Homotypic FADD interactions through a conserved RXDLL motif are required for death receptor-induced apoptosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology
Link
http://www.nature.com/articles/4401855.pdf
Reference33 articles.
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3. Huang B, Eberstadt M, Olejniczak ET, Meadows RP and Fesik SW (1996) NMR structure and mutagenesis of the Fas (APO-1/CD95) death domain. Nature 384: 638–641
4. Eberstadt M, Huang B, Chen Z, Meadows RP, Ng SC, Zheng L, Lenardo MJ and Fesik SW (1998) NMR structure and mutagenesis of the FADD (Mort1) death-effector domain. Nature 392: 941–945
5. Muzio M, Chinnaiyan AM, Kischkel FC, O’Rourke K, Shevchenko A, Ni J, Scaffidi C, Bretz JD, Zhang M, Gentz R, Mann M, Krammer PH, Peter ME and Dixit VM (1996) FLICE, a novel FADD-homologous ICE/CED-3-like protease, is recruited to the CD95 (Fas/APO-1) death--inducing signaling complex. Cell 85: 817–827
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