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Items: 1 to 20 of 44

1.
A Nonlinear Mixed Effects Approach for Modeling the Cell-To-Cell Variability of Mig1 Dynamics in Yeast
Joachim Almquist, Loubna Bendrioua, Caroline Beck Adiels, Mattias Goksör, Stefan Hohmann, Mats Jirstrand
PLoS One. 2015; 10(4): e0124050. Published online 2015 Apr 20. doi: 10.1371/journal.pone.0124050
Correction in:
PLoS One. 2015; 10(6): e0131657.
PMCID:
PMC4404321
AbstractArticlePDF–2.6M
2.
Environment-specific combinatorial cis-regulation in synthetic promoters
Jason Gertz, Barak A Cohen
Mol Syst Biol. 2009; 5: 244. Published online 2009 Feb 17. doi: 10.1038/msb.2009.1
PMCID:
PMC2657533
AbstractArticlePDF–1.7M
3.
Combinatorial control of gene expression by the three yeast repressors Mig1, Mig2 and Mig3
Jakub Orzechowski Westholm, Niklas Nordberg, Eva Murén, Adam Ameur, Jan Komorowski, Hans Ronne
BMC Genomics. 2008; 9: 601. Published online 2008 Dec 16. doi: 10.1186/1471-2164-9-601
PMCID:
PMC2631581
AbstractArticlePDF–395K
4.
Analysis of the mechanism by which glucose inhibits maltose induction of MAL gene expression in Saccharomyces.
Z Hu, Y Yue, H Jiang, B Zhang, P W Sherwood, C A Michels
Genetics. 2000 Jan; 154(1): 121–132. doi: 10.1093/genetics/154.1.121
PMCID:
PMC1460925
SummaryPDF–198K
5.
The catalytic efficiency of yeast ribonuclease III depends on substrate specific product release rate
Marc-Andre Comeau, Daniel A. Lafontaine, Sherif Abou Elela
Nucleic Acids Res. 2016 Sep 19; 44(16): 7911–7921. Published online 2016 Jun 1. doi: 10.1093/nar/gkw507
PMCID:
PMC5027489
AbstractArticlePDF–2.9M
6.
Yeast importin-β is required for nuclear import of the Mig2 repressor
Alejandra Fernández-Cid, Montserrat Vega, Pilar Herrero, Fernando Moreno
BMC Cell Biol. 2012; 13: 31. Published online 2012 Nov 6. doi: 10.1186/1471-2121-13-31
PMCID:
PMC3531251
AbstractArticlePDF–1.4M
7.
Regulation of conditional gene expression by coupled transcription repression and RNA degradation
Mathieu Lavoie, Dongling Ge, Sherif Abou Elela
Nucleic Acids Res. 2012 Jan; 40(2): 871–883. Published online 2011 Sep 20. doi: 10.1093/nar/gkr759
PMCID:
PMC3258148
AbstractArticlePDF–1.8M
8.
Two zinc-finger-containing repressors are responsible for glucose repression of SUC2 expression.
L L Lutfiyya, M Johnston
Mol Cell Biol. 1996 Sep; 16(9): 4790–4797. doi: 10.1128/mcb.16.9.4790
PMCID:
PMC231480
SummaryPDF–939K
9.
Characterization of three related glucose repressors and genes they regulate in Saccharomyces cerevisiae.
L L Lutfiyya, V R Iyer, J DeRisi, M J DeVit, P O Brown, M Johnston
Genetics. 1998 Dec; 150(4): 1377–1391. doi: 10.1093/genetics/150.4.1377
PMCID:
PMC1460414
SummaryPDF–523K
10.
Mutations in SIN4 and RGR1 Cause Constitutive Expression of MAL Structural Genes in Saccharomyces cerevisiae
Xin Wang, Corinne A. Michels
Genetics. 2004 Oct; 168(2): 747–757. doi: 10.1534/genetics.104.029611
PMCID:
PMC1448850
AbstractArticlePDF–197K
11.
A putative bet hedging strategy buffers budding yeast against environmental instability
Laura E. Bagamery, Quincey A. Justman, Ethan C. Garner, Andrew W. Murray
Curr Biol. Author manuscript; available in PMC 2021 Dec 7.
Published in final edited form as: Curr Biol. 2020 Dec 7; 30(23): 4563–4578.e4. Published online 2020 Sep 24. doi: 10.1016/j.cub.2020.08.092
PMCID:
PMC7726042
AbstractArticlePDF–1.9M
12.
