Garelli, A., Gontijo, A. M., Miguela, V., Caparrós, E., & Domínguez, M. (2012) · Science · doi:10.1126/science.1216735 · Cited by 504 · see citing works

Diabetic Larvae and Obese Flies—Emerging Studies of Metabolism in Drosophila

Baker, K. D., & Thummel, C. S. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.09.002 · Cited by 467 · see citing works

Electrical Silencing of Drosophila Pacemaker Neurons Stops the Free-Running Circadian Clock

Nitabach, M. N., Blau, J., & Holmes, T. C. (2002) · Cell · doi:10.1016/s0092-8674(02)00737-7 · Cited by 452 · see citing works

ATP-sensitive K+ channels and insulin secretion: their role in health and disease

Ashcroft, F., & Gribble, F. (1999) · Diabetologia · doi:10.1007/s001250051247 · Cited by 435 · see citing works

Identification of G protein-coupled receptors for Drosophila PRXamide peptides, CCAP, corazonin, and AKH supports a theory of ligand-receptor coevolution

Park, Y., Kim, Y., & Adams, M. E. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.162276199 · Cited by 388 · see citing works

Molecular mechanisms of metabolic regulation by insulin in Drosophila

Teleman, A. A. (2009) · Biochemical Journal · doi:10.1042/bj20091181 · Cited by 387 · see citing works

Drosophila Short Neuropeptide F Regulates Food Intake and Body Size

Lee, K., You, K., Choo, J., Han, Y., & Yu, K. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407842200 · Cited by 348 · see citing works

Regulatory peptides in fruit fly midgut

Veenstra, J. A., Agricola, H., & Sellami, A. (2008) · Cell and Tissue Research · doi:10.1007/s00441-008-0708-3 · Cited by 325 · see citing works

Enteric Neurons and Systemic Signals Couple Nutritional and Reproductive Status with Intestinal Homeostasis

Cognigni, P., Bailey, A. P., & Miguel‐Aliaga, I. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2010.12.010 · Cited by 325 · see citing works

Neuropeptides and their precursors in the fruitfly, Drosophila melanogaster☆

Broeck, J. V. (2001) · Peptides · doi:10.1016/s0196-9781(00)00376-4 · Cited by 321 · see citing works

A comparative review of short and long neuropeptide F signaling in invertebrates: Any similarities to vertebrate neuropeptide Y signaling?

Nässel, D. R., & Wegener, C. (2011) · Peptides · doi:10.1016/j.peptides.2011.03.013 · Cited by 316 · see citing works

Molecular identification of the insect adipokinetic hormone receptors

Staubli, F., Jørgensen, T. J. D., Cazzamali, G., Williamson, M. P., Lenz, C., Søndergaard, L., Roepstorff, P., & Grimmelikhuijzen, C. J. P. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.052556499 · Cited by 302 · see citing works

Isolation and structure of corazonin, a cardioactive peptide from the American cockroach

Veenstra, J. A. (1989) · FEBS Letters · doi:10.1016/0014-5793(89)80727-6 · Cited by 291 · see citing works

Role of insulin-like signalling in Drosophila lifespan

Giannakou, M. E., & PARTRIDGE, L. (2007) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2007.02.007 · Cited by 283 · see citing works

Candidate Gustatory Interneurons Modulating Feeding Behavior in the Drosophila Brain

Melcher, C., & Pankratz, M. J. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030305 · Cited by 278 · see citing works

Identification of a Neural Circuit that Underlies the Effects of Octopamine on Sleep:Wake Behavior

Crocker, A. J., Shahidullah, M., Levitan, I. B., & Sehgal, A. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.032 · Cited by 275 · see citing works

Identification of the gregarization-associated dark-pigmentotropin in locusts through an albino mutant

Tawfik, A. I., Tanaka, S., LOOF, A. D., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.12.7083 · Cited by 270 · see citing works

A novel diuretic hormone receptor inDrosophila: evidence for conservation of CGRP signaling

Johnson, E. C., Shafer, O. T., Trigg, J. S., Park, J. H., Schooley, D. A., Dow, J. A. T., & Taghert, P. H. (2005) · Journal of Experimental Biology · doi:10.1242/jeb.01529 · Cited by 254 · see citing works

A glucagon-like endocrine pathway in<i>Drosophila</i>modulates both lipid and carbohydrate homeostasis

Bharucha, K. N., Tarr, P., & Zipursky, S. L. (2008) · Journal of Experimental Biology · doi:10.1242/jeb.016451 · Cited by 239 · see citing works

Drosophila short neuropeptide F signalling regulates growth by ERK-mediated insulin signalling

Lee, K., Kwon, O., Lee, J. H., Kwon, K., Min, K., Jung, S., Kim, A., You, K., Tatar, M., & Yu, K. (2008) · Nature Cell Biology · doi:10.1038/ncb1710 · Cited by 230 · see citing works

