Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Milena, Ugrin"'
Publikováno v:
Children, Vol 11, Iss 7, p 785 (2024)
(1) Background: Thalassemia syndromes are common monogenic disorders that represent a significant global health issue. No systematic epidemiological or molecular investigations on thalassemias in the Croatian population have been reported to date. (2
Externí odkaz:
https://doaj.org/article/06007a3f638546c4bdbc123f6e6c3f42
Autor:
Teodora Karan-Đurašević, Milena Ugrin, Vojin Vukovic, Darko Antic, Sanja Stankovic, Irena Marjanovic, Tatjana Kostic, Vladimir Otasevic, Kristina Tomic, Sofija Sarac, Biljana Mihaljevic, Sonja Pavlovic, Nataša Tošić
Publikováno v:
HemaSphere, Vol 7, p e1785725 (2023)
Externí odkaz:
https://doaj.org/article/90568f52a111473e8ba1a3e6a1614c67
Autor:
Marina Andjelkovic, Anita Skakic, Milena Ugrin, Vesna Spasovski, Kristel Klaassen, Sonja Pavlovic, Maja Stojiljkovic
Publikováno v:
Life, Vol 12, Iss 9, p 1396 (2022)
Glycogen storage diseases (GSDs) are rare metabolic monogenic disorders characterized by an excessive accumulation of glycogen in the cell. However, monogenic disorders are not simple regarding genotype–phenotype correlation. Genes outside the majo
Externí odkaz:
https://doaj.org/article/2766184829b64a1280d95fe749804944
Autor:
Milena Ugrin, Jelena Dinic, Sanja Jeremic, Sandra Dragicevic, Bojana Banovic Djeri, Aleksandra Nikolic
Publikováno v:
Nanomaterials, Vol 11, Iss 9, p 2322 (2021)
Bacterial nanocellulose (BNC) stands out among polymers as a promising biomaterial due to its mechanical strength, hydrophilicity, biocompatibility, biodegradability, low toxicity and renewability. The use of scaffolds based on BNC for 3D cell cultur
Externí odkaz:
https://doaj.org/article/21f5988f447945b98cef1898eea4dd8a
Autor:
Natasa Tosic, Milena Ugrin, Irena Marjanovic, Tatjana Kostic, Vojin Vukovic, Kristina Tomic, Vladimir Otasevic, Darko Antic, Biljana Mihaljevic, Sonja Pavlovic, Teodora Karan‐Djurasevic
Publikováno v:
International Journal of Laboratory Hematology. 45:64-71
The B-cell lymphoma/leukaemia 11A (BCL11A) gene encodes a Krüppel-like transcription factor involved in lymphocyte development during normal haematopoiesis. Aberrant expression of BCL11A has been observed in several haematological malignancies, incl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0372b3bb9c6ae3b7149ca6e63aa019ba
https://doi.org/10.1111/ijlh.13969
https://doi.org/10.1111/ijlh.13969
Autor:
Nikola, Jovanović, Milica, Lazarević, Vladimir J, Cvetković, Vesna, Nikolov, Jelena, Kostić Perić, Milena, Ugrin, Sonja, Pavlović, Tatjana, Mitrović
Publikováno v:
International journal of molecular sciences. 23(21)
A single-institution observational study with 43 newly diagnosed diffuse gliomas defined the isocitrate dehydrogenase 1 and 2 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::21452b4f05f039048a8164bbf6dddc3c
https://pubmed.ncbi.nlm.nih.gov/36361838
https://pubmed.ncbi.nlm.nih.gov/36361838
Autor:
Sonja Pavlovic, Bojan Ristivojevic, Jovana Komazec, Branka Zukic, Vera Zdravkovic, Milena Ugrin, Teodora Karan-Djurasevic
Publikováno v:
Molecular Biology Reports. 47:6759-6768
Maturity-onset diabetes of the young (MODY) is a form of monogenic diabetes caused by the variants in MODY-related genes. In addition to coding variants, variants in the promoter region of MODY-related genes can cause the disease as well. In this stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c737d27196a5a6c0df407fd76f4f081
https://doi.org/10.1007/s11033-020-05734-7
https://doi.org/10.1007/s11033-020-05734-7
Autor:
Kristel, Klaassen, Sara, Stanković, Maja, Đorđević Milošević, Božica, Kecman, Marina, Andjelkovic, Anita, Skakić, Vesna, Spasovski, Milena, Ugrin, Jovana, Komazec, Marina, Parezanović, Nikola, Jocić, Nina, Stevanović, Sonja, Pavlovic, Maja, Stojiljković
Publikováno v:
Genetics & Applications; 2024 Special Issue, p41-41, 1p
Autor:
Anita Skakic, Maja Stojiljkovic, Iva Milacic, Sonja Pavlovic, Kristel Klaassen, Milena Ugrin, Jovana Komazec
Publikováno v:
Genetika, Vol 49, Iss 2, Pp 457-467 (2017)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is one of the most common endocrine diseases, yet genetic diagnosis is among the most complicated of all monogenic disorders. It has an overall incidence of 1:10000-1:20000, it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6da53eb9a5f9bae3fcd729dbc1bc67f0
https://doi.org/10.2298/gensr1702457u
https://doi.org/10.2298/gensr1702457u
Autor:
Sanja Srzentic, Kristel Klaassen, Gordana Nikcevic, Branka Zukic, Vesna Spasovski, Biljana Stankovic, Maja Djordjevic, Milena Ugrin, Sonja Pavlovic, Nikola Kotur, Maja Stojiljkovic
Publikováno v:
Journal of Applied Genetics. 58:79-85
Phenylketonuria (PKU) is a metabolic disease caused by mutations in the phenylalanine hydroxylase (PAH) gene. Although the PAH genotype remains the main determinant of PKU phenotype severity, genotype-phenotype inconsistencies have been reported. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07f2acaedb47467cfc2a00135877ce5f
https://doi.org/10.1007/s13353-016-0359-0
https://doi.org/10.1007/s13353-016-0359-0