Gene · 7516
Papers1,770
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
741 to 760 of 1,770
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Identification of biomarkers of immune checkpoint blockade efficacy in recurrent or refractory solid tumor malignancies. | Oncotarget | 2020 | 32110280 | PubTator, text mining | PubMed |
| Genetic Variants Detected Using Cell-Free DNA from Blood and Tumor Samples in Patients with Inflammatory Breast Cancer. | Int J Mol Sci | 2020 | 32075053 | PubTator, text mining | PubMed |
| Detection of Molecular Signatures of Homologous Recombination Deficiency in Prostate Cancer with or without BRCA1/2 Mutations. | Clin Cancer Res | 2020 | 32071115 | PubTator, text mining | PubMed |
| Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency. | Mol Genet Genomic Med | 2020 | 32048466 | PubTator, text mining | PubMed |
| FANCL gene mutations in premature ovarian insufficiency. | Hum Mutat | 2020 | 32048394 | PubTator, text mining | PubMed |
| Genetic Predisposition to Breast and Ovarian Cancers: How Many and Which Genes to Test? | Int J Mol Sci | 2020 | 32046255 | PubTator, text mining | PubMed |
| BRG1 Activates Proliferation and Transcription of Cell Cycle-Dependent Genes in Breast Cancer Cells. | Cancers (Basel) | 2020 | 32033115 | PubTator, text mining | PubMed |
| Detection of Germline Mutations in Breast Cancer Patients with Clinical Features of Hereditary Cancer Syndrome Using a Multi-Gene Panel Test. | Cancer Res Treat | 2020 | 32019277 | PubTator, text mining | PubMed |
| Bioinformatics-based screening of key genes for transformation of liver cirrhosis to hepatocellular carcinoma. | J Transl Med | 2020 | 32000807 | PubTator, text mining | PubMed |
| Association between DNA damage repair gene somatic mutations and immune-related gene expression in ovarian cancer. | Cancer Med | 2020 | 31991061 | PubTator, text mining | PubMed |
| Effect of eleutheroside B1 on non‑coding RNAs and protein profiles of influenza A virus‑infected A549 cells. | Int J Mol Med | 2020 | 31985023 | PubTator, text mining | PubMed |
| Fanconi anemia and the underlying causes of genomic instability. | Environ Mol Mutagen | 2020 | 31983075 | PubTator, text mining | PubMed |
| Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic Anemia. | Biol Blood Marrow Transplant | 2020 | 31982544 | PubTator, text mining | PubMed |
| Applications of Next Generation Sequencing to the Analysis of Familial Breast/Ovarian Cancer. | High Throughput | 2020 | 31936873 | PubTator, text mining | PubMed |
| Implementation and use of whole exome sequencing for metastatic solid cancer. | EBioMedicine | 2020 | 31923800 | PubTator, text mining | PubMed |
| Rad51 paralogs and the risk of unselected breast cancer: A case-control study. | PLoS One | 2020 | 31905201 | PubTator, text mining | PubMed |
| Fanconi Anemia DNA Repair Pathway as a New Mechanism to Exploit Cancer Drug Resistance. | Mini Rev Med Chem | 2020 | 31902358 | PubTator, text mining | PubMed |
| A Patient-Derived Glioblastoma Organoid Model and Biobank Recapitulates Inter- and Intra-tumoral Heterogeneity. | Cell | 2020 | 31883794 | PubTator, text mining | PubMed |
| A toxicogenomic approach for the risk assessment of the food contaminant acetamide. | Toxicol Appl Pharmacol | 2020 | 31881176 | PubTator, text mining | PubMed |
| Homologous recombination repair intermediates promote efficient de novo telomere addition at DNA double-strand breaks. | Nucleic Acids Res | 2020 | 31828313 | 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/v1/7516/papers?page=38