Mice with a conditional deletion of Talpid3 (KIAA0586) – a model for Joubert syndrome

Lignende værker

• KIAA0586 is mutated in Joubert syndrome
  af: Bachmann-Gagescu, Ruxandra, et al.
  Udgivet: (2015)
• TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)
  af: Stephen, Louise A, et al.
  Udgivet: (2015)
• Mutations in human homologue of chicken talpid3 gene (KIAA0586) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes
  af: Malicdan, May Christine V, et al.
  Udgivet: (2015)
• Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
  af: Roosing, Susanne, et al.
  Udgivet: (2015)
• The Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formation
  af: Yin, Yili, et al.
  Udgivet: (2009)