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.
161 to 180 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Construction of recombinant Marek's disease virus co-expressing σB and σC of avian reoviruses. | Front Vet Sci | 2024 | 39301286 | PubTator, text mining | PubMed |
| Recombinant Marek's disease virus type 1 provides full protection against H9N2 influenza A virus in chickens. | Vet Microbiol | 2024 | 39243669 | PubTator, text mining | PubMed |
| Whole-Exome Analysis for Polish Caucasian Patients with Retinal Dystrophies and the Creation of a Reference Genomic Database for the Polish Population. | Genes (Basel) | 2024 | 39202371 | PubTator, text mining | PubMed |
| Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene. | Cell J | 2024 | 39154239 | PubTator, text mining | PubMed |
| Otolith function in Usher type II syndrome. | Acta Otolaryngol | 2024 | 39151018 | PubTator, text mining | PubMed |
Prognostic mutations identified by whole-exome sequencing and validation of the Molecular International Prognostic Scoring System in myelodysplastic syndromes after allogeneic haematopoietic stem cell transplantation. | Br J Haematol | 2024 | 39138006 | PubTator, text mining | PubMed |
| Investigating Splice Defects in USH2A Using Targeted Long-Read Sequencing. | Cells | 2024 | 39120292 | PubTator, text mining | PubMed |
| Relationship between genotype, phenotype, and refractive status in patients of inherited retinal degeneration. | Eye (Lond) | 2024 | 39090253 | PubTator, text mining | PubMed |
| RNA variant assessment using transactivation and transdifferentiation. | Am J Hum Genet | 2024 | 39084224 | PubTator, text mining | PubMed |
| Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal Genes. | Genes (Basel) | 2024 | 39062705 | PubTator, text mining | PubMed |
| Clinical Genetic Testing for Hearing Loss: Implications for Genetic Counseling and Gene-Based Therapies. | Biomedicines | 2024 | 39062005 | PubTator, text mining | PubMed |
| A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy. | BMC Ophthalmol | 2024 | 39044131 | PubTator, text mining | PubMed |
| Usher syndrome in the United Arab Emirates. | Ophthalmic Genet | 2024 | 39016003 | PubTator, text mining | PubMed |
| Pseudorabies virus tegument protein US2 antagonizes antiviral innate immunity by targeting cGAS-STING signaling pathway. | Front Immunol | 2024 | 39015575 | PubTator, text mining | PubMed |
| Adaptive optics retinal imaging in patients with usher syndrome. | Front Ophthalmol (Lausanne) | 2024 | 38984112 | PubTator, text mining | PubMed |
| Comparison of strain specific pathogenicity of Herpes Simplex Virus Type 1 by high-throughput sequencing. | J Virol Methods | 2024 | 38971379 | PubTator, text mining | PubMed |
| Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. | Cell Genom | 2024 | 38944039 | PubTator, text mining | PubMed |
| Optimised, Broad NGS Panel for Inherited Eye Diseases to Diagnose 1000 Patients in Poland. | Biomedicines | 2024 | 38927562 | PubTator, text mining | PubMed |
| Whole-exome sequencing screening for candidate genes and variants associated with primary sporadic keratoconus in Chinese patients. | Exp Eye Res | 2024 | 38908538 | PubTator, text mining | PubMed |
| Structural Variants and Implicated Processes Associated with Familial Tourette Syndrome. | Int J Mol Sci | 2024 | 38891944 | 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/v1/7399/papers?page=9