Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Smiljana, Ristić"'
Autor:
Jasna Nekić, Ivana Stanković Matić, Valentino Rački, Dolores Janko Labinac, Vladimira Vuletić, Miljenko Kapović, Smiljana Ristić, Borut Peterlin, Nada Starčević Čizmarević
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 13, p 7412 (2024)
The aim of the present study was to investigate the impact of CCR5 Δ32 and CTLA-4 polymorphisms on the response to IFN-β treatment in our cohort of MS patients from Croatia and Slovenia. Genomic DNA was obtained from 295 MS patients (230 female; 65
Externí odkaz:
https://doaj.org/article/46e03153d63e4f93abf09b19cb0ddc04
Autor:
Smiljana Ristić, Sandra Milić, Tanja Tatalović, Matea Bilobrk, Dobrica Rončević, Božena Ćurko-Cofek, Vesna Barac-Latas, Nada Starčević Čizmarević
Publikováno v:
Balkan Medical Journal, Vol 40, Iss 3, Pp 229-231 (2023)
Externí odkaz:
https://doaj.org/article/562e93d93e7a460a9d1362437a059684
Autor:
Sergej Nadalin, Sanja Dević Pavlić, Vjekoslav Peitl, Dalibor Karlović, Lena Zatković, Smiljana Ristić, Alena Buretić-Tomljanović, Hrvoje Jakovac
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 20, p 12180 (2022)
We investigated whether a functional insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme (ACE) influenced antipsychotic treatment. At baseline, and after 8 weeks of treatment with various antipsychotic medications, we assessed pati
Externí odkaz:
https://doaj.org/article/5accf85a9e274e519b5ebf52f0595d62
Autor:
Ales Maver, Polona Lavtar, Smiljana Ristić, Sanja Stopinšek, Saša Simčič, Keli Hočevar, Juraj Sepčić, Jelena Drulović, Tatjana Pekmezović, Ivana Novaković, Hodžić Alenka, Gorazd Rudolf, Saša Šega, Nada Starčević-Čizmarević, Anja Palandačić, Gordana Zamolo, Miljenko Kapović, Tina Likar, Borut Peterlin
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract The genetic etiology and the contribution of rare genetic variation in multiple sclerosis (MS) has not yet been elucidated. Although familial forms of MS have been described, no convincing rare and penetrant variants have been reported to da
Externí odkaz:
https://doaj.org/article/e4072727c70249fda8baa63505e6bb7c
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Background: Over the past two decades, various novel disease-modifying drugs for multiple sclerosis (MS) have been approved. However, there is high variability in the patient response to the available medications, which is hypothesized to be partly a
Externí odkaz:
https://doaj.org/article/05270995bc1f4e4db94f5fbd5676daf4
Autor:
Polona Lavtar, Gorazd Rudolf, Aleš Maver, Alenka Hodžić, Nada Starčević Čizmarević, Maja Živković, Saša Šega Jazbec, Zalika Klemenc Ketiš, Miljenko Kapović, Evica Dinčić, Ranko Raičević, Juraj Sepčić, Luca Lovrečić, Aleksandra Stanković, Smiljana Ristić, Borut Peterlin
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0190601 (2018)
Prevalence of multiple sclerosis varies with geographic latitude. We hypothesized that this fact might be partially associated with the influence of latitude on circadian rhythm and consequently that genetic variability of key circadian rhythm regula
Externí odkaz:
https://doaj.org/article/140d9813c2514d76bf87cca171b73809
Autor:
Nada, Starčević Čizmarević, Božena, Ćurko-Cofek, Vesna, Barac-Latas, Borut, Peterlin, Smiljana, Ristić
Publikováno v:
Biomedical Reports
Volume 16
Issue 2
Biomed Rep
Volume 16
Issue 2
Biomed Rep
Increasing evidence supports the potential role of iron metabolism in multiple sclerosis (MS). Previous studies examining the association between polymorphisms of the hemochromatosis gene (HFE) and susceptibility to MS have yielded inconsistent resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32069497033033b84b899cfbd2f7dc1a
https://doi.org/10.3892/br.2021.1495
https://doi.org/10.3892/br.2021.1495
Autor:
Nada Starčević Čizmarević, Luca Lovrečić, Aleš Maver, Borut Peterlin, Aida Zečkanović, Smiljana Ristić
Publikováno v:
Biomed Rep
Biomedical Reports
Volume 15
Issue 6
Biomedical Reports
Volume 15
Issue 6
Pattern recognition receptors, such as specific nucleotide binding oligomerization domain protein 2, and their polymorphisms may be involved in the pathogenesis of multiple sclerosis (MS). They may also play a role in the forma tion of neutralizing a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1f416737efa546dbe3a6ec39e0580fe
https://pubmed.ncbi.nlm.nih.gov/34667597
https://pubmed.ncbi.nlm.nih.gov/34667597
Publikováno v:
Journal of Infection
Volume 83
Issue 3
Volume 83
Issue 3
We have read with great interest several recent articles on the insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme (ACE) gene and its potential relevance to the risk of a SARS-CoV-2 infection and the severity of the consequent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4acd49a0b1f5f9558c9008724535e26
https://www.bib.irb.hr/1140010
https://www.bib.irb.hr/1140010
Publikováno v:
Croatian Medical Journal
Volume 61
Issue 6
Volume 61
Issue 6
A study was conducted to compare CCR5-?32 mutation frequency in 39 European countries with the prevalence and mortality of COVID-19, as of June 1, 2020. Multiple regression analyses revealed that the partial correlation coefficients of the CCR5-?32 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55456b3241f0016db5742be15c991c99
https://doi.org/10.3325/cmj.2020.61.525
https://doi.org/10.3325/cmj.2020.61.525