Gastric cancer phenotype
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| Myc | associated_with | Gastric cancer | — | 1 |
Mentioned in (33)
Papers in which this entity is mentioned.
- Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
- Analysis of 10,478 cancer genomes identifies candidate driver genes and opportunities for precision oncology. (2024)
- The Application of Long-Read Sequencing to Cancer. (2024)
- Deterministic evolution and stringent selection during preneoplasia. (2023)
- Towards understandings of serine/arginine-rich splicing factors. (2023)
- RNA splicing dysregulation and the hallmarks of cancer. (2023)
- Nucleosome footprinting in plasma cell-free DNA for the pre-surgical diagnosis of ovarian cancer. (2022)
- Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA. (2022)
- Application of third-generation sequencing in cancer research. (2021)
- Therapeutic Implications of Germline Testing in Patients With Advanced Cancers. (2021)
- Macrophage Polarization States in the Tumor Microenvironment. (2021)
- Emerging Roles of SRSF3 as a Therapeutic Target for Cancer. (2020)
- Neoadjuvant checkpoint blockade for cancer immunotherapy. (2020)
- Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors. (2020)
- Establishing guidelines to harmonize tumor mutational burden (TMB): in silico assessment of variation in TMB quantification across diagnostic platforms: phase I of the Friends of Cancer Research TMB Harmonization Project. (2020)
- Liquid versus tissue biopsy for detecting acquired resistance and tumor heterogeneity in gastrointestinal cancers. (2019)
- The mutational footprints of cancer therapies. (2019)
- VCF2CNA: A tool for efficiently detecting copy-number alterations in VCF genotype data and tumor purity. (2019)
- Genome-wide cell-free DNA fragmentation in patients with cancer. (2019)
- Comprehensive analysis of structural variants in breast cancer genomes using single molecule sequencing (2019)
- Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
- Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients. (2017)
- Substantial contribution of extrinsic risk factors to cancer development. (2016)
- Prognostic value of inflammation-based scores in patients with osteosarcoma. (2016)
- CtBP2 is an independent prognostic marker that promotes GLI1 induced epithelial-mesenchymal transition in hepatocellular carcinoma. (2015)
- Endocannabinoids are conserved inhibitors of the Hedgehog pathway. (2015)
- Condensins are Required for Maintenance of Nuclear Architecture. (2014)
- PyClone: statistical inference of clonal population structure in cancer. (2014)
- Differential expression profiles of glycosphingolipids in human breast cancer stem cells vs. cancer non-stem cells. (2013)
- Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy. (2013)
- Blood cell origin of circulating microRNAs: a cautionary note for cancer biomarker studies. (2012)
- Significant differences in global genomic DNA methylation by gender and race/ethnicity in peripheral blood. (2011)
- Environmental programming of stress responses through DNA methylation: life at the interface between a dynamic environment and a fixed genome. (2005)
Merged raw entities (1)
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 |
|---|---|---|---|
| gastric cancer | phenotype | 33 | 63 |