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Stefania Dell'Orso

Researcher at National Institutes of Health

Publications -  38
Citations -  2568

Stefania Dell'Orso is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Biology & Gene. The author has an hindex of 17, co-authored 25 publications receiving 1606 citations. Previous affiliations of Stefania Dell'Orso include United States Department of Energy Office of Science.

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The NAD+-Dependent SIRT1 Deacetylase Translates a Metabolic Switch into Regulatory Epigenetics in Skeletal Muscle Stem Cells

TL;DR: It is reported that during the transition from quiescence to proliferation, skeletal muscle stem cells experience a metabolic switch from fatty acid oxidation to glycolysis, revealing how metabolic cues can be mechanistically translated into epigenetic modifications that regulate skeletal muscle cell biology.
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Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease.

TL;DR: Using a genotype-driven approach, this disorder is identified that connects seemingly unrelated adult-onset inflammatory syndromes and is named the VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome.
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eRNAs Promote Transcription by Establishing Chromatin Accessibility at Defined Genomic Loci

TL;DR: The data suggest that eRNAs contribute to establishing a cell-type-specific transcriptional circuitry by directing chromatin-remodeling events by regulating genomic access of the transcriptional complex to defined regulatory regions.
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Polycomb EZH2 controls self-renewal and safeguards the transcriptional identity of skeletal muscle stem cells

TL;DR: It is reported that EZH2, the enzymatic subunit of the Polycomb-repressive complex 2 (PRC2), is expressed in both Pax7+/Myf5⁻ stem cells and Pax7/My f5+ committed myogenic precursors and is required for homeostasis of the adult SC pool.
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Single cell analysis of adult mouse skeletal muscle stem cells in homeostatic and regenerative conditions

TL;DR: Single cell RNA sequencing of adult muscle stem cells and primary myoblasts from homeostatic or regenerating muscles identifies distinct clusters of cell types with partially overlapping but distinct transcriptional signatures.