Publications

ZORA Publication List

Publications

• 2026

  • Wang, H., Li, X., Zhai, K., Rhodes, J., Sang, T., Zhao, J., Gao, Y., Ma, S., Song, B., Pan, Q., Hu, M., Xin, P., Chu, J., Wang, P., Zipfel, C., & Zhou, J.-M. (2026). A regulatory network promotes apoplastic alkalinization to prime plant immunity in tissues distal to site of infection Cell, 189, 1389-1406.e19. https://doi.org/10.1016/j.cell.2026.01.027
  • Toth, R., Choi, S., Le Naour--Vernet, M., Schwanke, F., Johnson, J. L., Tee, E. E., Yaron-Barir, T. M., Khochaba, E., Derbyshire, P., Colo, A., Köster, P., Huntsman, E. M., Herold, L., Lee, Y., Fernández-Fernández, Á. D., Ahn, H.-K., Dindas, J., Bjornson, M., Rhodes, J., … et al. (2026). Motif-based substrate mapping of the receptor-like cytoplasmic kinase BIK1 reveals novel components and regulatory nodes of plant immunity Nature Plants, 12, 465–480. https://doi.org/10.1038/s41477-025-02218-z
  • Bernasconi, Z., Herger, A. G., Caro, M. D. P., Kunz, L., Müller, M. C., Stirnemann, U., Outram, M. A., Widrig, V., Neidhart, M., Isaksson, J., Schudel, S., Rösli, S., Wicker, T., Bender, K. W., Zipfel, C., Dodds, P. N., Figueroa, M., Sánchez-Martín, J., & Keller, B. (2026). Virulence on Pm4 kinase-based resistance is determined by two divergent wheat powdery mildew effectors Nature Plants, 12, 164–178. https://doi.org/10.1038/s41477-025-02180-w
  • Song, B., Choi, S., Kong, L., Kim, S.-I., Fliegmann, J., Li, X., Gao, Y., DeFalco, T. A., Hu, M., Li, M., Zhao, Y., Wang, H., Ma, S., Shan, L., Nürnberger, T., He, P., Zipfel, C., & Zhou, J.-M. (2026). New alleles of Arabidopsis BIK1 reinforce its predominant role in pattern-triggered immunity and caution interpretations of other reported functions Nature Plants, 12, 284–293. https://doi.org/10.1038/s41477-025-02187-3

• 2025

  • Snoeck, S., Zhang, L., Studer, V., Kim, G., Fernández-Fernández, Á. D., Nürnberger, T., & Zipfel, C. (2025). β-sheet stabilization of the island domain underlies ligand-induced LRR-RP activation of plant immune signaling Nature Communications, 16, 10958. https://doi.org/10.1038/s41467-025-66119-7
  • Yu, X., Liu, J., Wang, W., Shen, J., Shi, K., Li, J.-F., Ye, J., Rhodes, J., Zipfel, C., Li, C., Li, J., Yan, J., Lu, Y., & Cai, Y. (2025). Plant-derived peptides: From identification to agronomic applications Molecular Plant, 18, 1963–1982. https://doi.org/10.1016/j.molp.2025.11.004
  • Yue, L., Wang, L., Neuhäuser, B., Zhang, S., Herren, G., Jung, E., Kim, G., Goto, Y., Fernández-Fernández, Á. D., Heuberger, M., Ludewig, U., Zipfel, C., & Keller, B. (2025). Cytoplasmic calcium influx mediated by Lr14a regulates stomatal immunity against leaf rust in wheat Current Biology, 35, 5750-5761.e4. https://doi.org/10.1016/j.cub.2025.10.033
  • Hou, X., Bender, K. W., Fernández-Fernández, Á. D., Kadler, G., Gupta, S., Häfliger, M., Guérin, A., Diet, A., Roffler, S., Campanini, D. A., Wicker, T., Zipfel, C., & Ringli, C. (2025). The Arabidopsis phosphatase PP2C12 negatively regulates LRX-RALF-FER-mediated cell wall integrity sensing The EMBO Journal, 45, 243–260. https://doi.org/10.1038/s44318-025-00614-x
  • Zhang, S., Liu, S., Lai, H.-F., Bender, K. W., Kim, G., Caflisch, A., & Zipfel, C. (2025). Author Correction: Reverse engineering of the pattern recognition receptor FLS2 reveals key design principles of broader recognition spectra against evading flg22 epitopes Nature Plants, 11, 2437. https://doi.org/10.1038/s41477-025-02166-8
  • Lintz, J., Goto, Y., Bender, K. W., Bchini, R., Dubrulle, G., Cawston, E., Zipfel, C., Duplessis, S., & Petre, B. (2025). Genetically clustered antifungal phytocytokines and receptor protein family members cooperate to trigger plant immune signaling Journal of Experimental Botany, 76, 4910–4922. https://doi.org/10.1093/jxb/erae297
  • Biermann, D., von Arx, M., Munzert-Eberlein, K. S., Xhelilaj, K., Séré, D., Stegmann, M., Vert, G., Wolf, S., Engelsdorf, T., Zipfel, C., & Gronnier, J. (2025). A RALF-brassinosteroid signaling circuit regulates Arabidopsis hypocotyl cell shape Current Biology, 35, 5002-5017.e5. https://doi.org/10.1016/j.cub.2025.09.016
  • Zhang, S., Liu, S., Lai, H.-F., Bender, K. W., Kim, G., Caflisch, A., & Zipfel, C. (2025). Reverse engineering of the pattern recognition receptor FLS2 reveals key design principles of broader recognition spectra against evading flg22 epitopes Nature Plants, 11, 1642–1657. https://doi.org/10.1038/s41477-025-02050-5
  • Makechemu, M., Goto, Y., Schmid, M. W., Zbinden, H., Widrig, V., Kaufmann, M., Pothier, J. F., Keller, B., & Zipfel, C. (2025). Chitin Soil Amendment Triggers Systemic Plant Disease Resistance Through Enhanced Pattern‐Triggered Immunity Plant Biotechnology Journal, 23, 5032–5044. https://doi.org/10.1111/pbi.70282
  • Saake, P., Brands, M., Endeshaw, A. B., Stolze, S. C., Westhoff, P., Balcke, G. U., Hensel, G., Holton, N., Zipfel, C., Tissier, A., Nakagami, H., & Zuccaro, A. (2025). Ergosterol‐induced immune response in barley involves phosphorylation of phosphatidylinositol phosphate metabolic enzymes and activation of diterpene biosynthesis New Phytologist, 246, 1236–1255. https://doi.org/10.1111/nph.70022
  • Snoeck, S., Johanndrees, O., Nürnberger, T., & Zipfel, C. (2025). Plant pattern recognition receptors: from evolutionary insight to engineering Nature Reviews. Genetics, 26, 268–278. https://doi.org/10.1038/s41576-024-00793-z
  • Herold, L., Choi, S., He, S. Y., & Zipfel, C. (2025). The conserved AvrE family of bacterial effectors: functions and targets during pathogenesis Trends in Microbiology, 33, 184–193. https://doi.org/10.1016/j.tim.2024.08.007
  • Herold, L., Ordon, J., Hua, C., Kohorn, B. D., Nürnberger, T., DeFalco, T. A., & Zipfel, C. (2025). Arabidopsis WALL-ASSOCIATED KINASES are not required for oligogalacturonide-induced signaling and immunity Plant Cell, 37, koae317. https://doi.org/10.1093/plcell/koae317

• 2024

  • Keppler, A., Roulier, M., Pfeilmeier, S., Petti, G. C., Sintsova, A., Maier, B. A., Bortfeld-Miller, M., Sunagawa, S., Zipfel, C., & Vorholt, J. A. (2024). Plant microbiota feedbacks through dose-responsive expression of general non-self response genes Nature Plants, 11, 74–89. https://doi.org/10.1038/s41477-024-01856-z
  • Goto, Y., Kadota, Y., Mbengue, M., Lewis, J. D., Matsui, H., Maki, N., Ngou, B. P. M., Sklenar, J., Derbyshire, P., Shibata, A., Ichihashi, Y., Guttman, D. S., Nakagami, H., Suzuki, T., Menke, F. L. H., Robatzek, S., Desveaux, D., Zipfel, C., & Shirasu, K. (2024). The leucine-rich repeat receptor kinase QSK1 regulates PRR-RBOHD complexes targeted by the bacterial effector HopF2Pto Plant Cell, 36, 4932–4951. https://doi.org/10.1093/plcell/koae267
  • Gonçalves Dias, M., Doss, B., Rawat, A., Siegel, K. R., Mahathanthrige, T., Sklenar, J., Rodriguez Gallo, M. C., Derbyshire, P., Dharmasena, T., Cameron, E., Uhrig, R. G., Zipfel, C., Menke, F. L. H., & Monaghan, J. (2024). Subfamily C7 Raf‐like kinases MRK1, RAF26, and RAF39 regulate immune homeostasis and stomatal opening in Arabidopsis thaliana New Phytologist, 244, 2278–2294. https://doi.org/10.1111/nph.20198
  • Zhai, K., Rhodes, J., & Zipfel, C. (2024). A peptide-receptor module links cell wall integrity sensing to pattern-triggered immunity Nature Plants, 10, 2027–2037. https://doi.org/10.1038/s41477-024-01840-7
  • Moreira, C. J. S., Escórcio, R., Bento, A., Bjornson, M., Herold, L., Tomé, A. S., Martins, C., Fanuel, M., Martins, I., Bakan, B., Zipfel, C., & Silva Pereira, C. (2024). Cutin-Derived Oligomers Induce Hallmark Plant Immune Responses Journal of Experimental Botany, 75, 5146–5161. https://doi.org/10.1093/jxb/erae254
  • Snoeck, S., Lee, H. K., Schmid, M. W., Bender, K. W., Neeracher, M. J., Fernández-Fernández, A. D., Santiago, J., & Zipfel, C. (2024). Leveraging coevolutionary insights and AI-based structural modeling to unravel receptor–peptide ligand-binding mechanisms Proceedings of the National Academy of Sciences of the United States of America, 121, :e2400862121. https://doi.org/10.1073/pnas.2400862121
  • Kaufmann, M., Li, L., Van Poucke, C., Rhyner, N., De Tender, C., Uyttendaele, M., Heyndrickx, M., Zipfel, C., Pothier, J. F., & Bart, C. (2024). Soil type and associated microbiomes influences chitin’s growth-promotion effect in lettuce Phytobiomes Journal, 8, 248–261. https://doi.org/10.1094/pbiomes-12-23-0132-r
  • Cabre, L., Jing, L., Makechemu, M., Heluin, K., El Khamlichi, S., Leprince, J., Kiefer-Meyer, M. C., Pluchon, S., Mollet, J.-C., Zipfel, C., & Nguema-Ona, E. (2024). Additive and Specific Effects of Elicitor Treatments on the Metabolic Profile of Arabidopsis thaliana Molecular Plant-Microbe Interactions, 37, 112–126. https://doi.org/10.1094/mpmi-04-23-0051-r
  • Goto, Y., Maki, N., Sklenar, J., Derbyshire, P., Menke, F. L. H., Zipfel, C., Kadota, Y., & Shirasu, K. (2024). The phagocytosis oxidase/Bem1p domain-containing protein PB1CP negatively regulates the NADPH oxidase RBOHD in plant immunity New Phytologist, 241, 1763–1779. https://doi.org/10.1111/nph.19302
  • Rhodes, J., & Zipfel, C. (2024). Identification of Bioactive Phytocytokines Using Transcriptomic Data and Plant Bioassays In A. Schaller (Ed.), Plant Peptide Hormones and Growth Factors (pp. 23–35). Springer. https://doi.org/10.1007/978-1-0716-3511-7_2

