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Items: 1 to 20 of 29

1.
Coordination of adjacent domains mediates TACC3–ch-TOG–clathrin assembly and mitotic spindle binding
Fiona E. Hood, Samantha J. Williams, Selena G. Burgess, Mark W. Richards, Daniel Roth, Anne Straube, Mark Pfuhl, Richard Bayliss, Stephen J. Royle
J Cell Biol. 2013 Aug 5; 202(3): 463–478. doi: 10.1083/jcb.201211127
PMCID:
PMC3734082
AbstractArticlePDF–4.5M
2.
Transforming acidic coiled-coil protein-3 (Tacc3) acts as a negative regulator of Notch signaling through binding to CDC10 /Ankyrin repeats
Sharon Bargo, Ahmed Raafat, David McCurdy, Idean Amirjazil, Youmin Shu, June Traicoff, Joshua Plant, Barbara K. Vonderhaar, Robert Callahan
Biochem Biophys Res Commun. Author manuscript; available in PMC 2011 Oct 1.
Published in final edited form as: Biochem Biophys Res Commun. 2010 Oct 1; 400(4): 606–612. Published online 2010 Sep 6. doi: 10.1016/j.bbrc.2010.08.111
PMCID:
PMC2964058
AbstractArticlePDF–411K
3.
Male meiotic spindle poles are stabilized by TACC3 and cKAP5/chTOG differently from female meiotic or somatic mitotic spindles in mice
Calvin Simerly, Emily Robertson, Caleb Harrison, Sydney Ward, Charlize George, Jasmine Deleon, Carrie Hartnett, Gerald Schatten
Sci Rep. 2024; 14: 4808. Published online 2024 Feb 27. doi: 10.1038/s41598-024-55376-z
PMCID:
PMC10899211
AbstractArticlePDF–8.5M
4.
Aurora kinase A is essential for meiosis in mouse oocytes
Cecilia S. Blengini, Patricia Ibrahimian, Michaela Vaskovicova, David Drutovic, Petr Solc, Karen Schindler
PLoS Genet. 2021 Apr; 17(4): e1009327. Published online 2021 Apr 26. doi: 10.1371/journal.pgen.1009327
PMCID:
PMC8102010
AbstractArticlePDF–3.8M
5.
Regulating the ARNT/TACC3 axis: Multiple approaches to manipulating protein/protein interactions with small molecules
Yirui Guo, Carrie L. Partch, Jason Key, Paul B. Card, Victor Pashkov, Anjana Patel, Richard K. Bruick, Heiko Wurdak, Kevin H. Gardner
ACS Chem Biol. Author manuscript; available in PMC 2014 Mar 15.
Published in final edited form as: ACS Chem Biol. 2013 Mar 15; 8(3): 626–635. Published online 2012 Dec 26. doi: 10.1021/cb300604u
PMCID:
PMC3600089
AbstractArticlePDF–4.0M
6.
The Centrosomal, Putative Tumor Suppressor Protein TACC2 Is Dispensable for Normal Development, and Deficiency Does Not Lead to Cancer
Michael M. Schuendeln, Roland P. Piekorz, Christian Wichmann, Youngsoo Lee, Peter J. McKinnon, Kelli Boyd, Yutaka Takahashi, James N. Ihle
Mol Cell Biol. 2004 Jul; 24(14): 6403–6409. doi: 10.1128/MCB.24.14.6403-6409.2004
PMCID:
PMC434246
AbstractArticlePDF–451K
7.
The centrosomal protein TACC3 is essential for hematopoietic stem cell function and genetically interfaces with p53-regulated apoptosis
Roland P. Piekorz, Angelika Hoffmeyer, Christopher D. Duntsch, Catriona McKay, Hideaki Nakajima, Veronika Sexl, Linda Snyder, Jerold Rehg, James N. Ihle
EMBO J. 2002 Feb 15; 21(4): 653–664. doi: 10.1093/emboj/21.4.653
PMCID:
PMC125348
AbstractArticlePDF–405K
8.
