Alteration of nephrocystins and IFT-A proteins causes similar ciliary phenotypes leading to Nephronophthisis

Lignende værker

• Nephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargos
  af: Zhao, Chengtian, et al.
  Udgivet: (2011)
• Mainzer-Saldino syndrome is a ciliopathy caused by mutations in the IFT140 gene
  af: Perrault, I, et al.
  Udgivet: (2012)
• Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6
  af: Delous, Marion, et al.
  Udgivet: (2009)
• Renal Ciliopathies: Sorting Out Therapeutic Approaches for Nephronophthisis
  af: Stokman, Marijn F., et al.
  Udgivet: (2021)
• Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations
  af: Roepman, Ronald, et al.
  Udgivet: (2005)