Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Vedrana Makević"'
Autor:
Vedrana Makević, Ivan D. Milovanovich, Nevena Popovac, Radmila Janković, Jelena Trajković, Andrija Vuković, Bojana Milosević, Jovan Jevtić, Silvio R. de Luka, Andjelija Ž. Ilić
Publikováno v:
Fractal and Fractional, Vol 7, Iss 8, p 619 (2023)
Inflammatory bowel disease (IBD), which encompasses two different phenotypes—Crohn’s disease (CD) and ulcerative colitis (UC)—consists of chronic, relapsing disorders of the gastrointestinal tract. In 20–30% of cases, the disease begins in th
Externí odkaz:
https://doaj.org/article/f7cee56609724bb9aed657fb5541dea2
Autor:
Vedrana Makević, Ivan D. Milovanovich, Nevena Popovac, Saša Janković, Vesna Janković, Srđan Stefanović, Zoran Bukumirić, Silvio R. De Luka
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03276c67ca88d5abe17592c682189234
https://doi.org/10.2139/ssrn.4355092
https://doi.org/10.2139/ssrn.4355092
Autor:
Sara Milojevic, Arijit Ghosh, Vedrana Makevic, Maja Stojkovic, Maria Capovilla, Tomislav Tosti, Dejan Budimirovic, Dragana Protic
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 14, p 7949 (2024)
Fragile X syndrome (FXS) is caused by the full mutation in the FMR1 gene on the Xq27.3 chromosome region. It is the most common monogenic cause of autism spectrum disorder (ASD) and inherited intellectual disability (ID). Besides ASD and ID and other
Externí odkaz:
https://doaj.org/article/ef7162aa2fa44d239b1b9c523b45fa57
Autor:
Maja Stojkovic, Milan Petrovic, Maria Capovilla, Sara Milojevic, Vedrana Makevic, Dejan B. Budimirovic, Louise Corscadden, Shuhan He, Dragana Protic
Publikováno v:
Biology, Vol 13, Iss 6, p 432 (2024)
Fragile X syndrome (FXS), the most common monogenic cause of inherited intellectual disability and autism spectrum disorder, is caused by a full mutation (>200 CGG repeats) in the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene. Individuals with
Externí odkaz:
https://doaj.org/article/1af7cf936b0f46f084fd0eb8e156dd9c
Autor:
Milutin Parlić, Milan Parlic, Vedrana Makević, Vladimir Jakšić, Aleksandra Ilic, Sandra Milanović
Publikováno v:
Facta Universitatis, Series: Physical Education and Sport. :337
A fast reaction to visual stimuli is important for the success of any athlete. A fast reaction time enables a quick response in key situations. We have studied how age, sport engagement, moderate physical activity and lateralization affect the simple
Autor:
Jelena Trajković, Vedrana Makevic, Milica Pesic, Sofija Pavković-Lučić, Sara Milojevic, Smiljana Cvjetkovic, Randi Hagerman, Dejan B. Budimirovic, Dragana Protic
Publikováno v:
Genes, Vol 14, Iss 1, p 87 (2022)
Fragile X syndrome (FXS) is a global neurodevelopmental disorder caused by the expansion of CGG trinucleotide repeats (≥200) in the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene. FXS is the hallmark of Fragile X-associated disorders (FXD) and
Externí odkaz:
https://doaj.org/article/0b503870fd834c73b08e190f28c19fb6