Allatostatin-A neurons inhibit feeding behavior in adult Drosophila

Hergarden, A. C., Tayler, T. D., & Anderson, D. J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1200778109 · Cited by 214 · see citing works

Corazonin receptor signaling in ecdysis initiation

Kim, Y., Spalovská, I., Cho, K.-H., Zitnanova, I., Park, Y., Adams, M. E., & Žitňan, D. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0305291101 · Cited by 206 · see citing works

Reduction of DILP2 in Drosophila Triages a Metabolic Phenotype from Lifespan Revealing Redundancy and Compensation among DILPs

Broughton, S. J., Alic, N., Slack, C., Bass, T. M., Ikeya, T., Vinti, G., Tommasi, A. M., Driege, Y., Hafen, E., & Partridge, L. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003721 · Cited by 194 · see citing works

Expression of the Ciona intestinalis Alternative Oxidase (AOX) in Drosophila Complements Defects in Mitochondrial Oxidative Phosphorylation

Fernández‐Ayala, D. J. M., Sanz, A., Vartiainen, S., Kemppainen, K. K., Babušiak, M., Mustalahti, E., Costa, R., Tuomela, T., Zeviani, M., Chung, J., et al. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.03.004 · Cited by 181 · see citing works

A large population of diverse neurons in the Drosophilacentral nervous system expresses short neuropeptide F, suggesting multiple distributed peptide functions

Nässel, D. R., Enell, L. E., Santos, J. G., Wegener, C., & Johard, H. A. D. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-90 · Cited by 179 · see citing works

Localization of an insulin-like peptide in brains of two flies

Cao, C., & Brown, M. R. (2001) · Cell and Tissue Research · doi:10.1007/s004410100367 · Cited by 172 · see citing works

TheDhgene ofDrosophila melanogasterencodes a diuretic peptide that acts through cyclic AMP

Cabrero, P., Radford, J. C., Broderick, K. E., Costes, L., Veenstra, J. A., Spana, E. P., Davies, S. A., & Dow, J. A. T. (2002) · Journal of Experimental Biology · doi:10.1242/jeb.205.24.3799 · Cited by 163 · see citing works

Characterization of the short neuropeptide F receptor from Drosophila melanogaster

Mertens, I., Meeusen, T., Huybrechts, R., LOOF, A. D., & Schoofs, L. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02351-3 · Cited by 142 · see citing works

DILP‐producing median neurosecretory cells in the Drosophila brain mediate the response of lifespan to nutrition

Broughton, S. J., Slack, C., Alic, N., Metaxakis, A., Bass, T. M., Driege, Y., & Partridge, L. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00558.x · Cited by 124 · see citing works

Intrinsic neurons of <i>Drosophila</i> mushroom bodies express short neuropeptide F: Relations to extrinsic neurons expressing different neurotransmitters

Johard, H. A. D., Enell, L. E., Gustafsson, E., Trifilieff, P., Veenstra, J. A., & Nässel, D. R. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21636 · Cited by 120 · see citing works

Insulin-producing cells in the brain of adult Drosophila are regulated by the serotonin 5-HT1A receptor

Luo, J., Becnel, J., Nichols, C. D., & Nässel, D. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0789-0 · Cited by 114 · see citing works

Regulation of insulin-producing cells in the adult Drosophila brain via the tachykinin peptide receptor DTKR

Birse, R. T., Söderberg, J. A. E., Luo, J., et al. (2011) · Journal of Experimental Biology · doi:10.1242/jeb.062091 · Cited by 112 · see citing works

Molecular cloning and functional expression of a corazonin receptor

Cazzamali, G., Saxild, N. P. E., & Grimmelikhuijzen, C. J. P. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02398-7 · Cited by 111 · see citing works

Neuroanatomical studies of period gene expression in the hawkmoth, Manduca sexta

Wise, S. K., Davis, N. T., Tyndale, E., Noveral, J., Folwell, M. G., Bedian, V., Emery, I. F., & Siwicki, K. K. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10242 · Cited by 109 · see citing works

Corazonin Neurons Function in Sexually Dimorphic Circuitry That Shape Behavioral Responses to Stress in Drosophila

Zhao, Y., Bretz, C. A., Hawksworth, S. A., Hirsh, J., & Johnson, E. C. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009141 · Cited by 104 · see citing works

A nucleostemin family GTPase, NS3, acts in serotonergic neurons to regulate insulin signaling and control body sizePreprint

Kaplan, D. D., Zimmermann, G., Suyama, K. L., Meyer, T., & Scott, M. P. (2008) · Genes & Development · doi:10.1101/gad.1670508 · Cited by 104 · see citing works