• 2023

  • Goto, Y., Kadota, Y., Mbengue, M., Lewis, J. D., Matsui, H., Maki, N., Sklenar, J., Derbyshire, P., Shibata, A., Ichihashi, Y., Guttman, D. S., Nakagami, H., Suzuki, T., Menke, F. L. H., Robatzek, S., Desveaux, D., Zipfel, C., & Shirasu, K. (2023). The leucine-rich repeat receptor kinase QSK1 is a novel regulator of PRR-RBOHD complex and is employed by the bacterial effector HopF2$_{Pto}$ to modulate plant immunity (No. 571443; BioRxiv). https://doi.org/10.1101/2023.12.13.571443
  • Dias, M. G., Doss, B., Rawat, A., Siegel, K. R., Mahathanthrige, T., Sklenar, J., Derbyshire, P., Dharmasena, T., Cameron, E., Zipfel, C., Menke, F. L. H., & Monaghan, J. (2023). Subfamily C7 Raf-like kinases MRK1, RAF26, and RAF39 regulate immune homeostasis and stomatal opening in Arabidopsis thaliana (No. 569073; BioRxiv). https://doi.org/10.1101/2023.11.29.569073
  • Wanke, A., van Boerdonk, S., Mahdi, L. K., Wawra, S., Neidert, M., Chandrasekar, B., Saake, P., Saur, I. M. L., Derbyshire, P., Holton, N., Menke, F. L. H., Brands, M., Pauly, M., Acosta, I. F., Zipfel, C., & Zuccaro, A. (2023). A GH81-type β-glucan-binding protein enhances colonization by mutualistic fungi in barley Current Biology, 33, 5071-5084.e7. https://doi.org/10.1016/j.cub.2023.10.048
  • Yang, H., Kim, X., Skłenar, J., Aubourg, S., Sancho-Andrés, G., Stahl, E., Guillou, M.-C., Gigli-Bisceglia, N., Tran Van Canh, L., Bender, K. W., Stintzi, A., Reymond, P., Sánchez-Rodríguez, C., Testerink, C., Renou, J.-P., Menke, F. L. H., Schaller, A., Rhodes, J., & Zipfel, C. (2023). Subtilase-mediated biogenesis of the expanded family of SERINE RICH ENDOGENOUS PEPTIDES Nature Plants, 9, 2085–2094. https://doi.org/10.1038/s41477-023-01583-x
  • Lintz, J., Goto, Y., Bender, K. W., Bchini, R., Dubrulle, G., Cawston, E., Zipfel, C., Duplessis, S., & Petre, B. (2023). Genetically-clustered antifungal phytocytokines and receptor proteins function together to trigger plant immune signaling (No. 568785; BioRxiv). https://doi.org/10.1101/2023.11.27.568785
  • Kesten, C., Leitner, V., Dora, S., Sims, J. W., Dindas, J., Zipfel, C., De Moraes, C. M., & Sanchez-Rodriguez, C. (2023). Soil-borne fungi alter the apoplastic purinergic signaling in plants by deregulating the homeostasis of extracellular ATP and its metabolite adenosine ELife, 12, online. https://doi.org/10.7554/eLife.92913
  • Blekemolen, M. C., Liu, Z., Stegman, M., Zipfel, C., Shan, L., & Takken, F. L. W. (2023). The PTI-suppressing Avr2 effector from Fusarium oxysporum suppresses mono-ubiquitination and plasma membrane dissociation of BIK1 Molecular Plant Pathology, 24, 1273–1286. https://doi.org/10.1111/mpp.13369
  • Mühlenbeck, H., Tsutsui, Y., Lemmon, M. A., Bender, K. W., & Zipfel, C. (2023). Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling (No. 554490; BioRxiv). https://doi.org/10.1101/2023.08.23.554490
  • Pršić, J., Gilliard, G., Ibrahim, H., Argüelles-Arias, A., Rondelli, V., Crowet, J.-M., Genva, M., Luzuriaga-Loaiza, W. P., Deboever, E., Nasir, M. N., Lins, L., Mathelie-Guinlet, M., Boubsi, F., Eschrig, S., Ranf, S., Dorey, S., Coninck, B. D., Nürnberger, T., Mongrand, S., … Ongena, M. (2023). Mechanosensing and Sphingolipid-Docking Mediate Lipopeptide-Induced Immunity in Arabidopsis (No. 547613; BioRxiv). https://doi.org/10.1101/2023.07.04.547613
  • George, J., Stegmann, M., Monaghan, J., Bailey-Serres, J., & Zipfel, C. (2023). Arabidopsis translation initiation factor binding protein CBE1 negatively regulates accumulation of the NADPH oxidase respiratory burst oxidase homolog D Journal of Biological Chemistry, 299, 105018. https://doi.org/10.1016/j.jbc.2023.105018
  • Bender, K. W., & Zipfel, C. (2023). Paradigms of receptor kinase signaling in plants Biochemical Journal, 480, 835–854. https://doi.org/10.1042/BCJ20220372
  • Adero, M. O., Tripathi, J. N., Oduor, R. O., Zipfel, C., & Tripathi, L. (2023). Transgenic expression of Arabidopsis ELONGATION FACTOR-TU RECEPTOR (AtEFR) gene in banana enhances resistance to Banana Xanthomonas Wilt disease (No. 543870; BioRxiv). https://doi.org/10.1101/2023.06.06.543870
  • Moreira, C. J. S., Escórcio, R., Bento, A., Bjornson, M., Tomé, A. S., Martins, C., Fanuel, M., Martins, I., Bakan, B., Zipfel, C., & Pereira, C. S. (2023). Cutin-Derived Oligomers Act as Damage-Associated Molecular Patterns in Arabidopsis thaliana (No. 540997; BioRxiv). https://doi.org/10.1101/2023.05.16.540997
  • Hurst, C. H., Turnbull, D., Xhelilaj, K., Myles, S., Pflughaupt, R. L., Kopischke, M., Davies, P., Jones, S., Robatzek, S., Zipfel, C., Gronnier, J., & Hemsley, P. A. (2023). S-acylation stabilizes ligand-induced receptor kinase complex formation during plant pattern-triggered immune signaling Current Biology, 33, 1588-1596.e6. https://doi.org/10.1016/j.cub.2023.02.065
  • Wanke, A., van Boerdonk, S., Mahdi, L. K., Wawra, S., Neidert, M., Chandrasekar, B., Saake, P., Saur, I. M. L., Derbyshire, P., Holton, N., Menke, F. L. H., Brands, M., Pauly, M., Acosta, I. F., Zipfel, C., & Zuccaro, A. (2023). A GH81-type β-glucan-binding protein facilitates colonization by mutualistic fungi in barley (No. 536646; BioRxiv). https://doi.org/10.1101/2023.04.12.536646
  • Smokvarska, M., Bayle, V., Maneta-Peyret, L., Fouillen, L., Poitout, A., Dongois, A., Fiche, J.-B., Gronnier, J., Garcia, J., Höfte, H., Nolmann, M., Zipfel, C., Maurel, C., Moreau, P., Jaillais, Y., & Martiniere, A. (2023). The receptor kinase FERONIA regulates phosphatidylserine localization at the cell surface to modulate ROP signaling Science Advances, 9, eadd4791. https://doi.org/10.1126/sciadv.add4791
  • Chu, J., Monte, I., DeFalco, T. A., Köster, P., Derbyshire, P., Menke, F. L. H., & Zipfel, C. (2023). Conservation of the PBL-RBOH immune module in land plants Current Biology, 33, 1130-1137.e5. https://doi.org/10.1016/j.cub.2023.01.050
  • Wang, Q., Aliaga Fandino, A. C., Graeff, M., DeFalco, T. A., Zipfel, C., & Hardtke, C. S. (2023). A phosphoinositide hub connects CLE peptide signaling and polar auxin efflux regulation Nature Communications, 14, 423. https://doi.org/10.1038/s41467-023-36200-0
  • Hurst, C. H., Turnbull, D., Xhelilaj, K., Myles, S., Pflughaupt, R. L., Kopischke, M., Davies, P., Jones, S., Robatzek, S., Zipfel, C., Gronnier, J., & Hemsley, P. A. (2023). S-acylation stabilizes ligand-induced receptor kinase complex formation during plant pattern-triggered immune signalling (No. 457756; BioRxiv). https://doi.org/10.1101/2021.08.30.457756
  • Li, L., Kaufmann, M., Makechemu, M., Van Poucke, C., De Keyser, E., Uyttendaele, M., Zipfel, C., Cottyn, B., & Pothier, J. F. (2023). Assessment of transcriptional reprogramming of lettuce roots in response to chitin soil amendment Frontiers in Plant Science, 14, 1158068. https://doi.org/10.3389/fpls.2023.1158068
  • Mühlenbeck, H., Tsutsui, Y., Lemmon, M. A., Bender, K. W., & Zipfel, C. (2023). Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling ELife, online. https://doi.org/10.7554/elife.92110.1
  • Adero, M., Tripathi, J. N., Oduor, R., Zipfel, C., & Tripathi, L. (2023). Transgenic expression of Arabidopsis ELONGATION FACTOR-TU RECEPTOR (AtEFR) gene in banana enhances resistance against Xanthomonas campestris pv. musacearum PLoS ONE, 18, online. https://doi.org/10.1371/journal.pone.0290884

