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cloning and expression analysis of a protein kinase C (show PKC ELISA Kits) gene, PKCmu, and its regulation of the promoter region (PKCmu)
PKD1 (show PKD1 ELISA Kits) contributes to the regulation of physiological angiogenesis and lymphangiogenesis during zebrafish development and is essential for tumor angiogenesis.
None of the Polymorphous low-grade adenocarcinoma (PLGA) lacking PRKD1 somatic mutations or PRKD gene family rearrangements harboured somatic mutations in the kinase domains of the PRKD2 (show PKD2 ELISA Kits) or PRKD3 (show PRKD3 ELISA Kits) genes.
A single nucleotide polymorphism located within the fourth intron of PRKD1 (rs57803087) was strongly associated with DPP-4 (show DPP4 ELISA Kits) inhibitor response in patients with type 2 diabetes
Mutation in PRKD1 gene is associated with congenital heart defects.
Bradykinin stimulates myofibroblast migration through protein kinase D-mediated activation of COX-2 (show COX2 ELISA Kits) and Hsp27 (show HSPB1 ELISA Kits).
Lysophosphatidic acid/PKD-1 (show PKD1 ELISA Kits) signaling leads to nuclear accumulation of histone deacetylase 7 (show HDAC7 ELISA Kits), where it interacts with forkhead box protein O1 (show FOXO1 ELISA Kits) to suppress endothelial CD36 (show CD36 ELISA Kits) transcription and mediates silencing of antiangiogenic switch, resulting in proangiogenic and proarteriogenic reprogramming.
This study discovered and characterized a novel, highly conserved N-terminal domain, comprising 92 amino acids, which mediates dimerization of Protein Kinase D (PKD) isoforms, PKD1 (show PKD1 ELISA Kits), PKD2 (show PKD2 ELISA Kits), and PKD3 (show PRKD3 ELISA Kits) monomers.
MC stimulation by physical contact with T cells results in PKD activation, leading to the phosphorylation of p38 (show CRK ELISA Kits), degranulation and release of cytokines. Understanding the molecular events associated with T cell-induced MC activation might lead to therapeutic approaches for controlling T cell-mediated inflammatory processes in which MC participate.
Data suggest the role of the phospholipase C epsilon (show PLCL1 ELISA Kits)-Protein kinase D-PEA15 (show PEA15 ELISA Kits) protein-ribosomal S6 kinase (show RPS6KB1 ELISA Kits)-IkappaB-NF-kappa B (show NFKB1 ELISA Kits) pathway in facilitating inflammation and inflammation-associated carcinogenesis in the colon.
PRKD1 Mutation is not associated with Solid Tumors and Leukemias.
Knockdown of PKD1 (show PKD1 ELISA Kits) did not affect NMDAR (show GRIN1 ELISA Kits) internalization but prevented the phosphorylation and inhibition of remaining surface NMDARs and NMDAR (show GRIN1 ELISA Kits)-mediated synaptic functions.
These findings imply that PKD1 (show PKD1 ELISA Kits) plays a critical regulatory role in Group B streptococci (GBS (show GNB5 ELISA Kits))-induced proinflammatory reactions and sepsis, and inhibition of PKD1 (show PKD1 ELISA Kits) activation together with antibiotic treatment in GBS (show GNB5 ELISA Kits)-infected neonates could be an effective way to control GBS (show GNB5 ELISA Kits) diseases.
Our studies demonstrate that PKD1 (show PKD1 ELISA Kits)/2 is a key regulator of MVB maturation and exosome secretion, and constitutes a mediator of the DGK alpha (show DGKA ELISA Kits) effect on MVB secretory traffic.
Our results show that AKAP13 (show AKAP13 ELISA Kits)-PKD1 (show PKD1 ELISA Kits) signaling is critical for transcriptional regulation of key contractile, cell death, and metabolic pathways during the development of compensatory hypertrophy in vivo.
PKD1 (show PKD1 ELISA Kits) acts downstream of TGFalpha and Kras, to mediate formation of ductal structures through activation of the Notch (show NOTCH1 ELISA Kits) pathway.
Results reveal that whereas protein kinase D1 and protein kinase D2 (show PKD2 ELISA Kits) are essential for neuronal polarity, there exists a functional redundancy between the two proteins.
PKD controls synaptic plasticity and learning by regulating actin stability in dendritic spines.
regulatory kinase of eNOS (show NOS3 ELISA Kits) in endothelial cells whose activity orchestrates mammalian vascular tone
Overexpression of constitutively active PKD1 (show PKD1 ELISA Kits) in rodent heart results in dilated cardiomyopathy.
PKD1 (show PKD1 ELISA Kits)-deficient keratinocytes showed an increase in transglutaminase expression and activity, indicating an anti-differentiative role of PKD1 (show PKD1 ELISA Kits). Furthermore, the PKD1 (show PKD1 ELISA Kits)-deficient keratinocytes exhibited decreased proliferation.
AngII activates PKD via a mechanism involving Src family kinases and PKC, to underlie increased aldosterone production.
Data indicate that Ser738/742-to-glutamate (show GRIN2A ELISA Kits) protein kinase D mutant increased AngII-induced CREB (show CREB1 ELISA Kits) protein and activating transcription factor 2 (show ATF2 ELISA Kits) phosphorylation, and phospho-CREB (show CREB1 ELISA Kits) binding to the steroidogenic acute regulatory protein (show STAR ELISA Kits) promoter.
These results indicate that PKD is downstream of PLD (show PLD ELISA Kits) and suggest that PKD is one of the mechanisms through which PLD (show PLD ELISA Kits) promotes aldosterone production in response to AngII in adrenal glomerulosa cells.
PKD mediates acute AngII-induced aldosterone secretion.
Protein kinase D-HDAC5 pathway plays an important role in VEGF regulation of gene transcription and angiogenesis
PRKD1 is a serine/threonine kinase that regulates a variety of cellular functions, including membrane receptor signaling, transport at the Golgi, protection from oxidative stress at the mitochondria, gene transcription, and regulation of cell shape, motility, and adhesion (summary by Eiseler et al., 2009
protein kinase D1
, protein kinase C, mu
, serine/threonine-protein kinase D1-like
, protein kinase C mu type
, protein kinase D
, serine/threonine-protein kinase D1
, protein kinase C mu