AML phenotype

Aliases

acute myeloid leukemia

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Mentioned in (29)

Papers in which this entity is mentioned.

• Machine learning for genetics-based classification and treatment response prediction in cancer of unknown primary. (2023)
• Comprehensive analysis of mutational signatures reveals distinct patterns and molecular processes across 27 pediatric cancers. (2023)
• RNA splicing dysregulation and the hallmarks of cancer. (2023)
• Application of third-generation sequencing in cancer research. (2021)
• NUP98-NSD1 Driven MDS/MPN in Childhood Masquerading as JMML. (2021)
• The repertoire of mutational signatures in human cancer. (2020)
• Diverse noncoding mutations contribute to deregulation of cis-regulatory landscape in pediatric cancers. (2020)
• Single-Cell RNA-Seq Reveals AML Hierarchies Relevant to Disease Progression and Immunity. (2019)
• Super-enhancers: critical roles and therapeutic targets in hematologic malignancies. (2019)
• Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia. (2019)
• Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours. (2018)
• Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
• The Immune Landscape of Cancer. (2018)
• Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
• Clinical Assessment and Diagnosis of Germline Predisposition to Hematopoietic Malignancies: The University of Chicago Experience. (2017)
• Small molecule inhibition of cAMP response element binding protein in human acute myeloid leukemia cells. (2016)
• The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS. (2015)
• Clonal evolution in hematological malignancies and therapeutic implications. (2014)
• Signatures of mutational processes in human cancer. (2013)
• A rare population of CD24(+)ITGB4(+)Notch(hi) cells drives tumor propagation in NSCLC and requires Notch3 for self-renewal. (2013)
• Mutational heterogeneity in cancer and the search for new cancer-associated genes. (2013)
• An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia. (2012)
• Molecular genetics of B-precursor acute lymphoblastic leukemia. (2012)
• Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. (2012)
• Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
• Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations. (2012)
• Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
• BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
• Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009)

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