Clinical and Molecular Characterization of a Novel Selenocysteine Insertion Sequence-Binding Protein 2 (SBP2) Gene Mutation (R128X)

Những quyển sách tương tự

• The Syndrome of Inherited Partial SBP2 Deficiency in Humans
  Bằng: Dumitrescu, Alexandra M., et al.
  Được phát hành: (2010)
• Selenocysteine insertion sequence binding protein 2 (Sbp2) in the sex-specific regulation of selenoprotein gene expression in mouse pancreatic islets
  Bằng: Chellan, B., et al.
  Được phát hành: (2020)
• A Novel Homozygous Selenocysteine Insertion Sequence Binding Protein 2 (SECISBP2, SBP2) Gene Mutation in a Turkish Boy
  Bằng: Çatli, Gönül, et al.
  Được phát hành: (2018)
• The Redox State of SECIS Binding Protein 2 Controls Its Localization and Selenocysteine Incorporation Function
  Bằng: Papp, Laura V., et al.
  Được phát hành: (2006)
• SECIS–SBP2 interactions dictate selenocysteine incorporation efficiency and selenoprotein hierarchy
  Bằng: Low, Susan C., et al.
  Được phát hành: (2000)