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Items: 1 to 20 of 58

1.
Regulation of human cortical interneuron development by the chromatin remodeling protein CHD2
E. M. A. Lewis, G. Chapman, K. Kaushik, J. Determan, I. Antony, K. Meganathan, M. Narasimhan, P. Gontarz, B. Zhang, K. L. Kroll
Sci Rep. 2022; 12: 15636. Published online 2022 Sep 17. doi: 10.1038/s41598-022-19654-y
PMCID:
PMC9482661
AbstractArticlePDF–9.6M
2.
Novel Loss-of-Function Variants in CHD2 Cause Childhood-Onset Epileptic Encephalopathy in Chinese Patients
Xu Wang, Di Cui, Changhong Ding, Chunhong Chen, Xiaohui Wang, Fang Fang, Hong Jin, Xiaotun Ren
Genes (Basel) 2022 May; 13(5): 908. Published online 2022 May 19. doi: 10.3390/genes13050908
PMCID:
PMC9140428
AbstractArticlePDF–1.2M
3.
CHD2-Related CNS Pathologies
Marc-Michel Wilson, David C. Henshall, Susan M. Byrne, Gary P. Brennan
Int J Mol Sci. 2021 Jan; 22(2): 588. Published online 2021 Jan 8. doi: 10.3390/ijms22020588
PMCID:
PMC7827033
AbstractArticlePDF–809K
4.
A regulatory role for CHD2 in myelopoiesis
Farzaneh Shahin Varnoosfaderani, Anna Palau, Wenbo Dong, Jenna Persson, Mickaël Durand-Dubief, J Peter Svensson, Andreas Lennartsson
Epigenetics. 2020; 15(6-7): 702–714. Published online 2020 Jan 10. doi: 10.1080/15592294.2019.1710913
PMCID:
PMC7574388
AbstractArticlePDF–3.8M
5.
Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report
Alice Poisson, Nicolas Chatron, Audrey Labalme, Pierre Fourneret, Dorothée Ville, Marie Laure Mathieu, Damien Sanlaville, Caroline Demily, Gaëtan Lesca
BMC Med Genet. 2020; 21: 10. Published online 2020 Jan 8. doi: 10.1186/s12881-019-0946-0
PMCID:
PMC6950831
AbstractArticlePDF–1.2M
6.
CHD2 variants are a risk factor for photosensitivity in epilepsy
Elizabeth C. Galizia, Candace T. Myers, Costin Leu, Carolien G. F. de Kovel, Tatiana Afrikanova, Maria Lorena Cordero-Maldonado, Teresa G. Martins, Maxime Jacmin, Suzanne Drury, V. Krishna Chinthapalli, Hiltrud Muhle, Manuela Pendziwiat, Thomas Sander, Ann-Kathrin Ruppert, Rikke S. Møller, Holger Thiele, Roland Krause, Julian Schubert, Anna-Elina Lehesjoki, Peter Nürnberg, Holger Lerche, for the EuroEPINOMICS CoGIE Consortium, Aarno Palotie, Antonietta Coppola, Salvatore Striano, Luigi Del Gaudio, Christopher Boustred, Amy L. Schneider, Nicholas Lench, Bosanka Jocic-Jakubi, Athanasios Covanis, Giuseppe Capovilla, Pierangelo Veggiotti, Marta Piccioli, Pasquale Parisi, Laura Cantonetti, Lynette G. Sadleir, Saul A. Mullen, Samuel F. Berkovic, Ulrich Stephani, Ingo Helbig, Alexander D. Crawford, Camila V. Esguerra, Dorothee G. A. Kasteleijn-Nolst Trenité, Bobby P. C. Koeleman, Heather C. Mefford, Ingrid E. Scheffer, Sanjay M. Sisodiya
Brain. 2015 May; 138(5): 1198–1207. Published online 2015 Mar 16. doi: 10.1093/brain/awv052
PMCID:
PMC4407192
AbstractArticlePDF–464K
7.
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures
Rhys H. Thomas, Lin Mei Zhang, Gemma L. Carvill, John S. Archer, Sinéad B. Heavin, Simone A. Mandelstam, Dana Craiu, Samuel F. Berkovic, Deepak S. Gill, Heather C. Mefford, Ingrid E. Scheffer
Neurology. 2015 Mar 3; 84(9): 951–958. doi: 10.1212/WNL.0000000000001305
PMCID:
PMC4351660
AbstractArticlePDF–887K
8.
