Peroxisomal multifunctional protein-2: The enzyme, the patients and the knockout mouse model

This publication has 153 references indexed in Scilit:

• Response of SCP-2L Domain of Human MFE-2 to Ligand Removal: Binding Site Closure and Burial of Peroxisomal Targeting Signal
  Journal of Molecular Biology, 2002
• D-bifunctional protein deficiency with fetal ascites, polyhydramnios, and contractures of hands and toes
  The Journal of Pediatrics, 2001
• Crystal structure of the liganded SCP-2-like domain of human peroxisomal multifunctional enzyme type 2 at 1.75 Å resolution 1 1Edited by R. Huber
  Journal of Molecular Biology, 2001
• Characterization of the Promoter Region of the Human Peroxisomal Multifunctional Enzyme Type 2 Gene
  Biochemical and Biophysical Research Communications, 2001
• Complementation Analysis of Fibroblasts from Peroxisomal Fatty Acid Oxidation Deficient Patients Shows High Frequency of Bifunctional Enzyme Deficiency Plus Intragenic Complementation: Unequivocal Evidence for Differential Defects in the Same Enzyme Protein
  Biochemical and Biophysical Research Communications, 1997
• Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case
  Brain and Development, 1997
• Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups
  The Journal of Pediatrics, 1995
• A case of pseudo-Zellweger syndrome with a possible bifunctional enzyme deficiency but detectable enzyme protein
  Brain and Development, 1993
• Complementation Analysis of Patients with Intact Peroxisomes and Impaired Peroxisomal β-Oxidation
  Biochemical Medicine and Metabolic Biology, 1993
• Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activities
  The Journal of Pediatrics, 1986