N-methyl-d-aspartate receptor signaling results in Aurora kinase-catalyzed CPEB phosphorylation and αCaMKII mRNA polyadenylation at synapses
Yi-Shuian Huang, Mi-Young Jung, Madathia Sarkissian, Joel D. Richter
EMBO J. 2002 May 1; 21(9): 2139–2148. doi: 10.1093/emboj/21.9.2139
PMCID:
PMC125376
AbstractArticlePDF–428K
9.
TACC3 is required for the proper mitosis of sclerotome mesenchymal cells during formation of the axial skeleton
Ryoji Yao, Yasuko Natsume, Tetsuo Noda
Cancer Sci. 2007 Apr; 98(4): 555–562. Published online 2007 Mar 14. doi: 10.1111/j.1349-7006.2007.00433.x
PMCID:
PMC11158658
AbstractArticlePDF–311K
10.
The Centrosomal Adaptor TACC3 and the Microtubule Polymerase chTOG Interact via Defined C-terminal Subdomains in an Aurora-A Kinase-independent Manner
Harish C. Thakur, Madhurendra Singh, Luitgard Nagel-Steger, Jana Kremer, Daniel Prumbaum, Eyad Kalawy Fansa, Hakima Ezzahoini, Kazem Nouri, Lothar Gremer, André Abts, Lutz Schmitt, Stefan Raunser, Mohammad R. Ahmadian, Roland P. Piekorz
J Biol Chem. 2014 Jan 3; 289(1): 74–88. Published online 2013 Nov 22. doi: 10.1074/jbc.M113.532333
PMCID:
PMC3879581
AbstractArticlePDF–4.1M
11.
DOCK7 interacts with TACC3 to regulate interkinetic nuclear migration and cortical neurogenesis
Yu-Ting Yang, Chia-Lin Wang, Linda Van Aelst
Nat Neurosci. Author manuscript; available in PMC 2013 Mar 1.
Published in final edited form as: Nat Neurosci. 2012 Sep; 15(9): 1201–1210. Published online 2012 Jul 29. doi: 10.1038/nn.3171
PMCID:
PMC3431462
AbstractArticlePDF–4.1M
12.
NDEL1 Phosphorylation by Aurora-A Kinase Is Essential for Centrosomal Maturation, Separation, and TACC3 Recruitment
Daisuke Mori, Yoshihisa Yano, Kazuhito Toyo-oka, Noriyuki Yoshida, Masami Yamada, Masami Muramatsu, Dongwei Zhang, Hideyuki Saya, Yoko Y. Toyoshima, Kazuhisa Kinoshita, Anthony Wynshaw-Boris, Shinji Hirotsune
Mol Cell Biol. 2007 Jan; 27(1): 352–367. Published online 2006 Oct 23. doi: 10.1128/MCB.00878-06
PMCID:
PMC1800650
AbstractArticlePDF–2.3M
13.
Cep120 and TACCs Control Interkinetic Nuclear Migration and the Neural Progenitor Pool
Zhigang Xie, Lily Y. Moy, Kamon Sanada, Ying Zhou, Joshua J. Buchman, Li-Huei Tsai
Neuron. Author manuscript; available in PMC 2009 Feb 13.
Published in final edited form as: Neuron. 2007 Oct 4; 56(1): 79–93. doi: 10.1016/j.neuron.2007.08.026
PMCID:
PMC2642594
AbstractArticlePDF–3.1M
14.
Structure-function evolution of the Transforming acidic coiled coil genes revealed by analysis of phylogenetically diverse organisms
Ivan H Still, Ananthalakshmy K Vettaikkorumakankauv, Anthony DiMatteo, Ping Liang
BMC Evol Biol. 2004; 4: 16. Published online 2004 Jun 18. doi: 10.1186/1471-2148-4-16
PMCID:
PMC441373
AbstractArticlePDF–1.2M
15.
Gene expression analysis of the embryonic subplate
Franziska M. Oeschger, Wei-Zhi Wang, Sheena Lee, Fernando García-Moreno, André M. Goffinet, Mariona Arbones, Sonia Rakic, Zoltán Molnár
Cereb Cortex. Author manuscript; available in PMC 2016 Aug 3.
