Datasets

Latest additions:
2026-07-22
15:20
[DZNE-2026-00776] Dataset
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Dataset: Replication files for: Identifying Multi-omics Signatures that characterize Responders to Plant-based Dietary Interventions, v1.0
Zenodo () [10.5281/zenodo.17535871]
This repository contains original unprocessed data and code for the replication of our paper Identifying Multi-omics Signatures that characterize Responders to Plant-based Dietary Interventions..

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2026-07-22
15:13
[DZNE-2026-00775] Dataset
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Dataset: Replication files for: Identifying Multi-omics Signatures that characterize Responders to Plant-based Dietary Interventions, v2
Zenodo () [10.5281/zenodo.20546705]
This repository contains original unprocessed data and code for the replication of our paper Identifying Multi-omics Signatures that characterize Responders to Plant-based Dietary Interventions from a Randomized Trial..

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2026-07-07
13:01
[DZNE-2026-00681] Dataset
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Dataset: Hnrnpa1 is essential for early zebrafish development and lipid metabolism
Gene Expression Omnibus ()
RNA binding proteins have multiple diverse cellular functions and are often mis- regulated in disease. Despite their many cellular functions and implications in disease, very little is known about their physiological functions. [...]
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2026-06-23
14:59
[DZNE-2026-00666] Dataset
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Dataset: The retrotransposable element-silencing factor Daxx controls microglia identity and function in the adult brain
Gene Expression Omnibus ()
Death domain-associated protein (Daxx) is one of the two main H3.3 chaperones in mammalian cells and acts as key repressor of RTEs of viral origin. In present study, we found that Daxx is an IFN-stimulated gene mediating repression of RTEs and IFN-stimulated genes (ISGs) upon inflammatory stimuli in microglia. [...]
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2026-06-23
14:57
[DZNE-2026-00665] Dataset
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Dataset: The retrotransposable element-silencing factor Daxx controls microglia identity and function in the adult brain
Gene Expression Omnibus ()
Death domain-associated protein (Daxx) is one of the two main H3.3 chaperones in mammalian cells and acts as key repressor of RTEs of viral origin. In the present study, we found that Daxx is an IFN-stimulated gene mediating repression of RTEs and IFN-stimulated genes (ISGs) upon inflammatory stimuli in microglia. [...]
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2026-06-23
14:55
[DZNE-2026-00664] Dataset
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Dataset: The retrotransposable element-silencing factor Daxx controls microglia identity and function in the adult brain [RNA-seq]
Gene Expression Omnibus ()
Death domain-associated protein (Daxx) is one of the two main H3.3 chaperones in mammalian cells and acts as key repressor of RTEs of viral origin. In present study, we found that Daxx is an IFN-stimulated gene mediating repression of RTEs and IFN-stimulated genes (ISGs) upon inflammatory stimuli in microglia. [...]
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2026-06-23
14:53
[DZNE-2026-00663] Dataset
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Dataset: The retrotransposable element-silencing factor Daxx controls microglia identity and function in the adult brain [ATAC-seq]
Gene Expression Omnibus ()
Death domain-associated protein (Daxx) is one of the two main H3.3 chaperones in mammalian cells and acts as key repressor of RTEs of viral origin. In present study, we found that Daxx is an IFN-stimulated gene mediating repression of RTEs and IFN-stimulated genes (ISGs) upon inflammatory stimuli in microglia. [...]
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2026-05-13
11:28
[DZNE-2026-00519] Dataset
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Data from: Microglial motility is modulated by neuronal activity and correlates with dendritic spine plasticity in the hippocampus of awake mice
Dryad () [10.5061/dryad.63xsj3v68]
Microglia, the resident immune cells of the brain, play a complex role in health and disease. They actively survey the brain parenchyma by physically interacting with other cells and structurally shaping the brain. [...]

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2026-05-13
11:26
[DZNE-2026-00518] Dataset
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Dataset: Data from: A human iPSC model of tauopathies engineered for 4R tau isoform expression endogenously develops late-stage neuronal tau pathology
Dryad () [10.5061/dryad.8cz8w9h6g]
Tauopathies, such as Alzheimer’s disease and Frontotemporal Dementia, are common neurodegenerative diseases characterized by misfolding, hyperphosphorylation, and aggregation of Tau. Molecular mechanisms underlying Tauopathies are still poorly understood, in part due to a lack of human models endogenously developing major disease hallmarks. [...]

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2026-05-13
11:22
[DZNE-2026-00517] Dataset
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Dataset: Supplemental Material, Marchetti Giovanni and Gaia Tavosanis, Manuscript submitted to Current Biology, 2017, v3
Mendeley () [10.17632/x6xdc297bc.3]
Supplemental material for manuscript submitted to Current Biology, 2017..

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