Reversion of the Jun-induced oncogenic phenotype by enhanced synthesis of sialosyllactosylceramide (GM3 ganglioside). [electronic resource]
- Proceedings of the National Academy of Sciences of the United States of America Nov 2004
- 16204-9 p. digital
Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
0027-8424
10.1073/pnas.0407297101 doi
Animals Antigens, CD--metabolism Base Sequence Cell Adhesion Cell Division Cell Line, Transformed Chick Embryo Down-Regulation G(M3) Ganglioside--biosynthesis Genes, jun Integrin alpha5beta1--metabolism Membrane Glycoproteins--metabolism Mice Molecular Sequence Data Oncogene Protein p65(gag-jun)--physiology Phenotype RNA, Messenger--genetics Sialyltransferases--genetics Tetraspanin 29 Transfection