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Wind, N. de
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Lebbink, J.H.; Drost, M.; Wind, N. de
2016
DNA mismatch repair: from biophysics to bedside
Article / Letter to editor
metadata only
Yang, Y.R.; Liu, Z.B.; Wang, F.L.; Temviriyanukul, P.; Ma, X.L.; Tu, Y.F.; ... ; Guo, C.X.
2015
FANCD2 and REV1 cooperate in the protection of nascent DNA strands in response to replication stress
Article / Letter to editor
metadata only
Jansen, J.G.; Tsaalbi-Shtylik, A.; Wind, N. de
2015
Post-translesion synthesis repair
Article / Letter to editor
metadata only
Tsaalbi-Shtylik, A.; Jansen, J.G.; Wind, N. de
2015
When mismatch repair met translesion synthesis
Article / Letter to editor
metadata only
Parsons, M.T.; Whiley, P.J.; Beesley, J.; Drost, M.; Wind, N. de; Thompson, B.A.; ... ; Australasian Colorectal Canc
2015
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity
Article / Letter to editor
metadata only
Tomas-Roca, L.; Tsaalbi-Shtylik, A.; Jansen, J.G.; Singh, M.K.; Epstein, J.A.; Altunoglu, U.; ... ; Bokhoven, H. van
2015
De novo mutations in PLXND1 and REV3L cause Mobius syndrome
Article / Letter to editor
metadata only
Jansen, J.G.; Tsaalbi-Shtylik, A.; Wind, N. de
2015
Roles of mutagenic translesion synthesis in mammalian genome stability, health and disease
Article / Letter to editor
metadata only
Tsaalbi-Shtylik, A.; Ferras, C.; Pauw, B.; Hendriks, G.; Temviriyanukul, P.; Carlee, L.; ... ; Wind, N. de
2015
Excision of translesion synthesis errors orchestrates responses to helix-distorting DNA lesions
Article / Letter to editor
metadata only
Cohen, I.S.; Bar, C.; Paz-Elizur, T.; Ainbinder, E.; Leopold, K.; Wind, N. de; ... ; Livneh, Z.
2015
DNA lesion identity drives choice of damage tolerance pathway in murine cell chromosomes
Article / Letter to editor
metadata only
Wit, N.; Buoninfante, O.A.; Berk, P.C.M. van den; Jansen, J.G.; Hogenbirk, M.A.; Wind, N. de; Jacobs, H.
2015
Roles of PCNA ubiquitination and TLS polymerases kappa and eta in the bypass of methyl methanesulfonate-induced DNA damage
Article / Letter to editor
metadata only
Jansen, J.G.; Temviriyanukul, P.; Wit, N.; Delbos, F.; Reynaud, C.A.; Jacobs, H.; Wind, N. de
2014
Redundancy of mammalian Y family DNA polymerases in cellular responses to genomic DNA lesions induced by ultraviolet light
Article / Letter to editor
metadata only
Oberbeck, N.; Langevin, F.; King, G.; Wind, N. de; Crossan, G.P.; Patel, K.J.
2014
Maternal Aldehyde Elimination during Pregnancy Preserves the Fetal Genome
Article / Letter to editor
metadata only
Tsaalbi-Shtylik, A.; Moser, J.; Mullenders, L.H.F.; Jansen, J.G.; Wind, N. de
2014
Persistently stalled replication forks inhibit nucleotide excision repair in trans by sequestering Replication protein A
Article / Letter to editor
metadata only
Wind, N. de; Buermeyer, A.B.; Hanawalt, P.C.
2014
In memory of John Bruce Hays (1937-2014)
Article / Letter to editor
metadata only
Farrell, M.P.; Hughes, D.J.; Drost, M.; Wallace, A.J.; Cummins, R.J.; Fletcher, T.A.; ... ; Gallagher, D.J.
2013
Multivariate analysis of MLH1 c.1664T > C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity
Article / Letter to editor
metadata only
Drost, M.; Koppejan, H.; Wind, N. de
2013
Inactivation of DNA Mismatch Repair by Variants of Uncertain Significance in the PMS2 Gene
Article / Letter to editor
metadata only
Krijger, P.H.L.; Tsaalbi-Shtylik, A.; Wit, N.; Berk, P.C.M. van den; Wind, N. de; Jacobs, H.
2013
Rev1 is essential in generating G to C transversions downstream of the Ung2 pathway but not the Msh2+Ung2 hybrid pathway
Article / Letter to editor
metadata only
Rasmussen, L.J.; Heinen, C.D.; Royer-Pokora, B.; Drost, M.; Tavtigian, S.; Hofstra, R.M.W.; Wind, N. de
2013
Response to: Design of a Core Classification Process for DNA Mismatch Repair Variations of A Priori Unknown Functional Significance
Article / Letter to editor
metadata only
Drost, M.; Lutzen, A.; Hees, S. van; Ferreira, D.; Calleja, F.; Zonneveld, J.B.M.; ... ; Wind, N. de
2013
Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome
Article / Letter to editor
metadata only
Andersen, S.D.; Liberti, S.E.; Lutzen, A.; Drost, M.; Bernstein, I.; Nilbert, M.; ... ; Rasmussen, L.J.
2012
Functional characterization of MLH1 missense variants identified in lynch syndrome patients
Article / Letter to editor
metadata only
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