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Items: 4


Characterization of the mammalian family of DCN-type NEDD8 E3 ligases.

Keuss MJ, Thomas Y, Mcarthur R, Wood NT, Knebel A, Kurz T.

J Cell Sci. 2016 Apr 1;129(7):1441-54. doi: 10.1242/jcs.181784. Epub 2016 Feb 18.


Oncogenic function of SCCRO5/DCUN1D5 requires its Neddylation E3 activity and nuclear localization.

Bommeljé CC, Weeda VB, Huang G, Shah K, Bains S, Buss E, Shaha M, Gönen M, Ghossein R, Ramanathan SY, Singh B.

Clin Cancer Res. 2014 Jan 15;20(2):372-81. doi: 10.1158/1078-0432.CCR-13-1252. Epub 2013 Nov 5.


Constitutional 11q14-q22 chromosome deletion syndrome in a child with neuroblastoma MYCN single copy.

Passariello A, De Brasi D, Defferrari R, Genesio R, Tufano M, Mazzocco K, Capasso M, Migliorati R, Martinsson T, Siani P, Nitsch L, Tonini GP.

Eur J Med Genet. 2013 Nov;56(11):626-34. doi: 10.1016/j.ejmg.2013.08.005. Epub 2013 Sep 13.


In vitro biological characterization of DCUN1D5 in DNA damage response.

Guo W, Li GJ, Xu HB, Xie JS, Shi TP, Zhang SZ, Chen XH, Huang ZG.

Asian Pac J Cancer Prev. 2012;13(8):4157-62.

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