Cargando…
FPGS relapse-specific mutations in relapsed childhood acute lymphoblastic leukemia
Although the cure rate for childhood acute lymphoblastic leukemia (ALL) has exceeded 80% with contemporary therapy, relapsed ALL remains a leading cause of cancer-related death in children. Relapse-specific mutations can be identified by comprehensive genome sequencing and might have clinical signif...
Autores principales: | Yu, Sung-Liang, Zhang, Hui, Ho, Bing-Ching, Yu, Chih-Hsiang, Chang, Chia-Ching, Hsu, Yin-Chen, Ni, Yu-Ling, Lin, Kai-Hsin, Jou, Shiann-Tarng, Lu, Meng-Yao, Chen, Shu-Huey, Wu, Kang-Hsi, Wang, Shih-Chung, Chang, Hsiu-Hao, Pui, Ching-Hon, Yang, Jun J., Zhang, Jinghui, Lin, Dong-Tsamn, Lin, Shu-Wha, Ma, Xiaotu, Yang, Yung-Li |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374087/ https://www.ncbi.nlm.nih.gov/pubmed/32694622 http://dx.doi.org/10.1038/s41598-020-69059-y |
Ejemplares similares
-
TP53 alterations in relapsed childhood acute lymphoblastic leukemia
por: Yu, Chih‐Hsiang, et al.
Publicado: (2019) -
Targeted sequencing to identify genetic alterations and prognostic markers in pediatric T-cell acute lymphoblastic leukemia
por: Chang, Ya-Hsuan, et al.
Publicado: (2021) -
Philadelphia chromosome-negative B-cell acute lymphoblastic leukaemia with kinase fusions in Taiwan
por: Hsu, Yin-Chen, et al.
Publicado: (2021) -
A Double Negative Loop Comprising ETV6/RUNX1 and MIR181A1 Contributes to Differentiation Block in t(12;21)-Positive Acute Lymphoblastic Leukemia
por: Yang, Yung-Li, et al.
Publicado: (2015) -
Determination of NUDT15 variants by targeted sequencing can identify compound heterozygosity in pediatric acute lymphoblastic leukemia patients
por: Yu, Chih-Hsiang, et al.
Publicado: (2020)