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

Identification and abundance of miRNA in chicken hypothalamus tissue determined by Solexa sequencing

Sun, G., Li, M., Li, G. X., Tian, Y., Han, R. L., & Kang, X. T. (2012) · Genetics and Molecular Research · doi:10.4238/2012.october.2.2 · Cited by 14

Assaying Protein Kinase Activity with Radiolabeled ATP

Karra, A. S., Stippec, S., & Cobb, M. H. (2017) · Journal of Visualized Experiments · doi:10.3791/55504 · Cited by 14

Recent Progress of Adenosine Receptor Modulators in the Development of Anticancer Chemotherapeutic Agents

Marwein, S., Mishra, B., De, U. C., & Acharya, P. C. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190716141851 · Cited by 14

Inhibitory effects of SEL201 in acute myeloid leukemia

Kościuczuk, E. M., Kar, A. K., Blyth, G. T., Fischietti, M., Abedin, S. M., Mina, A. A., Siliezar, R., Rzymski, T., Brzózka, K. D., Eklund, E. A., et al. (2019) · Oncotarget · doi:10.18632/oncotarget.27388 · Cited by 14

Macrophage migration inhibitory factor anti-thrombin III complexes are decreased in bladder cancer patient serum: Complex formation as a mechanism of inactivation

Meyer‐Siegler, K. L., Cox, J., Leng, L., Bucala, R., & Vera, P. L. (2009) · Cancer Letters · doi:10.1016/j.canlet.2009.08.025 · Cited by 14

A functional polymorphism in the promoter of ERK5 gene interacts with tobacco smoking to increase the risk of lung cancer in Chinese populations

Qiu, F., Yang, L., Fang, W., Li, Y., Yang, R., Yang, X., Deng, J., Huang, B., Xie, C., Zhou, Y., et al. (2013) · Mutagenesis · doi:10.1093/mutage/get033 · Cited by 14

Mxi2 sustains ERK1/2 phosphorylation in the nucleus by preventing ERK1/2 binding to phosphatases

Casar, B., Rodríguez, J., Gibor, G., Seger, R., & Crespo, P. (2011) · Biochemical Journal · doi:10.1042/bj20110870 · Cited by 13

LncRNA Riken Attenuated Sevoflurane-Induced Neuroinflammation by Regulating the MicroRNA-101a/MKP-1/JNK Pathway

Hou, Q., Li, S., Zhang, B., Chu, H., Ni, C., Fei, X., & Zheng, H. (2021) · Neurotoxicity Research · doi:10.1007/s12640-021-00443-w · Cited by 13

c-MYC Protein Stability Is Sustained by MAPKs in Colorectal Cancer

Signorile, M. L., Grossi, V., Fasano, C., Forte, G., Disciglio, V., Sanese, P., Marco, K. D., Rocca, F. L., Armentano, R., Valentini, A. M., et al. (2022) · Cancers · doi:10.3390/cancers14194840 · Cited by 14

Novel Biomarkers and Therapeutic Targets for Melanoma

Sabag, N., Yakobson, A., Retchkiman, M., & Silberstein, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911656 · Cited by 14

Regulation of ERK2 activity by dynamic S-acylation

Azizi, S., Qiu, T., Brookes, N., & Dickinson, B. C. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113135 · Cited by 13

Monophosphothreonyl extracellular signal-regulated kinases 1 and 2 (ERK1/2) are formed endogenously in intact cardiac myocytes and are enzymically active

Sugden, P. H., Markou, T., Fuller, S. J., Tham, E. L., Molkentin, J. D., Paterson, H. F., & Clerk, A. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.10.024 · Cited by 13

Requirement of Apoptosis-Inducing Kinase 1 for the Induction of Bronchial Asthma following Stimulation with Ovalbumin

Takada, E., Furuhata, M., Nakae, S., Ichijo, H., Sudo, K., & Mizuguchi, J. (2013) · International Archives of Allergy and Immunology · doi:10.1159/000353240 · Cited by 13

Proteasome inhibition modulates kinase activation in neural cells: Relevence to ubiquitination, ribosomes, and survival

Zhang, L., Ebenezer, P. J., Dasuri, K., Bruce‐Keller, A. J., Liu, Y., & Keller, J. N. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22147 · Cited by 13

