Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.

Παρόμοια τεκμήρια

• Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.
  ανά: Schram, A W, κ.ά.
  Έκδοση: (1986)
• Topography of very-long-chain-fatty-acid-activating activity in peroxisomes from rat liver.
  ανά: Lageweg, W, κ.ά.
  Έκδοση: (1991)
• Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
  ανά: Brul, S, κ.ά.
  Έκδοση: (1988)
• Peroxisomal Fatty Acid Uptake Mechanism in Saccharomyces cerevisiae
  ανά: van Roermund, Carlo W. T., κ.ά.
  Έκδοση: (2012)
• Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.
  ανά: Heikoop, J C, κ.ά.
  Έκδοση: (1990)