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Page 1
Autoimmune lymphoproliferative syndrome with somatic Fas mutations.
Holzelova E, Vonarbourg C, Stolzenberg MC, Arkwright PD, Selz F, Prieur AM, Blanche S, Bartunkova J, Vilmer E, Fischer A, Le Deist F, Rieux-Laucat F. Holzelova E, et al. Among authors: selz f. N Engl J Med. 2004 Sep 30;351(14):1409-18. doi: 10.1056/NEJMoa040036. N Engl J Med. 2004. PMID: 15459302 Free article.
Novel mutations in the RFXANK gene: RFX complex containing in-vitro-generated RFXANK mutant binds the promoter without transactivating MHC II.
Wiszniewski W, Fondaneche MC, Louise-Plence P, Prochnicka-Chalufour A, Selz F, Picard C, Le Deist F, Eliaou JF, Fischer A, Lisowska-Grospierre B. Wiszniewski W, et al. Among authors: selz f. Immunogenetics. 2003 Feb;54(11):747-55. doi: 10.1007/s00251-002-0521-1. Epub 2003 Jan 16. Immunogenetics. 2003. PMID: 12618906
Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease.
Cavazzana-Calvo M, Hacein-Bey S, de Saint Basile G, Gross F, Yvon E, Nusbaum P, Selz F, Hue C, Certain S, Casanova JL, Bousso P, Deist FL, Fischer A. Cavazzana-Calvo M, et al. Among authors: selz f. Science. 2000 Apr 28;288(5466):669-72. doi: 10.1126/science.288.5466.669. Science. 2000. PMID: 10784449 Clinical Trial.
40 results