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Items: 1 to 20 of 30

1.
A Genome-Wide siRNA Screen Implicates Spire1/2 in SipA-Driven Salmonella Typhimurium Host Cell Invasion
Daniel Andritschke, Sabrina Dilling, Mario Emmenlauer, Tobias Welz, Fabian Schmich, Benjamin Misselwitz, Pauli Rämö, Klemens Rottner, Eugen Kerkhoff, Teiji Wada, Josef M. Penninger, Niko Beerenwinkel, Peter Horvath, Christoph Dehio, Wolf-Dietrich Hardt
PLoS One. 2016; 11(9): e0161965. Published online 2016 Sep 14. doi: 10.1371/journal.pone.0161965
PMCID:
PMC5023170
AbstractArticlePDF–2.9M
2.
Role of the C-terminal Extension of Formin 2 in Its Activation by Spire Protein and Processive Assembly of Actin Filaments
Pierre Montaville, Sonja Kühn, Christel Compper, Marie-France Carlier
J Biol Chem. 2016 Feb 12; 291(7): 3302–3318. Published online 2015 Dec 14. doi: 10.1074/jbc.M115.681379
PMCID:
PMC4751376
AbstractArticlePDF–4.4M
3.
Spire and Formin 2 Synergize and Antagonize in Regulating Actin Assembly in Meiosis by a Ping-Pong Mechanism
Pierre Montaville, Antoine Jégou, Julien Pernier, Christel Compper, Bérengère Guichard, Binyam Mogessie, Melina Schuh, Guillaume Romet-Lemonne, Marie-France Carlier
PLoS Biol. 2014 Feb; 12(2): e1001795. Published online 2014 Feb 25. doi: 10.1371/journal.pbio.1001795
PMCID:
PMC3934834
AbstractArticlePDF–2.8M
4.
Spire1 and Myosin Vc promote Ca2+-evoked externalization of von Willebrand factor in endothelial cells
Anna Holthenrich, Julian Terglane, Johannes Naß, Magdalena Mietkowska, Eugen Kerkhoff, Volker Gerke
Cell Mol Life Sci. 2022 Feb; 79(2): 96. Published online 2022 Jan 27. doi: 10.1007/s00018-021-04108-x
PMCID:
PMC8794916
AbstractArticlePDF–1.5M
5.
A mitochondria-anchored isoform of the actin-nucleating spire protein regulates mitochondrial division
Uri Manor, Sadie Bartholomew, Gonen Golani, Eric Christenson, Michael Kozlov, Henry Higgs, James Spudich, Jennifer Lippincott-Schwartz
eLife. 2015; 4: e08828. Published online 2015 Aug 25. doi: 10.7554/eLife.08828
PMCID:
PMC4574297
AbstractArticlePDF–6.5M
6.
Molecular Basis of Actin Nucleation Factor Cooperativity: CRYSTAL STRUCTURE OF THE SPIR-1 KINASE NON-CATALYTIC C-LOBE DOMAIN (KIND)·FORMIN-2 FORMIN SPIR INTERACTION MOTIF (FSI) COMPLEX
Kornelius Zeth, Markos Pechlivanis, Annette Samol, Sandra Pleiser, Clemens Vonrhein, Eugen Kerkhoff
J Biol Chem. 2011 Sep 2; 286(35): 30732–30739. Published online 2011 Jun 26. doi: 10.1074/jbc.M111.257782
PMCID:
PMC3162434
AbstractArticlePDF–2.8M
7.
Identification of a Short Spir Interaction Sequence at the C-terminal End of Formin Subgroup Proteins
Markos Pechlivanis, Annette Samol, Eugen Kerkhoff
J Biol Chem. 2009 Sep 11; 284(37): 25324–25333. Published online 2009 Jul 15. doi: 10.1074/jbc.M109.030320
PMCID:
PMC2757234
AbstractArticlePDF–2.4M
8.
DNA damage induces nuclear actin filament assembly by Formin-2 and Spire-1/2 that promotes efficient DNA repair
Brittany J Belin, Terri Lee, R Dyche Mullins
eLife. 2015; 4: e07735. Published online 2015 Aug 19. doi: 10.7554/eLife.07735
Correction in:
eLife. 2015; 4: e11935.
