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The Gcn4 Transcription Factor Reduces Protein Synthesis Capacity and Extends Yeast Lifespan [RNA-Seq]
PubMed Full text in PMC Similar studies SRA Run Selector
The Gcn4 Transcription Factor Reduces Protein Synthesis Capacity and Extends Yeast Lifespan
PubMed Full text in PMC Similar studies
The Gcn4 Transcription Factor Reduces Protein Synthesis Capacity and Extends Yeast Lifespan [ChIP-Seq]
Ssd1 and Gcn2 suppress global translational efficiency in replicatively aged yeast, while their activation in young cells extends lifespan
Multiomics of GCN4-dependent replicative lifespan extension models reveals Gcn4 as a regulator of protein turnover in yeast
Gcn4 binding in coding regions can activate internal and canonical 5’ promoters in yeast [RNA-seq]
Gcn4 binding in coding regions can activate internal and canonical 5’ promoters in yeast [ChIP-seq]
eIF4F complex dynamics are important for the activation of the integrated stress response
Chemical genomics study of Snf1 as a gene repressor
PubMed Full text in PMC Similar studies Analyze with GEO2R
Time-course expression data during assurance of the chronological longevity by caloric restriction in budding yeast
PubMed Similar studies Analyze with GEO2R
Fhl1 and lfh1 ChIP-chip
Genome-wide nucleosome position maps in Saccharomyces cerevisiae
The role of Sgf73 occupancy
CAN1 Arginine Permease Deficiency Extends Yeast Replicative Lifespan via Translational Activation of Stress Response Genes
The specific DNA sequence recognized by the yeast transcription factor Gcn4 is sufficient to predict high-affinity binding on a genome-wide scale
Genome-wide Ifh1p occupancy at the OX growth phase and RC quiescent phase of the yeast metabolic cycle
Binding data for nine transcription factors for S. cerevisiae salt response
Deficiency of the RNA-binding protein Cth2 extends yeast replicative lifespan by alleviating its repressive effects on mitochondrial function
Chronological Aging of Yeast in the Absence of Caloric Restriction: Cell Immobilization Uncouples Reproduction from Metabolism
A ribosome assembly stress response regulates transcription to maintain proteome homeostasis
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