Differential regulation and properties of MAPKs

Mitogen-Activated Protein Kinase Pathways Mediated by ERK, JNK, and p38 Protein Kinases

Johnson, G. L., & Lapadat, R. (2002) · Science · doi:10.1126/science.1072682 · Cited by 4,295

Mammalian Mitogen-Activated Protein Kinase Signal Transduction Pathways Activated by Stress and Inflammation

Kyriakis, J. M., & Avruch, J. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.807 · Cited by 3,400

A central role for JNK in obesity and insulin resistance

Hirosumi, J., Tuncman, G., Chang, L., Görgün, C. Z., Uysal, K. T., Maeda, K., Karin, M., & Hotamisligil, G. S. (2002) · Nature · doi:10.1038/nature01137 · Cited by 3,359

A protein kinase involved in the regulation of inflammatory cytokine biosynthesis

Lee, J. C., Laydon, J. T., McDonnell, P., Gallagher, T. F., Kumar, S., Green, D., McNulty, D. E., Blumenthal, M. J., Keys, J., vatter, S. W. L., et al. (1994) · Nature · doi:10.1038/372739a0 · Cited by 3,266

Protein Tyrosine Phosphatases in the Human Genome

Alonso, A., Sasin, J., Bottini, N., Friedberg, I., Friedberg, I., Osterman, A., Godzik, A., Hunter, T., Dixon, J., & Mustelin, T. (2004) · Cell · doi:10.1016/j.cell.2004.05.018 · Cited by 1,886

Identification of an oncoprotein- and UV-responsive protein kinase that binds and potentiates the c-Jun activation domain.

Hibi, M., Lin, A., Smeal, T., Minden, A., & Karin, M. (1993) · Genes & Development · doi:10.1101/gad.7.11.2135 · Cited by 1,886

Signal Transduction through MAP Kinase Cascades

Lewis, T. S., Shapiro, P. S., & Ahn, N. G. (1998) · Advances in cancer research · doi:10.1016/s0065-230x(08)60765-4 · Cited by 1,759

Conditional ablation of MAPK7 expression in chondrocytes impairs endochondral bone formation in limbs and adaptation of chondrocytes to hypoxia

Yang, X., Zhong, D., Gao, W., Liao, Z., Chen, Y., Zhang, S., Zhou, H., Su, P., & Xu, C. (2020) · Cell & Bioscience · doi:10.1186/s13578-020-00462-8 · Cited by 18

Induction of apoptosis by Shikonin through ROS-mediated intrinsic and extrinsic apoptotic pathways in primary effusion lymphoma

Alam, M. M., Kariya, R., Boonnate, P., Kawaguchi, A., & Okada, S. (2021) · Translational Oncology · doi:10.1016/j.tranon.2020.101006 · Cited by 18

The Effects of CD73 on Gastrointestinal Cancer Progression and Treatment

Sun, P., Zheng, X. W., & Li, X. (2022) · Journal of Oncology · doi:10.1155/2022/4330329 · Cited by 18

Abiotic Stress in Plants

Gong, Y., Rao, L., & Yu, D. (2013) · InTech eBooks · doi:10.5772/55865 · Cited by 18

Targeted agents for the treatment of metastatic melanoma

Dancey, J. E., & Monzon (2012) · OncoTargets and Therapy · doi:10.2147/ott.s21259 · Cited by 18

Phosphorylation of the M3/6 dual-specificity phosphatase enhances the activation of JNK by arsenite

Cotsiki, M., Oehrl, W., Samiotaki, M. K., Theodosiou, A., & Panayotou, G. (2011) · Cellular Signalling · doi:10.1016/j.cellsig.2011.10.015 · Cited by 18

T-Cell-Specific Deletion of Map3k1 Reveals the Critical Role for Mekk1 and Jnks in Cdkn1b-Dependent Proliferative Expansion

Suddason, T., Anwar, S., Charlaftis, N., & Gallagher, E. D. (2016) · Cell Reports · doi:10.1016/j.celrep.2015.12.047 · Cited by 18

