TERT gene
Evidence from:
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all sources
Related entities (6)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| TERT | risk_factor_for | breast cancer | — | 1 |
| TERT | protective_against | cellular senescence | — | 1 |
| TERT | risk_factor_for | idiopathic pulmonary fibrosis | — | 1 |
| TERT | risk_factor_for | lung cancer | — | 1 |
| TERT | regulates | telomere length | — | 1 |
| TERT | regulates | Telomeres | — | 1 |
Mentioned in (48)
Papers in which this entity is mentioned.
- Stratified Medicine Pediatrics: Cell-Free DNA and Serial Tumor Sequencing Identifies Subtype-Specific Cancer Evolution and Epigenetic States. (2025)
- Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
- Multigenerational cell tracking of DNA replication and heritable DNA damage. (2025)
- Functional analysis of cancer-associated germline risk variants. (2025)
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- The Application of Long-Read Sequencing to Cancer. (2024)
- RNA splicing dysregulation and the hallmarks of cancer. (2023)
- Cell-free DNA technologies for the analysis of brain cancer. (2022)
- Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
- Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
- Integrated Genomic Analysis Identifies Driver Genes and Cisplatin-Resistant Progenitor Phenotype in Pediatric Liver Cancer. (2021)
- Application of third-generation sequencing in cancer research. (2021)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes. (2021)
- Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
- Immuno-genomic landscape of osteosarcoma. (2020)
- Pan-cancer analysis of whole genomes. (2020)
- Diverse noncoding mutations contribute to deregulation of cis-regulatory landscape in pediatric cancers. (2020)
- Extrachromosomal circular DNA drives oncogenic genome remodeling in neuroblastoma. (2020)
- The Clonal Evolution of Metastatic Osteosarcoma as Shaped by Cisplatin Treatment. (2019)
- Rapid and reversible suppression of ALT by DAXX in osteosarcoma cells. (2019)
- The role and robustness of the Gini coefficient as an unbiased tool for the selection of Gini genes for normalising expression profiling data. (2019)
- Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
- Enhanced detection of circulating tumor DNA by fragment size analysis. (2018)
- Genome doubling shapes the evolution and prognosis of advanced cancers. (2018)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes (2018)
- Patterns and mechanisms of structural variations in human cancer. (2018)
- Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
- Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients. (2017)
- CScape: a tool for predicting oncogenic single-point mutations in the cancer genome. (2017)
- A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
- Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma. (2017)
- PGBD5 promotes site-specific oncogenic mutations in human tumors. (2017)
- Global analysis of somatic structural genomic alterations and their impact on gene expression in diverse human cancers. (2016)
- Landscape of somatic mutations in 560 breast cancer whole-genome sequences. (2016)
- Evolutionary Insights into RNA trans-Splicing in Vertebrates. (2016)
- Recurrent somatic mutations in regulatory regions of human cancer genomes. (2015)
- A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis. (2015)
- Oncogenic fusion protein EWS-FLI1 is a network hub that regulates alternative splicing. (2015)
- Genome-wide analysis of noncoding regulatory mutations in cancer. (2014)
- Gene expression signatures affected by alcohol-induced DNA methylomic deregulation in human embryonic stem cells. (2014)
- Cancer genome landscapes. (2013)
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
- Computational approaches to identify functional genetic variants in cancer genomes. (2013)
- Pan-cancer patterns of somatic copy number alteration. (2013)
- Molecular mechanisms of long noncoding RNAs. (2011)
- Linking functional decline of telomeres, mitochondria and stem cells during ageing. (2010)
- Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. (2009)
- MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings. (2008)
Merged raw entities (4)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| tert | gene | 48 | 154 |
| telomerase | gene | 1 | 2 |
| human tert | gene | — | — |
| telomerase reverse transcriptase | gene | — | — |