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KCNJ5(T158A)increases CYP11B2 (显示 CYP11B2 ELISA试剂盒) expression and production of aldosterone, corticosterone and hybrid steroids by upregulating both acute and chronic regulatory events in aldosterone production, and verapamil blocks KCNJ5(T158A)-mediated pathways leading to aldosterone production.
These findings expand on the clinical spectrum of phenotypes associated with KCNJ5 mutations and implicate these mutations in the pathogenesis of hypertension associated with increased aldosterone response to ACTH (显示 POMC ELISA试剂盒) stimulation.
KCNJ5 mutations predominate in large zona fasciculata (ZF)-like Aldosterone-producing Adenomas.
Mutations in KCNJ5 cause the excessive autonomous aldosterone secretion of Aldosterone-producing Adenomas.
KCNJ5 genetic mutation plays a role in the development of primary aldosteronism in aldosterone producing adenomas.
Study provides new evidence, indicating that some glutamate receptor ionotropic kainate 4 (显示 GRIK4 ELISA试剂盒) variants modulate the response to electroconvulsive therapy in patients with depression resistant to treatment, suggesting a role for kainate receptor modulation.
documented for the first time the expression of inflammation-related genes in aldosterone-producing adenomas (APAs) and the correlation of their expression levels with the KCNJ5 mutation status and mRNA expression levels of steroidogenic enzymes, indicating the pathophysiological relevance of inflammation-related genes in APAs
GIRK1 (显示 KCNJ3 ELISA试剂盒)/GIRK4 hetero-tetramers are not activated by Na+, but rather are in a permanent state of high responsiveness to G proteins beta-gamma, suggesting that the GIRK1 (显示 KCNJ3 ELISA试剂盒) subunit functions like a GIRK4 subunit with Na+ permanently bound.
japanese Aldosterone-Producing Adenoma patients may have distinct features including a higher prevalence of KCNJ5 mutations, no gender difference in the frequency of these mutations, and characteristics similar to the zona glomerulosa.
Novel somatic KCNJ5 variants likely cause adenomas by loss of potassium selectivity, similar to previously described mutations.
These results provide a novel molecular mechanism for autocrine negative feedback regulation of insulin (显示 INS ELISA试剂盒) secretion.
study establishes the role of f-channels in cardiac automaticity and indicates that arrhythmia related to HCN loss-of-function may be managed by pharmacological or genetic inhibition of GIRK4 channels
Data indicate taht m2R-RGS6 (显示 RGS6 ELISA试剂盒)-IKACh pathway sets heart rate variability independently from the autonomic input.
Therefore, the lack of proper functioning of the cardio-protective K(ATP) system in the mdx (显示 DMD ELISA试剂盒) cardiomyocytes may be part of the mechanism contributing to development of cardiac disease in dystrophic patients.
Data suggest HL-1 (显示 ASGR1 ELISA试剂盒) cells express GIRK1 (显示 KCNJ3 ELISA试剂盒)/4 and M2 muscarinic receptors and are a good model to study acetylcholine-activated potassium currents.
Data show that the composition of the Kir3.1 (显示 KCNJ3 ELISA试剂盒) and Kir (显示 GEM ELISA试剂盒) 3.4 subunits of the G protein-gated potassium channel (显示 KCNAB2 ELISA试剂盒) changes during embryonic development.
These data implicate GIRK4-containing channels in signaling crucial to energy homeostasis and body weight.
Blockade of K(ATP) channels further diminished (approximately 45%) the repayment of flow debt (显示 PLXNB2 ELISA试剂盒) in lean but not metabolic syndrome swine.
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins. It may associate with two other G-protein-activated potassium channels to form a heteromultimeric pore-forming complex.
CBF1 interacting corepressor
, CBF1-interacting corepressor
, corepressor interacting with RBPJ 1
, G protein-activated inward rectifier potassium channel 4
, cardiac ATP-sensitive potassium channel
, heart KATP channel
, inward rectifier K+ channel KIR3.4
, cardiac inward rectifier
, inward rectifier K(+) channel Kir3.4
, potassium channel, inwardly rectifying subfamily J member 5
, inward rectifying K channel
, potassium inwardly-rectifying channel J5