Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras.

Ítems similars

• Constitutive activation of fibroblast growth factor receptor 3 by the transmembrane domain point mutation found in achondroplasia.
  per: Webster, M K, et al.
  Publicat: (1996)
• Activating mutations in the extracellular domain of the fibroblast growth factor receptor 2 function by disruption of the disulfide bond in the third immunoglobulin-like domain
  per: Robertson, Scott C., et al.
  Publicat: (1998)
• FGFR2 mutation in a Chinese family with unusual Crouzon syndrome
  per: Li, Zi-Li, et al.
  Publicat: (2016)
• Medical genetics: advances in brief: Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
  per: Ravine, D
  Publicat: (1994)
• Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome
  per: Glaser, Rivka L., et al.
  Publicat: (2000)