pDest490-OPN-a Citations (3)

Originally described in: An osteopontin fragment is essential for tumor cell invasion in hepatocellular carcinoma.
Takafuji V, Forgues M, Unsworth E, Goldsmith P, Wang XW Oncogene. 2007 Sep 27. 26(44):6361-71. PubMed Journal

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Articles Citing pDest490-OPN-a

Articles
Hypophosphatemic osteomalacia and bone sclerosis caused by a novel homozygous mutation of the FAM20C gene in an elderly man with a mild variant of Raine syndrome. Takeyari S, Yamamoto T, Kinoshita Y, Fukumoto S, Glorieux FH, Michigami T, Hasegawa K, Kitaoka T, Kubota T, Imanishi Y, Shimotsuji T, Ozono K. Bone. 2014 Oct;67:56-62. doi: 10.1016/j.bone.2014.06.026. Epub 2014 Jun 27. PubMed
Functional analysis of mutant FAM20C in Raine syndrome with FGF23-related hypophosphatemia. Kinoshita Y, Hori M, Taguchi M, Fukumoto S. Bone. 2014 Oct;67:145-51. doi: 10.1016/j.bone.2014.07.009. Epub 2014 Jul 12. PubMed
Osteopontin as a novel substrate for the proprotein convertase 5/6 (PCSK5) in bone. Hoac B, Susan-Resiga D, Essalmani R, Marcinkiweicz E, Seidah NG, McKee MD. Bone. 2018 Feb;107:45-55. doi: 10.1016/j.bone.2017.11.002. Epub 2017 Nov 7. PubMed

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