Impaired Repair of Ionizing Radiation-Induced DNA Damage in Cockayne Syndrome Cells von Cramers, Patricia, Verhoeven, Esther E, Filon, A. Ronald, Rockx, Davy A. P, Santos, Susy J, van der Leer, Anneke A, Kleinjans, Jos C. S, van Zeeland, Albert A, Mullenders, Leon H. F

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Cisplatin and doxorubicin repress Vascular Endothelial Growth Factor expression and differentially down-regulate Hypoxia-inducible Factor I activity in human ovarian cancer cells von Duyndam, Monique C.A., van Berkel, Maria P.A., Dorsman, Josephine C., Rockx, Davy A.P., Pinedo, Herbert M., Boven, Epie

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Aberrant Epstein-Barr virus persistence in HIV carriers is characterized by anti-Epstein-Barr virus IgA and high cellular viral loads with restricted transcription von STEVENS, Servi J. C, SMITS, Paul H. M, VERKUIJLEN, Sandra A. W. M, ROCKX, Davy A. P, VAN GORP, Eric C. M, MULDER, Jan W, MIDDELDORP, Jaap M

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UV-Induced Inhibition of Transcription Involves Repression of Transcription Initiation and Phosphorylation of RNA Polymerase II von Davy A. P. Rockx, Mason, Rebecca, van Hoffen, Anneke, Barton, Michelle Craig, Citterio, Elisabetta, Bregman, David B., van Zeeland, Albert A., Vrieling, Harry, Leon H. F. Mullenders

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The iron-sulfur cluster assembly network component NARFL is a key element in the cellular defense against oxidative stress von Corbin, Monique V., Rockx, Davy A.P., Oostra, Anneke B., Joenje, Hans, Dorsman, Josephine C.

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Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption von Meyer, Stefan, Stevens, Adam, Paredes, Roberto, Schneider, Marion, Walker, Michael J, Williamson, Andrew J K, Gonzalez-Sanchez, Maria-Belen, Smetsers, Stephanie, Dalal, Vineet, Teng, Hsiang Ying, White, Daniel J, Taylor, Sam, Muter, Joanne, Pierce, Andrew, de Leonibus, Chiara, Rockx, Davy A P, Rooimans, Martin A, Spooncer, Elaine, Stauffer, Stacey, Biswas, Kajal, Godthelp, Barbara, Dorsman, Josephine, Clayton, Peter E, Sharan, Shyam K, Whetton, Anthony D

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Coregulation of FANCA and BRCA1 in human cells von Haitjema, Anneke, Mol, Berber M, Kooi, Irsan E, Massink, Maarten PG, Jørgensen, Jens AL, Rockx, Davy AP, Rooimans, Martin A, de Winter, Johan P, Meijers-Heijboer, Hanne, Joenje, Hans, Dorsman, Josephine C

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

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

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Identification of the Fanconi anemia complementation group I gene, FANCI von 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

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

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A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51 von 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, Altelaar, Maarten, 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

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Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma von Smetsers, Stephanie, Muter, Joanne, Bristow, Claire, Patel, Leena, Chandler, Kate, Bonney, Denise, Wynn, Robert F., Whetton, Anthony D., Will, Andrew M., Rockx, Davy, Joenje, Hans, Strathdee, Gordon, Shanks, Jonathan, Klopocki, Eva, Gille, Johan J. P., Dorsman, Josephine, Meyer, Stefan

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