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Philipson, Louis
One or more keywords matched the following items that are connected to Philipson, Louis
Item TypeName
Concept Potassium Channels, Inwardly Rectifying
Academic Article K+ channels: generating excitement in pancreatic beta-cells.
Academic Article Insulin gene mutations as a cause of permanent neonatal diabetes.
Academic Article Diagnosis and treatment of neonatal diabetes: a United States experience.
Academic Article Action potentials and insulin secretion: new insights into the role of Kv channels.
Academic Article Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.
Academic Article Functional expression of an epitope-tagged G protein-coupled K+ channel (GIRK1).
Academic Article Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism.
Academic Article ATP-sensitive K+ channels: paradigm lost, paradigm regained.
Academic Article Pas de deux or more: the sulfonylurea receptor and K+ channels.
Academic Article Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA.
Academic Article 5-amino-imidazole carboxamide riboside acutely potentiates glucose-stimulated insulin secretion from mouse pancreatic islets by KATP channel-dependent and -independent pathways.
Academic Article Tooth discoloration in patients with neonatal diabetes after transfer onto glibenclamide: a previously unreported side effect.
Academic Article Sulfonylurea treatment before genetic testing in neonatal diabetes: pros and cons.
Academic Article Update on diabetes classification.
Academic Article Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes.
Academic Article Patients with KCNJ11-related diabetes frequently have neuropsychological impairments compared with sibling controls.
Academic Article Preservation of Reduced Numbers of Insulin-Positive Cells in Sulfonylurea-Unresponsive KCNJ11-Related Diabetes.
Academic Article Pancreatic Histopathology of Human Monogenic Diabetes Due to Causal Variants in KCNJ11, HNF1A, GATA6, and LMNA.
Academic Article Developmental defects and impaired network excitability in a cerebral organoid model of KCNJ11 p.V59M-related neonatal diabetes.
Academic Article A loss-of-function mutation in KCNJ11 causing sulfonylurea-sensitive diabetes in early adult life.
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  • Potassium Channels Inwardly Rectifying