Molecular Cloning and Characterization of a Full-length Complementary DNA Encoding Human Acid Ceramidase
Open Access
- 1 December 1996
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 271 (51) , 33110-33115
- https://doi.org/10.1074/jbc.271.51.33110
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Neurodegenerative course in ceramidase deficiency (Farber disease) correlates with the residual lysosomal ceramide turnover in cultured living patient cellsJournal of the Neurological Sciences, 1995
- Purification, Characterization, and Biosynthesis of Human Acid CeramidaseJournal of Biological Chemistry, 1995
- Ceramide: an intracellular signal for apoptosisTrends in Biochemical Sciences, 1995
- Biosynthesis of sphingolipids: Dihydroceramide and not sphinganine is desaturated by cultured cellsBiochemical and Biophysical Research Communications, 1992
- Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDaAnalytical Biochemistry, 1987
- Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNANature, 1987
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979
- FARBER'S DISEASE AS A CERAMIDOSIS: CLINICAL, RADIOLOGICAL AND BIOCHEMICAL ASPECTSActa Paediatrica, 1978
- DNA sequencing with chain-terminating inhibitorsProceedings of the National Academy of Sciences, 1977
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970