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Select item 71498421.

The mutational burden and oligogenic inheritance in Klippel-Feil syndrome

Ziquan Li, Sen Zhao, Siyi Cai, Yuanqiang Zhang, Lianlei Wang, Yuchen Niu, Xiaoxin Li, Jianhua Hu, Jingdan Chen, Shengru Wang, Huizi Wang, Gang Liu, Ye Tian, Zhihong Wu, Terry Jianguo Zhang, DISCO (Deciphering Disorders Involving Scoliosis and COmorbidities) study, Yipeng Wang, Nan Wu

BMC Musculoskelet Disord. 2020; 21: 220. Published online 2020 Apr 11. doi: 10.1186/s12891-020-03229-x

PMCID:: PMC7149842

Abstract Article PDF–614K

Select item 68926272.

Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication

Matteo Zanella, Alessandro Vitriolo, Alejandro Andirko, Pedro Tiago Martins, Stefanie Sturm, Thomas O’Rourke, Magdalena Laugsch, Natascia Malerba, Adrianos Skaros, Sebastiano Trattaro, Pierre-Luc Germain, Marija Mihailovic, Giuseppe Merla, Alvaro Rada-Iglesias, Cedric Boeckx, Giuseppe Testa

Sci Adv. 2019 Dec; 5(12): eaaw7908. Published online 2019 Dec 4. doi: 10.1126/sciadv.aaw7908

PMCID:: PMC6892627

Abstract Article PDF–5.5M

Select item 63560813.

Quantitative Proteomics of the Mitotic Chromosome Scaffold Reveals the Association of BAZ1B with Chromosomal Axes

Shinya Ohta, Takako Taniguchi, Nobuko Sato, Mayako Hamada, Hisaaki Taniguchi, Juri Rappsilber

Mol Cell Proteomics. 2019 Feb; 18(2): 169–181. Published online 2018 Sep 28. doi: 10.1074/mcp.RA118.000923

PMCID:: PMC6356081

Abstract Article PDF–3.0M

Select item 32512574.

WSTF does it all: a multifunctional protein in transcription, repair and replication

Chris Barnett, Jocelyn E. Krebs

Biochem Cell Biol. Author manuscript; available in PMC 2012 Jan 4.

Published in final edited form as: Biochem Cell Biol. 2011 Feb; 89(1): 12–23. doi: 10.1139/O10-114

Correction in:: Biochem Cell Biol. 2015 Aug; 93(4): 421.

PMCID:: PMC3251257

Abstract Article PDF–2.6M

Select item 86114145.

Downregulation of Williams syndrome transcription factor (WSTF) suppresses glioblastoma cell growth and invasion by inhibiting PI3K/AKT signal pathway

Liyuan Yang, Chunfu Du, Hui Chen, Zhengwen Diao

Eur J Histochem. 2021 Nov 2; 65(4): 3255. Published online 2021 Nov 17. doi: 10.4081/ejh.2021.3255

PMCID:: PMC8611414

Abstract Article PDF–1.0M

Select item 79000716.

Both variants of A1CF and BAZ1B genes are associated with gout susceptibility: a replication study and meta-analysis in a Japanese population

Makoto Kawaguchi, Akiyoshi Nakayama, Yuka Aoyagi, Takahiro Nakamura, Seiko Shimizu, Yusuke Kawamura, Mikiya Takao, Takashi Tamura, Asahi Hishida, Mako Nagayoshi, Mitsuo Nagase, Keiko Ooyama, Hiroshi Ooyama, Nariyoshi Shinomiya, Hirotaka Matsuo

Hum Cell. 2021; 34(2): 293–299. Published online 2021 Jan 31. doi: 10.1007/s13577-021-00485-4

PMCID:: PMC7900071

Abstract Article PDF–470K

Select item 56367917.

Non-canonical reader modules of BAZ1A promote recovery from DNA damage

Mariano Oppikofer, Meredith Sagolla, Benjamin Haley, Hui-Min Zhang, Sarah K. Kummerfeld, Jawahar Sudhamsu, E. Megan Flynn, Tianyi Bai, Jennifer Zhang, Claudio Ciferri, Andrea G. Cochran

Nat Commun. 2017; 8: 862. Published online 2017 Oct 11. doi: 10.1038/s41467-017-00866-0

PMCID:: PMC5636791

Abstract Article PDF–4.6M

Select item 52881758.

