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

Informazioni relative al progetto

STREAMLINE

ID dell’accordo di sovvenzione: 101060201

DOI

10.3030/101060201

Progetto chiuso

Data della firma CE 15 Maggio 2022

Data di avvio 1 Luglio 2022

Data di completamento 30 Giugno 2025

Finanziato da

• Widening participation and spreading excellence

Costo totale

€ 1 162 391,00

Contributo UE

€ 1 162 391,00

Coordinato da

INSTITUT ZA MOLEKULARNU GENETIKU I GENETICKO INZENJERSTVO
Serbia

CORDIS fornisce collegamenti ai risultati finali pubblici e alle pubblicazioni dei progetti ORIZZONTE.

I link ai risultati e alle pubblicazioni dei progetti del 7° PQ, così come i link ad alcuni tipi di risultati specifici come dataset e software, sono recuperati dinamicamente da .OpenAIRE .

Risultati finali

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

Pubblicazioni

Conference proceedings (10)

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

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

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

Autori: Simeunović, Ivana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Kostić, Jovana; Stevanović, Milena
Pubblicato in: 8th Congress of the Serbian Neuroscience Society, 2023
Editore: Serbian Neuroscience Society

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

Autori: Kostić, Jovana; Drakulić, Danijela; Čuturilo, Goran; Petter, Olena; Perić, Mina; Simeunović, Ivana; Harwood J., Adrian; Stevanović, Milena; Kovačević-Grujičić, Nataša
Pubblicato in: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Editore: 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

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

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

Autori: Kostić, Jovana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Simeunović, Ivana; Stevanović, Milena
Pubblicato in: 8th Congress of the Serbian Neuroscience Society, 2023
Editore: 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

Autori: Drakulić, Danijela; Harwood, Adrian; Petrakis, Spyros; Linden, David; Stevanović, Milena
Pubblicato in: VII Congress of the serbian genetic society, 2024
Editore: 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

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

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

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

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

Autori: Lazić, Adrijana; Drakulić, Danijela; Kovačević-Grujičić, Nataša; Perić, Mina; Petrakis, Spyros; Linden, David; Harwood, Adrian; Stevanović, Milena
Pubblicato in: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Editore: 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

Autori: Simeunović, Ivana; Čuturilo, Goran; Kovačević-Grujičić, Nataša; Petter, Olena; Perić, Mina; Kostić, Jovana; Harwood J., Adrian; Stevanović, Milena; Drakulić, Danijela
Pubblicato in: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Editore: 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

Autori: Sylvester, Amy L.; Hensenne, Eva; Ivanov, Dimo; Poser, Benedikt A.; Linden, David E. J.; van Amelsvoort, Thérèse; Vingerhoets, Claudia
Pubblicato in: 2025
Editore: 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

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

Peer reviewed articles (2)

Intranuclear inclusions of polyQ-expanded ATXN1 sequester RNA molecules

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

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

Autori: Marijana Rakonjac, Goran Cuturilo, Natasa Kovacevic-Grujicic, Ivana Simeunovic, Jovana Kostic, Milena Stevanovic, Danijela Drakulic
Pubblicato in: Children, Numero 11, 2024, ISSN 2227-9067
Editore: MDPI AG
DOI: 10.3390/children11040489