HeLa cohort

Aliases

HeLa cells

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Mentioned in (22)

Papers in which this entity is mentioned.

• FET fusion oncoproteins disrupt physiologic DNA repair and create a targetable opportunity for ATR inhibitor therapy. (2025)
• Global impact of unproductive splicing on human gene expression. (2024)
• Towards understandings of serine/arginine-rich splicing factors. (2023)
• Joint single-cell measurements of nuclear proteins and RNA in vivo. (2021)
• Integrative reconstruction of cancer genome karyotypes using InfoGenomeR. (2021)
• Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
• Alternative Lengthening of Telomeres through Two Distinct Break-Induced Replication Pathways. (2019)
• GeneGini: Assessment via the Gini Coefficient of Reference "Housekeeping" Genes and Diverse Human Transporter Expression Profiles. (2018)
• PASSPORT-seq: A Novel High-Throughput Bioassay to Functionally Test Polymorphisms in Micro-RNA Target Sites. (2018)
• Evolutionary Insights into RNA trans-Splicing in Vertebrates. (2016)
• APOBEC-induced mutations in human cancers are strongly enriched on the lagging DNA strand during replication. (2016)
• The Hitchhiker's guide to Hi-C analysis: practical guidelines. (2015)
• A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
• Genome-wide analysis of noncoding regulatory mutations in cancer. (2014)
• Dynamic analyses of alternative polyadenylation from RNA-seq reveal a 3'-UTR landscape across seven tumour types. (2014)
• Long noncoding RNA EWSAT1-mediated gene repression facilitates Ewing sarcoma oncogenesis. (2014)
• EWS-FLI1 utilizes divergent chromatin remodeling mechanisms to directly activate or repress enhancer elements in Ewing sarcoma. (2014)
• Oncogenic ETS fusions deregulate E2F3 target genes in Ewing sarcoma and prostate cancer. (2013)
• Mutational heterogeneity in cancer and the search for new cancer-associated genes. (2013)
• Circular RNAs are the predominant transcript isoform from hundreds of human genes in diverse cell types. (2012)
• Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. (2011)
• EWS, but not EWS-FLI-1, is associated with both TFIID and RNA polymerase II: interactions between two members of the TET family, EWS and hTAFII68, and subunits of TFIID and RNA polymerase II complexes. (1998)

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