KRAS^G12 mutant induces the release of the WSTF/NRG3 complex, and contributes to an oncogenic paracrine signaling pathway

Yan Liu, Shu-Qing Wang, Yue-Hong Long, Su Chen, Yu-Feng Li, Jing-Hua Zhang

Oncotarget. 2016 Aug 16; 7(33): 53153–53164. Published online 2016 Jul 16. doi: 10.18632/oncotarget.10625

PMCID:: PMC5288175

Abstract Article PDF–8.6M

Select item 30125969.

Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study

Weihong Tang, Saonli Basu, Xiaoxiao Kong, James S. Pankow, Nena Aleksic, Adrian Tan, Mary Cushman, Eric Boerwinkle, Aaron R. Folsom

Blood. 2010 Dec 2; 116(23): 5032–5036. Prepublished online 2010 Aug 27. doi: 10.1182/blood-2010-05-283739

PMCID:: PMC3012596

Abstract Article

Select item 147956410.

The chromatin remodelling complex WSTF–SNF2h interacts with nuclear myosin 1 and has a role in RNA polymerase I transcription

Piergiorgio Percipalle, Nathalie Fomproix, Erica Cavellán, Renate Voit, Georg Reimer, Tim Krüger, Johan Thyberg, Ulrich Scheer, Ingrid Grummt, Ann-Kristin Östlund Farrants

EMBO Rep. 2006 May; 7(5): 525–530. Published online 2006 Mar 3. doi: 10.1038/sj.embor.7400657

PMCID:: PMC1479564

Abstract Article PDF–209K

Select item 301736911.

Mutation skew in genes identified by genome-wide association study of hypertriglyceridemia

Christopher T. Johansen, Jian Wang, Matthew B. Lanktree, Henian Cao, Adam D. McIntyre, Matthew R. Ban, Rebecca A. Martins, Brooke A. Kennedy, Reina G. Hassell, Maartje E. Visser, Stephen M. Schwartz, Benjamin F. Voight, Roberto Elosua, Veikko Salomaa, Christopher J. O'Donnell, Geesje M. Dallinga-Thie, Sonia S. Anand, Salim Yusuf, Murray W. Huff, Sekar Kathiresan, Robert A. Hegele

Nat Genet. Author manuscript; available in PMC 2011 Jan 7.

Published in final edited form as: Nat Genet. 2010 Aug; 42(8): 684–687. Published online 2010 Jul 25. doi: 10.1038/ng.628

PMCID:: PMC3017369

Abstract Article PDF–62K

Select item 285449912.

WSTF regulates the function of H2A.X via a novel tyrosine kinase activity

Andrew Xiao, Haitao Li, David Shechter, Sung Hee Ahn, Laura A. Fabrizio, Hediye Erdjument-Bromage, Satoko Ishibe-Murakami, Bin Wang, Paul Tempst, Kay Hofmann, Dinshaw J. Patel, Stephen J. Elledge, C. David Allis

Nature. Author manuscript; available in PMC 2010 Apr 14.

Published in final edited form as: Nature. 2009 Jan 1; 457(7225): 57–62. Published online 2008 Dec 17. doi: 10.1038/nature07668

PMCID:: PMC2854499

Abstract Article PDF–688K

Select item 661480013.

De novo phosphorylation of H2AX by WSTF regulates transcription-coupled homologous recombination repair

Jae-Hoon Ji, Sunwoo Min, Sunyoung Chae, Geun-Hyoung Ha, Yonghyeon Kim, Yeon-Ji Park, Chang-Woo Lee, Hyeseong Cho

Nucleic Acids Res. 2019 Jul 9; 47(12): 6299–6314. Published online 2019 May 2. doi: 10.1093/nar/gkz309

PMCID:: PMC6614800

Abstract Article PDF–24M

Select item 401167614.

