Gnas gene
Evidence from:
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all sources
No related entities found.
Mentioned in (14)
Papers in which this entity is mentioned.
- Tumour-wide RNA splicing aberrations generate actionable public neoantigens. (2025)
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- Alternative splicing events as peripheral biomarkers for motor learning deficit caused by adverse prenatal environments. (2023)
- Epigenetic analysis of cell-free DNA by fragmentomic profiling. (2022)
- Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncology. (2021)
- Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring. (2020)
- Cannabinoids Exacerbate Alcohol Teratogenesis by a CB1-Hedgehog Interaction. (2019)
- Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy. (2019)
- Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018)
- Statistical algorithms improve accuracy of gene fusion detection. (2017)
- Recurrent somatic mutations in regulatory regions of human cancer genomes. (2015)
- Integrative clinical genomics of advanced prostate cancer. (2015)
- MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
- High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. (2012)
Merged raw entities (3)
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 |
|---|---|---|---|
| gnas | gene | 23 | 68 |
| gαs | gene | 1 | 3 |
| gαs/olf | gene | — | — |