Results 1 to 10 of about 183,974 (371)

An overview of mammalian p38 mitogen-activated protein kinases, central regulators of cell stress and receptor signaling [version 1; peer review: 2 approved] [PDF]

open access: yesF1000Research, 2020
The p38 family is a highly evolutionarily conserved group of mitogen-activated protein kinases (MAPKs) that is involved in and helps co-ordinate cellular responses to nearly all stressful stimuli.
Jiahuai Han, Jianfeng Wu, John Silke
doaj   +3 more sources

Heat Shock Factor 1 Is a Substrate for p38 Mitogen-Activated Protein Kinases. [PDF]

open access: hybridMol Cell Biol, 2016
Heat shock factor 1 (HSF1) monitors the structural integrity of the proteome. Phosphorylation at S326 is a hallmark for HSF1 activation, but the identity of the kinase(s) phosphorylating this site has remained elusive. We show here that the dietary agent
Dayalan Naidu S   +13 more
europepmc   +4 more sources

Src Family Kinases and p38 Mitogen-Activated Protein Kinases Regulate Pluripotent Cell Differentiation in Culture. [PDF]

open access: goldPLoS ONE, 2016
Multiple pluripotent cell populations, which together comprise the pluripotent cell lineage, have been identified. The mechanisms that control the progression between these populations are still poorly understood.
Boon Siang Nicholas Tan   +9 more
doaj   +4 more sources

Functions of p38 MAP Kinases in the Central Nervous System

open access: yesFrontiers in Molecular Neuroscience, 2020
Mitogen-activated protein (MAP) kinases are a central component in signaling networks in a multitude of mammalian cell types. This review covers recent advances on specific functions of p38 MAP kinases in cells of the central nervous system.
Prita R. Asih   +5 more
doaj   +1 more source

Time courses of changes in phospho- and total- MAP kinases in the cochlea after intense noise exposure. [PDF]

open access: yesPLoS ONE, 2013
Mitogen-activated protein kinases (MAP kinases) are intracellular signaling kinases activated by phosphorylation in response to a variety of extracellular stimuli.
Yukihide Maeda   +4 more
doaj   +1 more source

Co-regulation of the transcription controlling ATF2 phosphoswitch by JNK and p38

open access: yesNature Communications, 2020
The ATF2 transcription factor is phosphorylated by different mitogen-activated protein (MAP) kinases. Here, the authors show that the functionally distinct MAP kinases JNK and p38 control ATF2 through different binding sites and differential ...
Klára Kirsch   +13 more
doaj   +1 more source

DUSP1 is a novel target for enhancing pancreatic cancer cell sensitivity to gemcitabine. [PDF]

open access: yesPLoS ONE, 2014
Pancreatic ductal adenocarcinoma (PDAC) is a deadly cancer with a poor prognosis that is characterized by excessive mitogenic pathway activation and marked chemoresistance to a broad spectrum of chemotherapeutic drugs.
Fang Liu   +3 more
doaj   +1 more source

Stress Relief Techniques: p38 MAPK Determines the Balance of Cell Cycle and Apoptosis Pathways

open access: yesBiomolecules, 2021
Protein signaling networks are formed from diverse and inter-connected cell signaling pathways converging into webs of function and regulation. These signaling pathways both receive and conduct molecular messages, often by a series of post-translation ...
Robert H. Whitaker, Jeanette Gowen Cook
doaj   +1 more source

Role of p38 mitogen-activated protein kinase isoforms in murine skin inflammation induced by 12-O-tetradecanoylphorbol 13-acetate [PDF]

open access: yes, 2011
p38 mitogen-activated protein kinase plays a pivotal role in skin inflammation. The purpose of this study was to investigate the role of the various p38 isoforms. p38 beta/delta-knockout-C57BL/6 mice were generated, studied in a 12-O-tetradecanoylphorbol
Arthur, J. Simon C.   +6 more
core   +3 more sources

Mitogen Activated Protein kinase signal transduction pathways in the prostate

open access: yesCell Communication and Signaling, 2004
The biochemistry of the mitogen activated protein kinases ERK, JNK, and p38 have been studied in prostate physiology in an attempt to elucidate novel mechanisms and pathways for the treatment of prostatic disease.
Koul Sweaty   +3 more
doaj   +1 more source

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