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PDK2/PARL (Montrer PARL Protéines) senses defects in mitochondrial bioenergetics.
The data demonstrate potential roles of PDK2 and ABCG2 polymorphisms in the metabolic phenotypes of Tibetan gout patients.
High glycolysis and PDK2 overexpression are closely linked to cisplatin resistance in head and neck cancer cells, which can be reversed by PDK2 nhibition.
both PDK 1 (Montrer PDK1 Protéines) and 2 isoforms are overexpressed in cutaneous melanoma compared to nevi, this expression being associated with the expression of the mTOR (Montrer FRAP1 Protéines) pathway effectors and independent of the BRAF (Montrer BRAF Protéines) mutational status
The findings of the present study reveal a novel survival pathway that functionally couples the unique glycolytic phenotype in cancer cells to hypoxia resistance via a PDK2-dependent mechanism that switches Bnip3 (Montrer BNIP3 Protéines) from cell death to survival.
The final compound of this series, 2-[(2,4-dihydroxyphenyl)sulfonyl]isoindoline-4,6-diol, designated PS10, inhibits all four PDK isoforms with IC50 = 0.8 muM for PDK2.
Germline mutations in PKD2 (Montrer PKD2 Protéines) gene is associated with autosomal-dominant polycystic kidney disease.
we for the first time demonstrated that a low-nutrient condition drives cancer cells to utilize glycolysis to produce ATP, and this increases the Warburg effect through a novel mechanism involving ROS (Montrer ROS1 Protéines)/AMPK (Montrer PRKAA1 Protéines)-dependent activation of PDK.
Mitochondrial activation by inhibition of PDKII suppresses HIF1a (Montrer HIF1A Protéines) signaling and angiogenesis in cancer.
Inactivation of pyruvate dehydrogenase kinase 2 by mitochondrial reactive oxygen species.
our results suggest that PDK2/4 can be a potential target for the development of pharmacotherapy for the treatment of acute inflammatory pain
The current study reports that increasing hepatic PDC (Montrer PDC Protéines) activity by inhibition of PDK2 ameliorates hepatic steatosis and insulin (Montrer INS Protéines) sensitivity by regulating TCA cycle anaplerosis and ketogenesis. The findings suggest PDK2 is a potential therapeutic target for nonalcoholic fatty liver disease.
PDK2/4 induction and the subsequent lactate surge induce the metabolic shift in the diabetic dorsal root ganglion thereby contributing to the pathogenesis of painful diabetic neuropathy.
Double-knockout mice with global deletion of PDK2 and PDK4 (Montrer PDK4 Protéines), which results in constitutively activated pyruvate dehydrogenase (Montrer PDP Protéines), preferentially oxidize glucose in muscle.
The Pdk4 (Montrer PDK4 Protéines) gene knockdown led to better glucose tolerance than the Pdk2 gene knockdown.
loss of both Pdk2 and Pdk4 (Montrer PDK4 Protéines) attenuated HSC (Montrer FUT1 Protéines) quiescence, glycolysis, and transplantation capacity.
Results established that wild-type p53 (Montrer TP53 Protéines) prevents manifestation of the Warburg effect by controlling Pdk2. These findings elucidate a new mechanism by which p53 (Montrer TP53 Protéines) suppresses tumorigenesis acting at the level of cancer cell metabolism.
PDK2 activity is essential, even at rest, in regulation of carbohydrate oxidation and production of reducing equivalents for the electron transport chain.
mitochondrial ND2 mutation contributes to HIF1alpha (Montrer HIF1A Protéines) accumulation via increased ROS (Montrer ROS1 Protéines) production, up-regulation of PDK2, attenuating PDH (Montrer PDP Protéines) activity, thereby increasing pyruvate, resulting in HIF1alpha (Montrer HIF1A Protéines) stabilization
This gene encodes a member of the pyruvate dehydrogenase kinase family. The encoded protein phosphorylates pyruvate dehydrogenase, down-regulating the activity of the mitochondrial pyruvate dehydrogenase complex. Overexpression of this gene may play a role in both cancer and diabetes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
PDH kinase 2
, pyruvate dehydrogenase kinase, isoenzyme 2
, pyruvate dehydrogenase, lipoamide, kinase isozyme 2, mitochondrial
, [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 2, mitochondrial
, pyruvate dehydrogenase 2
, pyruvate dehydrogenase kinase, isozyme 2
, PDK P45
, pyruvate dehydrogenase kinase 2 subunit p45 (PDK2)