PMCID:
PMC4577826
AbstractArticlePDF–5.4M
9.
Spire-Type Actin Nucleators Cooperate with Formin-2 to Drive Asymmetric Oocyte Division
Sybille Pfender, Vitaliy Kuznetsov, Sandra Pleiser, Eugen Kerkhoff, Melina Schuh
Curr Biol. 2011 Jun 7; 21(11): 955–960. doi: 10.1016/j.cub.2011.04.029
PMCID:
PMC3128265
AbstractArticle
10.
The polarity protein Inturned links NPHP4 to Daam1 to control the subapical actin network in multiciliated cells
Takayuki Yasunaga, Sylvia Hoff, Christoph Schell, Martin Helmstädter, Oliver Kretz, Sebastian Kuechlin, Toma A. Yakulov, Christina Engel, Barbara Müller, Robert Bensch, Olaf Ronneberger, Tobias B. Huber, Soeren S. Lienkamp, Gerd Walz
J Cell Biol. 2015 Dec 7; 211(5): 963–973. doi: 10.1083/jcb.201502043
PMCID:
PMC4674276
AbstractArticlePDF–2.5M
11.
Genome-Wide Association Study of Antibody Response to Smallpox Vaccine
Inna G. Ovsyannikova, Richard B. Kennedy, Megan O'Byrne, Robert M. Jacobson, V. Shane Pankratz, Gregory A. Poland
Vaccine. Author manuscript; available in PMC 2013 Jun 13.
Published in final edited form as: Vaccine. 2012 Jun 13; 30(28): 4182–4189. Published online 2012 Apr 25. doi: 10.1016/j.vaccine.2012.04.055
PMCID:
PMC3367131
AbstractArticlePDF–1.3M
12.
Nuclear actin interactome analysis links actin to KAT14 histone acetyl transferase and mRNA splicing
Tiina Viita, Salla Kyheröinen, Bina Prajapati, Jori Virtanen, Mikko J. Frilander, Markku Varjosalo, Maria K. Vartiainen
J Cell Sci. 2019 Apr 15; 132(8): jcs226852. Published online 2019 Apr 17. doi: 10.1242/jcs.226852
PMCID:
PMC6503952
AbstractArticle
13.
A dual-activity topoisomerase complex regulates mRNA translation and turnover
Shuaikun Su, Yutong Xue, Alexei Sharov, Yongqing Zhang, Seung Kyu Lee, Jennifer L Martindale, Wen Li, Wai Lim Ku, Keji Zhao, Supriyo De, Weiping Shen, Payel Sen, Myriam Gorospe, Dongyi Xu, Weidong Wang
Nucleic Acids Res. 2022 Jul 8; 50(12): 7013–7033. Published online 2022 Jun 24. doi: 10.1093/nar/gkac538
PMCID:
PMC9262614
AbstractArticlePDF–3.6M
14.
Large-scale mapping of human protein–protein interactions by mass spectrometry
Rob M Ewing, Peter Chu, Fred Elisma, Hongyan Li, Paul Taylor, Shane Climie, Linda McBroom-Cerajewski, Mark D Robinson, Liam O'Connor, Michael Li, Rod Taylor, Moyez Dharsee, Yuen Ho, Adrian Heilbut, Lynda Moore, Shudong Zhang, Olga Ornatsky, Yury V Bukhman, Martin Ethier, Yinglun Sheng, Julian Vasilescu, Mohamed Abu-Farha, Jean-Philippe Lambert, Henry S Duewel, Ian I Stewart, Bonnie Kuehl, Kelly Hogue, Karen Colwill, Katharine Gladwish, Brenda Muskat, Robert Kinach, Sally-Lin Adams, Michael F Moran, Gregg B Morin, Thodoros Topaloglou, Daniel Figeys
Mol Syst Biol. 2007; 3: 89. Published online 2007 Mar 13. doi: 10.1038/msb4100134
PMCID:
PMC1847948
AbstractArticlePDF–440K
15.
