Strengthening regional stem cells based research for advancement of multi modal innovative strategy for modelling neurodevelopmental disorders

Informacje na temat projektu

STREAMLINE

Identyfikator umowy o grant: 101060201

DOI

10.3030/101060201

Projekt został zamknięty

Data podpisania przez KE 15 Maja 2022

Data rozpoczęcia 1 Lipca 2022

Data zakończenia 30 Czerwca 2025

Finansowanie w ramach

• Widening participation and spreading excellence

Koszt całkowity

€ 1 162 391,00

Wkład UE

€ 1 162 391,00

Koordynowany przez

INSTITUT ZA MOLEKULARNU GENETIKU I GENETICKO INZENJERSTVO
Serbia

CORDIS oferuje możliwość skorzystania z odnośników do publicznie dostępnych publikacji i rezultatów projektów realizowanych w ramach programów ramowych HORYZONT.

Odnośniki do rezultatów i publikacji związanych z poszczególnymi projektami 7PR, a także odnośniki do niektórych konkretnych kategorii wyników, takich jak zbiory danych i oprogramowanie, są dynamicznie pobierane z systemu OpenAIRE .

Rezultaty

Documents, reports (6)

Data Management Plan developed
Risk list created
Dissemination, exploitation and communication plan created

Report on dissemination exploitation and communication plan

First report on virtual trainings by experts from partner institutions

Report on virtual trainings by experts from partner institutions

Project management handbook developed
First report on short-term staff exchanges and workshops

Report on shortterm staff exchanges and workshops

Websites, patent fillings, videos etc. (1)

Launch of the Project's motto and logos and the Project's website

Launch of the Projects motto and logos and the Projects website

Publikacje

Conference proceedings (10)

PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS WITH 22Q11.2 MICRODELETION: A MODEL SYSTEM FOR INVESTIGATING NEURODEVELOPMENTAL DISORDER

Autorzy: Simeunović, Ivana; Čuturilo, Goran; Kovačević-Grujičić, Nataša; Petter, Olena; Perić, Mina; Kostić, Jovana; Stanisavljević Ninković, Danijela; Harwood J., Adrian; Stevanović, Milena; Drakulić, Danijela
Opublikowane w: VII Congress of the serbian genetic society, 2024
Wydawca: Serbian Genetic Society

Analysis of cohort of patients with 22q11.2 deletion syndrome - a single-center experience from Serbia

Autorzy: Simeunović, Ivana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Kostić, Jovana; Stevanović, Milena
Opublikowane w: 8th Congress of the Serbian Neuroscience Society, 2023
Wydawca: Serbian Neuroscience Society

Establishment of induced pluripotent stem cells from patients with 22q11.2 duplication syndrome as a model system for studying neurodevelopmental disorders

Autorzy: Kostić, Jovana; Drakulić, Danijela; Čuturilo, Goran; Petter, Olena; Perić, Mina; Simeunović, Ivana; Harwood J., Adrian; Stevanović, Milena; Kovačević-Grujičić, Nataša
Opublikowane w: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Wydawca: Institute of Molecular Genetics and Genetic Engineering (IMGGE), University of Belgrade

STREAMLINE HUB: a high capacity hub for research of neurodevelopmental disorders in the Western Balkan region

Autorzy: Drakulić, Danijela; Petrakis, Spyros; Harwood, Adrian J.; Linden, David; Lazić, Andrijana; Kovačević-Grujičić, Nataša; Stevanović, Milena
Opublikowane w: Hemijska industrija (Chemical Industry), 2024
Wydawca: Association of Chemical Engineers of Serbia

Genomic and clinical findings in patients with 22q11.2 duplication syndrome

Autorzy: Kostić, Jovana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Simeunović, Ivana; Stevanović, Milena
Opublikowane w: 8th Congress of the Serbian Neuroscience Society, 2023
Wydawca: Serbian Neuroscience Society

ESTABLISHMENT OF A MODEL SYSTEM FOR STUDYING NEURODEVELOPMENTAL DISORDERS USING INDUCED PLURIPOTENT STEM CELLS DERIVED FROM PATIENTS WITH 22Q11.2 DELETION SYNDROME

