Cargando…
Whole-Exome Sequencing of ETV6/RUNX1 in Four Childhood Acute Lymphoblastic Leukaemia Cases
BACKGROUND: ETV6/RUNX1 gene fusion is the most frequently seen chromosomal abnormality in childhood acute lymphobastic leukamia (ALL). However, additional genetic changes are known to be required for the development of this type of leukaemia. Therefore, we here aimed to assess the somatic mutational...
Autores principales: | Zakaria, Zubaidah, Othman, Norodiyah, Ismail, Azli, Kamaluddin, Nor Rizan, Esa, Ezalia, Rahman, Eni Juraida Abdul, Yusoff, Yuslina Mat, Fauzi, Fazlin Mohd, Keoh, Ten Sew |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
West Asia Organization for Cancer Prevention
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494233/ https://www.ncbi.nlm.nih.gov/pubmed/28548470 http://dx.doi.org/10.22034/APJCP.2017.18.4.1169 |
Ejemplares similares
-
Chromosomal Aberrations in ETV6/RUNX1-positive Childhood Acute Lymphoblastic Leukemia using 244K Oligonucleotide Array Comparative Genomic Hybridization
por: Zakaria, Zubaidah, et al.
Publicado: (2012) -
Identification of FLT3 and NPM1 Mutations in Patients with Acute Myeloid Leukaemia
por: Yusoff, Yuslina Mat, et al.
Publicado: (2019) -
Prevalence of BCR-ABL T315I Mutation in Malaysian Patients with Imatinib-Resistant Chronic Myeloid Leukemia
por: Yusoff, Yuslina Mat, et al.
Publicado: (2018) -
Circulating cytokines and small molecules follow distinct expression patterns in acute myeloid leukaemia
por: Islam, Mirazul, et al.
Publicado: (2017) -
Comprehensive analysis of mutations and clonal evolution patterns in a cohort of patients with cytogenetically normal acute myeloid leukemia
por: Mat Yusoff, Yuslina, et al.
Publicado: (2021)