[56] Molecular genetic analysis of fission yeast Schizosaccharomyces pombe

Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombe

Kim, D.-U., Hayles, J., Kim, D., Wood, V., Park, H.-O., Won, M., Yoo, H.-S., Duhig, T., Nam, M., Palmer, G., et al. (2010) · Nature Biotechnology · doi:10.1038/nbt.1628 · Cited by 742 · see citing works

SREBP pathway responds to sterols and functions as an oxygen sensor in fission yeast.

Hughes, A. L., Todd, B. L., & Espenshade, P. J. (2005) · Cell · doi:10.1016/j.cell.2005.01.012 · Cited by 320 · see citing works

Chromosomal Inheritance of Epigenetic States in Fission Yeast During Mitosis and Meiosis

Grewal, S. I. S., & Klar, A. J. S. (1996) · Cell · doi:10.1016/s0092-8674(00)80080-x · Cited by 260 · see citing works

A role for Hsp90 in cell cycle control: Wee1 tyrosine kinase activity requires interaction with Hsp90.

Aligue, R., Akhavan‐Niak, H., & Russell, P. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06956.x · Cited by 261 · see citing works

Molecular Identification of a Eukaryotic, Stretch-Activated Nonselective Cation Channel

Kanzaki, M., Nagasawa, M., Kojima, I., Sato, C., Naruse, K., Sokabe, M., & Iida, H. (1999) · Science · doi:10.1126/science.285.5429.882 · Cited by 213 · see citing works

A PP1-PP2A phosphatase relay controls mitotic progression

Grallert, A., Boke, E., Hagting, A., Hodgson, B., Connolly, Y., Griffiths, J. R., Smith, D. L., Pines, J., & Hagan, I. M. (2015) · Nature · doi:10.1038/nature14019 · Cited by 188 · see citing works

Sterol regulatory element binding protein is a principal regulator of anaerobic gene expression in fission yeast.

Todd, B. L., Stewart, E. V., Burg, J. S., Hughes, A. L., & Espenshade, P. J. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.7.2817-2831.2006 · Cited by 172 · see citing works

A global profile of replicative polymerase usage

Daigaku, Y., Keszthelyi, A., Müller, C. A., Miyabe, I., Brooks, T., Retkute, R., Hubank, M., Nieduszynski, C. A., & Carr, A. M. (2015) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2962 · Cited by 169 · see citing works

A coordinated global control over cellular transcription

Zhurinsky, J., Leonhard, K., Watt, S., Marguerat, S., Bähler, J., & Nurse, P. (2010) · Current Biology · doi:10.1016/j.cub.2010.10.002 · Cited by 148 · see citing works

Epigenetic inheritance mediated by coupling of RNAi and histone H3K9 methylation

Yu, R., Wang, X., & Moazed, D. (2018) · Nature · doi:10.1038/s41586-018-0239-3 · Cited by 128 · see citing works

Fission yeast pkl1 is a kinesin-related protein involved in mitotic spindle function.

Pidoux, A. L., LeDizet, M., & Cande, W. Z. (1996) · Molecular Biology of the Cell · doi:10.1091/mbc.7.10.1639 · Cited by 115 · see citing works

A Mutation in γ-Tubulin Alters Microtubule Dynamics and Organization and Is Synthetically Lethal with the Kinesin-like Protein Pkl1p

Paluh, J. L., Nogales, E., Oakley, B. R., McDonald, K., Pidoux, A. L., & Cande, W. Z. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.4.1225 · Cited by 125 · see citing works

<i>pkl1</i>⁺and<i>klp2</i>⁺: Two Kinesins of the Kar3 Subfamily in Fission Yeast Perform Different Functions in Both Mitosis and Meiosis

Troxell, C. L., Sweezy, M. A., West, R. R., Reed, K. D., Carson, B. D., Pidoux, A. L., Cande, W. Z., & McIntosh, J. R. (2001) · Molecular Biology of the Cell · doi:10.1091/mbc.12.11.3476 · Cited by 106 · see citing works

Recovery from DNA damage checkpoint arrest by PP1-mediated inhibition of Chk1

den Elzen, N. R., & O'Connell, M. J. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600105 · Cited by 102 · see citing works

Evolutionary and Functional Conservation of the DNA Non-homologous End-joining Protein, XLF/Cernunnos

Hentges, P., Ahnesorg, P., Pitcher, R. S., Bruce, C. K., Kysela, B., Green, A. J., Bianchi, J., Wilson, T. E., Jackson, S. P., & Doherty, A. J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m608727200 · Cited by 88 · see citing works

Zinc Finger Protein Prz1 Regulates Ca2+ but Not Cl− Homeostasis in Fission Yeast

Hirayama, S., Sugiura, R., Lu, Y., Maeda, T., Kawagishi, K., Yokoyama, M., Tohda, H., Giga-Hama, Y., Shuntoh, H., & Kuno, T. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212900200 · Cited by 87 · see citing works