Leishmania mexicana promastigotes down regulate JNK and p-38 MAPK activation: Role in the inhibition of camptothecin-induced apoptosis of monocyte-derived dendritic cells

Rodríguez-González, J., Wilkins‐Rodríguez, A. A., Argueta, J., Aguirre‐García, M., & Gutiérrez‐Kobeh, L. (2016) · Experimental Parasitology · doi:10.1016/j.exppara.2015.12.005 · Cited by 18

The Stress-Response MAP Kinase Signaling in Cardiac Arrhythmias

Ai, X., Yan, J., Carrillo, E., & Ding, W. (2016) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/112_2016_8 · Cited by 18

Comparative transcriptome analysis of salt tolerance mechanism of Meyerozyma guilliermondii W2 under NaCl stress

Yang, H., Liao, Y., Zhang, J., & Wang, X.-L. (2019) · 3 Biotech · doi:10.1007/s13205-019-1817-2 · Cited by 18

Hepatospecific ablation of p38α MAPK governs liver regeneration through modulation of inflammatory response to CCl4-induced acute injury

Fortier, M., Cadoux, M., Boussetta, N., Pham, S., Donné, R., Couty, J., Desdouets, C., & Celton‐Morizur, S. (2019) · Scientific Reports · doi:10.1038/s41598-019-51175-z · Cited by 19

Effects of sodium fluoride on MAPKs signaling pathway in the gills of a freshwater teleost, Cyprinus carpio

Cao, J., Chen, J., Wang, J., Klerks, P. L., & Xie, L. (2014) · Aquatic Toxicology · doi:10.1016/j.aquatox.2014.04.007 · Cited by 18

The Effects of p38 MAPK Inhibition Combined with G-CSF Administration on the Hematoimmune System in Mice with Irradiation Injury

Li, D., Wang, Y., Wu, H., Lu, L., Wang, X., Zhang, J., Zhang, H., Fan, S., Fan, F., Zhou, D., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062921 · Cited by 18

TheSalmonellaTyphimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 inSaccharomyces cerevisiae

Fernández-Piñar, P., Alemán, A., Sondek, J., Dohlman, H. G., Molina, M., & Martı́n, H. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-03-0243 · Cited by 18

Proteomic responses of BEAS-2B cells to nontoxic and toxic chromium: Protein indicators of cytotoxicity conversion

Bruno, M., Ross, J. A., & Ge, Y. (2016) · Toxicology Letters · doi:10.1016/j.toxlet.2016.08.025 · Cited by 20

Anti-inflammatory and antiviral activities of cynanversicoside A and cynanversicoside C isolated from Cynanchun paniculatum in influenza A virus-infected mice pulmonary microvascular endothelial cells

Wei, P., Zhang, T., Dong, H., Chen, Q., Mu, X., & Hu, G. (2017) · Phytomedicine · doi:10.1016/j.phymed.2017.09.009 · Cited by 18

c-Jun N-terminal kinase regulates apoptosis in endometrial cancer cells

Reno, E. M., Haughian, J. M., Jackson, T. A., Thorne, A. M., & Bradford, A. P. (2009) · APOPTOSIS · doi:10.1007/s10495-009-0354-6 · Cited by 18

Effects and Mechanisms of Nonylphenol on Corticosterone Release in Rat Zona Fasciculata-Reticularis Cells

Chang, L., Wun, W.-S. A., & Wang, P. S. (2010) · Toxicological Sciences · doi:10.1093/toxsci/kfq274 · Cited by 18

Rat ERK2 E320K

th, C. A. T., Cormier, K. W., Juang, Y.-C., Goldsmith, E. J., & Cobb, M. H. (2019) · Worldwide Protein Data Bank · doi:10.2210/pdb6ots/pdb · Cited by 18

pH-responsive targeted nanoparticles release ERK-inhibitor in the hypoxic zone and sensitize free gemcitabine in mutant K-Ras-addicted pancreatic cancer cells and mouse model

