Folyóiratcikkek tallózása szerző szerint "Kool M"

A találatok rendezése: Rendezés: Találatok:

  • Atypical teratoid/rhabdoid tumor arising in a malignant glioma 
    Bozzai, Barbara; Hasselblatt M; Turányi, Eszter; Fruhwald MC; Siebert R; Bens S; Schneppenheim R; Kool M; Stelczer G; Hortobagyi T; Hauser, Péter (2017)
    Atypical teratoid/rhabdoid tumor (AT/RT), a highly malignant brain tumor in young children, usually arises de novo and has only rarely been described as a secondary malignancy. Here, we present a case of a child with ...
  • Cribriform neuroepithelial tumor: Molecular characterization of a SMARCB1-deficient non-rhabdoid tumor with favorable long-term outcome. 
    Johann PD; Hovestadt V; Thomas C; Jeibmann A; Hess K; Bens S; Oyen F; Hawkins C; Pierson CR; Aldape K; Kim SP; Widing E; Sumerauer D; Hauser, Péter; van Landeghem F; Ryzhova M; Korshunov A; Capper D; Jones DT; Pfister SM; Schneppenheim R; Siebert R; Paulus W; Fruhwald MC; Kool M; Hasselblatt M (2017)
    Rhabdoid phenotype and loss of SMARCB1 expression in a brain tumor are characteristic features of atypical teratoid/rhabdoid tumors (ATRT). Rare non-rhabdoid brain tumors showing cribriform growth pattern and SMARCB1 loss ...
  • Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma 
    Northcott PA; Lee C; Zichner T; Stutz AM; Erkek S; Kawauchi D; Shih DJ; Hovestadt V; Zapatka M; Sturm D; Jones DT; Kool M; Remke M; Cavalli FM; Zuyderduyn S; Bader GD; VandenBerg S; Esparza LA; Ryzhova M; Wang W; Wittmann A; Stark S; Sieber L; Seker-Cin H; Linke L; Kratochwil F; Jager N; Buchhalter I; Imbusch CD; Zipprich G; Raeder B; Schmidt S; Diessl N; Wolf S; Wiemann S; Brors B; Lawerenz C; Eils J; Warnatz HJ; Risch T; Yaspo ML; Weber UD; Bartholomae CC; von Kalle C; Turányi, Eszter; Hauser, Péter; Sanden E; Darabi A; Siesjo P; Sterba J; Zitterbart K; Sumerauer D; van Sluis P; Versteeg R; Volckmann R; Koster J; Schuhmann MU; Ebinger M; Grimes HL; Robinson GW; Gajjar A; Mynarek M; von Hoff K; Rutkowski S; Pietsch T; Scheurlen W; Felsberg J; Reifenberger G; Kulozik AE; von Deimling A; Witt O; Eils R; Gilbertson RJ; Korshunov A; Taylor MD; Lichter P; Korbel JO; Wechsler-Reya RJ; Pfister SM (2014)
    Medulloblastoma is a highly malignant paediatric brain tumour currently treated with a combination of surgery, radiation and chemotherapy, posing a considerable burden of toxicity to the developing child. Genomics has ...
  • Evaluation of age-dependent treatment strategies for children and young adults with pineoblastoma 
    Mynarek M; Pizer B; Dufour C; van Vuurden D; Garami, Miklós; Massimino M; Fangusaro J; Davidson T; Gil-da-Costa MJ; Sterba J; Benesch M; Gerber N; Juhnke BO; Kwiecien R; Pietsch T; Kool M; Clifford S; Ellison DW; Giangaspero F; Wesseling P; Gilles F; Gottardo N; Finlay JL; Rutkowski S; von Hoff K (2017)
  • Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas 
    Fontebasso AM; Schwartzentruber J; Khuong-Quang D-A; Liu X-Y; Sturm D; Korshunov A; Jones DTW; Witt H; Kool M; Albrecht S; Fleming A; Hadjadj D; Busche S; Lepage P; Montpetit A; Staffa A; Gerges N; Zakrzewska M; Zakrzewski K; Liberski PP; Hauser, Péter; Garami, Miklós; Klekner, Álmos; Bognár, László; Zadeh G; Faury D; Pfister SM; Jabado N; Majewski J (2013)
    Recurrent mutations affecting the histone H3.3 residues Lys27 or indirectly Lys36 are frequent drivers of pediatric high-grade gliomas (over 30 % of HGGs). To identify additional driver mutations in HGGs, we investigated ...
  • Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age 
    Fontebasso AM; Shirinian M; Khuong-Quang DA; Bechet D; Gayden T; Kool M; De Jay N; Jacob K; Gerges N; Hutter B; Seker-Cin H; Witt H; Montpetit A; Brunet S; Lepage P; Bourret G; Klekner, Álmos; Bognar L; Hauser, Péter; Garami, Miklós; Farmer JP; Montes JL; Atkinson J; Lambert S; Kwan T; Korshunov A; Tabori U; Collins VP; Albrecht S; Faury D; Pfister SM; Paulus W; Hasselblatt M; Jones DT; Jabado N (2015)
    Pilocytic astrocytoma (PA) is the most common brain tumor in children but is rare in adults, and hence poorly studied in this age group. We investigated 222 PA and report increased aneuploidy in older patients. Aneuploid ...
  • Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis 
    Hasselblatt M; Thomas C; Hovestadt V; Schrimpf D; Johann P; Johann P; Bens S; Oyen F; Peetz-Dienhart S; Crede Y; Wefers A; Vogel H; Riemenschneider MJ; Antonelli M; Giangaspero F; Bernardo MC; Giannini C; Ud Din N; Perry A; Keyvani K; van Landeghem F; Sumerauer D; Hauser, Péter; Capper D; Korshunov A; Jones DT; Pfister SM; Schneppenheim R; Siebert R; Fruhwald MC; Kool M (2016)