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Clinical application of whole-genome sequencing in patients with primary immunodeficiency.
Mousallem T, Urban TJ, McSweeney KM, Kleinstein SE, Zhu M, Adeli M, Parrott RE, Roberts JL, Krueger B, Buckley RH, Goldstein DB. Mousallem T, et al. Among authors: parrott re. J Allergy Clin Immunol. 2015 Aug;136(2):476-9.e6. doi: 10.1016/j.jaci.2015.02.040. Epub 2015 May 14. J Allergy Clin Immunol. 2015. PMID: 25981738 Free PMC article.
T-B+NK+ severe combined immunodeficiency caused by complete deficiency of the CD3zeta subunit of the T-cell antigen receptor complex.
Roberts JL, Lauritsen JP, Cooney M, Parrott RE, Sajaroff EO, Win CM, Keller MD, Carpenter JH, Carabana J, Krangel MS, Sarzotti M, Zhong XP, Wiest DL, Buckley RH. Roberts JL, et al. Among authors: parrott re. Blood. 2007 Apr 15;109(8):3198-206. doi: 10.1182/blood-2006-08-043166. Epub 2006 Dec 14. Blood. 2007. PMID: 17170122 Free PMC article.
CD45-deficient severe combined immunodeficiency caused by uniparental disomy.
Roberts JL, Buckley RH, Luo B, Pei J, Lapidus A, Peri S, Wei Q, Shin J, Parrott RE, Dunbrack RL Jr, Testa JR, Zhong XP, Wiest DL. Roberts JL, et al. Among authors: parrott re. Proc Natl Acad Sci U S A. 2012 Jun 26;109(26):10456-61. doi: 10.1073/pnas.1202249109. Epub 2012 Jun 11. Proc Natl Acad Sci U S A. 2012. PMID: 22689986 Free PMC article.
Post-transplantation B cell function in different molecular types of SCID.
Buckley RH, Win CM, Moser BK, Parrott RE, Sajaroff E, Sarzotti-Kelsoe M. Buckley RH, et al. Among authors: parrott re. J Clin Immunol. 2013 Jan;33(1):96-110. doi: 10.1007/s10875-012-9797-6. Epub 2012 Sep 22. J Clin Immunol. 2013. PMID: 23001410 Free PMC article.
A nonsense mutation in IKBKB causes combined immunodeficiency.
Mousallem T, Yang J, Urban TJ, Wang H, Adeli M, Parrott RE, Roberts JL, Goldstein DB, Buckley RH, Zhong XP. Mousallem T, et al. Among authors: parrott re. Blood. 2014 Sep 25;124(13):2046-50. doi: 10.1182/blood-2014-04-571265. Epub 2014 Aug 18. Blood. 2014. PMID: 25139357 Free PMC article.
23 results