Results 281 to 290 of about 3,477,167 (351)
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Proteinase inhibitors in Ascarida
Parasitology Today, 1994Ascaris suum and A. lumbricoides are intestinal parasites that survive in a hostile hydrolytic environment They contain low-molecular-weight proteins that can inactivate most of the proteinases present in the worm's surroundings. Jeffrey Hawley, Mark Martzen and Robert Peanasky suggest that host specificity of these nematodes may be associated with the
J H, Hawley, M R, Martzen, R J, Peanasky
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British Medical Bulletin, 1995
The primary agents responsible for cartilage and bone destruction in joint diseases are active proteinases degrading collagen and proteoglycan. All four main classes of proteolytic enzymes are involved in either the normal turnover of connective tissue or its pathological destruction.
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The primary agents responsible for cartilage and bone destruction in joint diseases are active proteinases degrading collagen and proteoglycan. All four main classes of proteolytic enzymes are involved in either the normal turnover of connective tissue or its pathological destruction.
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Proteinases and Proteinase Inhibitors
1992The peritoneal cavity is well endowed with proteinases both in the parietal and viseral peritoneum as well as in the peritoneal fluid. Proteinases have a major role in activating and modulating the complement, coagulation, kinin, fibrinolytic, and extracellular matrix remodeling systems, and thus are critical components of the peritoneal response to ...
Gere S. diZerega, Kathleen E. Rodgers
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Proteinase and Proteinase Inhibitor Localization in the Human Placenta
International Journal of Gynecological Pathology, 1989Standard immunoperoxidase techniques were used to investigate the distribution of the intracellular proteinase cathepsin D, two serine proteinase inhibitors--alpha 1-antitrypsin (alpha 1-AT) and alpha 1-antichymotrypsin (alpha 1-AChy)--and plasma fibrin stabilizing factor XIII (FXIII) in paraffin-embedded tissues from early and late intrauterine ...
U, Earl +3 more
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Acrosomal Proteinase and Proteinase Inhibitor of Human Spermatozoa
Science, 1972The acrosomal proteinase of human spermatozoa was characterized and differs from other human proteinases. The enzyme has optimal activity at p H 8.0, is inactive below p H 5.0 or above p H 10.5, requires calcium for maximum activity, hydrolyzes fibrinogen, gelatin, and
L J, Zaneveld +2 more
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Proteinase inhibitors as antileishmanial agents
Transactions of the Royal Society of Tropical Medicine and Hygiene, 1982Leishmania mexicana mexicana amastigote proteinase activity was largely inhibited by low concentrations of leupeptin, antipain and two epoxysuccinates, compounds known to affect cysteine proteinases. Of these inhibitors, only two had leishmanicidal activity. trans-Dicyclohexylepoxysuccinate at 10 microgram/ml inhibited the in vitro transformation of L.
G H, Coombs, D T, Hart, J, Capaldo
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Serine proteinase inhibitors in the Compositae: distribution, polymorphism and properties
Alexander V Konarev, I N Anisimova
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?1-Proteinase inhibitor and mucus proteinase inhibitor in human lung emphysema
The Clinical Investigator, 1992The role of the antiproteases alpha 1-proteinase inhibitor (alpha 1PI) and mucus proteinase inhibitor (MPI) in human lung emphysema was investigated by measuring their amount and functional activity against trypsin, leukocyte elastase, and pancreatic elastase in the bronchoalveolar lavage fluid (BALF).
G, Trefz +4 more
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Proteinase 3 phosphonic inhibitors
Biochimie, 2019Neutrophils are one of the most important military services of the armed forces of the immune system, a crucial line of defense against bacterial or fungal onslaughts. One of their mechanisms of action relies on the production of serine proteases.
Renata Grzywa +3 more
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Plant Serine Proteinase Inhibitors
Protein & Peptide Letters, 2005Evidence that establishes the mechanism of the classes of plant proteinase inhibitors (PIs) is evaluated. Of the eight classes of PIs, six are unique to plants. Except for plant serpins, there is evidence that PIs from all other classes form tight binding complexes with their target proteinases, and that they follow the standard mechanism of inhibition.
John, Christeller, William, Laing
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