Dutta, D., Ray, P., De, A., Ghosh, A., Hazra, R. S., Ghosh, P., Banerjee, S., Díaz, F. J., Upadhyay, S. P., Quadir, M., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0297749 · Cited by 17

Stress-activated MAPKs and CRM1 regulate the subcellular localization of Net1A to control cell motility and invasion

Ulu, A., Oh, W., Zuo, Y., & Frost, J. A. (2018) · Journal of Cell Science · doi:10.1242/jcs.204644 · Cited by 17

The Pseudokinase TRIB1 in Immune Cells and Associated Disorders

Danger, R., Feseha, Y., & Brouard, S. (2022) · Cancers · doi:10.3390/cancers14041011 · Cited by 17

ARAF suppresses ERBB3 expression and metastasis in a subset of lung cancers

Mooz, J., Riegel, K., Hari, P. S., Sadanandam, A., Marini, F., Klein, M., Werner, U., Roth, W., Wilken‐Schmitz, A., Tegeder, I., et al. (2022) · Science Advances · doi:10.1126/sciadv.abk1538 · Cited by 17

Sphingosine-1-phosphate receptor 3 is a non-hormonal target to counteract endometriosis-associated fibrosis

Bernacchioni, C., Rossi, M., Vannuzzi, V., Prisinzano, M., Seidita, I., Raeispour, M., Muccilli, A., Castiglione, F., Bruni, P., Petraglia, F., et al. (2023) · Fertility and Sterility · doi:10.1016/j.fertnstert.2023.12.007 · Cited by 17

Integrated analysis reveals that STAT3 is central to the crosstalk between HER/ErbB receptor signaling pathways in human mammary epithelial cells

Gong, C., Zhang, Y., Shankaran, H., & Resat, H. (2014) · Molecular BioSystems · doi:10.1039/c4mb00471j · Cited by 17

β, β-Dimethylacrylshikonin induces mitochondria-dependent apoptosis of human lung adenocarcinoma cells in vitro via p38 pathway activation

Wang, H., & Ma, X. (2014) · Acta Pharmacologica Sinica · doi:10.1038/aps.2014.108 · Cited by 17

Regulation of tristetraprolin expression by mitogen‐activated protein kinase phosphatase‐1

Huotari, N., Hömmö, T., Taimi, V., Nieminen, R. M., Moilanen, E., & Korhonen, R. (2012) · Apmis · doi:10.1111/j.1600-0463.2012.02927.x · Cited by 17

Cultured rat hepatocytes upregulate Akt and ERK in an ErbB-2-dependent manner

Scheving, L. A., Stevenson, M. C., Zhang, X., & Russell, W. E. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00597.2007 · Cited by 17

Cellular and Molecular Mechanisms of REM Sleep Homeostatic Drive: A Plausible Component for Behavioral Plasticity

Datta, S., & Oliver, M. D. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00063 · Cited by 18

Mechanism of CK2.3, a Novel Mimetic Peptide of Bone Morphogenetic Protein Receptor Type IA, Mediated Osteogenesis

Vrathasha, V., Weidner, H., & Nohe, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20102500 · Cited by 18

Nodularin-triggered apoptosis and hyperphosphorylation of signaling proteins in cultured rat hepatocytes

Ufelmann, H., & Schrenk, D. (2014) · Toxicology in Vitro · doi:10.1016/j.tiv.2014.08.008 · Cited by 17

CD40 and B-cell receptor signalling induce MAPK family members that can either induce or repress Bcl-6 expression

Batlle, A., Papadopoulou, V., Gomes, A., Willimott, S., Melo, J. V., Naresh, K. N., Lam, E. W. ‐., & Wagner, S. D. (2009) · Molecular Immunology · doi:10.1016/j.molimm.2009.02.003 · Cited by 17

Intact T cell receptor signaling by CD4+ T cells cultured in the rotating wall‐vessel bioreactor