• 2022

  • Yu, G., Derkacheva, M., Rufian, J. S., Brillada, C., Kowarschik, K., Jiang, S., Derbyshire, P., Ma, M., DeFalco, T. A., Morcillo, R. J. L., Stransfeld, L., Wei, Y., Zhou, J., Menke, F. L. H., Trujillo, M., Zipfel, C., & Macho, A. P. (2022). The Arabidopsis E3 ubiquitin ligase PUB4 regulates BIK1 and is targeted by a bacterial type-III effector The EMBO Journal, 41, e107257. https://doi.org/10.15252/embj.2020107257
  • Fan, L., Fröhlich, K., Melzer, E., Pruitt, R. N., Albert, I., Zhang, L., Joe, A., Hua, C., Song, Y., Albert, M., Kim, S.-T., Weigel, D., Zipfel, C., Chae, E., Gust, A. A., & Nürnberger, T. (2022). Genotyping-by-sequencing-based identification of Arabidopsis pattern recognition receptor RLP32 recognizing proteobacterial translation initiation factor IF1 Nature Communications, 13, 1294. https://doi.org/10.1038/s41467-022-28887-4
  • Noble, J. A., Bielski, N. V., Liu, M.-C. J., DeFalco, T. A., Stegmann, M., Nelson, A. D. L., McNamara, K., Sullivan, B., Dinh, K. K., Khuu, N., Hancock, S., Shiu, S.-H., Zipfel, C., Cheung, A. Y., Beilstein, M. A., & Palanivelu, R. (2022). Evolutionary analysis of the LORELEI gene family in plants reveals regulatory subfunctionalization Plant Physiology, 190, 2539–2556. https://doi.org/10.1093/plphys/kiac444
  • Rhodes, J., Zipfel, C., Jones, J. D. G., & Ngou, B. P. M. (2022). Concerted actions of PRR- and NLR-mediated immunity Essays in Biochemistry, 66, 501–511. https://doi.org/10.1042/ebc20220067
  • Köster, P., DeFalco, T. A., & Zipfel, C. (2022). Ca 2+ signals in plant immunity The EMBO Journal, 41, e110741. https://doi.org/10.15252/embj.2022110741
  • Rhodes, J., Roman, A.-O., Bjornson, M., Brandt, B., Derbyshire, P., Wyler, M., Schmid, M. W., Menke, F. L. H., Santiago, J., & Zipfel, C. (2022). Perception of a conserved family of plant signalling peptides by the receptor kinase HSL3 ELife, 11, e74687. https://doi.org/10.7554/elife.74687
  • Krishna, P. S., Woodcock, S. D., Pfeilmeier, S., Bornemann, S., Zipfel, C., & Malone, J. G. (2022). Pseudomonas syringae addresses distinct environmental challenges during plant infection through the coordinated deployment of polysaccharides Journal of Experimental Botany, 73, 2206–2221. https://doi.org/10.1093/jxb/erab550
  • DeFalco, T. A., Anne, P., James, S. R., Willoughby, A. C., Schwanke, F., Johanndrees, O., Genolet, Y., Derbyshire, P., Wang, Q., Rana, S., Pullen, A.-M., Menke, F. L. H., Zipfel, C., Hardtke, C. S., & Nimchuk, Z. L. (2022). A conserved module regulates receptor kinase signalling in immunity and development Nature Plants, 8, 356–365. https://doi.org/10.1038/s41477-022-01134-w
  • Schumacher, I., Menghini, D., Ovinnikov, S., Hauenstein, M., Fankhauser, N., Zipfel, C., Hörtensteiner, S., & Aubry, S. (2022). Evolution of chlorophyll degradation is associated with plant transition to land The Plant Journal, 109, 1473–1488. https://doi.org/10.1111/tpj.15645
  • Gronnier, J., Franck, C. M., Stegmann, M., DeFalco, T. A., Abarca, A., von Arx, M., Dünser, K., Lin, W., Yang, Z., Kleine-Vehn, J., Ringli, C., & Zipfel, C. (2022). Regulation of immune receptor kinase plasma membrane nanoscale organization by a plant peptide hormone and its receptors ELife, 22, e74162. https://doi.org/10.7554/elife.74162
  • Dindas, J., DeFalco, T. A., Yu, G., Zhang, L., David, P., Bjornson, M., Thibaud, M.-C., Custódio, V., Castrillo, G., Nussaume, L., Macho, A. P., & Zipfel, C. (2022). Direct inhibition of phosphate transport by immune signaling in Arabidopsis Current Biology, 32, 488–495. https://doi.org/10.1016/j.cub.2021.11.063

• 2021

  • Kolodziej, M. C., Singla, J., Sánchez-Martín, J., Zbinden, H., Šimková, H., Karafiátová, M., Doležel, J., Gronnier, J., Poretti, M., Glauser, G., Zhu, W., Köster, P., Zipfel, C., Wicker, T., Krattinger, S. G., & Keller, B. (2021). A membrane-bound ankyrin repeat protein confers race-specific leaf rust disease resistance in wheat Nature Communications, 12, 956. https://doi.org/10.1038/s41467-020-20777-x
  • Rhodes, J., Yang, H., Moussu, S., Boutrot, F., Santiago, J., & Zipfel, C. (2021). Perception of a divergent family of phytocytokines by the Arabidopsis receptor kinase MIK2 Nature Communications, 12, 705. https://doi.org/10.1038/s41467-021-20932-y
  • Piazza, S., Campa, M., Pompili, V., Costa, L. D., Salvagnin, U., Nekrasov, V., Zipfel, C., & Malnoy, M. (2021). The Arabidopsis pattern recognition receptor EFR enhances fire blight resistance in apple Horticulture Research, 8, 204. https://doi.org/10.1038/s41438-021-00639-3
  • Abarca, A., Franck, C. M., & Zipfel, C. (2021). Family-wide evaluation of RAPID ALKALINIZATION FACTOR peptides Plant Physiology, 187, 996–1010. https://doi.org/10.1093/plphys/kiab308
  • DeFalco, T. A., & Zipfel, C. (2021). Molecular mechanisms of early plant pattern-triggered immune signaling (Corrections) Molecular Cell, 81, 4346. https://doi.org/10.1016/j.molcel.2021.09.028
  • Schellenberger, R., Crouzet, J., Nickzad, A., Shu, L.-J., Kutschera, A., Gerster, T., Borie, N., Dawid, C., Cloutier, M., Villaume, S., Dhondt-Cordelier, S., Hubert, J., Cordelier, S., Mazeyrat-Gourbeyre, F., Schmid, C., Ongena, M., Renault, J.-H., Haudrechy, A., Hofmann, T., … Dorey, S. (2021). Bacterial rhamnolipids and their 3-hydroxyalkanoate precursors activate Arabidopsis innate immunity through two independent mechanisms Proceedings of the National Academy of Sciences of the United States of America, 118, e2101366118. https://doi.org/10.1073/pnas.2101366118
  • Bender, K. W., Couto, D., Kadota, Y., Macho, A. P., Sklenar, J., Derbyshire, P., Bjornson, M., DeFalco, T. A., Petriello, A., Font Farre, M., Schwessinger, B., Ntoukakis, V., Stransfeld, L., Jones, A. M. E., Menke, F. L. H., & Zipfel, C. (2021). Activation loop phosphorylaton of a non-RD receptor kinase initiates plant innate immune signaling Proceedings of the National Academy of Sciences of the United States of America, 118, e2108242118. https://doi.org/10.1073/pnas.2108242118
  • DeFalco, T. A., & Zipfel, C. (2021). Molecular mechanisms of early plant pattern-triggered immune signaling Molecular Cell, 81, 3449–3467. https://doi.org/10.1016/j.molcel.2021.07.029
  • Mühlenbeck, H., Bender, K. W., & Zipfel, C. (2021). Importance of tyrosine phosphorylation for transmembrane signaling in plants Biochemical Journal, 478, 2759–2774. https://doi.org/10.1042/bcj20210202
  • Mitre, L. K., Teixeira‐Silva, N. S., Rybak, K., Magalhães, D. M., de Souza‐Neto, R. R., Robatzek, S., Zipfel, C., & de Souza, A. A. (2021). The Arabidopsis immune receptor EFR increases resistance to the bacterial pathogens Xanthomonas and Xylella in transgenic sweet orange Plant Biotechnology Journal, 19, 1294–1296. https://doi.org/10.1111/pbi.13629
  • Aubry, S., Christ, B., Kräutler, B., Martinoia, E., Thomas, H., & Zipfel, C. (2021). An evergreen mind and a heart for the colors of fall Journal of Experimental Botany, 72, 4625–4633. https://doi.org/10.1093/jxb/erab162
  • Bjornson, M., & Zipfel, C. (2021). Plant immunity: Crosstalk between plant immune receptors Current Biology, 31, R796–R798. https://doi.org/10.1016/j.cub.2021.04.080
  • Bjornson, M., Pimprikar, P., Nürnberger, T., & Zipfel, C. (2021). The transcriptional landscape of Arabidopsis thaliana pattern-triggered immunity Nature Plants, 7, 579–586. https://doi.org/10.1038/s41477-021-00874-5
  • Grubb, L. E., Derbyshire, P., Dunning, K. E., Zipfel, C., Menke, F. L. H., & Monaghan, J. (2021). Large-scale identification of ubiquitination sites on membrane-associated proteins in Arabidopsis thaliana seedlings Plant Physiology, 185, 1483–1488. https://doi.org/10.1093/plphys/kiab023
  • Holmes, D. R., Bredow, M., Thor, K., Pascetta, S. A., Sementchoukova, I., Siegel, K. R., Zipfel, C., & Monaghan, J. (2021). A novel allele of the Arabidopsis thaliana MACPF protein CAD1 results in deregulated immune signaling Genetics, 217, iyab022. https://doi.org/10.1093/genetics/iyab022
  • Sánchez-Martín, J., Widrig, V., Herren, G., Wicker, T., Zbinden, H., Gronnier, J., Spörri, L., Praz, C. R., Heuberger, M., Kolodziej, M. C., Isaksson, J., Steuernagel, B., Karafiátová, M., Doležel, J., Zipfel, C., & Keller, B. (2021). Wheat Pm4 resistance to powdery mildew is controlled by alternative splice variants encoding chimeric proteins Nature Plants, 7, 327–341. https://doi.org/10.1038/s41477-021-00869-2

