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Abnormal lysosomal hydrolases excreted by cultured fibroblasts in I-cell disease (mucolipidosis II)

Published in: Biochemical and Biophysical Research Communications

Date of publication: December 1, 1975

Language: English

Main subject: cell biology, biochemistry, biophysics

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Cites articles 12

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Title

Authors

January 1, 1961

Studies on glucosaminidase. 4. The fluorimetric assay of N-acetyl-beta-glucosaminidase
September 1, 1965

The gel-filtration behaviour of proteins related to their molecular weights over a wide range
August 1, 1967

Mutant enzymatic and cytological phenotypes in cultured human fibroblasts
April 1, 1968

Glucose 6-phosphate dehydrogenase from human erythrocytes: Molecular weight determination by gel filtration
April 1, 1971

Electrophoretic characterization of glucose dehydrogenase, β-glucuronidase, and N-acetyl-β-glucosaminidase from placenta and gestational serum
November 1, 1972

A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomes
May 1, 1973

Analysis of N-acetyl- -D-glucosaminidase in mucolipidosis II (I-cell disease).
November 1, 1974

Studies on the pathogenetic mechanism of I-cell disease in cultured fibroblasts
January 1, 1974

Immunochemical characterization of human beta-D-N-acetyl hexosaminidase from normal individuals and patients with Tay-Sachs disease. I. Antigenic differences between hexosaminidase A and hexosaminidase B
January 1, 1974

Differences between the N-acetyl hexosaminidase isozymes in serum and tissues
November 1, 1974

Isozymes of human alpha-L-fucosidase detectable by starch gel electrophoresis
March 1, 1974

A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts

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