Simons, D. M., Gardner, E. M., & Lelkes, P. I. (2010) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22502 · Cited by 17

Multi-stage virtual screening of natural products against p38α mitogen-activated protein kinase: predictive modeling by machine learning, docking study and molecular dynamics simulation

Yang, R., Zha, X., Gao, X., Wang, K., Cheng, B., & Yan, B. (2022) · Heliyon · doi:10.1016/j.heliyon.2022.e10495 · Cited by 16

Osmoregulation, physiological metabolism, and oxidative stress responses to water salinity in adult males of Chinese mitten crabs (Eriocheir sinensis)

Wang, X., Guo, Z., Lei, X., Wang, S., Wan, J.-W., Liu, H., Chen, Y., Zhao, Y., Wang, G., Wang, Q., et al. (2022) · Aquaculture International · doi:10.1007/s10499-022-00998-1 · Cited by 16

Sensitivity analysis predicts that the ERK–pMEK interaction regulates ERK nuclear translocation

Radhakrishnan, K., Edwards, J. S., Lidke, D. S., Jovin, T. M., Wilson, B. S., & Oliver, J. M. (2009) · IET Systems Biology · doi:10.1049/iet-syb.2009.0010 · Cited by 16

Panhistone deacetylase inhibitors inhibit proinflammatory signaling pathways to ameliorate interleukin-18-induced cardiac hypertrophy

Majumdar, G., Rooney, R. J., Johnson, I. M., & Raghow, R. (2011) · Physiological Genomics · doi:10.1152/physiolgenomics.00048.2011 · Cited by 16

The MAP kinase ERK and its scaffold protein MP1 interact with the chromatin regulator Corto during Drosophilawing tissue development

Mouchel‐Vielh, E., Rougeot, J., Decoville, M., & Peronnet, F. (2011) · BMC Developmental Biology · doi:10.1186/1471-213x-11-17 · Cited by 16

Compound K protects MIN6N8 pancreatic β‐cells against palmitate‐induced apoptosis through modulating SAPK/JNK activation

Kim, K., Kim, D., & Kim, Y. H. (2009) · Cell Biology International · doi:10.1042/cbi20090020 · Cited by 16

microRNA let-7c is essential for the anisomycin-elicited apoptosis in Jurkat T cells by linking JNK1/2 to AP-1/STAT1/STAT3 signaling

Zhou, Z., Lu, X., Wang, J., Xiao, J., Liu, J., & Xing, F. (2016) · Scientific Reports · doi:10.1038/srep24434 · Cited by 16

The small G protein RAS2 is involved in the metabolic compensation of the circadian clock in the circadian model Neurospora crassa

Gyöngyösi, N., Szőke, A., Ella, K., & Káldi, K. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.804922 · Cited by 17

Dual-specificity phosphatase 4 is upregulated during skeletal muscle atrophy and modulates extracellular signal-regulated kinase activity

Haddock, A. N., Labuzan, S. A., Haynes, A. E., Hayes, C. S., Kakareka, K. M., & Waddell, D. S. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00234.2018 · Cited by 15

MKP-1 Modulates Mitochondrial Transcription Factors, Oxidative Phosphorylation, and Glycolysis

Bauerfeld, C. P., Talwar, H. S., Zhang, K., Liu, Y., & Samavati, L. (2020) · ImmunoHorizons · doi:10.4049/immunohorizons.2000015 · Cited by 16

Atrial fibrillation

Brundel, B. J. J. M., Ai, X., Hills, M. T., Kuipers, M. F., Lip, G. Y. H., & de Groot, N. M. S. (2016) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2016.17 · Cited by 18

Interaction of Kinase-Interaction-Motif Protein Tyrosine Phosphatases with the Mitogen-Activated Protein Kinase ERK2

Francis, D. M., Koveal, D., Tortajada, A., Page, R., & Peti, W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091934 · Cited by 16

