A lysosomal storage disorder in mice: A model of Niemann‐Pick disease
- 1 December 1982
- journal article
- conference paper
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 5 (4), 239-240
- https://doi.org/10.1007/bf02179154
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Sphingomyelinosis, a new mutation in the mouseJournal of Heredity, 1982
- A Practical Chromogenic Procedure for the Detection of Homozygotes and Heterozygous Carriers of Niemann-Pick DiseaseNew England Journal of Medicine, 1975
- Lipid storage disease in a Siamese cat.1970
- The Metabolism of SphingomyelinPublished by Elsevier ,1966
- METABOLISM OF SPHINGOMYELIN .I. PURIFICATION AND PROPERTIES OF A SPHINGOMYELIN-CLEAVING ENZYME FROM RAT LIVER TISSUE1966
- Foam-cell Reticulosis of Mice: An Inherited Condition Resembling Gaucher's and Niemann-Pick DiseasesJournal of Medical Genetics, 1965
- A SIMPLE METHOD FOR THE ISOLATION AND PURIFICATION OF TOTAL LIPIDES FROM ANIMAL TISSUESJournal of Biological Chemistry, 1957
- Simple Rapid Microtechnic for Serum Total CholesterolAmerican Journal of Clinical Pathology, 1957
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951