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

Información del proyecto

STREAMLINE

Identificador del acuerdo de subvención: 101060201

DOI

10.3030/101060201

Proyecto cerrado

Fecha de la firma de la CE 15 Mayo 2022

Fecha de inicio 1 Julio 2022

Fecha de finalización 30 Junio 2025

Financiado con arreglo a

• Widening participation and spreading excellence

Coste total

€ 1 162 391,00

Aportación de la UE

€ 1 162 391,00

Coordinado por

INSTITUT ZA MOLEKULARNU GENETIKU I GENETICKO INZENJERSTVO
Serbia

CORDIS proporciona enlaces a los documentos públicos y las publicaciones de los proyectos de los programas marco HORIZONTE.

Los enlaces a los documentos y las publicaciones de los proyectos del Séptimo Programa Marco, así como los enlaces a algunos tipos de resultados específicos, como conjuntos de datos y «software», se obtienen dinámicamente de OpenAIRE .

Resultado final

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

Publicaciones

Conference proceedings (10)

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

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

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

Autores: Simeunović, Ivana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Kostić, Jovana; Stevanović, Milena
Publicado en: 8th Congress of the Serbian Neuroscience Society, 2023
Editor: Serbian Neuroscience Society

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

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

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

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

Autores: Kostić, Jovana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Simeunović, Ivana; Stevanović, Milena
Publicado en: 8th Congress of the Serbian Neuroscience Society, 2023
Editor: 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

Autores: Drakulić, Danijela; Harwood, Adrian; Petrakis, Spyros; Linden, David; Stevanović, Milena
Publicado en: VII Congress of the serbian genetic society, 2024
Editor: 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

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

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

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

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

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

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

Autores: Sylvester, Amy L.; Hensenne, Eva; Ivanov, Dimo; Poser, Benedikt A.; Linden, David E. J.; van Amelsvoort, Thérèse; Vingerhoets, Claudia
Publicado en: 2025
Editor: 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

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

Peer reviewed articles (2)

Intranuclear inclusions of polyQ-expanded ATXN1 sequester RNA molecules

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

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

Autores: Marijana Rakonjac, Goran Cuturilo, Natasa Kovacevic-Grujicic, Ivana Simeunovic, Jovana Kostic, Milena Stevanovic, Danijela Drakulic
Publicado en: Children, Edición 11, 2024, ISSN 2227-9067
Editor: MDPI AG
DOI: 10.3390/children11040489