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Anke van den Berg
prof. dr.

I work as a clinical molecular biologist in the department of Pathology. In this function I supervise and implement advanced molecular diagnostic techniques. Within my research line, I focus on the molecular pathogenesis of B-cell Hodgkin and non-Hodgkin lymphoma. The specific fields of interest are genomic aberrations, genetic susceptibility, and the role of small and long noncoding RNAs. I have several international collaborations and am PI and co-PI in various projects.

Brain death causes structural and inflammatory changes in donor intestine
Published in: Transplantation Proceedings
Brain death donors are frequently used for transplantation. Previous studies showed that brain death (BD) negatively affects the immunological and inflammatory status of both liver and kidney. Objective. Therefore we studied the inflammatory and morphological changes in donor small intestine after brain death induction. Methods. BD was induced in rats by slow inflation of an epidural balloon catheter. Three groups (n = 6) were compared, 1 hour, 4 hours BID and sham operated controls. The liver was used as a reference to confirm our previous findings. Intestinal injury...
Dimeric galectin-1 induces IL-10 production in T-lymphocytes: an important tool in the regulation of the immune response
Published in: The Journal of Pathology
J. Van der Leij, Anke van den Berg, T. Blokzijl, G. Harms, H. van Goor, Peter Zwiers, Robert van Weeghel, Sibrand Poppema, Lydia Visser
Enhanced ecto-apyrase activity of stimulated endothelial or mesangial cells is downregulated by glucocorticolds in vitro
Published in: European Journal of Pharmacology
Jola Jovita Kapojos, Anke van den Berg, Theo Borghuis, B. Banas, Sipkje Huitema, Klaas Poelstra, W.W Bakker
Development of lymphoma in Autoimmune Lymphoproliferative Syndrome (ALPS) and its relationship to Fas gene mutations
Published in: Leukemia and Lymphoma
Autoimmune Lymphoproliferative Syndrome (ALPS) is generally the result of a mutation in genes associated with apoptosis, like Fas, Fas ligand, Casp 8 and Casp 10. As a result, the normal homeostasis of T- and B-lymphocytes is disturbed and a proliferation of polyclonal T lymphocytes occurs. This leads to hepatosplenomegaly and lymphadenopathy and in most patients also to autoimmune phenomena like anemia and thrombocytopenia. The proliferating T cells are TCRalphabeta and/or TCRgammadelta positive but lack both CD4 and CD8. Hence they are termed double negative (DN) T cells. In...
Sibrand Poppema, Ewerton Maggio, Anke van den Berg
Prolonged survival of rat islet xenografts in mice after CD45RB monotherapy
Published in: Transplantation
Lydia Visser, Sibrand Poppema, Bart de Haan, Pieter Klok, J. Van der Leij, Anke van den Berg, P. de Vos