Found: 26
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Refinement of IKZF1 status in pediatric Philadelphia-positive acute lymphoblastic leukemia.
- Published in:
- 2015
- By:
- Publication type:
- letter
KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia.
- Published in:
- Leukemia (08876924), 2015, v. 29, n. 8, p. 1656, doi. 10.1038/leu.2015.107
- By:
- Publication type:
- Article
ERG deletion is associated with CD2 and attenuates the negative impact of IKZF1 deletion in childhood acute lymphoblastic leukemia.
- Published in:
- Leukemia (08876924), 2015, v. 29, n. 5, p. 1222, doi. 10.1038/leu.2015.77
- By:
- Publication type:
- Article
Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients.
- Published in:
- Leukemia (08876924), 2015, v. 29, n. 2, p. 297, doi. 10.1038/leu.2014.205
- By:
- Publication type:
- Article
ERG deletion is associated with CD2 and attenuates the negative impact of IKZF1 deletion in childhood acute lymphoblastic leukemia.
- Published in:
- Leukemia (08876924), 2014, v. 28, n. 1, p. 182, doi. 10.1038/leu.2013.282
- By:
- Publication type:
- Article
Poor prognosis for P2RY8-CRLF2 fusion but not for CRLF2 over-expression in children with intermediate risk B-cell precursor acute lymphoblastic leukemia.
- Published in:
- Leukemia (08876924), 2012, v. 26, n. 10, p. 2245, doi. 10.1038/leu.2012.101
- By:
- Publication type:
- Article
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.
- Published in:
- Leukemia (08876924), 2012, v. 26, n. 5, p. 902, doi. 10.1038/leu.2011.302
- By:
- Publication type:
- Article
Very early/early relapses of acute lymphoblastic leukemia show unexpected changes of clonal markers and high heterogeneity in response to initial and relapse treatment.
- Published in:
- Leukemia (08876924), 2011, v. 25, n. 8, p. 1305, doi. 10.1038/leu.2011.89
- By:
- Publication type:
- Article
The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL-BFM 2000 protocol can be separated from FBXW7 loss of function.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Bimodal distribution of genomic MLL breakpoints in infant acute lymphoblastic leukemia treatment.
- Published in:
- 2010
- By:
- Publication type:
- letter
Long-term results of five consecutive trials in childhood acute lymphoblastic leukemia performed by the ALL-BFM study group from 1981 to 2000.
- Published in:
- Leukemia (08876924), 2010, v. 24, n. 2, p. 265, doi. 10.1038/leu.2009.257
- By:
- Publication type:
- Article
Asymmetric multiplex-polymerase chain reaction--a high throughput method for detection and sequencing genomic fusion sites in t(4;11).
- Published in:
- British Journal of Haematology, 2004, v. 124, n. 1, p. 47, doi. 10.1046/j.1365-2141.2003.04740.x
- By:
- Publication type:
- Article
Minimal residual disease-directed risk stratification using real-time quantitative PCR analysis of immunoglobulin and T-cell receptor gene rearrangements in the international multicenter trial AIEOP-BFM ALL 2000 for childhood acute lymphoblastic leukemia.
- Published in:
- Leukemia (08876924), 2008, v. 22, n. 4, p. 771, doi. 10.1038/leu.2008.5
- By:
- Publication type:
- Article
Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case–control study.
- Published in:
- Leukemia (08876924), 2007, v. 21, n. 2, p. 320, doi. 10.1038/sj.leu.2404474
- By:
- Publication type:
- Article
Consensus guidelines for microarray gene expression analyses in leukemia from three European leukemia networks.
- Published in:
- Leukemia (08876924), 2006, v. 20, n. 8, p. 1385, doi. 10.1038/sj.leu.2404274
- By:
- Publication type:
- Article
Mutational screen reveals a novel JAK2 mutation, L611S, in a child with acute lymphoblastic leukemia.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Immunosurveillance of childhood ALL: polymorphic interferon-?alleles are associated with age at diagnosis and clinical risk groups.
- Published in:
- Leukemia (08876924), 2005, v. 19, n. 1, p. 44, doi. 10.1038/sj.leu.2403553
- By:
- Publication type:
- Article
The GSTT1 deletion polymorphism is associated with initial response to glucocorticoids in childhood acute lymphoblastic leukemia.
- Published in:
- Leukemia (08876924), 2004, v. 18, n. 11, p. 1920, doi. 10.1038/sj.leu.2403521
- By:
- Publication type:
- Article
A novel TPMT missense mutation associated with TPMT deficiency in a 5-year-old boy with ALL.
- Published in:
- Leukemia (08876924), 2003, v. 17, n. 7, p. 1422, doi. 10.1038/sj.leu.2402981
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- Publication type:
- Article
Infant acute lymphoblastic leukemia--combined cytogenetic immunophenotypical and molecular analysis of 77 cases.
- Published in:
- Leukemia (08876924), 2002, v. 16, n. 9, p. 1685, doi. 10.1038/sj.leu.2402595
- By:
- Publication type:
- Article
Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life.
- Published in:
- 2000
- By:
- Publication type:
- commentary
Topoisomerase II inhibitors induce DNA double-strand breaks at a specific site within the AML1 locus.
- Published in:
- 1997
- By:
- Publication type:
- journal article
ABERACE TRANSKRIPČNÍHO FAKTORU IKAROS (IKZF1) MAJÍ VÝZNAMNÝ NEGATIVNÍ VLIV NA PROGNÓZU AKUTNÍ LYMFOBLASTICKÉ LEUKEMIE U DĚTÍ.
- Published in:
- Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie, 2012, v. 67, n. 5, p. 321
- By:
- Publication type:
- Article
Transplantation of allogeneic CD34-selected stem cells after fludarabine-based conditioning regimen for children with mucopolysaccharidosis 1H (M. Hurler).
- Published in:
- Bone Marrow Transplantation, 2005, v. 35, n. 3, p. 265, doi. 10.1038/sj.bmt.1704786
- By:
- Publication type:
- Article
Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.
- Published in:
- Clinical Pharmacology & Therapeutics, 2017, v. 101, n. 5, p. 684, doi. 10.1002/cpt.540
- By:
- Publication type:
- Article