tallózása szerző szerint "Sturm D"

A találatok rendezése: Rendezés: Találatok:

  • Development of the SIOPE DIPG network, registry and imaging repository: a collaborative effort to optimize research into a rare and lethal disease 
    van Zanten SE; Baugh J; Chaney B; De Jongh D; Aliaga ES; Barkhof F; Noltes J; De Wolf R; Van Dijk J; Cannarozzo A; Damen-Korbijn CM; Lieverst JA; Colditz N; Hoffmann M; Warmuth-Metz M; Bison B; Jones DT; Sturm D; Gielen GH; Jones C; Hulleman E; Calmon R; Castel D; Varlet P; Giraud G; Slavc I; Van Gool S; Jacobs S; Jadrijevic-Cvrlje F; Sumerauer D; Nysom K; Pentikainen V; Kivivuori SM; Leblond P; Entz-Werle N; von Bueren AO; Kattamis A; Hargrave DR; Hauser P; Garami, Miklós; Thorarinsdottir HK; Pears J; Gandola L; Rutkauskiene G; Janssens GO; Torsvik IK; Perek-Polnik M; Gil-da-Costa MJ; Zheludkova O; Shats L; Deak L; Kitanovski L; Cruz O; La Madrid AM; Holm S; Gerber N; Kebudi R; Grundy R; Lopez-Aguilar E; Zapata-Tarres M; Emmerik J; Hayden T; Bailey S; Biassoni V; Massimino M; Grill J; Vandertop WP; Kaspers GJ; Fouladi M; Kramm CM; van Vuurden DG; members of the SIOPE DIPG Network (2017)
    Diffuse intrinsic pontine glioma (DIPG) is a rare and deadly childhood malignancy. After 40 years of mostly single-center, often non-randomized trials with variable patient inclusions, there has been no improvement in ...
  • 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 ...
  • Erratum: Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma (Nature (2012) 482 (226-231)) 
    Schwartzentruber J; Korshunov A; Liu X-Y; Jones DTW; Pfaff E; Jacob K; Sturm D; Fontebasso AM; Quang D-AK; Tönjes M; Hovestadt V; Albrecht S; Kool M; Nantel A; Konermann C; Lindroth A; Jäger N; Rausch T; Ryzhova M; Korbel JO; Hielscher T; Hauser, Péter; Garami, Miklós; Klekner, Álmos; Bognár, László; Ebinger M; Schuhmann MU; Scheurlen W; Pekrun A; Frühwald MC; Roggendorf W; Kramm C; Dürken M; Atkinson J; Lepage P; Montpetit A; Zakrzewska M; Zakrzewski K; Liberski PP; Dong Z; Siegel P; Kulozik AE; Zapatka M; Guha A; Malkin D; Felsberg J; Reifenberger G; Von Deimling A; Ichimura K; Collins VP; Witt H; Milde T; Witt O; Zhang C; Castelo-Branco P; Lichter P; Faury D; Tabori U; Plass C; Majewski J; Pfister SM; Jabado N (2012)
  • 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 ...
  • Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma. 
    Fontebasso AM; Papillon-Cavanagh S; Schwartzentruber J; Nikbakht H; Gerges N; Fiset PO; Bechet D; Faury D; De Jay N; Ramkissoon LA; Corcoran A; Jones DT; Sturm D; Johann P; Tomita T; Goldman S; Nagib M; Bendel A; Goumnerova L; Bowers DC; Leonard JR; Rubin JB; Alden T; Browd S; Geyer JR; Leary S; Jallo G; Cohen K; Gupta N; Prados MD; Carret AS; Ellezam B; Crevier L; Klekner, Álmos; Bognár, László; Hauser, Péter; Garami, Miklós; Myseros J; Dong Z; Siegel PM; Malkin H; Ligon AH; Albrecht S; Pfister SM; Ligon KL; Majewski J; Jabado N; Kieran MW (2014)
    Pediatric midline high-grade astrocytomas (mHGAs) are incurable with few treatment targets identified. Most tumors harbor mutations encoding p.Lys27Met in histone H3 variants. In 40 treatment-naive mHGAs, 39 analyzed by ...