The Anti‐ HIV Microbicide Candidate RC ‐101 Inhibits Pathogenic Vaginal Bacteria Without Harming Endogenous Flora or Mucosa

Eade, C. R., Cole, A. L., Diaz, C., Rohan, L. C., Parniak, M. A., Marx, P. A., Tarwater, P. M., Gupta, P., & Cole, A. M. (2012) · American Journal of Reproductive Immunology · doi:10.1111/aji.12036 · Cited by 16

Mechanisms of GnRH-Induced Extracellular Signal-Regulated Kinase Nuclear Localization

Caunt, C. J., Perrett, R. M., Fowkes, R. C., & McArdle, C. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040077 · Cited by 16

Hyperthermia Differently Affects Connexin43 Expression and Gap Junction Permeability in Skeletal Myoblasts and HeLa Cells

Antanavičiūtė, I., Mildažienė, V., Stankevıčıus, E., Herdegen, T., & Skeberdis, V. A. (2014) · Mediators of Inflammation · doi:10.1155/2014/748290 · Cited by 16

p38δ mitogen-activated protein kinase regulates skin homeostasis and tumorigenesis

Efimova, T. (2010) · Cell Cycle · doi:10.4161/cc.9.3.10541 · Cited by 16

Visualization of the spatial and temporal dynamics of MAPK signaling using fluorescence imaging techniques

Tomida, T. (2014) · The Journal of Physiological Sciences · doi:10.1007/s12576-014-0332-9 · Cited by 17

Acute exposure of L6 myotubes to cis-9, trans-11 and trans-10, cis-12 conjugated linoleic acid isomers stimulates glucose uptake by modulating Ca2+/calmodulin-dependent protein kinase II

Mohankumar, S. K., Taylor, C. G., Siemens, L., & Zahradka, P. C. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.05.005 · Cited by 16

The inhibitory effect of CIL-102 on the growth of human astrocytoma cells is mediated by the generation of reactive oxygen species and induction of ERK1/2 MAPK

Teng, C., Kuo, H., Cheng, H.-C., Wang, T.-C., & Sze, C. (2012) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2012.05.025 · Cited by 16

Ginkgo Biloba L. Extract Reduces H2O2-Induced Bone Marrow Mesenchymal Stem Cells Cytotoxicity by Regulating Mitogen-Activated Protein Kinase (MAPK) Signaling Pathways and Oxidative Stress

Wang, A., Yang, Q., Li, Q., Wang, X., Hao, S., Wang, J., & Ren, M. (2018) · Medical Science Monitor · doi:10.12659/msm.910718 · Cited by 16

ΔNp63α modulates phosphorylation of p38 MAP kinase in regulation of cell cycle progression and cell growth

Wang, L., Xia, W., Chen, H., & Xiao, Z. J. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.12.185 · Cited by 16

Hypoxia-Induced Phenotypic Transformation of Corpus Cavernosum Smooth Muscle Cells After Cavernous Nerve Crush Injury by Down-Regulating P38 Mitogen-Activated Protein Kinase Expression

Chen, S., Huang, X., Kong, X., Sun, Z., Zhao, F., Huang, W., Ye, M., Ma, K., Tao, T., & Lv, B. (2019) · Sexual Medicine · doi:10.1016/j.esxm.2019.08.005 · Cited by 16

Differential regulation of HSP70 expression by the JNK kinases SEK1 and MKK7 in mouse embryonic stem cells treated with cadmium

Nishitai, G., & Matsuoka, M. (2008) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21743 · Cited by 16

Neural Influences on Tumor Progression Within the Central Nervous System

Lv, W., & Wang, Y. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70097 · Cited by 15

Genome-wide identification of the MAPK gene family in turbot and its involvement in abiotic and biotic stress responses

Zheng, W., Xu, X., Zechen, E., Liu, Y., & Chen, S. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.1005401 · Cited by 15

Repeated Use of Morphine Induces Anxiety by Affecting a Proinflammatory Cytokine Signaling Pathway in the Prefrontal Cortex in Rats

