scispace - formally typeset
N

Nazif Maqani

Researcher at University of Virginia

Publications -  13
Citations -  477

Nazif Maqani is an academic researcher from University of Virginia. The author has contributed to research in topics: Saccharomyces cerevisiae & Cohesin. The author has an hindex of 8, co-authored 13 publications receiving 413 citations. Previous affiliations of Nazif Maqani include University of Virginia Health System.

Papers
More filters
Journal ArticleDOI

A Microarray-Based Genetic Screen for Yeast Chronological Aging Factors

TL;DR: The identification of multiple novel effectors of yeast chronological lifespan will greatly aid in the elucidation of mechanisms that cells and organisms utilize in slowing down the aging process.
Journal ArticleDOI

The NEF4 Complex Regulates Rad4 Levels and Utilizes Snf2/Swi2-Related ATPase Activity for Nucleotide Excision Repair

TL;DR: A complex system for globally regulating repair activity in vivo by controlling turnover of Rad4 is suggested, and genetic analysis uncovered new interactions between NEF4 and Rad23, a repair factor that links repair to proteasome function.
Journal ArticleDOI

Caloric Restriction Extends Yeast Chronological Life Span by Optimizing the Snf1 (AMPK) Signaling Pathway.

TL;DR: It is concluded that CR maximizes Snf1 activity throughout and beyond the diauxic shift, thus optimizing the coordination of nucleocytosolic acetyl-CoA production with massive reorganization of the transcriptome and respiratory metabolism.
Journal ArticleDOI

Calorie restriction effects on silencing and recombination at the yeast rDNA

TL;DR: It is shown that in contrast to previous reports, Sir2 is not stimulated by CR to strengthen silencing of multiple reporter genes in the rDNA of S. cerevisiae, and CR does modestly reduce the frequency of rDNA recombination, although in a SIR2‐independent manner.
Journal ArticleDOI

Isonicotinamide enhances Sir2 protein-mediated silencing and longevity in yeast by raising intracellular NAD+ concentration.

TL;DR: This study determined that isonicotinamide (INAM) stimulates Sir2 through an additional mechanism in vivo, which involves elevation of the intracellular NAD+ concentration, and provides evidence suggesting that INAM influences the expression of multiple NAD+ biosynthesis and salvage pathways to promote homeostasis during stationary phase.