Human CHD2 Is a Chromatin Assembly ATPase Regulated by Its Chromo- and DNA-binding Domains
Jessica C. Liu, Catarina G. Ferreira, Timur Yusufzai
J Biol Chem. 2015 Jan 2; 290(1): 25–34. Published online 2014 Nov 10. doi: 10.1074/jbc.M114.609156
PMCID:
PMC4281729
AbstractArticlePDF–1.1M
9.
PARP1 Links CHD2-Mediated Chromatin Expansion and H3.3 Deposition to DNA Repair by Non-homologous End-Joining
Martijn S. Luijsterburg, Inge de Krijger, Wouter W. Wiegant, Rashmi G. Shah, Godelieve Smeenk, Anton J.L. de Groot, Alex Pines, Alfred C.O. Vertegaal, Jacqueline J.L. Jacobs, Girish M. Shah, Haico van Attikum
Mol Cell. 2016 Feb 18; 61(4): 547–562. doi: 10.1016/j.molcel.2016.01.019
PMCID:
PMC4769320
AbstractArticle
10.
De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome
Arvid Suls, Johanna A. Jaehn, Angela Kecskés, Yvonne Weber, Sarah Weckhuysen, Dana C. Craiu, Aleksandra Siekierska, Tania Djémié, Tatiana Afrikanova, Padhraig Gormley, Sarah von Spiczak, Gerhard Kluger, Catrinel M. Iliescu, Tiina Talvik, Inga Talvik, Cihan Meral, Hande S. Caglayan, Beatriz G. Giraldez, José Serratosa, Johannes R. Lemke, Dorota Hoffman-Zacharska, Elzbieta Szczepanik, Nina Barisic, Vladimir Komarek, Helle Hjalgrim, Rikke S. Møller, Tarja Linnankivi, Petia Dimova, Pasquale Striano, Federico Zara, Carla Marini, Renzo Guerrini, Christel Depienne, Stéphanie Baulac, Gregor Kuhlenbäumer, Alexander D. Crawford, Anna-Elina Lehesjoki, Peter A.M. de Witte, Aarno Palotie, Holger Lerche, Camila V. Esguerra, Peter De Jonghe, Ingo Helbig, the EuroEPINOMICS RES Consortium
Am J Hum Genet. 2013 Nov 7; 93(5): 967–975. doi: 10.1016/j.ajhg.2013.09.017
PMCID:
PMC3824114
AbstractArticlePDF–564K
11.
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
Gemma L. Carvill, Sinéad B. Heavin, Simone C. Yendle, Jacinta M. McMahon, Brian J. O’Roak, Joseph Cook, Adiba Khan, Michael O Dorschner, Molly Weaver, Sophie Calvert, Stephen Malone, Geoffrey Wallace, Thorsten Stanley, Ann M. E. Bye, Andrew Bleasel, Katherine B. Howell, Sara Kivity, Mark T. Mackay, Victoria Rodriguez-Casero, Richard Webster, Amos Korczyn, Zaid Afawi, Nathanel Zelnick, Tally Lerman-Sagie, Dorit Lev, Rikke S. Møller, Deepak Gill, Danielle M. Andrade, Jeremy L. Freeman, Lynette G. Sadleir, Jay Shendure, Samuel F. Berkovic, Ingrid E. Scheffer, Heather C. Mefford
Nat Genet. Author manuscript; available in PMC 2014 Jan 1.
Published in final edited form as: Nat Genet. 2013 Jul; 45(7): 825–830. Published online 2013 May 26. doi: 10.1038/ng.2646
PMCID:
PMC3704157
ArticlePDF–667K
12.
CHD1 and CHD2 are positive regulators of HIV-1 gene expression
Melissa J Rodgers, David J Banks, Kenneth A Bradley, John AT Young
Virol J. 2014; 11: 180. Published online 2014 Oct 8. doi: 10.1186/1743-422X-11-180
PMCID:
PMC4283154
AbstractArticlePDF–963K
13.
Non-EST based prediction of exon skipping and intron retention events using Pfam information
Michael Hiller, Klaus Huse, Matthias Platzer, Rolf Backofen
Nucleic Acids Res. 2005; 33(17): 5611–5621. Published online 2005 Oct 4. doi: 10.1093/nar/gki870
PMCID:
PMC1243800
AbstractArticlePDF–140K
14.
Characterization of the CHD family of proteins
Trevor Woodage, Munira A. Basrai, Andreas D. Baxevanis, Philip Hieter, Francis S. Collins
Proc Natl Acad Sci U S A. 1997 Oct 14; 94(21): 11472–11477. doi: 10.1073/pnas.94.21.11472
PMCID:
PMC23509
AbstractArticlePDF–338K
15.
