Impaired Repair of Ionizing Radiation-Induced DNA Damage in Cockayne Syndrome Cells by 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 by 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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UV-Induced Inhibition of Transcription Involves Repression of Transcription Initiation and Phosphorylation of RNA Polymerase II by 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 by 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 by 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 by 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 by 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 by 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 by 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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Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma by 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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