MTMT-ben szereplő publikációk tallózása szerző szerint "Nicholas, K Foreman"

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  • Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma 
    Sturm, Dominik; Witt, Hendrik; Hovestadt, Volker; Khuong-Quang, Dong-Anh; Jones, David TW; Carolin, Konermann; Elke, Pfaff; Martje, Tönjes; Martin, Sill; Sebastian, Bender; Marcel, Kool; Marc, Zapatka; Natalia, Becker; Manuela, Zucknick; Thomas, Hielscher; Xiao-Yang, Liu; Adam, M Fontebasso; Marina, Ryzhova; Steffen, Albrecht; Karine, Jacob; Marietta, Wolter; Martin, Ebinger; Martin, U Schuhmann; Timothy, van Meter; Michael, C Frühwald; Holger, Hauch; Arnulf, Pekrun; Bernhard, Radlwimmer; Tim, Niehues; Gregor, von Komorowski; Matthias, Dürken; Andreas, E Kulozik; Jenny, Madden; Andrew, Donson; Nicholas, K Foreman; Rachid, Drissi; Maryam, Fouladi; Wolfram, Scheurlen; Andreas, von Deimling; Camelia, Monoranu; Wolfgang, Roggendorf; Christel, Herold-Mende; Andreas, Unterberg; Christof, M Kramm; Jörg, Felsberg; Christian, Hartmann; Benedikt, Wiestler; Wolfgang, Wick; Till, Milde; Olaf, Witt; Anders, M Lindroth; Jeremy, Schwartzentruber; Damien, Faury; Adam, Fleming; Magdalena, Zakrzewska; Pawel, P Liberski; Krzysztof, Zakrzewski; Hauser, Péter; Garami, Miklós; Klekner, Álmos; Bognár, László; Sorana, Morrissy; Florence, Cavalli; Michael, D Taylor; Peter, van Sluis; Jan, Koste; Rogier, Versteeg; Richard, Volckmann; Tom, Mikkelsen; Kenneth, Aldape; Guido, Reifenberger; V Peter, Collins; Jacek, Majewski; Andrey, Korshunov; Peter, Lichter; Christoph, Plass; Nada, Jabado; Stefan, M Pfister; (2012)
    Glioblastoma (GBM) is a brain tumor that carries a dismal prognosis and displays considerable heterogeneity. We have recently identified recurrent H3F3A mutations affecting two critical amino acids (K27 and G34) of histone ...
  • Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors 
    Torchia, Jonathon; Golbourn, Brian; Feng, Shengrui; Ho, King Ching; Sin-Chan, Patrick; Alexandre, Vasiljevic; Joseph, D Norman; Paul, Guilhamon; Livia, Garzia; Natalia, R Agamez; Mei, Lu; Tiffany, S Chan; Daniel, Picard; Pasqualino, de Antonellis; Dong-Anh, Khuong-Quang; Aline, C Planello; Constanze, Zeller; Dalia, Barsyte-Lovejoy; Lucie, Lafay-Cousin; Louis, Letourneau; Mathieu, Bourgey; Man, Yu; Deena, MA Gendoo; Misko, Dzamba; Mark, Barszczyk; Tiago, Medina; Alexandra, N Riemenschneider; A Sorana, Morrissy; Young-Shin, Ra; Vijay, Ramaswamy; Marc, Remke; Christopher, P Dunham; Stephen, Yip; Ho-Keung, Ng; Jian-Qiang, Lu; Vivek, Mehta; Vivek, Mehta; Steffen, Albrecht; Jose, Pimentel; Jennifer, A Chan; Gino, R Somers; Claudia, C Faria; Lucia, Roque; Maryam, Fouladi; Lindsey, M Hoffman; Andrew, S Moore; Yin, Wang; Seung, Ah Choi; Jordan, R Hansford; Daniel, Catchpoole; Diane, K Birks; Nicholas, K Foreman; Doug, Strother; Álmos, Klekner; László, Bognár; Garami, Miklós; Hauser, Péter; Hortobágyi, Tibor; Beverly, Wilson; Juliette, Hukin; Anne-Sophie, Carret; Timothy, E Van Meter; Eugene, I Hwang; Amar, Gajjar; Shih-Hwa, Chiou; Hideo, Nakamura; Helen, Toledano; Iris, Fried; Daniel, Fults; Takafumi, Wataya; Chris, Fryer; David, D Eisenstat; Katrin, Scheinemann; Adam, J Fleming; Donna, L Johnston; Jean, Michaud; Shayna, Zelcer; Robert, Hammond; Samina, Afzal; David, A Ramsay; Nongnuch, Sirachainan; Suradej, Hongeng; Noppadol, Larbcharoensub; Richard, G Grundy; Rishi, R Lulla; Jason, R Fangusaro; Harriet, Druker; Ute, Bartels; Ronald, Grant; David, Malkin; C Jane, McGlade; Theodore, Nicolaides; Tarik, Tihan; Joanna, Phillips; Jacek, Majewski; Alexandre, Montpetit; Guillaume, Bourque; Gary, D Bader; Alyssa, T Reddy; G Yancey, Gillespie; Monika, Warmuth-Metz; Stefan, Rutkowski; Uri, Tabori; Mathieu, Lupien; Michael, Brudno; Ulrich, Sch€uller; Torsten, Pietsch; Alexander, R Judkins; Cynthia, E Hawkins; Eric, Bouffet; Seung-Ki, Kim; Peter, B Dirks; Michael, D Taylor; Anat, Erdreich-Epstein; Cheryl, H Arrowsmith; Daniel, D De Carvalho; James, T Rutka; Nada, Jabado; Annie, Huang (2016)
    We recently reported that atypical teratoid rhabdoid tumors (ATRTs) comprise at least two transcriptional subtypes with different clinical outcomes; however, the mechanisms underlying therapeutic heterogeneity remained ...