Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next‐generation sequencing approaches-Reference-Cited by-同舟云学术

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Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next‐generation sequencing approaches

Published:2020-01-08 Issue:1 Volume:38 Page:82-88
ISSN:0278-0232
Container-title:Hematological Oncology
language:en
Short-container-title:Hematological Oncology

Author:

Kim Borahm¹,Kim Esl²,Lee Seung‐Tae¹^ORCID,Cheong June‐Won³,Lyu Chuhl Joo⁴,Min Yoo Hong³,Choi Jong Rak¹

Affiliation:

1. Department of Laboratory MedicineYonsei University College of Medicine Seoul South Korea

2. Brain Korea 21 PLUS Project for Medical ScienceYonsei University Seoul South Korea

3. Department of Internal MedicineYonsei University College of Medicine Seoul South Korea

4. Department of PediatricsYonsei University College of Medicine Seoul South Korea

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

Cancer Research,Oncology,Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hon.2709

Reference27 articles.

1. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia

2. Cytogenetics in acute leukemia

3. ClustVis: a web tool for visualizing clustering of multivariate data using Principal Component Analysis and heatmap

4. Intrinsic differences between the catalytic properties of the oncogenic NUP214-ABL1 and BCR-ABL1 fusion protein kinases

5. NUP214-ABL1 fusion defines a rare subtype of B-cell precursor acute lymphoblastic leukemia that could benefit from tyrosine kinase inhibitors

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