Control of Metabolism and Growth Through Insulin-Like Peptides inDrosophila

Géminard, C., Arquier, N., Layalle, S., Bourouis, M., Slaidina, M., Delanoue, R., Bjordal, M., Ohanna, M., Ma, M., Colombani, J., et al. (2006) · Diabetes · doi:10.2337/db06-s001 · Cited by 102 · see citing works

Insulin Signaling, Lifespan and Stress Resistance Are Modulated by Metabotropic GABA Receptors on Insulin Producing Cells in the Brain of Drosophila

Enell, L. E., Kapan, N., Söderberg, J. A. E., Kahsai, L., & Nässel, D. R. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015780 · Cited by 101 · see citing works

Functional characterization of a neuropeptide F‐like receptor from Drosophila melanogaster

Feng, G., Reale, V., Chatwin, H. M., Kennedy, K., Venard, R., Ericsson, C., Yu, K., Evans, P. D., & Hall, L. M. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02719.x · Cited by 101 · see citing works

Insulin-Like Peptides

Antonova, Y., Arik, A. J., Moore, W., Riehle, M. A., & Brown, M. R. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-384749-2.10002-0 · Cited by 101 · see citing works

Immunocytochemical localization of Diploptera punctata allatostatin‐like peptide in Drosophila melanogaster

Yoon, J. G., & Stay, B. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903630310 · Cited by 100 · see citing works

Does corazonin signal nutritional stress in insects?

Veenstra, J. A. (2009) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2009.09.008 · Cited by 99 · see citing works

Isolation and Structure of the Drosophila Corazonin Gene

Veenstra, J. A. (1994) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1994.2458 · Cited by 96 · see citing works

In search for a common denominator for the diverse functions of arthropod corazonin: A role in the physiology of stress?

Boerjan, B., Verleyen, P., Huybrechts, J., Schoofs, L., & LOOF, A. D. (2009) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2009.09.004 · Cited by 92 · see citing works

Comparative analysis ofCorazonin‐encoding genes (Crz's) inDrosophilaspecies and functional insights intoCrz‐expressing neurons

Choi, Y. J., Lee, G., Hall, J. C., & Park, J. H. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20419 · Cited by 86 · see citing works

Corazonin in insects

Predel, R., Neupert, S., Russell, W. K., Scheibner, O., & Nachman, R. J. (2006) · Peptides · doi:10.1016/j.peptides.2006.10.011 · Cited by 83 · see citing works

Role of Corticotropin-Releasing Factor Receptor-2 in Stress-Induced Suppression of Pulsatile Luteinizing Hormone Secretion in the Rat

Li, X. F., Bowe, J. E., Lightman, S. L., & O’Byrne, K. T. (2004) · Endocrinology · doi:10.1210/en.2004-0950 · Cited by 77 · see citing works

Increased uncoupling protein (UCP) activity in Drosophila insulin-producing neurons attenuates insulin signaling and extends lifespan

Fridell, Y.-W. C., Hoh, M., Kréneisz, O., Hosier, S., Chang, C.-Y., Scantling, D. R., Mulkey, D. K., & Helfand, S. L. (2009) · Aging · doi:10.18632/aging.100067 · Cited by 75 · see citing works

Glucose increases activity and Ca2+ in insulin-producing cells of adult Drosophila

Kréneisz, O., Chen, X., Fridell, Y.-W. C., & Mulkey, D. K. (2010) · Neuroreport · doi:10.1097/wnr.0b013e3283409200 · Cited by 74 · see citing works

JNK signaling in insulin‐producing cells is required for adaptive responses to stress in Drosophila

Karpac, J., Hull‐Thompson, J., Falleur, M., & Jasper, H. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00476.x · Cited by 74 · see citing works

Developmental regulation and functions of the expression of the neuropeptide corazonin in Drosophila melanogaster

Lee, G., Kim, K., Kikuno, K., Wang, Z., Choi, Y., & Park, J. H. (2007) · Cell and Tissue Research · doi:10.1007/s00441-007-0549-5 · Cited by 69 · see citing works

Distribution of metabotropic receptors of serotonin, dopamine, GABA, glutamate, and short neuropeptide F in the central complex of Drosophila

Kahsai, L., Carlsson, M. A., Winther, Å. M. E., & Nässel, D. R. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.02.007 · Cited by 65 · see citing works

Postembryonic development of corazonin‐containing neurons and neurosecretory cells in the blowfly, Phormia terraenovae

Cantera, R., Veenstra, J. A., & Nässel, D. R. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500405 · Cited by 59 · see citing works

Stress-Induced Suppression of the Gonadotropin-Releasing Hormone Pulse Generator in the Female Rat: A Novel Neural Action for Calcitonin Gene-Related Peptide

