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Page 1
Defective TLR9-driven STAT3 activation in B cells of patients with CVID.
Borzutzky A, Rauter I, Fried A, Rachid R, McDonald DR, Hammarstrom L, Grimbacher B, Abraham RS, Geha RS. Borzutzky A, et al. Among authors: grimbacher b. Clin Immunol. 2018 Dec;197:40-44. doi: 10.1016/j.clim.2018.08.008. Epub 2018 Aug 23. Clin Immunol. 2018. PMID: 30145329
ICOS deficiency in patients with common variable immunodeficiency.
Salzer U, Maul-Pavicic A, Cunningham-Rundles C, Urschel S, Belohradsky BH, Litzman J, Holm A, Franco JL, Plebani A, Hammarstrom L, Skrabl A, Schwinger W, Grimbacher B. Salzer U, et al. Among authors: grimbacher b. Clin Immunol. 2004 Dec;113(3):234-40. doi: 10.1016/j.clim.2004.07.002. Clin Immunol. 2004. PMID: 15507387
Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.
Finck A, Van der Meer JW, Schäffer AA, Pfannstiel J, Fieschi C, Plebani A, Webster AD, Hammarström L, Grimbacher B. Finck A, et al. Among authors: grimbacher b. Eur J Hum Genet. 2006 Jul;14(7):867-75. doi: 10.1038/sj.ejhg.5201634. Epub 2006 Apr 26. Eur J Hum Genet. 2006. PMID: 16639407
Deconstructing common variable immunodeficiency by genetic analysis.
Schäffer AA, Salzer U, Hammarström L, Grimbacher B. Schäffer AA, et al. Among authors: grimbacher b. Curr Opin Genet Dev. 2007 Jun;17(3):201-12. doi: 10.1016/j.gde.2007.04.002. Epub 2007 Apr 27. Curr Opin Genet Dev. 2007. PMID: 17467261 Review.
343 results