Specific ER quality control components required for biogenesis of the plant innate immune receptor EFR

Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana

Clough, S. J., & Bent, A. F. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00343.x · Cited by 22,014

The plant immune system

Jones, J. D. G., & Dangl, J. L. (2006) · Nature · doi:10.1038/nature05286 · Cited by 13,177

Plant pathogens and integrated defence responses to infection

Dangl, J. L., & Jones, J. D. G. (2001) · Nature · doi:10.1038/35081161 · Cited by 3,959

Host-Microbe Interactions: Shaping the Evolution of the Plant Immune Response

Chisholm, S. T., Coaker, G., Day, B., & Staskawicz, B. J. (2006) · Cell · doi:10.1016/j.cell.2006.02.008 · Cited by 2,957

FLS2

Gómez‐Gómez, L., & Boller, T. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)80265-8 · Cited by 2,319

A multicolored set of in vivo organelle markers for co‐localization studies in Arabidopsis and other plants

Nelson, B. K., Cai, X., & Nebenführ, A. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03212.x · Cited by 2,086

Perception of the Bacterial PAMP EF-Tu by the Receptor EFR Restricts Agrobacterium-Mediated Transformation

Zipfel, C., Kunze, G., Chinchilla, D., Caniard, A., Jones, J. D. G., Boller, T., & Felix, G. (2006) · Cell · doi:10.1016/j.cell.2006.03.037 · Cited by 2,068

A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence

Chinchilla, D., Zipfel, C., Robatzek, S., Kemmerling, B., Nürnberger, T., Jones, J. D. G., Felix, G., & Boller, T. (2007) · Nature · doi:10.1038/nature05999 · Cited by 1,923

Bacterial disease resistance in Arabidopsis through flagellin perception

Zipfel, C., Robatzek, S., Navarro, L., Oakeley, E. J., Jones, J. D. G., Felix, G., & Boller, T. (2004) · Nature · doi:10.1038/nature02485 · Cited by 1,793

Plants have a sensitive perception system for the most conserved domain of bacterial flagellin

Felix, G., Duran, J. D., Volko, S. M., & Boller, T. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00265.x · Cited by 1,719

Salicylic acid signalling: new insights and prospects at a quarter-century milestone

Liu, X., Rockett, K. S., Kørner, C. J., & Pajerowska-Mukhtar, K. M. (2015) · Essays in Biochemistry · doi:10.1042/bse0580101 · Cited by 48

Plant ERD2‐like proteins function as endoplasmic reticulum luminal protein receptors and participate in programmed cell death during innate immunity

Xu, G., Li, S., Xie, K., Zhang, Q., Wang, Y., Tang, Y., Liu, D., Hong, Y., He, C., & Liu, Y. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.05053.x · Cited by 46

The function of calreticulin in plant immunity

Qiu, Y., Xi, J. H., Du, L., & Poovaiah, B. W. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.20721 · Cited by 46

An important role of l ‐fucose biosynthesis and protein fucosylation genes in Arabidopsis immunity

Zhang, L., Paasch, B. C., Chen, J., Day, B., & He, S. Y. (2018) · New Phytologist · doi:10.1111/nph.15639 · Cited by 47

Transcriptome reprogramming during severe dehydration contributes to physiological and metabolic changes in the resurrection plant Haberlea rhodopensis

Liu, J., Moyankova, D., Lin, C.-T., Mladenov, P., Sun, R., Djilianov, D. L., & Deng, X. (2018) · BMC Plant Biology · doi:10.1186/s12870-018-1566-0 · Cited by 46

PAWH1 and PAWH2 are plant-specific components of an Arabidopsis endoplasmic reticulum-associated degradation complex

Lin, L. L., Zhang, C.-C., Chen, Y., Wang, Y., Wang, D., Liu, X., Wang, M., Mao, J., Zhang, J., Xing, W., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11480-7 · Cited by 46

An update on evolutionary, structural, and functional studies of receptor-like kinases in plants

Liu, J., Li, W., Wu, G., & Ali, K. (2024) · Frontiers in Plant Science · doi:10.3389/fpls.2024.1305599 · Cited by 45

