poor prognosis phenotype
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| Ctbp2 | risk_factor_for | poor prognosis | — | 1 |
| Ctbp2 | biomarker_for | poor prognosis | — | 1 |
Mentioned in (52)
Papers in which this entity is mentioned.
- A guide to transcriptomic deconvolution in cancer. (2026)
- Whole-genome landscapes of 1,364 breast cancers. (2026)
- Nanopore-based cell-free DNA fragmentation and methylation profiles from the cerebral spinal fluid of patients with lung cancer brain metastases. (2025)
- Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
- Chromosomal instability as a driver of cancer progression. (2025)
- Functional analysis of cancer-associated germline risk variants. (2025)
- Tumor-informed deep sequencing of ctDNA detects minimal residual disease and predicts relapse in osteosarcoma. (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)
- ENPP1 Immunobiology as a Therapeutic Target. (2023)
- Machine learning for genetics-based classification and treatment response prediction in cancer of unknown primary. (2023)
- Towards understandings of serine/arginine-rich splicing factors. (2023)
- RNA splicing dysregulation and the hallmarks of cancer. (2023)
- Circulating Tumor DNA Is Associated with Response and Survival in Patients with Advanced Leiomyosarcoma. (2022)
- Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncology. (2021)
- 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)
- Integrative reconstruction of cancer genome karyotypes using InfoGenomeR. (2021)
- Macrophage Polarization States in the Tumor Microenvironment. (2021)
- Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
- NUP98-NSD1 Driven MDS/MPN in Childhood Masquerading as JMML. (2021)
- Immuno-genomic landscape of osteosarcoma. (2020)
- Inferring structural variant cancer cell fraction. (2020)
- Emerging Roles of SRSF3 as a Therapeutic Target for Cancer. (2020)
- Super-enhancers: critical roles and therapeutic targets in hematologic malignancies. (2019)
- How I diagnose and manage Philadelphia chromosome-like acute lymphoblastic leukemia. (2019)
- VCF2CNA: A tool for efficiently detecting copy-number alterations in VCF genotype data and tumor purity. (2019)
- Genome-Informed Targeted Therapy for Osteosarcoma. (2019)
- Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors. (2018)
- Detection of Somatic Structural Variants Enables Quantification and Characterization of Circulating Tumor DNA in Children With Solid Tumors. (2018)
- Genome doubling shapes the evolution and prognosis of advanced cancers. (2018)
- The Immune Landscape of Cancer. (2018)
- Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
- Copy number signatures and mutational processes in ovarian carcinoma. (2018)
- 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)
- DNA Methylation Analysis: Choosing the Right Method. (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)
- Systematic pan-cancer analysis of tumour purity. (2015)
- Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays. (2014)
- Dynamic analyses of alternative polyadenylation from RNA-seq reveal a 3'-UTR landscape across seven tumour types. (2014)
- A rare population of CD24(+)ITGB4(+)Notch(hi) cells drives tumor propagation in NSCLC and requires Notch3 for self-renewal. (2013)
- Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
- Pan-cancer patterns of somatic copy number alteration. (2013)
- Myeloid cells in tumor inflammation. (2012)
- Molecular genetics of B-precursor acute lymphoblastic leukemia. (2012)
- Patient-derived tumour xenografts as models for oncology drug development. (2012)
- "CRASH"ing with the worm: insights into L1CAM functions and mechanisms. (2010)
- Fewer permutations, more accurate P-values. (2009)
- Three-dimensional brain growth abnormalities in childhood-onset schizophrenia visualized by using tensor-based morphometry. (2008)
- Adrenomedullin signaling is necessary for murine lymphatic vascular development. (2008)
- Gender and Alcoholic Subtypes. (1996)
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 |
|---|---|---|---|
| poor prognosis | phenotype | 52 | 70 |
| poor survival outlook | phenotype | 1 | 1 |
| extremely poor prognosis | phenotype | — | — |