Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mirela Mackic-Djurovic"'
Publikováno v:
Asian Journal of Medical Sciences, Vol 9, Iss 5, Pp 12-16 (2018)
Background: The causes of infertility and recurrent spontaneous abortions are diverse and numerous – including non-genetic and genetic factors – whereby the importance of genetic factors in pathogenesis of infertility is becoming more and more co
Externí odkaz:
https://doaj.org/article/5a7e02c564a74017bd80c1cf82aaa5ee
Autor:
Grażyna Adler, Amina Valjevac, Karolina Skonieczna-Żydecka, Mirela Mackic-Djurovic, Miłosz Parczewski, Anna Urbańska, Nermin Nusret Salkic
Publikováno v:
Biomolecules & Biomedicine, Vol 14, Iss 3 (2014)
Recent evidence has demonstrated the role of CCR5Δ32 in a variety of human diseases: from infectious and inflammatory diseases to cancer. Several studies have confirmed that genetic variants in chemokine receptor CCR5 gene are correlated with suscep
Externí odkaz:
https://doaj.org/article/1fd5eb2db8ff4fa4a4825284aa784ac7
Autor:
Naris Pojskić, Mirela Mackic-Djurovic, Dunja Rukavina, Amir Zahirović, Adaleta Durmić-Pašić, Belma Kalamujic-Stroil, Ćazim Crnkić
Publikováno v:
Genetika, Vol 51, Iss 2, Pp 619-627 (2019)
In the present study modern technology of DNA extraction and automatic genotyping was applied in Bosnian and Herzegovinian autochthonous horse breed by using 17-Plex horse genotyping kit. The study was aimed at investigating usefulness of the 17-plex
Publikováno v:
Medical Archives
Background: The gene for 5,10-methylenetetrahydrofolate reductase (NAD(P)H) or MTHFR gene encodes protein methylenetetrahydrofolate reductase (MTHFR), an enzyme important in folate metabolism. Aim: The aim of this study was to determine the frequenci
Publikováno v:
Medical Archives
Introduction One of the important causes of male infertility is aberration at the chromosomes. Aim The main purpose of this study was to determine the frequency and types of chromosomal aberration in infertile/sterile men whose samples were analyzed
Autor:
Meliha Stomornjak-Vukadin, Radmila Malesevic, Lejla Mehinovic, Mirza Kozaric, Tijana Jaros, Ilvana Kurtovic-Basic, Slavica Ibrulj, Mirela Mackic-Djurovic, Amina Kurtovic-Kozaric, Semir Mesanovic
Publikováno v:
European journal of obstetrics, gynecology, and reproductive biology. 206
Objective This study examines trends in total and live birth prevalence of trisomy 21 (T21) with regard to increasing maternal age and the introduction of prenatal diagnosis in Bosnia and Herzegovina. Method The prenatal detection was introduced in J
Autor:
Amela Bećiragić, Halima Resić, Amina Valjevac, Mirela Mackic-Djurovic, Lejla Alic, Emina Kiseljaković, Sabaheta Hasić
Publikováno v:
Medical Archives
Introduction: Renalase is a protein secreted in kidneys and considered as a blood pressure modulator. High rates of hypertension and its regulation in patients on hemodialysis demands search for potential cause and treatment. The aim of this study wa
Publikováno v:
Medical archives (Sarajevo, Bosnia and Herzegovina). 67(4)
Introduction: The invention and use of antibiotics in treating infections is one of the greatest achievements of the twentieth century medicine. Antibiotics are one of the categories of pharmaceuticals with a broad and increasing application. Goal: T
Association of Parental Age and the Type of Down Syndrome on the Territory of Bosnia and Herzegovina
Autor:
Mirela Mackic-Djurovic, Mia Sotonica, Sabaheta Hasić, Slavka Ibrulj, Radivoj Jadrić, Emina Kiseljaković
Publikováno v:
Medical Archives
BACKGROUND One of the complications aneurysms subarachnoid hemorrhage is the development of vasospasm, which is the leading cause of disability and death from ruptured cerebral aneurysm. AIM To evaluate the significance of previous comorbidities on e
Autor:
Anna Urbańska, Nermin N. Salkic, Grażyna Adler, Miłosz Parczewski, Mirela Mackic-Djurovic, Amina Valjevac, Karolina Skonieczna-Żydecka
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Bosnian Journal of Basic Medical Sciences, Vol 14, Iss 3 (2014)
Europe PubMed Central
Bosnian Journal of Basic Medical Sciences, Vol 14, Iss 3 (2014)
Recent evidence has demonstrated the role of CCR5Δ32 in a variety of human diseases: from infectious and inflammatory diseases to cancer. Several studies have confirmed that genetic variants in chemokine receptor CCR5 gene are correlated with suscep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c60a6cb3be08de855f0abf470495a24
http://www.scopus.com/inward/record.url?eid=2-s2.0-84928107748&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84928107748&partnerID=MN8TOARS