Gene · 5981
Papers2,391
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
101 to 120 of 2,391
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| A genome-wide approach for the discovery of novel repeat expansion disorders in the Undiagnosed Diseases Network cohort. | Genet Med | 2025 | 40417743 | PubTator, text mining | PubMed |
| Polydatin sensitizes osteosarcoma cells to methotrexate through suppressing the H19/H3K27me3/H3K9me3 mediated folate metabolism regulatory axis. | Bioorg Chem | 2025 | 40381463 | PubTator, text mining | PubMed |
| Structural and molecular basis of PCNA-activated FAN1 nuclease function in DNA repair. | Nat Commun | 2025 | 40368897 | PubTator, text mining | PubMed |
| A FAN1 point mutation associated with accelerated Huntington's disease progression alters its PCNA-mediated assembly on DNA. | Nat Commun | 2025 | 40368883 | PubTator, text mining | PubMed |
Folate-Associated Gene Expression in Primary Tumors Is Associated With Tumor Response and Progression-Free Survival of Patients With Metastatic Colorectal Cancer Undergoing 5-FU/Leucovorin-Based Combination Chemotherapy. | Cancer Med | 2025 | 40357991 | PubTator, text mining | PubMed |
| Heterozygous and Homozygous RFC1 AAGGG Repeat Expansions are Common in Idiopathic Peripheral Neuropathy. | medRxiv | 2025 | 40313272 | PubTator, text mining | PubMed |
| The genetic landscape of sporadic adult-onset degenerative ataxia: a multi-modal genetic study of 377 consecutive patients from the longitudinal multi-centre SPORTAX cohort. | EBioMedicine | 2025 | 40273470 | PubTator, text mining | PubMed |
| CANVAS as example of genetic and clinical complexity of RFC1-related disorders. | Neurol Neurochir Pol | 2025 | 40241639 | PubTator, text mining | PubMed |
| Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies. | J Peripher Nerv Syst | 2025 | 40211677 | PubTator, text mining | PubMed |
| Comment on "Spectrum disorder of RFC1 expansions/CANVAS: Clinical and electrophysiological characterization of a group of 31 patients". | Clin Neurophysiol | 2025 | 40204545 | PubTator, text mining | PubMed |
| Hereditary Ataxias in Argentina. | Cerebellum | 2025 | 40198507 | PubTator, text mining | PubMed |
| ONT in Clinical Diagnostics of Repeat Expansion Disorders: Detection and Reporting Challenges. | Int J Mol Sci | 2025 | 40141365 | PubTator, text mining | PubMed |
| Optical genome mapping enables accurate testing of large repeat expansions. | Genome Res | 2025 | 40113266 | PubTator, text mining | PubMed |
| The Spectrum of Peripheral-Vestibular Deficits and Their Change Over Time in CANVAS/RFC1-Related Ataxia Systematic Review and Meta-Analysis of Quantitative Head-Impulse Testing. | Cerebellum | 2025 | 40111638 | PubTator, text mining | PubMed |
| Development of Immunostaining Protocols for 3D Visualization of Pericytes in Human Retinal Flatmounts. | J Histochem Cytochem | 2025 | 40098221 | PubTator, text mining | PubMed |
| Knockdown of RFC2 Prevents the Proliferation, Migration and Invasion of Cervical Cancer Cells. | Anticancer Res | 2025 | 40037867 | PubTator, text mining | PubMed |
| Targeted Long-Read Sequencing as a Single Assay Improves the Diagnosis of Spastic-Ataxia Disorders. | Ann Clin Transl Neurol | 2025 | 40007153 | PubTator, text mining | PubMed |
| Prognostic value of folate-associated gene expression in stage II colon cancer. | J Cancer Res Clin Oncol | 2025 | 39998667 | PubTator, text mining | PubMed |
| Prime Editing: Mechanistic Insights and DNA Repair Modulation. | Cells | 2025 | 39996750 | PubTator, text mining | PubMed |
| Movement Disorders in Hereditary Cerebellar Ataxia. | Mov Disord Clin Pract | 2025 | 39936868 | 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/v1/5981/papers?page=6