BIRC2–BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia von Roohollahi, Khashayar, de Jong, Yvonne, Pai, Govind, Zaini, Mohamad Amr, de Lint, Klaas, Sie, Daoud, Rooimans, Martin A., Rockx, Davy, Hoskins, Elizabeth E., Ameziane, Najim, Wolthuis, Rob, Joenje, Hans, Wells, Susanne I., Dorsman, Josephine

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Update of the human and mouse Fanconi anemia genes von Dong, Hongbin, Nebert, Daniel W, Bruford, Elspeth A, Thompson, David C, Joenje, Hans, Vasiliou, Vasilis

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Publisher Correction: BIRC2–BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia von Roohollahi, Khashayar, de Jong, Yvonne, Pai, Govind, Zaini, Mohamad Amr, de Lint, Klaas, Sie, Daoud, Rooimans, Martin A., Rockx, Davy, Hoskins, Elizabeth E., Ameziane, Najim, Wolthuis, Rob, Joenje, Hans, Wells, Susanne I., Dorsman, Josephine

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SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype von Schindler, Detlev, Rouse, John, de Winter, Johan P, Stoepker, Chantal, Hain, Karolina, Schuster, Beatrice, Hilhorst-Hofstee, Yvonne, Rooimans, Martin A, Steltenpool, Jurgen, Oostra, Anneke B, Eirich, Katharina, Korthof, Elisabeth T, Nieuwint, Aggie W M, Jaspers, Nicolaas G J, Bettecken, Thomas, Joenje, Hans

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Loss of Rb proteins causes genomic instability in the absence of mitogenic signaling von van Harn, Tanja, Foijer, Floris, van Vugt, Marcel, Banerjee, Ruby, Yang, Fentang, Oostra, Anneke, Joenje, Hans, te Riele, Hein

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A Histone-Fold Complex and FANCM Form a Conserved DNA-Remodeling Complex to Maintain Genome Stability von 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, Décaillet, Chantal, Stasiak, Andrzej, Stasiak, Alicja Z., Stone, Stacie, Hoatlin, Maureen E., Schindler, Detlev, Woodcock, Christopher L., Joenje, Hans, Sen, Ranjan, de Winter, Johan P., Li, Lei, Seidman, Michael M., Whitby, Matthew C., Myung, Kyungjae, Constantinou, Angelos, Wang, Weidong

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A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M von de Winter, Johan P, Wang, Weidong, Meetei, Amom Ruhikanta, Medhurst, Annette L, Ling, Chen, Xue, Yutong, Singh, Thiyam Ramsing, Bier, Patrick, Steltenpool, Jurgen, Stone, Stacie, Dokal, Inderjeet, Mathew, Christopher G, Hoatlin, Maureen, Joenje, Hans

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The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J von Wiegant, Wouter W, De Winter, Johan P, Rooimans, Martin A, Waisfisz, Quinten, Pals, Gerard, Hiom, Kevin, Elghalbzouri-Maghrani, Elhaam, Levitus, Marieke, Joenje, Hans, Vries, Yne de, Hussain, Shobbir, Zdzienicka, Ma gorzata Z, Steltenpool, Jûrgen, Godthelp, Barbara C, Mathew, Christopher G, Arwert, Fré

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Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors von D'Andrea, Alan D, Taniguchi, Toshiyasu, Tischkowitz, Marc, Ameziane, Najim, Hodgson, Shirley V, Mathew, Christopher G, Joenje, Hans, Mok, Samuel C

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A "late-but-fitter revertant cell" explains the high frequency of revertant mosaicism in epidermolysis bullosa von van den Akker, Peter C, Pasmooij, Anna M G, Joenje, Hans, Hofstra, Robert M W, Te Meerman, Gerard J, Jonkman, Marcel F

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A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome von Meetei, Amom Ruhikanta, Sechi, Salvatore, Wallisch, Michael, Yang, Dafeng, Young, Mary K., Joenje, Hans, Hoatlin, Maureen E., Wang, Weidong

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Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M von Singh, Thiyam Ramsing, Bakker, Sietske T., Agarwal, Sheba, Jansen, Michael, Grassman, Elke, Godthelp, Barbara C., Ali, Abdullah Mahmood, Du, Chang-hu, Rooimans, Martin A., Fan, Qiang, Wahengbam, Kebola, Steltenpool, Jurgen, Andreassen, Paul R., Williams, David A., Joenje, Hans, de Winter, Johan P., Meetei, Amom Ruhikanta

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Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis von de Winter, Johan P., Joenje, Hans, Nieuwint, Aggie W. M., Oostra, Anneke B.

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Spontaneous abrogation of the G2 DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients von Ceccaldi, Raphael, Briot, Delphine, Larghero, Jérôme, Vasquez, Nadia, Dubois d’Enghien, Catherine, Chamousset, Delphine, Noguera, Maria-Elena, Waisfisz, Quinten, Hermine, Olivier, Pondarre, Corinne, Leblanc, Thierry, Gluckman, Eliane, Joenje, Hans, Stoppa-Lyonnet, Dominique, Socié, Gérard, Soulier, Jean

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

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Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes von Levitus, Marieke, Rooimans, Martin A., Steltenpool, Jûrgen, Cool, Nicolle F.C., Oostra, Anneke B., Mathew, Christopher G., Hoatlin, Maureen E., Waisfisz, Quinten, Arwert, Fré, de Winter, Johan P., Joenje, Hans

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Metabolism: alcohol, DNA and disease von Joenje, Hans

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The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2 von 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

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Evidence for subcomplexes in the Fanconi anemia pathway von Medhurst, Annette L., Laghmani, El Houari, Steltenpool, Jurgen, Ferrer, Miriam, Fontaine, Chantal, de Groot, Jan, Rooimans, Martin A., Scheper, Rik J., Meetei, Amom Ruhikanta, Wang, Weidong, Joenje, Hans, de Winter, Johan P.

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The Fanconi anemia pathway of genomic maintenance von Levitus, Marieke, Joenje, Hans, de Winter, Johan P

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