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.
61 to 80 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Listening Effort and Its Relation to Spatial Localization, and Vestibular and Visual Impairment in Usher Syndrome-Our Experience. | Audiol Res | 2025 | 41440504 | PubTator, text mining | PubMed |
| Erratum: Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles. | Mol Ther Methods Clin Dev | 2025 | 41376777 | PubTator, text mining | PubMed |
| The Landscape of Genetic Variation and Disease Risk in Romania: A Single-Center Study of Autosomal Recessive Carrier Frequencies and Molecular Variants. | Int J Mol Sci | 2025 | 41303398 | PubTator, text mining | PubMed |
| Identification of pathogenic variants for the development of ultra-long axial length in myopic children. | PLoS One | 2025 | 41259386 | PubTator, text mining | PubMed |
| Epidemiological and genetic insights of Usher syndrome in Turkish population: A cross-sectional preliminary study from University of Health Sciences, Turkey. | J Int Med Res | 2025 | 41200749 | PubTator, text mining | PubMed |
| USH2A-Mutated Human Retinal Organoids Model Rod-Cone Dystrophy. | Invest Ophthalmol Vis Sci | 2025 | 41182029 | PubTator, text mining | PubMed |
| Identification and validation of selenium metabolism-related genes in lung adenocarcinoma prognosis using bioinformatics analysis. | Front Genet | 2025 | 41170198 | PubTator, text mining | PubMed |
| Cystoid Macular Lesions in Inherited Retinal Diseases: Prevalence, Characteristics, and Genetic Associations in a Hungarian Cohort. | Genes (Basel) | 2025 | 41153429 | PubTator, text mining | PubMed |
| Identification of a variant in the USH1G gene in a family with Usher syndrome | Biomedica | 2025 | 41060164 | PubTator, text mining | PubMed |
| A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF. | Hum Genomics | 2025 | 41053850 | PubTator, text mining | PubMed |
| Exploring exon excision as a therapeutic intervention strategy for the future treatment of ADGRV1-associated retinitis pigmentosa. | Mol Ther Nucleic Acids | 2025 | 41036464 | PubTator, text mining | PubMed |
| Evolving Threats: Adaptive Mechanisms of Monkeypox Virus (MPXV) in the 2022 Global Outbreak and Their Implications for Vaccine Strategies. | Viruses | 2025 | 41012622 | PubTator, text mining | PubMed |
| Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays. | Biomedicines | 2025 | 41007806 | PubTator, text mining | PubMed |
| In Vitro Silencing of MHC-I in Keratinocytes by Herpesvirus US11 Protein to Model Alloreactive Suppression. | Eur Burn J | 2025 | 40981095 | PubTator, text mining | PubMed |
| Exon Skipping Therapy Restores Ciliary Function in USH2A-Related Retinal Degeneration. | Invest Ophthalmol Vis Sci | 2025 | 40970667 | PubTator, text mining | PubMed |
| Virion proteomics of genetically intact HCMV reveals a regulator of envelope glycoprotein composition that protects against humoral immunity. | Proc Natl Acad Sci U S A | 2025 | 40966292 | PubTator, text mining | PubMed |
| Identification of Tumor Antigens and Immune Subtypes in Hepatocellular Carcinoma From a Multiomics Perspective. | Cancer Rep (Hoboken) | 2025 | 40948427 | PubTator, text mining | PubMed |
| Primary Acute Myeloid Leukemia with Concomitant BCR∷ABL and NPM1 Mutation. | Clin Lab | 2025 | 40923740 | PubTator, text mining | PubMed |
| Four novel genetic mutations are associated with patent foramen ovale in Tibetan population using whole exome sequencing. | Front Genet | 2025 | 40901676 | PubTator, text mining | PubMed |
| Cystoid Macular Edema in Non-Syndromic Retinitis Pigmentosa: Associations With Causative Genes in a Large Cohort. | Invest Ophthalmol Vis Sci | 2025 | 40900079 | 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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GET https://conductscience.org/api/genes/v1/7399/papers?page=4