dr. D.S. (Dineke) Verbeek

Associate professor (Tenure track) /adjunct hoogleraar

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E-mail:
d.s.verbeek umcg.nl

Research

  1. 2021
  2. 2020
  3. 2019
  4. 2018
  5. Bazov, I., Sarkisyan, D., Kononenko, O., Watanabe, H., Taqi, M. M., Stålhandske, L., Verbeek, D. S., Mulder, J., Rajkowska, G., Sheedy, D., Kril, J., Sun, X., Syvänen, A-C., Yakovleva, T., & Bakalkin, G. (2018). Neuronal Expression of Opioid Gene is Controlled by Dual Epigenetic and Transcriptional Mechanism in Human Brain. Cerebral Cortex, 28(9), 3129-3142. https://doi.org/10.1093/cercor/bhx181
  6. Müller, C., Zidek, L. M., Ackermann, T., de Jong, T., Liu, P., Kliche, V., Zaini, M. A., Kortman, G., Harkema, L., Verbeek, D. S., Tuckermann, J. P., von Maltzahn, J., de Bruin, A., Guryev, V., Wang, Z-Q., & Calkhoven, C. F. (2018). Reduced expression of C/EBPβ-LIP extends health- and lifespan in mice. eLife, 7. https://doi.org/10.7554/eLife.34985
  7. 2017
  8. Nibbeling, E. A. R., Duarri, A., Verschuuren-Bemelmans, C. C., Fokkens, M. R., Karjalainen, J. M., Smeets, C. J. L. M., de Boer-Bergsma, J. J., van der Vries, G., Dooijes, D., Bampi, G. B., van Diemen, C., Brunt, E., Ippel, E., Kremer, B., Vlak, M., Adir, N., Wijmenga, C., Warrenburg, B. P. C. V. D., Franke, L., ... Verbeek, D. S. (2017). Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. Brain, 140(11), 2860-2878. https://doi.org/10.1093/brain/awx251
  9. Morelli, F. F., Verbeek, D. S., Bertacchini, J., Vinet, J., Mediani, L., Marmiroli, S., Cenacchi, G., Nasi, M., De Biasi, S., Brunsting, J. F., Lammerding, J., Pegoraro, E., Angelini, C., Tupler, R., Alberti, S., & Carra, S. (2017). Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function. Cell reports, 20(9), 2100-2115. https://doi.org/10.1016/j.celrep.2017.08.018
  10. Kononenko, O., Bazov, I., Watanabe, H., Gerashchenko, G., Dyachok, O., Verbeek, D. S., Alkass, K., Druid, H., Andersson, M., Mulder, J., Svenningsen, A. F., Rajkowska, G., Stockmeier, C. A., Krishtal, O., Yakovleva, T., & Bakalkin, G. (2017). Opioid precursor protein isoform is targeted to the cell nuclei in the human brain. Biochimica et Biophysica Acta-General Subjects, 1861(2), 246-255. https://doi.org/10.1016/j.bbagen.2016.11.002
  11. 2016
  12. 2015
  13. Smets, K., Duarri , A., Deconinck, T., Ceulemans, B., van de Warrenburg, B. P., Zuechner, S., Gonzalez, M. A., Schuele, R., Synofzik, M., Van der Aa, N., De Jonghe, P., Verbeek, D. S., & Baets, J. (2015). First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy. BMC MEDICAL GENETICS, 16, [51]. https://doi.org/10.1186/s12881-015-0200-3
  14. Duarri , A., Nibbeling, E. A. R., Fokkens, M. R., Meijer, M., Boerrigter, M., Verschuuren - Bemelmans, C. C., Kremer, B. P. H., van de Warrenburg, B. P., Dooijes, D., Boddeke, E., Sinke, R. J., & Verbeek, D. S. (2015). Functional Analysis Helps to Define KCNC3 Mutational Spectrum in Dutch Ataxia Cases. PLoS ONE, 10(3), [e0116599]. https://doi.org/10.1371/journal.pone.0116599
