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Items: 19

1.
Casein kinase 1 is required for efficient removal of Rec8 during meiosis I
Cornelia Rumpf, Lubos Cipak, Andrej Dudas, Zsigmond Benko, Miroslava Pozgajova, Christian G Riedel, Gustav Ammerer, Karl Mechtler, Juraj Gregan
Cell Cycle. 2010 Jul 1; 9(13): 2657–2662. Published online 2010 Jul 1. doi: 10.4161/cc.9.13.12146
PMCID:
PMC3083834
AbstractArticlePDF–834K
2.
Characterization of two protein kinases from Schizosaccharomyces pombe involved in the regulation of DNA repair.
N Dhillon, M F Hoekstra
EMBO J. 1994 Jun 15; 13(12): 2777–2788. doi: 10.1002/j.1460-2075.1994.tb06571.x
PMCID:
PMC395157
SummaryPage BrowsePDF–3.3M
3.
The kinase domain of CK1 enzymes contains the localization cue essential for compartmentalized signaling at the spindle pole
Zachary C. Elmore, Rodrigo X. Guillen, Kathleen L. Gould
Mol Biol Cell. 2018 Jul 1; 29(13): 1664–1674. doi: 10.1091/mbc.E18-02-0129
PMCID:
PMC6080649
AbstractArticlePDF–3.0M
4.
Casein Kinase 1 Regulates Sterol Regulatory Element-binding Protein (SREBP) to Control Sterol Homeostasis
Rita T. Brookheart, Chih-Yung S. Lee, Peter J. Espenshade
J Biol Chem. 2014 Jan 31; 289(5): 2725–2735. Published online 2013 Dec 10. doi: 10.1074/jbc.M113.511899
PMCID:
PMC3908405
AbstractArticlePDF–1.3M
5.
Budding and fission yeast casein kinase I isoforms have dual-specificity protein kinase activity.
M F Hoekstra, N Dhillon, G Carmel, A J DeMaggio, R A Lindberg, T Hunter, J Kuret
Mol Biol Cell. 1994 Aug; 5(8): 877–886. doi: 10.1091/mbc.5.8.877
PMCID:
PMC301108
SummaryPage BrowsePDF–2.1M
6.
AMPKα Subunit Ssp2 and Glycogen Synthase Kinases Gsk3/Gsk31 are involved in regulation of sterol regulatory element-binding protein (SREBP) activity in fission yeast
Hao Miao, Qiannan Liu, Guanglie Jiang, Wen Zhang, Kun Liu, Xiang Gao, Yujie Huo, Si Chen, Toshiaki Kato, Norihiro Sakamoto, Takayoshi Kuno, Yue Fang
PLoS One. 2020; 15(2): e0228845. Published online 2020 Feb 13. doi: 10.1371/journal.pone.0228845
PMCID:
PMC7018046
AbstractArticlePDF–1.5M
7.
Casein Kinase 1 and Phosphorylation of Cohesin Subunit Rec11 (SA3) Promote Meiotic Recombination through Linear Element Formation
Naina Phadnis, Lubos Cipak, Silvia Polakova, Randy W. Hyppa, Ingrid Cipakova, Dorothea Anrather, Lucia Karvaiova, Karl Mechtler, Gerald R. Smith, Juraj Gregan
PLoS Genet. 2015 May; 11(5): e1005225. Published online 2015 May 20. doi: 10.1371/journal.pgen.1005225
Correction in:
PLoS Genet. 2015 Jun; 11(6): e1005343.
PMCID:
PMC4439085
AbstractArticlePDF–1.7M
8.
Dialogue between centrosomal entrance and exit scaffold pathways regulates mitotic commitment
Kuan Yoow Chan, Marisa Alonso-Nuñez, Agnes Grallert, Kayoko Tanaka, Yvonne Connolly, Duncan L. Smith, Iain M. Hagan
J Cell Biol. 2017 Sep 4; 216(9): 2795–2812. doi: 10.1083/jcb.201702172
PMCID:
PMC5584178
AbstractArticlePDF–3.2M
9.
Characterisation of Schizosaccharomyces pombe rad31, a UBA-related gene required for DNA damage tolerance.
M Shayeghi, C L Doe, M Tavassoli, F Z Watts
Nucleic Acids Res. 1997 Mar 15; 25(6): 1162–1169. doi: 10.1093/nar/25.6.1162
PMCID:
PMC146553
SummaryPDF–221K
10.
Mitotic spindle formation in the absence of Polo kinase
Juyoung Kim, Gohta Goshima
Proc Natl Acad Sci U S A. 2022 Mar 22; 119(12): e2114429119. Published online 2022 Mar 14. doi: 10.1073/pnas.2114429119
PMCID:
PMC8944928
AbstractArticlePDF–3.1M
11.
CK1 is required for a mitotic checkpoint that delays cytokinesis
Alyssa E. Johnson, Jun-Song Chen, Kathleen L. Gould
Curr Biol. Author manuscript; available in PMC 2014 Oct 7.
Published in final edited form as: Curr Biol. 2013 Oct 7; 23(19): 1920–1926. Published online 2013 Sep 19. doi: 10.1016/j.cub.2013.07.077
PMCID:
PMC4078987
AbstractArticlePDF–1.0M
12.
