(Q28287890)

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

3-D structural and functional characterization of the purified KATP channel complex Kir6.2-SUR1.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Cloning and functional expression of the cDNA encoding an inwardly-rectifying potassium channel expressed in pancreatic beta-cells and in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Association and stoichiometry of K(ATP) channel subunits

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

A family of sulfonylurea receptors determines the pharmacological properties of ATP-sensitive K+ channels

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

A novel sulfonylurea receptor forms with BIR (Kir6.2) a smooth muscle type ATP-sensitive K+ channel

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Regulation of glucagon release in mouse -cells by KATP channels and inactivation of TTX-sensitive Na+ channels.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Patch-clamp characterisation of somatostatin-secreting -cells in intact mouse pancreatic islets

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

A novel glucose-sensing mechanism contributing to glucagon-like peptide-1 secretion from the GLUTag cell line

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Properties of cloned ATP-sensitive K+ currents expressed in Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Morphological changes in pancreatic islets of KATP channel-deficient mice: the involvement of KATP channels in the survival of insulin cells and the maintenance of islet architecture

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Roles of ATP-sensitive K+ channels in cell survival and differentiation in the endocrine pancreas

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Sulfonylurea stimulation of insulin secretion

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Gene targeting approach to clarification of ion channel function: studies of Kir6.x null mice

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Distribution and phenotype of neurons containing the ATP-sensitive K+ channel in rat brain

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Neuroprotection by KATP channels.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Protection against hypoxic-ischemic injury in transgenic mice overexpressing Kir6.2 channel pore in forebrain

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

ATP-sensitive K+ channels in the hypothalamus are essential for the maintenance of glucose homeostasis.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Behavioral phenotyping of mice lacking the K ATP channel subunit Kir6.2.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

KATP channels depress force by reducing action potential amplitude in mouse EDL and soleus muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Kir6.2 is required for adaptation to stress

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Cellular remodeling in heart failure disrupts K(ATP) channel-dependent stress tolerance

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

ATP-sensitive K+ channel knockout compromises the metabolic benefit of exercise training, resulting in cardiac deficits

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Cardiac ATP-sensitive K+ channels: regulation by intracellular nucleotides and K+ channel-opening drugs

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Genetic disruption of Kir6.2, the pore-forming subunit of ATP-sensitive K+ channel, predisposes to catecholamine-induced ventricular dysrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Role of sarcolemmal K(ATP) channels in cardioprotection against ischemia/reperfusion injury in mice

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

ATP-sensitive and inwardly rectifying potassium channels in smooth muscle

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: deficiency of pancreatic D cells or hyperactivity of B cells?

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's role

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Hyperinsulinism in infancy: from basic science to clinical disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Familial hyperinsulinism caused by an activating glucokinase mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemia

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Loss of functional KATP channels in pancreatic beta-cells causes persistent hyperinsulinemic hypoglycemia of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

A novel KCNJ11 mutation associated with congenital hyperinsulinism reduces the intrinsic open probability of beta-cell ATP-sensitive potassium channels

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Targeted Overactivity of β Cell KATP Channels Induces Profound Neonatal Diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

The prevalent Glu23Lys polymorphism in the potassium inward rectifier 6.2 (KIR6.2) gene is associated with impaired glucagon suppression in response to hyperglycemia

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Permanent diabetes mellitus in the first year of life

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Neonatal and very-early-onset diabetes mellitus

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Neonatal diabetes mellitus: chromosomal analysis in transient and permanent cases.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Neonatal diabetes mellitus due to complete glucokinase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Activating Mutations in the KCNJ11 Gene Encoding the ATP-Sensitive K+ Channel Subunit Kir6.2 Are Rare in Clinically Defined Type 1 Diabetes Diagnosed Before 2 Years

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Relapsing diabetes can result from moderately activating mutations in KCNJ11.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 Gene encoding the Kir6.2 subunit of the beta-cell potassium adenosine triphosphate channel

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Functional analysis of a structural model of the ATP-binding site of the KATP channel Kir6.2 subunit.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Molecular mechanism for ATP-dependent closure of the K+ channel Kir6.2

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Molecular basis for Kir6.2 channel inhibition by adenine nucleotides

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Functional effects of naturally occurring KCNJ11 mutations causing neonatal diabetes on cloned cardiac KATP channels

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Tissue specificity of sulfonylureas: studies on cloned cardiac and beta-cell K(ATP) channels.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Pathways in beta-cell stimulus-secretion coupling as targets for therapeutic insulin secretagogues

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Differential sensitivity of beta-cell and extrapancreatic K(ATP) channels to gliclazide.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

The interaction of nucleotides with the tolbutamide block of cloned ATP-sensitive K+ channel currents expressed in Xenopus oocytes: a reinterpretation.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Sulfonylurea and non-sulfonylurea hypoglycemic agents: pharmachological properties and tissue selectivity

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

High-dose glibenclamide can replace insulin therapy despite transitory diarrhea in early-onset diabetes caused by a novel R201L Kir6.2 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Sulfonylurea induced beta-cell apoptosis in cultured human islets

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Beta-cell toxicity of ATP-sensitive K+ channel-blocking insulin secretagogues

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

High-affinity interactions between peptides and heat shock protein 70 augment CD8+ T lymphocyte immune responses

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

The tolbutamide site of SUR1 and a mechanism for its functional coupling to K(ATP) channel closure.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R2

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Functional effects of mutations at F35 in the NH2-terminus of Kir6.2 (KCNJ11), causing neonatal diabetes, and response to sulfonylurea therapy.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects.

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021

KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features

1 reference

https://api.crossref.org/works/10.1016%2FS1262-3636%2807%2970311-7

7 January 2021