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Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma.
Tasaka, Keiji; Ueno, Hiroo; Yamasaki, Kai; Okuno, Takahiro; Isobe, Tomoya; Kimura, Shunsuke; Umeda, Katsutsugu; Hara, Junichi; Ogawa, Seishi; Takita, Junko.
Afiliación
  • Tasaka K; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Ueno H; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Yamasaki K; Department of Pediatric Hematology and Oncology, Osaka City General Hospital, Osaka, Japan.
  • Okuno T; Department of Pathology, Osaka City General Hospital, Osaka, Japan.
  • Isobe T; Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Kimura S; Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Umeda K; Department of Pediatrics, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan.
  • Hara J; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Ogawa S; Cancer Consultation and Support Center, Osaka City General Hospital, Osaka, Japan.
  • Takita J; Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Cancer Sci ; 113(4): 1535-1541, 2022 Apr.
Article en En | MEDLINE | ID: mdl-34971484

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Feocromocitoma / Neoplasias de las Glándulas Suprarrenales / Neuroblastoma Límite: Humans Idioma: En Revista: Cancer Sci Año: 2022 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Feocromocitoma / Neoplasias de las Glándulas Suprarrenales / Neuroblastoma Límite: Humans Idioma: En Revista: Cancer Sci Año: 2022 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido