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Sonia Vanina Forcales

Researcher at University of Barcelona

Publications -  22
Citations -  2205

Sonia Vanina Forcales is an academic researcher from University of Barcelona. The author has contributed to research in topics: Chromatin & Cellular differentiation. The author has an hindex of 13, co-authored 19 publications receiving 2026 citations. Previous affiliations of Sonia Vanina Forcales include Sanford-Burnham Institute for Medical Research & Sapienza University of Rome.

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Studying arrhythmogenic right ventricular dysplasia with patient-specific iPSCs

TL;DR: This study is the first to demonstrate that induction of adult-like metabolism has a critical role in establishing an adult-onset disease model using patient-specific iPSCs, and revealed crucial pathogenic insights that metabolic derangement in adult- like metabolic milieu underlies ARVD/C pathologies, enabling us to propose novel disease-modifying therapeutic strategies.
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p38 pathway targets SWI-SNF chromatin-remodeling complex to muscle-specific loci.

TL;DR: An unexpected function of differentiation-activated p38 is identified in converting external cues into chromatin modifications at discrete loci, by selectively targeting SWI-SNF to muscle-regulatory elements.
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TNF/p38α/Polycomb Signaling to Pax7 Locus in Satellite Cells Links Inflammation to the Epigenetic Control of Muscle Regeneration

TL;DR: An inflammation-activated signaling in muscle stem (satellite) cells is identified, by which the polycomb repressive complex 2 (PRC2) represses Pax7 expression during muscle regeneration, establishing the biological link between p38/ PRC2 signaling to Pax7 and satellite cell decision to proliferate or differentiate.
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p38-dependent phosphorylation of the mRNA decay-promoting factor KSRP controls the stability of select myogenic transcripts.

TL;DR: It is demonstrated that p38 alpha and beta isoforms also control muscle-gene expression posttranscriptionally, by stabilizing critical myogenic transcripts, by establishing a biochemical link between differentiation-activated p38 signaling and turnover of myogenic mRNAs.