Novel <scp><i>IKZF1</i></scp> rearrangement identified in a patient with blastic plasmacytoid dendritic cell neoplasm decreased haematopoietic stem cell function and promoted plasmacytoid dendritic cell abnormality-Reference-Cited by-同舟云学术

Novel IKZF1 rearrangement identified in a patient with blastic plasmacytoid dendritic cell neoplasm decreased haematopoietic stem cell function and promoted plasmacytoid dendritic cell abnormality

Published:2024-04-15 Issue:6 Volume:204 Page:2496-2500
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Yin Le¹²³,Yu Qian¹,Zhang Huifang¹²³,Zhu Hongkai¹²³,Deng Zeyu¹²³,Xing Cheng¹²³,Wang Peilong¹²³,Zeng Xiangju⁴,Cheng Zhao¹²³,Sheng Yue¹²³,Peng Hongling¹²³⁵^ORCID

Affiliation:

1. Division of Hematology, Second Xiangya Hospital Central South University Changsha Hunan China

2. Institute of Molecular Hematology, Central South University Changsha Hunan China

3. Hunan Engineering Research Center of Cell Immunotherapy for Hematopoietic Malignancies Changsha Hunan China

4. Department of Outpatient The Second Xiangya Hospital of Central South University Changsha Hunan China

5. Hunan Key Laboratory of Tumor Models and Individualized Medicine Changsha Hunan China

Funder

Huxiang Youth Talent Support Program

National Natural Science Foundation of China

International Centre for Genetic Engineering and Biotechnology

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.19429

Reference9 articles.

1. Blastic Plasmacytoid Dendritic Cell Neoplasm

2. Exome sequencing reveals novel and recurrent mutations with clinical impact in blastic plasmacytoid dendritic cell neoplasm

3. Targeted ultra-deep sequencing reveals recurrent and mutually exclusive mutations of cancer genes in blastic plasmacytoid dendritic cell neoplasm

4. CLTC-ALKfusion as a primary event in congenital blastic plasmacytoid dendritic cell neoplasm

5. Blastic plasmacytoid dendritic cell neoplasm with leukemic manifestation and ETV6 gene rearrangement: A case report