Snf1 AMPK positively regulates ER-phagy via expression control of Atg39 autophagy receptor in yeast ER stress response
Tomoaki Mizuno, Kei Muroi, Kenji Irie
PLoS Genet. 2020 Sep; 16(9): e1009053. Published online 2020 Sep 28. doi: 10.1371/journal.pgen.1009053
PMCID:
PMC7544123
AbstractArticlePDF–2.7M
13.
The β subunit of yeast AMP-activated protein kinase directs substrate specificity in response to alkaline stress
Dakshayini G. Chandrashekarappa, Rhonda R. McCartney, Allyson F. O’Donnell, Martin C. Schmidt
Cell Signal. Author manuscript; available in PMC 2017 Dec 1.
Published in final edited form as: Cell Signal. 2016 Dec; 28(12): 1881–1893. Published online 2016 Aug 31. doi: 10.1016/j.cellsig.2016.08.016
PMCID:
PMC5067241
AbstractArticlePDF–2.8M
14.
Expression of GUT1, which encodes glycerol kinase in Saccharomyces cerevisiae, is controlled by the positive regulators Adr1p, Ino2p and Ino4p and the negative regulator Opi1p in a carbon source-dependent fashion.
M Grauslund, J M Lopes, B Rønnow
Nucleic Acids Res. 1999 Nov 15; 27(22): 4391–4398. doi: 10.1093/nar/27.22.4391
PMCID:
PMC148721
SummaryPDF–411K
15.
Repressors and Upstream Repressing Sequences of the Stress-Regulated ENA1 Gene in Saccharomyces cerevisiae: bZIP Protein Sko1p Confers HOG-Dependent Osmotic Regulation
Markus Proft, Ramón Serrano
Mol Cell Biol. 1999 Jan; 19(1): 537–546. doi: 10.1128/mcb.19.1.537
PMCID:
PMC83911
AbstractArticlePDF–789K
16.
The Filamentous Growth MAPK Pathway Responds to Glucose Starvation Through the Mig1/2 Transcriptional Repressors in Saccharomyces cerevisiae
Sheelarani Karunanithi, Paul J. Cullen
Genetics. 2012 Nov; 192(3): 869–887. doi: 10.1534/genetics.112.142661
PMCID:
PMC3522164
AbstractArticlePDF–5.4M
17.
Regulatory Network Connecting Two Glucose Signal Transduction Pathways in Saccharomyces cerevisiae
Aneta Kaniak, Zhixiong Xue, Daniel Macool, Jeong-Ho Kim, Mark Johnston
Eukaryot Cell. 2004 Feb; 3(1): 221–231. doi: 10.1128/EC.3.1.221-231.2004
PMCID:
PMC329515
AbstractArticlePDF–675K
18.
A glucose-starvation response governs endocytic trafficking and eisosomal retention of surface cargoes in budding yeast
Kamilla M. E. Laidlaw, Daniel D. Bisinski, Sviatlana Shashkova, Katherine M. Paine, Malaury A. Veillon, Mark C. Leake, Chris MacDonald
J Cell Sci. 2021 Jan 15; 134(2): jcs257733. Published online 2021 Jan 25. doi: 10.1242/jcs.257733
PMCID:
PMC7860119
AbstractArticle
19.
Distributed and dynamic intracellular organization of extracellular information
Alejandro A. Granados, Julian M. J. Pietsch, Sarah A. Cepeda-Humerez, Iseabail L. Farquhar, Gašper Tkačik, Peter S. Swain
Proc Natl Acad Sci U S A. 2018 Jun 5; 115(23): 6088–6093. Published online 2018 May 21. doi: 10.1073/pnas.1716659115
PMCID:
PMC6003323
AbstractArticlePDF–1.3M
20.
Association of improved oxidative stress tolerance and alleviation of glucose repression with superior xylose-utilization capability by a natural isolate of Saccharomyces cerevisiae
Cheng Cheng, Rui-Qi Tang, Liang Xiong, Ronald E. Hector, Feng-Wu Bai, Xin-Qing Zhao
Biotechnol Biofuels. 2018; 11: 28. Published online 2018 Feb 5. doi: 10.1186/s13068-018-1018-y
PMCID:
PMC5798184
AbstractArticlePDF–2.2M

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