Henrik Lilljebjörn
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- 2013
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Mark
SOCS2 is dispensable for BCR/ABL1-induced chronic myeloid leukemia-like disease and for normal hematopoietic stem cell function.
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- Contribution to journal › Article
- 2012
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Mark
Whole-exome sequencing of pediatric acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
Myeloid malignancies with acquired trisomy 21 as the sole cytogenetic change are clinically highly variable and display a heterogeneous pattern of copy number alterations and mutations(a).
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- Contribution to journal › Article
- 2011
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Mark
Genomic characterization of ETV6/RUNX1-positive acute lymphoblastic leukemia
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- Thesis › Doctoral thesis (compilation)
- 2010
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Mark
Integrative analysis of gene expression and copy number alterations using canonical correlation analysis
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- Contribution to journal › Article
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Mark
The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias
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- Contribution to journal › Article
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Mark
Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma.
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- Contribution to journal › Article
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Mark
Genetic analysis of dasatinib-treated chronic myeloid leukemia rapidly developing into acute myeloid leukemia with monosomy 7 in Philadelphia-negative cells.
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- Contribution to journal › Article
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Mark
Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.
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- Contribution to journal › Article