Loss of all three calreticulins, CRT1, CRT2 and CRT3, causes enhanced sensitivity to water stress in Arabidopsis

Kim, J. H., Nguyen, N. H., Nguyen, N. T., Hong, S., & Lee, H. (2013) · Plant Cell Reports · doi:10.1007/s00299-013-1497-z · Cited by 46

Overexpression of a Triticum aestivum Calreticulin gene (TaCRT1) Improves Salinity Tolerance in Tobacco

Xiang, Y., Lü, Y., Song, M., Wang, Y., Xu, W., Wu, L., Wang, H., & Ma, Z. (2015) · PLoS ONE · doi:10.1371/journal.pone.0140591 · Cited by 45

Cell Death Signaling From Endoplasmic Reticulum Stress: Plant-Specific and Conserved Features

Simoni, E. B., Oliveira, C. C., Fraga, O. T., Reis, P. A. B., & Fontes, E. P. B. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.835738 · Cited by 42

Post-Translational Modifications of Proteins Have Versatile Roles in Regulating Plant Immune Responses

Yin, J., Yi, H., Chen, X., & Wang, J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112807 · Cited by 44

Arabidopsis Clade I TGA Factors Regulate Apoplastic Defences against the Bacterial Pathogen Pseudomonas syringae through Endoplasmic Reticulum-Based Processes

Wang, L., & Fobert, P. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077378 · Cited by 45

Altered glycosylation of exported proteins, including surface immune receptors, compromises calcium and downstream signaling responses to microbe-associated molecular patterns in Arabidopsis thaliana

Trempel, F., Kajiura, H., Ranf, S., Grimmer, J., Westphal, L., Zipfel, C., Scheel, D., Fujiyama, K., & Lee, J. (2016) · BMC Plant Biology · doi:10.1186/s12870-016-0718-3 · Cited by 44

Differentiation between MAMP Triggered Defenses in Arabidopsis thaliana

Vetter, M., Karasov, T. L., & Bergelson, J. M. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006068 · Cited by 41

Dual impact of ambient humidity on the virulence of Magnaporthe oryzae and basal resistance in rice

Qiu, J., Liu, Z., Xie, J., Lan, B., Shen, Z., Shi, H., Lin, F., Shen, X., & Kou, Y. (2022) · Plant Cell & Environment · doi:10.1111/pce.14452 · Cited by 40

Genome-Wide Computational Function Prediction of Arabidopsis Proteins by Integration of Multiple Data Sources

Kourmpetis, Y. A. I., van Dijk, A. D. J., van Ham, R. C. H. J., & ter Braak, C. J. F. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.162164 · Cited by 39

Weighted gene co-expression network analysis unveils gene networks associated with the Fusarium head blight resistance in tetraploid wheat

Sari, E., Cabral, A. L., Polley, B., Tan, Y., Hsueh, E., Konkin, D. J. F., Knox, R. E., Ruan, Y., & Fobert, P. R. (2019) · BMC Genomics · doi:10.1186/s12864-019-6161-8 · Cited by 39

Several MAMPs, including chitin fragments, enhanceAtPep-triggered oxidative burst independently of wounding

Klauser, D., Flury, P., Boller, T., & Bartels, S. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.25346 · Cited by 38

Chaperones of the endoplasmic reticulum are required for Ve1 ‐mediated resistance to V erticillium

Liebrand, T. W. H., Kombrink, A., Zhang, Z., Sklenář, J., Jones, A. M. E., Robatzek, S., Thomma, B. P. H. J., & JOOSTEN, M. H. A. J. (2013) · Molecular Plant Pathology · doi:10.1111/mpp.12071 · Cited by 40

Plant Cells under Attack: Unconventional Endomembrane Trafficking during Plant Defense

Ruano, G., & Scheuring, D. (2020) · Plants · doi:10.3390/plants9030389 · Cited by 38

WRKY7, -11 and -17 transcription factors are modulators of the bZIP28 branch of the unfolded protein response during PAMP-triggered immunity in Arabidopsis thaliana

Arraño‐Salinas, P., Dominguez-Figueroa, J. D., Herrera‐Vásquez, A., Zavala, D., Medina, J., Vicente‐Carbajosa, J., Meneses, C., Canessa, P., Moreno, A. A., & Blanco‐Herrera, F. (2018) · Plant Science · doi:10.1016/j.plantsci.2018.09.019 · Cited by 36

