Corneal Opacification in Infancy [PDF]
, 1972 The purpose of this paper is to present a systematic classification of the more important conditions that can manifest as corneal opacification in early infancy and to state its differential diagnostic ...
Ching, Florencio C.
core +1 more source
Heparanase deglycanation of syndecan-1 is required for binding of the epithelial-restricted prosecretory mitogen lacritin [PDF]
, 2006 Cell surface heparan sulfate (HS) proteoglycans are carbohydrate-rich regulators of cell migratory, mitogenic, secretory, and inflammatory activity that bind and present soluble heparin-binding growth factors (e.g., fibroblast growth factor, Wnt, Hh ...
Beck, Shannon L. +8 more
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Recommendations on clinical trial design for treatment of Mucopolysaccharidosis Type III [PDF]
, 2017 Background Mucopolysaccharidosis type III is a progressive, neurodegenerative lysosomal storage disorder for which there is currently no effective therapy. Though numerous potential therapies are in development, there are several challenges to conducting
Bigger, Brian +12 more
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Chondroitin Sulfate Proteoglycans Are Associated with the Lesions of Alzheimer\u27s Disease [PDF]
, 1993 Chondroitin sulfate proteoglycans (CSPG) are extracellular matrix proteins inhibitory to neurite outgrowth in vitro and correlated with decreased neurite outgrowth after CNS injury.
Canning, David R. +3 more
core
European Journal of Biochemistry, 1989 The hydrophobic cell-surface proteoglycans of mouse mammary epithelial cells were purified by gel filtration, ion-exchange chromatography, and liposome incorporation. The size of the proteoglycans appeared to be directly proportional to the size of their
G. David, H. van den Berghe
semanticscholar +1 more source
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1編 正常小児の尿中酸性ムコ多糖類の排泄パターン [PDF]
, 1972 Qualitative and quantitative determination of urinary acid mucopolysaccharide (AMPS) have been studied by several methods including ECTEOLA cellulose column chromatography, Dowex I-X 2 column chromatography, electrophoresis, and enzymatic digestion with
南 良二
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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
semanticscholar +1 more source
Structure of glassy lithium sulfate films sputtered in nitrogen (LISON): Insight from Raman spectroscopy and ab initio calculations [PDF]
, 2007 Raman spectra of thin solid electrolyte films obtained by sputtering a lithium sulfate target in nitrogen plasma are measured and compared to ab initio electronic structure calculations for clusters composed of 28 atoms. Agreement between measured and calculated spectra is obtained when oxygen atoms are replaced by nitrogen atoms and when the nitrogen ...
arxiv +1 more source
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
core
Role of heparan sulfate as a tissue-specific regulator of FGF-4 and FGF receptor recognition [PDF]
, 2001 FGF signaling uses receptor tyrosine kinases that form high-affinity complexes with FGFs and heparan sulfate (HS) proteoglycans at the cell surface.
Allen, Benjamin L. +2 more
core +3 more sources