Gene · 3981
Papers3,259
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1,141 to 1,160 of 3,259
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Multiple cerebral cavernous malformations in association with a Dubowitz-like syndrome. | J Cerebrovasc Endovasc Neurosurg | 2020 | 32596139 | PubTator, text mining | PubMed |
| Small Molecule Inhibitors Confirm Ubiquitin-Dependent Removal of TOP2-DNA Covalent Complexes. | Mol Pharmacol | 2020 | 32587095 | PubTator, text mining | PubMed |
| Dominantly Inherited Hereditary Nonpolyposis Colorectal Cancer Not Caused by MMR Genes. | J Clin Med | 2020 | 32585810 | PubTator, text mining | PubMed |
| New Frontiers in Prostate Cancer Treatment: Are We Ready for Drug Combinations with Novel Agents? | Cells | 2020 | 32580469 | PubTator, text mining | PubMed |
| Druggable binding sites in the multicomponent assemblies that characterise DNA double-strand-break repair through non-homologous end joining. | Essays Biochem | 2020 | 32579168 | PubTator, text mining | PubMed |
| DNA double-strand breaks induce H2Ax phosphorylation domains in a contact-dependent manner. | Nat Commun | 2020 | 32572033 | PubTator, text mining | PubMed |
| Base Excision Repair in the Immune System: Small DNA Lesions With Big Consequences. | Front Immunol | 2020 | 32547565 | PubTator, text mining | PubMed |
| Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformations. | Eur J Med Genet | 2020 | 32534991 | PubTator, text mining | PubMed |
| Precise breakpoint detection in a patient with 9p- syndrome. | Cold Spring Harb Mol Case Stud | 2020 | 32532883 | PubTator, text mining | PubMed |
| Competitive Growth Assay of Mutagenized Chlamydomonas reinhardtii Compatible With the International Space Station Veggie Plant Growth Chamber. | Front Plant Sci | 2020 | 32523594 | PubTator, text mining | PubMed |
| Diagnosis of radiosensitive severe combined immunodeficiency disease (RS-SCID) by Comet Assay, management of bone marrow transplantation. | Immunobiology | 2020 | 32517885 | PubTator, text mining | PubMed |
| Synergistic gene editing in human iPS cells via cell cycle and DNA repair modulation. | Nat Commun | 2020 | 32513994 | PubTator, text mining | PubMed |
| Pathological mutations in PNKP trigger defects in DNA single-strand break repair but not DNA double-strand break repair. | Nucleic Acids Res | 2020 | 32504494 | PubTator, text mining | PubMed |
| The XRCC4 rs1805377 polymorphism is not associated with the risk of cancer: An updated meta-analysis. | J Int Med Res | 2020 | 32493081 | PubTator, text mining | PubMed |
| Pharmacological methods to transcriptionally modulate double-strand break DNA repair. | Int Rev Cell Mol Biol | 2020 | 32475473 | PubTator, text mining | PubMed |
| H3K36 dimethylation by MMSET promotes classical non-homologous end-joining at unprotected telomeres. | Oncogene | 2020 | 32472076 | PubTator, text mining | PubMed |
| LIG4 syndrome: clinical and molecular characterization in a Chinese cohort. | Orphanet J Rare Dis | 2020 | 32471509 | PubTator, text mining | PubMed |
| A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer. | Cancer Epidemiol Biomarkers Prev | 2020 | 32467344 | PubTator, text mining | PubMed |
| Improving Precise CRISPR Genome Editing by Small Molecules: Is there a Magic Potion? | Cells | 2020 | 32466303 | PubTator, text mining | PubMed |
| Genome Editing Fidelity in the Context of DNA Sequence and Chromatin Structure. | Front Cell Dev Biol | 2020 | 32457906 | 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/v1/3981/papers?page=58