The endoplasmic reticulum-quality control component SDF2 is essential for XA21-mediated immunity in rice

Park, C., Sharma, R. A., Lefebvre, B., Canlas, P. E., & Ronald, P. C. (2013) · Plant Science · doi:10.1016/j.plantsci.2013.05.003 · Cited by 36

ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants

Tintor, N., & Saijo, Y. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00065 · Cited by 34

Receptor-Like Kinases and Regulation of Plant Innate Immunity

He, K., & Wu, Y. (2016) · The Enzymes · doi:10.1016/bs.enz.2016.09.003 · Cited by 36

Association analysis for resistance to Striga hermonthica in diverse tropical maize inbred lines

Stanley, A. E., Menkir, A., Ifie, B. E., Paterne, A. A., Unachukwu, N. N., Meseka, S. K., Mengesha, W., Bossey, B., Kwadwo, O., Tongoona, P. B., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-03566-4 · Cited by 35

Arabidopsis p24δ5 and p24δ9 facilitate Coat Protein I‐dependent transport of the K/ HDEL receptor ERD 2 from the Golgi to the endoplasmic reticulum

Montesinos, J. C., Pastor‐Cantizano, N., Robinson, D. G., Marcote, M. J., & Aniento, F. (2014) · The Plant Journal · doi:10.1111/tpj.12700 · Cited by 34

Susceptibility factor RTP1 negatively regulates Phytophthora parasitica resistance via modulating UPR regulators bZIP60 and bZIP28

Qiang, X., Liu, X., Wang, X., Zheng, Q., Kang, L., Gao, X., Wei, Y., Wu, W., Zhao, H. G., & Shan, W. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab126 · Cited by 34

The Function of Rac Small GTPase and Associated Proteins in Rice Innate Immunity

Kawano, Y., Chen, L., & Shimamoto, K. (2010) · Rice · doi:10.1007/s12284-010-9049-4 · Cited by 33

N‐linked glycosylation of At VSR 1 is important for vacuolar protein sorting in A rabidopsis

Shen, J., Ding, Y., Gao, C., Rojo, E., & Jiang, L. (2014) · The Plant Journal · doi:10.1111/tpj.12696 · Cited by 33

Arabidopsis Endoplasmic Reticulum-Localized UBAC2 Proteins Interact with PAMP-INDUCED COILED-COIL to Regulate Pathogen-Induced Callose Deposition and Plant Immunity

Wang, Z., Li, X., Wang, X., Liu, N., Xu, B., Peng, Q., Guo, Z., Fan, B., Zhu, C., & Chen, Z. (2019) · The Plant Cell · doi:10.1105/tpc.18.00334 · Cited by 32

Quantitative proteomics analysis reveals resistance differences of banana cultivar ‘Brazilian’ to Fusarium oxysporum f. sp. cubense races 1 and 4

Dong, H., Li, Y., Fan, H., Zhou, D., & Li, H. (2019) · Journal of Proteomics · doi:10.1016/j.jprot.2019.05.004 · Cited by 31

A lineage-specific Exo70 is required for receptor kinase–mediated immunity in barley

Holden, S., Bergum, M., Green, P., Bettgenhaeuser, J., Hernández-Pinzón, I., Thind, A., Clare, S., Russell, J. M., Hubbard, A., Taylor, J., et al. (2022) · Science Advances · doi:10.1126/sciadv.abn7258 · Cited by 29

Identification of defense-related genes newly-associated with tomato flower abscission

Meir, S., Philosoph‐Hadas, S., Sundaresan, S., Selvaraj, K. S. V., Burd, S., Ophir, R., Kochanek, K. S. B., Reid, M. S., Jiang, C., & Lers, A. (2011) · Plant Signaling & Behavior · doi:10.4161/psb.6.4.15043 · Cited by 31

Requirement of a Homolog of Glucosidase II β-Subunit for EFR-Mediated Defense Signaling in Arabidopsis thaliana

von Numers, N., Survila, M., Aalto, M. K., Batoux, M., Heino, P. I., Palva, E. T., & Li, J. (2010) · Molecular Plant · doi:10.1093/mp/ssq017 · Cited by 31

