Enhanced proteolytic degradation of normal β-galactosidase in the lysosomal storage disease with combined β-galactosidase and neuraminidase deficiency
- 21 April 1982
- journal article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology
- Vol. 703 (1), 69-76
- https://doi.org/10.1016/0167-4838(82)90012-7
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Atypical expression of ß-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalitiesClinical Genetics, 2008
- Correction of combined β-galactosidase/neuraminidase deficiency in human fibroblastsBiochemical and Biophysical Research Communications, 1981
- Genetic heterogeneity in human neuraminidase deficiencyNature, 1980
- Prenatal diagnosis of sialidosis with combined neuraminidase and ø‐galactosidase deficiencyClinical Genetics, 1979
- Mucolipidosis I — A sialidosisAmerican Journal of Medical Genetics, 1977
- The role of glycosidically bound mannose in the assimilation of β-galactosidase by generalized gangliosidosis fibroblastsBiochemical and Biophysical Research Communications, 1976
- Increased levels of sialic acid associated with a sialidase deficiency in I-cell disease (mucolipidosis II) fibroblastsBiochemical and Biophysical Research Communications, 1976
- Active-site-directed irreversible inhibition of E. coliβ-galactosidase by the ‘hot’ carbonium ion precursor, β-D-galactopyranosylmethyl-p-nitrophenyltriazeneJournal of the Chemical Society, Chemical Communications, 1976
- Genetic heterogeneity in GM1-gangliosidosisNature, 1975
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970