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Human Molecular Genetics|August 15, 2009
The DNA methylome of pediatric acute lymphoblastic leukemiaJosef Davidsson, Henrik Lilljebjörn, Anna Andersson, et al.Cancer Research|March 22, 2003
A novel gene, MSI2, encoding a putative RNA-binding protein is recurrently rearranged at disease progression of chronic myeloid leukemia and forms a fusion gene with HOXA9 as a result of the cryptic t(7;17)(p15;q23)Aikaterini Barbouti, Mattias Höglund, Bertil Johansson, et al.Blood|June 28, 2003
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemiaKajsa Paulsson, Ioannis Panagopoulos, Sakari Knuutila, et al.Genes, Chromosomes & Cancer|October 19, 2007
FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patternsAnna Andersson, Kajsa Paulsson, Henrik Lilljebjörn, et al.British Journal of Haematology|December 6, 2008
The t(X;7)(q22;q34) in paediatric T-cell acute lymphoblastic leukaemia results in overexpression of the insulin receptor substrate 4 gene through illegitimate recombination with the T-cell receptor beta locusKristina Karrman, Eigil Kjeldsen, Carin Lassen, et al.Genes, Chromosomes & Cancer|January 1, 2003
Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G-banding analysisChieu B Diep, Luis A Parada, Manuel R Teixeira, et al.British Journal of Cancer|December 26, 2025
Lifetime risk of solid tumors and leukemia in Down Syndrome: a population-based Swedish matched cohort studyAlexandra Wachtmeister, Benedicte Bang, Ida Nordgren, et al.Genes, Chromosomes & Cancer|September 12, 2018
Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis: A single center experience of 296 casesLinda Olsson, Kristina B Lundin-Ström, Anders Castor, et al.Genes, Chromosomes & Cancer|October 3, 2007
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemiaKajsa Paulsson, Andrea Horvat, Bodil Strömbeck, et al.Journal of Hematology & Oncology|April 24, 2015
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 CDKN2AKristina Karrman, Anders Castor, Mikael Behrendtz, et al.Pageof 12