Regulation of SOBIR 1 accumulation and activation of defense responses in bir1–1 by specific components of ER quality control

Sun, T., Zhang, Q., Gao, M., & Zhang, Y. (2014) · The Plant Journal · doi:10.1111/tpj.12425 · Cited by 29

Protein Changes in Response to Lead Stress of Lead-Tolerant and Lead-Sensitive Industrial Hemp Using SWATH Technology

Xia, C., Hong, L., Yang, Y., Yanping, X., Huang, X., & Deng, G. (2019) · Genes · doi:10.3390/genes10050396 · Cited by 29

Long Chain Acyl-Coenzyme A Synthetase 4 (BnLACS4) Gene from Brassica napus Enhances the Yeast Lipid Contents

Tan, X., Zheng, X., Zhang, Z., Wang, Z., Xia, H., Lu, C., & Gu, S. (2014) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(13)60583-3 · Cited by 28

Systematic deletion of the ER lectin chaperone genes reveals their roles in vegetative growth and male gametophyte development in Arabidopsis

Vu, K. V., Nguyen, N. T., Jeong, C. Y., Lee, Y., Lee, H., & Hong, S. (2016) · The Plant Journal · doi:10.1111/tpj.13435 · Cited by 28

Modulation of ERQC and ERAD: A Broad-Spectrum Spanner in the Works of Cancer Cells?

Tax, G., Lia, A., Santino, A., & Roversi, P. (2019) · Journal of Oncology · doi:10.1155/2019/8384913 · Cited by 28

Clamping, bending, and twisting inter-domain motions in the misfold-recognizing portion of UDP-glucose: Glycoprotein glucosyltransferase

Modenutti, C. P., Capurro, J. I. B., Ibba, R., Alonzi, D. S., Song, M. N., Vasiljević, S., Kumar, A., Chandran, A. V., Tax, G., Marti, L., et al. (2020) · Structure · doi:10.1016/j.str.2020.11.017 · Cited by 28

Modulating Plant Calcium for Better Nutrition and Stress Tolerance

Robertson, D. (2013) · ISRN Botany · doi:10.1155/2013/952043 · Cited by 28

Plant Pathogens Utilize Effectors to Hijack the Host Endoplasmic Reticulum as Part of Their Infection Strategy

Jing, M., & Wang, Y. (2020) · Engineering · doi:10.1016/j.eng.2020.03.003 · Cited by 27

Phytophthora infection signals‐induced translocation of NAC089 is required for endoplasmic reticulum stress response‐mediated plant immunity

Ai, G., Zhu, H., Fu, X., Liu, J., Li, T., Cheng, Y., Zhou, Y., Yang, K., Pan, W., Zhang, H., et al. (2021) · The Plant Journal · doi:10.1111/tpj.15425 · Cited by 27

Predominant Golgi Residency of the Plant K/HDEL Receptor Is Essential for Its Function in Mediating ER Retention

Silva‐Alvim, F. A. L., An, J., Alvim, J. C., Foresti, O., Grippa, A., Pelgrom, A. J. E., Adams, T. L., Hawes, C. R., & Denecke, J. (2018) · The Plant Cell · doi:10.1105/tpc.18.00426 · Cited by 27

FLS2-BAK1 Extracellular Domain Interaction Sites Required for Defense Signaling Activation

Koller, T., & Bent, A. F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111185 · Cited by 26

Exploitation of Tolerance of Wheat Kernel Weight and Shape-Related Traits from Aegilops tauschii under Heat and Combined Heat-Drought Stresses

Elhadi, G. M. I., Kamal, N. M., Gorafi, Y. S. A., Yamasaki, Y., Takata, K., Tahir, I. S. A., Itam, M., Tanaka, H., & Tsujimoto, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041830 · Cited by 26

Directed Evolution of FLS2 towards Novel Flagellin Peptide Recognition

Helft, L., Thompson, M., & Bent, A. F. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157155 · Cited by 26

Diverging functions among calreticulin isoforms in higher plants

Thelin, L., Mutwil, M., Sommarin, M., & Persson, S. (2011) · Plant Signaling & Behavior · doi:10.4161/psb.6.6.15339 · Cited by 25

