Pages that link to "Q41520261"
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The following pages link to Thoas Fioretos (Q41520261):
Displaying 50 items.
- RNA-seq identifies clinically relevant fusion genes in leukemia including a novel MEF2D/CSF1R fusion responsive to imatinib (Q27852644) (← links)
- Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13) (Q28116183) (← links)
- Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11) (Q28183334) (← links)
- CRK proto-oncogene maps to human chromosome band 17p13 (Q28262715) (← links)
- Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS (Q28296815) (← links)
- Isodicentric 7p, idic(7)(q11.2), in acute myeloid leukemia associated with older age and favorable response to induction chemotherapy: a new clinical entity? (Q31913737) (← links)
- Recurrent and multiple bladder tumors show conserved expression profiles (Q33347849) (← links)
- Gene expression signatures in childhood acute leukemias are largely unique and distinct from those of normal tissues and other malignancies. (Q33538325) (← links)
- Integrative analysis of gene expression and copy number alterations using canonical correlation analysis (Q33557657) (← links)
- 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 repeats (Q33909470) (← links)
- Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations. (Q34244973) (← links)
- The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias (Q34465221) (← links)
- Deregulation of cyclin D2 by juxtaposition with T-cell receptor alpha/delta locus in t(12;14)(p13;q11)-positive childhood T-cell acute lymphoblastic leukemia. (Q34503575) (← links)
- Cytogenetic and molecular genetic evolution of chronic myeloid leukemia. (Q34580136) (← links)
- Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpres (Q34646535) (← links)
- Modeling chronic myeloid leukemia in immunodeficient mice reveals expansion of aberrant mast cells and accumulation of pre-B cells. (Q35044993) (← links)
- Activation of human telomerase reverse transcriptase through gene fusion in clear cell sarcoma of the kidney (Q35496976) (← links)
- 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 CDKN2A (Q35545539) (← links)
- Ebf1 heterozygosity results in increased DNA damage in pro-B cells and their synergistic transformation by Pax5 haploinsufficiency (Q35784511) (← links)
- Antibodies targeting human IL1RAP (IL1R3) show therapeutic effects in xenograft models of acute myeloid leukemia. (Q36008395) (← links)
- A glioma classification scheme based on coexpression modules of EGFR and PDGFRA. (Q37627927) (← links)
- Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1. (Q38357026) (← links)
- Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study (Q38485684) (← links)
- Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression. (Q38487737) (← links)
- The emerging complexity of gene fusions in cancer (Q38496502) (← links)
- Threshold-free high-power methods for the ontological analysis of genome-wide gene-expression studies (Q38516220) (← links)
- An improved method for detecting and delineating genomic regions with altered gene expression in cancer (Q38610956) (← links)
- Whole-exome sequencing of pediatric acute lymphoblastic leukemia. (Q39685818) (← links)
- Modeling the human 8p11-myeloproliferative syndrome in immunodeficient mice. (Q39862996) (← links)
- Deregulation of the Wilms' tumour gene 1 protein (WT1) by BCR/ABL1 mediates resistance to imatinib in human leukaemia cells. (Q40087603) (← links)
- Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations. (Q40428994) (← links)
- An EcoRI polymorphism at the insulin receptor locus on a fragment comprising exons 4 to 8. (Q40507764) (← links)
- Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer (Q41520220) (← links)
- Regional localization and developmental expression of the BCR gene in rodent brain (Q42954773) (← links)
- Genetic analysis of dasatinib-treated chronic myeloid leukemia rapidly developing into acute myeloid leukemia with monosomy 7 in Philadelphia-negative cells (Q43062695) (← links)
- Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia (Q43718577) (← links)
- Prognostic implications of BCL6 rearrangement in uniformly treated patients with diffuse large B-cell lymphoma--a Nordic Lymphoma Group study. (Q43822819) (← links)
- Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL. (Q43825958) (← links)
- Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate (Q44489093) (← links)
- Establishment and phenotypic characterization of human U937 cells with inducible P210 BCR/ABL expression reveals upregulation of CEACAM1 (CD66a). (Q44719689) (← links)
- Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients. (Q44826208) (← links)
- Identification of genes differentially regulated by the P210 BCR/ABL1 fusion oncogene using cDNA microarrays (Q44897414) (← links)
- Impact of malignant stem cell burden on therapy outcome in newly diagnosed chronic myeloid leukemia patients (Q45340032) (← links)
- Smad4 binds Hoxa9 in the cytoplasm and protects primitive hematopoietic cells against nuclear activation by Hoxa9 and leukemia transformation (Q45869110) (← links)
- Expression of P190 and P210 BCR/ABL1 in normal human CD34( ) cells induces similar gene expression profiles and results in a STAT5-dependent expansion of the erythroid lineage. (Q46168248) (← links)
- Selective killing of candidate AML stem cells by antibody targeting of IL1RAP. (Q46526054) (← links)
- The FLT3 inhibitor PKC412 in combination with cytostatic drugs in vitro in acute myeloid leukemia. (Q46932190) (← links)
- FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns (Q46944335) (← links)
- Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia. (Q46971359) (← links)
- Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies (Q47428347) (← links)