The structure-specific endonuclease Ercc1–Xpf is required for targeted gene replacement in embryonic stem cells

Por Niedernhofer, Laura J., Essers, Jeroen, Weeda, Geert, Beverloo, Berna, de Wit, Jan, Muijtjens, Manja, Odijk, Hanny, Hoeijmakers, Jan H.J., Kanaar, Roland
Publicado em 2001

Mutation of the mouse Rad17 gene leads to embryonic lethality and reveals a role in DNA damage-dependent recombination

Por Budzowska, Magda, Jaspers, Iris, Essers, Jeroen, de Waard, Harm, van Drunen, Ellen, Hanada, Katsuhiro, Beverloo, Berna, Hendriks, Rudolf W, de Klein, Annelies, Kanaar, Roland, Hoeijmakers, Jan H, Maas, Alex
Publicado em 2004

Restricted 12p Amplification and RAS Mutation in Human Germ Cell Tumors of the Adult Testis

Por Roelofs, Helene, Mostert, Marijke C., Pompe, Kirsten, Zafarana, Gaetano, van Oorschot, Monique, van Gurp, Ruud J. H. L. M., Gillis, Ad J. M., Stoop, Hans, Beverloo, Berna, Oosterhuis, J. Wolter, Bokemeyer, Carsten, Looijenga, Leendert H. J.
Publicado em 2000

CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer

Por Ling, Hui, Spizzo, Riccardo, Atlasi, Yaser, Nicoloso, Milena, Shimizu, Masayoshi, Redis, Roxana S., Nishida, Naohiro, Gafà, Roberta, Song, Jian, Guo, Zhiyi, Ivan, Cristina, Barbarotto, Elisa, De Vries, Ingrid, Zhang, Xinna, Ferracin, Manuela, Churchman, Mike, van Galen, Janneke F., Beverloo, Berna H., Shariati, Maryam, Haderk, Franziska, Estecio, Marcos R., Garcia-Manero, Guillermo, Patijn, Gijs A., Gotley, David C., Bhardwaj, Vikas, Shureiqi, Imad, Sen, Subrata, Multani, Asha S., Welsh, James, Yamamoto, Ken, Taniguchi, Itsuki, Song, Min-Ae, Gallinger, Steven, Casey, Graham, Thibodeau, Stephen N., Le Marchand, Loïc, Tiirikainen, Maarit, Mani, Sendurai A., Zhang, Wei, Davuluri, Ramana V., Mimori, Koshi, Mori, Masaki, Sieuwerts, Anieta M., Martens, John W.M., Tomlinson, Ian, Negrini, Massimo, Berindan-Neagoe, Ioana, Foekens, John A., Hamilton, Stanley R., Lanza, Giovanni, Kopetz, Scott, Fodde, Riccardo, Calin, George A.
Publicado em 2013

Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections

Por Bertoli-Avella, Aida M., Gillis, Elisabeth, Morisaki, Hiroko, Verhagen, Judith M.A., de Graaf, Bianca M., van de Beek, Gerarda, Gallo, Elena, Kruithof, Boudewijn P.T., Venselaar, Hanka, Myers, Loretha A., Laga, Steven, Doyle, Alexander J., Oswald, Gretchen, van Cappellen, Gert W.A., Yamanaka, Itaru, van der Helm, Robert M., Beverloo, Berna, de Klein, Annelies, Pardo, Luba, Lammens, Martin, Evers, Christina, Devriendt, Koenraad, Dumoulein, Michiel, Timmermans, Janneke, Bruggenwirth, Hennie T., Verheijen, Frans, Rodrigus, Inez, Baynam, Gareth, Kempers, Marlies, Saenen, Johan, Van Craenenbroeck, Emeline M., Minatoya, Kenji, Matsukawa, Ritsu, Tsukube, Takuro, Kubo, Noriaki, Hofstra, Robert, Goumans, Marie Jose, Bekkers, Jos A., Roos-Hesselink, Jolien W., van de Laar, Ingrid M.B.H., Dietz, Harry C., Van Laer, Lut, Morisaki, Takayuki, Wessels, Marja W., Loeys, Bart L.
Publicado no J Am Coll Cardiol (2015)