Unmasking host and microbial strategies in the Agrobacterium-plant defense tango

Hwang, E. E., Wang, M. B., Bravo, J. E., & Banta, L. M. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00200 · Cited by 25

TabZIP74 Acts as a Positive Regulator in Wheat Stripe Rust Resistance and Involves Root Development by mRNA Splicing

Wang, F., Lin, R., Li, Y., Wang, P., Feng, J., Chen, W., & Xu, S. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01551 · Cited by 24

The Crucial Role of Demannosylating Asparagine-Linked Glycans in ERADicating Misfolded Glycoproteins in the Endoplasmic Reticulum

Zhang, J., Wu, J., Liu, L., & Li, J. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2020.625033 · Cited by 24

Arabidopsis ERdj3B coordinates with ERECTA-family receptor kinases to regulate ovule development and the heat stress response

Leng, Y.-J., Yao, Y.-S., Yang, K., Wu, P.-X., Xia, Y., Zuo, C.-R., Luo, J.-H., Wang, P., Liu, Y.-Y., Zhang, X., et al. (2022) · The Plant Cell · doi:10.1093/plcell/koac226 · Cited by 25

The evolutionary history of calreticulin and calnexin genes in green plants

Del‐Bem, L. (2011) · Genetica · doi:10.1007/s10709-010-9544-y · Cited by 24

Loss of Arabidopsis p24 function affects ERD2 trafficking and Golgi structure, and activates the unfolded protein response

Pastor‐Cantizano, N., Bernat-Silvestre, C., Marcote, M. J., & Aniento, F. (2017) · Journal of Cell Science · doi:10.1242/jcs.203802 · Cited by 24

The nematode effector calreticulin competes with the high mobility group protein OsHMGB1 for binding to the rice calmodulin‐like protein OsCML31 to enhance rice susceptibility to Meloidogyne graminicola

Liu, J., Zhang, J., Wei, Y., Su, W., Li, W., Wang, B., Peng, D., Gheysen, G., Peng, H., & Dai, L. (2024) · Plant Cell & Environment · doi:10.1111/pce.14848 · Cited by 23

Double-faced role of Bcl-2-associated athanogene 7 in plant–Phytophthora interaction

Zhou, Y., Yang, K., Cheng, M., Cheng, Y., Li, Y., Ai, G., Bai, T., Xu, R., Duan, W., Peng, H. F., et al. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab252 · Cited by 23

Cotton Bollworm (H. armigera) Effector PPI5 Targets FKBP17‐2 to Inhibit ER Immunity and JA/SA Responses, Enhancing Insect Feeding

Wang, Y., Zhu, C., Chen, G., Li, X., Zhu, M., Alariqi, M., Hussian, A., Ma, W., Lindsey, K., Zhang, X., et al. (2024) · Advanced Science · doi:10.1002/advs.202407826 · Cited by 23

Key roles of calreticulin and calnexin proteins in plant perception under stress conditions: a review.

Garg, G., Yadav, S. K., Ruchi, & Yadav, G. (2015) · Advances in life sciences · Cited by 22

(De)Activation (Ir)Reversibly or Degradation: Dynamics of Post-Translational Protein Modifications in Plants

Muleya, V., Lois, L. M., Chahtane, H., Thomas, L. A., Chiapello, M., & Marondedze, C. (2022) · Life · doi:10.3390/life12020324 · Cited by 21

Powdery mildew effectors AVR A1 and BEC1016 target the ER J‐domain protein Hv ERdj3B required for immunity in barley

Li, Z., Zapata, V. V., Elmore, J. M., Li, X., Xie, W., Deb, S., Tian, X., Banerjee, S., Jørgensen, H. J. L., Pedersen, C., et al. (2024) · Molecular Plant Pathology · doi:10.1111/mpp.13463 · Cited by 20

GANAB and N-Glycans Substrates Are Relevant in Human Physiology, Polycystic Pathology and Multiple Sclerosis: A Review

De Masi, R., & Orlando, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137373 · Cited by 20

