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Gabriel G. Perrone

Researcher at University of Sydney

Publications -  35
Citations -  2293

Gabriel G. Perrone is an academic researcher from University of Sydney. The author has contributed to research in topics: Saccharomyces cerevisiae & Glutathione. The author has an hindex of 20, co-authored 35 publications receiving 2139 citations. Previous affiliations of Gabriel G. Perrone include University of Western Sydney & University of Manchester.

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Complex cellular responses to reactive oxygen species

TL;DR: Genome-wide analyses of yeast provide insight into cellular responses to reactive oxygen species (ROS), but no one oxidant is representative of 'oxidative stress' despite the widespread use of a single compound such as H(2)O(2).
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Reactive oxygen species and yeast apoptosis.

TL;DR: The nature of the ROS involved, the damage they cause to cells, the responses of S. cerevisiae to ROS are summarised, and those aspects in which ROS affect cell integrity that may be relevant to the apoptotic process are discussed.
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The yeast Saccharomyces cerevisiae contains two glutaredoxin genes that are required for protection against reactive oxygen species.

TL;DR: Grx1 and Grx2 function differently in the cell, and it is suggested that glutaredoxins may act as one of the primary defenses against mixed disulfides formed following oxidative damage to proteins.
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Glutathione and catalase provide overlapping defenses for protection against hydrogen peroxide in the yeast Saccharomyces cerevisiae

TL;DR: There are two lines of evidence that indicate catalases are required in the absence of GSH; firstly, strains that lack both catalase A and T accumulate increased levels of oxidized glutathione following treatment with hydrogen peroxide; and secondly, deletion ofCatalase genes exacerbates the hydrogen perox sensitivity of glr1 and gsh1 mutants.
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Genetic basis of arsenite and cadmium tolerance in Saccharomyces cerevisiae.

TL;DR: In this article, a genome-wide screening of the Saccharomyces cerevisiae haploid and homozygous diploid deletion mutant collections was carried out to gain insight into metal action and cellular tolerance mechanisms.