2015
DOI: 10.1016/j.bbrc.2015.07.119
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Overexpression of Arl6ip5 in osteoblast regulates RANKL subcellualr localization

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Cited by 3 publications
(4 citation statements)
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“…Furthermore, JWA binds to a variety of proteins (Figure 1C). The NH 2 terminus of JWA is important for the binding between JWA and the receptor activator of NF-kB ligand (RANKL), thus inhibiting osteoclastogenesis [39]. The region between 103rd-117th aa of JWA protein is required for homodimer and heterodimer formation with ADP-ribosylation factor-like 6 interacting protein 1 (ARL6IP1) [40].…”
Section: The Structure and Functions Of Jwamentioning
confidence: 99%
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“…Furthermore, JWA binds to a variety of proteins (Figure 1C). The NH 2 terminus of JWA is important for the binding between JWA and the receptor activator of NF-kB ligand (RANKL), thus inhibiting osteoclastogenesis [39]. The region between 103rd-117th aa of JWA protein is required for homodimer and heterodimer formation with ADP-ribosylation factor-like 6 interacting protein 1 (ARL6IP1) [40].…”
Section: The Structure and Functions Of Jwamentioning
confidence: 99%
“…This suggests that JWA regulates self-protein stability mainly through protein phosphorylation and ubiquitination of its intracellular signaling molecules [32,37,45]. JWA binds to multiple proteins and participates in the regulation of signaling networks [22,35,[38][39][40][41]46,48,49]. (D) Potential modification sites of JWA from the Phosphosite tool (http://www.phosphosite.org (accessed on 15 August 2022)) [50].…”
Section: The Structure and Functions Of Jwamentioning
confidence: 99%
See 2 more Smart Citations