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Items: 1 to 20 of 58

1.
Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder
Masaki Nishioka, An-a Kazuno, Takumi Nakamura, Naomi Sakai, Takashi Hayama, Kumiko Fujii, Koji Matsuo, Atsuko Komori, Mizuho Ishiwata, Yoshinori Watanabe, Takashi Oka, Nana Matoba, Muneko Kataoka, Ahmed N. Alkanaq, Kohei Hamanaka, Takashi Tsuboi, Toru Sengoku, Kazuhiro Ogata, Nakao Iwata, Masashi Ikeda, Naomichi Matsumoto, Tadafumi Kato, Atsushi Takata
Nat Commun. 2021; 12: 3750. Published online 2021 Jun 18. doi: 10.1038/s41467-021-23453-w
PMCID:
PMC8213845
ArticlePDF–2.9M
2.
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J.M. Dingemans, Sarah J. Goodman, Michelle T. Siu, Cheryl Cytrynbaum, Sanaa Choufani, Ny Hoang, Susan Walker, Zain Awamleh, Joshua Charkow, Stephen Meyn, Rolph Pfundt, Tuula Rinne, Thatjana Gardeitchik, Bert B.A. de Vries, A. Chantal Deden, Erika Leenders, Michael Kwint, Constance T.R.M. Stumpel, Servi J.C. Stevens, Jeroen R. Vermeulen, Jeske V.T. van Harssel, Danielle G.M. Bosch, Koen L.I. van Gassen, Ellen van Binsbergen, Christa M. de Geus, Hein Brackel, Maja Hempel, Davor Lessel, Jonas Denecke, Anne Slavotinek, Jonathan Strober, Amy Crunk, Leandra Folk, Ingrid M. Wentzensen, Hui Yang, Fanggeng Zou, Francisca Millan, Richard Person, Yili Xie, Shuxi Liu, Lilian B. Ousager, Martin Larsen, Laura Schultz-Rogers, Eva Morava, Eric W. Klee, Ian R. Berry, Jennifer Campbell, Kristin Lindstrom, Brianna Pruniski, Ann M. Neumeyer, Jessica A. Radley, Chanika Phornphutkul, Berkley Schmidt, William G. Wilson, Katrin Õunap, Karit Reinson, Sander Pajusalu, Arie van Haeringen, Claudia Ruivenkamp, Roos Cuperus, Fernando Santos-Simarro, María Palomares-Bralo, Marta Pacio-Míguez, Alyssa Ritter, Elizabeth Bhoj, Elin Tønne, Kristian Tveten, Gerarda Cappuccio, Nicola Brunetti-Pierri, Leah Rowe, Jason Bunn, Margarita Saenz, Konrad Platzer, Mareike Mertens, Oana Caluseriu, Małgorzata J.M. Nowaczyk, Ronald D. Cohn, Peter Kannu, Ebba Alkhunaizi, David Chitayat, Stephen W. Scherer, Han G. Brunner, Lisenka E.L.M. Vissers, Tjitske Kleefstra, David A. Koolen, Rosanna Weksberg
Am J Hum Genet. 2021 Jun 3; 108(6): 1053–1068. Published online 2021 Apr 27. doi: 10.1016/j.ajhg.2021.04.008
PMCID:
PMC8206150
ArticlePDF–3.1M
3.
Cryo-EM structure of human SRCAP complex
Yangyang Feng, Yuan Tian, Zihan Wu, Yanhui Xu
Cell Res. 2018 Nov; 28(11): 1121–1123. Published online 2018 Oct 18. doi: 10.1038/s41422-018-0102-y
PMCID:
PMC6218446
ArticlePDF–895K
4.
Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome
Wenke Seifert, Peter Meinecke, Gabriele Krüger, Eva Rossier, Wolfram Heinritz, Achim Wüsthof, Denise Horn
BMC Med Genet. 2014; 15: 127. Published online 2014 Nov 30. doi: 10.1186/s12881-014-0127-0
PMCID:
PMC4412025
ArticlePDF–1.0M
5.
Gene Reactivation by 5-Aza-2′-Deoxycytidine–Induced Demethylation Requires SRCAP–Mediated H2A.Z Insertion to Establish Nucleosome Depleted Regions
Xiaojing Yang, Houtan Noushmehr, Han Han, Claudia Andreu-Vieyra, Gangning Liang, Peter A. Jones
PLoS Genet. 2012 Mar; 8(3): e1002604. Published online 2012 Mar 29. doi: 10.1371/journal.pgen.1002604
PMCID:
PMC3315468
ArticlePDF–2.0M
6.
Loss of H2A.Z Is Not Sufficient to Determine Transcriptional Activity of Snf2-Related CBP Activator Protein or p400 Complexes
Tamara A. Bowman, Madeline M. Wong, Linda K. Cox, Joseph J. Baldassare, John C. Chrivia
Int J Cell Biol. 2011; 2011: 715642. Published online 2011 May 29. doi: 10.1155/2011/715642
PMCID:
PMC3140016
ArticlePDF–946K
7.
