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| Home > Publications Database > Dataset: RNA-seq of human post-mortem brain tissue of the frontal lobe from patients with FTD and healthy controls > print |
| 001 | 279466 | ||
| 005 | 20250710100949.0 | ||
| 037 | _ | _ | |a DZNE-2025-00793 |
| 100 | 1 | _ | |a Menden, Kevin |0 P:(DE-2719)2812499 |b 0 |
| 245 | _ | _ | |a Dataset: RNA-seq of human post-mortem brain tissue of the frontal lobe from patients with FTD and healthy controls |
| 260 | _ | _ | |c 2023 |b ArrayExpress |
| 336 | 7 | _ | |a MISC |2 BibTeX |
| 336 | 7 | _ | |a Dataset |b dataset |m dataset |0 PUB:(DE-HGF)32 |s 1752049801_18333 |2 PUB:(DE-HGF) |
| 336 | 7 | _ | |a Chart or Table |0 26 |2 EndNote |
| 336 | 7 | _ | |a Dataset |2 DataCite |
| 336 | 7 | _ | |a DATA_SET |2 ORCID |
| 336 | 7 | _ | |a ResearchData |2 DINI |
| 520 | _ | _ | |a Understanding the molecular mechanisms underlying frontotemporal dementia (FTD) is essential for the development of successful therapies. Systematic studies on human post-mortem brain tissue of patients with genetic subtypes of FTD are currently lacking. The Risk and Modyfing Factors of Frontotemporal Dementia (RiMod-FTD) consortium therefore has generated multi-omics datasets for genetic subtypes of FTD to identify common and distinct molecular mechanisms disturbed in disease. This experiment contains data from RNA-sequencing of human post-mortem brain tissue of the frontal lobe from patients with FTD caused by mutations in GRN, MAPT or C9orf72 and healthy controls. |
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| 700 | 1 | _ | |a Heutink, Peter |0 P:(DE-2719)2810728 |b 1 |
| 856 | 4 | _ | |u https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-MTAB-12647 |
| 909 | C | O | |o oai:pub.dzne.de:279466 |p VDB |
| 910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 0 |6 P:(DE-2719)2812499 |
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| 980 | _ | _ | |a dataset |
| 980 | _ | _ | |a VDB |
| 980 | _ | _ | |a I:(DE-2719)1040260 |
| 980 | _ | _ | |a UNRESTRICTED |
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