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المؤلفون: Philip S. Stewart, Jean-Paul Dehaye, Carole Nagant, Michel Vandenbranden, Betsey Pitts, J. G. Bolscher, K. Nazmi
المساهمون: Orale Biochemie (OII, ACTA), Oral Biochemistry
المصدر: Antimicrobial Agents and Chemotherapy, 56(11), 5698-5708. American Society for Microbiology
Antimicrobial agents and chemotherapy, 56(11), 5698-5708. American Society for Microbiology
Nagant, C, Pitts, B, Nazmi, K, Vandenbranden, M, Bolscher, J G, Stewart, P S & Dehaye, J-P 2012, ' Identification of peptides derived from the human antimicrobial peptide LL-37 active against biofilms formed by Pseudomonas aeruginosa using a library of truncated fragments ', Antimicrobial agents and chemotherapy, vol. 56, no. 11, pp. 5698-5708 . https://doi.org/10.1128/AAC.00918-12Testمصطلحات موضوعية: Cell Membrane Permeability, Spectrophotometry, Infrared, Cell Survival, medicine.medical_treatment, Antimicrobial peptides, Molecular Sequence Data, Peptide, medicine.disease_cause, Cathelicidin, Microbiology, Species Specificity, SDG 3 - Good Health and Well-being, Cathelicidins, Peptide Library, medicine, Human Umbilical Vein Endothelial Cells, Humans, Pharmacology (medical), Amino Acid Sequence, Peptide library, Peptide sequence, Mechanisms of Action: Physiological Effects, Pharmacology, chemistry.chemical_classification, Microbial Viability, biology, L-Lactate Dehydrogenase, Pseudomonas aeruginosa, Cell Membrane, Biofilm, biology.organism_classification, Peptide Fragments, Anti-Bacterial Agents, Infectious Diseases, Biochemistry, chemistry, Biofilms, Bacteria, Antimicrobial Cationic Peptides, Propidium
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ab59609fc6621958e15ed5a310760a8Test
https://doi.org/10.1128/aac.00918-12Test -
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المؤلفون: Tomoko Komiyama, Joel A. Swanson, Robert S. Fuller
المصدر: Antimicrobial Agents and Chemotherapy. 49:3875-3882
مصطلحات موضوعية: Proteases, Anthrax toxin, Bacterial Toxins, Blotting, Western, Receptors, Cell Surface, Endocytosis, medicine.disease_cause, Microbiology, Antimalarials, Mice, Chloroquine, medicine, Animals, Pharmacology (medical), Protease inhibitor (pharmacology), Mechanisms of Action: Physiological Effects, Furin, Cells, Cultured, Serpins, Pharmacology, Antigens, Bacterial, L-Lactate Dehydrogenase, biology, Toxin, Macrophages, Proteins, biology.organism_classification, Virology, Bacillus anthracis, Infectious Diseases, biology.protein, Algorithms, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecabf9dead306b0a2cdc6a85e468f463Test
https://doi.org/10.1128/aac.49.9.3875-3882.2005Test -
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المؤلفون: Patrick J. Brennan, Takemasa Takii, Chiyoji Abe, John T. Belisle, Kikuo Onozaki, Yoshifumi Yamamoto, Taku Chiba
المصدر: Antimicrobial Agents and Chemotherapy. 46:2533-2539
مصطلحات موضوعية: Cell Survival, medicine.drug_class, Antitubercular Agents, Colony Count, Microbial, Drug Evaluation, Preclinical, Microbial Sensitivity Tests, Biology, Antimycobacterial, Microbiology, Mycobacterium tuberculosis, Minimum inhibitory concentration, Isoniazid, medicine, Humans, Pharmacology (medical), Cytotoxicity, Cells, Cultured, Ethambutol, Antibacterial agent, Pharmacology, L-Lactate Dehydrogenase, Fibroblasts, biology.organism_classification, Pyrazinamide, Infectious Diseases, Susceptibility, Streptomycin, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99012356df9526a9126fbce85a52a556Test
https://doi.org/10.1128/aac.46.8.2533-2539.2002Test