Caterina Berti

Summary

Affiliation: San Raffaele Scientific Institute
Country: Italy

Publications

  1. pmc Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules
    Caterina Berti
    Telethon Institute of Genetics and Medicine, 80131 Naples, Italy
    BMC Cell Biol 5:9. 2004
  2. ncbi X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum
    Francesca De Falco
    Telethon Institute of Genetics and Medicine, Naples, Italy
    Am J Med Genet A 120:222-8. 2003

Collaborators

  • Francesca De Falco
  • Germ├ín RodrIguez Criado
  • Sylvie Odent
  • Rosa Ferrentino
  • Silvia Cainarca
  • Harindar Jawanda
  • Robin Winter
  • Andrea Ballabio
  • Jan Liebelt
  • Amit Rastogi
  • Nick Dennis
  • David Chitayat
  • Brunella Franco
  • Olaf Rittinger
  • Germana Meroni
  • Grazia Andolfi

Detail Information

Publications2

  1. pmc Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules
    Caterina Berti
    Telethon Institute of Genetics and Medicine, 80131 Naples, Italy
    BMC Cell Biol 5:9. 2004
    ..Mid1 acts as an E3 ubiquitin ligase, regulating PP2A degradation on microtubules...
  2. ncbi X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum
    Francesca De Falco
    Telethon Institute of Genetics and Medicine, Naples, Italy
    Am J Med Genet A 120:222-8. 2003
    ..The low frequency of mutations in MID1 and the high variability of the phenotype suggest the involvement of other genes in the OS phenotype...