DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair

由 de Laat, Wouter L., Appeldoorn, Esther, Sugasawa, Kaoru, Weterings, Eric, Jaspers, Nicolaas G.J., Hoeijmakers, Jan H.J.
出版 1998

Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome

由 Horibata, Katsuyoshi, Iwamoto, Yuka, Kuraoka, Isao, Jaspers, Nicolaas G. J., Kurimasa, Akihiro, Oshimura, Mitsuo, Ichihashi, Masamitsu, Tanaka, Kiyoji
出版 2004

The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF Complex

由 Faridounnia, Maryam, Wienk, Hans, Kovačič, Lidija, Folkers, Gert E., Jaspers, Nicolaas G. J., Kaptein, Robert, Hoeijmakers, Jan H. J., Boelens, Rolf
發表在 J Biol Chem (2015)

Dynamics of Relative Chromosome Position during the Cell Cycle

由 Essers, Jeroen, van Cappellen, Wiggert A., Theil, Arjan F., van Drunen, Ellen, Jaspers, Nicolaas G.J., Hoeijmakers, Jan H.J., Wyman, Claire, Vermeulen, Wim, Kanaar, Roland
出版 2005

Cerebro-Oculo-Facio-Skeletal Syndrome with a Nucleotide Excision–Repair Defect and a Mutated XPD Gene, with Prenatal Diagnosis in a Triplet Pregnancy

由 Graham, Jr., John M., Anyane-Yeboa, Kwame, Raams, Anja, Appeldoorn, Esther, Kleijer, Wim J., Garritsen, Victor H., Busch, David, Edersheim, Terri G., Jaspers, Nicolaas G. J.
出版 2001

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene

由 Taylor, Elaine M., Broughton, Bernard C., Botta, Elena, Stefanini, Miria, Sarasin, Alain, Jaspers, Nicolaas G. J., Fawcett, Heather, Harcourt, Susan A., Arlett, Colin F., Lehmann, Alan R.
出版 1997

Definition of a Short Region of XPG Necessary for TFIIH Interaction and Stable Recruitment to Sites of UV Damage

由 Thorel, Fabrizio, Constantinou, Angelos, Dunand-Sauthier, Isabelle, Nouspikel, Thierry, Lalle, Philippe, Raams, Anja, Jaspers, Nicolaas G. J., Vermeulen, Wim, Shivji, Mahmud K. K., Wood, Richard D., Clarkson, Stuart G.
出版 2004

First Reported Patient with Human ERCC1 Deficiency Has Cerebro-Oculo-Facio-Skeletal Syndrome with a Mild Defect in Nucleotide Excision Repair and Severe Developmental Failure

由 Jaspers, Nicolaas G. J., Raams, Anja, Silengo, Margherita Cirillo, Wijgers, Nils, Niedernhofer, Laura J., Robinson, Andria Rasile, Giglia-Mari, Giuseppina, Hoogstraten, Deborah, Kleijer, Wim J., Hoeijmakers, Jan H. J., Vermeulen, Wim
出版 2007

Pollitt syndrome patients carry mutation in TTDN1

由 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.
發表在 Meta Gene (2014)

MicroRNA-mediated gene silencing modulates the UV-induced DNA-damage response

由 Pothof, Joris, Verkaik, Nicole S, van IJcken, Wilfred, Wiemer, Erik A C, Ta, Van T B, van der Horst, Gijsbertus T J, Jaspers, Nicolaas G J, van Gent, Dik C, Hoeijmakers, Jan H J, Persengiev, Stephan P
出版 2009

Transcription-Associated Breaks in Xeroderma Pigmentosum Group D Cells from Patients with Combined Features of Xeroderma Pigmentosum and Cockayne Syndrome

由 Theron, Therina, Fousteri, Maria I., Volker, Marcel, Harries, Lorna W., Botta, Elena, Stefanini, Miria, Fujimoto, Mitsuo, Andressoo, Jaan-Olle, Mitchell, Jay, Jaspers, Nicolaas G. J., McDaniel, Lisa D., Mullenders, Leon H., Lehmann, Alan R.
出版 2005

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

由 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.
發表在 PLoS One (2015)

ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination

由 Shehata, Laila, Simeonov, Dimitre R., Raams, Anja, Wolfe, Lynne, Vanderver, Adeline, Li, Xueli, Huang, Yan, Garner, Shannon, Boerkoel, Cornelius F., Thurm, Audrey, Herman, Gail E., Tifft, Cynthia J., He, Miao, Jaspers, Nicolaas G.J., Gahl, William A.
出版 2014

Molecular analysis of mutations in DNA polymerase η in xeroderma pigmentosum-variant patients

由 Broughton, Bernard C., Cordonnier, Agnes, Kleijer, Wim J., Jaspers, Nicolaas G. J., Fawcett, Heather, Raams, Anja, Garritsen, Victor H., Stary, Anne, Avril, Marie-Françoise, Boudsocq, François, Masutani, Chikahide, Hanaoka, Fumio, Fuchs, Robert P., Sarasin, Alain, Lehmann, Alan R.
出版 2002

A new type of radiosensitive T(–)B(–)NK(+) severe combined immunodeficiency caused by a LIG4 mutation

由 van der Burg, Mirjam, van Veelen, Lieneke R., Verkaik, Nicole S., Wiegant, Wouter W., Hartwig, Nico G., Barendregt, Barbara H., Brugmans, Linda, Raams, Anja, Jaspers, Nicolaas G.J., Zdzienicka, Malgorzata Z., van Dongen, Jacques J.M., van Gent, Dik C.
出版 2006

Brca2 (XRCC11) Deficiency Results in Radioresistant DNA Synthesis and a Higher Frequency of Spontaneous Deletions

由 Kraakman-van der Zwet, Maria, Overkamp, Wilhelmina J. I., van Lange, Rebecca E. E., Essers, Jeroen, van Duijn-Goedhart, Annemarie, Wiggers, Ingrid, Swaminathan, Srividya, van Buul, Paul P. W., Errami, Abdellatif, Tan, Raoul T. L., Jaspers, Nicolaas G. J., Sharan, Shyam K., Kanaar, Roland, Zdzienicka, Małgorzata Z.
出版 2002

SMARCAL1 Deficiency Predisposes to Non-Hodgkin Lymphoma and Hypersensitivity to Genotoxic Agents In vivo

由 Baradaran-Heravi, Alireza, Raams, Anja, Lubieniecka, Joanna, Cho, Kyoung Sang, DeHaai, Kristi A., Basiratnia, Mitra, Mari, Pierre-Olivier, Xue, Yutong, Rauth, Michael, Olney, Ann Haskins, Shago, Mary, Choi, Kunho, Weksberg, Rosanna A., Nowaczyk, Malgorzata J.M., Wang, Weidong, Jaspers, Nicolaas G.J., Boerkoel, Cornelius F.
出版 2012

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

由 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
出版 2014

Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue

由 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
發表在 Hum Mol Genet (2017)

Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy

由 Nakabayashi, Kazuhiko, Amann, Daniela, Ren, Yan, Saarialho-Kere, Ulpu, Avidan, Nili, Gentles, Simone, MacDonald, Jeffrey R., Puffenberger, Erik G., Christiano, Angela M., Martinez-Mir, Amalia, Salas-Alanis, Julio C., Rizzo, Renata, Vamos, Esther, Raams, Anja, Les, Clifford, Seboun, Eric, Jaspers, Nicolaas G. J., Beckmann, Jacques S., Jackson, Charles E., Scherer, Stephen W.
出版 2005