ITAMs versus ITIMs: striking a balance during cell regulation

[1] The inositol phosphatase SHIP inhibits Akt/PKB activation in B cells [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (51) : 33922 - 33928

[2] CYTOPLASMIC DOMAIN HETEROGENEITY AND FUNCTIONS OF IGG FC-RECEPTORS IN LYMPHOCYTES-B [J]. SCIENCE, 1992, 256 (5065) : 1808 - 1812

[3] Crippling of CD3-ζ ITAMs does not impair T cell receptor signaling [J]. IMMUNITY, 1999, 10 (04) : 409 - 420

[4] Positive selection through a motif in the αβ T cell receptor [J]. SCIENCE, 1998, 281 (5378) : 835 - 838

[5] Sequential involvement of Lck and SHP-1 with MHC-recognizing receptors on NK cells inhibits FcR-initiated tyrosine kinase activation [J]. IMMUNITY, 1996, 5 (06) : 629 - 638

[6] SLP-76 is a direct substrate of SHP-1 recruited to killer cell inhibitory receptors [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) : 27518 - 27523

[7] Spontaneous autoimmune disease in FcγRIIB-deficient mice results from strain-specific epistasis [J]. IMMUNITY, 2000, 13 (02) : 277 - 285

[8] Molecular basis of the recruitment of the SH2 domain-containing inositol 5-phosphatases SHIP1 and SHIP2 by FcγRIIB [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) : 37357 - 37364

[9] Brumbaugh KM, 1996, J IMMUNOL, V157, P2804

[10] A novel phosphotyrosine motif with a critical amino acid at position-2 for the SH2 domain-mediated activation of the tyrosine phosphatase SHP-1 [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (20) : 13066 - 13072

[1] The inositol phosphatase SHIP inhibits Akt/PKB activation in B cells [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (51) : 33922 - 33928

[2] CYTOPLASMIC DOMAIN HETEROGENEITY AND FUNCTIONS OF IGG FC-RECEPTORS IN LYMPHOCYTES-B [J]. SCIENCE, 1992, 256 (5065) : 1808 - 1812

[3] Crippling of CD3-ζ ITAMs does not impair T cell receptor signaling [J]. IMMUNITY, 1999, 10 (04) : 409 - 420

[4] Positive selection through a motif in the αβ T cell receptor [J]. SCIENCE, 1998, 281 (5378) : 835 - 838

[5] Sequential involvement of Lck and SHP-1 with MHC-recognizing receptors on NK cells inhibits FcR-initiated tyrosine kinase activation [J]. IMMUNITY, 1996, 5 (06) : 629 - 638

[6] SLP-76 is a direct substrate of SHP-1 recruited to killer cell inhibitory receptors [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) : 27518 - 27523

[7] Spontaneous autoimmune disease in FcγRIIB-deficient mice results from strain-specific epistasis [J]. IMMUNITY, 2000, 13 (02) : 277 - 285

[8] Molecular basis of the recruitment of the SH2 domain-containing inositol 5-phosphatases SHIP1 and SHIP2 by FcγRIIB [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) : 37357 - 37364

[9] Brumbaugh KM, 1996, J IMMUNOL, V157, P2804

[10] A novel phosphotyrosine motif with a critical amino acid at position-2 for the SH2 domain-mediated activation of the tyrosine phosphatase SHP-1 [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (20) : 13066 - 13072