FcγRIV : A novel FcR with distinct IgG subclass specificity
By F. Nimmerjahn, P. Bruhns, Kentaro Horiuchi, J. Ravetch. 2005
657 citations recorded by the source corpus.
Subfields: Immunology, Molecular Biology, Radiology, Nuclear Medicine and Imaging
View Paper: https://www.semanticscholar.org/paper/e45ef06c10ad7e30ce12d0e068a44cc61f60ca05
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Immunology
- James P. Allison
- J. Wolchok
- Sergio A. Quezada
- K. Peggs
- H. Yagita
- J. Ravetch
- Lieping Chen
- F. Nimmerjahn
In Molecular Biology
In Radiology, Nuclear Medicine and Imaging
Citations in the corpus
- Fc-dependent depletion of tumor-infiltrating regulatory T cells co-defines the efficacy of anti–CTLA-4 therapy against melanoma (2013, background): “In mice, ADCC is regulated predominantly by the low-affinity receptors FcRIII and FcRIV (Nimmerjahn et al., 2005; Nimmerjahn et al., 2010; Setiady et al., 2010), and to a lesser extent by the highaffinity FcRI (Fossati-Jimack et al., 2000; Tedder et al., 2006; Hamaguchi et al., 2006).”
- IgEb immune complexes activate macrophages through FcγRIV binding (2007, background): “FcγRIV is encoded by the gene Fcgr4 (also called Fcgr3a , Fcrl3 and CD16-2”