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Volumn 321, Issue 5889, 2008, Pages 663-668

Essential cytoplasmic translocation of a cytokine receptor-assembled signaling complex

Author keywords

[No Author keywords available]

Indexed keywords

CD40 ANTIGEN; CYTOKINE RECEPTOR; I KAPPA B KINASE GAMMA; INHIBITOR OF APOPTOSIS PROTEIN 1; INHIBITOR OF APOPTOSIS PROTEIN 2; MEMBRANE RECEPTOR; MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE KINASE KINASE 1; PROTEASOME; PROTEIN KINASE; TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED FACTOR 2; TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED FACTOR 3; UBIQUITIN CONJUGATING ENZYME 13;

EID: 48749090228     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1157340     Document Type: Article
Times cited : (190)

References (35)
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    • The monoclonal antibody has been generated against a branched peptide corresponding to the region containing K63 of one ubiquitin chain and the C-terminal portion of another chain. It does not recognize ubiquitin attached to any other lysine residue of ubiquitin including K48
    • The monoclonal antibody has been generated against a branched peptide corresponding to the region containing K63 of one ubiquitin chain and the C-terminal portion of another chain. It does not recognize ubiquitin attached to any other lysine residue of ubiquitin including K48.
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    • We thank V. M. Dixit (Genentech) for his excellent suggestions, X. Wang (University of Texas Southwestern Medical School) for SM, J. DiDonato (Cleveland Clinic) and G. Courtois (INSERM U697) for IKKγ-deficient cells, R. Fonseca (Mayo Clinic) for c-IAP-deficient cells, and J. Reed and Z. Ronai (Burnham) for c-IAP2 and TRAF2 expression vectors, respectively. Work was supported by NIH grant AI043477 and a Leukemia and Lymphoma Society SCOR (7332-06) project to M.K, who is an American Cancer Society Research Professor. A.M, P.-H.T, and J.-L.L. were supported in part by The Mochida Memorial Foundation for Medical and Pharmaceutical Research, American Lung Association of California, and Life Science Foundation, respectively. H.W. and D.A.A.V were supported by the NIH (AI52199, a Cancer Center Support CORE grant (CA21765, and the American Lebanese Syrian Associated Charities ALSAC
    • We thank V. M. Dixit (Genentech) for his excellent suggestions, X. Wang (University of Texas Southwestern Medical School) for SM, J. DiDonato (Cleveland Clinic) and G. Courtois (INSERM U697) for IKKγ-deficient cells, R. Fonseca (Mayo Clinic) for c-IAP-deficient cells, and J. Reed and Z. Ronai (Burnham) for c-IAP2 and TRAF2 expression vectors, respectively. Work was supported by NIH grant AI043477 and a Leukemia and Lymphoma Society SCOR (7332-06) project to M.K., who is an American Cancer Society Research Professor. A.M., P.-H.T., and J.-L.L. were supported in part by The Mochida Memorial Foundation for Medical and Pharmaceutical Research, American Lung Association of California, and Life Science Foundation, respectively. H.W. and D.A.A.V were supported by the NIH (AI52199), a Cancer Center Support CORE grant (CA21765), and the American Lebanese Syrian Associated Charities (ALSAC).


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