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Biochimica Et Biophysica Acta|April 7, 1975
Studies on the mechanism of metabolic stimulation in polymorphonuclear leucocytes during phagocytosis. I. Evidence for superoxide anion involvement in the oxidation of NADPH2P Patriarca, P Dri, K Kakinuma, et al.
Quaderni Sclavo Di Diagnostica Clinica E Di Laboratorio|December 1, 1978
[Pathogenicity of E. coli: biological aspects and problems related to laboratory diagnosis (author's transl)]P Patriarca, F Cian, G De Nicola, et al.
Rapid Communications in Mass Spectrometry : RCM|May 20, 2011
Fully automated software solution for protein quantitation by global metabolic labeling with stable isotopesL V Bindschedler, R Cramer
Infection and Immunity|August 1, 1985
Kinetics of assembly and decay of complement components on Escherichia coli O111:B4 preparation of stable intermediatesG Rottini, F Tedesco, M Basaglia, et al.
European Journal of Immunology|May 1, 1995
Human eosinophil peroxidase enhances tumor necrosis factor and hydrogen peroxide release by human monocyte-derived macrophagesP Spessotto, P Dri, R Bulla, et al.
Infection and Immunity|August 1, 1995
Leptospira icterohemorrhagiae and leptospire peptidolgycans induce endothelial cell adhesiveness for polymorphonuclear leukocytesA Dobrina, E Nardon, E Vecile, et al.
Toxicon : Official Journal of the International Society on Toxinology|May 1, 1997
Biologically active polypeptides in the venom of the jellyfish Rhopilema nomadicaL Gusmani, M Avian, B Galil, et al.
Surgical Endoscopy|March 17, 2007
Laparoscopic versus open incisional hernia repair: an open randomized controlled studyS Olmi, A Scaini, G C Cesana, et al.
Journal of Immunological Methods|December 27, 1985
A simple method to obtain pure granule-rich eosinophil fragments (cytosomes) from normal human bloodG Zabucchi, B Skerlavaj, R Menegazzi, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 1994
Hereditary eosinophil peroxidase deficiency: immunochemical and spectroscopic studies and evidence for a compound heterozygosity of the defectM Romano, P Patriarca, C Melo, et al.
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