Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Vera Bunjevacki"'
Autor:
Branka Popovic, Nela Maksimovic, Vera Milic, Tatjana Damnjanovic, Vera Bunjevacki, Maja Krajinovic, Nemanja Damjanov, Biljana Jekic, Dubravka Vejnovic, Ivana Novakovic
Publikováno v:
Expert Opinion on Drug Metabolism & Toxicology
Background: Methotrexate (MTX), a folate analogue, is the most commonly used disease-modifying drug in the treatment of rheumatoid arthritis (RA). However, high interindividual differences in drug response are present among RA patients.Research desig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6ef0509c1c0baff160397131e9dc562
https://doi.org/10.1080/17425255.2019.1563594
https://doi.org/10.1080/17425255.2019.1563594
Autor:
Vera Bunjevacki, Nela Maksimovic, Vera Milic, Maja Krajinovic, Ljiljana Lukovic, Sofija Pavković-Lučić, Ivana Novakovic, Tatjana Damnjanovic, Biljana Jekic, Nemanja Damjanov, Dubravka Vejnovic, Goran Radunovic
Publikováno v:
Genetika, Vol 48, Iss 1, Pp 395-408 (2016)
A folate analogue methotrexate (MTX) is the most commonly used disease-modifying drug in the treatment of rheumatoid arthritis. However, the clinical response of RA patients treated with MTX shows interindividual differences and 30% of patients disco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db1b399fad430ddcb8746fbb79116879
https://doi.org/10.2298/gensr1601395v
https://doi.org/10.2298/gensr1601395v
Autor:
Suzana Cvjeticanin, Ivana Novakovic, Vera Bunjevacki, Nada Majkic-Singh, S. Slavko, Dragana Cvetković, Biljana Jekic, Tatjana Damnjanovic, Ljiljana Lukovic, Nela Maksimovic
Publikováno v:
Archives of Biological Sciences, Vol 66, Iss 2, Pp 729-734 (2014)
The effect of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism on serum lipid profiles is controversial. We randomly selected 530 healthy schoolchildren that were included in the Yugoslav Study of the Precursors of Atheroscler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6e61c3144f0de0ebc6a3d301e6444b9
http://www.doiserbia.nb.rs/img/doi/0354-4664/2014/0354-46641402729D.pdf
http://www.doiserbia.nb.rs/img/doi/0354-4664/2014/0354-46641402729D.pdf
Autor:
Andrija Bogdanovic, Vera Bunjevacki, Momcilo Ristanovic, Ljiljana Lukovic, Nela Maksimovic, Ivana Novakovic, Suzana Cvjeticanin, Biljana Jekic, Tatjana Damnjanovic
Publikováno v:
Archives of Biological Sciences, Vol 66, Iss 3, Pp 1055-1059 (2014)
Myelodysplastic syndromes (MDS) are clonal hematologic stem cell disorders with an as yet unknown molecular pathology. Genetic instability has been proposed as a cause of MDS. Mutations in the NBS1 gene, whose product nibrin (p95) is involved in DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34b194697f3f1e0e72279fb512a2dec5
http://www.doiserbia.nb.rs/img/doi/0354-4664/2014/0354-46641403055B.pdf
http://www.doiserbia.nb.rs/img/doi/0354-4664/2014/0354-46641403055B.pdf
Autor:
Nela Maksimovic, Vera Bunjevacki, Tatjana Damnjanovic, Dubravka Vejnovic, Ivana Novakovic, Ljiljana Lukovic, Maja Krajinovic, Nemanja Damjanov, Vera Milic, Biljana Jekic
Publikováno v:
Pharmacogenomics. 17(15)
Aim: Our aim was to explore the influence of 9-bp insertion/deletion and variable number of 9 bp elements (63/91) length polymorphism in noncoding interfering RNA and major promoter of DHFR gene on methotrexate (MTX) efficacy and toxicity in patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afe53abf6114a441a26a9ee3429ef99f
https://pubmed.ncbi.nlm.nih.gov/27636122
https://pubmed.ncbi.nlm.nih.gov/27636122
