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Items: 1 to 20 of 28

1.
A yeast nuclear gene, MRS1, involved in mitochondrial RNA splicing: nucleotide sequence and mutational analysis of two overlapping open reading frames on opposite strands.
J Kreike, M Schulze, F Ahne, B F Lang
EMBO J. 1987 Jul; 6(7): 2123–2129. doi: 10.1002/j.1460-2075.1987.tb02479.x
PMCID:
PMC553604
SummaryPage BrowsePDF–1.4M
2.
Multiple Molecular Mechanisms Cause Reproductive Isolation between Three Yeast Species
Jui-Yu Chou, Yin-Shan Hung, Kuan-Huei Lin, Hsin-Yi Lee, Jun-Yi Leu
PLoS Biol. 2010 Jul; 8(7): e1000432. Published online 2010 Jul 20. doi: 10.1371/journal.pbio.1000432
PMCID:
PMC2907292
AbstractArticlePDF–2.9M
3.
The Mrs1 Splicing Factor Binds the bI3 Group I Intron at Each of Two Tetraloop-Receptor Motifs
Caia D. S. Duncan, Kevin M. Weeks
PLoS One. 2010; 5(2): e8983. Published online 2010 Feb 1. doi: 10.1371/journal.pone.0008983
PMCID:
PMC2813881
AbstractArticlePDF–629K
4.
Recruitment of intron-encoded and co-opted proteins in splicing of the bI3 group I intron RNA
Gurminder S. Bassi, Daniela M. de Oliveira, Malcolm F. White, Kevin M. Weeks
Proc Natl Acad Sci U S A. 2002 Jan 8; 99(1): 128–133. Published online 2002 Jan 2. doi: 10.1073/pnas.012579299
PMCID:
PMC117526
AbstractArticlePDF–204K
5.
A DExH/D-box protein coordinates the two steps of splicing in a group I intron
Abby L. Bifano, Mark G. Caprara
J Mol Biol. Author manuscript; available in PMC 2009 Nov 14.
Published in final edited form as: J Mol Biol. 2008 Nov 14; 383(3): 667–682. Published online 2008 Sep 4. doi: 10.1016/j.jmb.2008.08.070
PMCID:
PMC2643062
AbstractArticlePDF–1.4M
6.
Mne1 Is a Novel Component of the Mitochondrial Splicing Apparatus Responsible for Processing of a COX1 Group I Intron in Yeast
Talina Watts, Oleh Khalimonchuk, Rachel Z. Wolf, Edward M. Turk, Georg Mohr, Dennis R. Winge
J Biol Chem. 2011 Mar 25; 286(12): 10137–10146. Published online 2011 Jan 21. doi: 10.1074/jbc.M110.205625
PMCID:
PMC3060465
AbstractArticlePDF–1.9M
7.
Splicing of Yeast aI5β Group I Intron Requires SUV3 to Recycle MRS1 via Mitochondrial Degradosome-promoted Decay of Excised Intron Ribonucleoprotein (RNP)
Edward M. Turk, Mark G. Caprara
J Biol Chem. 2010 Mar 19; 285(12): 8585–8594. Published online 2010 Jan 11. doi: 10.1074/jbc.M109.090761
PMCID:
PMC2838280
AbstractArticlePDF–5.3M
8.
RSC Chromatin-Remodeling Complex Is Important for Mitochondrial Function in Saccharomyces cerevisiae
Yuko Imamura, Feifei Yu, Misaki Nakamura, Yuhki Chihara, Kyo Okane, Masahiro Sato, Muneyoshi Kanai, Ryoko Hamada, Masaru Ueno, Masashi Yukawa, Eiko Tsuchiya
PLoS One. 2015; 10(6): e0130397. Published online 2015 Jun 18. doi: 10.1371/journal.pone.0130397
PMCID:
PMC4472808
AbstractArticlePDF–1.0M
9.
A chemical-genetic screen to unravel the genetic network of CDC28/CDK1 links ubiquitin and Rad6–Bre1 to cell cycle progression
Christine Zimmermann, Pierre Chymkowitch, Vegard Eldholm, Christopher D. Putnam, Jessica M. Lindvall, Manja Omerzu, Magnar Bjørås, Richard D. Kolodner, Jorrit M. Enserink
Proc Natl Acad Sci U S A. 2011 Nov 15; 108(46): 18748–18753. Published online 2011 Oct 31. doi: 10.1073/pnas.1115885108
PMCID:
PMC3219101
AbstractArticlePDF–1.4M
10.
The ribosome receptors Mrx15 and Mba1 jointly organize cotranslational insertion and protein biogenesis in mitochondria
Braulio Vargas Möller-Hergt, Andreas Carlström, Katharina Stephan, Axel Imhof, Martin Ott
Mol Biol Cell. 2018 Oct 1; 29(20): 2386–2396. doi: 10.1091/mbc.E18-04-0227
PMCID:
PMC6233058
AbstractArticlePDF–2.0M
11.
