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Merck

[The use of genetic angiogenesis inductors in surgical treatment of chronic lower limb ischemia].

Khirurgiia (2013-03-19)
A V Gavrilenko, D A Voronov, N P Bochkov
RESUMO

The efficacy and safety of gene-engineering recombinant constructions with endothelial growth factor gene and angiogenin for the treatment of the chronic lower limb ischemia were studied. 134 patients were included in prospective controlled study. The main group, who received both traditional treatment and genetic therapy, consisted of 74 patients. The rest 60 patients were included into the control group. Of 74 patients from the main group, genetic therapy was used together with conservative means in 39 patients and with reconstructive vascular operations in 35 patients. The gene-engineering angiogenesis stimulation therapy proved to be effective and safe. The combination of angiogenesis genetic stimulation with reconstructive vascular surgery demonstrated significantly better results, then monotherapy.

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Ribonuclease A, Type I-A, powder, ≥60% RNase A basis (SDS-PAGE), ≥50 Kunitz units/mg protein
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Ribonuclease A, for molecular biology, ≥70 Kunitz units/mg protein, lyophilized
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Ribonuclease A, Type III-A, ≥85% RNase A basis (SDS-PAGE), 85-140 Kunitz units/mg protein
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Ribonuclease A, (Solution of 50% glycerol, 10mM Tris-HCL pH 8.0)
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Ribonuclease A, Type I-AS, 50-100 Kunitz units/mg protein
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Ribonuclease A, Type XII-A, ≥90% (SDS-PAGE), 75-125 Kunitz units/mg protein
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Ribonuclease A, Type II-A, ≥60% (SDS-PAGE), >= 60 Kunitz units/mg protein
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Ribonuclease B from bovine pancreas, BioReagent, ≥50 Kunitz units/mg protein, ≥80% (SDS-PAGE)
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Ribonuclease A, Type X-A, ≥90% (SDS-PAGE), ≥70 Kunitz units/mg protein
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Ribonuclease A-agarose, ammonium sulfate suspension, 400-1,000 units/g agarose (One ml gel will yield 12-30 units)