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1 inimized, thereby reducing signaling via the immunoreceptor tyrosine-based inhibition motif.
2 Fc gamma RIIB cytoplasmic domain termed the immunoreceptor tyrosine-based inhibition motif.
3 sine phosphatase SHP-1 through a cytoplasmic immunoreceptor tyrosine-based inhibition motif.
4 FcgammaRIIB mediates inhibitory signals via immunoreceptor tyrosine-based inhibition motifs.
5 cross-linking or the presence of functional immunoreceptor tyrosine-based inhibition motifs.
6 smic tail or by introducing mutations in the immunoreceptor tyrosine-based inhibition motifs.
8 pport a role for CEACAM1 as a novel class of immunoreceptor tyrosine-based inhibition motif-bearing r
10 Thus, gp49B1 is an immunoreceptor tyrosine-based inhibition motif-containin
11 Deletion of the immunoreceptor tyrosine-based inhibition motif-containin
12 nce IKKYRLQ conforms poorly to the concensus immunoreceptor tyrosine-based inhibition motifs found in
14 Fc epsilon RI with a receptor containing an immunoreceptor tyrosine-based inhibition motif, has ther
17 ive intracellular signaling by virtue of two immunoreceptor tyrosine-based inhibition motifs in its c
20 ype Ig superfamily domains and two consensus immunoreceptor tyrosine-based inhibition motifs in the c
21 the cytoplasmic domains of gB (gBcyt) via an immunoreceptor tyrosine-based inhibition motif (ITIM) an
22 city of NK cells, despite the presence of an immunoreceptor tyrosine-based inhibition motif (ITIM) in
23 The present study identifies a canonical immunoreceptor tyrosine-based inhibition motif (ITIM) in
24 uitment of the tyrosine phosphatase SHP-1 to immunoreceptor tyrosine-based inhibition motif (ITIM) se
26 ion by FcgammaRIIB is mediated solely by its immunoreceptor tyrosine-based inhibition motif (ITIM) th
27 e sequence I/VxYxxL, often referred to as an immunoreceptor tyrosine-based inhibition motif (ITIM), b
28 tor pair that recruited components to CD33's immunoreceptor tyrosine-based inhibition motif (ITIM), i
29 5SHIP binds directly a phosphorylated motif, immunoreceptor tyrosine-based inhibition motif (ITIM), p
30 brane receptor-like protein that contains an immunoreceptor tyrosine-based inhibition motif (ITIM), w
31 iciently phosphorylated in the absence of an immunoreceptor tyrosine-based inhibition motif (ITIM)-be
33 ositol 5'-phosphatase (SHIP) is recruited to immunoreceptor tyrosine-based inhibition motif (ITIM)-co
34 oss-linking, Fgr becomes associated with the immunoreceptor tyrosine-based inhibition motif (ITIM)-co
35 ell inhibitory receptors, and B22, shares an immunoreceptor tyrosine-based inhibition motif (ITIM).
36 egulation was dependent upon the presence of immunoreceptor tyrosine-based inhibition motifs (ITIM) w
38 ne region, and a cytoplasmic tail containing immunoreceptor tyrosine-based inhibition motifs (ITIMs)
39 xes held on FDCs decreases the activation of immunoreceptor tyrosine-based inhibition motifs (ITIMs),
40 are controlled by receptors with cytoplasmic immunoreceptor tyrosine-based inhibition motifs (ITIMs).
41 ealed that these processes require the ITIM (immunoreceptor tyrosine-based inhibition motif) of the r
42 regulatory cellular responses whereby gp49B1 immunoreceptor tyrosine-based inhibition motifs rapidly
43 at least in part, because the phosphorylated immunoreceptor tyrosine-based inhibition motifs recruit
44 ack FcgammaRII, were incapable of preventing immunoreceptor tyrosine-based inhibition motif signaling
45 he cytoplasmic domain of gp49B1 contains two immunoreceptor tyrosine-based inhibition motifs that are
46 s), dampening immune responses via cytosolic immunoreceptor tyrosine-based inhibition motifs that rec
47 tyrosine-based activation motifs) and ITIMs (immunoreceptor tyrosine-based inhibition motifs) that ac
48 1, a member of the Ig superfamily containing immunoreceptor tyrosine-based inhibition motifs, with th
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