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Items: 1 to 20 of 25

1.
Variants in ALX4 and their association with genitourinary defects
Ching H. Chen, Juan C. Bournat, Nathan Wilken, Jill A. Rosenfeld, Jason Zhang, Abhishek Seth, Carolina J. Jorgez
Andrology. Author manuscript; available in PMC 2023 Jul 4.
Published in final edited form as: Andrology. 2020 Sep; 8(5): 1243–1255. Published online 2020 Jul 16. doi: 10.1111/andr.12815
PMCID:
PMC10318892
AbstractArticlePDF–847K
2.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
3.
Impact of cytosine methylation on DNA binding specificities of human transcription factors
Yimeng Yin, Ekaterina Morgunova, Arttu Jolma, Eevi Kaasinen, Biswajyoti Sahu, Syed Khund-Sayeed, Pratyush K. Das, Teemu Kivioja, Kashyap Dave, Fan Zhong, Kazuhiro R. Nitta, Minna Taipale, Alexander Popov, Paul A. Ginno, Silvia Domcke, Jian Yan, Dirk Schübeler, Charles Vinson, Jussi Taipale
Science. Author manuscript; available in PMC 2021 Mar 30.
Published in final edited form as: Science. 2017 May 5; 356(6337): eaaj2239. doi: 10.1126/science.aaj2239
PMCID:
PMC8009048
AbstractArticlePDF–2.6M
4.
Overexpression of Aristaless-Like Homeobox-4 Inhibits Proliferation, Invasion, and EMT in Hepatocellular Carcinoma Cells
Yao Shi, Xiaoke Sun, Xiafen He
Oncol Res. 2017; 25(1): 11–18. Published online 2017 Jan 2. doi: 10.3727/096504016X14685034103833
PMCID:
PMC7840740
AbstractArticlePDF–2.1M
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.
AMPK Interactome Reveals New Function in Non-homologous End Joining DNA Repair
Zhen Chen, Chao Wang, Antrix Jain, Mrinal Srivastava, Mengfan Tang, Huimin Zhang, Xu Feng, Litong Nie, Dan Su, Yun Xiong, Sung Yun Jung, Jun Qin, Junjie Chen
Mol Cell Proteomics. 2020 Mar; 19(3): 467–477. Published online 2020 Jan 3. doi: 10.1074/mcp.RA119.001794
PMCID:
PMC7050103
AbstractArticlePDF–1.8M
7.
ALX4, an epigenetically down regulated tumor suppressor, inhibits breast cancer progression by interfering Wnt/β-catenin pathway
Juntang Yang, Fei Han, Wenbin Liu, Hongqiang Chen, Xianglin Hao, Xiao Jiang, Li Yin, Yongsheng Huang, Jia Cao, Huidong Zhang, Jinyi Liu
J Exp Clin Cancer Res. 2017; 36: 170. Published online 2017 Nov 28. doi: 10.1186/s13046-017-0643-9
PMCID:
PMC5706407
AbstractArticlePDF–5.0M
8.
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
9.
HOXB13 and ALX4 induce SLUG expression for the promotion of EMT and cell invasion in ovarian cancer cells
Hong Yuan, Hiroaki Kajiyama, Satoko Ito, Dan Chen, Kiyosumi Shibata, Michinari Hamaguchi, Fumitaka Kikkawa, Takeshi Senga
Oncotarget. 2015 May 30; 6(15): 13359–13370. Published online 2015 Apr 10. doi: 10.18632/oncotarget.3673
PMCID:
PMC4537020
AbstractArticlePDF–6.3M
10.
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
11.
Solution NMR Structures of Homeodomains from Human Proteins ALX4, ZHX1, and CASP8AP2 Contribute to the Structural Coverage of the Human Cancer Protein Interaction Network
Xianzhong Xu, Surya VSRK Pulavarti, Alexander Eletsky, Yuanpeng Janet Huang, Thomas B. Acton, Rong Xiao, John K. Everett, Gaetano T. Montelione, Thomas Szyperski
J Struct Funct Genomics. Author manuscript; available in PMC 2015 Dec 1.
