Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma-Reference-Cited by-同舟云学术

Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma

Published:2021-12-31 Issue: Volume: Page:
ISSN:1347-9032
Container-title:Cancer Science
language:en
Short-container-title:Cancer Science

Author:

Tasaka Keiji¹^ORCID,Ueno Hiroo¹,Yamasaki Kai²,Okuno Takahiro³,Isobe Tomoya⁴,Kimura Shunsuke⁴⁵,Umeda Katsutsugu¹^ORCID,Hara Junichi⁶^ORCID,Ogawa Seishi⁷⁸⁹,Takita Junko¹

Affiliation:

1. Department of Pediatrics Graduate School of Medicine Kyoto University Kyoto Japan

2. Department of Pediatric Hematology and Oncology Osaka City General Hospital

3. Department of Pathology Osaka City General Hospital

4. Department of Pediatrics Graduate School of Medicine The University of Tokyo Tokyo Japan

5. Department of Pediatrics Hiroshima University Graduate School of Biomedical Sciences Hiroshima Japan

6. Cancer Consultation and Support Center Osaka City General Hospital

7. Department of Pathology and Tumor Biology Graduate School of Medicine Kyoto University Kyoto Japan

8. Institute for the Advanced Study of Human Biology (WPI‐ASHBi) Kyoto University Kyoto Japan

9. Department of Medicine Center for Hematology and Regenerative Medicine Karolinska Institute Stockholm Sweden

Publisher

Wiley

Subject

Cancer Research,Oncology,General Medicine

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1. Cytoplasmic HIF-2α as tissue biomarker to identify metastatic sympathetic paraganglioma;Scientific Reports;2023-07-18

2. Case Report: Composite pheochromocytoma with ganglioneuroma component: A report of three cases;Frontiers in Endocrinology;2022-09-14

3. Cytoplasmic HIF-2α correlates to proliferation and predicts worse outcome in sympathetic paraganglioma;2022-05-29