A Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense Mutation

Lignende værker

• A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation
  af: Ashraf, Hassan, et al.
  Udgivet: (2014)
• Crystallization and preliminary X-ray analysis of the NKX2.5 homeodomain in complex with DNA
  af: Genis, Caroli, et al.
  Udgivet: (2008)
• Crystal Structure of the Human NKX2.5 Homeodomain in Complex with DNA Target
  af: Pradhan, Lagnajeet, et al.
  Udgivet: (2012)
• Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein
  af: Kasahara, Hideko, et al.
  Udgivet: (2001)
• Identification of the In Vivo Casein Kinase II Phosphorylation Site within the Homeodomain of the Cardiac Tisue-Specifying Homeobox Gene Product Csx/Nkx2.5
  af: Kasahara, Hideko, et al.
  Udgivet: (1999)