KRAS gene
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| KRAS | interacts_with | alcohol | — | 1 |
| KRAS | expressed_in | anterior cingulate cortex | — | 1 |
Mentioned in (85)
Papers in which this entity is mentioned.
- Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
- Chromosomal instability as a driver of cancer progression. (2025)
- Three-dimensional genome landscape of primary human cancers. (2025)
- Tracing the evolution of single-cell 3D genomes in Kras-driven cancers. (2025)
- MYC ecDNA promotes intratumour heterogeneity and plasticity in PDAC. (2025)
- Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. (2024)
- Synthetic augmentation of cancer cell line multi-omic datasets using unsupervised deep learning. (2024)
- Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme. (2024)
- Analysis of 10,478 cancer genomes identifies candidate driver genes and opportunities for precision oncology. (2024)
- Combination of genomic instability score and TP53 status for prognosis prediction in lung adenocarcinoma. (2023)
- Combined low-pass whole genome and targeted sequencing in liquid biopsies for pediatric solid tumors. (2023)
- Machine learning for genetics-based classification and treatment response prediction in cancer of unknown primary. (2023)
- Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA. (2022)
- Single-cell analysis of hepatoblastoma identifies tumor signatures that predict chemotherapy susceptibility using patient-specific tumor spheroids. (2022)
- Single-cell genomic variation induced by mutational processes in cancer. (2022)
- Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
- Evaluating the transcriptional fidelity of cancer models. (2021)
- Micro-RNA-125a mediates the effects of hypomethylating agents in chronic myelomonocytic leukemia. (2021)
- Potential Role of S-Palmitoylation in Cancer Stem Cells of Lung Adenocarcinoma. (2021)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes. (2021)
- : batch effect adjustment for RNA-seq count data. (2020)
- Inferring structural variant cancer cell fraction. (2020)
- Single-cell RNA landscape of intratumoral heterogeneity and immunosuppressive microenvironment in advanced osteosarcoma. (2020)
- Longitudinal therapy monitoring of ALK-positive lung cancer by combined copy number and targeted mutation profiling of cell-free DNA. (2020)
- Liquid versus tissue biopsy for detecting acquired resistance and tumor heterogeneity in gastrointestinal cancers. (2019)
- CHASMplus Reveals the Scope of Somatic Missense Mutations Driving Human Cancers. (2019)
- The Network of Cancer Genes (NCG): a comprehensive catalogue of known and candidate cancer genes from cancer sequencing screens. (2019)
- How I diagnose and manage Philadelphia chromosome-like acute lymphoblastic leukemia. (2019)
- Assessment of tumor mutation burden calculation from gene panel sequencing data. (2019)
- RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
- Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
- Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours. (2018)
- Detection of Somatic Structural Variants Enables Quantification and Characterization of Circulating Tumor DNA in Children With Solid Tumors. (2018)
- Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
- Widespread Selection for Oncogenic Mutant Allele Imbalance in Cancer. (2018)
- Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018)
- Genome doubling shapes the evolution and prognosis of advanced cancers. (2018)
- The Immune Landscape of Cancer. (2018)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes (2018)
- Molecular profiling and sequential somatic mutation shift in hypermutator tumours harbouring POLE mutations. (2018)
- Copy number signatures and mutational processes in ovarian carcinoma. (2018)
- OncoKB: A Precision Oncology Knowledge Base. (2017)
- Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
- Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
- One-Carbon Metabolism in Health and Disease. (2017)
- Integrated analysis of gene expression and copy number identified potential cancer driver genes with amplification-dependent overexpression in 1,454 solid tumors. (2017)
- Allele-Specific HLA Loss and Immune Escape in Lung Cancer Evolution. (2017)
- Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients. (2017)
- Copy-number signatures and mutational processes in ovarian carcinoma (2017)
- Clinical Assessment and Diagnosis of Germline Predisposition to Hematopoietic Malignancies: The University of Chicago Experience. (2017)
- An open access pilot freely sharing cancer genomic data from participants in Texas. (2016)
- Integrated digital error suppression for improved detection of circulating tumor DNA. (2016)
- Fragment Length of Circulating Tumor DNA. (2016)
- The clinical trial landscape in oncology and connectivity of somatic mutational profiles to targeted therapies. (2016)
- Oxidative stress signaling to chromatin in health and disease. (2016)
- Development and clinical application of an integrative genomic approach to personalized cancer therapy. (2016)
- Establishment of human iPSC-based models for the study and targeting of glioma initiating cells. (2016)
- Genomic Characterization of Brain Metastases Reveals Branched Evolution and Potential Therapeutic Targets. (2015)
- Recurrent somatic mutations in regulatory regions of human cancer genomes. (2015)
- Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia. (2015)
- MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
- RADIA: RNA and DNA integrated analysis for somatic mutation detection. (2014)
- Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. (2014)
- An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. (2014)
- Clonal evolution in hematological malignancies and therapeutic implications. (2014)
- Cancer genome landscapes. (2013)
- Clinical whole-exome sequencing for the diagnosis of mendelian disorders. (2013)
- A simple consensus approach improves somatic mutation prediction accuracy. (2013)
- A rare population of CD24(+)ITGB4(+)Notch(hi) cells drives tumor propagation in NSCLC and requires Notch3 for self-renewal. (2013)
- Emerging landscape of oncogenic signatures across human cancers. (2013)
- Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
- Computational approaches to identify functional genetic variants in cancer genomes. (2013)
- Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy. (2013)
- The genomic landscape of hypodiploid acute lymphoblastic leukemia. (2013)
- Zebrafish models of human liver development and disease. (2013)
- LIN28B promotes growth and tumorigenesis of the intestinal epithelium via Let-7. (2013)
- High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. (2012)
- Molecular genetics of B-precursor acute lymphoblastic leukemia. (2012)
- Patient-derived tumour xenografts as models for oncology drug development. (2012)
- GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers. (2011)
- DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing. (2010)
- Cellular metabolic stress: considering how cells respond to nutrient excess. (2010)
- Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. (2009)
- Identification of a small molecule inhibitor of the hedgehog signaling pathway: effects on basal cell carcinoma-like lesions. (2003)
- Disruption of hyaluronan synthase-2 abrogates normal cardiac morphogenesis and hyaluronan-mediated transformation of epithelium to mesenchyme. (2000)
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 |
|---|---|---|---|
| kras | gene | 85 | 244 |
| k-ras | gene | — | — |