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Molecular Biology of the Cell|December 3, 2004
Dynamics of relative chromosome position during the cell cycleJeroen Essers, Wiggert A van Cappellen, Arjan F Theil, et al.
Mutation Research|August 22, 2006
Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2Barbara C Godthelp, Paul P W van Buul, Nicolaas G J Jaspers, et al.
Journal of Inherited Metabolic Disease|December 20, 2024
Altered lipid profile and reduced neuronal support in human induced pluripotent stem cell-derived astrocytes from adrenoleukodystrophy patientsRoberto Montoro Ferrer, Yorrick R J Jaspers, Inge M E Dijkstra, et al.
Cardiovascular Drugs and Therapy|February 19, 2013
Gastroprotection in low-dose aspirin users for primary and secondary prevention of ACS: results of a cost-effectiveness analysis including complianceN L de Groot, H G M van Haalen, B M R Spiegel, et al.
Frontiers in Cell and Developmental Biology|September 9, 2020
Comparison of the Diagnostic Performance of C26:0-Lysophosphatidylcholine and Very Long-Chain Fatty Acids Analysis for Peroxisomal DisordersYorrick R J Jaspers, Sacha Ferdinandusse, Inge M E Dijkstra, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2016
Low performance of bleeding risk models in the very elderly with atrial fibrillation using vitamin K antagonistsJ Jaspers Focks, S P G van Vugt, M T H Albers-Akkers, et al.
Molecular and Cellular Biology|December 2, 2004
Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damageFabrizio Thorel, Angelos Constantinou, Isabelle Dunand-Sauthier, et al.
Human Mutation|September 16, 2006
Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationshipsElena Botta, Judith Offman, Tiziana Nardo, et al.
Molecular and Cellular Biology|June 17, 2004
The structure-specific endonuclease Ercc1-Xpf is required to resolve DNA interstrand cross-link-induced double-strand breaksLaura J Niedernhofer, Hanny Odijk, Magda Budzowska, et al.
American Journal of Human Genetics|February 3, 2007
First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failureNicolaas G J Jaspers, Anja Raams, Margherita Cirillo Silengo, et al.
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