Results 251 to 260 of about 89,565 (294)
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Enzyme Replacement for Lysosomal Diseases

Annual Review of Medicine, 2006
Following the demonstration of the nature of the enzymatic defects in the sphingolipid storage disorders in the mid-1960s, consideration was directed to the development of therapy for patients with these conditions. High on the list of possibilities was enzyme supplementation or replacement.
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Inhibition of Lysosomal Enzymes by Dapsone

Archives of Dermatology, 1974
The possible inhibition of lysosomal enzymes by dapsone (diaminodiphenylsulfone) was studied. Experimentally induced hypervitaminosis A in rabbits results in loss of chondroitin sulfate from cartilage matrix through the release of lysosomal enzymes. In this study, thinning and decreased toluidine blue and Alcian blue staining of tracheal and articular
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Transport of Lysosomal Enzymes

2005
More than 50 acid hydrolases involved in the ordered lysosomal degradation of a variety of proteins, lipids, carbohydrates, and nucleic acids have been identified. The hydrolases are enclosed by a membrane containing a set of highly glycosylated lysosomal membrane proteins.
Stephan Storch, Thomas Braulke
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Biosynthesis of lysosomal enzymes

Trends in Biochemical Sciences, 1980
During their synthesis lysosomal enzymes are subjected to extensive processing, which involves both the protein and the sugar moieties of these molecules. The many modifications to the sugars appear to play a decisive role in sorting those molecules to be delivered into the lysosomes from those to be secreted.
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Lysosomal enzymes in invertebrate leucocytes

Journal of Cellular and Comparative Physiology, 1964
A, JANOFF, E, HAWRYLKO
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Lysosomal enzymes in amniotic fluid

Clinica Chimica Acta, 1972
J, Butterworth   +3 more
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LYSOSOMAL ENZYMES

1981
Earl H. Harrison, William E. Bowers
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Lysosomal Enzymes

1978
R. B. Zurier, K. Krakauer
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Lysosomal enzyme activities in phenylketonuria

Molecular Genetics and Metabolism, 2011
Francesco, Porta   +5 more
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