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Browsing by Author Linden, David
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | 22q11.2 Deletion syndrome as a tool for modelling and research of neurodevelopmental disorders | Lazić, Adrijana; Drakulić, Danijela   ; Kovačević-Grujičić, Nataša ; Perić, Mina ; Petrakis, Spyros; Linden, David; Harwood, Adrian; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2024 | ESTABLISHMENT OF A MODEL SYSTEM FOR STUDYING NEURODEVELOPMENTAL DISORDERS USING INDUCED PLURIPOTENT STEM CELLS DERIVED FROM PATIENTS WITH 22Q11.2 DELETION SYNDROME | Drakulić, Danijela ; Harwood, Adrian; Petrakis, Spyros; Linden, David; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2023 | "Mindds-Connect" - Federated Data Sharing Platform for Neurodevelopmental Disorders and Rare Genetic Mutations | Mihaljevic, Marina; Huremagic, Benjamin; Harwood, Janet; Jorge, Paola; Teles, Natalia; Novakowska, Beata; Vandeweyer, Geert; Drakulic, Danijela ; Van, Amelsvoort Therese; Linden, David;
Straccia, Marco; Vermeersch, Joris; Harwood, Adrian;
| Conference Paper | Mp. category will be shown later |
| 2024 | STREAMLINE HUB: a high capacity hub for research of neurodevelopmental disorders in the Western Balkan region | Drakulić, Danijela ; Petrakis, Spyros; Harwood, Adrian J.; Linden, David; Lazić, Andrijana ; Kovačević-Grujičić, Nataša ; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2025 | Transcriptomic profiling of iPSC-derived astrocytes from patients with 22q11.2 deletion syndrome | Simeunović, 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 ; | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |