Lista de obras - Karen E Cosgrove - Dominio Público Uruguay

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland

artículo científico publicado en 1999

ATP-sensitive potassium channels and efaroxan-induced insulin release in the electrofusion-derived BRIN-BD11 beta-cell line

artículo científico publicado en 1999

Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism

artículo científico

Affinity isolation of imidazoline binding proteins from rat brain using 5-amino-efaroxan as a ligand

artículo científico publicado en 1999

Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-Channel

artículo científico publicado en 2015

BPDZ 154 activates adenosine 5'-triphosphate-sensitive potassium channels: in vitro studies using rodent insulin-secreting cells and islets isolated from patients with hyperinsulinism

artículo científico publicado en 2002

Can network biology unravel the aetiology of congenital hyperinsulinism?

artículo científico publicado en 2013

Characterization of ion channels in stimulus-secretion coupling in pancreatic islets

artículo científico publicado en 1997

Engineering a glucose-responsive human insulin-secreting cell line from islets of Langerhans isolated from a patient with persistent hyperinsulinemic hypoglycemia of infancy

artículo científico publicado en 1999

From congenital hyperinsulinism to diabetes mellitus: the role of pancreatic beta-cell KATP channels.

artículo científico publicado en 2005

Genetics and pathophysiology of hyperinsulinism in infancy.

artículo científico publicado en 2004

Glucose modulation of insulin mRNA levels is dependent on transcription factor PDX-1 and occurs independently of changes in intracellular Ca2+.

artículo científico publicado en 2000

Human embryonic stem cells: possibilities for human cell transplantation.

artículo científico publicado en 2005

Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Defects in the Function of Pancreatic β-Cell Adenosine Triphosphate-Sensitive Potassium Channels

artículo científico publicado en 2005

Hyperinsulinism in infancy: from basic science to clinical disease.

artículo científico publicado en 2004

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity

artículo científico publicado en 2004

Hyperinsulinism of infancy: the regulated release of insulin by KATP channel-independent pathways.

artículo científico publicado en 2001

Hyperinsulinism of infancy: towards an understanding of unregulated insulin release. European Network for Research into Hyperinsulinism in Infancy.

artículo científico publicado en 2000

In vitro recovery of ATP-sensitive potassium channels in β-cells from patients with congenital hyperinsulinism of infancy ⬇️

artículo científico publicado en 2011

Increased Plasma Incretin Concentrations Identifies a Subset of Patients with Persistent Congenital Hyperinsulinism without KATP Channel Gene Defects

article

Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p.

artículo científico publicado en 2004

Integrating genetic and imaging investigations into the clinical management of congenital hyperinsulinism.

artículo científico

Network analysis: a new approach to study endocrine disorders

artículo científico publicado en 2014

PAX4 enhances beta-cell differentiation of human embryonic stem cells

artículo científico publicado en 2008

Potassium Channels, Sulphonylurea Receptors and Control of Insulin Release

artículo científico publicado en 1999

Reduced Glycemic Variability in Diazoxide-Responsive Children with Congenital Hyperinsulinism Using Supplemental Omega-3-Polyunsaturated Fatty Acids; A Pilot Trial with MaxEPA(R.).

artículo científico publicado en 2014

The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism

article

Uncontrolled insulin secretion from a childhood pancreatic beta-cell adenoma is not due to the functional loss of ATP-sensitive potassium channels.

artículo científico publicado en 2002

Verapamil, a phenylalkylamine Ca 2 + channel blocker, inhibits ATP-sensitive K + channels in insulin-secreting cells from rats

scientific article published on 01 December 1997

Y-26763: ATP-sensitive K+ channel activation and the inhibition of insulin release from human pancreatic beta-cells

artículo científico publicado en 2004

Lista de obras de Karen E Cosgrove

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland

ATP-sensitive potassium channels and efaroxan-induced insulin release in the electrofusion-derived BRIN-BD11 beta-cell line

Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism

Affinity isolation of imidazoline binding proteins from rat brain using 5-amino-efaroxan as a ligand

Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-Channel

BPDZ 154 activates adenosine 5'-triphosphate-sensitive potassium channels: in vitro studies using rodent insulin-secreting cells and islets isolated from patients with hyperinsulinism

Can network biology unravel the aetiology of congenital hyperinsulinism?

Characterization of ion channels in stimulus-secretion coupling in pancreatic islets

Engineering a glucose-responsive human insulin-secreting cell line from islets of Langerhans isolated from a patient with persistent hyperinsulinemic hypoglycemia of infancy

From congenital hyperinsulinism to diabetes mellitus: the role of pancreatic beta-cell KATP channels.

Genetics and pathophysiology of hyperinsulinism in infancy.

Glucose modulation of insulin mRNA levels is dependent on transcription factor PDX-1 and occurs independently of changes in intracellular Ca2+.

Human embryonic stem cells: possibilities for human cell transplantation.

Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Defects in the Function of Pancreatic β-Cell Adenosine Triphosphate-Sensitive Potassium Channels

Hyperinsulinism in infancy: from basic science to clinical disease.

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity

Hyperinsulinism of infancy: the regulated release of insulin by KATP channel-independent pathways.

Hyperinsulinism of infancy: towards an understanding of unregulated insulin release. European Network for Research into Hyperinsulinism in Infancy.

In vitro recovery of ATP-sensitive potassium channels in β-cells from patients with congenital hyperinsulinism of infancy ⬇️

Increased Plasma Incretin Concentrations Identifies a Subset of Patients with Persistent Congenital Hyperinsulinism without KATP Channel Gene Defects

Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p.

Integrating genetic and imaging investigations into the clinical management of congenital hyperinsulinism.

Network analysis: a new approach to study endocrine disorders

PAX4 enhances beta-cell differentiation of human embryonic stem cells

Potassium Channels, Sulphonylurea Receptors and Control of Insulin Release

Reduced Glycemic Variability in Diazoxide-Responsive Children with Congenital Hyperinsulinism Using Supplemental Omega-3-Polyunsaturated Fatty Acids; A Pilot Trial with MaxEPA(R.).

The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism

Uncontrolled insulin secretion from a childhood pancreatic beta-cell adenoma is not due to the functional loss of ATP-sensitive potassium channels.

Verapamil, a phenylalkylamine Ca 2 + channel blocker, inhibits ATP-sensitive K + channels in insulin-secreting cells from rats

Y-26763: ATP-sensitive K+ channel activation and the inhibition of insulin release from human pancreatic beta-cells