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Davide Ruggero

Researcher at University of California, San Francisco

Publications -  118
Citations -  20361

Davide Ruggero is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Translation (biology) & EIF4E. The author has an hindex of 49, co-authored 111 publications receiving 17167 citations. Previous affiliations of Davide Ruggero include Fox Chase Cancer Center & University of Bologna.

Papers
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Journal ArticleDOI

ERα is an RNA-binding protein sustaining tumor cell survival and drug resistance.

TL;DR: In this article, the authors show that ERα RNA binding function is uncoupled from its activity to bind DNA and critical for breast cancer progression, and they also show ERα-associated mRNAs sustain cancer cell fitness and elicit cellular responses to stress.
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Enhanced MET translation and signaling sustains K-Ras driven proliferation under anchorage-independent growth conditions

TL;DR: The results indicate that enhanced Met expression and signaling is essential for anchorage-independent growth of K-Ras mutant cancer cells and suggests that pharmacological inhibitors of Met could be effective for K- Ras mutant tumor patients.
Patent

MTOR Modulators and Uses Thereof

TL;DR: In this paper, the authors provide methods and compositions for selective modulation of certain protein kinases, and especially mTor complexes, which are particularly useful in inhibiting mTor selectively for therapeutic applications.
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Parallel measurement of dynamic changes in translation rates in single cells

TL;DR: This study has developed a reporter system to measure real-time changes of translation rates in human or mouse individual cells by conjugating translation regulatory motifs to sequences encoding a nuclear targeted fluorescent protein and a controllable destabilization domain.
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Nuclear TARBP2 Drives Oncogenic Dysregulation of RNA Splicing and Decay.

TL;DR: Using xenograft mouse models, it is found that TARBP2 affects tumor growth in the lung and that this is dependent on TarBP2-mediated destabilization of ABCA3 and FOXN3 and ZNF143 is established as an upstream regulator of TAR BP2 expression.