Telomeres avoid end detection by severing the checkpoint signal transduction pathway

Carneiro, T., Khair, L., Reis, C. C., Borges, V., Moser, B. A., Nakamura, T. M., & Ferreira, M. G. (2010) · Nature · doi:10.1038/nature09353 · Cited by 75 · see citing works

Glutathione Reductase and a Mitochondrial Thioredoxin Play Overlapping Roles in Maintaining Iron-Sulfur Enzymes in Fission Yeast

Song, J.-Y., Cha, J., Lee, J., & Roe, J.-H. (2006) · Eukaryotic Cell · doi:10.1128/ec.00244-06 · Cited by 55 · see citing works

UV irradiation induces a postreplication DNA damage checkpoint

Callegari, A. J., & Kelly, T. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607343103 · Cited by 51 · see citing works

Gcn5 facilitates Pol II progression, rather than recruitment to nucleosome-depleted stress promoters, in Schizosaccharomyces pombe

Sansó, M., Vargas-Pérez, I., Quintales, L., Antequera, F., Ayté, J., & Hidalgo, E. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr255 · Cited by 51 · see citing works

Protein complexes at the microtubule organizing center regulate bipolar spindle assembly

Rodriguez, A. S., Killilea, A. N., Batac, J., Filopei, J., Simeonov, D., Lin, I., & Paluh, J. L. (2008) · Cell Cycle · doi:10.4161/cc.7.9.5808 · Cited by 38 · see citing works

Pyruvate kinase variant of fission yeast tunes carbon metabolism, cell regulation, growth and stress resistance

Kamrad, S., Grossbach, J., Rodríguez‐López, M., Mülleder, M., Townsend, S., Cappelletti, V., Stojanovski, G., Correia‐Melo, C., Picotti, P., Beyer, A., et al. (2020) · Molecular Systems Biology · doi:10.15252/msb.20199270 · Cited by 40 · see citing works

β(1,3)-Glucanosyl-Transferase Activity Is Essential for Cell Wall Integrity and Viability of Schizosaccharomyces pombe

de Medina-Redondo, M., Arnáiz-Pita, Y., Clavaud, C., Fontaine, T., del Rey, F., Latgé, J. P., & Vázquez de Aldana, C. R. (2010) · PLoS ONE · doi:10.1371/journal.pone.0014046 · Cited by 39 · see citing works

Functional interactions among members of the meiotic initiation complex in fission yeast

Steiner, S., Kohli, J., & Ludin, K. (2010) · Current Genetics · doi:10.1007/s00294-010-0296-0 · Cited by 34 · see citing works

Alternative Excision Repair Pathway of UV-damaged DNA inSchizosaccharomyces pombe Operates Both in Nucleus and in Mitochondria

Yasuhira, S., & Yasui, A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.16.11824 · Cited by 34 · see citing works

The Schizosaccharomyces pombe PPR protein Ppr10 associates with a novel protein Mpa1 and acts as a mitochondrial translational activator

Wang, Y., Yan, J., Zhang, Q., Ma, X., Zhang, J., Su, M., Wang, X., & Huang, Y. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx127 · Cited by 34 · see citing works

The signal peptide peptidase SppA is involved in sterol regulatory element‐binding protein cleavage and hypoxia adaptation in <i>Aspergillus nidulans</i>

Bat‐Ochir, C., Kwak, J., Koh, S., Jeon, M., Chung, D., Lee, Y., & Chae, S. (2016) · Molecular Microbiology · doi:10.1111/mmi.13341 · Cited by 33 · see citing works

ATP insertion opposite 8-oxo-deoxyguanosine by Pol4 mediates error-free tolerance in Schizosaccharomyces pombe

Sastre-Moreno, G., Sánchez, A., Esteban, V., & Blanco, L. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku711 · Cited by 19 · see citing works

Bin1 Interacts with and Restrains the DNA End-Binding Protein Complex Ku

Ramalingam, A., Farmer, G. E., Stamato, T., & Prendergast, G. C. (2007) · Cell Cycle · doi:10.4161/cc.6.15.4514 · Cited by 18 · see citing works

Schizosaccharomyces pombe Ppr10 and mpa1 together mediate mitochondrial translational initiation

Luo, Y., Wang, Y., & Huang, Y. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100869 · Cited by 10 · see citing works

<scp>RNAi</scp> reveals a unique set of kinesins mediating chloroplast motility in the giant cytoplasm of <i>Bryopsis</i> (Ulvophyceae), a coenocytic green alga

Ogawa, H. A., Ochiai, K. K., Shirae‐Kurabayashi, M., & Goshima, G. (2026) · Journal of Phycology · doi:10.1111/jpy.70118 · Cited by 1 · see citing works