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Sebastiano Sciarretta

Researcher at Sapienza University of Rome

Publications -  238
Citations -  15994

Sebastiano Sciarretta is an academic researcher from Sapienza University of Rome. The author has contributed to research in topics: Autophagy & Medicine. The author has an hindex of 45, co-authored 203 publications receiving 12313 citations. Previous affiliations of Sebastiano Sciarretta include Rutgers University & University of Salerno.

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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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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky, +2983 more
- 08 Feb 2021 - 
TL;DR: In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
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Endogenous Drp1 Mediates Mitochondrial Autophagy and Protects the Heart Against Energy Stress

TL;DR: Investigation of the role of dynamin-related protein 1 (Drp1), a GTPase that mediates mitochondrial fission, in mediating mitochondrial autophagy, ventricular function, and stress resistance in the heart found disruption of Drp1 induces mitochondrial elongation, inhibits mitochondrial autophileagy, and causes mitochondrial dysfunction, thereby promoting cardiac dysfunction and increased susceptibility to ischemia/reperfusion.
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Mst1 inhibits autophagy by promoting the interaction between Beclin1 and Bcl-2

TL;DR: It is suggested that Mst1 coordinately regulates autophagy and apoptosis by phosphorylating Beclin1 and consequently modulating a three-way interaction among Bcl-2 proteins, Becl in1 and Bax.
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A Typical Immune T/B Subset Profile Characterizes Bicuspid Aortic Valve: In an Old Status?

TL;DR: Patients with bicuspid valve disease show a quantitative reduction of T and B lymphocyte cell subsets, and future studies are encouraged to understand the molecular mechanisms underlying this observation and its pathophysiological significance.