The RSF1 Histone-Remodelling Factor Facilitates DNA Double-Strand Break Repair by Recruiting Centromeric and Fanconi Anaemia Proteins

Fabio Pessina, Noel F. Lowndes

PLoS Biol. 2014 May; 12(5): e1001856. Published online 2014 May 6. doi: 10.1371/journal.pbio.1001856

Correction in:: PLoS Biol. 2017 Feb; 15(2): e1002595.

Expression of Concern in:: PLoS Biol. 2024 May; 22(5): e3002635.

PMCID:: PMC4011676

Abstract Article PDF–3.0M

Select item 359166715.

The Proteomic Investigation of Chromatin Functional Domains Reveals Novel Synergisms among Distinct Heterochromatin Components

Monica Soldi, Tiziana Bonaldi

Mol Cell Proteomics. 2013 Mar; 12(3): 764–780. Published online 2013 Jan 14. doi: 10.1074/mcp.M112.024307

PMCID:: PMC3591667

Abstract Article PDF–2.8M

Select item 12599316.

WSTF–ISWI chromatin remodeling complex targets heterochromatic replication foci

Ludmila Bozhenok, Paul A. Wade, Patrick Varga-Weisz

EMBO J. 2002 May 1; 21(9): 2231–2241. doi: 10.1093/emboj/21.9.2231

Correction in:: EMBO J. 2002 Jun 17; 21(12): 3212.

PMCID:: PMC125993

Abstract Article PDF–315K

Select item 448608917.

Nuclear myosin 1 contributes to a chromatin landscape compatible with RNA polymerase II transcription activation

Bader Almuzzaini, Aishe A. Sarshad, Ann-Kristin Östlund Farrants, Piergiorgio Percipalle

BMC Biol. 2015; 13: 35. Published online 2015 Jun 5. doi: 10.1186/s12915-015-0147-z

PMCID:: PMC4486089

Abstract Article PDF–2.6M

Select item 307163018.

Genome-Wide Meta-Analysis Identifies Regions on 7p21 (AHR) and 15q24 (CYP1A2) As Determinants of Habitual Caffeine Consumption

Marilyn C. Cornelis, Keri L. Monda, Kai Yu, Nina Paynter, Elizabeth M. Azzato, Siiri N. Bennett, Sonja I. Berndt, Eric Boerwinkle, Stephen Chanock, Nilanjan Chatterjee, David Couper, Gary Curhan, Gerardo Heiss, Frank B. Hu, David J. Hunter, Kevin Jacobs, Majken K. Jensen, Peter Kraft, Maria Teresa Landi, Jennifer A. Nettleton, Mark P. Purdue, Preetha Rajaraman, Eric B. Rimm, Lynda M. Rose, Nathaniel Rothman, Debra Silverman, Rachael Stolzenberg-Solomon, Amy Subar, Meredith Yeager, Daniel I. Chasman, Rob M. van Dam, Neil E. Caporaso

PLoS Genet. 2011 Apr; 7(4): e1002033. Published online 2011 Apr 7. doi: 10.1371/journal.pgen.1002033

PMCID:: PMC3071630

Abstract Article PDF–281K

Select item 360510319.

Nuclear Myosin 1c Facilitates the Chromatin Modifications Required to Activate rRNA Gene Transcription and Cell Cycle Progression

Aishe Sarshad, Fatemeh Sadeghifar, Emilie Louvet, Raffaele Mori, Stefanie Böhm, Bader Al-Muzzaini, Anna Vintermist, Nathalie Fomproix, Ann-Kristin Östlund, Piergiorgio Percipalle

PLoS Genet. 2013 Mar; 9(3): e1003397. Published online 2013 Mar 21. doi: 10.1371/journal.pgen.1003397

PMCID:: PMC3605103

Abstract Article PDF–3.5M

Select item 275814220.

A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia

Robert A. Hegele, Matthew R. Ban, Neil Hsueh, Brooke A. Kennedy, Henian Cao, Guang Yong Zou, Sonia Anand, Salim Yusuf, Murray W. Huff, Jian Wang

Hum Mol Genet. 2009 Nov 1; 18(21): 4189–4194. Published online 2009 Aug 5. doi: 10.1093/hmg/ddp361

PMCID:: PMC2758142

Abstract Article PDF–81K

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