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Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency.
Fliegauf M, Bryant VL, Frede N, Slade C, Woon ST, Lehnert K, Winzer S, Bulashevska A, Scerri T, Leung E, Jordan A, Keller B, de Vries E, Cao H, Yang F, Schäffer AA, Warnatz K, Browett P, Douglass J, Ameratunga RV, van der Meer JW, Grimbacher B. Fliegauf M, et al. Among authors: bryant vl. Am J Hum Genet. 2015 Sep 3;97(3):389-403. doi: 10.1016/j.ajhg.2015.07.008. Epub 2015 Aug 13. Am J Hum Genet. 2015. PMID: 26279205 Free PMC article.
The Expanding Spectrum of NFkB1 Deficiency.
Bryant VL, Tangye SG. Bryant VL, et al. J Clin Immunol. 2016 Aug;36(6):531-2. doi: 10.1007/s10875-016-0310-5. Epub 2016 Jun 23. J Clin Immunol. 2016. PMID: 27338826 No abstract available.
The TNF Receptor Superfamily-NF-κB Axis Is Critical to Maintain Effector Regulatory T Cells in Lymphoid and Non-lymphoid Tissues.
Vasanthakumar A, Liao Y, Teh P, Pascutti MF, Oja AE, Garnham AL, Gloury R, Tempany JC, Sidwell T, Cuadrado E, Tuijnenburg P, Kuijpers TW, Lalaoui N, Mielke LA, Bryant VL, Hodgkin PD, Silke J, Smyth GK, Nolte MA, Shi W, Kallies A. Vasanthakumar A, et al. Among authors: bryant vl. Cell Rep. 2017 Sep 19;20(12):2906-2920. doi: 10.1016/j.celrep.2017.08.068. Epub 2017 Sep 7. Cell Rep. 2017. PMID: 28889989 Free article.
Life, death, and antibodies.
Bryant VL, Hodgkin PD. Bryant VL, et al. Science. 2017 Oct 13;358(6360):171-172. doi: 10.1126/science.aap8728. Science. 2017. PMID: 29026032 No abstract available.
Epistatic interactions between mutations of TACI (TNFRSF13B) and TCF3 result in a severe primary immunodeficiency disorder and systemic lupus erythematosus.
Ameratunga R, Koopmans W, Woon ST, Leung E, Lehnert K, Slade CA, Tempany JC, Enders A, Steele R, Browett P, Hodgkin PD, Bryant VL. Ameratunga R, et al. Among authors: bryant vl. Clin Transl Immunology. 2017 Oct 20;6(10):e159. doi: 10.1038/cti.2017.41. eCollection 2017 Oct. Clin Transl Immunology. 2017. PMID: 29114388 Free PMC article.
50 results