The structure of the XPF-ssDNA complex underscores the distinct roles of the XPF and ERCC1 helix- hairpin-helix domains in ss/ds DNA recognition

Autor: Das, D., Folkers, G.E., van Dijk, M., Jaspers, N.G.J., Hoeijmakers, J.H.J., Kaptein, R., Boelens, R., NMR Spectroscopy, Dep Scheikunde, Sub NMR Spectroscopy

Publikováno v: Das, D, Folkers, G, van Dijk, M, Jaspers, N G J, Hoeijmakers, J H J, Kaptein, R & Boelens, R 2012, ' The structure of the XPF-ssDNA complex underscores the distinct roles of the XPF and ERCC1 helix-hairpin-helix domains in ss/ds DNA recognition ', Structure, vol. 20, no. 4, pp. 667-75 . https://doi.org/10.1016/j.str.2012.02.009
Structure, 20(4), 667-675. Cell Press
Structure, 20(4), 667-75. Cell Press
Structure, 20(4), 667. Cell Press
Structure

SummaryHuman XPF/ERCC1 is a structure-specific DNA endonuclease that nicks the damaged DNA strand at the 5′ end during nucleotide excision repair. We determined the structure of the complex of the C-terminal domain of XPF with 10 nt ssDNA. A positi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab80c0b680c3a6b6ffe3861ddcc36eee
https://research.vu.nl/en/publications/72e213d4-9b4f-4c24-8bd0-6ab0d952717b

Verouderingstheorieën.

Autor: Jaspers, N.G.J., Vermeij, W.P., Marcoen, A.A., Aartsen, M.J., Thomése, G.C.F.

Publikováno v: Inleiding in de Gerontologie en Geriatrie; 2016, p9-20, 12p

Phenotypic heterogeneity in the XPB DNA helicase gene ( ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.

Autor: Oh, Kyu-Seon, Khan, Sikandar G., Jaspers, N.G.J., Raams, Anja, Ueda, Takahiro, Lehmann, Alan, Friedmann, Peter S., Emmert, Steffen, Gratchev, Alexi, Lachlan, Katherine, Lucassan, Anneke, Baker, Carl C., Kraemer, Kenneth H.

Publikováno v: Human Mutation; Nov2006, Vol. 27 Issue 11, p1092-1103, 12p

Co-dominance of radioresistant DNA synthesis in a group of AT-like Chinese hamster cell mutants.

Autor: Verhaegh, G.W.C.T., Jaspers, N.G.J., Lohman, P.H.M., Zdzienicka, M.Z.

Publikováno v: Cytogenetics & Cell Genetics; 1993, Vol. 63 Issue 3, p176-180, 5p

Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2

Autor: Godthelp, B.C., van Buul, P.P.W., Jaspers, N.G.J., Elghalbzouri-Maghrani, E., van Duijn-Goedhart, A., Arwert, F., Joenje, H., Zdzienicka, M.Z.

Publikováno v: Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis; October 2006, Vol. 601 Issue: 1-2 p191-201, 11p