Results 21 to 30 of about 389 (140)

Chondroitin Sulfate Proteoglycans Are Associated with the Lesions of Alzheimer\u27s Disease [PDF]

open access: yes, 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  

Identification of genetic variants associated with a wide spectrum of phenotypes clinically diagnosed as Sanfilippo and Morquio syndromes using whole genome sequencing [PDF]

open access: yes, 2023
Mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders (LSDs). MPSs are caused by excessive accumulation of mucopolysaccharides due to missing or deficiency of enzymes required for the degradation of specific macromolecules. MPS I-IV, MPS
Anne C. B. Thuesen   +13 more
core   +1 more source

Chondroitin sulphate mediated fusion of brain: neural folds in rat embryons [PDF]

open access: yes, 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
core   +2 more sources

A Minireview Of Cellulose Nanocrystals And Its Potential Integration As Co-product In Bioethanol Production [PDF]

open access: yes, 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  

Some side effects of heparin, heparinoids, and their antagonists [PDF]

open access: yes, 1966
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/117045/1/cpt196673379 ...
Coon, William W., Willis, Park W.
core   +1 more source

Recommendations on clinical trial design for treatment of Mucopolysaccharidosis Type III [PDF]

open access: yes, 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
core   +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]

open access: yes, 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
core   +1 more source

Profiling of pathway-specific changes in gene expression following growth of human cancer cell lines transplanted into mice [PDF]

open access: yes, 2003
Background Tumor cells cultured in vitro are widely used to investigate the molecular biology of cancers and to evaluate responses to drugs and other agents.
Brichory, Franck M   +7 more
core   +2 more sources

An investigation of total and 35S-labeled mucopolysaccharides in intestinal wall kidney of cattle, sheep and swine [PDF]

open access: yes, 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
core   +1 more source

Heparinases: cloning, expression and structural requirements for activity [PDF]

open access: yes, 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
core   +1 more source

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