LINC00665 sponges miR-641 to promote the progression of breast cancer by targeting the SNF2-related CREBBP activator protein (SRCAP)
Wen Cao, Xiaojing Liu, Weijia Su, Hao Liang, Huiru Tang, Weiliang Zhang, Shuhong Huang, Ningning Dang, Aiguo Qiao
Bioengineered. 2022; 13(2): 4573–4586. Published online 2022 Feb 12. doi: 10.1080/21655979.2022.2031402
PMCID:
PMC8974044
ArticlePDF–3.5M
8.
Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome
Rebecca L. Hood, Matthew A. Lines, Sarah M. Nikkel, Jeremy Schwartzentruber, Chandree Beaulieu, Małgorzata J.M. Nowaczyk, Judith Allanson, Chong Ae Kim, Dagmar Wieczorek, Jukka S. Moilanen, Didier Lacombe, Gabriele Gillessen-Kaesbach, Margo L. Whiteford, Caio Robledo D.C. Quaio, Israel Gomy, Debora R. Bertola, Beate Albrecht, Konrad Platzer, George McGillivray, Ruobing Zou, D. Ross McLeod, Albert E. Chudley, Bernard N. Chodirker, Janet Marcadier, FORGE Canada Consortium, Jacek Majewski, Dennis E. Bulman, Susan M. White, Kym M. Boycott
Am J Hum Genet. 2012 Feb 10; 90(2): 308–313. doi: 10.1016/j.ajhg.2011.12.001
PMCID:
PMC3276662
ArticlePDF–440K
9.
Purification and Assay of the Human INO80 and SRCAP Chromatin Remodeling Complexes
Yong Cai, Jingji Jin, Aaron J. Gottschalk, Tingting Yao, Joan W. Conaway, Ronald C. Conaway
Methods. Author manuscript; available in PMC 2011 May 11.
Published in final edited form as: Methods. 2006 Dec; 40(4): 312–317. doi: 10.1016/j.ymeth.2006.06.023
PMCID:
PMC3092633
ArticlePDF–381K
10.
Identification and characterization of the two isoforms of the vertebrate H2A.Z histone variant
Ryo Matsuda, Tetsuya Hori, Hiroshi Kitamura, Kozo Takeuchi, Tatsuo Fukagawa, Masahiko Harata
Nucleic Acids Res. 2010 Jul; 38(13): 4263–4273. Published online 2010 Mar 18. doi: 10.1093/nar/gkq171
PMCID:
PMC2910051
ArticlePDF–869K
11.
Adenovirus DNA Binding Protein Interacts with the SNF2-Related CBP Activator Protein (SrCap) and Inhibits SrCap-Mediated Transcription
Xiequn Xu, Isaac Chackalaparampil, M. Alexandra Monroy, Maria T. Cannella, Elizabeth Pesek, John Chrivia, Peter Yaciuk
J Virol. 2001 Nov; 75(21): 10033–10040. doi: 10.1128/JVI.75.21.10033-10040.2001
PMCID:
PMC114578
ArticlePDF–1.5M
12.
The catalytic subunit of the SWR1 remodeler is a histone chaperone for the H2A.Z-H2B dimer
Jingjun Hong, Hanqiao Feng, Feng Wang, Anand Ranjan, Jianhong Chen, Jiansheng Jiang, Rodolfo Ghirlando, T. Sam Xiao, Carl Wu, Yawen Bai
Mol Cell. Author manuscript; available in PMC 2015 Feb 6.
Published in final edited form as: Mol Cell. 2014 Feb 6; 53(3): 498–505. doi: 10.1016/j.molcel.2014.01.010
PMCID:
PMC3940207
ArticlePDF–1.6M
13.
Hepatitis C Virus NS3 Protein Can Activate the Notch-Signaling Pathway through Binding to a Transcription Factor, SRCAP
Atsushi Iwai, Tsutomu Takegami, Takuya Shiozaki, Tadaaki Miyazaki
PLoS One. 2011; 6(6): e20718. Published online 2011 Jun 6. doi: 10.1371/journal.pone.0020718
PMCID:
PMC3108961
ArticlePDF–760K
14.
Human SRCAP and Drosophila melanogaster DOM Are Homologs That Function in the Notch Signaling Pathway
Joel C. Eissenberg, Madeline Wong, John C. Chrivia
Mol Cell Biol. 2005 Aug; 25(15): 6559–6569. doi: 10.1128/MCB.25.15.6559-6569.2005
PMCID:
PMC1190335
ArticlePDF–744K
15.
Suppression of SRCAP chromatin remodelling complex and restriction of lymphoid lineage commitment by Pcid2
Buqing Ye, Benyu Liu, Liuliu Yang, Guanling Huang, Lu Hao, Pengyan Xia, Shuo Wang, Ying Du, Xiwen Qin, Pingping Zhu, Jiayi Wu, Nobuo Sakaguchi, Junyan Zhang, Zusen Fan
Nat Commun. 2017; 8: 1518. Published online 2017 Nov 15. doi: 10.1038/s41467-017-01788-7
PMCID:
PMC5686073
ArticlePDF–4.8M
16.
