未登录Disruption of MeCP2-TCF20 complex underlies distinct neurodevelopmental disordersMeCP2-TCF20复合体的破坏是不同的神经发育障碍的基础
Zhou, Jian; Hamdan, Hamdan; Yalamanchili, Hari Krishna; Pang, Kaifang; Pohodich, Amy E.; Lopez, Joanna; Shao, Yingyao; Oses-Prieto, Juan A.; Li, Lifang; Kim, Wonho; Durham, Mark A.; Bajikar, Sameer S.; Palmer, Donna J.; Ng, Philip; Thompson, Michelle L.; Bebin, E. Martina; Mueller, Amelie J.; Kuechler, Alma; Kampmeier, Antje; Haack, Tobias B.; Burlingame, Alma L.; Liu, Zhandong; Rasband, Matthew N.; Zoghbi, Huda Y. .png)
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收藏SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in femalesSPEN单倍功能不全导致神经发育障碍重叠近端1p36缺失综合征，并伴有女性X染色体的表观特征Radio, Francesca Clementina; Pang, Kaifang; Ciolfi, Andrea; Levy, Michael A.; Hernandez-Garcia, Andres; Pedace, Lucia; Pantaleoni, Francesca; Liu, Zhandong; de Boer, Elke; Jackson, Adam; Bruselles, Alessandro; McConkey, Haley; Stellacci, Emilia; Lo Cicero, Stefania; Motta, Marialetizia; Carrozzo, Rosalba; Dentici, Maria Lisa; McWalter, Kirsty; Desai, Megha; Monaghan, Kristin G.; Telegrafi, Aida; Philippe, Christophe; Vitobello, Antonio; Au, Margaret; Grand, Katheryn; Sanchez-Lara, Pedro A.; Baez, Joanne; Lindstrom, Kristin; Kulch, Peggy; Sebastian, Jessica; Madan-Khetarpal, Suneeta; Roadhouse, Chelsea; MacKenzie, Jennifer J.; Monteleone, Berrin; Saunders, Carol J.; Cuevas, July K. Jean; Cross, Laura; Zhou, Dihong; Hartley, Taila; Sawyer, Sarah L.; Monteiro, Fabiola Paoli; Secches, Tania Vertemati; Kok, Fernando; Schultz-Rogers, Laura E.; Macke, Erica L.; Morava, Eva; Klee, Eric W.; Kemppainen, Jennifer; Iascone, Maria; Selicorni, Angelo; Tenconi, Romano; Amor, David J.; Pais, Lynn; Gallacher, Lyndon; Turnpenny, Peter D.; Stals, Karen; Ellard, Sian; Cabet, Sara; Lesca, Gaetan; Pascal, Joset; Steindl, Katharina; Ravid, Sarit; Weiss, Karin; Castle, Alison M. R.; Carter, Melissa T.; Kalsner, Louisa; de Vries, Bert B. A.; van Bon, Bregje W.; Wevers, Marijke R.; Pfundt, Rolph; Stegmann, Alexander P. A.; Kerr, Bronwyn; Kingston, Helen M.; Chandler, Kate E.; Sheehan, Willow; Elias, Abdallah F.; Shinde, Deepali N.; Towne, Meghan C.; Robin, Nathaniel H.; Goodloe, Dana; Vanderver, Adeline; Sherbini, Omar; Bluske, Krista; Hagelstrom, R. Tanner; Zanus, Caterina; Faletra, Flavio; Musante, Luciana; Kurtz-Nelson, Evangeline C.; Earl, Rachel K.; Anderlid, Britt-Marie; Morin, Gilles; van Slegtenhorst, Marjon; Diderich, Karin E. M.; Brooks, Alice S.; Gribnau, Joost; Boers, Ruben G.; Finestra, Teresa Robert; Carter, Lauren B.; Rauch, Anita; Gasparini, Paolo; Boycott, Kym M.; Barakat, Tahsin Stefan; Graham, John M., Jr.; Faivre, Laurence; Banka, Siddharth; Wang, Tianyun; Eichler, Evan E.; Priolo, Manuela; Dallapiccola, Bruno; Vissers, Lisenka E. L. M.; Sadikovic, Bekim; Scott, Daryl A.; Holder, Jimmy Lloyd, Jr.; Tartaglia, Marco 分享 收藏 分享 收藏 BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorderBAZ2B单倍体不足是发育迟缓，智力障碍和自闭症谱系障碍的原因Scott, Tiana M.; Guo, Hui; Eichler, Evan E.; Rosenfeld, Jill A.; Pang, Kaifang; Liu, Zhandong; Lalani, Seema; Bi, Weimin; Yang, Yaping; Bacino, Carlos A.; Streff, Haley; Lewis, Andrea M.; Koenig, Mary K.; Thiffault, Isabelle; Bellomo, Allison; Everman, David B.; Jones, Julie R.; Stevenson, Roger E.; Bernier, Raphael; Gilissen, Christian; Pfundt, Rolph; Hiatt, Susan M.; Cooper, Gregory M.; Holder, Jimmy L.; Scott, Daryl A. 分享 收藏 A kinome-wide RNAi screen identifies ERK2 as a druggable regulator of Shank3 stabilityWang, Li; Adamski, Carolyn J.; Bondar, Vitaliy V.; Craigen, Evelyn; Collette, John R.; Pang, Kaifang; Han, Kihoon; Jain, Antrix; Y. Jung, Sung; Liu, Zhandong; Sifers, Richard N.; Holder, J. Lloyd, Jr.; Zoghbi, Huda Y. 分享 收藏 An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 functionWang, Li; Pang, Kaifang; Han, Kihoon; Adamski, Carolyn J.; Wang, Wei; He, Lingjie; Lai, Jason K.; Bondar, Vitaliy V.; Duman, Joseph G.; Richman, Ronald; Tolias, Kimberley F.; Barth, Patrick; Palzkill, Timothy; Liu, Zhandong; Holder, J. Lloyd, Jr.; Zoghbi, Huda Y. 分享 收藏 High-Throughput Functional Analysis Distinguishes Pathogenic, Nonpathogenic, and Compensatory Transcriptional Changes in NeurodegenerationAl-Ramahi, Ismael; Lu, Boxun; Di Paola, Simone; Pang, Kaifang; de Haro, Maria; Peluso, Ivana; Gallego-Flores, Tatiana; Malik, Nazish T.; Erikson, Kelly; Bleiberg, Benjamin A.; Avalos, Matthew; Fan, George; Rivers, Laura Elizabeth; Laitman, Andrew M.; Diaz-Garcia, Javier R.; Hild, Marc; Palacino, James; Liu, Zhandong; Medina, Diego L.; Botas, Juan 分享 收藏 Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion SyndromeYin, Jiani; Chen, Wu; Chao, Eugene S.; Soriano, Sirena; Wang, Li; Wang, Wei; Cummock, Steven E.; Tao, Huifang; Pang, Kaifang; Liu, Zhandong; Pereira, Fred A.; Samaco, Rodney C.; Zoghbi, Huda Y.; Xue, Mingshan; Schaaf, Christian P. 分享 收藏 Post-transcriptional regulation of SHANK3 expression by microRNAs related to multiple neuropsychiatric disordersChoi, Su-Yeon; Pang, Kaifang; Kim, Joo Yeon; Ryu, Jae Ryun; Kang, Hyojin; Liu, Zhandong; Kim, Won-Ki; Sun, Woong; Kim, Hyun; Han, Kihoon 分享 收藏 分享 收藏 
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