prof. dr. B.J.L. (Bart) Eggen



  1. 2019
  2. 2018
  3. Sribudiani, Y., Chauhan, R. K., Alves, M. M., Petrova, L., Brosens, E., Harrison, C., ... Hofstra, R. M. W. (2018). Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease. Gastroenterology, 155(1), 118-129.e6.
  4. 2017
  5. Wlodarczyk, A., Holtman, I. R., Krueger, M., Yogev, N., Bruttger, J., Khorooshi, R., ... Owens, T. (2017). A novel microglial subset plays a key role in myelinogenesis in developing brain. The EMBO Journal, 36(22), 3292-3308.
  6. Gui, H., Schriemer, D., Cheng, W. W., Chauhan, R. K., Antinolo, G., Berrios, C., ... Hofstra, R. M. W. (2017). Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes. Genome Biology, 18(48).
  7. 2016
  8. Vinet, J., Vainchtein, I. D., Spano, C., Giordano, C., Bordini, D., Curia, G., ... Biagini, G. (2016). Microglia are Less Pro-Inflammatory than Myeloid Infiltrates in the Hippocampus of Mice Exposed to Status Epilepticus. Glia, 64(8), 1350-1362.
  9. Janova, H., Boettcher, C., Holtman, I. R., Regen, T., van Rossum, D., Goetz, A., ... Hanisch, U-K. (2016). CD14 is a key organizer of microglial responses to CNS infection and injury. Glia, 64(4), 635-649.
  10. 2015
  11. Holtman, I. R., Noback, M., Bijlsma, M., Duong, K. N., van der Geest, M. A., Ketelaars, P. T., ... Boddeke, H. W. G. M. (2015). Glia Open Access Database (GOAD): A comprehensive gene expression encyclopedia of glia cells in health and disease. Glia, 63(9), 1495-1506.
  12. 2014
  13. Raj, D. D. A., Jaarsma, D., Holtman, I. R., Olah, M., Ferreira, F. M., Schaafsma, W., ... Boddeke, H. W. G. M. (2014). Priming of microglia in a DNA-repair deficient model of accelerated aging. Neurobiology of Aging, 35(9), 2147-2160.
  14. Bsibsi, M., Peferoen, L. A. N., Holtman, I. R., Nacken, P. J., Gerritsen, W. H., Witte, M. E., ... van Noort, J. M. (2014). Demyelination during multiple sclerosis is associated with combined activation of microglia/macrophages by IFN-gamma and alpha B-crystallin. Acta Neuropathologica, 128(2), 215-229.
  15. 2013
  16. Alves, M. M., Sribudiani, Y., Brouwer, R. W. W., Amiel, J., Antinolo, G., Borrego, S., ... Hofstra, R. M. W. (2013). Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model. Developmental Biology, 382(1), 320-329.
  17. 2012
  18. 2010
  19. Alves, M. M. M., Osinga, J., Verheij, J. B. G. M., Metzger, M., Eggen, B. J. L., & Hofstra, R. M. W. (2010). Mutations in SCG10 Are Not Involved in Hirschsprung Disease. PLoS ONE, 5(12), [15144].
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