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Articles by Kerem Ozdemir
Total Records ( 2 ) for Kerem Ozdemir
  Muhammed Arabaci , Yasin Yilmaz , Saltuk Bugrahan Ceyhun , Orhan Erdogan , Hakan Galip Dorlay , Ibrahim Diler , Suleyman Akhan , Mehmet Kocabas , Kerem Ozdemir , Hasan Koyun and Seyrani Koncagul
  S. aurata is a marine fish living along the Atlantic coasts of Europe and the Mediterranean Sea. It is an important food species, so that its production reached 128,943 t in the European aquaculture in 2008. However, little is known on its biology, in particular the efective and census sizes, distribution, spawning grounds and behaviour. Also the species subdivision still needs to be clarified. In this review, studies related with gilthead sea bream populations and problems with the clarification of gilthead seabream population structure in hatchery and wild were reviewed. Also, it was intensified on potential research areas, having importance in determination of population structure of gilthead seabream such as morphology and behaviour in hatchery and wild. Determination of the genetic structure of S. aurata populations based on behaviour and morphology will not only contribute greatly to biological clarification of the species but also will help the development strategy for conservation of natural stocks (e.g., protecting the stopover points) and the determination of reference stocks, which is important for the culture of gilthead seabream to use in the genetic improvement programmes.
  Metin Ertas , Kerem Ozdemir and Ekrem Atalan
  Recently with the advancement of molecular methods, studies that determine intraspecific genetic polymorphisms have yielded substantial results. The aim of this study was to use Random Amplified Polymorphic DNA PCR (RAPD-PCR) analysis to determine the differences among Micromonospora species isolated from the soil. M3 medium with antibiotics was used to isolate the species from the soil and 65 Micromonospora species were identified. Total DNA analysis was performed for the different color groups which were obtained as a result analysis of the species. Sm5R, Sm6F, DAF4, M13, 27F and 1492R primers were used for RAPD-PCR analysis and the band profiles of the species were obtained. The dendrogram generated according to the simple matching coefficient method clearly showed the differences detected among the species. A total of seven groups were identified along with two main groups. Five of these groups had a single member, one had 3 and one had 2 members.
 
 
 
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