Defense strategies for plant health: Disease resistance and tolerance

Tang, Z., Mou, R., & Xu, G. (2025) · The Plant Cell · doi:10.1093/plcell/koaf186 · Cited by 19

Comparative Label-Free Quantitative Proteomics Analysis Reveals the Essential Roles of N-Glycans in Salt Tolerance by Modulating Protein Abundance in Arabidopsis

Liu, C., Niu, G., Li, X., Zhang, H., Chen, H., Hou, D., Lan, P., & Hong, Z. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.646425 · Cited by 19

The participation of plant cell organelles in compatible and incompatible potato virus Y-tobacco and -potato plant interaction

Otulak-Kozieł, K., & Garbaczewska, G. (2013) · Acta Physiologiae Plantarum · doi:10.1007/s11738-013-1389-4 · Cited by 19

Emerging roles of molecular chaperones in plant innate immunity

Chen, L., & Shimamoto, K. (2010) · Journal of General Plant Pathology · doi:10.1007/s10327-010-0286-6 · Cited by 19

Knock-down of protein phosphatase 2A subunit B’γ promotes phosphorylation of CALRETICULIN 1 in Arabidopsis thaliana

Trotta, A., Konert, G., Rahikainen, M. M., Aro, E., & Kangasjärvi, S. (2011) · Plant Signaling & Behavior · doi:10.4161/psb.6.11.17829 · Cited by 18

ER Quality Control Components UGGT and STT3a Are Required for Activation of Defense Responses in Bir1-1

Zhang, Q., Sun, T., & Zhang, Y. (2015) · PLoS ONE · doi:10.1371/journal.pone.0120245 · Cited by 16

Molecular cloning and transcriptional activity of a new Petunia calreticulin gene involved in pistil transmitting tract maturation, progamic phase, and double fertilization

Lenartowski, R., Suwińska, A., Prusińska, J., Gumowski, K., & Lenartowska, M. (2013) · Planta · doi:10.1007/s00425-013-1971-4 · Cited by 16

Correlation of trichome density and length and polyphenol fluorescence with susceptibility of five cucurbits to Didymella bryoniae

Rennberger, G., Keinath, A. P., & Hess, M. (2016) · Journal of Plant Diseases and Protection · doi:10.1007/s41348-016-0050-z · Cited by 16

Arabidopsis DOK 1 encodes a functional dolichol kinase involved in reproduction

Kanehara, K., Cho, Y., Lin, Y., Chen, C., Yu, C., & Nakamura, Y. (2014) · The Plant Journal · doi:10.1111/tpj.12727 · Cited by 16

Pattern-Triggered Oxidative Burst and Seedling Growth Inhibition Assays in Arabidopsis thaliana

Bredow, M., Sementchoukova, I., Siegel, K. R., & Monaghan, J. (2019) · Journal of Visualized Experiments · doi:10.3791/59437 · Cited by 16

A Model for ERD2 Function in Higher Plants

Robinson, D. G., & Aniento, F. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00343 · Cited by 16

POD1-SUN-CRT3 chaperone complex guards the ER sorting of LRR receptor kinases in Arabidopsis

Xue, Y., Meng, J., Jia, P., Zhang, Z.-R., Li, H., & Yang, W. (2022) · Nature Communications · doi:10.1038/s41467-022-30179-w · Cited by 15

The K/HDEL receptor does not recycle but instead acts as a Golgi-gatekeeper

Alvim, J. C., Bolt, R. M., An, J., Kamisugi, Y., Cuming, A. C., Silva‐Alvim, F. A. L., Concha, J. O., daSilva, L. L. P., Hu, M., Hirsz, D., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-37056-0 · Cited by 15

Endoplasmic reticulum calnexins participate in the primary root growth response to phosphate deficiency

Montpetit, J., Clúa, J., Hsieh, Y.-F., Vogiatzaki, E., Müller, J., Abel, S., Strasser, R., & Poirier, Y. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac595 · Cited by 14

iNID: An Analytical Framework for Identifying Network Models for Interplays among Developmental Signaling in Arabidopsis

Choi, D., Choi, J., Kang, B., Lee, S., Cho, Y., Hwang, I., & Hwang, D. (2014) · Molecular Plant · doi:10.1093/mp/sst173 · Cited by 14

