Hepatic acid mucopolysaccharides in the mucopolysaccharidoses type I, II and 3.
暂无分享,去创建一个
[1] J. A. Cifonelli,et al. L-iduronidase in cultured human fibroblasts and liver. , 1971, Biochemical and biophysical research communications.
[2] E. Neufeld,et al. Inborn errors of mucopolysaccharide metabolism. , 1970, Science.
[3] M. Haust,et al. The mucopolysaccharidoses types I, II, and 3: urinary findings in 23 cases. , 1970, Clinical biochemistry.
[4] V. Feleki,et al. Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3. , 1970, Clinical biochemistry.
[5] R. Matalon,et al. The Hurler and Hunter syndromes. , 1969, The American journal of medicine.
[6] R. Matalon,et al. Acid mucopolysaccharides in cultured human fibroblasts. , 1969, Lancet.
[7] N. Ferrante,et al. The glycosaminoglycans of human term placenta , 1969 .
[8] N. Aronson,et al. Catabolism of mucopolysaccharides by rat liver lysosomes in vivo. , 1968, The Journal of biological chemistry.
[9] R. Matalon,et al. The structure of acid mucopolysaccharides produced by Hurler fibroblasts in tissue culture. , 1968, Proceedings of the National Academy of Sciences of the United States of America.
[10] L. Fransson. Structure of dermatan sulfate. 3. The hybrid structure of dermatan sulfate from umbilical cord. , 1968, The Journal of biological chemistry.
[11] J. A. Cifonelli,et al. Structural studies on heparitin sulfate of normal and Hurler tissues. , 1967, The Journal of biological chemistry.
[12] L. Fransson,et al. Structure of dermatan sulfate. II. Characterization of products obtained by hyaluronidase digestion of dermatan sulfate. , 1967, The Journal of biological chemistry.
[13] L. Fransson,et al. Structure of dermatan sulfate. I. Degradation by testicular hyaluronidase. , 1967, The Journal of biological chemistry.
[14] E. Balazs,et al. Determination of the hexosamine content of macro-molecules with manual and automated techniques using the p-dimethylaminobenzaldehyde reaction , 1966 .
[15] R. Matalon,et al. Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture. , 1966, Proceedings of the National Academy of Sciences of the United States of America.
[16] V. McKusick,et al. THE GENETIC MUCOPOLYSACCHARIDOSES , 1965, Medicine.
[17] H. Hers. INBORN LYSOSOMAL DISEASES. , 1965, Gastroenterology.
[18] T. Nikkari,et al. Determination of glucosamine and galactosamine by gas chromatography. , 1965, Journal of chromatography.
[19] R. Good,et al. Mental retardation associated with acid mucopolysacchariduria (heparitin sulfate type) , 1963 .
[20] T BITTER,et al. A modified uronic acid carbazole reaction. , 1962, Analytical biochemistry.
[21] H. Flood,et al. A Modification for the Determination of Sulphate in Mucopolysaccharides by the Benzidine Method. , 1962 .
[22] K. Meyer,et al. Hurler's syndrome. , 1961, Arthritis and rheumatism.
[23] S. Schiller,et al. A method for the separation of acid mucopolysaccharides: its application to the isolation of heparin from the skin of rats. , 1961, The Journal of biological chemistry.
[24] A. Linker,et al. Sulfated Mucopolysaccharides of Urine and Organs in Gargoylism (Hurler's Syndrome) II. Additional Studies.∗ , 1959 .
[25] A. Linker,et al. Excretion of Sulfated Mucopolysaccharides in Gargoylism. (Hurler's Syndrome)∗ , 1958, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.
[26] Z. Dische,et al. A new specific color reaction of hexuronic acids. , 1947, The Journal of biological chemistry.
[27] Brown Ah. Determination of pentose in the presence of large quantities of glucose. , 1946 .