Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes.

Benzer Materyaller

• Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects.
  Yazar:: Shimomura, K, ve diğerleri
  Baskı/Yayın Bilgisi: (2006)
• Functional effects of mutations at F35 in the NH2-terminus of Kir6.2 (KCNJ11), causing neonatal diabetes, and response to sulfonylurea therapy.
  Yazar:: Proks, P, ve diğerleri
  Baskı/Yayın Bilgisi: (2006)
• An in-frame deletion in Kir6.2 (KCNJ11) causing neonatal diabetes reveals a site of interaction between Kir6.2 and SUR1.
  Yazar:: Craig, T, ve diğerleri
  Baskı/Yayın Bilgisi: (2009)
• The first clinical case of a mutation at residue K185 of Kir6.2 (KCNJ11): a major ATP-binding residue.
  Yazar:: Shimomura, K, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Functional analysis of two Kir6.2 (KCNJ11) mutations, K170T and E322K, causing neonatal diabetes.
  Yazar:: Tarasov, A, ve diğerleri
  Baskı/Yayın Bilgisi: (2007)