A new peak in the ALPS

Nature Medicine

Volumn 5, Issue 8, 1999, Pages 876-877

  Fischer, Alain ^a   Rieux Laucat, Frédéric ^a   Le Deist, Françoise ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE; LIGAND; TUMOR NECROSIS FACTOR RECEPTOR;

APOPTOSIS; AUTOIMMUNE DISEASE; AUTOIMMUNITY; GENETIC ASSOCIATION; HUMAN; IMMUNOPATHOGENESIS; LYMPHOCYTE PROLIFERATION; LYMPHOPROLIFERATIVE DISEASE; MISSENSE MUTATION; MOLECULAR DYNAMICS; PRIORITY JOURNAL; PROTEIN FAMILY; SHORT SURVEY; SIGNAL TRANSDUCTION;

ANIMALS; ANTIGENS, CD95; APOPTOSIS; AUTOIMMUNITY; CASPASES; HOMEOSTASIS; HUMANS; LYMPHOCYTES; LYMPHOPROLIFERATIVE DISORDERS; MICE; MUTATION; SIGNAL TRANSDUCTION;

EID: 0032799123     PISSN: 10788956     EISSN: None     Source Type: Journal    
DOI: 10.1038/11313     Document Type: Short Survey

References (10)

1. Ashkenazi, A. & Dixit, V.M. Death receptors: signaling and modulation. Science 281, 1305-1308 (1998).
2. Thornberry, N.A. & Lazebnik, Y. Caspases: Enemies within. Science 281, 1312-1316 (1998).
3. Rieux-Laucat, F. et al. Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity. Science 268, 1347-1349 (1995).
4. Fisher, G.H. et al. Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. Cell 81, 935-946 (1995).
5. Drappa, J., Vaishnew, A.K., Sullivan, K.E., Chu, J.L. & Elkon, K. B. Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity. N. Engl. J. Med. 355, 1643-1649 (1996).
6. Dianzani, U. et al. Deficiency of the Fas-associated pathway without Fas gene mutations in pediatric patients with autoimmunity and lymphoproliferation. Blood 89, 2871-2879 (1997).
7. Sneller M.C. et al. Clinical, immunologic and genetic features of an autoimmune lymphoproliferative syndrome associated with abnormal lymphocytic apoptosis. Blood 89, 1341-1348 (1997).
8. Wang, J. et al. Inherited human caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II. Cell 98, 47-58 (1999).
9. Ridge, J.P., DiRosa, F. & Matzinger, P. A conditioned dendritic cell can be a temporal bridge between a CD4+ T-helper and a T-killer cell. Nature 381, 434-438 (1998).
10. McDermott, M.F. et al. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 97, 133-144 (1999).