Bacterial effectors target BAK1-associated receptor complexes

Lu, D., He, P., & Shan, L. (2010) · Communicative & Integrative Biology · doi:10.4161/cib.3.2.10301 · Cited by 14

Rice BiP3 regulates immunity mediated by the PRRs XA3 and XA21 but not immunity mediated by the NB-LRR protein, Pi5

Park, C., Song, M., Kim, C., Jeon, J., & Ronald, P. C. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.04.093 · Cited by 14

Differences in gene expression profiles at the early stage of Solanum lycopersicum infection with mild and severe variants of potato spindle tuber viroid

Więsyk, A., Lirski, M., Fogtman, A., Zagórski‐Ostoja, W., & Góra‐Sochacka, A. (2020) · Virus Research · doi:10.1016/j.virusres.2020.198090 · Cited by 13

Identification and genomic characterization of major effect bacterial blight resistance locus (BB-13) in Upland cotton (Gossypium hirsutum L.)

Gowda, S. A., Shrestha, N., Harris, T. M., Phillips, A. Z., Fang, H., Sood, S., Zhang, K., Bourland, F. M., Bart, R. S., & Kuraparthy, V. (2022) · Theoretical and Applied Genetics · doi:10.1007/s00122-022-04229-2 · Cited by 13

A Model for the Biosynthesis and Transport of Plasma Membrane-Associated Signaling Receptors to the Cell Surface

Popescu, S. C. (2012) · Frontiers in Plant Science · doi:10.3389/fpls.2012.00071 · Cited by 13

Isolation and Characterization of Pepper Genes Interacting with the CMV-P1 Helicase Domain

Choi, Y., Kang, M., Lee, J., Kang, W., Hwang, J., Kwon, J., & Kang, B. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146320 · Cited by 12

Tight genetic linkage of genes causing hybrid necrosis and pollinator isolation between young species

Li, C., Binaghi, M., Pichon, V., Cannarozzi, G. M., Freitas, L. B., Hanemian, M., & Kuhlemeier, C. J. (2023) · Nature Plants · doi:10.1038/s41477-023-01354-8 · Cited by 12

Comparative transcriptome of compatible and incompatible interaction of Erysiphe pisi and garden pea reveals putative defense and pathogenicity factors

Bhosle, S. M., & Makandar, R. (2021) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiab006 · Cited by 12

Identification of Phytaspase Interactors via the Proximity-Dependent Biotin-Based Identification Approach

Teplova, A. D., Serebryakova, M. V., Galiullina, R. A., Chichkova, N. V., & Vartapetian, A. B. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222313123 · Cited by 12

Functional role of formate dehydrogenase 1 (FDH1) for host and nonhost disease resistance against bacterial pathogens

Lee, S., Vemanna, R. S., Oh, S., Rojas, C. M., Oh, Y., Kaundal, A., Kwon, T., Lee, H., Senthil‐Kumar, M., & Mysore, K. S. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264917 · Cited by 12

Comprehensive genomic characterization and expression analysis of calreticulin gene family in tomato

Muhammad, T., Yang, T., Wang, B., Yang, H., Tuerdiyusufu, D., Wang, J., & Yu, Q. (2024) · Frontiers in Plant Science · doi:10.3389/fpls.2024.1397765 · Cited by 12

An illustration of optimal selected glycosidase for N-glycoproteins deglycosylation and crystallization

Tang, J., Sun, Y., Han, Z., & Shi, W. Q. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.10.138 · Cited by 11

Lumi-Map, a Real-Time Luciferase Bioluminescence Screen of Mutants Combined with MutMap, Reveals Arabidopsis Genes Involved in PAMP-Triggered Immunity

Kato, H., Onai, K., Abe, A., Shimizu, M., Takagi, H., Tateda, C., Utsushi, H., Singkarabanit-Ogawa, S., Kitakura, S., Ono, E., et al. (2020) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-05-20-0118-ta · Cited by 11

Identification of virulence associated milRNAs and their bidirectional targets in Rhizoctonia solani and maize during infection

Meng, H., Wang, S., Yang, W., Ding, X., Li, N., Chu, Z., & Li, X. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-02930-w · Cited by 11

