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Frances M. Ashcroft
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Activating mutations in the gene encoding Kir6.2 alter fetal and postnatal growth and also cause neonatal diabetes
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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
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K-ATP channels promote the differential degeneration of dopaminergic midbrain neurons
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Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes
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beta-cell death and mass in syngeneically transplanted islets exposed to short- and long-term hyperglycemia
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