Sialic acid storage diseases. A multiple lysosomal transport defect for acidic monosaccharides.

Lignende værker

• Defective glucuronic acid transport from lysosomes of infantile free sialic acid storage disease fibroblasts.
  af: Blom, H J, et al.
  Udgivet: (1990)
• Functional reconstitution of the lysosomal sialic acid carrier into proteoliposomes.
  af: Mancini, G M, et al.
  Udgivet: (1992)
• Defective lysosomal release of glycoprotein-derived sialic acid in fibroblasts from patients with sialic acid storage disease.
  af: Mendla, K, et al.
  Udgivet: (1988)
• Studies on the defect underlying the lysosomal storage of sialic acid in Salla disease. Lysosomal accumulation of sialic acid formed from N-acetyl-mannosamine or derived from low density lipoprotein in cultured mutant fibroblasts.
  af: Renlund, M, et al.
  Udgivet: (1986)
• Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15.
  af: Schleutker, J, et al.
  Udgivet: (1995)