Pretraga

Rezultati

SOX3 function in glioblastoma cells [2022]

Marjanović, Jelena; Drakulić, Danijela ; Garcia, Idoia; Vuković, Vladanka; Aldaz, Paula; Garros-Regulez, Laura; Sampron, Nicolas; Matheu, Ander; Stevanović, Milena

RTL in peripheral blood of CD patients as a potential predictor of the disease outcome [2024]

Stevanović, Bojana ; Milovanović, Ivan ; Kosić, Marija ; Popović, Branka

Exploring the knowledge of genetics laboratories on CFTR modulator therapy eligibility: findings and reflections during external quality assessment [2024]

Laudus, Nele; Torkler, Heike; Yamamoto, Raina; Raynal, Caroline; Audrezet, Marie-Pierre; Badenas, Celia; Radojkovic, Dragica P; Seia, Manuela; Giannone, Valentina; Dequeker, Els

Loss-of-function of AMFR causes autosomal recessive hereditary spastic paraplegia by altering lipid metabolism [2023]

Deng, Ruizhi; ...; Capo, Ivan Dj ; ...; (broj, koautora 27)

case-control study of association of FV HR2 6775A > G polymorphisms with thrombosis in Montenegrin patients; Haplotype analysis between FV 1691G > A and FV HR2 6775A > G polymorphisms [2024]

Teofilov, Sladjana; Miljanovic, Olivera; Ostojic, Tatjana; Bulatovic, Milena; Perovic, Sasa; Djordjevic, Natasa

Multidisciplinary investigation of backward-speech trait suggests a link between RIC3, RIPK1, ZBED5 and working memory [2016]

Preković, Stefan; Filipović Đurđević, Dušica M. ; Csifcsák, Gábor; Šveljo, Olivera ; Stojković, Oliver V. ; Newbury, Dianne F.

Applications of the new tool: VUS Notifier [2025]

Domazet, Milan; Ugrin, Milena M ; Andjelkovic, Marina Z ; Klaassen, Kristel M ; Skakic, Anita ; Komazec, Jovana ; Spasovski, Vesna M ; Todorovic, Sasa; Stojiljkovic, Maja M

Unravelling phenylalanine-induced neuronal dysfunction: transcriptome analysis of NT2-derived neurons highlights neurite impairment and synaptic connectivity [2025]

Stankovic, Sara; Lazic, Andrijana ; Parezanovic, Marina V; Andjelkovic, Marina Z; Ugrin, Milena M; Stevanovic, Milena J ; Pavlovic, Sonja T; Stojiljkovic, Maja M; Klaassen, Kristel M

Chromosomal microarray analysis in children with syndromic short stature [2024]

Maksimović, Nela ; Damnjanović, Tatjana M. ; Jekić, Biljana B. ; Grk, Milka B. ; Dušanović-Pjević, Marija G. ; Đuranović, Ana S. ; Rašić, Milica ; Barzegar, Parsa; El Hayani, Badr; Perović, Dijana

One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans [2017]

Howard, Heidi C.; van, El Carla G.; Forzano, Francesca; Radojković, Dragica ; Rial-Sebbag, Emmanuelle; de, Wert Guido; Borry, Pascal; Cornel, Martina C.