Peroxisomal organization in normal and cerebrohepatorenal (Zellweger) syndrome fibroblasts.

Lignende værker

• Multiple Peroxisomal Enzymatic Deficiency Disorders: A Comparative Biochemical and Morphologic Study of Zellweger Cerebrohepatorenal Syndrome and Neonatal Adrenoleukodystrophy
  af: Vamecq, Joseph, et al.
  Udgivet: (1986)
• Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
  af: Brul, S, et al.
  Udgivet: (1988)
• Metabolism of saturated and polyunsaturated fatty acids by normal and Zellweger syndrome skin fibroblasts.
  af: Street, J M, et al.
  Udgivet: (1989)
• Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.
  af: Schram, A W, et al.
  Udgivet: (1986)
• In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid.
  af: Kase, B F, et al.
  Udgivet: (1985)