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Vinay V. Eapen

Researcher at Brandeis University

Publications -  25
Citations -  6133

Vinay V. Eapen is an academic researcher from Brandeis University. The author has contributed to research in topics: DNA damage & Autophagy. The author has an hindex of 15, co-authored 22 publications receiving 5499 citations. Previous affiliations of Vinay V. Eapen include Harvard University.

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DNA damage checkpoint triggers autophagy to regulate the initiation of anaphase.

TL;DR: It is found that hyperactivation of the cytoplasm-to-vacuole (CVT) autophagy pathway causes the permanent G2/M arrest of cells with a single DSB that is reflected in the nuclear exclusion of both Esp1 and Pds1.
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Respiratory Supercomplexes Promote Mitochondrial Efficiency and Growth in Severely Hypoxic Pancreatic Cancer.

TL;DR: Investigating how PDAC cells survive in the near absence of oxygen finds that PDAC cell lines grow robustly in oxygen tensions down to 0.1%, maintaining mitochondrial morphology, membrane potential, and the oxidative metabolic activity required for the synthesis of key metabolites for proliferation.
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Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

Daniel J. Klionsky, +2522 more
- 01 Jan 2016 - 
TL;DR: Author(s): Klionsky, DJ; Abdelmohsen, K; Abe, A; Abedin, MJ; Abeliovich, H; A Frozena, AA; Adachi, H, Adeli, K, Adhihetty, PJ; Adler, SG; Agam, G; Agarwal, R; Aghi, MK; Agnello, M; Agostinis, P; Aguilar, PV; Aguirre-Ghis
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Proteomic Analysis Identifies Ribosome Reduction as an Effective Proteotoxic Stress Response

TL;DR: The results suggest that a major source of toxicity of trivalent arsenic derives from misfolding of newly synthesized proteins and identifies ribosome reduction as a rapid, effective, and reversible proteotoxic stress response.
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A pathway of targeted autophagy is induced by DNA damage in budding yeast

TL;DR: It is demonstrated that global genotoxic damage or even a single unrepaired double-strand break (DSB) initiates a previously undescribed and selective pathway of autophagy that is referred to as genotoxin-induced targeted Autophagy (GTA), which is distinct from starvation-induced autophagic pathways.