Gene · 5378
Papers1,886
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
701 to 720 of 1,886
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Sex in Symbiodiniaceae dinoflagellates: genomic evidence for independent loss of the canonical synaptonemal complex. | Sci Rep | 2020 | 32555361 | PubTator, text mining | PubMed |
| Clinicopathologic characteristics of resectable colorectal cancer with mismatch repair protein defects in Chinese population: Retrospective case series and literature review. | Medicine (Baltimore) | 2020 | 32541478 | PubTator, text mining | PubMed |
| MICA ∗012:01 Allele Facilitates the Metastasis of KRAS-Mutant Colorectal Cancer. | Front Genet | 2020 | 32528529 | PubTator, text mining | PubMed |
| Prenatal exposure to bisphenol A alters the transcriptome-interactome profiles of genes associated with Alzheimer's disease in the offspring hippocampus. | Sci Rep | 2020 | 32528016 | PubTator, text mining | PubMed |
| Actionable Strategies to Target Multiple Myeloma Plasma Cell Resistance/Resilience to Stress: Insights From "Omics" Research. | Front Oncol | 2020 | 32500036 | PubTator, text mining | PubMed |
| Advances in DNA Repair-Emerging Players in the Arena of Eukaryotic DNA Repair. | Int J Mol Sci | 2020 | 32486270 | PubTator, text mining | PubMed |
| Yeast mismatch repair components are required for stable inheritance of gene silencing. | PLoS Genet | 2020 | 32469861 | PubTator, text mining | PubMed |
| Clinical Implications of DNA Repair Defects in High-Grade Serous Ovarian Carcinomas. | Cancers (Basel) | 2020 | 32455819 | PubTator, text mining | PubMed |
| Relationship between MLH1, PMS2, MSH2 and MSH6 gene-specific alterations and tumor mutational burden in 1057 microsatellite instability-high solid tumors. | Int J Cancer | 2020 | 32449172 | PubTator, text mining | PubMed |
| ATAC-seq identifies thousands of extrachromosomal circular DNA in cancer and cell lines. | Sci Adv | 2020 | 32440553 | PubTator, text mining | PubMed |
| An NMF-Based Methodology for Selecting Biomarkers in the Landscape of Genes of Heterogeneous Cancer-Associated Fibroblast Populations. | Bioinform Biol Insights | 2020 | 32425511 | PubTator, text mining | PubMed |
| High tumor mutation burden is associated with DNA damage repair gene mutation in breast carcinomas. | Diagn Pathol | 2020 | 32393302 | PubTator, text mining | PubMed |
| Mutation analysis of related genes in hamartoma polyp tissue of Peutz-Jeghers syndrome. | World J Gastroenterol | 2020 | 32390703 | PubTator, text mining | PubMed |
| Colorectal Adenomas-Genetics and Searching for New Molecular Screening Biomarkers. | Int J Mol Sci | 2020 | 32380676 | PubTator, text mining | PubMed |
| Development and validation of next generation sequencing based 35-gene hereditary cancer panel. | Hered Cancer Clin Pract | 2020 | 32368312 | PubTator, text mining | PubMed |
| Exploration of the role of serum ghrelin in the diagnosis and treatment of digestive tract malignancies. | J Int Med Res | 2020 | 32366148 | PubTator, text mining | PubMed |
| Male Breast Cancer: Results of the Application of Multigene Panel Testing to an Italian Cohort of Patients. | Diagnostics (Basel) | 2020 | 32365798 | PubTator, text mining | PubMed |
| Mechanisms and therapeutic implications of hypermutation in gliomas. | Nature | 2020 | 32322066 | PubTator, text mining | PubMed |
| A reference map of the human binary protein interactome. | Nature | 2020 | 32296183 | PubTator, text mining | PubMed |
| Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families. | Breast Cancer Res | 2020 | 32295625 | PubTator, text mining | PubMed |
gene-search-2026-11-11-0.2.0
Sources 12
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
- GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
- HGNCCC0
- NCBI GenePublic domain (US government)
- NIH's project files and grant-paper linksPublic domain
- Open TargetsCC0 1.0
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
- GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
- HGNCCC0: https://www.genenames.org/about/license/
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/5378/papers?page=36