• 2020

  • Steinbrenner, A. D., Muñoz-Amatriaín, M., Chaparro, A. F., Aguilar-Venegas, J. M., Lo, S., Okuda, S., Glauser, G., Dongiovanni, J., Shi, D., Hall, M., Crubaugh, D., Holton, N., Zipfel, C., Abagyan, R., Turlings, T. C. J., Close, T. J., Huffaker, A., & Schmelz, E. A. (2020). A receptor-like protein mediates plant immune responses to herbivore-associated molecular patterns Proceedings of the National Academy of Sciences of the United States of America, 117, 31510–31518. https://doi.org/10.1073/pnas.2018415117
  • Kato, H., Onai, K., Abe, A., Shimizu, M., Takagi, H., Tateda, C., Utsushi, H., Singkarabanit-Ogawa, S., Kitakura, S., Ono, E., Zipfel, C., Takano, Y., Ishiura, M., & Terauchi, R. (2020). Lumi-Map, a real-time luciferase bioluminescence screen of mutants combined with MutMap, reveals Arabidopsis genes involved in PAMP-triggered immunity Molecular Plant-Microbe Interactions, 33, 1366–1380. https://doi.org/10.1094/mpmi-05-20-0118-ta
  • Bjornson, M., Kajala, K., Zipfel, C., & Ding, P. (2020). Low-cost and high-throughput RNA-seq library preparation for illumina sequencing from plant tissue Bio-Protocol, 10, e3799. https://doi.org/10.21769/bioprotoc.3799
  • Thor, K., Jiang, S., Michard, E., George, J., Scherzer, S., Huang, S., Dindas, J., Derbyshire, P., Leitão, N., DeFalco, T. A., Köster, P., Hunter, K., Kimura, S., Gronnier, J., Stransfeld, L., Kadota, Y., Bücherl, C. A., Charpentier, M., Wrzaczek, M., … Zipfel, C. (2020). The calcium-permeable channel OSCA1.3 regulates plant stomatal immunity Nature, 585, 569–573. https://doi.org/10.1038/s41586-020-2702-1
  • Cheval, C., Samwald, S., Johnston, M. G., de Keijzer, J., Breakspear, A., Liu, X., Bellandi, A., Kadota, Y., Zipfel, C., & Faulkner, C. (2020). Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants Proceedings of the National Academy of Sciences of the United States of America, 117, 9621–9629. https://doi.org/10.1073/pnas.1907799117
  • Cheung, A. Y., Qu, L.-J., Russinova, E., Zhao, Y., & Zipfel, C. (2020). Update on Receptors and Signaling Plant Physiology, 182, 1527–1530. https://doi.org/10.1104/pp.20.00275
  • Zhou, Y., Vroegop-Vos, I. A., Van Dijken, A. J. H., Van der Does, D., Zipfel, C., Pieterse, C. M. J., & Van Wees, S. C. M. (2020). Carbonic anhydrases CA1 and CA4 function in atmospheric CO2-modulated disease resistance Planta, 251, 75. https://doi.org/10.1007/s00425-020-03370-w
  • Caro, M. del P., Holton, N., Conti, G., Venturuzzi, A. L., Martínez‐Zamora, M. G., Zipfel, C., Asurmendi, S., & Díaz‐Ricci, J. C. (2020). The fungal subtilase AsES elicits a PTI‐like defence response in Arabidopsis thaliana plants independently of its enzymatic activity Molecular Plant Pathology, 21, 147–159. https://doi.org/10.1111/mpp.12881

• 2019

  • Galindo‐Trigo, S., Blanco‐Touriñán, N., DeFalco, T. A., Wells, E. S., Gray, J. E., Zipfel, C., & Smith, L. M. (2019). Cr RLK 1L receptor‐like kinases HERK 1 and ANJEA are female determinants of pollen tube reception EMBO Reports, e48466. https://doi.org/10.15252/embr.201948466
  • Amorim-Silva, V., Garcia-Moreno, A., Castillo, A. G., Lakhssassi, N., Del Valle, A. E., Perez-Sancho, J., Li, Y., Pose, D., Perez-Rodriguez, J., Lin, J., Valpuesta, V., Borsani, O., Zipfel, C., Macho, A. P., & Botella, M. A. (2019). TTL proteins scaffold brassinosteroid signaling components at the plasma membrane to optimize signal transduction in Arabidopsis Plant Cell, 31, 1807–1828. https://doi.org/10.1105/tpc.19.00150
  • Xiao, Y., Stegmann, M., Han, Z., DeFalco, T. A., Parys, K., Xu, L., Belkhadir, Y., Zipfel, C., & Chai, J. (2019). Mechanisms of RALF peptide perception by a heterotypic receptor complex Nature, 572, 270–274. https://doi.org/10.1038/s41586-019-1409-7
  • Wong, J. E. M. M., Nadzieja, M., Madsen, L. H., Bücherl, C. A., Dam, S., Sandal, N. N., Couto, D., Derbyshire, P., Uldum-Berentsen, M., Schroeder, S., Schwämmle, V., Nogueira, F. C. S., Asmussen, M. H., Thirup, S., Radutoiu, S., Blaise, M., Andersen, K. R., Menke, F. L. H., Zipfel, C., & Stougaard, J. (2019). A Lotus japonicus cytoplasmic kinase connects Nod factor perception by the NFR5 LysM receptor to nodulation Proceedings of the National Academy of Sciences of the United States of America, 116, 14339–14348. https://doi.org/10.1073/pnas.1815425116
  • Lammertz, M., Kuhn, H., Pfeilmeier, S., Malone, J., Zipfel, C., Kwaaitaal, M., Lin, N.-C., Kvitko, B. H., & Panstruga, R. (2019). Widely Conserved Attenuation of Plant MAMP-Induced Calcium Influx by Bacteria Depends on Multiple Virulence Factors and May Involve Desensitization of Host Pattern Recognition Receptors Molecular Plant-Microbe Interactions, 32, 608–621. https://doi.org/10.1094/MPMI-10-18-0291-R
  • Brulé, D., Villano, C., Davies, L. J., Trdá, L., Claverie, J., Héloir, M.-C., Chiltz, A., Adrian, M., Darblade, B., Tornero, P., Stransfeld, L., Boutrot, F., Zipfel, C., Dry, I. B., & Poinssot, B. (2019). The grapevine (Vitis vinifera) LysM receptor kinases VvLYK1-1 and VvLYK1-2 mediate chitooligosaccharide-triggered immunity Plant Biotechnology Journal, 17, 812–825. https://doi.org/10.1111/pbi.13017
  • Pfeilmeier, S., George, J., Morel, A., Roy, S., Smoker, M., Stransfeld, L., Downie, J. A., Peeters, N., Malone, J. G., & Zipfel, C. (2019). Expression of the Arabidopsis thaliana immune receptor EFR in Medicago truncatula reduces infection by a root pathogenic bacterium, but not nitrogen‐fixing rhizobial symbiosis Plant Biotechnology Journal, 17, 569–579. https://doi.org/10.1111/pbi.12999
  • Wan, W., Zhang, L., Pruitt, R., Zaidem, M., Brugman, R., Ma, X., Krol, E., Perraki, A., Kilian, J., Grossmann, G., Stahl, M., Shan, L., Zipfel, C., van Kan, J. A. L., Hedrich, R., Weigel, D., Gust, A. A., & Nürnberger, T. (2019). Comparing Arabidopsis receptor kinase and receptor protein‐mediated immune signaling reveals BIK1‐dependent differences New Phytologist, 221, 2080–2095. https://doi.org/10.1111/nph.15497
  • Kadota, Y., Liebrand, T. W. H., Goto, Y., Sklenar, J., Derbyshire, P., Menke, F. L. H., Torres, M.-A., Molina, A., Zipfel, C., Coaker, G., & Shirasu, K. (2019). Quantitative phosphoproteomic analysis reveals common regulatory mechanisms between effector- and PAMP-triggered immunity in plants New Phytologist, 221, 2160–2175. https://doi.org/10.1111/nph.15523

