Molecules and Cells

Cited by CrossRef (12)

  1. George Komis, Olga Šamajová, Miroslav Ovečka, Jozef Šamaj. Cell and Developmental Biology of Plant Mitogen-Activated Protein Kinases. Annu. Rev. Plant Biol. 2018;69:237
    https://doi.org/10.1146/annurev-arplant-042817-040314
  2. Brant T. McNeece, Keshav Sharma, Gary W. Lawrence, Kathy S. Lawrence, Vincent P. Klink. The mitogen activated protein kinase (MAPK) gene family functions as a cohort during the Glycine max defense response to Heterodera glycines. Plant Physiology and Biochemistry 2019;137:25
    https://doi.org/10.1016/j.plaphy.2019.01.018
  3. Tao Chen, Kai Bi, Yanli Zhao, Xueliang Lyu, Zhixiao Gao, Ying Zhao, Yanping Fu, Jiasen Cheng, Jiatao Xie, Daohong Jiang. MAPKK Inhibitor U0126 Inhibits Plasmodiophora brassicae Development. Phytopathology® 2018;108:711
    https://doi.org/10.1094/PHYTO-07-17-0240-R
  4. Zong-You Lv, Wen-Jing Sun, Rui Jiang, Jun-Feng Chen, Xiao Ying, Lei Zhang, Wan-Sheng Chen. Phytohormones jasmonic acid, salicylic acid, gibberellins, and abscisic acid are key mediators of plant secondary metabolites. World J Tradit Chin Med 2021;7:307
    https://doi.org/10.4103/wjtcm.wjtcm_20_21
  5. Rishi Khatri, Shankar R. Pant, Keshav Sharma, Prakash M. Niraula, Bisho R. Lawaju, Kathy S. Lawrence, Nadim W. Alkharouf, Vincent P. Klink. Glycine max Homologs of DOESN'T MAKE INFECTIONS 1, 2, and 3 Function to Impair Heterodera glycines Parasitism While Also Regulating Mitogen Activated Protein Kinase Expression. Front. Plant Sci. 2022;13
    https://doi.org/10.3389/fpls.2022.842597
  6. Mengzhu Zeng, Bowen Wan, Lei Wang, Zhiyuan Chen, Yachun Lin, Wenwu Ye, Yan Wang, Yuanchao Wang. Identification and characterization of L-type lectin receptor-like kinases involved in Glycine max–Phytophthora sojae interaction. Planta 2021;254
    https://doi.org/10.1007/s00425-021-03789-9
  7. Jean Bigeard, Heribert Hirt. Nuclear Signaling of Plant MAPKs. Front. Plant Sci. 2018;9
    https://doi.org/10.3389/fpls.2018.00469
  8. Miroslava Hrbáčková, Ivan Luptovčiak, Kateřina Hlaváčková, Petr Dvořák, Michaela Tichá, Olga Šamajová, Dominik Novák, Hanna Bednarz, Karsten Niehaus, Miroslav Ovečka, Jozef Šamaj. Overexpression of alfalfa SIMK promotes root hair growth, nodule clustering and shoot biomass production. Plant Biotechnol J 2021;19:767
    https://doi.org/10.1111/pbi.13503
  9. Savithri Purayannur, Kamal Kumar, Vemula Chandra Kaladhar, Praveen Kumar Verma. Phylogenomic analysis of MKKs and MAPKs from 16 legumes and detection of interacting pairs in chickpea divulge MAPK signalling modules. Sci Rep 2017;7
    https://doi.org/10.1038/s41598-017-04913-0
  10. Jun Yin, Xiaomin Guan, Heng Zhang, Longxiang Wang, Hao Li, Qing Zhang, Tao Chen, Zeyuan Xu, Zonglie Hong, Yangrong Cao, Zhongming Zhang. An MAP kinase interacts with LHK1 and regulates nodule organogenesis in Lotus japonicus. Sci. China Life Sci. 2019;62:1203
    https://doi.org/10.1007/s11427-018-9444-9
  11. Sebastian Pfeilmeier, Jeoffrey George, Arry Morel, Sonali Roy, Matthew Smoker, Lena Stransfeld, J. Allan Downie, Nemo Peeters, Jacob G. Malone, Cyril Zipfel. 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 Biotechnol J 2019;17:569
    https://doi.org/10.1111/pbi.12999
  12. Xin Cui, Ji Hyung Jun, Xiaolan Rao, Camille Bahr, Elisabeth Chapman, Stephen Temple, Richard A. Dixon. Leaf layer-based transcriptome profiling for discovery of epidermal-selective promoters in Medicago truncatula. Planta 2022;256
    https://doi.org/10.1007/s00425-022-03920-4