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Study propose a model for sequential roles of MPK12, HT1, and GHR1 in the ABA-independent regulation of SLAC1 during CO2-induced stomatal closure.
MPK9 (show MAPK9 ELISA Kits) and MPK12 are positive regulators of salicylic acid signaling in Arabidopsis guard cells.
MPK9 (show MAPK9 ELISA Kits) and MPK12 are key regulators mediating both abscisic acid (ABA) and Methyl jasmonate (MeJA) signalling in guard cells.
MPK9 (show MAPK9 ELISA Kits) and MPK12 function redundantly downstream of extracellular reactive oxygen production and intracellular accumulation, cytosolic alkalisation and Ca(2 (show CA2 ELISA Kits)+)cytosolic oscillation in yeast elcictor-induced stomatal closure
MPK9 (show MAPK9 ELISA Kits) and MPK12 act downstream of ROS (show ROS1 ELISA Kits) and cytosolic Ca2 (show CA2 ELISA Kits)+ and upstream of anion channels in the guard cell abscisic acid signaling cascade.
MAP kinases MPK9 (show MAPK9 ELISA Kits) and MPK12 are preferentially expressed in guard cells and positively regulate ROS (show ROS1 ELISA Kits)-mediated ABA signaling.
MPK12 is both a physiological substrate of IBR5 and a novel negative regulator of auxin signaling.
There was significant association between p38gamma expression and esophageal squamous cell carcinoma clinical stage, lymph nodes metastases, and tumor volume. p38delta (show MAPK1/3 ELISA Kits) overexpression can promote tumorigenesis in nude mice model xenografted with Eca109 cells whose basal level of p38delta (show MAPK1/3 ELISA Kits) was stably over-expressed and p38gamma was stably knocked down.
This study reveals a novel pathway that directly links ErbB4 (show ERBB4 ELISA Kits) and p38gamma to the transcriptional machinery of NKx2.5 (show NKX2-5 ELISA Kits)-GATA4 (show GATA4 ELISA Kits) complex which is critical for cardiomyocyte formation during mammalian heart development.
during interphase ERK3 (show MAPK4 ELISA Kits) is mainly resident in the nucleoplasm in association with ribonuclear proteins involved in early pre-mRNA splicing, it undergoes cell cycle-dependent redistribution and, during apoptosis
Taken together our data suggest that as cells initiate adhesion to matrix increasing levels of ERK3 (show MAPK4 ELISA Kits) at the cell periphery are required to orchestrate cell morphology changes which can then drive migratory behavior.
p38gamma and p38delta (show MAPK1/3 ELISA Kits) reprogram liver metabolism by modulating neutrophil infiltration and provide a potential target for NAFLD (show TSC2 ELISA Kits) therapy
analysis of how allosteric regulation of p38gamma and PTPN3 (show PTPN3 ELISA Kits) involves a PDZ domain (show INADL ELISA Kits)-modulated complex formation
Thus, in endothelial cells p38alpha (show MAPK14 ELISA Kits) mediates apoptotic signaling, whereas p38beta (show MAPK11 ELISA Kits) and p38gamma transduce survival signaling
p38gamma Mitogen-activated protein kinase signals through phosphorylating its phosphatase PTPH1 in regulating ras protein oncogenesis and stress response.
SEPW1 (show SEPW1 ELISA Kits) silencing increases MKK4 (show MAP2K4 ELISA Kits), which activates p38gamma, p38delta (show MAPK1/3 ELISA Kits), and JNK2 (show MAPK9 ELISA Kits) to phosphorylate p53 (show TP53 ELISA Kits) on Ser (show SIGLEC1 ELISA Kits)-33 and cause a transient G(1) arrest.
phosphorylation at Ser (show SIGLEC1 ELISA Kits)-118 is required for ER to bind both p38gamma and c-Jun (show JUN ELISA Kits), thereby promoting ER relocation from ERE to AP-1 (show FOSB ELISA Kits) promoter sites.
p38gamma mitogen-activated protein kinase (show MAPK1 ELISA Kits) mediates inflammatory signaling to promote colon tumorigenesis
p38gamma and p38delta (show MAPK1/3 ELISA Kits) control heart growth by modulating mTOR (show FRAP1 ELISA Kits) pathway through DEPTOR (show DEPTOR ELISA Kits) phosphorylation and subsequent degradation.
Findings provide genetic evidence that p38gamma and p38delta (show MAPK1/3 ELISA Kits) have essential roles in skin tumour development.
Together, our results establish that p38gamma and p38delta (show MAPK1/3 ELISA Kits) are central to colitis-associated colon cancer formation through regulation of hematopoietic cell response to injury, and validate p38gamma and p38kappa as potential targets for cancer therapy.
An energetic signal may trigger phosphorylation of the p38-gamma isoform which may explain how contractions differentially activate signaling pathways.
p38gamma and p38delta (show MAPK1/3 ELISA Kits) are crucial regulators of inflammatory joint destruction in collagen-induced arthritis.
p38gamma and p38delta (show MAPK1/3 ELISA Kits) kinases regulate the Toll-like receptor 4 (TLR4 (show TLR4 ELISA Kits))-induced cytokine production by controlling ERK1/2 (show MAPK1/3 ELISA Kits) protein kinase (show CDK7 ELISA Kits) pathway activation
results indicate that p38gamma and p38delta (show MAPK1/3 ELISA Kits) have a role in the suppression of tumor development
Activation of members of the mitogen-activated protein kinase family is a major mechanism for transduction of extracellular signals. Stress-activated protein kinases are one subclass of MAP kinases. The protein encoded by this gene functions as a signal transducer during differentiation of myoblasts to myotubes.
mitogen-activated protein kinase 12
, MAP kinase 12
, MAPK 12
, extracellular signal-regulated kinase 6
, stress-activated protein kinase 3
, MAP kinase p38 gamma
, mitogen-activated protein kinase 3
, mitogen-activated protein kinase p38 gamma
, mitogen activated protein kinase 12
, stress activated protein kinase 3
, SAP kinase-3