• 2018

  • Kunwar, S., Iriarte, F., Fan, Q., da Silva, E. E., Ritchie, L., Nguyen, N. S., Freeman, J. H., Stall, R. E., Jones, J. B., Minsavage, G. V., Colee, J., Scott, J. W., Vallad, G. E., Zipfel, C., Horvath, D., Westwood, J., Hutton, S. F., & Paret, M. L. (2018). Transgenic Expression of EFR and Bs2 Genes for Field Management of Bacterial Wilt and Bacterial Spot of Tomato Phytopathology, 108, 1402–1411. https://doi.org/10.1094/phyto-12-17-0424-r
  • Perraki, A., DeFalco, T. A., Derbyshire, P., Avila, J., Séré, D., Sklenar, J., Qi, X., Stransfeld, L., Schwessinger, B., Kadota, Y., Macho, A. P., Jiang, S., Couto, D., Torii, K. U., Menke, F. L. H., & Zipfel, C. (2018). Phosphocode-dependent functional dichotomy of a common co-receptor in plant signalling Nature, 561, 248–252. https://doi.org/10.1038/s41586-018-0471-x
  • Bender, K. W., & Zipfel, C. (2018). Plant G-protein activation: connecting to plant receptor kinases Cell Research, 28, 697–698. https://doi.org/10.1038/s41422-018-0046-2
  • Smakowska-Luzan, E., Mott, G. A., Parys, K., Stegmann, M., Howton, T. C., Layeghifard, M., Neuhold, J., Lehner, A., Kong, J., Grünwald, K., Weinberger, N., Satbhai, S. B., Mayer, D., Busch, W., Madalinski, M., Stolt-Bergner, P., Provart, N. J., Mukhtar, M. S., Zipfel, C., … Belkhadir, Y. (2018). An extracellular network of Arabidopsis leucine-rich repeat receptor kinases Nature, 553, 342–346. https://doi.org/10.1038/nature25184
  • Ziemann, S., van der Linde, K., Lahrmann, U., Acar, B., Kaschani, F., Colby, T., Kaiser, M., Ding, Y., Schmelz, E., Huffaker, A., Holton, N., Zipfel, C., & Doehlemann, G. (2018). An apoplastic peptide activates salicylic acid signalling in maize Nature Plants, 4, 172–180. https://doi.org/10.1038/s41477-018-0116-y
  • Wang, J., Grubb, L. E., Wang, J., Liang, X., Li, L., Gao, C., Ma, M., Feng, F., Li, M., Li, L., Zhang, X., Yu, F., Xie, Q., Chen, S., Zipfel, C., Monaghan, J., & Zhou, J.-M. (2018). A Regulatory Module Controlling Homeostasis of a Plant Immune Kinase Molecular Cell, 69, 493-504.e6. https://doi.org/10.1016/j.molcel.2017.12.026
  • Engelsdorf, T., Gigli-Bisceglia, N., Veerabagu, M., McKenna, J. F., Vaahtera, L., Augstein, F., Van der Does, D., Zipfel, C., & Hamann, T. (2018). The plant cell wall integrity maintenance and immune signaling systems cooperate to control stress responses inArabidopsis thaliana Science Signaling, 11, eaao3070. https://doi.org/10.1126/scisignal.aao3070
  • Perraki, A., Gronnier, J., Gouguet, P., Boudsocq, M., Deroubaix, A.-F., Simon, V., German-Retana, S., Legrand, A., Habenstein, B., Zipfel, C., Bayer, E., Mongrand, S., & Germain, V. (2018). REM1.3’s phospho-status defines its plasma membrane nanodomain organization and activity in restricting PVX cell-to-cell movement. PLoS Pathogens, 14, e1007378. https://doi.org/10.1371/journal.ppat.1007378
  • Liu, Q., Vain, T., Viotti, C., Doyle, S. M., Tarkowská, D., Novák, O., Zipfel, C., Sitbon, F., Robert, S., & Hofius, D. (2018). Vacuole Integrity Maintained by DUF300 Proteins Is Required for Brassinosteroid Signaling Regulation Molecular Plant, 11, 553–567. https://doi.org/10.1016/j.molp.2017.12.015

• 2017

  • Stegmann, M., & Zipfel, C. (2017). Complex regulation of plant sex by peptides Science, 358, 1544–1545. https://doi.org/10.1126/science.aar4190
  • D’Ambrosio, J. M., Couto, D., Fabro, G., Scuffi, D., Lamattina, L., Munnik, T., Andersson, M. X., Álvarez, M. E., Zipfel, C., & Laxalt, A. M. (2017). Phospholipase C2 Affects MAMP-Triggered Immunity by Modulating ROS Production Plant Physiology, 175, 970–981. https://doi.org/10.1104/pp.17.00173
  • Boschi, F., Schvartzman, C., Murchio, S., Ferreira, V., Siri, M. I., Galván, G. A., Smoker, M., Stransfeld, L., Zipfel, C., Vilaró, F. L., & Dalla-Rizza, M. (2017). Enhanced Bacterial Wilt Resistance in Potato Through Expression of Arabidopsis EFR and Introgression of Quantitative Resistance from Solanum commersonii Frontiers in Plant Science, 8, 1642. https://doi.org/10.3389/fpls.2017.01642
  • Imkampe, J., Halter, T., Huang, S., Schulze, S., Mazzotta, S., Schmidt, N., Manstretta, R., Postel, S., Wierzba, M., Yang, Y., van Dongen, W. M. A. M., Stahl, M., Zipfel, C., Goshe, M. B., Clouse, S., de Vries, S. C., Tax, F., Wang, X., & Kemmerling, B. (2017). The Arabidopsis Leucine-Rich Repeat Receptor Kinase BIR3 Negatively Regulates BAK1 Receptor Complex Formation and Stabilizes BAK1 Plant Cell, 29, 2285–2303. https://doi.org/10.1105/tpc.17.00376
  • Boutrot, F., & Zipfel, C. (2017). Function, Discovery, and Exploitation of Plant Pattern Recognition Receptors for Broad-Spectrum Disease Resistance Annual Review of Phytopathology, 55, 257–286. https://doi.org/10.1146/annurev-phyto-080614-120106
  • Singh, V., Perraki, A., Kim, S. Y., Shrivastava, S., Lee, J. H., Zhao, Y., Schwessinger, B., Oh, M.-H., Marshall-Colon, A., Zipfel, C., & Huber, S. C. (2017). Tyrosine-610 in the Receptor Kinase BAK1 Does Not Play a Major Role in Brassinosteroid Signaling or Innate Immunity Frontiers in Plant Science, 8, 1273. https://doi.org/10.3389/fpls.2017.01273
  • Van der Does, D., Boutrot, F., Engelsdorf, T., Rhodes, J., McKenna, J. F., Vernhettes, S., Koevoets, I., Tintor, N., Veerabagu, M., Miedes, E., Segonzac, C., Roux, M., Breda, A. S., Hardtke, C. S., Molina, A., Rep, M., Testerink, C., Mouille, G., Höfte, H., … Zipfel, C. (2017). The Arabidopsis leucine-rich repeat receptor kinase MIK2/LRR-KISS connects cell wall integrity sensing, root growth and response to abiotic and bioticstresses PLoS Genetics, 13, e1006832. https://doi.org/10.1371/journal.pgen.1006832
  • Mendy, B., Wang’ombe, M. W., Radakovic, Z. S., Holbein, J., Ilyas, M., Chopra, D., Holton, N., Zipfel, C., Grundler, F. M. W., & Siddique, S. (2017). Arabidopsis leucine-rich repeat receptor–like kinase NILR1 is required for induction of innate immunity to parasitic nematodes PLoS Pathogens, 13, e1006284. https://doi.org/10.1371/journal.ppat.1006284
  • Souza, C. de A., Li, S., Lin, A. Z., Boutrot, F., Grossmann, G., Zipfel, C., & Somerville, S. C. (2017). Cellulose-Derived Oligomers Act as Damage-Associated Molecular Patterns and Trigger Defense-Like Responses Plant Physiology, 173, 2383–2398. https://doi.org/10.1104/pp.16.01680
  • Zipfel, C., & Oldroyd, G. E. D. (2017). Plant signalling in symbiosis and immunity Nature, 543, 328–336. https://doi.org/10.1038/nature22009
  • Bender, K. W., Blackburn, R. K., Monaghan, J., Derbyshire, P., Menke, F. L. H., Zipfel, C., Goshe, M. B., Zielinski, R. E., & Huber, S. C. (2017). Autophosphorylation-based Calcium (Ca2+) Sensitivity Priming and Ca2+/Calmodulin Inhibition of Arabidopsis thaliana Ca2+-dependent Protein Kinase 28 (CPK28) Journal of Biological Chemistry, 292, 3988–4002. https://doi.org/10.1074/jbc.m116.763243
  • Bücherl, C. A., Jarsch, I. K., Schudoma, C., Segonzac, C., Mbengue, M., Robatzek, S., MacLean, D., Ott, T., & Zipfel, C. (2017). Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains ELife, 6, e25114. https://doi.org/10.7554/elife.25114
  • Shubchynskyy, V., Boniecka, J., Schweighofer, A., Simulis, J., Kvederaviciute, K., Stumpe, M., Mauch, F., Balazadeh, S., Mueller-Roeber, B., Boutrot, F., Zipfel, C., & Meskiene, I. (2017). Protein phosphatase AP2C1 negatively regulates basal resistance and defense responses to Pseudomonas syringae Journal of Experimental Botany, 68, 1169–1183. https://doi.org/10.1093/jxb/erw485
  • Stegmann, M., Monaghan, J., Smakowska-Luzan, E., Rovenich, H., Lehner, A., Holton, N., Belkhadir, Y., & Zipfel, C. (2017). The receptor kinase FER is a RALF-regulated scaffold controlling plant immune signaling Science, 355, 287–289. https://doi.org/10.1126/science.aal2541

