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Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.
Osborne AJ, Breno M, Borsa NG, Bu F, Frémeaux-Bacchi V, Gale DP, van den Heuvel LP, Kavanagh D, Noris M, Pinto S, Rallapalli PM, Remuzzi G, Rodríguez de Cordoba S, Ruiz A, Smith RJH, Vieira-Martins P, Volokhina E, Wilson V, Goodship THJ, Perkins SJ. Osborne AJ, et al. Among authors: volokhina e. J Immunol. 2018 Apr 1;200(7):2464-2478. doi: 10.4049/jimmunol.1701695. Epub 2018 Mar 2. J Immunol. 2018. PMID: 29500241 Free PMC article.
Analysis of rare variants in the C3 gene in patients with age-related macular degeneration.
Duvvari MR, Paun CC, Buitendijk GH, Saksens NT, Volokhina EB, Ristau T, Schoenmaker-Koller FE, van de Ven JP, Groenewoud JM, van den Heuvel LP, Hofman A, Fauser S, Uitterlinden AG, Klaver CC, Hoyng CB, de Jong EK, den Hollander AI. Duvvari MR, et al. Among authors: volokhina eb. PLoS One. 2014 Apr 15;9(4):e94165. doi: 10.1371/journal.pone.0094165. eCollection 2014. PLoS One. 2014. PMID: 24736606 Free PMC article.
A novel method for direct measurement of complement convertases activity in human serum.
Blom AM, Volokhina EB, Fransson V, Strömberg P, Berghard L, Viktorelius M, Mollnes TE, López-Trascasa M, van den Heuvel LP, Goodship TH, Marchbank KJ, Okroj M. Blom AM, et al. Among authors: volokhina eb. Clin Exp Immunol. 2014 Oct;178(1):142-53. doi: 10.1111/cei.12388. Clin Exp Immunol. 2014. PMID: 24853370 Free PMC article.
53 results