Glycosaminoglycan accumulation with partial deficiency of ?-glucuronidase in the C3H strain of mice
- 1 December 1978
- journal article
- research article
- Published by Springer Nature in Biochemical Genetics
- Vol. 16 (11-12) , 1079-1084
- https://doi.org/10.1007/bf00484528
Abstract
Young (60–80 days) mice of the low β-glucuronidase strain, C3H/HeJ, showed no differences in hepatic levels of glycosaminoglycans (GAGs) when compared to the randombred, “normal” Swiss-Webster mice of the same age. However, by 12 months of age hepatic GAG is nearly twice as high in C3H/HeJ mice as in Swiss-Webster mice. Studies of β-glucuronidase, β-galactosidase, and N-acetyl-β-glucosaminidase in four tissues of the two types of mice at the two ages revealed that glucuronidase was the only enzyme with lower activity in the C3H/HeJ strain.This publication has 12 references indexed in Scilit:
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