Ahmadi, S., Talvar, S. M., Masoudi, K., & Zobeiri, M. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03144-3 · Cited by 15

Capsular polysaccharide from the marine bacterium Cobetia marina induces apoptosis via both caspase-dependent and mitochondria-mediated pathways in HL-60 cells

Kokoulin, M. S., Kuzmich, A. S., Filshtein, A. P., Prassolov, V., & Romanenko, L. A. (2024) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2024.122791 · Cited by 15

A focus on c-Jun-N-terminal kinase signaling in sepsis-associated multiple organ dysfunction: Mechanisms and therapeutic strategies

Gagnani, R., Srivastava, M., Suri, M., Singh, H., Navik, U. S., & Bali, A. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113552 · Cited by 15

MAPK13 phosphorylates PHGDH and promotes its degradation via chaperone-mediated autophagy during liver injury

Xing, R., Liu, R., Man, Y., Liu, C., Zhang, Y., Gao, H., & Yang, W. (2025) · Cell Discovery · doi:10.1038/s41421-024-00758-w · Cited by 16

Differential regulation of mitogen-activated protein kinase signaling pathways in human with different types of mitral valvular disease

Chang, C. D., Zhang, C., Zhao, X., Kuang, X., Tang, H., & Xiao, X. (2012) · Journal of Surgical Research · doi:10.1016/j.jss.2012.05.028 · Cited by 15

Caspase and mitogen activated protein kinase pathways are involved in Solanum lyratum herba induced apoptosis

Lee, J.-H., Lee, Y.-H., Lee, H., Lee, H., Lee, E., Ahn, K. S., Shim, B. S., Bae, H., Choi, S., Ahn, K.-S., et al. (2009) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2009.02.013 · Cited by 15

p38 MAPK contributes to CD54 expression and the enhancement of phagocytic activity during macrophage development

Cui, J., Zhu, N., Wang, Q., Yu, M., Feng, J., Li, Y., Zhang, J., & Shen, B. (2009) · Cellular Immunology · doi:10.1016/j.cellimm.2008.12.003 · Cited by 15

cAMP-activated Nr4a1 expression requires ERK activity and is modulated by MAPK phosphatase-1 in MA-10 Leydig cells

Garcia, M. M. M. S., Gorostizaga, A., Brion, L., González-Calvar, S. I., & Paz, C. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2015.01.041 · Cited by 18

Modulation of albumin-induced endoplasmic reticulum stress in renal proximal tubule cells by upregulation of mapk phosphatase-1

Gorostizaga, A., Garcia, M. M. M. S., Acquier, A. B., Gomez, N. V., Maloberti, P. M., Méndez, C. F., & Paz, C. (2013) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2013.08.009 · Cited by 15

Molecular characterization of a p38 mitogen-activated protein kinase gene from Scylla paramamosain and its expression profiles during pathogenic challenge

Yu, Z., Geng, Y., Huang, A., Wang, K., Huang, X., Chen, D., Ou, Y., & Wang, J. (2017) · Journal of Invertebrate Pathology · doi:10.1016/j.jip.2017.01.001 · Cited by 15

Neuroprotective effects of N-acetyl cysteine on primary hippocampus neurons against hydrogen peroxide-induced injury are mediated via inhibition of mitogen-activated protein kinases signal transduction and antioxidative action

Wu, W., Liu, B., Xie, C., Xia, X., & Zhang, Y. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.8699 · Cited by 15

Allosteric Modulation of JNK Docking Site Interactions with ATP-Competitive Inhibitors

Lombard, C. K., Davis, A. L., Inukai, T., & Maly, D. J. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b00776 · Cited by 16

Dual-Specificity Phosphatases in Neuroblastoma Cell Growth and Differentiation

Nunes‐Xavier, C. E., Zaldumbide, L., Aurtenetxe, O., Almaraz, R. L., Lopez, J. I., & Pulido, R. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20051170 · Cited by 15

