The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging. - Wikidata - awgldk - TriplyDB

The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

http://www.wikidata.org/entity/Q37041325

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Lessons from C. elegans: signaling pathways for longevity Alpha-Ketoglutarate: Physiological Functions and Applications Long live FOXO: unraveling the role of FOXO proteins in aging and longevity A Genetic Cascade of let-7-ncl-1-fib-1 Modulates Nucleolar Size and rRNA Pool in Caenorhabditis elegans HIF-1 modulates dietary restriction-mediated lifespan extension via IRE-1 in Caenorhabditis elegans The Drosophila FoxA ortholog Fork head regulates growth and gene expression downstream of Target of rapamycin Lifespan-extending effects of royal jelly and its related substances on the nematode Caenorhabditis elegans ETS-4 is a transcriptional regulator of life span in Caenorhabditis elegans Manipulation of behavioral decline in Caenorhabditis elegans with the Rag GTPase raga-1 Genome-wide identification of binding sites defines distinct functions for Caenorhabditis elegans PHA-4/FOXA in development and environmental response Mechanisms of aging-related proteinopathies in Caenorhabditis elegans Transcriptional and epigenetic regulation of autophagy in aging TOR signaling and rapamycin influence longevity by regulating SKN-1/Nrf and DAF-16/FoxO Haploinsufficiency of akt1 prolongs the lifespan of mice C. elegans S6K Mutants Require a Creatine-Kinase-like Effector for Lifespan Extension Global Proteomics Analysis of the Response to Starvation in C. elegans RVB1/RVB2: running rings around molecular biology.A metabolic signature of long life in Caenorhabditis elegans A two-tiered compensatory response to loss of DNA repair modulates aging and stress response pathways.Dynamic chromatin organization during foregut development mediated by the organ selector gene PHA-4/FoxA Açai palm fruit (Euterpe oleracea Mart.) pulp improves survival of flies on a high fat diet Genetic variation in neurodegenerative diseases and its accessibility in the model organism Caenorhabditis elegans.The new biology of ageing.With TOR, less is more: a key role for the conserved nutrient-sensing TOR pathway in aging drr-2 encodes an eIF4H that acts downstream of TOR in diet-restriction-induced longevity of C. elegans.Dietary restriction and aging, 2009.Germline signaling mediates the synergistically prolonged longevity produced by double mutations in daf-2 and rsks-1 in C. elegans.RNAi screening implicates a SKN-1-dependent transcriptional response in stress resistance and longevity deriving from translation inhibition.The metabolite α-ketoglutarate extends lifespan by inhibiting ATP synthase and TOR.Expression profile of Caenorhabditis elegans mutant for the Werner syndrome gene ortholog reveals the impact of vitamin C on development to increase life span.The general control nonderepressible-2 kinase mediates stress response and longevity induced by target of rapamycin inactivation in Caenorhabditis elegans Role of TOR signaling in aging and related biological processes in Drosophila melanogaster Converging pathways in lifespan regulation A Krüppel-like factor downstream of the E3 ligase WWP-1 mediates dietary-restriction-induced longevity in Caenorhabditis elegans.Autophagy and lipid metabolism coordinately modulate life span in germline-less C. elegans.S6K links cell fate, cell cycle and nutrient response in C. elegans germline stem/progenitor cells Intestinal apical polarity mediates regulation of TORC1 by glucosylceramide in C. elegans The nucleolus of Caenorhabditis elegans.Mitochondrial deficiency: a double-edged sword for aging and neurodegeneration.Mondo complexes regulate TFEB via TOR inhibition to promote longevity in response to gonadal signals

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The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

http://www.wikidata.org/entity/Q37041325

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on September 2008

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

@en

The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

@nl

type

label

The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

@en

The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

@nl

prefLabel

The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

@en

The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging.

@nl

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J.CUB.2008.07.097

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Current Biology

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The Target of Rapamycin pathway antagonizes pha-4/FoxA to control development and aging

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Karyn L Sheaffer

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P2860

The foxa2 gene controls the birth and spontaneous degeneration of dopamine neurons in old age

Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action

A dynamic scaffold of pre-snoRNP factors facilitates human box C/D snoRNP assembly

Statistics review 12: survival analysis

Whole-genome analysis of temporal gene expression during foregut development

New genes tied to endocrine, metabolic, and dietary regulation of lifespan from a Caenorhabditis elegans genomic RNAi screen.

Long-term starvation and ageing induce AGE-1/PI 3-kinase-dependent translocation of DAF-16/FOXO to the cytoplasm

A role for autophagy in the extension of lifespan by dietary restriction in C. elegans

TOR signaling in growth and metabolism

Systematic functional analysis of the Caenorhabditis elegans genome using RNAi

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1355-1364

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scholarly article

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10.1016/J.CUB.2008.07.097

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18

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Dustin L Updike

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2008-09-01T00:00:00Z

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23269311

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