DNA methylome, R-loop and clinical exome profiling of patients with sporadic amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the death of motor neurons, the aetiology of which is essentially unknown. Here, we present an integrative epigenomic study in blood samples from seven clinically characterised sporadic ALS patients to elucida...
Elmentve itt :
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| Dokumentumtípus: | Cikk |
| Megjelent: |
2024
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| Sorozat: | SCIENTIFIC DATA
11 No. 1 |
| Tárgyszavak: | |
| doi: | 10.1038/s41597-024-02985-y |
| mtmt: | 34534306 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/37555 |
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| 024 | 7 | |a 34534306 |2 mtmt | |
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| 100 | 1 | |a Feró Orsolya | |
| 245 | 1 | 0 | |a DNA methylome, R-loop and clinical exome profiling of patients with sporadic amyotrophic lateral sclerosis |h [elektronikus dokumentum] / |c Feró Orsolya |
| 260 | |c 2024 | ||
| 300 | |a 12 | ||
| 490 | 0 | |a SCIENTIFIC DATA |v 11 No. 1 | |
| 520 | 3 | |a Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the death of motor neurons, the aetiology of which is essentially unknown. Here, we present an integrative epigenomic study in blood samples from seven clinically characterised sporadic ALS patients to elucidate molecular factors associated with the disease. We used clinical exome sequencing (CES) to study DNA variants, DNA-RNA hybrid immunoprecipitation sequencing (DRIP-seq) to assess R-loop distribution, and reduced representation bisulfite sequencing (RRBS) to examine DNA methylation changes. The above datasets were combined to create a comprehensive repository of genetic and epigenetic changes associated with the ALS cases studied. This repository is well-suited to unveil new correlations within individual patients and across the entire patient cohort. The molecular attributes described here are expected to guide further mechanistic studies on ALS, shedding light on the underlying genetic causes and facilitating the development of new epigenetic therapies to combat this life-threatening disease. | |
| 650 | 4 | |a Klinikai orvostan | |
| 700 | 0 | 1 | |a Varga Dóra |e aut |
| 700 | 0 | 1 | |a Nagy Éva |e aut |
| 700 | 0 | 1 | |a Karányi Zsolt |e aut |
| 700 | 0 | 1 | |a Sipos Éva |e aut |
| 700 | 0 | 1 | |a Engelhardt József |e aut |
| 700 | 0 | 1 | |a Török Nóra |e aut |
| 700 | 0 | 1 | |a Balogh István |e aut |
| 700 | 0 | 1 | |a Vető Borbála |e aut |
| 700 | 0 | 1 | |a Likó István |e aut |
| 700 | 0 | 1 | |a Fóthi Ábel |e aut |
| 700 | 0 | 1 | |a Szabó Zoltán |e aut |
| 700 | 0 | 1 | |a Halmos Gábor |e aut |
| 700 | 0 | 1 | |a Vécsei László |e aut |
| 700 | 0 | 1 | |a Arányi Tamás |e aut |
| 700 | 0 | 1 | |a Székvölgyi Lóránt |e aut |
| 856 | 4 | 0 | |u http://publicatio.bibl.u-szeged.hu/37555/1/FeroOrsolya_DNAmethylomeR-loopandclinicalexomeprofilingofpatientswithsporadicamyotrophiclateralsclerosis_41597_2024_Article_2985.pdf |z Dokumentum-elérés |