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms
Karsten Boldt, Jeroen van Reeuwijk, Qianhao Lu, Konstantinos Koutroumpas, Thanh-Minh T. Nguyen, Yves Texier, Sylvia E. C. van Beersum, Nicola Horn, Jason R. Willer, Dorus A. Mans, Gerard Dougherty, Ideke J. C. Lamers, Karlien L. M. Coene, Heleen H. Arts, Matthew J. Betts, Tina Beyer, Emine Bolat, Christian Johannes Gloeckner, Khatera Haidari, Lisette Hetterschijt, Daniela Iaconis, Dagan Jenkins, Franziska Klose, Barbara Knapp, Brooke Latour, Stef J. F. Letteboer, Carlo L. Marcelis, Dragana Mitic, Manuela Morleo, Machteld M. Oud, Moniek Riemersma, Susan Rix, Paulien A. Terhal, Grischa Toedt, Teunis J. P. van Dam, Erik de Vrieze, Yasmin Wissinger, Ka Man Wu, Gordana Apic, Philip L. Beales, Oliver E. Blacque, Toby J. Gibson, Martijn A. Huynen, Nicholas Katsanis, Hannie Kremer, Heymut Omran, Erwin van Wijk, Uwe Wolfrum, François Kepes, Erica E. Davis, Brunella Franco, Rachel H. Giles, Marius Ueffing, Robert B. Russell, Ronald Roepman, UK10K Rare Diseases Group
Nat Commun. 2016; 7: 11491. Published online 2016 May 13. doi: 10.1038/ncomms11491
PMCID:
PMC4869170
AbstractArticlePDF–2.0M
16.
Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing
Teng Fei, Yiwen Chen, Tengfei Xiao, Wei Li, Laura Cato, Peng Zhang, Maura B. Cotter, Michaela Bowden, Rosina T. Lis, Shuang G. Zhao, Qiu Wu, Felix Y. Feng, Massimo Loda, Housheng Hansen He, X. Shirley Liu, Myles Brown
Proc Natl Acad Sci U S A. 2017 Jun 27; 114(26): E5207–E5215. Published online 2017 Jun 13. doi: 10.1073/pnas.1617467114
PMCID:
PMC5495225
AbstractArticlePDF–1.3M
17.
The RNA-mediated estrogen receptor α interactome of hormone-dependent human breast cancer cell nuclei
Giovanni Nassa, Giorgio Giurato, Annamaria Salvati, Valerio Gigantino, Giovanni Pecoraro, Jessica Lamberti, Francesca Rizzo, Tuula A. Nyman, Roberta Tarallo, Alessandro Weisz
Sci Data. 2019; 6: 173. Published online 2019 Sep 16. doi: 10.1038/s41597-019-0179-2
PMCID:
PMC6746822
AbstractArticlePDF–2.0M
18.
Quantitative mapping of RNA-mediated nuclear estrogen receptor β interactome in human breast cancer cells
Giorgio Giurato, Giovanni Nassa, Annamaria Salvati, Elena Alexandrova, Francesca Rizzo, Tuula A. Nyman, Alessandro Weisz, Roberta Tarallo
Sci Data. 2018; 5: 180031. Published online 2018 Mar 6. doi: 10.1038/sdata.2018.31
PMCID:
PMC5839158
AbstractArticlePDF–1.9M
19.
RNA-binding activity of TRIM25 is mediated by its PRY/SPRY domain and is required for ubiquitination
Nila Roy Choudhury, Gregory Heikel, Maryia Trubitsyna, Peter Kubik, Jakub Stanislaw Nowak, Shaun Webb, Sander Granneman, Christos Spanos, Juri Rappsilber, Alfredo Castello, Gracjan Michlewski
BMC Biol. 2017; 15: 105. Published online 2017 Nov 8. doi: 10.1186/s12915-017-0444-9
PMCID:
PMC5678581
AbstractArticlePDF–3.2M
20.
PLEKHA4/kramer Attenuates Dishevelled Ubiquitination to Modulate Wnt and Planar Cell Polarity Signaling
Adnan Shami Shah, Alex G. Batrouni, Dongsung Kim, Amith Punyala, Wendy Cao, Chun Han, Michael L. Goldberg, Marcus B. Smolka, Jeremy M. Baskin
Cell Rep. Author manuscript; available in PMC 2019 Jun 26.
Published in final edited form as: Cell Rep. 2019 May 14; 27(7): 2157–2170.e8. doi: 10.1016/j.celrep.2019.04.060
PMCID:
PMC6594551
AbstractArticlePDF–1.4M

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