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Items: 1 to 20 of 23

1.
The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers
Martina Oravcová, Minghua Nie, Nicola Zilio, Shintaro Maeda, Yasaman Jami-Alahmadi, Eros Lazzerini-Denchi, James A Wohlschlegel, Helle D Ulrich, Takanori Otomo, Michael N Boddy
eLife. 2022; 11: e79676. Published online 2022 Nov 14. doi: 10.7554/eLife.79676
PMCID:
PMC9708086
AbstractArticlePDF–8.5M
2.
Molecular basis for DNA recognition by the maternal pioneer transcription factor FoxH1
Radoslaw Pluta, Eric Aragón, Nicholas A. Prescott, Lidia Ruiz, Rebeca A. Mees, Blazej Baginski, Julia R. Flood, Pau Martin-Malpartida, Joan Massagué, Yael David, Maria J. Macias
Nat Commun. 2022; 13: 7279. Published online 2022 Nov 26. doi: 10.1038/s41467-022-34925-y
PMCID:
PMC9701222
AbstractArticlePDF–4.3M
3.
A comprehensive analysis of FOX family in HCC and experimental evidence to support the oncogenic role of FOXH1
Xiwu Ouyang, Lemeng Feng, Lei Yao, Jingyu Zhang, Yao Xiao, Guodong Liu, Gewen Zhang, Zhiming Wang
Aging (Albany NY) 2022 Mar 15; 14(5): 2268–2286. Published online 2022 Mar 7. doi: 10.18632/aging.203934
PMCID:
PMC8954963
AbstractArticlePDF–3.0M
4.
Large‐scale whole‐exome sequencing association study identifies FOXH1 gene and sphingolipid metabolism pathway influencing major depressive disorder
Wei Zhou, Luan Chen, Bixuan Jiang, Yidan Sun, Mo Li, Hao Wu, Na Zhang, Xiaofang Sun, Shengying Qin
CNS Neurosci Ther. 2021 Nov; 27(11): 1425–1428. Published online 2021 Oct 11. doi: 10.1111/cns.13733
PMCID:
PMC8504519
AbstractArticlePDF–361K
5.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M
6.
Inhibition of MELK Protooncogene as an Innovative Treatment for Intrahepatic Cholangiocarcinoma
Antonio Cigliano, Maria Giulia Pilo, Marta Mela, Silvia Ribback, Frank Dombrowski, Giovanni Mario Pes, Antonio Cossu, Matthias Evert, Diego Francesco Calvisi, Kirsten Utpatel
Medicina (Kaunas) 2020 Jan; 56(1): 1. Published online 2019 Dec 18. doi: 10.3390/medicina56010001
PMCID:
PMC7023300
AbstractArticlePDF–4.9M
7.
Proteomic analyses reveal distinct chromatin-associated and soluble transcription factor complexes
Xu Li, Wenqi Wang, Jiadong Wang, Anna Malovannaya, Yuanxin Xi, Wei Li, Rudy Guerra, David H Hawke, Jun Qin, Junjie Chen
Mol Syst Biol. 2015 Jan; 11(1): 775. Published online 2015 Jan 21. doi: 10.15252/msb.20145504
PMCID:
PMC4332150
AbstractArticlePDF–2.8M
8.
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
Cornelius A. Rietveld, Tõnu Esko, Gail Davies, Tune H. Pers, Patrick Turley, Beben Benyamin, Christopher F. Chabris, Valur Emilsson, Andrew D. Johnson, James J. Lee, Christiaan de Leeuw, Riccardo E. Marioni, Sarah E. Medland, Michael B. Miller, Olga Rostapshova, Sven J. van der Lee, Anna A. E. Vinkhuyzen, Najaf Amin, Dalton Conley, Jaime Derringer, Cornelia M. van Duijn, Rudolf Fehrmann, Lude Franke, Edward L. Glaeser, Narelle K. Hansell, Caroline Hayward, William G. Iacono, Carla Ibrahim-Verbaas, Vincent Jaddoe, Juha Karjalainen, David Laibson, Paul Lichtenstein, David C. Liewald, Patrik K. E. Magnusson, Nicholas G. Martin, Matt McGue, George McMahon, Nancy L. Pedersen, Steven Pinker, David J. Porteous, Danielle Posthuma, Fernando Rivadeneira, Blair H. Smith, John M. Starr, Henning Tiemeier, Nicholas J. Timpson, Maciej Trzaskowski, André G. Uitterlinden, Frank C. Verhulst, Mary E. Ward, Margaret J. Wright, George Davey Smith, Ian J. Deary, Magnus Johannesson, Robert Plomin, Peter M. Visscher, Daniel J. Benjamin, David Cesarini, Philipp D. Koellinger
Proc Natl Acad Sci U S A. 2014 Sep 23; 111(38): 13790–13794. Published online 2014 Sep 8. doi: 10.1073/pnas.1404623111
Correction in:
Proc Natl Acad Sci U S A. 2015 Jan 27; 112(4): E380.
PMCID:
PMC4183313
AbstractArticlePDF–650K
9.
