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Human TCR alpha/beta+ CD4-CD8- double-negative T cells in patients with autoimmune lymphoproliferative syndrome express restricted Vbeta TCR diversity and are clonally related to CD8+ T cells.
Bristeau-Leprince A, Mateo V, Lim A, Magerus-Chatinet A, Solary E, Fischer A, Rieux-Laucat F, Gougeon ML. Bristeau-Leprince A, et al. Among authors: fischer a. J Immunol. 2008 Jul 1;181(1):440-8. doi: 10.4049/jimmunol.181.1.440. J Immunol. 2008. PMID: 18566410 Free article.
Cell-death signaling and human disease.
Rieux-Laucat F, Fischer A, Deist FL. Rieux-Laucat F, et al. Among authors: fischer a. Curr Opin Immunol. 2003 Jun;15(3):325-31. doi: 10.1016/s0952-7915(03)00042-6. Curr Opin Immunol. 2003. PMID: 12787759 Review.
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: fischer a. N Engl J Med. 2004 Sep 30;351(14):1409-18. doi: 10.1056/NEJMoa040036. N Engl J Med. 2004. PMID: 15459302 Free article.
Long-term immune reconstitution in RAG-1-deficient mice treated by retroviral gene therapy: a balance between efficiency and toxicity.
Lagresle-Peyrou C, Yates F, Malassis-Séris M, Hue C, Morillon E, Garrigue A, Liu A, Hajdari P, Stockholm D, Danos O, Lemercier B, Gougeon ML, Rieux-Laucat F, de Villartay JP, Fischer A, Cavazzana-Calvo M. Lagresle-Peyrou C, et al. Among authors: fischer a. Blood. 2006 Jan 1;107(1):63-72. doi: 10.1182/blood-2005-05-2032. Epub 2005 Sep 20. Blood. 2006. PMID: 16174758 Free article.
A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection.
de Villartay JP, Lim A, Al-Mousa H, Dupont S, Déchanet-Merville J, Coumau-Gatbois E, Gougeon ML, Lemainque A, Eidenschenk C, Jouanguy E, Abel L, Casanova JL, Fischer A, Le Deist F. de Villartay JP, et al. Among authors: fischer a. J Clin Invest. 2005 Nov;115(11):3291-9. doi: 10.1172/JCI25178. J Clin Invest. 2005. PMID: 16276422 Free PMC article.
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome.
Rigaud S, Fondanèche MC, Lambert N, Pasquier B, Mateo V, Soulas P, Galicier L, Le Deist F, Rieux-Laucat F, Revy P, Fischer A, de Saint Basile G, Latour S. Rigaud S, et al. Among authors: fischer a. Nature. 2006 Nov 2;444(7115):110-4. doi: 10.1038/nature05257. Nature. 2006. PMID: 17080092
5,285 results