Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A.
Författare
Summary, in English
Pediatric T-cell acute lymphoblastic leukemia (T-ALL) is a genetically heterogeneous disease that arises in a multistep fashion through acquisition of several genetic aberrations, subsequently giving rise to a malignant, clonal expansion of T-lymphoblasts. The aim of the present study was to identify additional as well as cooperative genetic events in T-ALL.
Avdelning/ar
- Genetiska och epigenetiska studier av barnleukemi
- Avdelningen för klinisk genetik
- Pediatrik, Lund
- Tumörmikromiljö
- BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation
Publiceringsår
2015
Språk
Engelska
Publikation/Tidskrift/Serie
Journal of Hematology & Oncology
Volym
8
Issue
1
Fulltext
- Available as PDF - 764 kB
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Länkar
Dokumenttyp
Artikel i tidskrift
Förlag
BioMed Central (BMC)
Ämne
- Medical Genetics
- Pediatrics
- Cancer and Oncology
Status
Published
Forskningsgrupp
- Genetic and epigenetic studies of pediatric leukemia
ISBN/ISSN/Övrigt
- ISSN: 1756-8722