Sex-biased and parental allele-specific gene regulation by KDM6A

por Ma, Wenxiu, Fang, He, Pease, Nicolas, Filippova, Galina N., Disteche, Christine M., Berletch, Joel B.
Publicado 2022

CTCF Expression is Essential for Somatic Cell Viability and Protection Against Cancer

por Bailey, Charles G, Metierre, Cynthia, Feng, Yue, Baidya, Kinsha, Filippova, Galina N, Loukinov, Dmitri I, Lobanenkov, Victor V, Semaan, Crystal, Rasko, John EJ
Publicado 2018

CTCF-mediated insulation and chromatin environment modulate Car5b escape from X inactivation

por Fang, He, Tronco, Ana R., Bonora, Giancarlo, Nguyen, Truong, Thakur, Jitendra, Berletch, Joel B., Filippova, Galina N., Henikoff, Steven, Shendure, Jay, Noble, William S., Disteche, Christine M., Deng, Xinxian
Publicado 2023

Trans- and cis-acting effects of Firre on epigenetic features of the inactive X chromosome

por Fang, He, Bonora, Giancarlo, Lewandowski, Jordan P., Thakur, Jitendra, Filippova, Galina N., Henikoff, Steven, Shendure, Jay, Duan, Zhijun, Rinn, John L., Deng, Xinxian, Noble, William S., Disteche, Christine M.
Publicado 2020

Loss of Maternal CTCF Is Associated with Peri-Implantation Lethality of Ctcf Null Embryos

por Moore, James M., Rabaia, Natalia A., Smith, Leslie E., Fagerlie, Sara, Gurley, Kay, Loukinov, Dmitry, Disteche, Christine M., Collins, Steven J., Kemp, Christopher J., Lobanenkov, Victor V., Filippova, Galina N.
Publicado 2012

The lncRNA Firre anchors the inactive X chromosome to the nucleolus by binding CTCF and maintains H3K27me3 methylation

por Yang, Fan, Deng, Xinxian, Ma, Wenxiu, Berletch, Joel B, Rabaia, Natalia, Wei, Gengze, Moore, James M, Filippova, Galina N, Xu, Jun, Liu, Yajuan, Noble, William S, Shendure, Jay, Disteche, Christine M
Publicado 2015

Asymmetric Bidirectional Transcription from the FSHD-Causing D4Z4 Array Modulates DUX4 Production

por Block, Gregory J., Petek, Lisa M., Narayanan, Divya, Amell, Amanda M., Moore, James M., Rabaia, Natalia A., Tyler, Ashlee, van der Maarel, Silvere M., Tawil, Rabi, Filippova, Galina N., Miller, Daniel G.
Publicado 2012

Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene

por Snider, Lauren, Geng, Linda N., Lemmers, Richard J. L. F., Kyba, Michael, Ware, Carol B., Nelson, Angelique M., Tawil, Rabi, Filippova, Galina N., van der Maarel, Silvère M., Tapscott, Stephen J., Miller, Daniel G.
Publicado 2010

SMCHD1 regulates a limited set of gene clusters on autosomal chromosomes

por Mason, Amanda G., Slieker, Roderick C., Balog, Judit, Lemmers, Richard J. L. F., Wong, Chao-Jen, Yao, Zizhen, Lim, Jong-Won, Filippova, Galina N., Ne, Enrico, Tawil, Rabi, Heijmans, Bas T., Tapscott, Stephen J., van der Maarel, Silvère M.
Publicado 2017

CTCF cis-Regulates Trinucleotide Repeat Instability in an Epigenetic Manner: A Novel Basis for Mutational Hot Spot Determination

por Libby, Randell T., Hagerman, Katharine A., Pineda, Victor V., Lau, Rachel, Cho, Diane H., Baccam, Sandy L., Axford, Michelle M., Cleary, John D., Moore, James M., Sopher, Bryce L., Tapscott, Stephen J., Filippova, Galina N., Pearson, Christopher E., La Spada, Albert R.
Publicado 2008

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

por Lemmers, Richard J.L.F., Tawil, Rabi, Petek, Lisa M., Balog, Judit, Block, Gregory J., Santen, Gijs W.E., Amell, Amanda M., van der Vliet, Patrick J., Almomani, Rowida, Straasheijm, Kirsten R., Krom, Yvonne D., Klooster, Rinse, Sun, Yu, den Dunnen, Johan T., Helmer, Quinta, Donlin-Smith, Colleen M., Padberg, George W., van Engelen, Baziel G.M., de Greef, Jessica C., Aartsma-Rus, Annemieke M., Frants, Rune R., de Visser, Marianne, Desnuelle, Claude, Sacconi, Sabrina, Filippova, Galina N., Bakker, Bert, Bamshad, Michael J., Tapscott, Stephen J., Miller, Daniel G., van der Maarel, Silvère M.
Publicado 2012