|1.||Szymanska, Paulina: 1 article (09/2009)|
|2.||Kusio, Monika: 1 article (09/2009)|
|3.||Popowska, Magdalena: 1 article (09/2009)|
|4.||Markiewicz, Zdzislaw: 1 article (09/2009)|
|5.||Ruzal, Sandra M: 1 article (03/2009)|
|6.||Sanchez-Rivas, Carmen: 1 article (03/2009)|
|7.||Palomino, María Mercedes: 1 article (03/2009)|
|8.||Eisenmenger, Michael: 1 article (08/2006)|
|9.||Gilliland, Stanley E: 1 article (08/2006)|
|10.||Dunford, Nurhan Turgut: 1 article (08/2006)|
03/01/1987 - "This may also partially explain how mutanolysin treatment alleviates cell wall-induced arthritis in the rat."
02/01/1986 - "Small fragments, derived from mutanolysin digestion, caused both an acute edematous reaction and transient arthritis. "
11/01/1984 - "Treatment of experimental erosive arthritis in rats by injection of the muralytic enzyme mutanolysin."
03/01/1987 - "The treatment of PG-APS-injected rats with a single intravenous injection of 0.4 mg of mutanolysin prevents the development of chronic arthritis, even when administration of the enzyme is delayed until severe acute arthritis has developed. "
06/01/1995 - "Mutanolysin, an enzyme which degrades peptidoglycan-polysaccharide from group A streptococci, exacerbated arthritis for the first 6 days but then diminished joint swelling from 12 to 21 days after surgery (P < 0.001). "
11/01/1984 - "In addition, rats treated with mutanolysin immediately after receiving an intraperitoneal injection of PG-APS developed a transient limb edema similar to that seen in rats after the injection of PG-APS digested to a small fragment size in vitro with mutanolysin. "
12/01/1982 - "Low-molecular-weight PG-PS ( congruent with30,000) derived from the mutanolysin digests and the PG-PS fragments isolated from phage-associated lysin digests also induced edema; however, a higher dose was required to elicit the same response as that produced by high-molecular-weight PG-PS fragments. "
03/01/2009 - "Whole cells or purified peptidoglycan from WT cultures grown in high salt medium showed increased autolysis and susceptibility to mutanolysin. "
09/01/2009 - "However, the pgdA mutant was more prone to autolysis induced by such agents as Triton X-100 and EDTA, and is more susceptible to the cationic antimicrobial peptides (CAMP) lysozyme and mutanolysin, using either peptidoglycan muramidases or autolysis-inducing agents. "
|4.||Antimicrobial Cationic Peptides
|5.||Octoxynol (Triton X 100)
|7.||Edetic Acid (EDTA)
|8.||streptococcal polysaccharide group A