Recurrent inactivating RASA2 mutations in melanoma.
Nature Genetics
Arafeh, Rand R; Qutob, Nouar N; Emmanuel, Rafi R; Keren-Paz, Alona A; Madore, Jason J; Elkahloun, Abdel A; Wilmott, James S JS; Gartner, Jared J JJ; Di Pizio, Antonella A; Winograd-Katz, Sabina S; Sindiri, Sivasish S; Rotkopf, Ron R; Dutton-Regester, Ken K; Johansson, Peter P; Pritchard, Antonia L AL; Waddell, Nicola N; Hill, Victoria K VK; Lin, Jimmy C JC; Hevroni, Yael Y; Rosenberg, Steven A SA; Khan, Javed J; Ben-Dor, Shifra S; Niv, Masha Y MY; Ulitsky, Igor I; Mann, Graham J GJ; Scolyer, Richard A RA; Hayward, Nicholas K NK; Samuels, Yardena Y
Chromosome 19 annotations with disease speciation: a first report from the Global Research Consortium.
Journal Of Proteome Research
Nilsson, Carol L CL; Berven, Frode F; Selheim, Frode F; Liu, Huiling H; Moskal, Joseph R JR; Kroes, Roger A RA; Sulman, Erik P EP; Conrad, Charles A CA; Lang, Frederick F FF; Andrén, Per E PE; Nilsson, Anna A; Carlsohn, Elisabet E; Lilja, Hans H; Malm, Johan J; Fenyö, David D; Subramaniyam, Devipriya D; Wang, Xiangdong X; Gonzales-Gonzales, Maria M; Dasilva, Noelia N; Diez, Paula P; Fuentes, Manuel M; Végvári, Ákos Á; Sjödin, Karin K; Welinder, Charlotte C; Laurell, Thomas T; Fehniger, Thomas E TE; Lindberg, Henrik H; Rezeli, Melinda M; Edula, Goutham G; Hober, Sophia S; Marko-Varga, György G