scholarly article | Q13442814 |
P356 | DOI | 10.1016/0006-291X(65)90413-4 |
P698 | PubMed publication ID | 4222532 |
P2093 | author name string | A Dorfman | |
J Knecht | |||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Hurler syndrome | Q25379699 |
P304 | page(s) | 509-515 | |
P577 | publication date | 1965-12-01 | |
P1433 | published in | Biochemical and Biophysical Research Communications | Q864228 |
P1476 | title | Structure of heparitin sulfate in tissues of the Hurler syndrome | |
P478 | volume | 21 |
Q68452905 | Biochemical definition of the mucopolysaccharidoses |
Q54433717 | Characterization of urinary peptoglycans in Morquio's disease. |
Q39894675 | Differentiation of connective tissues. |
Q72223143 | Epimerization of D-glucuronic acid to L-iduronic acid by deamination of heparins |
Q42154353 | Functional abnormalities of heparan sulfate in mucopolysaccharidosis-I are associated with defective biologic activity of FGF-2 on human multipotent progenitor cells |
Q36384007 | Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture |
Q93800237 | Increased urinary excretion of chondroitin sulfate A and C in Hunter's syndrome |
Q39735866 | Molecular size difference of urinary heparan sulfates from normal individuals and genetic mucopoly-saccharidoses |
Q35920065 | Ocular correlates of inborn metabolic defects |
Q72281633 | Stability of the biological activities of heparins to mild acid treatments |
Q34272120 | Study of the Hurler syndrome using cell culture: definition of the biochemical phenotype and the effects of ascorbic acid on the mutant cell |
Q33562639 | The structure of acid mucopolysaccharides produced by Hurler fibroblasts in tissue culture |
Q36540186 | Urinary excretion of glycosaminoglycans in the various forms of gargoylism |