Substrate specificities of the two genetically distinct human brain β-galactosidases

Author:

Tanaka Harumi,Suzuki Kunihiko

Publisher

Elsevier BV

Subject

Developmental Biology,Clinical Neurology,Molecular Biology,General Neuroscience

Reference27 articles.

1. Cerebroside galactosidase: a method for determination and a comparison with other lysosomal enzymes in developing rat brain;Bowen;J. Neurochem.,1969

2. Purification of GM1-ganglioside and ceramide lactoside β-galactosidase from rabbit brain;Callahan;Biochim. biophys. Acta (Amst.),1975

3. Lactosylceramidosis: catabolic enzyme defect of glycosphingolipid metabolism;Dawson;Science,1970

4. Gal, A. E., Brady, R. O., Pentchev, P. G., Furbish, F. S., Suzuki, K., Tanaka, H. and Schneider, E. L., A pracitcal chromogenic procedure for the diagnosis of Krabbe's disease, Submitted for publication.

5. Enzymatic hydrolysis of sphingolipids. V. hydrolysis of monosialoganglioside and hexosylceramides by rat brain β-galactosidase;Gatt;Biochim. biophys. Acta (Amst.),1967

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