Search Results - "Kosasih, Hansen J"
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PU.1 eviction at lymphocyte-specific chromatin domains mediates glucocorticoid response in acute lymphoblastic leukemia
Published in Nature communications (08-11-2024)“…The epigenetic landscape plays a critical role in cancer progression, yet its therapeutic potential remains underexplored. Glucocorticoids are essential…”
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Unusual PDGFRB fusion reveals novel mechanism of kinase activation in Ph-like B-ALL
Published in Leukemia (01-04-2023)Get full text
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3
Less is more: Depleting myeloid‐biased HSCs to restore immune function
Published in HemaSphere (01-07-2024)Get full text
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4
Targeting hyperactive platelet-derived growth factor receptor-β signaling in T-cell acute lymphoblastic leukemia and lymphoma
Published in Haematologica (Roma) (01-05-2024)“…T-cell acute lymphoblastic leukemia (T-ALL) and T-cell lymphoblastic lymphoma (T-LBL) are rare aggressive hematologic malignancies. Current treatment consists…”
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In vitro and in vivo modelling of mutant JAK3/STAT5 signaling in leukemia
Published in Heliyon (01-11-2023)“…Mutations within the IL7-R-JAK-STAT signaling pathway are important drivers of T-cell acute lymphoblastic leukemia (T-ALL). Here we describe the important…”
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ALLSorts: a RNA-Seq subtype classifier for B-Cell Acute Lymphoblastic Leukemia
Published in Blood advances (26-07-2022)“…B-cell acute lymphoblastic leukemia (B-ALL) is the most common childhood cancer. Subtypes within B-ALL are distinguished by characteristic structural variants…”
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The third generation AKR1C3-activated prodrug, ACHM-025, eradicates disease in preclinical models of aggressive T-cell acute lymphoblastic leukemia
Published in Blood cancer journal (New York) (06-11-2024)“…T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological malignancy that expresses high levels of the enzyme aldo-keto reductase family 1…”
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A novel MYB::PAIP1 oncogenic fusion in pediatric blastic plasmacytoid dendritic cell neoplasm (BPDCN) is dependent on BCL2 expression and is sensitive to venetoclax
Published in HemaSphere (01-02-2024)“…The huMCL1 mouse strain (human MCL1 gene knocked -into the murine Mcl1 locus) is phenotypically indistinguishable from wild-type C57BL/6 (WT). To determine…”
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Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL–USP2 fusions
Published in Leukemia (01-09-2019)Get full text
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10
In vivo activity of the second-generation proteasome inhibitor ixazomib against pediatric T-cell acute lymphoblastic leukemia xenografts
Published in Experimental hematology (01-04-2024)“…•Ixazomib is an orally available, reversible selective proteasome inhibitor•Ixazomib elicited IC50 values in the low nanomolar range in T-ALL cell models in…”
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Description of a novel subtype of acute myeloid leukemia defined by recurrent CBFB insertions
Published in Blood (16-02-2023)Get full text
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TALLSorts: a T-cell acute lymphoblastic leukemia subtype classifier using RNA-seq expression data
Published in Blood advances (26-12-2023)Get full text
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13
A Disintegrin and Metalloproteinase with Thrombospondin Motifs-5 (ADAMTS-5) Forms Catalytically Active Oligomers
Published in The Journal of biological chemistry (12-02-2016)“…The metalloproteinase ADAMTS-5 (Adisintegrin and metalloproteinase with thrombospondin motifs) degrades aggrecan, a proteoglycan essential for cartilage…”
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14
SFPQ-ABL1 and BCR-ABL1 use different signaling networks to drive B-cell acute lymphoblastic leukemia
Published in Blood advances (12-04-2022)“…Philadelphia-like (Ph-like) acute lymphoblastic leukemia (ALL) is a high-risk subtype of B-cell ALL characterized by a gene expression profile resembling…”
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MLL-TFE3: a novel and aggressive KMT2A fusion identified in infant leukemia
Published in Blood advances (13-10-2020)“…•A novel KMT2A-rearrangement, MLL-TFE3, was identified in an infant leukemia patient.•MLL-TFE3 expression produces aggressive leukemia in a mouse model…”
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The AKR1C3-Activated Prodrug, Achm-025, Eradicates Disease in Preclinical Models of Aggressive T-Cell Acute Lymphoblastic Leukemia
Published in Blood (02-11-2023)“…Introduction: T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive malignancy that is exceptionally difficult to cure after relapse. T-ALL expresses…”
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