Partitioning the transcriptional program induced by rapamycin among the effectors of the Tor proteins (Q73342523)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137008%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Partitioning the transcriptional program induced by rapamycin among the effectors of the Tor proteins (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137008%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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A F Shamji

1

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3 November 2019

F G Kuruvilla

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137008%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

S L Schreiber

series ordinal

3

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3 November 2019

publication date

1 December 2000

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3 November 2019

language of work or name

0 references

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3 November 2019

volume

10

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3 November 2019

issue

24

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3 November 2019

page(s)

1574-1581

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3 November 2019

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Chemistry and Biology of the Immunophilins and Their Immunosuppressive Ligands

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Targets for Cell Cycle Arrest by the Immunosuppressant Rapamycin in Yeast

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Structure of the FKBP12-rapamycin complex interacting with the binding domain of human FRAP

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TOR controls translation initiation and early G1 progression in yeast

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FKBP12-Rapamycin-associated Protein (FRAP) Autophosphorylates at Serine 2481 under Translationally Repressive Conditions

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Rapamycin-modulated transcription defines the subset of nutrient-sensitive signaling pathways directly controlled by the Tor proteins

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The TOR signaling cascade regulates gene expression in response to nutrients

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Nitrogen catabolite repression in Saccharomyces cerevisiae

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The GLN3 gene product is required for transcriptional activation of allantoin system gene expression in Saccharomyces cerevisiae

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The URE2 gene product of Saccharomyces cerevisiae plays an important role in the cellular response to the nitrogen source and has homology to glutathione s-transferases

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The TOR signalling pathway controls nuclear localization of nutrient-regulated transcription factors

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Tripartite regulation of Gln3p by TOR, Ure2p, and phosphatases

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Mechanism of metabolic control. Target of rapamycin signaling links nitrogen quality to the activity of the Rtg1 and Rtg3 transcription factors

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The 14-3-3 proteins positively regulate rapamycin-sensitive signaling

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Nutrients, via the Tor proteins, stimulate the association of Tap42 with type 2A phosphatases

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Tor proteins and protein phosphatase 2A reciprocally regulate Tap42 in controlling cell growth in yeast

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Regulation of ribosome biogenesis by the rapamycin-sensitive TOR-signaling pathway in Saccharomyces cerevisiae

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Exploring the Metabolic and Genetic Control of Gene Expression on a Genomic Scale

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Rapamycin Induces the G0 Program of Transcriptional Repression in Yeast by Interfering with the TOR Signaling Pathway

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Signalling between mitochondria and the nucleus regulates the expression of a new D-lactate dehydrogenase activity in yeast

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A transcriptional switch in the expression of yeast tricarboxylic acid cycle genes in response to a reduction or loss of respiratory function

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Lys80p ofSaccharomyces cerevisiae, previously proposed as a specific repressor ofLYS genes, is a pleiotropic regulatory factor identical to Mks1p

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Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137008%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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