• 2016

  • Xin, X.-F., Nomura, K., Aung, K., Velásquez, A. C., Yao, J., Boutrot, F., Chang, J. H., Zipfel, C., & He, S. Y. (2016). Bacteria establish an aqueous living space in plants crucial for virulence Nature, 539, 524–529. https://doi.org/10.1038/nature20166
  • Couto, D., & Zipfel, C. (2016). Regulation of pattern recognition receptor signalling in plants Nature Reviews. Immunology, 16, 537–552. https://doi.org/10.1038/nri.2016.77
  • Magalhães, D. M., Scholte, L. L. S., Silva, N. V., Oliveira, G. C., Zipfel, C., Takita, M. A., & de Souza, A. A. (2016). LRR-RLK family from two Citrus species: genome-wide identification and evolutionary aspects BMC Genomics, 17, 623. https://doi.org/10.1186/s12864-016-2930-9
  • Couto, D., Niebergall, R., Liang, X., Bücherl, C. A., Sklenar, J., Macho, A. P., Ntoukakis, V., Derbyshire, P., Altenbach, D., Maclean, D., Robatzek, S., Uhrig, J., Menke, F., Zhou, J.-M., & Zipfel, C. (2016). The Arabidopsis Protein Phosphatase PP2C38 Negatively Regulates the Central Immune Kinase BIK1 PLoS Pathogens, 12, e1005811. https://doi.org/10.1371/journal.ppat.1005811
  • Hegenauer, V., Fürst, U., Kaiser, B., Smoker, M., Zipfel, C., Felix, G., Stahl, M., & Albert, M. (2016). Detection of the plant parasite Cuscuta reflexa by a tomato cell surface receptor Science, 353, 478–481. https://doi.org/10.1126/science.aaf3919
  • Yeh, Y.-H., Panzeri, D., Kadota, Y., Huang, Y.-C., Huang, P.-Y., Tao, C.-N., Roux, M., Chien, H.-C., Chin, T.-C., Chu, P.-W., Zipfel, C., & Zimmerli, L. (2016). The Arabidopsis Malectin-Like/LRR-RLK IOS1 is Critical for BAK1-Dependent and BAK1-Independent Pattern-Triggered Immunity Plant Cell, 28, 1701–1721. https://doi.org/10.1105/tpc.16.00313
  • Kamoun, S., & Zipfel, C. (2016). Fungal pathogenesis: Host modulation every which way Nature Microbiology, 1, 16075. https://doi.org/10.1038/nmicrobiol.2016.75
  • Pfeilmeier, S., Saur, I. M., Rathjen, J. P., Zipfel, C., & Malone, J. G. (2016). High levels of cyclic-di-GMP in plant-associated Pseudomonas correlate with evasion of plant immunity Molecular Plant Pathology, 17, 521–531. https://doi.org/10.1111/mpp.12297
  • Saur, I. M. L., Kadota, Y., Sklenar, J., Holton, N. J., Smakowska, E., Belkhadir, Y., Zipfel, C., & Rathjen, J. P. (2016). NbCSPR underlies age-dependent immune responses to bacterial cold shock protein in Nicotiana benthamiana Proceedings of the National Academy of Sciences of the United States of America, 113, 3389–3394. https://doi.org/10.1073/pnas.1511847113
  • Kamoun, S., & Zipfel, C. (2016). Class uncorrected errors as misconduct Nature, 531, 173. https://doi.org/10.1038/531173e
  • Morales, J., Kadota, Y., Zipfel, C., Molina, A., & Torres, M.-A. (2016). The Arabidopsis NADPH oxidases RbohD and RbohF display differential expression patterns and contributions during plant immunity Journal of Experimental Botany, 67, 1663–1676. https://doi.org/10.1093/jxb/erv558
  • Yue, K., Sandal, P., Williams, E. L., Murphy, E., Stes, E., Nikonorova, N., Ramakrishna, P., Czyzewicz, N., Montero-Morales, L., Kumpf, R., Lin, Z., van de Cotte, B., Iqbal, M., Van Bel, M., Van De Slijke, E., Meyer, M. R., Gadeyne, A., Zipfel, C., De Jaeger, G., … De Smet, I. (2016). PP2A-3 interacts with ACR4 and regulates formative cell division in the Arabidopsis root Proceedings of the National Academy of Sciences of the United States of America, 113, 1447–1452. https://doi.org/10.1073/pnas.1525122113
  • Trempel, F., Kajiura, H., Ranf, S., Grimmer, J., Westphal, L., Zipfel, C., Scheel, D., Fujiyama, K., & Lee, J. (2016). Altered glycosylation of exported proteins, including surface immune receptors, compromises calcium and downstream signaling responses to microbe-associated molecular patterns in Arabidopsis thaliana BMC Plant Biology, 16, 31. https://doi.org/10.1186/s12870-016-0718-3
  • Kadota, Y., Macho, A. P., & Zipfel, C. (2016). Immunoprecipitation of Plasma Membrane Receptor-Like Kinases for Identification of Phosphorylation Sites and Associated Proteins In M. A. Botella & J. Botella (Eds.), Plant signal transduction (pp. 133–144). Springer. https://doi.org/10.1007/978-1-4939-3115-6_11

• 2015

  • Jiménez-Góngora, T., Kim, S.-K., Lozano-Durán, R., & Zipfel, C. (2015). Flg22-Triggered Immunity Negatively Regulates Key BR Biosynthetic Genes Frontiers in Plant Science, 6, 981. https://doi.org/10.3389/fpls.2015.00981
  • Gou, M., Zhang, Z., Zhang, N., Huang, Q., Monaghan, J., Yang, H., Shi, Z., Zipfel, C., & Hua, J. (2015). Opposing effects on two phases of defense responses from concerted actions of HSC70 and BON1 in Arabidopsis Plant Physiology, 169, 2304–2323. https://doi.org/10.1104/pp.15.00970
  • Patron, N. J., Orzaez, D., Marillonnet, S., Warzecha, H., Matthewman, C., Youles, M., Raitskin, O., Leveau, A., Farré, G., Rogers, C., Smith, A., Hibberd, J., Webb, A. A. R., Locke, J., Schornack, S., Ajioka, J., Baulcombe, D. C., Zipfel, C., Kamoun, S., … et al. (2015). Standards for plant synthetic biology: a common syntax for exchange of DNA parts New Phytologist, 208, 13–19. https://doi.org/10.1111/nph.13532
  • Rickett, L. M., Pullen, N., Hartley, M., Zipfel, C., Kamoun, S., Baranyi, J., & Morris, R. J. (2015). Incorporating prior knowledge improves detection of differences in bacterial growth rate BMC Systems Biology, 9, 60. https://doi.org/10.1186/s12918-015-0204-9
  • Kadota, Y., Shirasu, K., & Zipfel, C. (2015). Regulation of the NADPH Oxidase RBOHD During Plant Immunity Plant & Cell Physiology, 56, 1472–1480. https://doi.org/10.1093/pcp/pcv063
  • Monaghan, J., Matschi, S., Romeis, T., & Zipfel, C. (2015). The calcium-dependent protein kinase CPK28 negatively regulates the BIK1-mediated PAMP-induced calcium burst Plant Signaling & Behavior, 10, e1018497. https://doi.org/10.1080/15592324.2015.1018497
  • Macho, A. P., Lozano-Durán, R., & Zipfel, C. (2015). Importance of tyrosine phosphorylation in receptor kinase complexes Trends in Plant Science, 20, 269–272. https://doi.org/10.1016/j.tplants.2015.02.005
  • Couto, D., Stransfeld, L., Arruabarrena, A., Zipfel, C., & Lozano-Durán, R. (2015). Broad application of a simple and affordable protocol for isolating plant RNA BMC Research Notes, 8, 154. https://doi.org/10.1186/s13104-015-1119-7
  • Schoonbeek, H., Wang, H., Stefanato, F. L., Craze, M., Bowden, S., Wallington, E., Zipfel, C., & Ridout, C. J. (2015). Arabidopsis EF‐Tu receptor enhances bacterial disease resistance in transgenic wheat New Phytologist, 206, 606–613. https://doi.org/10.1111/nph.13356
  • Schwessinger, B., Bahar, O., Thomas, N., Holton, N., Nekrasov, V., Ruan, D., Canlas, P. E., Daudi, A., Petzold, C. J., Singan, V. R., Kuo, R., Chovatia, M., Daum, C., Heazlewood, J. L., Zipfel, C., & Ronald, P. C. (2015). Transgenic Expression of the Dicotyledonous Pattern Recognition Receptor EFR in Rice Leads to Ligand-Dependent Activation of Defense Responses PLoS Pathogens, 11, e1004809. https://doi.org/10.1371/journal.ppat.1004809
  • Macho, A. P., & Zipfel, C. (2015). Targeting of plant pattern recognition receptor-triggered immunity by bacterial type-III secretion system effectors Current Opinion in Microbiology, 23, 14–22. https://doi.org/10.1016/j.mib.2014.10.009
  • Holton, N., Nekrasov, V., Ronald, P. C., & Zipfel, C. (2015). The Phylogenetically-Related Pattern Recognition Receptors EFR and XA21 Recruit Similar Immune Signaling Components in Monocots and Dicots PLoS Pathogens, 11, e1004602. https://doi.org/10.1371/journal.ppat.1004602
  • Lozano-Durán, R., & Zipfel, C. (2015). Trade-off between growth and immunity: role of brassinosteroids Trends in Plant Science, 20, 12–19. https://doi.org/10.1016/j.tplants.2014.09.003

