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Alleles of 2 equine AMPK (show PRKAA1 ELISA Kits) gamma subunit genes had no causative role in polysaccharide storage myopathy in horses
PRKAG3-230 may be associated with sporadic Wolff-Parkinson-White (WPW) syndrome in a Taiwanese population.
The mTOR (show FRAP1 ELISA Kits) pathway was significantly associated with overall and estrogen receptor (show ESR1 ELISA Kits)-negative (ER-) breast cancer risk (P = 0.003 and 0.03, respectively). PRKAG3 (Padj = 0.0018) and RPS6KA3 (show RPS6KA3 ELISA Kits) (Padj = 0.061) were the leading genes for the associations with overall breast cancer risk and ER- breast cancer risk, respectively.
Data suggest different gamma-isoforms in AMPK (show PRKAA1 ELISA Kits) can have different effects on enzyme activation; here, activation of AMPK (show PRKAA1 ELISA Kits) by compound 991 is greater if AMPK (show PRKAA1 ELISA Kits) contains PRKAG2 (show PRKAG2 ELISA Kits) versus PRKAG1 (show PRKAG1 ELISA Kits) or PRKAG3.
Low PRKAA2 (show PRKAA2 ELISA Kits) expression is associated with follicular lymphoma.
Through the enhancement of skeletal muscle glucose uptake and increased mitochondrial content, the R225W mutation of the gene encoding AMP-activated protein kinase (AMPK (show PRKAA2 ELISA Kits))gamma(3)may significantly enhance exercise performance.
Purification and characterization of truncated human AMPK alpha 2 (show PRKAA2 ELISA Kits) beta 2 gamma 3 heterotrimer from baculovirus-infected insect cells
identified for the first time a mutation in the skeletal muscle-specific (show EIF3K ELISA Kits) regulatory gamma(3) subunit of AMPK (show PRKAA1 ELISA Kits) in humans
data show that different mutations in gamma3 exert different effects on allosteric regulation of alpha2beta2gamma3 complex by AMP (show APRT ELISA Kits), whereas we find no evidence for their role in regulating the level of phosphorylation of alpha2 by upstream kinases.
Genetic variability in PRKAG3 does not seem to have a major effect on glucose metabolism, but play a role in lipoprotein metabolism in humans.
Variants in genes for AMPKalpha2 (show PRKAA2 ELISA Kits) and AMPKgamma3 were not associated with PCOS or its component traits.
Association between polymorphism in bovine PRKAG3 gene and milk production traits.
Activity of glycogen synthase without the allosteric activator glucose 6-phosphate was decreased in gain of function AMPKgamma3(R200Q) relative to all other genotypes
allelic frequencies of PRKAG3 in several pig breeds
The variation in the promoter region of the porcine PRKAG3 gene has associations with meat quality phenotypes, including traits which are influenced by glycolytic potential and muscle metabolism in a breed-dependent manner.
PRKAG3 mutation influences muscle characteristics and promotes an oxidative phenotype to a varying degree among muscles with different functions
increased rate of glycogen synthesis following exercise in pigs carrying the PRKAG3 mutation correlates with an increased signalling response of Akt and its substrate, AS160.
Genetic variation of PRKAG3 was studied in indigenous breeds of China.
the R225Q mutation of PRKAG3 is associated with higher basal AMPK (show PRKAA1 ELISA Kits) activity and diminished AMP (show TMPRSS5 ELISA Kits) dependence
findings suggest that the R200Q mutation results in a constitutively active enzyme, leading to hyperaccumulation of glycogen (show GYS1 ELISA Kits) due to the increased influx of glucose
Data suggest that the AMPK (show PRKAA1 ELISA Kits)-TBC1D4 signaling axis is likely mediating the improved muscle insulin (show INS ELISA Kits) sensitivity after contraction/exercise and illuminates an important and physiologically relevant role of AMPK (show PRKAA1 ELISA Kits) in skeletal muscle.
gamma3-AMPK (show PRKAA1 ELISA Kits) down-regulation is a rapid physiological muscle response observed in mouse after running exercise or fasting, two situations leading to PPARbeta (show PPARD ELISA Kits) activation.
AMPK (show PRKAA1 ELISA Kits) acts as the primordial trigger for fasting- and exercise-induced adaptations in skeletal muscle and that activation of SIRT1 (show SIRT1 ELISA Kits) and its downstream signaling pathways are improperly triggered in AMPK (show PRKAA1 ELISA Kits)-deficient states.
Gamma3 subunit of AMPK (show PRKAA1 ELISA Kits) is highly expressed in fast-twitch glycolytic skeletal muscle, and wild-type gamma3 functions in the regulation of alpha1 catalytic activity, but it is not associated with changes in muscle glycogen (show GYS1 ELISA Kits) concentrations
functional studies of the protein kinase (show CDK7 ELISA Kits), AMP (show TMPRSS5 ELISA Kits)-activated, gamma 3 (AMPK3) isoform further support the close connection between glycogen (show GYS1 ELISA Kits) content and exercise performance in skeletal muscle
AMPKg3 is involved in the coordinated transcription of genes critical for lipid and glucose metabolism in white glycolytic skeletal muscle.
analysis of transcriptional regulation in skeletal muscle of AMP-activated protein kinase (show PRKAA2 ELISA Kits) gamma3 R225Q transgenic and knock-out mice
Expression of either wild type or mutant (R225Q) gamma3-subunit of AMPK (show PRKAA1 ELISA Kits) results in increased glycogen (show GYS1 ELISA Kits) concentrations in muscle, but the mechanisms underlying this alteration appear to be different.
AMPK (show PRKAA1 ELISA Kits) heterotrimeric complexes containing the AMPKgamma(3) subunit may play a specific role in linking circadian oscillators and energy metabolism in skeletal muscle.
Basal and A-769662-mediated IL-6 (show IL6 ELISA Kits) release provide evidence for a role of AMPK (show PRKAA1 ELISA Kits) in the regulation of IL-6 (show IL6 ELISA Kits) release from oxidative skeletal muscle.
The protein encoded by this gene is a regulatory subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This subunit is one of the gamma regulatory subunits of AMPK. It is dominantly expressed in skeletal muscle. Studies of the pig counterpart suggest that this subunit may play a key role in the regulation of energy metabolism in skeletal muscle.
5'-AMP-activated protein kinase subunit gamma-3
, AMP-activated protein kinase gamma 3 subunit
, protein kinase, AMP-activated, gamma 3 non-catatlytic subunit
, 5'-AMP-activated protein kinase gamma-3 non-catalytic subunit long form
, AMP-activated protein kinase gamma subunit
, protein kinase non-catalytic gamma subunit
, AMP-activated protein kinase, non-catalytic gamma-3 subunit
, AMP-activated protein kinase gamma 3
, AMPK-activated protein kinase gamma-3 subunit
, protein kinase, AMP-activated, gamma 3 non-catalytic subunit a
, protein kinase, AMP-activated, gamma 3 non-catalytic subunit
, AMP-activated protein kinase subunit gamma
, 5'-AMP-activated protein kinase subunit gamma-3-like
, 5'-AMP-activated protein kinase, gamma-3 subunit
, AMPK gamma-3 chain
, AMPK gamma3
, AMPK subunit gamma-3
, 5'-AMP-activated protein kinase gamma-3 subunit
, AMP-activated protein kinase gamma