Gene · 4437
Papers3,191
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
301 to 320 of 3,191
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Can MSH3 lowering stop HTT repeat expansion in its CAG tract? | Mol Ther | 2023 | 37236185 | PubTator, text mining | PubMed |
| Microsatellite Status Detection of Colorectal Cancer: Evaluation of Inconsistency between PCR and IHC. | J Cancer | 2023 | 37215453 | PubTator, text mining | PubMed |
| Extraordinary clinical response to ibrutinib in low-grade ovarian cancer guided by organoid drug testing. | NPJ Precis Oncol | 2023 | 37202426 | PubTator, text mining | PubMed |
| Microsatellite Instability: A Review of Molecular Epidemiology and Implications for Immune Checkpoint Inhibitor Therapy. | Cancers (Basel) | 2023 | 37190216 | PubTator, text mining | PubMed |
| Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington's disease. | Mol Ther | 2023 | 37177784 | PubTator, text mining | PubMed |
| Diverse genetic spectrum among patients who met the criteria of hereditary breast, ovarian and pancreatic cancer syndrome. | J Gynecol Oncol | 2023 | 37170728 | PubTator, text mining | PubMed |
| Dysregulation of DNA repair genes in Fuchs endothelial corneal dystrophy. | Exp Eye Res | 2023 | 37169279 | PubTator, text mining | PubMed |
| Hereditary colorectal, gastric, and pancreatic cancer: comprehensive review. | BJS Open | 2023 | 37165697 | PubTator, text mining | PubMed |
| A draft human pangenome reference. | Nature | 2023 | 37165242 | PubTator, text mining | PubMed |
| Deficiency in mammalian STN1 promotes colon cancer development via inhibiting DNA repair. | Sci Adv | 2023 | 37163605 | PubTator, text mining | PubMed |
| Multi-omic analysis in normal colon organoids highlights MSH4 as a novel marker of defective mismatch repair in Lynch syndrome and microsatellite instability. | Cancer Med | 2023 | 37162286 | PubTator, text mining | PubMed |
| Diversity and heterogeneity in human breast cancer adipose tissue revealed at single-nucleus resolution. | Front Immunol | 2023 | 37153595 | PubTator, text mining | PubMed |
| MSH2-MSH3 promotes DNA end resection during homologous recombination and blocks polymerase theta-mediated end-joining through interaction with SMARCAD1 and EXO1. | Nucleic Acids Res | 2023 | 37140056 | PubTator, text mining | PubMed |
| A novel quantitative trait locus implicates Msh3 in the propensity for genome-wide short tandem repeat expansions in mice. | Genome Res | 2023 | 37127331 | PubTator, text mining | PubMed |
| Efficacy of Nivolumab in Pediatric Cancers with High Mutation Burden and Mismatch Repair Deficiency. | Clin Cancer Res | 2023 | 37126021 | PubTator, text mining | PubMed |
| The role of DNA methylation in ovarian cancer chemoresistance: A narrative review. | Health Sci Rep | 2023 | 37123549 | PubTator, text mining | PubMed |
| Radiation‑induced pure red cell aplasia combined with acquired amegakaryocytic thrombocytopenia in a thymoma after rapid response to radiotherapy: A case report and literature review. | Exp Ther Med | 2023 | 37114181 | PubTator, text mining | PubMed |
| The Current Status of DNA-Repair-Directed Precision Oncology Strategies in Epithelial Ovarian Cancers. | Int J Mol Sci | 2023 | 37108451 | PubTator, text mining | PubMed |
| The Unique Spectrum of MUTYH Germline Mutations in Colombian Patients with Extracolonic Carcinomas. | Appl Clin Genet | 2023 | 37096204 | PubTator, text mining | PubMed |
| Candidate variants in DNA replication and repair genes in early-onset renal cell carcinoma patients referred for germline testing. | BMC Genomics | 2023 | 37095444 | 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.
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GET https://conductscience.org/api/genes/v1/4437/papers?page=16