• 2014

  • Etherington, G. J., Monaghan, J., Zipfel, C., & Maclean, D. (2014). Mapping mutations in plant genomes with the user-friendly web application CandiSNP Plant Methods, 10, 41. https://doi.org/10.1186/s13007-014-0041-7
  • Monaghan, J., Matschi, S., Shorinola, O., Rovenich, H., Matei, A., Segonzac, C., Malinovsky, F. G., Rathjen, J. P., Maclean, D., Romeis, T., & Zipfel, C. (2014). The Calcium-Dependent Protein Kinase CPK28 Buffers Plant Immunity and Regulates BIK1 Turnover Cell Host & Microbe, 16, 605–615. https://doi.org/10.1016/j.chom.2014.10.007
  • Segonzac, C., Macho, A. P., Sanmartín, M., Ntoukakis, V., Sánchez‐Serrano, J. J., & Zipfel, C. (2014). Negative control of BAK1 by protein phosphatase 2A during plant innate immunity The EMBO Journal, 33, 2069–2079. https://doi.org/10.15252/embj.201488698
  • Macho, A. P., & Zipfel, C. (2014). Plant PRRs and the Activation of Innate Immune Signaling Molecular Cell, 54, 263–272. https://doi.org/10.1016/j.molcel.2014.03.028
  • Kadota, Y., Sklenar, J., Derbyshire, P., Stransfeld, L., Asai, S., Ntoukakis, V., Jones, J. D., Shirasu, K., Menke, F., Jones, A., & Zipfel, C. (2014). Direct Regulation of the NADPH Oxidase RBOHD by the PRR-Associated Kinase BIK1 during Plant Immunity Molecular Cell, 54, 43–55. https://doi.org/10.1016/j.molcel.2014.02.021
  • Prince, D. C., Drurey, C., Zipfel, C., & Hogenhout, S. A. (2014). The Leucine-Rich Repeat Receptor-Like Kinase BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 and the Cytochrome P450 PHYTOALEXIN DEFICIENT3 Contribute to Innate Immunity to Aphids in Arabidopsis Plant Physiology, 164, 2207–2219. https://doi.org/10.1104/pp.114.235598
  • Macho, A. P., Schwessinger, B., Ntoukakis, V., Brutus, A., Segonzac, C., Roy, S., Kadota, Y., Oh, M.-H., Sklenar, J., Derbyshire, P., Lozano-Durán, R., Malinovsky, F. G., Monaghan, J., Menke, F. L. H., Huber, S. C., He, S. Y., & Zipfel, C. (2014). A Bacterial Tyrosine Phosphatase Inhibits Plant Pattern Recognition Receptor Activation Science, 343, 1509–1512. https://doi.org/10.1126/science.1248849
  • Lloyd, S. R., Schoonbeek, H., Trick, M., Zipfel, C., & Ridout, C. J. (2014). Methods to Study PAMP-Triggered Immunity in Brassica Species Molecular Plant-Microbe Interactions, 27, 286–295. https://doi.org/10.1094/mpmi-05-13-0154-fi
  • Trost, G., Vi, S. L., Czesnick, H., Lange, P., Holton, N., Giavalisco, P., Zipfel, C., Kappel, C., & Lenhard, M. (2014). Arabidopsis poly(A) polymerase PAPS1 limits founder-cell recruitment to organ primordia and suppresses the salicylic acid-independent immune response downstream of EDS1/PAD4 The Plant Journal, 77, 688–699. https://doi.org/10.1111/tpj.12421
  • Malinovsky, F. G., Batoux, M., Schwessinger, B., Youn, J. H., Stransfeld, L., Win, J., Kim, S.-K., & Zipfel, C. (2014). Antagonistic regulation of growth and immunity by the Arabidopsis basic helix-loop-helix transcription factor homolog of brassinosteroid enhanced expression2 interacting with increased leaf inclination1 binding bHLH1 Plant Physiology, 164, 1443–1455. https://doi.org/10.1104/pp.113.234625
  • Trdá, L., Fernandez, O., Boutrot, F., Héloir, M., Kelloniemi, J., Daire, X., Adrian, M., Clément, C., Zipfel, C., Dorey, S., & Poinssot, B. (2014). The grapevine flagellin receptor VvFLS2 differentially recognizes flagellin-derived epitopes from the endophytic growth-promoting bacterium Burkholderia phytofirmans and plant pathogenic bacteria New Phytologist, 201, 1371–1384. https://doi.org/10.1111/nph.12592

• 2013

  • Lozano-Durán, R., Macho, A. P., Boutrot, F., Segonzac, C., Somssich, I. E., & Zipfel, C. (2013). The transcriptional regulator BZR1 mediates trade-off between plant innate immunity and growth ELife, 2, e00983. https://doi.org/10.7554/elife.00983
  • Sun, Y., Li, L., Macho, A. P., Han, Z., Hu, Z., Zipfel, C., Zhou, J.-M., & Chai, J. (2013). Structural Basis for flg22-Induced Activation of the Arabidopsis FLS2-BAK1 Immune Complex Science, 342, 624–628. https://doi.org/10.1126/science.1243825
  • Zhang, W., Fraiture, M., Kolb, D., Löffelhardt, B., Desaki, Y., Boutrot, F. F. G., Tör, M., Zipfel, C., Gust, A. A., & Brunner, F. (2013). Arabidopsis receptor-like protein30 and receptor-like kinase suppressor of BIR1-1/EVERSHED mediate innate immunity to necrotrophic fungi Plant Cell, 25, 4227–4241. https://doi.org/10.1105/tpc.113.117010
  • Asai, S., Ichikawa, T., Nomura, H., Kobayashi, M., Kamiyoshihara, Y., Mori, H., Kadota, Y., Zipfel, C., Jones, J. D. G., & Yoshioka, H. (2013). The Variable Domain of a Plant Calcium-dependent Protein Kinase (CDPK) Confers Subcellular Localization and Substrate Recognition for NADPH Oxidase Journal of Biological Chemistry, 288, 14332–14340. https://doi.org/10.1074/jbc.m112.448910
  • Farid, A., Gro Malinovsky, F., Veit, C., Schoberer, J., Zipfel, C., & Strasser, R. (2013). Specialized Roles of the Conserved Subunit OST3/6 of the Oligosaccharyltransferase Complex in Innate Immunity and Tolerance to Abiotic Stresses Plant Physiology, 162, 24–38. https://doi.org/10.1104/pp.113.215509
  • Zipfel, C. (2013). Combined roles of ethylene and endogenous peptides in regulating plant immunity and growth Proceedings of the National Academy of Sciences of the United States of America, 110, 5748–5749. https://doi.org/10.1073/pnas.1302659110
  • Nicaise, V., Joe, A., Jeong, B., Korneli, C., Boutrot, F., Westedt, I., Staiger, D., Alfano, J. R., & Zipfel, C. (2013). Pseudomonas HopU1 modulates plant immune receptor levels by blocking the interaction of their mRNAs with GRP7 The EMBO Journal, 32, 701–712. https://doi.org/10.1038/emboj.2013.15

• 2012

  • Win, J., Chaparro-Garcia, A., Belhaj, K., Saunders, D. G. O., Yoshida, K., Dong, S., Schornack, S., Zipfel, C., Robatzek, S., Hogenhout, S. A., & Kamoun, S. (2012). Effector Biology of Plant-Associated Organisms: Concepts and Perspectives Cold Spring Harbor Symposia on Quantitative Biology, 77, 235–247. https://doi.org/10.1101/sqb.2012.77.015933
  • Segonzac, C., Nimchuk, Z. L., Beck, M., Tarr, P. T., Robatzek, S., Meyerowitz, E. M., & Zipfel, C. (2012). The Shoot Apical Meristem Regulatory Peptide CLV3 Does Not Activate Innate Immunity Plant Cell, 24, 3186–3192. https://doi.org/10.1105/tpc.111.091264
  • Monaghan, J., & Zipfel, C. (2012). Plant pattern recognition receptor complexes at the plasma membrane Current Opinion in Plant Biology, 15, 349–357. https://doi.org/10.1016/j.pbi.2012.05.006
  • Macho, A. P., Boutrot, F., Rathjen, J. P., & Zipfel, C. (2012). Aspartate Oxidase Plays an Important Role in Arabidopsis Stomatal Immunity Plant Physiology, 159, 1845–1856. https://doi.org/10.1104/pp.112.199810
  • Roux, M., & Zipfel, C. (2012). Receptor Kinase Interactions: Complexity of Signalling In F. Tax & B. Kemmerling (Eds.), Receptor-like kinases in plants : from development to defense (pp. 145–172). Springer. https://doi.org/10.1007/978-3-642-23044-8_9
  • Marshall, A., Aalen, R. B., Audenaert, D., Beeckman, T., Broadley, M. R., Butenko, M. A., Caño-Delgado, A. I., de Vries, S., Dresselhaus, T., Felix, G., Graham, N. S., Foulkes, J., Granier, C., Greb, T., Grossniklaus, U., Hammond, J. P., Heidstra, R., Hodgman, C., Hothorn, M., … De Smet, I. (2012). Tackling drought stress: receptor-like kinases present new approaches Plant Cell, 24, 2262–2278. https://doi.org/10.1105/tpc.112.096677

