Chondroitin sulphate mediated fusion of brain: neural folds in rat embryons [PDF]
, 2008 Producción CientíficaPrevious studies have demonstrated that during neural fold fusion in different species, an apical extracellular material rich in glycoconjugates is involved.
Alonso Revuelta, María Isabel +8 more
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The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.
Proceedings of the National Academy of Sciences of the United States of America, 1968 Hurler's syndrome is a genetically transmitted disorder of mucopolysaccharide metabolism, distinguished chemically by excessive intracellular accumulation and urinary excretion of chondroitin sulfate B and heparitin monosulfate, and clinically, by mental
J. Fratantoni, C. W. Hall, E. Neufeld
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A Minireview Of Cellulose Nanocrystals And Its Potential Integration As Co-product In Bioethanol Production [PDF]
, 2015 Cellulose nanocrystals appeared as important bio-based products and the collected information in term of production, characterization and application suggest that this nanomaterial could be easily extrapolated to bioethanol production.
Baeza J. +4 more
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Heparinases: cloning, expression and structural requirements for activity [PDF]
, 2011 Structural characteristics of heparin (Hep) and heparan sulfate (HS) have been determined using enzymes from Flavobacterium heparinum, a non-pathogenic soil bacterium.
Córdula, Carolina Ribeiro
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Some side effects of heparin, heparinoids, and their antagonists [PDF]
, 1966 Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/117045/1/cpt196673379 ...
Coon, William W., Willis, Park W.
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An investigation of total and 35S-labeled mucopolysaccharides in intestinal wall kidney of cattle, sheep and swine [PDF]
, 1967 Mucopolysaccharides (MPS) occur in the ground substance of connective tissue and have been isolated and identified from many diverse types of tissue.
Berry, Robert Kerns
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小児における尿中酸性ムコ多糖類の排泄パターンに関する研究 第II編 遺伝性酸性ムコ多糖代謝異常症*5例の尿中酸性ムコ多糖類の排泄パターン [PDF]
, 1972 Since Brante suggested that Hurler syndrome was mucopolysaccharidosis, urinary acid mucopolysaccharides (AMPS) have been of interest to investigators.
南 良二
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Characterization of a Mucopolysaccharidosis Type I and GalNAc Transferase deficiency double knockout mouse [PDF]
, 2018 The mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases (LSDs) which are characterized by the aberrant primary storage of glycosaminoglycans (GAGs) in lysosomes of multiple organ and tissue systems.
Gera, Karan
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Studies on the Urinary Cetylpyridinium Chloride-Precipitates and Non-Cetylpyridinium Chloride-Precipitates in Normal Children and the Patients with Mucopolys-accharidoses, Mucolipidoses and Lipidoses. ―Hyperglyeopeptiduria in Mucolipidoses― [PDF]
, 1974 Urinary cetylPyridinium chloride(CPC)-precipitates and non-CPC-precipitates in normal male children and seven patients with a new type of mucolipidosis, GM1-gangliosidosis type 1, I-cell disease, MPS I (Hurler type), MPS IV (Morquio type), Gauche's ...
千葉, 学道
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Regional distribution of acid mucopolysaccharides in the kidney.
Journal of Clinical Investigation, 1968 Kidneys from 20 dogs were dissected into cortical and medullary components and analysed for acid mucopolysaccharide content. Heparitin sulfate accounted for approximately 80% of cortical acid mucopolysaccharide, 10% was chondroitin sulfate B, and 10% was
C. Castor, J. A. Greene
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