Expanded Interactome of the Intrinsically Disordered Protein Dss1
Signe M. Schenstrøm, Caio A. Rebula, Michael H. Tatham, Ruth Hendus-Altenburger, Isabelle Jourdain, Ronald T. Hay, Birthe B. Kragelund, Rasmus Hartmann-Petersen
Cell Rep. 2018 Oct 23; 25(4): 862–870. Published online 2018 Oct 23. doi: 10.1016/j.celrep.2018.09.080
PMCID:
PMC6218214
AbstractArticlePDF–2.6M
13.
Conservation and Rewiring of Functional Modules Revealed by an Epistasis Map in Fission Yeast
Assen Roguev, Sourav Bandyopadhyay, Martin Zofall, Ke Zhang, Tamas Fischer, Sean R. Collins, Hongjing Qu, Michael Shales, Han-Oh Park, Jacqueline Hayles, Kwang-Lae Hoe, Dong-Uk Kim, Trey Ideker, Shiv I. Grewal, Jonathan S. Weissman, Nevan J. Krogan
Science. Author manuscript; available in PMC 2009 Sep 28.
Published in final edited form as: Science. 2008 Oct 17; 322(5900): 405–410. Published online 2008 Sep 25. doi: 10.1126/science.1162609
PMCID:
PMC2753251
AbstractArticlePDF–4.2M
14.
Yeast SREBP cleavage activation requires the Golgi Dsc E3 ligase complex
Emerson V. Stewart, Christine C. Nwosu, Zongtian Tong, Assen Roguev, Timothy D. Cummins, Dong-Uk Kim, Jacqueline Hayles, Han-Oh Park, Kwang-Lae Hoe, David W. Powell, Nevan J. Krogan, Peter J. Espenshade
Mol Cell. Author manuscript; available in PMC 2012 Apr 22.
Published in final edited form as: Mol Cell. 2011 Apr 22; 42(2): 160–171. doi: 10.1016/j.molcel.2011.02.035
PMCID:
PMC3083633
AbstractArticlePDF–1.3M
15.
A proteome-wide fission yeast interactome reveals network evolution principles from yeasts to human
Tommy V. Vo, Jishnu Das, Michael J. Meyer, Nicolas A. Cordero, Nurten Akturk, Xiaomu Wei, Benjamin J. Fair, Andrew G. Degatano, Robert Fragoza, Lisa G. Liu, Akihisa Matsuyama, Michelle Trickey, Sachi Horibata, Andrew Grimson, Hiroyuki Yamano, Minoru Yoshida, Frederick P. Roth, Jeffrey A. Pleiss, Yu Xia, Haiyuan Yu
Cell. Author manuscript; available in PMC 2017 Jan 14.
Published in final edited form as: Cell. 2016 Jan 14; 164(0): 310–323. doi: 10.1016/j.cell.2015.11.037
PMCID:
PMC4715267
AbstractArticlePDF–1.4M
16.
Hierarchical modularity and the evolution of genetic interactomes across species
Colm J. Ryan, Assen Roguev, Kristin Patrick, Jiewei Xu, Harlizawati Jahari, Zongtian Tong, Pedro Beltrao, Michael Shales, Hong Qu, Sean R. Collins, Joseph I. Kliegman, Lingli Jiang, Dwight Kuo, Elena Tosti, Hyun-Soo Kim, Winfried Edelmann, Michael-Christopher Keogh, Derek Greene, Chao Tang, Pádraig Cunningham, Kevan M. Shokat, Gerard Cagney, J. Peter Svensson, Christine Guthrie, Peter J. Espenshade, Trey Ideker, Nevan J. Krogan
Mol Cell. Author manuscript; available in PMC 2013 Jun 8.
Published in final edited form as: Mol Cell. 2012 Jun 8; 46(5): 691–704. doi: 10.1016/j.molcel.2012.05.028
PMCID:
PMC3380636
AbstractArticlePDF–2.1M
17.
Transcription and RNA-processing in fission yeast mitochondria
BERND SCHÄFER, MONIKA HANSEN, B. FRANZ LANG
RNA. 2005 May; 11(5): 785–795. doi: 10.1261/rna.7252205
PMCID:
PMC1370763
AbstractArticlePDF–474K
18.
The mitochondrial genome of the fission yeast Schizosaccharomyces pombe: highly homologous introns are inserted at the same position of the otherwise less conserved cox1 genes in Schizosaccharomyces pombe and Aspergillus nidulans.
B F Lang
EMBO J. 1984 Sep; 3(9): 2129–2136. doi: 10.1002/j.1460-2075.1984.tb02102.x
PMCID:
PMC557654
SummaryPage BrowsePDF–1.3M
19.
Nucleotide sequence of the gene encoding the small ribosomal RNA in the mitochondrial genome of the fission yeast Schizosaccharomyces pombe.
H Trinkl, B F Lang, K Wolf
Nucleic Acids Res. 1989 Aug 25; 17(16): 6730. doi: 10.1093/nar/17.16.6730
PMCID:
PMC318371
SummaryPage BrowsePDF–106K

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