Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Emina, Kiseljakovic"'
Autor:
Grazyna Adler, Izabela Uzar, Amina Valjevac, Emina Kiseljakovic, Emir Mahmutbegovic, Nermin N. Salkic, Mateusz A. Adler, Nevena Mahmutbegovic
Publikováno v:
Annals of Human Biology, Vol 49, Iss 3-4, Pp 210-215 (2022)
Background CYP3A5 enzyme encoded by CYP3A5 is important for drug metabolism in gut and liver, whereas P-glycoprotein by ABCB1, is an ATP-dependent drug efflux pump which exports endo- and exogenous substances outside the cell. Aim The study was to as
Externí odkaz:
https://doaj.org/article/5e06c2c236cc4e47895c4453cb573cf0
Autor:
Grażyna Adler, Mateusz A. Adler, Anna Urbańska, Karolina Skonieczna-Żydecka, Emina Kiseljakovic, Amina Valjevac, Miłosz Parczewski, Almira Hadzovic-Dzuvo
Publikováno v:
Annals of Human Biology, Vol 44, Iss 6, Pp 568-573 (2017)
Background: The ε2, ε3 and ε4 alleles of APOE gene have been associated with several diseases in different populations. Data on the frequency of alleles are used in both a clinical and evolutionary context. Although the data on frequency of these
Externí odkaz:
https://doaj.org/article/b3b67336e2474d9586799cfcb46f502c
Autor:
Grazyna, Adler, Izabela, Uzar, Amina, Valjevac, Emina, Kiseljakovic, Emir, Mahmutbegovic, Nermin N, Salkic, Mateusz A, Adler, Nevena, Mahmutbegovic
Publikováno v:
Annals of human biology. 49(3-4)
CYP3A5 enzyme encoded byThe study was to assess the prevalence ofOverall, 511 unrelated healthy subjects from Poland (In Poles, Belarusians and Bosnians the *3 allele ofIn compared populations, the distribution of
Autor:
Sabina Segalo, Emina Kiseljakovic, Emsel Papic, Anes Joguncic, Aleksandra Pasic, Mubera Sahinagic, Orhan Lepara, Lutvo Sporisevic
Publikováno v:
Acta Informatica Medica. 31:41
Background: Coronavirus disease 2019 (COVID-19) can cause a wide clinical spectrum, ranging from asymptomatic to severe disease with a high mortality rate. In view of the current pandemic and the increasing influx of patients into healthcare faciliti
Autor:
Jürgen-Christoph von Kleist-Retzow, Michaela Jaksch, Mark Helm, Rudolf J. Wiesner, Armine Hayrapetyan, Emina Kiseljakovic, Katharina Maniura-Weber, Myriam Möllers, Maria Bust
Publikováno v:
Nucleic Acids Research
We have studied the consequences of two homoplasmic, pathogenic point mutations (T7512C and G7497A) in the tRNA S e r ( U C N ) gene of mitochondrial (mt) DNA using osteosarcoma cybrids. We identified a severe reduction of tRNA S e r ( U C N ) to lev