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan KC Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang, Giovanna Pellecchia, Janet A Buchanan, Susan Walker, Christian R Marshall, Mohammed Uddin, Mehdi Zarrei, Eric Deneault, Lia D’Abate, Ada JS Chan, Stephanie Koyanagi, Tara Paton, Sergio L Pereira, Ny Hoang, Worrawat Engchuan, Edward J Higginbotham, Karen Ho, Sylvia Lamoureux, Weili Li, Jeffrey R MacDonald, Thomas Nalpathamkalam, Wilson WL Sung, Fiona J Tsoi, John Wei, Lizhen Xu, Anne-Marie Tasse, Emily Kirby, William Van Etten, Simon Twigger, Wendy Roberts, Irene Drmic, Sanne Jilderda, Bonnie MacKinnon Modi, Barbara Kellam, Michael Szego, Cheryl Cytrynbaum, Rosanna Weksberg, Lonnie Zwaigenbaum, Marc Woodbury-Smith, Jessica Brian, Lili Senman, Alana Iaboni, Krissy Doyle-Thomas, Ann Thompson, Christina Chrysler, Jonathan Leef, Tal Savion-Lemieux, Isabel M Smith, Xudong Liu, Rob Nicolson, Vicki Seifer, Angie Fedele, Edwin H Cook, Stephen Dager, Annette Estes, Louise Gallagher, Beth A Malow, Jeremy R Parr, Sarah J Spence, Jacob Vorstman, Brendan J Frey, James T Robinson, Lisa J Strug, Bridget A Fernandez, Mayada Elsabbagh, Melissa T Carter, Joachim Hallmayer, Bartha M Knoppers, Evdokia Anagnostou, Peter Szatmari, Robert H Ring, David Glazer, Mathew T Pletcher, Stephen W Scherer
Nat Neurosci. Author manuscript; available in PMC 2017 Oct 1.
Published in final edited form as: Nat Neurosci. 2017 Apr; 20(4): 602–611. Published online 2017 Mar 6. doi: 10.1038/nn.4524
PMCID:
PMC5501701
ArticlePDF–1.3M
17.
The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov, Brian J. O’Roak, Stephan J. Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A. Stessman, Kali Witherspoon, Laura Vives, Karynne E. Patterson, Joshua D. Smith, Bryan Paeper, Deborah A. Nickerson, Jeanselle Dea, Shan Dong, Luis E. Gonzalez, Jefferey D. Mandell, Shrikant M. Mane, Michael T. Murtha, Catherine A. Sullivan, Michael F. Walker, Zainulabedin Waqar, Liping Wei, A. Jeremy Willsey, Boris Yamrom, Yoon-ha Lee, Ewa Grabowska, Ertugrul Dalkic, Zihua Wang, Steven Marks, Peter Andrews, Anthony Leotta, Jude Kendall, Inessa Hakker, Julie Rosenbaum, Beicong Ma, Linda Rodgers, Jennifer Troge, Giuseppe Narzisi, Seungtai Yoon, Michael C. Schatz, Kenny Ye, W. Richard McCombie, Jay Shendure, Evan E. Eichler, Matthew W. State, Michael Wigler
Nature. Author manuscript; available in PMC 2015 May 13.
Published in final edited form as: Nature. 2014 Nov 13; 515(7526): 216–221. Published online 2014 Oct 29. doi: 10.1038/nature13908
PMCID:
PMC4313871
ArticlePDF–377K
18.
H2A.Z.2.2 is an alternatively spliced histone H2A.Z variant that causes severe nucleosome destabilization
Clemens Bönisch, Katrin Schneider, Sebastian Pünzeler, Sonja M. Wiedemann, Christina Bielmeier, Marco Bocola, H. Christian Eberl, Wolfgang Kuegel, Jürgen Neumann, Elisabeth Kremmer, Heinrich Leonhardt, Matthias Mann, Jens Michaelis, Lothar Schermelleh, Sandra B. Hake
Nucleic Acids Res. 2012 Jul; 40(13): 5951–5964. Published online 2012 Mar 29. doi: 10.1093/nar/gks267
PMCID:
PMC3401452
ArticlePDF–8.3M
19.
A Myc rather than core pluripotency module accounts for the shared signatures of embryonic stem and cancer cells
Jonghwan Kim, Andrew J. Woo, Jianlin Chu, Jonathan W. Snow, Yuko Fujiwara, Chul Geun Kim, Alan B. Cantor, Stuart H. Orkin
Cell. Author manuscript; available in PMC 2011 Apr 15.
Published in final edited form as: Cell. 2010 Oct 15; 143(2): 313–324. doi: 10.1016/j.cell.2010.09.010
PMCID:
PMC3018841
ArticlePDF–5.8M
20.
Structural and Functional Conservation of the NuA4 Histone Acetyltransferase Complex from Yeast to Humans
Yannick Doyon, William Selleck, William S. Lane, Song Tan, Jacques Côté
Mol Cell Biol. 2004 Mar; 24(5): 1884–1896. doi: 10.1128/MCB.24.5.1884-1896.2004
PMCID:
PMC350560
ArticlePDF–743K

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