Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
about
Functional properties of four splice variants of a human pancreatic tandem-pore K+ channel, TALK-1ATP-sensitive potassium channel (KATP channel) expression in the normal canine pancreas and in canine insulinomas.Neuroprotective role of ATP-sensitive potassium channels in cerebral ischemiaA novel KCNJ11 mutation associated with congenital hyperinsulinism reduces the intrinsic open probability of beta-cell ATP-sensitive potassium channelsPotassium channel regulation.Purinergic contribution to circulatory, metabolic, and adrenergic responses to acute hypoxemia in fetal sheep.Mutations in the linker domain of NBD2 of SUR inhibit transduction but not nucleotide bindingGenetic Variations in the Kir6.2 Subunit (KCNJ11) of Pancreatic ATP-Sensitive Potassium Channel Gene Are Associated with Insulin Response to Glucose Loading and Early Onset of Type 2 Diabetes in Childhood and Adolescence in Taiwan.Defective trafficking and function of KATP channels caused by a sulfonylurea receptor 1 mutation associated with persistent hyperinsulinemic hypoglycemia of infancy.K(ATP) channels and insulin secretion disorders.Diabetes and insulin secretion: whither KATP?Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescueMaternal protein restriction induces alterations in insulin signaling and ATP sensitive potassium channel protein in hypothalami of intrauterine growth restriction fetal ratsUpdate of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism.Current understanding of K ATP channels in neonatal diseases: focus on insulin secretion disorders.Membrane targeting of ATP-sensitive potassium channel. Effects of glycosylation on surface expression.Modulation of the trafficking efficiency and functional properties of ATP-sensitive potassium channels through a single amino acid in the sulfonylurea receptor.Sulfonylureas correct trafficking defects of ATP-sensitive potassium channels caused by mutations in the sulfonylurea receptor.A novel mutation in ABCC8 gene in a newborn with congenital hyperinsulinism -a case report.Prediabetes is associated with genetic variations in the gene encoding the Kir6.2 subunit of the pancreatic ATP-sensitive potassium channel (KCNJ11): A case-control study in a Han Chinese youth population.Molecular structure of human KATP in complex with ATP and ADP.Kir2.1 is important for efficient BMP signaling in mammalian face development.
P2860
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P2860
Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
description
2000 nî lūn-bûn
@nan
2000 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մարտին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
@ast
Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
@en
type
label
Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
@ast
Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
@en
prefLabel
Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
@ast
Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
@en
P2093
P1433
P1476
Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
@en
P2093
P304
P356
10.1046/J.1523-1755.2000.00918.X
P407
P577
2000-03-01T00:00:00Z
P5875
P6179
1029157049