TDP-43 promotes neurodegeneration by impairing chromatin remodeling
Amit Berson, Ashley Sartoris, Raffaella Nativio, Vivianna Van Deerlin, Jon B. Toledo, Sílvia Porta, Shichong Liu, Chia-Yu Chung, Benjamin A. Garcia, Virginia M.-Y. Lee, John Q. Trojanowski, F. Brad Johnson, Shelley L. Berger, Nancy M. Bonini
Curr Biol. Author manuscript; available in PMC 2018 Dec 4.
Published in final edited form as: Curr Biol. 2017 Dec 4; 27(23): 3579–3590.e6. Published online 2017 Nov 16. doi: 10.1016/j.cub.2017.10.024
PMCID:
PMC5720388
AbstractArticlePDF–2.1M
16.
Multidimensional Proteomics Reveals a Role of UHRF2 in the Regulation of Epithelial-Mesenchymal Transition (EMT)
Mi Lai, Lizhu Liang, Jiwei Chen, Naiqi Qiu, Sai Ge, Shuhui Ji, Tieliu Shi, Bei Zhen, Mingwei Liu, Chen Ding, Yi Wang, Jun Qin
Mol Cell Proteomics. 2016 Jul; 15(7): 2263–2278. Published online 2016 Apr 25. doi: 10.1074/mcp.M115.057448
PMCID:
PMC4937503
AbstractArticlePDF–4.6M
17.
Proteomic analysis reveals novel ligands and substrates for LNX1 E3 ubiquitin ligase
Joan A. Lenihan, Orthis Saha, Paul W. Young
PLoS One. 2017; 12(11): e0187352. Published online 2017 Nov 9. doi: 10.1371/journal.pone.0187352
PMCID:
PMC5679597
AbstractArticlePDF–10M
18.
SHLD2/FAM35A co‐operates with REV7 to coordinate DNA double‐strand break repair pathway choice
Steven Findlay, John Heath, Vincent M Luo, Abba Malina, Théo Morin, Yan Coulombe, Billel Djerir, Zhigang Li, Arash Samiei, Estelle Simo‐Cheyou, Martin Karam, Halil Bagci, Dolev Rahat, Damien Grapton, Elise G Lavoie, Christian Dove, Husam Khaled, Hellen Kuasne, Koren K Mann, Kathleen Oros Klein, Celia M Greenwood, Yuval Tabach, Morag Park, Jean‐Francois Côté, Jean‐Yves Masson, Alexandre Maréchal, Alexandre Orthwein
EMBO J. 2018 Sep 14; 37(18): e100158. Published online 2018 Aug 28. doi: 10.15252/embj.2018100158
PMCID:
PMC6138439
AbstractArticlePDF–1.1M
19.
Loci Associated with N-Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological Cancers
Gordan Lauc, Jennifer E. Huffman, Maja Pučić, Lina Zgaga, Barbara Adamczyk, Ana Mužinić, Mislav Novokmet, Ozren Polašek, Olga Gornik, Jasminka Krištić, Toma Keser, Veronique Vitart, Blanca Scheijen, Hae-Won Uh, Mariam Molokhia, Alan Leslie Patrick, Paul McKeigue, Ivana Kolčić, Ivan Krešimir Lukić, Olivia Swann, Frank N. van Leeuwen, L. Renee Ruhaak, Jeanine J. Houwing-Duistermaat, P. Eline Slagboom, Marian Beekman, Anton J. M. de Craen, André M. Deelder, Qiang Zeng, Wei Wang, Nicholas D. Hastie, Ulf Gyllensten, James F. Wilson, Manfred Wuhrer, Alan F. Wright, Pauline M. Rudd, Caroline Hayward, Yurii Aulchenko, Harry Campbell, Igor Rudan
PLoS Genet. 2013 Jan; 9(1): e1003225. Published online 2013 Jan 31. doi: 10.1371/journal.pgen.1003225
PMCID:
PMC3561084
AbstractArticlePDF–1.0M
20.
Interaction of LATS1 with SMAC links the MST2/Hippo pathway with apoptosis in an IAP-dependent manner
Lucía García-Gutiérrez, Emma Fallahi, Nourhan Aboud, Niall Quinn, David Matallanas
Cell Death Dis. 2022 Aug; 13(8): 692. Published online 2022 Aug 8. doi: 10.1038/s41419-022-05147-3
PMCID:
PMC9360443
AbstractArticlePDF–5.8M

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