Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

Por Oostra, Anneke B., Nieuwint, Aggie W. M., Joenje, Hans, de Winter, Johan P.
Publicado em 2012

Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome

Por van der Lelij, Petra, Oostra, Anneke B., Rooimans, Martin A., Joenje, Hans, de Winter, Johan P.
Publicado em 2010

Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1

Por van der Lelij, Petra, Chrzanowska, Krystyna H., Godthelp, Barbara C., Rooimans, Martin A., Oostra, Anneke B., Stumm, Markus, Zdzienicka, Małgorzata Z., Joenje, Hans, de Winter, Johan P.
Publicado em 2010

The Cellular Phenotype of Roberts Syndrome Fibroblasts as Revealed by Ectopic Expression of ESCO2

Por van der Lelij, Petra, Godthelp, Barbara C., van Zon, Wouter, van Gosliga, Djoke, Oostra, Anneke B., Steltenpool, Jûrgen, de Groot, Jan, Scheper, Rik J., Wolthuis, Rob M., Waisfisz, Quinten, Darroudi, Firouz, Joenje, Hans, de Winter, Johan P.
Publicado em 2009

Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function

Por de Lange, Job, Faramarz, Atiq, Oostra, Anneke B., de Menezes, Renee X., van der Meulen, Ida H., Rooimans, Martin A., Rockx, Davy A., Brakenhoff, Ruud H., van Beusechem, Victor W., King, Randall W., de Winter, Johan P., Wolthuis, Rob M. F.
Publicado no Nat Commun (2015)

Identification of the Fanconi Anemia Complementation Group I Gene, FANCI

Por Dorsman, Josephine C., Levitus, Marieke, Rockx, Davy, Rooimans, Martin A., Oostra, Anneke B., Haitjema, Anneke, Bakker, Sietske T., Steltenpool, Jûrgen, Schuler, Dezsö, Mohan, Sheila, Schindler, Detlev, Arwert, Fré, Pals, Gerard, Mathew, Christopher G., Waisfisz, Quinten, de Winter, Johan P., Joenje, Hans
Publicado no Cell Oncol (2007)

FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway

Por Ling, Chen, Ishiai, Masamichi, Ali, Abdullah Mahmood, Medhurst, Annette L, Neveling, Kornelia, Kalb, Reinhard, Yan, Zhijiang, Xue, Yutong, Oostra, Anneke B, Auerbach, Arleen D, Hoatlin, Maureen E, Schindler, Detlev, Joenje, Hans, de Winter, Johan P, Takata, Minoru, Meetei, Amom Ruhikanta, Wang, Weidong
Publicado em 2007

A ubiquitin-binding protein FAAP20 links RNF8-mediated ubiquitination to the Fanconi anemia DNA Repair network

Por Yan, Zhijiang, Guo, Rong, Paramasivam, Manikandan, Shen, Weiping, Ling, Chen, Fox, David, Wang, Yucai, Oostra, Anneke B., Kuehl, Julia, Lee, Duck-Yeon, Takata, Minoru, Hoatlin, Maureen E., Schindler, Detlev, Joenje, Hans, de Winter, Johan P., Li, Lei, Seidman, Michael M., Wang, Weidong
Publicado em 2012

A histone-fold complex and FANCM form a conserved DNA remodeling complex to maintain genome stability

Por Yan, Zhijiang, Delannoy, Mathieu, Ling, Chen, Daee, Danielle, Osman, Fekret, Muniandy, Parameswary A., Shen, Xi, Oostra, Anneke B., Du, Hansen, Steltenpool, Jurgen, Lin, Ti, Schuster, Beatrice, Decaillet, Chantal, Stasiak, Andrzej, Stasiak, Alicja Z., Stone, Stacie, Hoatlin, Maureen E., Schindler, Detlev, Woodcock, Chris, Joenje, Hans, Sen, Ranjan, de Winter, Johan P., Li, Lei, Seidman, Michael M., Whitby, Matthew C., Myung, Kyungjae, Constantinou, Angelos, Wang, Weidong
Publicado em 2010

A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

Por Ameziane, Najim, May, Patrick, Haitjema, Anneke, van de Vrugt, Henri J., van Rossum-Fikkert, Sari E., Ristic, Dejan, Williams, Gareth J., Balk, Jesper, Rockx, Davy, Li, Hong, Rooimans, Martin A., Oostra, Anneke B., Velleuer, Eunike, Dietrich, Ralf, Bleijerveld, Onno B., Maarten Altelaar, A. F., Meijers-Heijboer, Hanne, Joenje, Hans, Glusman, Gustavo, Roach, Jared, Hood, Leroy, Galas, David, Wyman, Claire, Balling, Rudi, den Dunnen, Johan, de Winter, Johan P., Kanaar, Roland, Gelinas, Richard, Dorsman, Josephine C.
Publicado no Nat Commun (2015)