Frédéric Rieux-Laucat
INSERM Unité 768
Hôpital Necker
Paris
France
Name/email consistency: high
- Inherited and somatic CD3zeta mutations in a patient with T-cell deficiency. Rieux-Laucat, F., Hivroz, C., Lim, A., Mateo, V., Pellier, I., Selz, F., Fischer, A., Le Deist, F. N. Engl. J. Med. (2006)
- Inherited and acquired death receptor defects in human Autoimmune Lymphoproliferative Syndrome. Rieux-Laucat, F. Curr. Dir. Autoimmun. (2006)
- Autoimmune lymphoproliferative syndromes: genetic defects of apoptosis pathways. Rieux-Laucat, F., Le Deist, F., Fischer, A. Cell Death Differ. (2003)
- Cell-death signaling and human disease. Rieux-Laucat, F., Fischer, A., Deist, F.L. Curr. Opin. Immunol. (2003)
- Lymphoproliferative syndrome with autoimmunity: A possible genetic basis for dominant expression of the clinical manifestations. Rieux-Laucat, F., Blachère, S., Danielan, S., De Villartay, J.P., Oleastro, M., Solary, E., Bader-Meunier, B., Arkwright, P., Pondaré, C., Bernaudin, F., Chapel, H., Nielsen, S., Berrah, M., Fischer, A., Le Deist, F. Blood (1999)
- Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome. Rieux-Laucat, F., Bahadoran, P., Brousse, N., Selz, F., Fischer, A., Le Deist, F., De Villartay, J.P. J. Clin. Invest. (1998)