Published in final edited form as: Cereb Cortex. 2012 Jun; 22(6): 1343–1359. Published online 2011 Aug 22. doi: 10.1093/cercor/bhr197
PMCID:
PMC4972418
AbstractArticlePDF–7.1M
16.
A Genome-Wide Screen to Identify Transcription Factors Expressed in Pelvic Ganglia of the Lower Urinary Tract
Carrie B. Wiese, Sara Ireland, Nicole L. Fleming, Jing Yu, M. Todd Valerius, Kylie Georgas, Han Sheng Chiu, Jane Brennan, Jane Armstrong, Melissa H. Little, Andrew P. McMahon, E. Michelle Southard-Smith
Front Neurosci. 2012; 6: 130. Published online 2012 Sep 12. doi: 10.3389/fnins.2012.00130
PMCID:
PMC3439845
AbstractArticlePDF–1.4M
17.
Spatio-temporal profile of postynaptic interactomes integrates components of complex brain disorders
Jing Li, Wangshu Zhang, Hui Yang, Daniel P. Howrigan, Brent Wilkinson, Tade Souaiaia, Oleg V. Evgrafov, Giulio Genovese, Veronica A. Clementel, Jennifer C. Tudor, Ted Abel, James A. Knowles, Benjamin M. Neale, Kai Wang, Fengzhu Sun, Marcelo P. Coba
Nat Neurosci. Author manuscript; available in PMC 2018 Aug 1.
Published in final edited form as: Nat Neurosci. 2017 Aug; 20(8): 1150–1161. Published online 2017 Jun 26. doi: 10.1038/nn.4594
PMCID:
PMC5645082
AbstractArticlePDF–2.3M
18.
Systematic Characterization of Human Protein Complexes Identifies Chromosome Segregation Proteins
James R.A. Hutchins, Yusuke Toyoda, Björn Hegemann, Ina Poser, Jean-Karim Hériché, Martina M. Sykora, Martina Augsburg, Otto Hudecz, Bettina A. Buschhorn, Jutta Bulkescher, Christian Conrad, David Comartin, Alexander Schleiffer, Mihail Sarov, Andrei Pozniakovsky, Mikolaj Michal Slabicki, Siegfried Schloissnig, Ines Steinmacher, Marit Leuschner, Andrea Ssykor, Steffen Lawo, Laurence Pelletier, Holger Stark, Kim Nasmyth, Jan Ellenberg, Richard Durbin, Frank Buchholz, Karl Mechtler, Anthony A. Hyman, Jan-Michael Peters
Science. Author manuscript; available in PMC 2010 Nov 22.
Published in final edited form as: Science. 2010 Apr 30; 328(5978): 593–599. Published online 2010 Apr 1. doi: 10.1126/science.1181348
PMCID:
PMC2989461
AbstractArticlePDF–2.2M
19.
A Systems Approach Reveals that the Myogenesis Genome Network Is Regulated by the Transcriptional Repressor RP58
Shigetoshi Yokoyama, Yoshiaki Ito, Hiroe Ueno-Kudoh, Hirohito Shimizu, Kenta Uchibe, Sonia Albini, Kazuhiko Mitsuoka, Shigeru Miyaki, Minako Kiso, Akane Nagai, Tomohiro Hikata, Tadahiro Osada, Noritsugu Fukuda, Satoshi Yamashita, Daisuke Harada, Valeria Mezzano, Masataka Kasai, Pier Lorenzo Puri, Yoshihide Hayashizaki, Haruo Okado, Megumi Hashimoto, Hiroshi Asahara
Dev Cell. Author manuscript; available in PMC 2011 Jun 7.
Published in final edited form as: Dev Cell. 2009 Dec; 17(6): 836–848. doi: 10.1016/j.devcel.2009.10.011
PMCID:
PMC3110151
AbstractArticlePDF–2.0M
20.
Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development
Francesco Bedogni, Robert F. Hevner
Front Mol Neurosci. 2021; 14: 686034. Published online 2021 Jul 12. doi: 10.3389/fnmol.2021.686034
PMCID:
PMC8313239
AbstractArticlePDF–1.6M

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