Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Tatjana Damnjanovic"'
Autor:
Nela Maksimovic, Vanja Vidovic, Tatjana Damnjanovic, Biljana Jekic, Nada Majkic Singh, Slavko Simeunovic, Dara Savic Bozovic, Stojko Vidovic, Ivana Novakovic
Publikováno v:
Archives of Medical Science, Vol 19, Iss 3, Pp 593-599 (2021)
Introduction Positive regulatory domain containing 16 (PRDM16) protein represents the key regulator of brown adipose tissue (BAT) development. It induces brown fat phenotype and represses white adipose tissue specific genes through the association wi
Externí odkaz:
https://doaj.org/article/160cb88bd27740d6b110cd35dd79238c
Autor:
Vanja Vidovic, Nela Maksimovic, Stojko Vidovic, Tatjana Damnjanovic, Irina Milovac, Ivana Novakovic
Publikováno v:
Genetika. 54:1375-1384
PPARGC1A is involved in many metabolic processes including normal mitochondrial biogenesis, oxidation of glucose and lipids and transport of glucose into skeletal muscles. Previous researches linked this polymorphism with the higher risk of developin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36c834c77a7f568060705010cf997d64
https://doi.org/10.2298/gensr2203375v
https://doi.org/10.2298/gensr2203375v
Autor:
Dijana Perovic, Tatjana Damnjanovic, Biljana Jekic, Marija Dusanovic‐Pjevic, Milka Grk, Ana Djuranovic, Milica Rasic, Ivana Novakovic, Nela Maksimovic
Publikováno v:
Journal of clinical laboratory analysis. 36(6)
Array-based genomic analysis is a gold standard for the detection of copy number variations (CNVs) as an important source of benign as well as pathogenic variations in humans. The introduction of chromosomal microarray (CMA) has led to a significant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca18e8647ae01d24c3d5e395b4e8622d
https://pubmed.ncbi.nlm.nih.gov/35441737
https://pubmed.ncbi.nlm.nih.gov/35441737
Autor:
Stojko Vidović, Biljana Jekic, D Marisavljević, N Majkić Singh, Nela Maksimovic, Vanja Vidović, Ivana Novakovic, Dejan Nikolic, Marina Stamenkovic-Radak, Tatjana Damnjanovic
Publikováno v:
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics, Vol 23, Iss 1, Pp 77-82 (2020)
Balkan Journal of Medical Genetics, Vol 23, Iss 1, Pp 77-82 (2020)
Brain-derived neurotrophic factor (BDNF) has an important role in energy balance. It suppresses food intake, reduces hepatic glucose production and converts white fat into brown fat in adipose tissue, leading to energy dissipation, lowered blood gluc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d65067bc1d12e8fb3a6da7ec23cb77c
https://doi.org/10.2478/bjmg-2020-0004
https://doi.org/10.2478/bjmg-2020-0004
Autor:
Vita Dolzan, Ivana Novakovic, Marija Dusanovic Pjevic, Milica Pešić, Vera Milic, Tatjana Damnjanovic, Milka Grk, Biljana Jekic, Nela Maksimovic
Publikováno v:
The Pharmacogenomics Journal. 20:784-791
Adenosine receptors ADORA2A and ADORA3 are part of the adenosine-mediated antiinflammatory pathway and are overexpressed in patients with Rheumatoid arthritis (RA). Methotrexate (MTX) antiinflammatory effects are partially mediated via increased rele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::374bada48318ef00fbb0a397cebf1a5e
https://doi.org/10.1038/s41397-020-0168-z
https://doi.org/10.1038/s41397-020-0168-z
Autor:
Milka Grk, Stojko Vidović, Tatjana Damnjanovic, Biljana Jekic, Irina Milovac, Vanja Vidović, Nela Maksimovic
Publikováno v:
Genetics & Applications. 3:38-41
Initial testing of children with psychomotor delays considers karyotype analysis and metabolic tests. However, introduction of Array Comparative Genomic Hybridization (ACGH) has become the standard method of diagnostics worldwide. ACGH is a highly se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ade7c3ac4b269881c992c4f4579d752
https://doi.org/10.31383/ga.vol3iss3pp38-41
https://doi.org/10.31383/ga.vol3iss3pp38-41
Autor:
Olgica Rakic, Nela Maksimovic, Tatjana Varljen, Tatjana Damnjanovic, Gordana Sekulovic, Ivana Novakovic, Biljana Jekic
Publikováno v:
Inflammation Research. 69:155-157
Interleukin-1-B (IL1B) is a proinflammatory cytokine that plays an important role in sepsis. The aim of this study was to evaluate the relationships between IL1B-511G/A polymorphism and susceptibility and outcome of early-onset sepsis (EOS) in preter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4712a043db014d2a5df2a200c255e564
https://doi.org/10.1007/s00011-019-01301-4
https://doi.org/10.1007/s00011-019-01301-4
Publikováno v:
Pharmacogenomics. 20:1235-1245
For many decades, methotrexate (MXT) has remained the drug of choice in the treatment of rheumatoid arthritis (RA). Unfortunately, a considerable number of patients do not achieve an appropriate therapeutic response. Pharmacogenetics studies do not g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dab63d9217759c500fde84e4fe3db3c
https://doi.org/10.2217/pgs-2019-0121
https://doi.org/10.2217/pgs-2019-0121
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:
Biljana Jekic, Ivana Novakovic, Milica Rankovic Janevski, Olgica Rakic, Nela Maksimovic, Tatjana Damnjanovic, Gordana Sekulovic, Tatjana Varljen
Publikováno v:
The Tohoku Journal of Experimental Medicine. 247:259-264
Early-onset neonatal sepsis (EOS) is diagnosed during the first 7 days of neonatal life and is the major cause of morbidity and mortality among preterm infants. Genetic predisposition may have an impact on EOS susceptibility and outcome. The aim of o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86e723d5cba667c3057f015302dc5579
https://doi.org/10.1620/tjem.247.259
https://doi.org/10.1620/tjem.247.259