Showing results (71-80 of 112) with videos related to
Sort By:
Pageof 12
British Journal of Haematology|September 27, 2006
Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2Jacqueline Schoumans, Bertil Johansson, Martin Corcoran, et al.Nature Genetics|May 12, 2015
The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemiaKajsa Paulsson, Henrik Lilljebjörn, Andrea Biloglav, et al.Genes, Chromosomes & Cancer|March 27, 2025
Discovery of Cis-Regulatory Mechanisms via Non-Coding Mutations in Acute Lymphoblastic LeukemiaEfe Aydın, Eleanor L Woodward, Gladys Telliam Dushime, et al.Molecular Cancer|February 24, 2004
Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patientsChieu B Diep, Manuel R Teixeira, Lin Thorstensen, et al.Leukemia & Lymphoma|April 20, 2016
Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemiaIngegerd Ivanov Öfverholm, Anh Nhi Tran, Linda Olsson, et al.Human Molecular Genetics|June 2, 2010
The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemiasHenrik Lilljebjörn, Charlotte Soneson, Anna Andersson, et al.American Journal of Hematology|June 20, 2015
Prognostic significance of high hyperdiploid and triploid/tetraploid adult acute myeloid leukemiaVladimir Lazarevic, Aldana Rosso, Gunnar Juliusson, et al.Blood|June 19, 2002
Involvement and functional impairment of the CD34(+)CD38(-)Thy-1(+) hematopoietic stem cell pool in myelodysplastic syndromes with trisomy 8Lars Nilsson, Ingbritt Astrand-Grundström, Kristina Anderson, et al.British Journal of Haematology|May 29, 2015
The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013Linda Olsson, Ingegerd Ivanov Öfverholm, Ulrika Norén-Nyström, et al.American Journal of Human Genetics|December 11, 2003
The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeatsAikaterini Barbouti, Pawel Stankiewicz, Chad Nusbaum, et al.Pageof 12