New therapeutic prospects for the glycosphingolipid lysosomal storage diseases

Biochemical Pharmacology

Volumn 56, Issue 4, 1998, Pages 421-430

  Platt, F M ^a   Butters, T D ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Glycosphingolipids; Imino sugars; Lysosomal storage diseases; N butyldeoxynojirimycin; Substrate deprivation; Tay Sachs disease

Indexed keywords

ALPHA GALACTOSIDASE; ALPHA LEVO FUCOSIDASE; AMINOSUGAR; ARYLSULFATASE; BETA GALACTOSIDASE; BETA N ACETYLHEXOSAMINIDASE; ENZYME INHIBITOR; GLUCOSIDASE; GLYCOSPHINGOLIPID; MIGLUSTAT;

ANIMAL CELL; BONE MARROW TRANSPLANTATION; DRUG METABOLISM; ENZYME ASSAY; ENZYME DEFICIENCY; ENZYME REPLACEMENT; GAUCHER DISEASE; GENE MUTATION; GENE THERAPY; GENOTYPE; HUMAN; IN VITRO STUDY; LYSOSOME STORAGE DISEASE; MACROPHAGE; MODEL; MOUSE; NONHUMAN; PRIORITY JOURNAL; REVIEW; TAY SACHS DISEASE;

EID: 0031714682     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-2952(98)00115-4     Document Type: Note

References (50)