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Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: correlation with phenotype and genotype

  • Published:2002-08 Issue:4 Volume:76 Page:262-270
  • ISSN:1096-7192
  • Container-title:Molecular Genetics and Metabolism
  • language:en
  • Short-container-title:Molecular Genetics and Metabolism

Author:

Orvisky Eduard,Park Joseph K,LaMarca Mary E,Ginns Edward I,Martin Brian M,Tayebi Nahid,Sidransky Ellen

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference37 articles.

1. Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestation;Orvisky;Pediatr. Res.,2000

2. Glucosylceramide and related compounds in normal tissues and in Gaucher disease;Suzuki,1989

3. Glucosylceramide lipidoses: Gaucher disease;Barranger,1989

4. Pathologic gene expression in Gaucher disease: up-regulation of cysteine proteinases including osteoclastic cathepsin K;Moran;Blood,2000

5. Twenty five years of the “psychosine hypothesis”: a personal perspective of its history and present status;Suzuki;Neurochem. Res.,1998

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