Pollitt syndrome patients carry mutation in TTDN1

por Swagemakers, Sigrid M.A., Jaspers, Nicolaas G.J., Raams, Anja, Heijsman, Daphne, Vermeulen, Wim, Troelstra, Christine, Kremer, Andreas, Lincoln, Stephen E., Tearle, Rick, Hoeijmakers, Jan H.J., van der Spek, Peter J.
Publicado 2014

Attenuated XPC Expression Is Not Associated with Impaired DNA Repair in Bladder Cancer

por Naipal, Kishan A. T., Raams, Anja, Bruens, Serena T., Brandsma, Inger, Verkaik, Nicole S., Jaspers, Nicolaas G. J., Hoeijmakers, Jan H. J., van Leenders, Geert J. L. H., Pothof, Joris, Kanaar, Roland, Boormans, Joost, van Gent, Dik C.
Publicado 2015

Cell-Autonomous Progeroid Changes in Conditional Mouse Models for Repair Endonuclease XPG Deficiency

por Barnhoorn, Sander, Uittenboogaard, Lieneke M., Jaarsma, Dick, Vermeij, Wilbert P., Tresini, Maria, Weymaere, Michael, Menoni, Hervé, Brandt, Renata M. C., de Waard, Monique C., Botter, Sander M., Sarker, Altaf H., Jaspers, Nicolaas G. J., van der Horst, Gijsbertus T. J., Cooper, Priscilla K., Hoeijmakers, Jan H. J., van der Pluijm, Ingrid
Publicado 2014

Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue

por Theil, Arjan F, Mandemaker, Imke K, van den Akker, Emile, Swagemakers, Sigrid M A, Raams, Anja, Wüst, Tatjana, Marteijn, Jurgen A, Giltay, Jacques C, Colombijn, Richard M, Moog, Ute, Kotzaeridou, Urania, Ghazvini, Mehrnaz, von Lindern, Marieke, Hoeijmakers, Jan H J, Jaspers, Nicolaas G J, van der Spek, Peter J, Vermeulen, Wim
Publicado 2017