Li, X. F., Bowe, J. E., Mitchell, J. C., Brain, S. D., Lightman, S. L., & O’Byrne, K. T. (2004) · Endocrinology · doi:10.1210/en.2003-1609 · Cited by 57 · see citing works

Analysis of Neuropeptide Expression and Localization in Adult Drosophila melanogaster Central Nervous System by Affinity Cell-Capture Mass Spectrometry

Yew, J. Y., Wang, Y., Barteneva, N. S., Dikler, S., Kutz‐Naber, K. K., Li, L., & Kravitz, E. A. (2009) · Journal of Proteome Research · doi:10.1021/pr800601x · Cited by 55 · see citing works

Processed short neuropeptide F peptides regulate growth through the ERK‐insulin pathway in Drosophila melanogaster

Lee, K., Hong, S.-H., Kim, A., et al. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.07.024 · Cited by 39 · see citing works

Fine-scale mapping of natural variation in fly fecundity identifies neuronal domain of expression and function of an aquaporin

Bergland, A. O., Chae, H.-S., Kim, Y.-J., & Tatar, M. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002631 · Cited by 35 · see citing works

Anopheles gambiae corazonin: gene structure, expression and effect on mosquito heart physiology

Hillyer, J. F., Estévez‐Lao, T. Y., Funkhouser-Jones, L. J., & Aluoch, V. A. (2012) · Insect Molecular Biology · doi:10.1111/j.1365-2583.2012.01140.x · Cited by 32 · see citing works

Spatial regulation of Corazonin neuropeptide expression requires multiple cis‐acting elements in Drosophila melanogaster

Choi, S., Lee, G., Monahan, P., et al. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21594 · Cited by 30 · see citing works

Nerve growth factor induces light adaptive cellular and synaptic plasticity in the outer retina of fish

Haamedi, S. N., Karten, H. J., & Djamgoz, M. B. A. (2001) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20010319)431:4 · Cited by 8 · see citing works

Transsynaptic mapping of second-order taste neurons in flies by trans-Tango

Talay, M., Richman, E. B., Snell, N. J., Hartmann, G. G., Fisher, J. D., Sorkaç, A., Santoyo, J. F., Chou-Freed, C., Nair, N., Johnson, M., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.011 · Cited by 301 · see citing works

Eat to reproduce: a key role for the insulin signaling pathway in adult insects

Badisco, L., Van Wielendaele, P., & Vanden Broeck, J. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00202 · Cited by 173 · see citing works

Systemic corazonin signalling modulates stress responses and metabolism in<i>Drosophila</i>

Kubrak, O. I., Lushchak, O. V., Zandawala, M., & Nässel, D. R. (2016) · Open Biology · doi:10.1098/rsob.160152 · Cited by 134 · see citing works

Regulation of ecdysone production in <i>Drosophila</i> by neuropeptides and peptide hormones

Kannangara, J. R., Mirth, C. K., & Warr, C. G. (2021) · Open Biology · doi:10.1098/rsob.200373 · Cited by 84 · see citing works

Corazonin signaling integrates energy homeostasis and lunar phase to regulate aspects of growth and sexual maturation in <i>Platynereis</i>

Andreatta, G., Broyart, C., Borghgraef, C., Vadiwala, K., Kozin, V., Polo, A., Bileck, A., Beets, I., Schoofs, L., Gerner, C., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910262116 · Cited by 61 · see citing works

RNaseH-mediated simultaneous piggyback knockdown of multiple genes in adult zebrafish

Raman, R., Ryon, M., & Jagadeeswaran, P. (2020) · Scientific Reports · doi:10.1038/s41598-020-76655-5 · Cited by 10 · see citing works

Knockdown of LIMD2 inhibits the progression of ovarian carcinoma through ERK1/2 pathway

Hu, H., Wang, Y., Dong, Y., et al. (2023) · Molecular Biology Reports · doi:10.1007/s11033-023-08733-6 · Cited by 2 · see citing works

Knockdown of ecdysteroid synthesis genes results in impaired molting and high mortality in Bactericera cockerelli (Hemiptera: Triozidae)

Paredes‐Montero, J. R., Arif, U., & Brown, J. K. (2022) · Pest Management Science · doi:10.1002/ps.6848 · Cited by 9 · see citing works

Supplementary Revised Figure S3 from MUC16 Regulates TSPYL5 for Lung Cancer Cell Growth and Chemoresistance by Suppressing p53

Lakshmanan, I., Salfity, S., Seshacharyulu, P., et al. (2023) · doi:10.1158/1078-0432.22465758

Supplementary Revised Figure S3 from MUC16 Regulates TSPYL5 for Lung Cancer Cell Growth and Chemoresistance by Suppressing p53

Lakshmanan, I., Salfity, S., Seshacharyulu, P., et al. (2023) · doi:10.1158/1078-0432.22465758.v1