Gene · 7399
Papers2,630
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1,001 to 1,020 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Differential Mutation Detection Capability Through Capture-Based Targeted Sequencing in Plasma Samples in Hepatocellular Carcinoma. | Front Oncol | 2021 | 33996539 | PubTator, text mining | PubMed |
| LRP1B mutation is associated with tumor HPV status and promotes poor disease outcomes with a higher mutation count in HPV-related cervical carcinoma and head & neck squamous cell carcinoma. | Int J Biol Sci | 2021 | 33994859 | PubTator, text mining | PubMed |
| Identification of four insertion sites for foreign genes in a pseudorabies virus vector. | BMC Vet Res | 2021 | 33980225 | PubTator, text mining | PubMed |
| Long-Read Sequencing to Unravel Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss. | Front Cell Dev Biol | 2021 | 33968938 | PubTator, text mining | PubMed |
| Genomic Alteration Characterization in Colorectal Cancer Identifies a Prognostic and Metastasis Biomarker: FAM83A|IDO1. | Front Oncol | 2021 | 33959500 | PubTator, text mining | PubMed |
| Target 5000: a standardized all-Ireland pathway for the diagnosis and management of inherited retinal degenerations. | Orphanet J Rare Dis | 2021 | 33952326 | PubTator, text mining | PubMed |
| Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort. | Genes (Basel) | 2021 | 33946315 | PubTator, text mining | PubMed |
| Structure and Membrane Targeting of the PDZD7 Harmonin Homology Domain (HHD) Associated With Hearing Loss. | Front Cell Dev Biol | 2021 | 33937240 | PubTator, text mining | PubMed |
| MRPL15 is a novel prognostic biomarker and therapeutic target for epithelial ovarian cancer. | Cancer Med | 2021 | 33934540 | PubTator, text mining | PubMed |
| USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families. | BMC Ophthalmol | 2021 | 33926394 | PubTator, text mining | PubMed |
| An Update on Gene Therapy for Inherited Retinal Dystrophy: Experience in Leber Congenital Amaurosis Clinical Trials. | Int J Mol Sci | 2021 | 33926102 | PubTator, text mining | PubMed |
| Antisense Oligonucleotide-Based Rescue of Aberrant Splicing Defects Caused by 15 Pathogenic Variants in ABCA4. | Int J Mol Sci | 2021 | 33924840 | PubTator, text mining | PubMed |
| Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies. | Genes (Basel) | 2021 | 33924653 | PubTator, text mining | PubMed |
| Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies. | Genes (Basel) | 2021 | 33921607 | PubTator, text mining | PubMed |
| Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy. | Int J Mol Sci | 2021 | 33920085 | PubTator, text mining | PubMed |
| Autosomal Recessive Retinitis Pigmentosa Associated with Three Novel REEP6 Variants in Chinese Population. | Genes (Basel) | 2021 | 33917198 | PubTator, text mining | PubMed |
| Human Mitoribosome Biogenesis and Its Emerging Links to Disease. | Int J Mol Sci | 2021 | 33917098 | PubTator, text mining | PubMed |
| Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations. | Mol Vis | 2021 | 33907365 | PubTator, text mining | PubMed |
| Increasing prediction accuracy of pathogenic staging by sample augmentation with a GAN. | PLoS One | 2021 | 33905431 | PubTator, text mining | PubMed |
| Clonal Architectures Predict Clinical Outcome in Gastric Adenocarcinoma Based on Genomic Variation, Tumor Evolution, and Heterogeneity. | Cell Transplant | 2021 | 33900127 | 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
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