Lactosyl Ceramidosis: Catabolic Enzyme Defect of Glycosphingolipid Metabolism-Reference-Cited by-同舟云学术

Lactosyl Ceramidosis: Catabolic Enzyme Defect of Glycosphingolipid Metabolism

Published:1970-10-30 Issue:3957 Volume:170 Page:556-558
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Dawson Glyn¹,Stein Arthur O.¹

Affiliation:

1. Departments of Pediatrics and Biochemistry, Joseph P. Kennedy, Jr., Mental Retardation Research Center, University of Chicago, Chicago, Illinois 60637

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference26 articles.

1. BRADY, R.O., METABOLISM OF GLUCOCEREBROSIDES .2. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHERS DISEASE, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 18: 221 (1965).

2. BRADY, R.O., ENZYMATIC DEFECT IN FABRYS DISEASE - CERAMIDETRIHEXOSIDASE DEFICIENCY, NEW ENGLAND JOURNAL OF MEDICINE 276: 1163 (1967).

3. Dawson G. in preparation.

4. EVANS, J.E., STRUCTURE OF BRAIN DIHEXOSYLCERAMIDE IN GLOBOID CELL LEUKODYSTROPHY, JOURNAL OF NEUROCHEMISTRY 16: 1393 (1969).

5. FOLCH, J, A SIMPLE METHOD FOR THE ISOLATION AND PURIFICATION OF TOTAL LIPIDES FROM ANIMAL TISSUES, JOURNAL OF BIOLOGICAL CHEMISTRY 226: 497 (1957).

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