Detection of Hepatic Phenylalanine 4-Hydroxylase in Classical Phenylketonuria

Ítems similars

• Identification of hepatic nuclear factor 1 binding sites in the 5′ flanking region of the human phenylalanine hydroxylase gene: Implication of a dual function of phenylalanine hydroxylase stimulator in the phenylalanine hydroxylation system
  per: Lei, Xiang-Dong, et al.
  Publicat: (1998)
• Mutagenesis of the regulatory domain of phenylalanine hydroxylase
  per: Wang, Guo-An, et al.
  Publicat: (2001)
• The role of phenylalanine in structure–function relationships of phenylalanine hydroxylase revealed by radiation target analysis
  per: Davis, Michael D., et al.
  Publicat: (1997)
• Mutations of the phenylalanine hydroxylase gene in patients with phenylketonuria in Shanxi, China
  per: Zhou, Yong-An, et al.
  Publicat: (2012)
• Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations
  per: Erlandsen, Heidi, et al.
  Publicat: (2004)