Quantitative traits associated with the Type 2 diabetes susceptibility allele in Kir6.2.

Benzer Materyaller

• Molecular basis of Kir6.2 mutations causing neonatal diabetes and neonatal diabetes with neurological features
  Yazar:: Proks, P, ve diğerleri
  Baskı/Yayın Bilgisi: (2005)
• A gating mutation at the internal mouth of the Kir6.2 pore is associated with DEND syndrome.
  Yazar:: Proks, P, ve diğerleri
  Baskı/Yayın Bilgisi: (2005)
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  Yazar:: Proks, P, ve diğerleri
  Baskı/Yayın Bilgisi: (2004)
• Glimepiride block of Kir6.2/SUR1 Kir6.2/SUR2A and Kir6.2/SUR2A and Kir6.2/SUR2B K-ATP channels.
  Yazar:: Ashcroft, F, ve diğerleri
  Baskı/Yayın Bilgisi: (2001)
• 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.
  Yazar:: Flanagan, SE, ve diğerleri
  Baskı/Yayın Bilgisi: (2006)