Results 1 to 10 of about 60,305 (309)

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

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   +2 more sources

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

open access: hybridMol Cell Biol, 2016
Dayalan Naidu S   +13 more
europepmc   +3 more sources

P38 mitogen-activated protein kinase and Parkinson’s disease [PDF]

open access: yesTranslational Neuroscience, 2018
AbstractParkinson’s disease, the second major neurodegenerative disease, has created a great impact on the elder people. Although the mechanisms underlying Parkinson’s disease are not fully understood, considerable evidence suggests that neuro-inflammation, oxidative stress, mitochondrial dysfunction, cell proliferation, differentiation and apoptosis ...
He Jianying   +4 more
openaire   +3 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

Crystal Structure of p38 Mitogen-activated Protein Kinase [PDF]

open access: yesJournal of Biological Chemistry, 1996
p38 mitogen-activated protein kinase is activated by environmental stress and cytokines and plays a role in transcriptional regulation and inflammatory responses. The crystal structure of the apo, unphosphorylated form of p38 kinase has been solved at 2.3 A resolution. The fold and topology of p38 is similar to ERK2 (Zhang, F., Strand, A., Robbins, D.,
K P, Wilson   +7 more
openaire   +2 more sources

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