BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 17015442)

  • 21. The TOR signalling pathway controls nuclear localization of nutrient-regulated transcription factors.
    Beck T; Hall MN
    Nature; 1999 Dec; 402(6762):689-92. PubMed ID: 10604478
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Five conditions commonly used to down-regulate tor complex 1 generate different physiological situations exhibiting distinct requirements and outcomes.
    Tate JJ; Cooper TG
    J Biol Chem; 2013 Sep; 288(38):27243-27262. PubMed ID: 23935103
    [TBL] [Abstract][Full Text] [Related]  

  • 23. NPR1 kinase and RSP5-BUL1/2 ubiquitin ligase control GLN3-dependent transcription in Saccharomyces cerevisiae.
    Crespo JL; Helliwell SB; Wiederkehr C; Demougin P; Fowler B; Primig M; Hall MN
    J Biol Chem; 2004 Sep; 279(36):37512-7. PubMed ID: 15247235
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Nuclear Gln3 Import Is Regulated by Nitrogen Catabolite Repression Whereas Export Is Specifically Regulated by Glutamine.
    Rai R; Tate JJ; Shanmuganatham K; Howe MM; Nelson D; Cooper TG
    Genetics; 2015 Nov; 201(3):989-1016. PubMed ID: 26333687
    [TBL] [Abstract][Full Text] [Related]  

  • 25. gln3 mutations dissociate responses to nitrogen limitation (nitrogen catabolite repression) and rapamycin inhibition of TorC1.
    Rai R; Tate JJ; Nelson DR; Cooper TG
    J Biol Chem; 2013 Jan; 288(4):2789-804. PubMed ID: 23223232
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cytoplasmic compartmentation of Gln3 during nitrogen catabolite repression and the mechanism of its nuclear localization during carbon starvation in Saccharomyces cerevisiae.
    Cox KH; Tate JJ; Cooper TG
    J Biol Chem; 2002 Oct; 277(40):37559-66. PubMed ID: 12140287
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Interaction with Tap42 is required for the essential function of Sit4 and type 2A phosphatases.
    Wang H; Wang X; Jiang Y
    Mol Biol Cell; 2003 Nov; 14(11):4342-51. PubMed ID: 14551259
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A domain in the transcription activator Gln3 specifically required for rapamycin responsiveness.
    Rai R; Tate JJ; Shanmuganatham K; Howe MM; Cooper TG
    J Biol Chem; 2014 Jul; 289(27):18999-9018. PubMed ID: 24847055
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Transduction of the nitrogen signal activating Gln3-mediated transcription is independent of Npr1 kinase and Rsp5-Bul1/2 ubiquitin ligase in Saccharomyces cerevisiae.
    Feller A; Boeckstaens M; Marini AM; Dubois E
    J Biol Chem; 2006 Sep; 281(39):28546-54. PubMed ID: 16864574
    [TBL] [Abstract][Full Text] [Related]  

  • 30. GATA Factor Regulation in Excess Nitrogen Occurs Independently of Gtr-Ego Complex-Dependent TorC1 Activation.
    Tate JJ; Georis I; Rai R; Vierendeels F; Dubois E; Cooper TG
    G3 (Bethesda); 2015 May; 5(8):1625-38. PubMed ID: 26024867
    [TBL] [Abstract][Full Text] [Related]  

  • 31. General Amino Acid Control and 14-3-3 Proteins Bmh1/2 Are Required for Nitrogen Catabolite Repression-Sensitive Regulation of Gln3 and Gat1 Localization.
    Tate JJ; Buford D; Rai R; Cooper TG
    Genetics; 2017 Feb; 205(2):633-655. PubMed ID: 28007891
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ammonia regulates VID30 expression and Vid30p function shifts nitrogen metabolism toward glutamate formation especially when Saccharomyces cerevisiae is grown in low concentrations of ammonia.
    van der Merwe GK; Cooper TG; van Vuuren HJ
    J Biol Chem; 2001 Aug; 276(31):28659-66. PubMed ID: 11356843
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Alterations in the Ure2 αCap domain elicit different GATA factor responses to rapamycin treatment and nitrogen limitation.
    Feller A; Georis I; Tate JJ; Cooper TG; Dubois E
    J Biol Chem; 2013 Jan; 288(3):1841-55. PubMed ID: 23184930
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Intranuclear function for protein phosphatase 2A: Pph21 and Pph22 are required for rapamycin-induced GATA factor binding to the DAL5 promoter in yeast.
    Georis I; Tate JJ; Feller A; Cooper TG; Dubois E
    Mol Cell Biol; 2011 Jan; 31(1):92-104. PubMed ID: 20974806
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Roles of URE2 and GLN3 in the proline utilization pathway in Saccharomyces cerevisiae.
    Xu S; Falvey DA; Brandriss MC
    Mol Cell Biol; 1995 Apr; 15(4):2321-30. PubMed ID: 7891726
    [TBL] [Abstract][Full Text] [Related]  

  • 36. PP2A phosphatase activity is required for stress and Tor kinase regulation of yeast stress response factor Msn2p.
    Santhanam A; Hartley A; Düvel K; Broach JR; Garrett S
    Eukaryot Cell; 2004 Oct; 3(5):1261-71. PubMed ID: 15470255
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Multiple Targets on the Gln3 Transcription Activator Are Cumulatively Required for Control of Its Cytoplasmic Sequestration.
    Rai R; Tate JJ; Cooper TG
    G3 (Bethesda); 2016 May; 6(5):1391-408. PubMed ID: 26976442
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Formalin can alter the intracellular localization of some transcription factors in Saccharomyces cerevisiae.
    Tate JJ; Cooper TG
    FEMS Yeast Res; 2008 Dec; 8(8):1223-35. PubMed ID: 19054131
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The TOR-controlled transcription activators GLN3, RTG1, and RTG3 are regulated in response to intracellular levels of glutamine.
    Crespo JL; Powers T; Fowler B; Hall MN
    Proc Natl Acad Sci U S A; 2002 May; 99(10):6784-9. PubMed ID: 11997479
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Multiple roles of Tap42 in mediating rapamycin-induced transcriptional changes in yeast.
    Düvel K; Santhanam A; Garrett S; Schneper L; Broach JR
    Mol Cell; 2003 Jun; 11(6):1467-78. PubMed ID: 12820961
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.