Association between metalloproteinases 2 and 9 activity and ERK1/2 phosphorylation status in head and neck cancers: An ex vivo study

Maggioni (2010) · Oncology Reports · doi:10.3892/or_00000957 · Cited by 13

Gene expression during testis development in Duroc boars

Lervik, S., Kristoffersen, A. B., Conley, L. N., Oskam, I. C., Hedegaard, J., Ropstad, E., & Olsaker, I. (2015) · animal · doi:10.1017/s1751731115000907 · Cited by 13

c-Jun N-terminal kinases 3 (JNK3) from orange-spotted grouper, Epinephelus coioides, inhibiting the replication of Singapore grouper iridovirus (SGIV) and SGIV-induced apoptosis

Guo, M., Wei, J., Zhou, Y., & Qin, Q. (2016) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2016.06.009 · Cited by 13

The Preventive Effect of Coffee Compounds on Dermatitis and Epidermal Pigmentation after Ultraviolet Irradiation in Mice

Yamate, Y., Hiramoto, K., & Sato, E. F. (2017) · Skin Pharmacology and Physiology · doi:10.1159/000455237 · Cited by 13

Gleditsia Saponin C Induces A549 Cell Apoptosis via Caspase-Dependent Cascade and Suppresses Tumor Growth on Xenografts Tumor Animal Model

Cheng, Y., He, W., & He, Y. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00988 · Cited by 13

Regulation of intrinsic polarity establishment by a differentiation-type MAPK pathway in S. cerevisiae

Prabhakar, A., Chow, J. L., Siegel, A. J., & Cullen, P. J. (2020) · Journal of Cell Science · doi:10.1242/jcs.241513 · Cited by 13

Studying molecular interactions in the intact organism: fluorescence correlation spectroscopy in the living zebrafish embryo

Dawes, M., Soeller, C., & Scholpp, S. (2020) · Histochemistry and Cell Biology · doi:10.1007/s00418-020-01930-5 · Cited by 13

Activation of transcription factor AP-1 in response to thermal injury in rat small intestine and IEC-6 cells

Zhang, Y., Zhao, H., Liu, T., Wan, C., Liu, X., Gao, Z., Hou, X., Jiang, L., & Liu, F. (2015) · BMC Gastroenterology · doi:10.1186/s12876-015-0309-z · Cited by 13

Intracellular mobility and nuclear trafficking of the stress-activated kinase JNK1 are impeded by hyperosmotic stress

Misheva, M., Kaur, G., Ngoei, K. R. W., Yeap, Y. Y. C., Ng, I. H. W., Wagstaff, K. M., Ng, D. C. H., Jans, D. A., & Bogoyevitch, M. A. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.10.017 · Cited by 13

Cross-talk between protein kinase A and the MAPK-activated protein kinases RSK1 and MK5

Kostenko, S., Shiryaev, A., Dumitriu, G., Gerits, N., & Moens, U. L. (2010) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2010.515593 · Cited by 13

JNK‐binding protein 1 regulates NF‐κB activation through TRAF2 and TAK1

Yamaguchi, T., Miyashita, C., Koyano, S., Kanda, H., Yoshioka, K., Shiba, T., Takamatsu, N., & Ito, M. (2009) · Cell Biology International · doi:10.1016/j.cellbi.2009.01.003 · Cited by 13

Improved insulin sensitivity with calorie restriction does not require reduced JNK1/2, p38, or ERK1/2 phosphorylation in skeletal muscle of 9-month-old rats

Sharma, N., Bhat, A. D., Kassa, A. D., Xiao, Y., Arias, E. B., & Cartee, G. D. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00372.2011 · Cited by 13

SPAG9/MKK3/p38 axis is a novel therapeutic target for liver cancer

Luo, S., Ren, B., Zou, G., Liu, J., Chen, W., Huang, Y., Chen, X., & Fu, Y. (2019) · Oncology Reports · doi:10.3892/or.2019.6987 · Cited by 13

Characterization of an Immune-Enhancing Polysaccharide Fraction Isolated from Heat-Processed Ginseng Derived from Panax ginseng C.A. Meyer

Kim, S. J., Shin, M., Kim, M., Baek, S., & Kang, K. S. (2021) · Applied Sciences · doi:10.3390/app112210835 · Cited by 12

