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Blood|October 8, 2008
A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroupsSarina Sulong, Anthony V Moorman, Julie A E Irving, et al.Blood|February 13, 2016
The ability to cross the blood-cerebrospinal fluid barrier is a generic property of acute lymphoblastic leukemia blastsMark T S Williams, Yasar M Yousafzai, Alex Elder, et al.Leukemia|May 12, 2016
The role of the RAS pathway in iAMP21-ALLS L Ryan, E Matheson, V Grossmann, et al.Blood|May 28, 2016
Integration of genetic and clinical risk factors improves prognostication in relapsed childhood B-cell precursor acute lymphoblastic leukemiaJulie A E Irving, Amir Enshaei, Catriona A Parker, et al.Haematologica|April 2, 2026
First-year results of the International Leukemia/Lymphoma Target Board for pediatric relapsed and refractory hematological malignanciesUri Ilan, Judith M Boer, Maaike Luesink, et al.Nature Genetics|May 11, 2010
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia riskAmy L Sherborne, Fay J Hosking, Rashmi B Prasad, et al.Pageof 4