Genomic insights into chromatin reprogramming to totipotency in embryos

por Ladstätter, Sabrina, Tachibana, Kikuë
Publicado 2019

The emergence of genome architecture and zygotic genome activation

por Vallot, Antoine, Tachibana, Kikuë
Publicado 2020

Centromere-specifying nucleosomes persist in aging mouse oocytes in the absence of nascent assembly

por Das, Arunika, Boese, Katelyn G., Tachibana, Kikue, Baek, Sung Hee, Lampson, Michael A., Black, Ben E.
Publicado 2023

Wapl releases Scc1-cohesin and regulates chromosome structure and segregation in mouse oocytes

por Silva, Mariana C.C., Powell, Sean, Ladstätter, Sabrina, Gassler, Johanna, Stocsits, Roman, Tedeschi, Antonio, Peters, Jan-Michael, Tachibana, Kikuë
Publicado 2020

A mechanism of cohesin‐dependent loop extrusion organizes zygotic genome architecture

por Gassler, Johanna, Brandão, Hugo B, Imakaev, Maxim, Flyamer, Ilya M, Ladstätter, Sabrina, Bickmore, Wendy A, Peters, Jan‐Michael, Mirny, Leonid A, Tachibana, Kikuë
Publicado 2017

MCM complexes are barriers that restrict cohesin-mediated loop extrusion

por Dequeker, Bart J. H., Scherr, Matthias J., Brandão, Hugo B., Gassler, Johanna, Powell, Sean, Gaspar, Imre, Flyamer, Ilya M., Lalic, Aleksandar, Tang, Wen, Stocsits, Roman, Davidson, Iain F., Peters, Jan-Michael, Duderstadt, Karl E., Mirny, Leonid A., Tachibana, Kikuë
Publicado 2022

Control of inducible gene expression links cohesin to hematopoietic progenitor self-renewal and differentiation

por Cuartero, Sergi, Weiss, Felix D., Dharmalingam, Gopuraja, Guo, Ya, Ing-Simmons, Elizabeth, Masella, Silvia, Robles-Rebollo, Irene, Xiao, Xiaolin, Wang, Yi-Fang, Barozzi, Iros, Djeghloul, Dounia, Amano, Mariane T., Niskanen, Henri, Petretto, Enrico, Dowell, Robin D., Tachibana, Kikuë, Kaikkonen, Minna U., Nasmyth, Kim A., Lenhard, Boris, Natoli, Gioacchino, Fisher, Amanda G., Merkenschlager, Matthias
Publicado 2018

Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder

por Kaiser, Fabian M.P., Gruenbacher, Sarah, Oyaga, Maria Roa, Nio, Enzo, Jaritz, Markus, Sun, Qiong, van der Zwaag, Wietske, Kreidl, Emanuel, Zopf, Lydia M., Dalm, Virgil A.S.H., Pel, Johan, Gaiser, Carolin, van der Vliet, Rick, Wahl, Lucas, Rietman, André, Hill, Louisa, Leca, Ines, Driessen, Gertjan, Laffeber, Charlie, Brooks, Alice, Katsikis, Peter D., Lebbink, Joyce H.G., Tachibana, Kikuë, van der Burg, Mirjam, De Zeeuw, Chris I., Badura, Aleksandra, Busslinger, Meinrad
Publicado 2022

Correction: Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder

por Kaiser, Fabian M.P., Gruenbacher, Sarah, Oyaga, Maria Roa, Nio, Enzo, Jaritz, Markus, Sun, Qiong, van der Zwaag, Wietske, Kreidl, Emanuel, Zopf, Lydia M., Dalm, Virgil A.S.H., Pel, Johan, Gaiser, Carolin, van der Vliet, Rick, Wahl, Lucas, Rietman, André, Hill, Louisa, Leca, Ines, Driessen, Gertjan, Laffeber, Charlie, Brooks, Alice, Katsikis, Peter D., Lebbink, Joyce H.G., Tachibana, Kikuë, van der Burg, Mirjam, De Zeeuw, Chris I., Badura, Aleksandra, Busslinger, Meinrad
Publicado 2022