Gene · 79840
Papers1,354
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
21 to 40 of 1,354
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Expanding the clinical spectrum of Cernunnos/XLF deficiency: a literature review of a rare cause of severe combined immunodeficiency including a novel case. | BMC Immunol | 2025 | 41225329 | PubTator, text mining | PubMed |
| A comprehensive genetic catalog of human double-strand break repair. | Science | 2025 | 41037600 | PubTator, text mining | PubMed |
| Smart technique for calculating fault current model parameters using short circuit current measurements. | Sci Rep | 2025 | 40790055 | PubTator, text mining | PubMed |
| PIPKIγ promotes non-homologous end joining through LIG4 to enhance radiotherapy resistance in triple-negative breast cancer. | Cell Death Dis | 2025 | 40744919 | PubTator, text mining | PubMed |
| Lactylation of XLF promotes non-homologous end-joining repair and chemoresistance in cancer. | Mol Cell | 2025 | 40680721 | PubTator, text mining | PubMed |
| PAXX/Ku interaction is rate limiting for repair of double-strand DNA breaks requiring end processing. | J Biol Chem | 2025 | 40659092 | PubTator, text mining | PubMed |
| NHEJ1 Splice Variants Associated With Bone Marrow Failure and Hematologic Malignancy. | Pediatr Blood Cancer | 2025 | 40580024 | PubTator, text mining | PubMed |
| Enhancing Specificity, Precision, Accessibility, Flexibility, and Safety to Overcome Traditional CRISPR/Cas Editing Challenges and Shape Future Innovations. | Adv Sci (Weinh) | 2025 | 40548648 | PubTator, text mining | PubMed |
| Distinct functions of PAXX and MRI during chromosomal end joining. | iScience | 2025 | 40546969 | PubTator, text mining | PubMed |
| Dynamic assemblies and coordinated reactions of non-homologous end joining. | Nature | 2025 | 40500445 | PubTator, text mining | PubMed |
| Nuclear VPS35 attenuates NHEJ repair by sequestering Ku protein. | Mol Med | 2025 | 40484931 | PubTator, text mining | PubMed |
| Centralized rapid genetic diagnosis of combined immunodeficiency in Japan. | Pediatr Int | 2025 | 40457861 | PubTator, text mining | PubMed |
| Newborn Screening Followed By Early Treatment is Essential to Improve Survival in SCID. | J Clin Immunol | 2025 | 40374985 | PubTator, text mining | PubMed |
Genetic variants in NHEJ1 and related DNA repair disorders: insights into phenotypic heterogeneity and links to hypoplastic myelodysplastic syndromes and familial hematological malignancies susceptibility. | Ann Hematol | 2025 | 40047910 | PubTator, text mining | PubMed |
| Fibroblast-based radiosensitivity assays as a clinically valuable tool for (severe) combined immunodeficiency syndromes. | Mutat Res Genet Toxicol Environ Mutagen | 2025 | 40044379 | PubTator, text mining | PubMed |
| Prime Editing: Mechanistic Insights and DNA Repair Modulation. | Cells | 2025 | 39996750 | PubTator, text mining | PubMed |
| A meta-analysis of epigenome-wide association studies of ultra-processed food consumption with DNA methylation in European children. | Clin Epigenetics | 2025 | 39773758 | PubTator, text mining | PubMed |
| Perspective in the Mechanisms for Repairing Sperm DNA Damage. | Reprod Sci | 2025 | 39333437 | PubTator, text mining | PubMed |
| FET fusion oncoproteins disrupt physiologic DNA repair and create a targetable opportunity for ATR inhibitor therapy. | bioRxiv | 2025 | 37205599 | PubTator, text mining | PubMed |
| Severe immunodeficiency spectrum associated with NHEJ1 gene mutation: Cernunnos/XLF deficiency | Biomedica | 2024 | 39836852 | 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/v1/79840/papers?page=2