Autorzy: Drakulić, Danijela; Harwood, Adrian; Petrakis, Spyros; Linden, David; Stevanović, Milena
Opublikowane w: VII Congress of the serbian genetic society, 2024
Wydawca: Serbian Genetic Society

Application of principal component analysis (PCA) and analytical hierarchy process (AHP) in analysis of articulatory characteristics of phonemes of children with 22q11.2 Deletion Syndrome

Autorzy: Drakulić, Danijela; Rakonjac, Marijana; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Kušić-Tišma, Jelena; Morić, Ivana; Zukić, Branka; Stevanović, Milena
Opublikowane w: 4th Belgrade Bioinformatics Conference, 2023
Wydawca: Institute of Molecular Genetics and Genetic Engineering, University of Belgrade

CHARACTERIZATION OF INDUCED PLURIPOTENT STEM CELLS FROM PATIENTS WITH 22Q11.2 DUPLICATION SYNDROME

Autorzy: Kostić, Jovana; Cuturilo, Goran; Drakulić, Danijela; Petter, Olena; Perić, Mina; Simeunović, Ivana; Stanisavljević Ninković, Danijela; Harwood J., Adrian; Stevanović, Milena; Kovačević-Grujicić, Nataša
Opublikowane w: VII Congress of the serbian genetic society, 2024
Wydawca: Serbian Genetic Society

22q11.2 Deletion syndrome as a tool for modelling and research of neurodevelopmental disorders

Autorzy: Lazić, Adrijana; Drakulić, Danijela; Kovačević-Grujičić, Nataša; Perić, Mina; Petrakis, Spyros; Linden, David; Harwood, Adrian; Stevanović, Milena
Opublikowane w: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Wydawca: Institute of Molecular Genetics and Genetic Engineering (IMGGE), University of Belgrade

Generation of induced pluripotent stem cells derived from patients with 22q11.2 deletion syndrome as a tool for studying neurodevelopmental disorders

Autorzy: Simeunović, Ivana; Čuturilo, Goran; Kovačević-Grujičić, Nataša; Petter, Olena; Perić, Mina; Kostić, Jovana; Harwood J., Adrian; Stevanović, Milena; Drakulić, Danijela
Opublikowane w: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Wydawca: Institute of Molecular Genetics and Genetic Engineering (IMGGE), University of Belgrade

Other (2)

Additional file 1 of Neural excitation/inhibition imbalance and neurodevelopmental pathology in human copy number variant syndromes: a systematic review

Autorzy: Sylvester, Amy L.; Hensenne, Eva; Ivanov, Dimo; Poser, Benedikt A.; Linden, David E. J.; van Amelsvoort, Thérèse; Vingerhoets, Claudia
Opublikowane w: 2025
Wydawca: BioMed Central Ltd
DOI: 10.6084/M9.FIGSHARE.29276451.V1

Neural excitation/inhibition imbalance and neurodevelopmental pathology in human copy number variant syndromes: a systematic review

Autorzy: Sylvester, Amy L.; Hensenne, Eva; Ivanov, Dimo; Poser, Benedikt A.; Linden, David E. J.; van Amelsvoort, Therese; Vingerhoets, Claudia
Opublikowane w: Journal of Neurodevelopmental Disorders, 2025
Wydawca: BioMed Central Ltd
DOI: 10.1186/S11689-025-09614-8

Peer reviewed articles (2)

Intranuclear inclusions of polyQ-expanded ATXN1 sequester RNA molecules

Autorzy: Ioannis Gkekas, Aimilia-Christina Vagiona, Nikolaos Pechlivanis, Georgia Kastrinaki, Katerina Pliatsika, Sebastian Iben, Konstantinos Xanthopoulos, Fotis E. Psomopoulos, Miguel A. Andrade-Navarro, Spyros Petrakis
Opublikowane w: Frontiers in Molecular Neuroscience, Numer 16, 2023, ISSN 1662-5099
Wydawca: Frontiers Media SA
DOI: 10.3389/FNMOL.2023.1280546

Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 Microdeletion

Autorzy: Marijana Rakonjac, Goran Cuturilo, Natasa Kovacevic-Grujicic, Ivana Simeunovic, Jovana Kostic, Milena Stevanovic, Danijela Drakulic
Opublikowane w: Children, Numer 11, 2024, ISSN 2227-9067
Wydawca: MDPI AG
DOI: 10.3390/children11040489