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Quantitative multiplex profiling of the complement system to diagnose complement-mediated diseases.
Willems E, Lorés-Motta L, Zanichelli A, Suffritti C, van der Flier M, van der Molen RG, Langereis JD, van Drongelen J, van den Heuvel LP, Volokhina E, van de Kar NC, Keizer-Garritsen J, Levin M, Herberg JA, Martinon-Torres F, Wessels HJ, de Breuk A, Fauser S, Hoyng CB, den Hollander AI, de Groot R, van Gool AJ, Gloerich J, de Jonge MI. Willems E, et al. Among authors: van der molen rg, den hollander ai, van gool aj, van drongelen j, van de kar nc, van der flier m, van den heuvel lp. Clin Transl Immunology. 2020 Dec 9;9(12):e1225. doi: 10.1002/cti2.1225. eCollection 2020. Clin Transl Immunology. 2020. PMID: 33318796 Free PMC article.
Biosynthetic homeostasis and resilience of the complement system in health and infectious disease.
Willems E, Alkema W, Keizer-Garritsen J, Suppers A, van der Flier M, Philipsen RHLA, van den Heuvel LP, Volokhina E, van der Molen RG, Herberg JA, Levin M, Wright VJ, Ahout IML, Ferwerda G, Emonts M, Boeddha NP, Rivero-Calle I, Torres FM, Wessels HJCT, de Groot R, van Gool AJ, Gloerich J, de Jonge MI. Willems E, et al. Among authors: van der molen rg, van gool aj, van der flier m, van den heuvel lp. EBioMedicine. 2019 Jul;45:303-313. doi: 10.1016/j.ebiom.2019.06.008. Epub 2019 Jun 29. EBioMedicine. 2019. PMID: 31262714 Free PMC article.
Effect of rare coding variants in the CFI gene on Factor I expression levels.
de Jong S, Volokhina EB, de Breuk A, Nilsson SC, de Jong EK, van der Kar NCAJ, Bakker B, Hoyng CB, van den Heuvel LP, Blom AM, den Hollander AI. de Jong S, et al. Among authors: den hollander ai, van der kar ncaj, van den heuvel lp. Hum Mol Genet. 2020 Aug 11;29(14):2313-2324. doi: 10.1093/hmg/ddaa114. Hum Mol Genet. 2020. PMID: 32510551 Free PMC article.
Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome.
de Jong S, de Breuk A, Bakker B, Katti S, Hoyng CB, Nilsson SC, Blom AM, van den Heuvel LP, den Hollander AI, Volokhina EB. de Jong S, et al. Among authors: den hollander ai, van den heuvel lp. Front Immunol. 2022 Jan 5;12:789897. doi: 10.3389/fimmu.2021.789897. eCollection 2021. Front Immunol. 2022. PMID: 35069568 Free PMC article. Clinical Trial.
Implications of genetic variation in the complement system in age-related macular degeneration.
de Jong S, Gagliardi G, Garanto A, de Breuk A, Lechanteur YTE, Katti S, van den Heuvel LP, Volokhina EB, den Hollander AI. de Jong S, et al. Among authors: den hollander ai, van den heuvel lp. Prog Retin Eye Res. 2021 Sep;84:100952. doi: 10.1016/j.preteyeres.2021.100952. Epub 2021 Feb 19. Prog Retin Eye Res. 2021. PMID: 33610747 Free article. Review.
Compound heterozygous mutations in the C6 gene of a child with recurrent infections.
Westra D, Kurvers RA, van den Heuvel LP, Würzner R, Hoppenreijs EP, van der Flier M, van de Kar NC, Warris A. Westra D, et al. Among authors: van de kar nc, van der flier m, van den heuvel lp. Mol Immunol. 2014 Apr;58(2):201-5. doi: 10.1016/j.molimm.2013.11.023. Epub 2013 Dec 30. Mol Immunol. 2014. PMID: 24378253
Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome.
Westra D, Volokhina EB, van der Molen RG, van der Velden TJ, Jeronimus-Klaasen A, Goertz J, Gracchi V, Dorresteijn EM, Bouts AH, Keijzer-Veen MG, van Wijk JA, Bakker JA, Roos A, van den Heuvel LP, van de Kar NC. Westra D, et al. Among authors: van der molen rg, van wijk ja, van de kar nc, van der velden tj, van den heuvel lp. Pediatr Nephrol. 2017 Feb;32(2):297-309. doi: 10.1007/s00467-016-3496-0. Epub 2016 Oct 7. Pediatr Nephrol. 2017. PMID: 27718086 Free PMC article.
389 results