Enhanced proliferation and differentiation of human mesenchymal stem cells in the gravity‐controlled environment

Nakaji‐Hirabayashi, T., Matsumura, K., Ishihara, R., Ishiguro, T., Nasu, H., Kanno, M., Ichida, S., & Hatashima, T. (2022) · Artificial Organs · doi:10.1111/aor.14251 · Cited by 12

Differences in p38-STAT3-S100A11 signaling after the administration of aristolochic acid I and IVa may account for the disparity in their nephrotoxicity

Xian, Z., Tian, J., Zhao, Y., Yan, Y., Li, C., Han, J., Zhang, Y., Wang, Y., Wang, L., Liu, S., et al. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154815 · Cited by 12

An insight into crosstalk among multiple signalling pathways contributing to the pathophysiology of PTSD and depressive disorders

‬‬‬‬‬‬‬Bommaraju, S., Dhokne, M. D., Arun, E. V., Srinivasan, K., Sharma, S. S., & Datusalia, A. K. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.110943 · Cited by 12

Pml and TAp73 interacting at nuclear body mediate imatinib‐induced p53‐independent apoptosis of chronic myeloid leukemia cells

Liu, H., Liu, C.-C., Yen, C., Gau, J., Wang, W., & Tzeng, C. (2009) · International Journal of Cancer · doi:10.1002/ijc.24329 · Cited by 12

Functional analysis of novel phosphorylation sites of CREB‐binding protein using mass spectrometry and mammalian two‐hybrid assays

Xia, Z., Guo, M., & Ma, H. (2011) · PROTEOMICS · doi:10.1002/pmic.201100121 · Cited by 12

2′-Nitroflavone induces apoptosis and modulates mitogen-activated protein kinase pathways in human leukaemia cells

Cárdenas, M., Blank, V. C., Marder, M., & Roguin, L. P. (2012) · Anti-Cancer Drugs · doi:10.1097/cad.0b013e328353f947 · Cited by 12

AtMPK6‐induced phosphorylation of AtERF72 enhances its DNA binding activity and interaction with TGA4/OBF4 in Arabidopsis

Park, H. C., Park, B., Kim, H. S., Kim, S. H., Lee, S. W., & Chung, W. S. (2020) · Plant Biology · doi:10.1111/plb.13196 · Cited by 12

PP2A Catalytic Subunit α promotes fibroblast activation and kidney fibrosis via ERK pathway

Lu, Q., Tan, M., Hou, Q., Wang, M., & Dai, C. (2021) · Cellular Signalling · doi:10.1016/j.cellsig.2021.110187 · Cited by 12

Exosome-mediated crosstalk between epithelial cells amplifies the cell injury cascade in CaOx stone formation

Yang, Y., Hong, S., Wang, Q., Wang, S., & Xun, Y. (2023) · Journal of Biological Engineering · doi:10.1186/s13036-023-00324-0 · Cited by 12

Identification of mitogen‐activated protein/extracellular signal‐responsive kinase kinase 2 as a novel partner of the scaffolding protein human homolog of disc‐large

Maïga, O., Philippe, M., Kotelevets, L., Chastre, E., Benadda, S., Pidard, D., Vranckx, R., & Walch, L. (2011) · FEBS Journal · doi:10.1111/j.1742-4658.2011.08192.x · Cited by 12

SR calcium handling dysfunction, stress-response signaling pathways, and atrial fibrillation

Ai, X. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00046 · Cited by 12

Signal Transduction Pathways (MAPKs, NF-κB, and C/EBP) Regulating COX-2 Expression in Nasal Fibroblasts from Asthma Patients with Aspirin Intolerance

García‐García, F. J., Mullol, J., Pérez-González, M., Pujols, L., Alobid, I., Roca‐Ferrer, J., & Picado, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051281 · Cited by 12

Amelogenin promotes odontoblast-like MDPC-23 cell differentiation via activation of ERK1/2 and p38 MAPK

Yao, N., Li, S., Jiang, Y., Qiu, S., & Tan, Y. (2011) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-011-0842-1 · Cited by 12

p38 MAP Kinase Mediated Proteoglycan Synthesis as a Target for the Prevention of Atherosclerosis

