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Items: 1 to 20 of 38

1.

Nuclear translocation of Gln3 in response to nutrient signals requires Golgi-to-endosome trafficking in Saccharomyces cerevisiae.

Puria R, Zurita-Martinez SA, Cardenas ME.

Proc Natl Acad Sci U S A. 2008 May 20;105(20):7194-9. doi: 10.1073/pnas.0801087105. Epub 2008 Apr 28.

2.

Tor pathway control of the nitrogen-responsive DAL5 gene bifurcates at the level of Gln3 and Gat1 regulation in Saccharomyces cerevisiae.

Georis I, Tate JJ, Cooper TG, Dubois E.

J Biol Chem. 2008 Apr 4;283(14):8919-29. doi: 10.1074/jbc.M708811200. Epub 2008 Feb 1.

3.

TOR regulation of AGC kinases in yeast and mammals.

Jacinto E, Lorberg A.

Biochem J. 2008 Feb 15;410(1):19-37. doi: 10.1042/BJ20071518. Review.

PMID:
18215152
4.
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6.

Cell growth control: little eukaryotes make big contributions.

De Virgilio C, Loewith R.

Oncogene. 2006 Oct 16;25(48):6392-415. Review.

PMID:
17041625
8.

Rapamycin activates Tap42-associated phosphatases by abrogating their association with Tor complex 1.

Yan G, Shen X, Jiang Y.

EMBO J. 2006 Aug 9;25(15):3546-55. Epub 2006 Jul 27.

9.

Ammonia-specific regulation of Gln3 localization in Saccharomyces cerevisiae by protein kinase Npr1.

Tate JJ, Rai R, Cooper TG.

J Biol Chem. 2006 Sep 22;281(38):28460-9. Epub 2006 Jul 24.

11.

Retrograde response to mitochondrial dysfunction is separable from TOR1/2 regulation of retrograde gene expression.

Giannattasio S, Liu Z, Thornton J, Butow RA.

J Biol Chem. 2005 Dec 30;280(52):42528-35. Epub 2005 Oct 27.

12.

Methionine sulfoximine treatment and carbon starvation elicit Snf1-independent phosphorylation of the transcription activator Gln3 in Saccharomyces cerevisiae.

Tate JJ, Rai R, Cooper TG.

J Biol Chem. 2005 Jul 22;280(29):27195-204. Epub 2005 May 23. Erratum in: J Biol Chem. 2007 Apr 27;282(17):13139.

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15.

Nutrient signaling through TOR kinases controls gene expression and cellular differentiation in fungi.

Rohde JR, Cardenas ME.

Curr Top Microbiol Immunol. 2004;279:53-72. Review.

PMID:
14560951
16.

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. Epub 2003 Jul 25.

18.

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.

19.

Domains of Gln3p interacting with karyopherins, Ure2p, and the target of rapamycin protein.

Carvalho J, Zheng XF.

J Biol Chem. 2003 May 9;278(19):16878-86. Epub 2003 Mar 5.

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