Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley- Ruvalcaba syndrome without germline PTEN mutations

Antzeko izenburuak

• Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.
  nork: Longy, M, et al.
  Argitaratua: (1998)
• Germline TTN variants are enriched in PTEN-wildtype Bannayan–Riley–Ruvalcaba syndrome
  nork: Yehia, Lamis, et al.
  Argitaratua: (2017)
• Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations
  nork: Yehia, Lamis, et al.
  Argitaratua: (2018)
• Germline PTEN Promoter Mutations and Deletions in Cowden/Bannayan-Riley-Ruvalcaba Syndrome Result in Aberrant PTEN Protein and Dysregulation of the Phosphoinositol-3-Kinase/Akt Pathway
  nork: Zhou, Xiao-Ping, et al.
  Argitaratua: (2003)
• Distinct Expression Profiles for PTEN Transcript and Its Splice Variants in Cowden Syndrome and Bannayan-Riley-Ruvalcaba Syndrome
  nork: Sarquis, Marta S., et al.
  Argitaratua: (2006)