Published in final edited form as: J Struct Funct Genomics. 2014 Dec; 15(4): 201–207. Published online 2014 Jun 19. doi: 10.1007/s10969-014-9184-z
PMCID:
PMC4239167
AbstractArticlePDF–556K
12.
Genome-Wide Association Study Identifies Eight Novel Loci Associated with Blood Pressure Responses to Interventions in Han Chinese
Jiang He, Tanika N. Kelly, Qi Zhao, Hongfan Li, Jianfeng Huang, Laiyuan Wang, Cashell E. Jaquish, Yun Ju Sung, Lawrence C. Shimmin, Fanghong Lu, Jianjun Mu, Dongsheng Hu, Xu Ji, Chong Shen, Dongshuang Guo, Jixiang Ma, Renping Wang, Jinjin Shen, Shengxu Li, Jing Chen, Hao Mei, Chung-Shiuan Chen, Shufeng Chen, Jichun Chen, Jianxin Li, Jie Cao, Xiangfeng Lu, Xigui Wu, Treva K. Rice, C. Charles Gu, Karen Schwander, L. Lee Hamm, Depei Liu, Dabeeru C. Rao, James E. Hixson, Dongfeng Gu
Circ Cardiovasc Genet. Author manuscript; available in PMC 2014 Dec 1.
Published in final edited form as: Circ Cardiovasc Genet. 2013 Dec; 6(6): 598–607. Published online 2013 Oct 28. doi: 10.1161/CIRCGENETICS.113.000307
PMCID:
PMC3952335
AbstractArticlePDF–5.3M
13.
ALX4 gain-of-function mutations in non-syndromic craniosynostosis
Garima Yagnik, Apar Ghuman, Sundon Kim, Cristina G. Stevens, Virginia Kimonis, Joan Stoler, Pedro Sanchez-Lara, Jonathan Bernstein, Cyril Naydenov, Hicham Drissi, Michael L. Cunningham, Jinoh Kim, Simeon A. Boyadjiev
Hum Mutat. Author manuscript; available in PMC 2013 Dec 1.
Published in final edited form as: Hum Mutat. 2012 Dec; 33(12): 1626–1629. Published online 2012 Aug 13. doi: 10.1002/humu.22166
PMCID:
PMC3495992
AbstractArticlePDF–661K
14.
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
15.
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
16.
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
17.
Performance of Epigenetic Markers SEPT9 and ALX4 in Plasma for Detection of Colorectal Precancerous Lesions
Marc Tänzer, Benjamin Balluff, Jürgen Distler, Kari Hale, Andreas Leodolter, Christoph Röcken, Bela Molnar, Roland Schmid, Catherine Lofton-Day, Tibor Schuster, Matthias P. A. Ebert
PLoS One. 2010; 5(2): e9061. Published online 2010 Feb 4. doi: 10.1371/journal.pone.0009061
PMCID:
PMC2816214
AbstractArticlePDF–101K
18.
Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk
Fotios Drenos, Philippa J. Talmud, Juan P. Casas, Liam Smeeth, Jutta Palmen, Steve E. Humphries, Aroon D. Hingorani
Hum Mol Genet. 2009 Jun 15; 18(12): 2305–2316. Published online 2009 Mar 31. doi: 10.1093/hmg/ddp159
PMCID:
PMC2685759
AbstractArticlePDF–530K
19.
High throughput SNP and expression analyses of candidate genes for non‐syndromic oral clefts
J W Park, J Cai, I McIntosh, E W Jabs, M D Fallin, R Ingersoll, J B Hetmanski, M Vekemans, T Attie‐Bitach, M Lovett, A F Scott, T H Beaty
J Med Genet. 2006 Jul; 43(7): 598–608. Published online 2006 Jan 13. doi: 10.1136/jmg.2005.040162
PMCID:
PMC2564555
AbstractArticlePDF–2.0M
20.
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.
O. Bartsch, W. Wuyts, W. Van Hul, J. T. Hecht, P. Meinecke, D. Hogue, W. Werner, B. Zabel, G. K. Hinkel, C. M. Powell, L. G. Shaffer, P. J. Willems
Am J Hum Genet. 1996 Apr; 58(4): 734–742.
PMCID:
PMC1914683
SummaryPage BrowsePDF–2.6M

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