Autor:
Vera Pravica, Vladimir Perovic, Radovan Mijanovic, Dijana Perovic, Vera Bunjevacki, Branka Bonaci-Nikolic
Publikováno v:
Immunology letters. 176
Common variable immunodeficiency (CVID) is a heterogeneous disease characterized by impaired B-cell differentiation and maturation accompanied with the defective antibody production. Several investigators addressed the possibility that disturbed cyto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ffcb0d63e70d0a67682bd5985e7bd8
https://pubmed.ncbi.nlm.nih.gov/27288995
https://pubmed.ncbi.nlm.nih.gov/27288995
Autor:
Tatjana Damnjanovic, Ana Andjelković, Suzana Cvjeticanin, Biljana Kastratovic-Kotlica, Dijana Perovic, Vidosava Rakocevic-Stojanovic, Slavko Brankovic, Biljana Jekic, Vera Bunjevacki, Vedrana Milic-Rasic, Nela Maksimovic, Ivana Novakovic, Ljiljana Lukovic
Publikováno v:
Archives of Biological Sciences, Vol 64, Iss 2, Pp 787-792 (2012)
Duchenne and Becker muscular dystrophy (DMD/BMD) are severe X-linked neuromuscular disorders caused by mutations in the dystrophin gene. Our aim was to optimize a quantitative real-time PCR method based on SYBR? Green I chemistry for routine diagnost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ac1ea7c7352c69bced1f9b32d7d8386
https://doi.org/10.2298/abs1202787m
https://doi.org/10.2298/abs1202787m
Autor:
Tatjana, Damnjanovic, Goran, Cuturilo, Nela, Maksimovic, Nikola, Dimitrijevic, Vesna, Mitic, Biljana, Jekic, Ljiljana, Lukovic, Vera, Bunjevacki, Tatjana, Varljen, Valerija, Dobricic, Ida, Jovanovic, Vladimir, Kostic, Ivana, Novakovic
Publikováno v:
The Turkish journal of pediatrics. 57(2)
Developmental delay and intellectual disabilities (DD/ID) are significant health problems affecting 3% of the human population. Submicroscopic chromosomal rearrangements involving subtelomeric regions are often considered to be the cause of unexplain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9f91531266e74bb413ce496a51fb07eb
https://pubmed.ncbi.nlm.nih.gov/26690596
https://pubmed.ncbi.nlm.nih.gov/26690596
Autor:
Vera Bunjevacki, Tatjana Damnjanovic, Ivana Novakovic, Ljiljana Lukovic, Branka Popovic, Nela Maksimovic, Biljana Jekic, Valerija Dobricic, Vladimir Perovic, Jelena Milasin
Publikováno v:
Archives of Biological Sciences, Vol 63, Iss 3, Pp 649-653 (2011)
Archives of Biological Sciences
Archives of Biological Sciences
Myelodysplastic syndromes (MDS) are rare in children and only a few studies have analyzed their molecular mechanisms. The NPM1 gene encodes for nucleophosmin (NPM) which regulates hematopoiesis. Mutations in exon 12 of the NPM1 cause the nucleophosmi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94bfe4c7580ca24a30a4a0eb56908150
http://www.doiserbia.nb.rs/img/doi/0354-4664/2011/0354-46641103649J.pdf
http://www.doiserbia.nb.rs/img/doi/0354-4664/2011/0354-46641103649J.pdf
Autor:
Milos Kuzmanovic, Gordana Bunjevacki, Vera Bunjevacki, Suzana Cvjeticanin, Tatjana Damnjanovic, Branka Popovic, Ivana Novakovic, Ljiljana Lukovic, Jelena Milasin, Biljana Jekic
Publikováno v:
Cancer Genetics & Cytogenetics
Myelodysplastic syndromes (MDS) are rare disorders in children. Molecular mechanisims underlying MDS in children are not yet completely understood. Considering the role of FMS and TP53 gene mutations in adult MDS patients, we analyzed nnutations of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5275e3904233975d0ef0fff38470c6cd
https://doi.org/10.1016/j.cancergencyto.2005.11.003
https://doi.org/10.1016/j.cancergencyto.2005.11.003