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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 (zeige MAPK9 Proteine) and MPK12 are positive regulators of salicylic acid signaling in Arabidopsis guard cells.
MPK9 (zeige MAPK9 Proteine) and MPK12 are key regulators mediating both abscisic acid (ABA) and Methyl jasmonate (MeJA) signalling in guard cells.
MPK9 (zeige MAPK9 Proteine) and MPK12 function redundantly downstream of extracellular reactive oxygen production and intracellular accumulation, cytosolic alkalisation and Ca(2 (zeige CA2 Proteine)+)cytosolic oscillation in yeast elcictor-induced stomatal closure
MPK9 (zeige MAPK9 Proteine) and MPK12 act downstream of ROS (zeige ROS1 Proteine) and cytosolic Ca2 (zeige CA2 Proteine)+ and upstream of anion channels in the guard cell abscisic acid signaling cascade.
MAP kinases MPK9 (zeige MAPK9 Proteine) and MPK12 are preferentially expressed in guard cells and positively regulate ROS (zeige ROS1 Proteine)-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 overexpression can promote tumorigenesis in nude mice model xenografted with Eca109 cells whose basal level of p38delta was stably over-expressed and p38gamma was stably knocked down.
This study reveals a novel pathway that directly links ErbB4 (zeige ERBB4 Proteine) and p38gamma to the transcriptional machinery of NKx2.5 (zeige NKX2-5 Proteine)-GATA4 (zeige GATA4 Proteine) complex which is critical for cardiomyocyte formation during mammalian heart development.
during interphase ERK3 (zeige MAPK4 Proteine) 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 (zeige MAPK4 Proteine) at the cell periphery are required to orchestrate cell morphology changes which can then drive migratory behavior.
p38gamma and p38delta reprogram liver metabolism by modulating neutrophil infiltration and provide a potential target for NAFLD therapy
analysis of how allosteric regulation of p38gamma and PTPN3 involves a PDZ domain-modulated complex formation
Thus, in endothelial cells p38alpha (zeige MAPK14 Proteine) mediates apoptotic signaling, whereas p38beta (zeige MAPK11 Proteine) 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 (zeige SEPW1 Proteine) silencing increases MKK4 (zeige MAP2K4 Proteine), which activates p38gamma, p38delta, and JNK2 (zeige MAPK9 Proteine) to phosphorylate p53 (zeige TP53 Proteine) on Ser (zeige SIGLEC1 Proteine)-33 and cause a transient G(1) arrest.
phosphorylation at Ser (zeige SIGLEC1 Proteine)-118 is required for ER to bind both p38gamma and c-Jun (zeige JUN Proteine), thereby promoting ER relocation from ERE to AP-1 (zeige FOSB Proteine) promoter sites.
p38gamma mitogen-activated protein kinase (zeige MAPK1 Proteine) mediates inflammatory signaling to promote colon tumorigenesis
p38gamma and p38delta control heart growth by modulating mTOR (zeige FRAP1 Proteine) pathway through DEPTOR (zeige DEPTOR Proteine) phosphorylation and subsequent degradation.
Findings provide genetic evidence that p38gamma and p38delta have essential roles in skin tumour development.
Together, our results establish that p38gamma and p38delta 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 are crucial regulators of inflammatory joint destruction in collagen-induced arthritis.
p38gamma and p38delta kinases regulate the Toll-like receptor 4 (TLR4 (zeige TLR4 Proteine))-induced cytokine production by controlling ERK1/2 protein kinase (zeige CDK7 Proteine) pathway activation
results indicate that p38gamma and p38delta 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