DNA damage phenotype
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Mentioned in (43)
Papers in which this entity is mentioned.
- Comprehensive repertoire of the chromosomal alteration and mutational signatures across 16 cancer types. (2026)
- FET fusion oncoproteins disrupt physiologic DNA repair and create a targetable opportunity for ATR inhibitor therapy. (2025)
- Multigenerational cell tracking of DNA replication and heritable DNA damage. (2025)
- Chromosomal instability as a driver of cancer progression. (2025)
- Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
- Gastrulation-stage alcohol exposure induces similar rates of craniofacial malformations in male and female C57BL/6J mice. (2024)
- ENPP1 Immunobiology as a Therapeutic Target. (2023)
- Comprehensive analysis of mutational signatures reveals distinct patterns and molecular processes across 27 pediatric cancers. (2023)
- Towards understandings of serine/arginine-rich splicing factors. (2023)
- Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smoking. (2022)
- Transcriptomic analyses of gastrulation-stage mouse embryos with differential susceptibility to alcohol. (2021)
- Loss of tumor protein 53 protects against alcohol-induced facial malformations in mice and zebrafish. (2021)
- Macrophage Polarization States in the Tumor Microenvironment. (2021)
- Best practices for variant calling in clinical sequencing. (2020)
- DNA mismatch repair promotes APOBEC3-mediated diffuse hypermutation in human cancers. (2020)
- Emerging Roles of SRSF3 as a Therapeutic Target for Cancer. (2020)
- Designing combination therapies with modeling chaperoned machine learning. (2019)
- RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
- A Compendium of Mutational Signatures of Environmental Agents. (2019)
- The Cancer Spliceome: Reprograming of Alternative Splicing in Cancer. (2018)
- MutationalPatterns: comprehensive genome-wide analysis of mutational processes. (2018)
- EWS/FLI Confers Tumor Cell Synthetic Lethality to CDK12 Inhibition in Ewing Sarcoma. (2018)
- HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures. (2017)
- Gene-environment interactions in development and disease. (2017)
- Copy-number signatures and mutational processes in ovarian carcinoma (2017)
- Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin. (2016)
- New insights into the generation and role of de novo mutations in health and disease. (2016)
- Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
- Evolutionary Insights into RNA trans-Splicing in Vertebrates. (2016)
- The Genetics of Fetal Alcohol Spectrum Disorders. (2016)
- A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
- Break-induced replication is a source of mutation clusters underlying kataegis. (2014)
- Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. (2014)
- Involvement of p53 in the repair of DNA double strand breaks: multifaceted Roles of p53 in homologous recombination repair (HRR) and non-homologous end joining (NHEJ). (2014)
- Ewing sarcoma protein: a key player in human cancer. (2013)
- RNA splicing: a new player in the DNA damage response. (2013)
- Mutational processes molding the genomes of 21 breast cancers. (2012)
- Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
- Massive genomic rearrangement acquired in a single catastrophic event during cancer development. (2011)
- BRCA1 and BRCA2: different roles in a common pathway of genome protection. (2011)
- Functional consequences of developmentally regulated alternative splicing. (2011)
- 3' end mRNA processing: molecular mechanisms and implications for health and disease. (2008)
- MDM2 and MDM4: p53 regulators as targets in anticancer therapy. (2007)
Merged raw entities (2)
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 |
|---|---|---|---|
| dna damage | phenotype | 67 | 138 |
| dna damage by aldehydes and alcohol | phenotype | — | — |