HEB and E2A function as SMAD/FOXH1 cofactors
Se-Jin Yoon, Andrea E. Wills, Edward Chuong, Rakhi Gupta, Julie C. Baker
Genes Dev. 2011 Aug 1; 25(15): 1654–1661. doi: 10.1101/gad.16800511
PMCID:
PMC3182016
AbstractArticlePDF–733K
10.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
11.
Maternal Genes and Facial Clefts in Offspring: A Comprehensive Search for Genetic Associations in Two Population-Based Cleft Studies from Scandinavia
Astanand Jugessur, Min Shi, Håkon Kristian Gjessing, Rolv Terje Lie, Allen James Wilcox, Clarice Ring Weinberg, Kaare Christensen, Abee Lowman Boyles, Sandra Daack-Hirsch, Truc Trung Nguyen, Lene Christiansen, Andrew Carl Lidral, Jeffrey Clark Murray
PLoS One. 2010; 5(7): e11493. Published online 2010 Jul 9. doi: 10.1371/journal.pone.0011493
PMCID:
PMC2901336
AbstractArticlePDF–778K
12.
SMAD proteins of oligodendroglial cells regulate transcription of JC virus early and late genes coordinately with the Tat protein of human immunodeficiency virus type 1
Michelle R. Stettner, Jonas A. Nance, Clayton A. Wright, Yayoi Kinoshita, Woong-Ki Kim, Susan Morgello, Jay Rappaport, Kamel Khalili, Jennifer Gordon, Edward M. Johnson
J Gen Virol. 2009 Aug; 90(Pt 8): 2005–2014. doi: 10.1099/vir.0.011072-0
PMCID:
PMC2871392
AbstractArticlePDF–408K
13.
An atlas of combinatorial transcriptional regulation in mouse and man
The FANTOM consortium and RIKEN Omics Science Center
Cell. Author manuscript; available in PMC 2011 Mar 5.
Published in final edited form as: Cell. 2010 Mar 5; 140(5): 744–752. doi: 10.1016/j.cell.2010.01.044
Correction in:
volume 141 on page 369
PMCID:
PMC2836267
AbstractArticlePDF–2.2M
14.
Oct25 Represses Transcription of Nodal/Activin Target Genes by Interaction with Signal Transducers during Xenopus Gastrulation
Ying Cao, Doreen Siegel, Franz Oswald, Walter Knöchel
J Biol Chem. 2008 Dec 5; 283(49): 34168–34177. doi: 10.1074/jbc.M803532200
PMCID:
PMC2662234
AbstractArticlePDF–703K
15.
Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
Erich Roessler, Maia V. Ouspenskaia, Jayaprakash D. Karkera, Jorge I. Vélez, Amy Kantipong, Felicitas Lacbawan, Peter Bowers, John W. Belmont, Jeffrey A. Towbin, Elizabeth Goldmuntz, Benjamin Feldman, Maximilian Muenke
Am J Hum Genet. 2008 Jul 11; 83(1): 18–29. Published online 2008 Jul 3. doi: 10.1016/j.ajhg.2008.05.012
PMCID:
PMC2443854
AbstractArticlePDF–2.5M
16.
Smad7 Antagonizes Transforming Growth Factor β Signaling in the Nucleus by Interfering with Functional Smad-DNA Complex Formation
Suping Zhang, Teng Fei, Lixia Zhang, Ran Zhang, Feng Chen, Yuanheng Ning, Yuna Han, Xin-Hua Feng, Anming Meng, Ye-Guang Chen
Mol Cell Biol. 2007 Jun; 27(12): 4488–4499. Published online 2007 Apr 16. doi: 10.1128/MCB.01636-06
PMCID:
PMC1900056
AbstractArticlePDF–696K
17.
Dual role of the Smad4/DPC4 tumor suppressor in TGFβ-inducible transcriptional complexes
Fang Liu, Celio Pouponnot, Joan Massagué
Genes Dev. 1997 Dec 1; 11(23): 3157–3167. doi: 10.1101/gad.11.23.3157
PMCID:
PMC316747
AbstractArticlePDF–1.1M
18.
DNA Cloning Using In Vitro Site-Specific Recombination
James L. Hartley, Gary F. Temple, Michael A. Brasch
Genome Res. 2000 Nov; 10(11): 1788–1795. doi: 10.1101/gr.143000
PMCID:
PMC310948
AbstractArticlePDF–1.7M
19.
Homeoprotein DLX-1 interacts with Smad4 and blocks a signaling pathway from activin A in hematopoietic cells
Shigeru Chiba, Kenichi Takeshita, Yoichi Imai, Keiki Kumano, Mineo Kurokawa, Shigeo Masuda, Kiyoshi Shimizu, Shuji Nakamura, Frank H. Ruddle, Hisamaru Hirai
Proc Natl Acad Sci U S A. 2003 Dec 23; 100(26): 15577–15582. Published online 2003 Dec 11. doi: 10.1073/pnas.2536757100
PMCID:
PMC307610
AbstractArticlePDF–457K
20.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K

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