Osman, N., Ballinger, M. L., Dadlani, H., Getachew, R., Burch, M. L., & Little, P. J. (2008) · Cardiovascular & Haematological Disorders - Drug Targets · doi:10.2174/187152908786786205 · Cited by 12

Effects of C‐Terminal Amelogenin Peptide on Proliferation of Human Cementoblast Lineage Cells

Yoshimi, Y., Kunimatsu, R., Hirose, N., Awada, T., Miyauchi, M., Takata, T., Li, W., Zhu, L., DenBesten, P., Tanne, K., et al. (2016) · Journal of Periodontology · doi:10.1902/jop.2016.150507 · Cited by 12

High glucose enhances cAMP level and extracellular signal-regulated kinase phosphorylation in Chinese hamster ovary cell: Usage of Br-cAMP in foreign protein β-galactosidase expression

Lin, H., Lee, T.-Y., Liu, T., & Tseng, C. (2017) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2017.02.010 · Cited by 12

Diethylcarbamazine attenuates the expression of pro-fibrogenic markers and hepatic stellate cells activation in carbon tetrachloride-induced liver fibrosis

de França, M. E. R., Rocha, S. W. S., de Oliveira, W. H., dos Santos, L. A. M., de Oliveira, A. G. V., Barbosa, K. P. S., Nunes, A. K. S., Rodrigues, G. B., Lós, D. B., & Peixoto, C. A. (2017) · Inflammopharmacology · doi:10.1007/s10787-017-0329-0 · Cited by 12

Kinetic and mechanistic studies of p38α MAP kinase phosphorylation by MKK 6

Wang, Y., Zhang, Y., Lu, C., Zhang, W., Deng, H., Wu, J., Wang, J., & Wang, Z. (2019) · FEBS Journal · doi:10.1111/febs.14762 · Cited by 10

Increase of Hspa1a and Hspa1b genes in the resting B cells of Sirt1 knockout mice

Han, Y. H., Kang, Y., Yu, J., Yu, S., Park, H., Shin, J., Park, S., & Kang, J. (2019) · Molecular Biology Reports · doi:10.1007/s11033-019-04876-7 · Cited by 12

Dissection of MAPK signaling specificity through protein engineering in a developmental context

Wengier, D. L., Lampard, G. R., & Bergmann, D. C. (2018) · BMC Plant Biology · doi:10.1186/s12870-018-1274-9 · Cited by 12

Computational analysis of receptor tyrosine kinase inhibitors and cancer metabolism: implications for treatment and discovery of potential therapeutic signatures

Li, J., Halfter, K., Zhang, M., Saad, C., Xu, K. L., Bauer, B., Huang, Y., Shi, L., & Mansmann, U. (2019) · BMC Cancer · doi:10.1186/s12885-019-5804-0 · Cited by 12

MAPK Erk5 in Leptin Receptor‒Expressing Neurons Controls Body Weight and Systemic Energy Homeostasis in Female Mice

Horie, T., Park, G., Inaba, Y., Hashiuchi, E., Iezaki, T., Tokumura, K., Fukasawa, K., Yamada, T., Hiraiwa, M., Kitaguchi, Y., et al. (2019) · Endocrinology · doi:10.1210/en.2019-00090 · Cited by 12

ERK3/MAPK6 is required for KRAS-mediated NSCLC tumorigenesis

Bogucka, K., Marini, F., Rosigkeit, S., Schlöder, J., Jonuleit, H., David, K. A., Schlackow, M., & Rajalingam, K. (2020) · Cancer Gene Therapy · doi:10.1038/s41417-020-00245-w · Cited by 14

The p38 mitogen-activated protein kinases modulate endothelial cell survival and tissue repair

Kanaji, N., Nelson, A. J., Allen‐Gipson, D., Sato, T., Nakanishi, M., Wang, X., Li, Y., Basma, H., Michalski, J., Farid, M., et al. (2011) · Inflammation Research · doi:10.1007/s00011-011-0405-7 · Cited by 11

Single-Well Monitoring of Protein−Protein Interaction and Phosphorylation−Dephosphorylation Events

Arcand, M., Roby, P., Bossé, R., Lipari, F., Padrós, J., Beaudet, L., Marcil, A., & Dahan, S. (2010) · Biochemistry · doi:10.1021/bi100253p · Cited by 12

Role of SB203580 in the regulation of human esophageal cancer cells under the effection of Diosgenin.

