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Yacine Graba

Researcher at Aix-Marseille University

Publications -  17
Citations -  5586

Yacine Graba is an academic researcher from Aix-Marseille University. The author has contributed to research in topics: Hox gene & Autophagy. The author has an hindex of 7, co-authored 16 publications receiving 5085 citations.

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Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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The emerging role of acetylation in the regulation of autophagy

TL;DR: How previously identified histone acetylases and deacetylases modify key autophagic effector proteins are summarized and discussed, and how this has an impact on physiological and pathological cellular processes are discussed.
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Cellular and molecular insights into Hox protein action.

TL;DR: The molecular and cellular scale mechanisms underlying the diverse roles of the Hox transcription factors during morphogenesis and organogenesis are discussed.
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Hox Proteins Mediate Developmental and Environmental Control of Autophagy

TL;DR: It is shown that Drosophila Hox proteins are potent repressors of the autophagic process, and that temporality is controlled by Pontin, a facultative component of the Brahma chromatin remodeling complex, which indicates that regulation of autophagy is an evolutionary conserved feature of H Cox proteins.
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The Hox proteins Ubx and AbdA collaborate with the transcription pausing factor M1BP to regulate gene transcription

TL;DR: Linking transcription factors, PcG proteins and paused Pol II states, these data identify a two‐step mechanism of Hox‐driven transcription, with M1BP binding leading to Pol II recruitment followed by AbdA targeting, which results in a change in the chromatin landscape and enhanced transcription.