Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Berna Ozbek-Celik"'
Autor:
Berna Ozbek-Celik, Damla Damar-Celik, Emel Mataraci-Kara, Cagla Bozkurt-Guzel, Paul B. Savage
Publikováno v:
Antibiotics, Vol 8, Iss 3, p 130 (2019)
Objectives: The ceragenins, or CSAs, were designed to mimic the activities of antimicrobial peptides and represent a new class of antimicrobial agent. The aim of this study was to comparatively investigate the antimicrobial activities of first/second
Externí odkaz:
https://doaj.org/article/bd9459ced299484ca5ba34c48035a23f
Autor:
Damla Damar Celik, Abdulkerim Karaynir, Hanife Salih Dogan, Bulent Bozdogan, Berna Ozbek Celik
Publikováno v:
Heliyon, Vol 10, Iss 17, Pp e36243- (2024)
Phages are ubiquitous in freshwater, seawater, soil, the human body, and sewage water. They are potent biopharmaceuticals against antimicrobial-resistant bacteria and offer a promising alternative for treating infectious diseases. Also, combining pha
Externí odkaz:
https://doaj.org/article/f017b4a00bf0411881ae67855daaa94d
Autor:
Emel Mataracı-Kara, Berna Ozbek-Celik, Mahmut Yıldız, Amaç Fatih Tuyun, Hatice Yıldırım, Merve Ataman, Nilüfer Bayrak
Publikováno v:
Medicinal Chemistry Research. 30:1728-1737
The aim of this study was to evaluate the antimicrobial activity of twenty-five Plastoquinone analogs synthesized previously in a panel of seven bacterial strains (three Gram-positive and four Gram-negative bacteria) and three fungi. PQ1, which does
Publikováno v:
Journal of Research in Pharmacy. 25:549-553
Publikováno v:
Journal of Chemotherapy. 33:216-227
Achromobacter species, which are recognized as emerging pathogens isolated from patients with cystic fibrosis, are capable of forming biofilm in the respiratory tract in patients and innate multidr...
Autor:
Berna Ozbek-Celik, Özlen Güzel-Akdemir, Görkem Ermut, Mehtap Özbek-Babuç, Muhammed Trawally, Hakan Ozdemir
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 151:1443-1452
The synthesis of a series of new 3-phenyl-5-sulfamoyl-N-(7/8/9-(non)substituted-3-oxo-1-thia-4-azaspiro[4.4]non/[4.5]dec-4-yl)-1H-indole-2-carboxamide derivatives and their subsequent testing for antibacterial activity is described in this paper. 4-S
Publikováno v:
Journal of Global Antimicrobial Resistance, Vol 22, Iss, Pp 713-717 (2020)
Damar-Çelik, D, Nørskov-Lauritsen, N & Özbek-Çelik, B 2020, ' Comparative in vitro activities of meropenem in combination with colistin, levofloxacin, or chloramphenicol against Achromobacter xylosoxidans strains isolated from patients with cystic fibrosis ', Journal of Global Antimicrobial Resistance, vol. 22, pp. 713-717 . https://doi.org/10.1016/j.jgar.2020.06.001
Damar-Çelik, D, Nørskov-Lauritsen, N & Özbek-Çelik, B 2020, ' Comparative in vitro activities of meropenem in combination with colistin, levofloxacin, or chloramphenicol against Achromobacter xylosoxidans strains isolated from patients with cystic fibrosis ', Journal of Global Antimicrobial Resistance, vol. 22, pp. 713-717 . https://doi.org/10.1016/j.jgar.2020.06.001
Objectives Achromobacter xylosoxidans is an emerging pathogen in cystic fibrosis (CF). Relatively little is known about its clinical impact and optimal management. In the present study, the in vitro bactericidal activities of meropenem, either alone
Publikováno v:
Archives of Microbiology. 202:2543-2550
The present study aims to examine the in vitro antifungal susceptibility patterns ofCandidaspecies isolated from hospital wastewater, and the efficacy of widely used disinfectants (sodium hypochlorite and benzalkonium chloride) against planktonic and
Publikováno v:
Current Microbiology. 77:2137-2142
The aim of this study is to investigate the combination of cefepime and sulbactam. Sulbactam, when administered , will effectively inhibit all Extended-spectrum beta lactamases (ESBLs) of the microorganism, while cefepime will inhibit the growth of t
Autor:
Emel Mataracı-Kara, Hatice Yıldırım, Nilüfer Bayrak, Amaç Fatih Tuyun, Mahmut Yıldız, Berna Ozbek-Celik
Publikováno v:
Drug Development Research.
In our pursuit of developing the novel, potent, and selective antimicrobial agents, we managed to obtain the quinolinequinone for their antimicrobial profile with minimal inhibitory concentrations (MICs) determined against a panel of seven bacterial