A nuclear role for the DEAD-box protein Dbp5 in tRNA export
Azra Lari, Arvind Arul Nambi Rajan, Rima Sandhu, Taylor Reiter, Rachel Montpetit, Barry P Young, Chris JR Loewen, Ben Montpetit
eLife. 2019; 8: e48410. Published online 2019 Aug 27. doi: 10.7554/eLife.48410
Correction in:
eLife. 2020; 9: e63264.
PMCID:
PMC6711706
AbstractArticlePDF–3.8M
12.
Proteomics of the Eukaryotic Transcription Machinery: Identification of Proteins Associated with Components of Yeast TFIID by Multidimensional Mass Spectrometry
Steven L. Sanders, Jennifer Jennings, Adrian Canutescu, Andrew J. Link, P. Anthony Weil
Mol Cell Biol. 2002 Jul; 22(13): 4723–4738. doi: 10.1128/MCB.22.13.4723-4738.2002
PMCID:
PMC133885
AbstractArticlePDF–399K
13.
Annotating novel genes by integrating synthetic lethals and genomic information
Daniel Schöner, Markus Kalisch, Christian Leisner, Lukas Meier, Marc Sohrmann, Mahamadou Faty, Yves Barral, Matthias Peter, Wilhelm Gruissem, Peter Bühlmann
BMC Syst Biol. 2008; 2: 3. Published online 2008 Jan 14. doi: 10.1186/1752-0509-2-3
PMCID:
PMC2258006
AbstractArticlePDF–523K
14.
Effect of Sec61 interaction with Mpd1 on endoplasmic reticulum-associated degradation
Fabio Pereira, Mandy Rettel, Frank Stein, Mikhail M. Savitski, Ian Collinson, Karin Römisch
PLoS One. 2019; 14(1): e0211180. Published online 2019 Jan 25. doi: 10.1371/journal.pone.0211180
PMCID:
PMC6347170
AbstractArticlePDF–16M
15.
The proteome of Saccharomyces cerevisiae mitochondria
Albert Sickmann, Jörg Reinders, Yvonne Wagner, Cornelia Joppich, René Zahedi, Helmut E. Meyer, Birgit Schönfisch, Inge Perschil, Agnieszka Chacinska, Bernard Guiard, Peter Rehling, Nikolaus Pfanner, Chris Meisinger
Proc Natl Acad Sci U S A. 2003 Nov 11; 100(23): 13207–13212. Published online 2003 Oct 23. doi: 10.1073/pnas.2135385100
PMCID:
PMC263752
AbstractArticlePDF–694K
16.
Systematic identification of genes involved in metabolic acid stress resistance in yeast and their potential as cancer targets
John J. Shin, Qurratulain Aftab, Pamela Austin, Jennifer A. McQueen, Tak Poon, Shu Chen Li, Barry P. Young, Calvin D. Roskelley, Christopher J. R. Loewen
Dis Model Mech. 2016 Sep 1; 9(9): 1039–1049. doi: 10.1242/dmm.023374
PMCID:
PMC5047693
AbstractArticle
17.
Protein Moonlighting Revealed by Noncatalytic Phenotypes of Yeast Enzymes
Adriana Espinosa-Cantú, Diana Ascencio, Selene Herrera-Basurto, Jiewei Xu, Assen Roguev, Nevan J. Krogan, Alexander DeLuna
Genetics. 2018 Jan; 208(1): 419–431. Published online 2017 Nov 10. doi: 10.1534/genetics.117.300377
PMCID:
PMC5753873
AbstractArticlePDF–1.5M
18.
Integrated multi-omics analyses reveal the pleiotropic nature of the control of gene expression by Puf3p
Christopher J. Kershaw, Joseph L. Costello, David Talavera, William Rowe, Lydia M. Castelli, Paul F. G. Sims, Christopher M. Grant, Mark P. Ashe, Simon J. Hubbard, Graham D. Pavitt
Sci Rep. 2015; 5: 15518. Published online 2015 Oct 23. doi: 10.1038/srep15518
PMCID:
PMC4616039
AbstractArticlePDF–2.2M
19.
The Complete Spectrum of Yeast Chromosome Instability Genes Identifies Candidate CIN Cancer Genes and Functional Roles for ASTRA Complex Components
Peter C. Stirling, Michelle S. Bloom, Tejomayee Solanki-Patil, Stephanie Smith, Payal Sipahimalani, Zhijian Li, Megan Kofoed, Shay Ben-Aroya, Kyungjae Myung, Philip Hieter
PLoS Genet. 2011 Apr; 7(4): e1002057. Published online 2011 Apr 28. doi: 10.1371/journal.pgen.1002057
PMCID:
PMC3084213
AbstractArticlePDF–710K
20.
A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria
Suzanne Hoppins, Sean R. Collins, Ann Cassidy-Stone, Eric Hummel, Rachel M. DeVay, Laura L. Lackner, Benedikt Westermann, Maya Schuldiner, Jonathan S. Weissman, Jodi Nunnari
J Cell Biol. 2011 Oct 17; 195(2): 323–340. doi: 10.1083/jcb.201107053
PMCID:
PMC3198156
AbstractArticlePDF–4.1M

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