The Meckel-Gruber Syndrome protein TMEM67 (meckelin) regulates basal body planar polarization and non-canonical Wnt signalling via Wnt5a and ROR2

Lignende værker

• The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway
  af: Abdelhamed, Zakia A., et al.
  Udgivet: (2015)
• The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity
  af: Leightner, Amanda C., et al.
  Udgivet: (2013)
• The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5
  af: Abdelhamed, Zakia A., et al.
  Udgivet: (2019)
• Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel–Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects
  af: Abdelhamed, Zakia A., et al.
  Udgivet: (2013)
• Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation
  af: Shim, Joon W., et al.
  Udgivet: (2019)