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Clinical and Experimental Dermatology|January 9, 2010
Spontaneous cure of American cutaneous leishmaniasis due to Leishmania naiffi in two Dutch infantry soldiersE M van der Snoek, A M Lammers, L M Kortbeek, et al.
The Journal of Biological Chemistry|June 19, 2015
The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF ComplexMaryam Faridounnia, Hans Wienk, Lidija Kovačič, et al.
Inflammatory Bowel Diseases|September 7, 2006
Azathioprine maintains first remission in newly diagnosed pediatric Crohn's diseaseGerald J Jaspers, Henkjan J Verkade, Johanna C Escher, et al.
Structure (London, England : 1993)|December 13, 2005
The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repairKonstantinos Tripsianes, Gert Folkers, Eiso Ab, et al.
Clinical Genetics|May 12, 2010
ERCC6 founder mutation identified in Finnish patients with COFS syndromeE Jaakkola, A Mustonen, P Olsen, et al.
Environment International|October 20, 2023
The contribution of PFAS to thyroid hormone-displacing activity in Dutch waters: A comparison between two in vitro bioassays with chemical analysisJ K H de Schepper, Y van Oorschot, R J Jaspers, et al.
Blood Cells, Molecules & Diseases|November 29, 2007
A novel (Leu183Pro-)mutation in the HFE-gene co-inherited with the Cys282Tyr mutation in two unrelated Dutch hemochromatosis patientsDorine W Swinkels, Hanka Venselaar, Erwin T Wiegerinck, et al.
DNA Repair|March 11, 2008
Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophyWim J Kleijer, Vincent Laugel, Mark Berneburg, et al.
DNA Repair|January 18, 2003
Anti-tumour compounds illudin S and Irofulven induce DNA lesions ignored by global repair and exclusively processed by transcription- and replication-coupled repair pathwaysNicolaas G J Jaspers, Anja Raams, Michael J Kelner, et al.
European Journal of Medical Genetics|September 7, 2011
A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12Oliver Bartsch, Detlev Schindler, Vera Beyer, et al.
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