Ding, W., Jiang, Y., Jiang, Y., Zhu, T., Xu, Y., Jiang, W., Zhu, W., Tang, Z., Ge, Z., Ma, T., et al. (2015) · PubMed Central · Cited by 12

Microsomal Prostaglandin E Synthase-1 Expression in Inflammatory Conditions Is Downregulated by Dexamethasone: Seminal Role of the Regulatory Phosphatase MKP-1

Tuure, L., Hämäläinen, M., Whittle, B. J. R., & Moilanen, E. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00646 · Cited by 13

Design, Synthesis, and Antitumor Activity Evaluation of Proteolysis-Targeting Chimeras as Degraders of Extracellular Signal-Regulated Kinases 1/2

Pan, P., He, Y., Geng, T., Li, Z., Li, Z., & Meng, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242216290 · Cited by 11

Translational Relevance of Secondary Intracellular Signaling Cascades Following Traumatic Spinal Cord Injury

Zavvarian, M.-M., Modi, A. D., Sadat, S., Hong, J., & Fehlings, M. G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115708 · Cited by 12

Protein Tyrosine Phosphatases in Metabolism: A New Frontier for Therapeutics

Bennett, A. M., & Tiganis, T. (2024) · Annual Review of Physiology · doi:10.1146/annurev-physiol-022724-105540 · Cited by 12

Transforming growth factor alpha: Key insights into physiological role, cancer therapeutics, and biomarker potential (A review)

Gaba, S., Sahu, M., Chauhan, N., & Jain, U. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.143212 · Cited by 12

EGFR signaling pathways are wired differently in normal 184A1L5 human mammary epithelial and MDA-MB-231 breast cancer cells

Speth, Z., Islam, T., Banerjee, K., & Resat, H. (2017) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-017-0389-3 · Cited by 11

Autophagy plays a protective role during Pseudomonas aeruginosa -induced apoptosis via ROS–MAPK pathway

Han, L., Ma, Q., Yu, J., Gong, Z., Ma, C., Xu, Y., Deng, G., & Wu, X. (2020) · Innate Immunity · doi:10.1177/1753425920952156 · Cited by 11

Causal roles of stress kinase JNK2 in DNA methylation and binge alcohol withdrawal-evoked behavioral deficits

Yang, M., Barrios, J., Yan, J., Zhao, W., Yuan, S., Dong, E., & Ai, X. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105375 · Cited by 11

Acacetin Alleviates Listeria monocytogenes Virulence Both In Vitro and In Vivo via the Inhibition of Listeriolysin O

Li, S., Xu, X., Wei, L., Wang, L., & Lv, Q. (2021) · Foodborne Pathogens and Disease · doi:10.1089/fpd.2021.0021 · Cited by 11

Inhibition of pro-collagen I expression by oxymatrine in hepatic stellate cells is mediated via nuclear translocation of Y-box binding protein 1

DU, M., Zhang, J., Xu, D., LI, W., Liu, J., & Liu, F. (2012) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4428 · Cited by 11

Tachykinin Peptide, Substance P, and Its Receptor NK-1R Play an Important Role in Alimentary Tract Mucosal Inflammation During Cytotoxic Therapy

Kumar, K. S., & Mohan, M. P. (2014) · Digestive Diseases and Sciences · doi:10.1007/s10620-014-3263-7 · Cited by 11

MAP kinase phosphatase-3 (MKP-3) is transcriptionally and post-translationally up-regulated by hCG and modulates cAMP-induced p21 expression in MA-10 Leydig cells

Garcia, M. M. M. S., Gomez, N. V., Gorostizaga, A., Acquier, A. B., González-Calvar, S. I., Méndez, C. F., & Paz, C. (2012) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2012.12.006 · Cited by 11

Pharmacological Analyses of Protein Kinases Regulating Egg Maturation in Marine Nemertean Worms: A Review and Comparison with Mammalian Eggs

Stricker, S. A., Escalona, J. R., Abernathy, S., & Marquardt, A. (2010) · Marine Drugs · doi:10.3390/md8082417 · Cited by 11

Suprafenacine, an Indazole-Hydrazide Agent, Targets Cancer Cells Through Microtubule Destabilization