• 2011

  • Ntoukakis, V., Schwessinger, B., Segonzac, C., & Zipfel, C. (2011). Cautionary Notes on the Use of C-Terminal BAK1 Fusion Proteins for Functional Studies Plant Cell, 23, 3871–3878. https://doi.org/10.1105/tpc.111.090779
  • Albrecht, C., Boutrot, F., Segonzac, C., Schwessinger, B., Gimenez-Ibanez, S., Chinchilla, D., Rathjen, J. P., de Vries, S. C., & Zipfel, C. (2011). Brassinosteroids inhibit pathogen-associated molecular pattern–triggered immune signaling independent of the receptor kinase BAK1 Proceedings of the National Academy of Sciences of the United States of America, 109, 303–308. https://doi.org/10.1073/pnas.1109921108
  • Denness, L., McKenna, J. F., Segonzac, C., Wormit, A., Madhou, P., Bennett, M., Mansfield, J., Zipfel, C., & Hamann, T. (2011). Cell Wall Damage-Induced Lignin Biosynthesis Is Regulated by a Reactive Oxygen Species- and Jasmonic Acid-Dependent Process in Arabidopsis Plant Physiology, 156, 1364–1374. https://doi.org/10.1104/pp.111.175737
  • Roux, M., Schwessinger, B., Albrecht, C., Chinchilla, D., Jones, A., Holton, N., Malinovsky, F. G., Tör, M., de Vries, S., & Zipfel, C. (2011). The Arabidopsis Leucine-Rich Repeat Receptor–Like Kinases BAK1/SERK3 and BKK1/SERK4 Are Required for Innate Immunity to Hemibiotrophic and Biotrophic Pathogens Plant Cell, 23, 2440–2455. https://doi.org/10.1105/tpc.111.084301
  • Segonzac, C., Feike, D., Gimenez-Ibanez, S., Hann, D. R., Zipfel, C., & Rathjen, J. P. (2011). Hierarchy and Roles of Pathogen-Associated Molecular Pattern-Induced Responses in Nicotiana benthamiana Plant Physiology, 156, 687–699. https://doi.org/10.1104/pp.110.171249
  • Schwessinger, B., Roux, M., Kadota, Y., Ntoukakis, V., Sklenar, J., Jones, A., & Zipfel, C. (2011). Phosphorylation-Dependent Differential Regulation of Plant Growth, Cell Death, and Innate Immunity by the Regulatory Receptor-Like Kinase BAK1 PLoS Genetics, 7, e1002046. https://doi.org/10.1371/journal.pgen.1002046
  • Liebminger, E., Veit, C., Pabst, M., Batoux, M., Zipfel, C., Altmann, F., Mach, L., & Strasser, R. (2011). β-N-Acetylhexosaminidases HEXO1 and HEXO3 Are Responsible for the Formation of Paucimannosidic N-Glycans in Arabidopsis thaliana Journal of Biological Chemistry, 286, 10793–10802. https://doi.org/10.1074/jbc.m110.178020
  • Segonzac, C., & Zipfel, C. (2011). Activation of plant pattern-recognition receptors by bacteria Current Opinion in Microbiology, 14, 54–61. https://doi.org/10.1016/j.mib.2010.12.005
  • Chaparro-Garcia, A., Wilkinson, R. C., Gimenez-Ibanez, S., Findlay, K., Coffey, M. D., Zipfel, C., Rathjen, J. P., Kamoun, S., & Schornack, S. (2011). The Receptor-Like Kinase SERK3/BAK1 Is Required for Basal Resistance against the Late Blight Pathogen Phytophthora infestans in Nicotiana benthamiana PLoS ONE, 6, e16608. https://doi.org/10.1371/journal.pone.0016608

• 2010

  • Zipfel, C., & Robatzek, S. (2010). Pathogen-Associated Molecular Pattern-Triggered Immunity: Veni, Vidi…? Plant Physiology, 154, 551–554. https://doi.org/10.1104/pp.110.161547
  • Malinovsky, F. G., Brodersen, P., Fiil, B. K., McKinney, L. V., Thorgrimsen, S., Beck, M., Nielsen, H. B., Pietra, S., Zipfel, C., Robatzek, S., Petersen, M., Hofius, D., & Mundy, J. (2010). Lazarus1, a DUF300 Protein, Contributes to Programmed Cell Death Associated with Arabidopsis acd11 and the Hypersensitive Response PLoS ONE, 5, e12586. https://doi.org/10.1371/journal.pone.0012586
  • Boutrot, F., Segonzac, C., Chang, K. N., Qiao, H., Ecker, J. R., Zipfel, C., & Rathjen, J. P. (2010). Direct transcriptional control of the Arabidopsis immune receptor FLS2 by the ethylene-dependent transcription factors EIN3 and EIL1 Proceedings of the National Academy of Sciences of the United States of America, 107, 14502–14507. https://doi.org/10.1073/pnas.1003347107
  • Lacombe, S., Rougon-Cardoso, A., Sherwood, E., Peeters, N., Dahlbeck, D., van Esse, H. P., Smoker, M., Rallapalli, G., Thomma, B. P. H. J., Staskawicz, B., Jones, J. D. G., & Zipfel, C. (2010). Interfamily transfer of a plant pattern-recognition receptor confers broad-spectrum bacterial resistance Nature Biotechnology, 28, 365–369. https://doi.org/10.1038/nbt.1613

• 2009

  • Nekrasov, V., Li, J., Batoux, M., Roux, M., Chu, Z.-H., Lacombe, S., Rougon, A., Bittel, P., Kiss-Papp, M., Chinchilla, D., van Esse, H. P., Jorda, L., Schwessinger, B., Nicaise, V., Thomma, B. P. H. J., Molina, A., Jones, J. D. G., & Zipfel, C. (2009). Control of the pattern-recognition receptor EFR by an ER protein complex in plant immunity The EMBO Journal, 28, 3428–3438. https://doi.org/10.1038/emboj.2009.262
  • Li, J., Chu, Z.-H., Batoux, M., Nekrasov, V., Roux, M., Chinchilla, D., Zipfel, C., & Jones, J. D. G. (2009). Specific ER quality control components required for biogenesis of the plant innate immune receptor EFR Proceedings of the National Academy of Sciences of the United States of America, 106, 15973–15978. https://doi.org/10.1073/pnas.0905532106
  • Zipfel, C. (2009). Early molecular events in PAMP-triggered immunity Current Opinion in Plant Biology, 12, 414–420. https://doi.org/10.1016/j.pbi.2009.06.003
  • Nicaise, V., Roux, M., & Zipfel, C. (2009). Recent Advances in PAMP-Triggered Immunity against Bacteria: Pattern Recognition Receptors Watch over and Raise the Alarm Plant Physiology, 150, 1638–1647. https://doi.org/10.1104/pp.109.139709

• 2008

  • Schwessinger, B., & Zipfel, C. (2008). News from the frontline: recent insights into PAMP-triggered immunity in plants Current Opinion in Plant Biology, 11, 389–395. https://doi.org/10.1016/j.pbi.2008.06.001
  • Wang, G., Ellendorff, U., Kemp, B., Mansfield, J. W., Forsyth, A., Mitchell, K., Bastas, K., Liu, C.-M., Woods-Tör, A., Zipfel, C., de Wit, P. J. G. M., Jones, J. D. G., Tör, M., & Thomma, B. P. H. J. (2008). A Genome-Wide Functional Investigation into the Roles of Receptor-Like Proteins in Arabidopsis Plant Physiology, 147, 503–517. https://doi.org/10.1104/pp.108.119487
  • Zipfel, C., & Rathjen, J. P. (2008). Plant Immunity: AvrPto Targets the Frontline Current Biology, 18, R218–R220. https://doi.org/10.1016/j.cub.2008.01.016
  • Zipfel, C. (2008). Pattern-recognition receptors in plant innate immunity Current Opinion in Immunology, 20, 10–16. https://doi.org/10.1016/j.coi.2007.11.003

• 2007

  • Chinchilla, D., Zipfel, C., Robatzek, S., Kemmerling, B., Nürnberger, T., Jones, J. D. G., Felix, G., & Boller, T. (2007). A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence Nature, 448, 497–500. https://doi.org/10.1038/nature05999

• 2006

  • Molinier, J., Ries, G., Zipfel, C., & Hohn, B. (2006). Transgeneration memory of stress in plants Nature, 442, 1046–1049. https://doi.org/10.1038/nature05022
  • Zipfel, C., Kunze, G., Chinchilla, D., Caniard, A., Jones, J. D. G., Boller, T., & Felix, G. (2006). Perception of the Bacterial PAMP EF-Tu by the Receptor EFR Restricts Agrobacterium-Mediated Transformation Cell, 125, 749–760. https://doi.org/10.1016/j.cell.2006.03.037

• 2005

  • Zipfel, C., & Felix, G. (2005). Plants and animals: a different taste for microbes? Current Opinion in Plant Biology, 8, 353–360. https://doi.org/10.1016/j.pbi.2005.05.004

• 2004

  • Kunze, G., Zipfel, C., Robatzek, S., Niehaus, K., Boller, T., & Felix, G. (2004). The N Terminus of Bacterial Elongation Factor Tu Elicits Innate Immunity in Arabidopsis Plants Plant Cell, 16, 3496–3507. https://doi.org/10.1105/tpc.104.026765
  • Navarro, L., Zipfel, C., Rowland, O., Keller, I., Robatzek, S., Boller, T., & Jones, J. D. G. (2004). The Transcriptional Innate Immune Response to flg22. Interplay and Overlap with Avr Gene-Dependent Defense Responses and Bacterial Pathogenesis Plant Physiology, 135, 1113–1128. https://doi.org/10.1104/pp.103.036749
  • Zipfel, C., Robatzek, S., Navarro, L., Oakeley, E. J., Jones, J. D. G., Felix, G., & Boller, T. (2004). Bacterial disease resistance in Arabidopsis through flagellin perception Nature, 428, 764–767. https://doi.org/10.1038/nature02485