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Genomic Amplifications and Distal 6q Loss: Novel Markers for Poor Survival in High-risk Neuroblastoma Patients.
Depuydt, Pauline; Boeva, Valentina; Hocking, Toby D; Cannoodt, Robrecht; Ambros, Inge M; Ambros, Peter F; Asgharzadeh, Shahab; Attiyeh, Edward F; Combaret, Valérie; Defferrari, Raffaella; Fischer, Matthias; Hero, Barbara; Hogarty, Michael D; Irwin, Meredith S; Koster, Jan; Kreissman, Susan; Ladenstein, Ruth; Lapouble, Eve; Laureys, Geneviève; London, Wendy B; Mazzocco, Katia; Nakagawara, Akira; Noguera, Rosa; Ohira, Miki; Park, Julie R; Pötschger, Ulrike; Theissen, Jessica; Tonini, Gian Paolo; Valteau-Couanet, Dominique; Varesio, Luigi; Versteeg, Rogier; Speleman, Frank; Maris, John M; Schleiermacher, Gudrun; De Preter, Katleen.
Afiliação
  • Depuydt P; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Boeva V; Cancer Research Institute Ghent, Ghent, Belgium.
  • Hocking TD; Institut Cochin, Inserm U1016, CNRS UMR 8104, Université Paris Descartes UMR-S1016, Paris, France.
  • Cannoodt R; Institut Curie, Inserm U900, Mines ParisTech, PSL Research University, Paris, France.
  • Ambros IM; Department of Human Genetics, McGill University, Montreal, Quebec, Canada.
  • Ambros PF; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Asgharzadeh S; Cancer Research Institute Ghent, Ghent, Belgium.
  • Attiyeh EF; Data Mining and Modelling for Biomedicine Group, VIB Center for Inflammation Research, Ghent, Belgium.
  • Combaret V; Children's Cancer Research Institute, Austria.
  • Defferrari R; Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
  • Fischer M; Children's Cancer Research Institute, Austria.
  • Hero B; Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
  • Hogarty MD; Division of Hematology/Oncology, Children's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, CA.
  • Irwin MS; Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Koster J; Center for Childhood Cancer Research, University of Pennsylvania, Philadelphia, PA.
  • Kreissman S; Department of Pediatrics, University of Pennsylvania, Philadelphia, PA.
  • Ladenstein R; Centre Léon-Bérard, Laboratoire de Recherche Translationnelle, Lyon, France.
  • Lapouble E; Department of Pathology, Istituto Giannina Gaslini, Genova, Italy.
  • Laureys G; Department of Experimental Pediatric Oncology, University of Cologne, Cologne, Germany.
  • London WB; University Children's Hospital Cologne, Medical Faculty, and Center for Molecular Medicine Cologne.
  • Mazzocco K; Department of Pediatric Oncology and Hematology, University of Cologne, Cologne, Germany.
  • Nakagawara A; Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Noguera R; Perelman School of Medicine (MDH), University of Pennsylvania, Philadelphia, PA.
  • Ohira M; Division of Hematology-Oncology, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Park JR; Department of Oncogenomics, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
  • Pötschger U; Department of Pediatrics, Duke University School of Medicine, Durham, NC.
  • Theissen J; Children's Cancer Research Institute, Austria.
  • Tonini GP; Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
  • Valteau-Couanet D; Genetic Somatic Unit.
  • Varesio L; Institut Curie, Paris, France.
  • Versteeg R; Department of Pediatric Hematology and Oncology, Ghent University Hospital, De Pintelaan, Ghent, Belgium.
  • Speleman F; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA.
  • Maris JM; Department of Pathology, Istituto Giannina Gaslini, Genova, Italy.
  • Schleiermacher G; Saga Medical Center KOSEIKAN, Saga, Japan.
  • De Preter K; Pathology Department, Medical School, University of Valencia, Valencia, Spain.
J Natl Cancer Inst ; 110(10): 1084-1093, 2018 10 01.
Article em En | MEDLINE | ID: mdl-29514301

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 6 / Amplificação de Genes / Deleção Cromossômica / Genômica / Neuroblastoma Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 6 / Amplificação de Genes / Deleção Cromossômica / Genômica / Neuroblastoma Idioma: En Ano de publicação: 2018 Tipo de documento: Article