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Luisa Di Stefano

Researcher at Harvard University

Publications -  19
Citations -  2538

Luisa Di Stefano is an academic researcher from Harvard University. The author has contributed to research in topics: Chromatin & Transcription factor. The author has an hindex of 13, co-authored 17 publications receiving 2338 citations. Previous affiliations of Luisa Di Stefano include European Institute of Oncology & Centre national de la recherche scientifique.

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Journal ArticleDOI

Identification of Functional Elements and Regulatory Circuits by Drosophila modENCODE

Sushmita Roy, +95 more
- 24 Dec 2010 - 
TL;DR: The Drosophila Encyclopedia of DNA Elements (modENCODE) project as mentioned in this paper has been used to map transcripts, histone modifications, chromosomal proteins, transcription factors, replication proteins and intermediates, and nucleosome properties across a developmental time course and in multiple cell lines.
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E2F1 represses β-catenin transcription and is antagonized by both pRB and CDK8

TL;DR: By retaining RB1 and amplifying CDK8, colorectal tumour cells select conditions that collectively suppress E2F1 and enhance the activity of β-catenin.
Journal ArticleDOI

E2F7, a novel E2F featuring DP‐independent repression of a subset of E2F‐regulated genes

TL;DR: E2F7 is a unique repressor of a subset of E2F target genes whose products are required for cell cycle progression and inhibition of E 2F7 expression results in specific derepression of these promoters.
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A SIRT1-LSD1 Corepressor Complex Regulates Notch Target Gene Expression and Development

TL;DR: A SIRT1 corepressor complex containing the histone H3K4 demethylase LSD1/KDM1A and several other LSD1-associated proteins is described, offering new insights into conserved mechanisms of epigenetic gene repression and regulation of development by Sirt1 in metazoans.
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Characterization of E2F8, a novel E2F-like cell-cycle regulated repressor of E2F-activated transcription.

TL;DR: Data suggest that E2F8 has an important role in turning of the expression of E 2F-target genes in the S-phase of the cell cycle, as well as a role for repressing E2f transcriptional activity.