Over-expression of Bcl2-associated athanogene 2 in oral cancer promotes cellular proliferation and is associated with poor prognosis

Liu, Y., & Wei, B. (2019) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2019.04.015 · Cited by 15

Transcriptional modulation of calcium‐permeable AMPA receptor subunits in glioblastoma by MEK–ERK1/2 inhibitors and their role in invasion

Ramaswamy, P., Nanjaiah, N. D., Prasad, C., & Goswami, K. (2019) · Cell Biology International · doi:10.1002/cbin.11279 · Cited by 15

Discovery of tofacitinib derivatives as orally active antitumor agents based on the scaffold hybridization strategy

Shi, X., Wang, S., Li, X., Yuan, X., Cao, L., Yu, B., & Liu, H. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.112601 · Cited by 15

Network pharmacology-based study on the mechanism of scutellarin against zearalenone-induced ovarian granulosa cell injury

Hu, P., Sun, N., Khan, A., Zhang, X., Sun, P., Sun, Y., Guo, J., Zheng, X., Yin, W. H., Fan, K., et al. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112865 · Cited by 15

KRAS Affects Adipogenic Differentiation by Regulating Autophagy and MAPK Activation in 3T3-L1 and C2C12 Cells

Yu, W., Chen, C., Peng, Y., Li, Z., Gao, Y., Liang, S., Yuan, B., Kim, N., Jiang, H., & Zhang, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413630 · Cited by 17

Quantitative phosphoproteomics reveals ectopic ATP synthase on mesenchymal stem cells to promote tumor progression via ERK/c-Fos pathway activation

Chang, Y., Wang, C., Yin, C.-F., Wu, C.-H., Huang, H., & Juan, H. (2022) · Molecular & Cellular Proteomics · doi:10.1016/j.mcpro.2022.100237 · Cited by 14

The Proinflammatory Cytokine, IL-6, and its Interference with bFGF Signaling and PSMA in Prostate Cancer Cells

Jemaa, A. B., Sallami, S., Ramarli, D., Colombatti, M., & Oueslati, R. (2012) · Inflammation · doi:10.1007/s10753-012-9586-7 · Cited by 15

Signals and Systems: Towards a Systems Biology of Signal Transduction

Gunawardena, J. (2008) · Proceedings of the IEEE · doi:10.1109/jproc.2008.925413 · Cited by 15

Loss of p38δ mitogen-activated protein kinase expression promotes oesophageal squamous cell carcinoma proliferation, migration and anchorage-independent growth

O'Callaghan, C., Fanning, L. J., Houston, A. M., & Barry, Ó. P. (2013) · International Journal of Oncology · doi:10.3892/ijo.2013.1968 · Cited by 15

Reactive oxygen species in signal transduction

Дробот, Л. Б. (2013) · The Ukrainian Biochemical Journal · doi:10.15407/ubj85.06.209 · Cited by 15

KIF15 promotes the evolution of gastric cancer cells through inhibition of reactive oxygen species‐mediated apoptosis

Tao, J., Sun, G., Li, Q., Zhi, X., Li, Z., He, Z., Chen, H., Zhou, A., Ye, J., Xu, G., et al. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.29743 · Cited by 15

Overexpression of FNTB and the activation of Ras induce hypertrophy and promote apoptosis and autophagic cell death in cardiomyocytes

Ding, J., Chen, Y. X., Chen, Y., Mou, Y., Sun, X. T., Dai, D., Zhao, C. Z., Yang, J., Hu, S., & Guo, X. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15533 · Cited by 15

Sprouty2 Interacts with Protein Kinase Cδ and Disrupts Phosphorylation of Protein Kinase D1

Chow, S. Y., Yu, C. Y., & Guy, G. R. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.021600 · Cited by 15

Extraction of Phosphorylated Proteins from Formalin-Fixed Cancer Cells and Tissues

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The atypical MAPK ERK 3 controls positive selection of thymocytes

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