A conserved basic residue cluster is essential for the protein quality control function of theArabidopsiscalreticulin 3

Liu, Y., & Li, J. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.23864 · Cited by 11

Potato DMP2 positively regulates plant immunity by modulating endoplasmic reticulum homeostasis

Bi, W., Chen, Y., Song, Y., Liu, J., Zhao, T., Sun, C., Qin, J., Tu, Z., Li, Y., Wang, X., et al. (2025) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13876 · Cited by 10

Plant's cellular response to biotic stress: A review

Chaurasia, S. K., Acharya, C., & Pandey, J. K. (2025) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2025.102718 · Cited by 12

The Arabidopsis thaliana SERK1 Kinase Domain Spontaneously Refolds to an Active State In Vitro

den Toorn, M. A., Huijbers, M. M. E., de Vries, S. C., & van Mierlo, C. P. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050907 · Cited by 10

Genome-wide identification, classification, and characterization of lectin gene superfamily in sweet orange (Citrus sinensis L.)

Ahmed, F. F., Dola, F. S., Zohra, F. T., Rahman, S. M., Konak, J. N., & Sarkar, M. A. R. (2023) · PLoS ONE · doi:10.1371/journal.pone.0294233 · Cited by 11

Plant G proteins interact with endoplasmic reticulum luminal protein receptors to regulate endoplasmic reticulum retrieval

Wang, S., Xie, K., Xu, G., Zhou, H., Guo, Q., Wu, J., Liao, Z., Liu, N., Wang, Y., & Liu, Y. (2018) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12648 · Cited by 10

Engineering plant leucine rich repeat-receptors for enhanced pattern-triggered immunity (PTI) and effector-triggered immunity (ETI)

Poltronieri, P., Brutus, A., Reca, I. B., Francocci, F., Cheng, X., & Stigliano, E. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816030-5.00001-x · Cited by 10

Ca 2+ , The Miracle Molecule in Plant Hormone Signaling During Abiotic Stress

Ray, S. D. (2017) · Wiley eBooks · doi:10.1002/9781118889022.ch21 · Cited by 10

Ubiquitin/Proteasome System in Plant Pathogen Responses

Sorel, M., Mooney, B., de Marchi, R., & Graciet, E. (2019) · Annual Plant Reviews online · doi:10.1002/9781119312994.apr0665 · Cited by 10

Phylogenetic analysis of plant calreticulin homologs

Wasąg, P., Grajkowski, T., Suwińska, A., Lenartowska, M., & Lenartowski, R. (2019) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2019.01.014 · Cited by 9

Control of pattern-recognition receptors by an ER protein complex in plant immunity

Nekrasov, V., Li, J., Roux, M. E., Batoux, M., Lacombe, S., Rougon‐Cardoso, A., Chu, Z., Kiss-Papp, M., Chinchilla, D., van Esse, H. P., et al. (2009) · Socio-Environmental Systems Modeling

Control of the pattern‐recognition receptor EFR by an ER protein complex in plant immunity

Nekrasov, V., Li, J., Batoux, M., Roux, M. E., Chu, Z., Lacombe, S., Rougon‐Cardoso, A., Bittel, P., Kiss-Papp, M., Chinchilla, D., et al. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.262 · Cited by 314

Receptor quality control in the endoplasmic reticulum for plant innate immunity

Saijo, Y., Tintor, N., Lu, X., Rauf, P., Pajerowska-Mukhtar, K. M., Häweker, H., Dong, X., Robatzek, S., & Schulze‐Lefert, P. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.263 · Cited by 261

EFR-Mediated Innate Immune Response in Arabidopsis thaliana is a Useful Tool for Identification of Novel ERQC Modulators

Lia, A., Gallo, A., Marti, L., Roversi, P., & Santino, A. (2018) · Genes · doi:10.3390/genes10010015 · Cited by 9

Requirement of a Homolog of Glucosidase II β-Subunit for EFR-Mediated Defense Signaling in Arabidopsis thaliana

von Numers, N., Survila, M., Aalto, M. K., Batoux, M., Heino, P. I., Palva, E. T., & Li, J. (2010) · Molecular Plant · doi:10.1093/mp/ssq017 · Cited by 31