  15. Groen, J. L., Andrade, A., Ritz, K., Jalalzadeh, H., Haagmans, M., Bradley, T. E. J., Jongejan, A., Verbeek, D. S., Nuernberg, P., Denome, S., Hennekam, R. C. M., Lipscombe, D., Baas, F., & Tijssen, M. A. J. (2015). CACNA1B mutation is linked to unique myoclonus-dystonia syndrome. Human Molecular Genetics, 24(4), 987-993. https://doi.org/10.1093/hmg/ddu513
  16. 2014
  17. Seidel, K., Kusters, B., den Dunnen, W. F. A., Bouzrou, M., Hageman, G., Korf, H. -W., Schelhaas, H. J., Verbeek, D., & Rueb, U. (2014). First patho-anatomical investigation of the brain of a SCA19 patient. Neuropathology and Applied Neurobiology, 40(5), 640-644. https://doi.org/10.1111/nan.12128
  18. 2013
  19. Jezierska, J., Stevanin, G., Watanabe, H., Fokkens, M. R., Zagnoli, F., Kok, J., Goas, J-Y., Bertrand, P., Robin, C., Brice, A., Bakalkin, G., Durr, A., & Verbeek, D. S. (2013). Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases. Journal of Neurology, 260(7), 1807-1812. https://doi.org/10.1007/s00415-013-6882-6
  20. 2012
  21. Duarri, A., Jezierska, J., Fokkens, M., Meijer, M., Schelhaas, H. J., den Dunnen, W. F. A., van Dijk, F., Verschuuren - Bemelmans, C., Hageman, G., van de Vlies, P., Küsters, B., van de Warrenburg, B. P., Kremer, B., Wijmenga, C., Sinke, R. J., Swertz, M. A., Kampinga, H. H., Boddeke, H., & Verbeek, D. S. (2012). Mutations in Potassium Channel KCND3 Cause Spinocerebellar Ataxia Type 19. Annals of Neurology, 72(6), 870-880. https://doi.org/10.1002/ana.23700
  22. Taqi, M. M., Warmlander, S. K. T. S., Yamskova, O., Madani, F., Bazov, I., Luo, J., Zubarev, R., Verbeek, D., Graslund, A., & Bakalkin, G. (2012). Conformation Effects of CpG Methylation on Single-Stranded DNA Oligonucleotides: Analysis of the Opioid Peptide Dynorphin-Coding Sequences. PLoS ONE, 7(6), [e39605]. https://doi.org/10.1371/journal.pone.0039605
  23. 2011
  24. 2010
  25. Bakalkin, G., Watanabe, H., Jezierska, J., Depoorter, C., Verschuuren - Bemelmans, C., Bazov, I., Artemenko, K. A., Yakovleva, T., Dooijes, D., Van de Warrenburg, B. P. C., Zubarev, R. A., Kremer, B., Knapp, P. E., Hauser, K. F., Wijmenga, C., Nyberg, F., Sinke, R. J., & Verbeek, D. S. (2010). Prodynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23. American Journal of Human Genetics, 87(5), 593-603. https://doi.org/10.1016/j.ajhg.2010.10.001
  26. 2009
  27. Muller, P. A. J., van de Sluis, B., Groot, A. J., Verbeek, D., Vonk, W. I. M., Maine, G. N., Burstein, E., Wijmenga, C., Vooijs, M., Reits, E., & Klomp, L. W. J. (2009). Nuclear-Cytosolic Transport of COMMD1 Regulates NF-kappa B and HIF-1 Activity. Traffic, 10(5), 514-527. https://doi.org/10.1111/j.1600-0854.2009.00892.x
  28. 2008
  29. 2005
  30. Verbeek, DS., van de Warrenburg, BPC., Hennekam, FAM., Dooijes, D., Ippel, PF., Verschuuren-Bemelmans, CC., Kremer, HPH., & Sinke, RJ. (2005). Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population. HUMAN GENETICS, 117(1), 88-91. https://doi.org/10.1007/s00439-005-1278-z
  31. 2004
  32. 2002

ID: 321781