Browsing eNauka

Browsing by Author Čuturilo, Goran

Showing results 1 to 16 of 16
Issue DateTitleAuthor(s)TypeМp-cat.
2019Analiza govorno-jezičkog, socio-emocionalnog i kognitivnog razvoja bolesnika sa heterozigotnom mikrodelecijom regiona q11.2 na hromozomu 22Rakonjac, MarijanaDoctoral theses
70M70
2022Detekcija i karakterizacija genomskih abnormalnosti kod novorođenčadi sa kritično teškim urođenim srčanim manamaMiletić, AleksandraDoctoral theses
70M70
2025Establishment and characterization of induced pluripotent stem cells from patients with 22q11.2 Duplication SyndromeKovačević-Grujičić, Nataša  ; Kostić, Jovana  ; Drakulić, Danijela  ; Perić, Mina  ; Simeunović, Ivana  ; Čuturilo, Goran; Petter, Olena; Harwood, Adrian; Stevanović, Milena  Conference Paper
Mp. category will be shown later
2025Establishment of a patient-derived induced pluripotent stem cells with 22q11.2 microdeletion: a model system for studying neurodevelopmental disordersDrakulić, Danijela  ; Kovačević-Grujičić, Nataša  ; Perić, Mina  ; Petter, Olena; Simeunović, Ivana  ; Kostić, Jovana  ; Čuturilo, Goran; Harwood, Adrian; Stevanović, Milena  Conference Paper
Mp. category will be shown later
2024Establishment of induced pluripotent stem cells derived from patients with 22q11.2 microdeletion as a tool for studying neurodevelopmental disordersSimeunović, Ivana  ; Čuturilo, Goran; Kovačević-Grujičić, Nataša  ; Petter, Olena; Perić, Mina  ; Kostić, Jovana  ; Stanisavljević Ninković, Danijela  ; Harwood, Adrian; Stevanović, Milena  ; Drakulić, Danijela  Конференцијски рад
Мп категорија ће бити приказана накнадно.
2023Establishment of induced pluripotent stem cells from patients with 22q11.2 duplication syndrome as a model system for studying neurodevelopmental disordersKostić, Jovana  ; Drakulić, Danijela  ; Čuturilo, Goran; Petter, Olena; Perić, Mina  ; Simeunović, Ivana  ; Harwood J., Adrian; Stevanović, Milena  ; Kovačević-Grujičić, Nataša  Конференцијски рад
Мп категорија ће бити приказана накнадно.
2025Expression of miR-185 during neural differentiation of induced pluripotent stem cells from patients with 22q11.2 Deletion SyndromeStanisavljević Ninković, Danijela  ; Simeunović, Ivana  ; Drakulić, Danijela  ; Kovačević-Grujičić, Nataša  ; Perić, Mina  ; Kostić, Jovana  ; Čuturilo, Goran; Petter, Olena; Harwood, Adrian; Stevanović, Milena  Конференцијски рад
Мп категорија ће бити приказана накнадно.
2023Generation of induced pluripotent stem cells derived from patients with 22q11.2 deletion syndrome as a tool for studying neurodevelopmental disordersSimeunović, Ivana  ; Čuturilo, Goran; Kovačević-Grujičić, Nataša  ; Petter, Olena; Perić, Mina  ; Kostić, Jovana  ; Harwood J., Adrian; Stevanović, Milena  ; Drakulić, Danijela  Конференцијски рад
Мп категорија ће бити приказана накнадно.
2024Generation of induced pluripotent stem cells from patients with 22q11.2 Duplication Syndrome as an in vitro model system for exploring neurodevelopmental disordersKostić, Jovana  ; Čuturilo, Goran; Drakulić, Danijela  ; Petter, Olena; Perić, Mina  ; Simeunović, Ivana  ; Stanisavljević Ninković, Danijela  ; Harwood, Adrian J.; Stevanović, Milena  ; Kovačević-Grujicić, Nataša  Conference Paper
Mp. category will be shown later
2011Komparativna studija molekularnog i molekularno-citogenetičkog pristupa u analizi mikrodelecije 22q11.2 kod bolesnika sa sindromatskim formama urođenih srčanih manaČuturilo, GoranDoctoral theses
70M70
2009Muvat-Vilsonov sindrom : prikaz bolesnikaČuturilo, Goran; Stefanović, Igor; Jovanović, Ida; Miletić-Grković, Slobodanka; Novaković, Ivana  Article
24M24
2024PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS WITH 22Q11.2 MICRODELETION: A MODEL SYSTEM FOR INVESTIGATING NEURODEVELOPMENTAL DISORDERSimeunović, Ivana  ; Čuturilo, Goran; Kovačević-Grujičić, Nataša  ; Petter, Olena; Perić, Mina  ; Kostić, Jovana  ; Stanisavljević Ninković, Danijela  ; Harwood J., Adrian; Stevanović, Milena  ; Drakulić, Danijela  Conference Paper
Mp. category will be shown later
2008Prenatal growth retardation, microcephaly, and eye coloboma in infant with multiple congenital anomalies - further delineation of presumed new dysmorphic syndromeČuturilo, Goran; Jovanović, Ida; Vukomanović, Goran; Đukić, Milan  ; Stefanović, Igor; Atanasković-Marković, Marina  Article
22M22
2024Psychological difficulties of parents of children with a rare genetic disorders: the contribution of intolerance of uncertainty, intolerance of distress and tendency towards worryČuturilo, Goran; Vukosavljević-Gvozden, Tatjana  ; Vukašinović, Nađa; Gvozden, Matija  Conference Paper
Mp. category will be shown later
2025Transcriptomic profiling of iPSC-derived astrocytes from patients with 22q11.2 deletion syndromeSimeunović, Ivana  ; Kovačević-Grujičić, Nataša  ; Perić, Mina  ; Petter, Olena; Ehrhart, Friederike; Kostić, Jovana  ; Lazić, Stefan  ; Čuturilo, Goran; de Nijs, Laurence; Linden, David;
Harwood, Adrian; Stevanović, Milena  ; Drakulić, Danijela  ;
Conference Paper
Mp. category will be shown later
2016Uticaj ginekoloških faktora na hematopoezni potencijal umbilikalne krviŠkorić, Dejan; Milovanović, Ivan; Sinđić, Marina; Čuturilo, GoranConference Paper
Mp. category will be shown later