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1 al transducing receptor betac subunit of the IL-5 receptor.
2 nteraction with the alpha chain of the human IL-5 receptor.
3 ls and monocytes from patients expressed the IL-5 receptor.
4 s with the alpha subunit of the interleukin (IL) 5 receptor.
5 colony stimulating factor, and the IL-3 and IL-5 receptors.
6 We describe MVF assays for the IL-1 and IL-5 receptors.
7 Ras activation through the GM-CSF, IL-3, and IL-5 receptors.
8 onent of the GM-CSF, interleukin (IL)-3, and IL-5 receptors.
10 is regulated by the restricted expression of IL-5 receptor alpha (IL-5Ralpha), a subunit of high-affi
11 inistration of 3 doses of benralizumab (anti-IL-5 receptor alpha antibody [n = 5]) or placebo (n = 4)
12 oth monomers were shown to interact with the IL-5 receptor alpha chain with 1:1 stoichiometry and aff
13 al analysis revealed unexpected affinity for IL-5 receptor alpha chain with variants containing E110W
15 of biologics, such as benralizumab (an anti-IL-5 receptor alpha humanised monoclonal antibody), has
16 Treatment with antibodies targeting IL-5 or IL-5 receptor alpha reduces the frequency of asthma exac
18 Benralizumab targets eosinophils by binding IL-5 receptor alpha, inducing apoptosis through antibody
20 This mutein was found to retain substantial IL-5 receptor alpha-chain binding but with selectively s
21 This result confirms recent findings that IL-5 receptor alpha-chain recognition can be supported b
22 d benralizumab, a monoclonal antibody to the IL-5 receptor alpha-chain, are comparatively limited, es
24 generated a 19-aa peptide that binds to the IL-5 receptor alpha/beta heterodimer complex with an aff
25 se findings highlight the cross-talk between IL-5 receptor and CD300f as a novel pathway regulating a
29 sL(+) B cells expressed higher levels of the IL-5 receptor, and treating B cells with IL-5 and CD40L
30 sitization, leukotriene modifiers, anti-IL-5/IL-5 receptor, anti-IL-4 receptor, and anti-IgE) and inv
31 have shown that dynamin-2 interacts with the IL-5 receptor-associated tyrosine kinases, Lyn and JAK2,
33 the atopic sensitized tissues with either an IL-5 receptor blocking antibody (IL-5ra) or the human re
35 ted monoclonal antibody directed against the IL-5 receptor, has powerful apoptotic effects on eosinop
38 logy is critically dependent on IL-5 and the IL-5 receptor (IL-5R), composed of a ligand binding alph
39 hils; in contrast, benralizumab binds to the IL-5 receptor (IL-5R), preventing IL-5 from binding and
41 e a novel signaling pathway activated by the IL-5 receptor in eosinophils involving the CrkL adapter
42 zumab, and benralizumab, inhibit the IL-5 or IL-5 receptor pathway; dupilumab blocks IL-4 and IL-13 t
43 omers stimulated cell proliferation of human IL-5 receptor positive cells with a concentration depend
47 ces including interleukin (IL-)-3, IL-4, and IL-5 receptor subunits, the p65 component of nuclear fac
49 te the therapeutic benefit of inhibiting the IL-5 receptor using benralizumab to treat severe rhinosi
51 ding alpha-chain of the human interleukin 5 (IL-5) receptor was expressed in its soluble form, lackin