Choi, B., Chattopadhaya, S., Le, T. N., Feng, L., Nguyen, Q. T., Lim, C. B., Harikishore, A., Nanga, R. P. R., Bharatham, N., Zhao, Y., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110955 · Cited by 11

Targets, Structures, and Recent Approaches in Malignant Melanoma Chemotherapy

de Matos, A. M., & Francisco, A. P. (2013) · ChemMedChem · doi:10.1002/cmdc.201300248 · Cited by 11

Decreased p44/42 Mitogen-Activated Protein Kinase Phosphorylation in Gender- or Hormone-Related But Not during Age-Related Adrenal Gland Growth in Mice

Bielohuby, M., Sawitzky, M., Johnsen, I. K., Wittenburg, D., Beuschlein, F., Wolf, E., & Hoeflich, A. (2008) · Endocrinology · doi:10.1210/en.2008-1055 · Cited by 9

Volume Regulation and Osmosensing in Animal Cells

Keith, C., & Kevin, S. (2008) · CRC Press eBooks · doi:10.1201/9780849380525-2 · Cited by 13

Critical Role of the Secondary Binding Pocket in Modulating the Enzymatic Activity of DUSP5 toward Phosphorylated ERKs

Talipov, M. R., Nayak, J., Lepley, M. A., Bongard, R. D., Sem, D. S., Ramchandran, R., & Rathore, R. (2016) · Biochemistry · doi:10.1021/acs.biochem.6b00498 · Cited by 10

c-Jun N-terminal kinase activity is required for efficient respiratory syncytial virus production

Caly, L., Li, H., Bogoyevitch, M. A., & Jans, D. A. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.01.005 · Cited by 11

Knock-down of filaggrin influences the mitogen-activated protein kinases signaling pathway in normal human epidermal keratinocytes

Wang, S., Qiu, L., Meng, X., & Dang, N. (2018) · médecine/sciences · doi:10.1051/medsci/201834f116 · Cited by 11

Identification of proteins that mediate the role of androgens in antler regeneration using label free proteomics in sika deer (Cervus nippon)

Akhtar, R. W., Liu, Z., Wang, D., Ba, H., Shah, S. A. H., & Li, C. (2019) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2019.113235 · Cited by 11

MiR-199-3p modulates the onset of puberty in rodents probably by regulating the expression of Kiss1 via the p38 MAPK pathway

Li, X., Xiao, J., Li, K., & Zhou, Y. (2020) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2020.110994 · Cited by 11

A Putative MAPK Kinase Kinase GeneSsos4is Involved in Mycelial Growth, Virulence, Osmotic Adaptation, and Sensitivity to Fludioxonil and is Essential for SsHog1 Phosphorylation inSclerotinia sclerotiorum

Li, T., Xiu, Q., Wang, J., Duan, Y., & Zhou, M. (2020) · Phytopathology · doi:10.1094/phyto-07-20-0292-r · Cited by 11

A Rab escort protein regulates the MAPK pathway that controls filamentous growth in yeast

Jamalzadeh, S., Pujari, A. N., & Cullen, P. J. (2020) · Scientific Reports · doi:10.1038/s41598-020-78470-4 · Cited by 11

MicroRNAs associated with signaling pathways and exercise adaptation in sarcopenia

Javanmardifard, Z., Shahrbanian, S., & Mowla, S. J. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119926 · Cited by 11

Map2k4δ — Identification and functional characterization of a novel Map2k4 splice variant

Haeusgen, W., Tüeffers, L., Herdegen, T., & Waetzig, V. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2014.01.028 · Cited by 11

Activation of mitogen activated protein kinase (MAPK) pathways after soman poisoning in rat cerebellar granule neurons

Pejchal, J., Österreicher, J., Kassa, J., Tichý, A., & Mokrý, J. (2007) · Journal of Applied Toxicology · doi:10.1002/jat.1323 · Cited by 11

Effects of diabetes on retinal pigment epithelial cell proliferation and mitogen-activated protein kinase signaling in dark Agouti rats

Al‐Hussaini, H., & Kilarkaje, N. (2014) · Experimental and Toxicologic Pathology · doi:10.1016/j.etp.2014.10.006 · Cited by 11

RFTN1 facilitates gastric cancer progression by modulating AKT/p38 signaling pathways

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