The proteomics of quiescent and nonquiescent cell differentiation in yeast stationary-phase cultures. - Wikidata - thesis-toulmin - TriplyDB

The proteomics of quiescent and nonquiescent cell differentiation in yeast stationary-phase cultures.

The proteomics of quiescent and nonquiescent cell differentiation in yeast stationary-phase cultures.

http://www.wikidata.org/entity/Q33810828

about

Amino acid homeostasis and chronological longevity in Saccharomyces cerevisiae The Stationary-Phase Cells of Saccharomyces cerevisiae Display Dynamic Actin Filaments Required for Processes Extending Chronological Life Span.SOD1 integrates signals from oxygen and glucose to repress respiration.Xbp1 directs global repression of budding yeast transcription during the transition to quiescence and is important for the longevity and reversibility of the quiescent state Spatial reorganization of telomeres in long-lived quiescent cells.Dressed to impress: impact of environmental adaptation on the Candida albicans cell wall Transcriptional profiling of a yeast colony provides new insight into the heterogeneity of multicellular fungal communities Similar environments but diverse fates: Responses of budding yeast to nutrient deprivation Adaptive Roles of SSY1 and SIR3 During Cycles of Growth and Starvation in Saccharomyces cerevisiae Populations Enriched for Quiescent or Nonquiescent Cells.Identification of a small molecule yeast TORC1 inhibitor with a multiplex screen based on flow cytometry Yeast colonies: a model for studies of aging, environmental adaptation, and longevity.Tor1 regulates protein solubility in Saccharomyces cerevisiae.PKA isoforms coordinate mRNA fate during nutrient starvation.Stratification of yeast cells during chronological aging by size points to the role of trehalose in cell vitality A Whole Genome Screen for Minisatellite Stability Genes in Stationary-Phase Yeast Cells Filamentation of Metabolic Enzymes in Saccharomyces cerevisiae.Key events during the transition from rapid growth to quiescence in budding yeast require posttranscriptional regulators.Predicting complex phenotype-genotype interactions to enable yeast engineering: Saccharomyces cerevisiae as a model organism and a cell factory.Differentiated cytoplasmic granule formation in quiescent and non-quiescent cells upon chronological aging Uncoupling reproduction from metabolism extends chronological lifespan in yeast.Molecular mechanisms linking the evolutionary conserved TORC1-Sch9 nutrient signalling branch to lifespan regulation in Saccharomyces cerevisiae.Aging and differentiation in yeast populations: elders with different properties and functions.Sociobiology of the budding yeast.Quasi-programmed aging of budding yeast: a trade-off between programmed processes of cell proliferation, differentiation, stress response, survival and death defines yeast lifespan.Quantitative proteomic comparison of stationary/G0 phase cells and tetrads in budding yeast.Proliferation/Quiescence: When to start? Where to stop? What to stock?Feasibility of protein turnover studies in prototroph Saccharomyces cerevisiae strains.Proliferation/quiescence: the controversial "aller-retour".Endoplasmic reticulum-associated degradation (ERAD) and free oligosaccharide generation in Saccharomyces cerevisiae.A multiple network learning approach to capture system-wide condition-specific responses.Increased lignocellulosic inhibitor tolerance of Saccharomyces cerevisiae cell populations in early stationary phase.Gearing up for survival - HSP-containing granules accumulate in quiescent cells and promote survival.Caloric restriction extends yeast chronological lifespan via a mechanism linking cellular aging to cell cycle regulation, maintenance of a quiescent state, entry into a non-quiescent state and survival in the non-quiescent state.Modified MuDPIT separation identified 4488 proteins in a system-wide analysis of quiescence in yeast.Preferential Ty1 retromobility in mother cells and nonquiescent stationary phase cells is associated with increased concentrations of total Gag or processed Gag and is inhibited by exposure to a high concentration of calcium.Lso2 is a conserved ribosome-bound protein required for translational recovery in yeast

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P2860

The proteomics of quiescent and nonquiescent cell differentiation in yeast stationary-phase cultures.

http://www.wikidata.org/entity/Q33810828

description

2011 nî lūn-bûn

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2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2011 թվականի փետրվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

The proteomics of quiescent an ...... ast stationary-phase cultures.

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The proteomics of quiescent an ...... ast stationary-phase cultures.

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The proteomics of quiescent an ...... ast stationary-phase cultures.

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The proteomics of quiescent an ...... ast stationary-phase cultures.

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MBC.E10-06-0499

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Molecular Biology of the Cell

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The proteomics of quiescent an ...... east stationary-phase cultures

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Bruce Edwards

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Chris P Allen

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Elaine E Manzanilla

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George S Davidson

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Larry Sklar

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Margaret Werner-Washburne

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Mark Carter

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Melissa R Wilson

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Osorio Meirelles

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Phillip H Tapia

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P2860

Structure, function and regulation of the vacuolar (H+)-ATPase

Noise in gene expression: origins, consequences, and control.

The molecular chaperone Hsp90 plays a role in the assembly and maintenance of the 26S proteasome

Global analysis of protein localization in budding yeast.

Toward the complete yeast mitochondrial proteome: multidimensional separation techniques for mitochondrial proteomics.

Functional profiling of the Saccharomyces cerevisiae genome

Genes determining yeast replicative life span in a long-lived genetic background.

Deletion of the phosphoglucose isomerase structural gene makes growth and sporulation glucose dependent in Saccharomyces cerevisiae.

Lipid rafts function in biosynthetic delivery of proteins to the cell surface in yeast.

Cloning and disruption of a gene required for growth on acetate but not on ethanol: the acetyl-coenzyme A synthetase gene of Saccharomyces cerevisiae.

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988-998

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10.1091/MBC.E10-06-0499

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7

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22

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21289090

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3069023

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