Gene · 4647
Papers1,877
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
241 to 260 of 1,877
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia-Alania. | PeerJ | 2023 | 36743950 | PubTator, text mining | PubMed |
| Identifying and Overcoming Challenges in Developing Effective Treatments for Usher 1B: A Workshop Report. | Transl Vis Sci Technol | 2023 | 36723965 | PubTator, text mining | PubMed |
| Identification of Relevant Protein Interactions with Partial Knowledge: A Complex Network and Deep Learning Approach. | Biology (Basel) | 2023 | 36671832 | PubTator, text mining | PubMed |
| Synaptotagmin-like protein 1 is a potential diagnostic and prognostic biomarker in endometrial cancer based on bioinformatics and experiments. | J Ovarian Res | 2023 | 36653850 | PubTator, text mining | PubMed |
| The LHX2-OTX2 transcriptional regulatory module controls retinal pigmented epithelium differentiation and underlies genetic risk for age-related macular degeneration. | PLoS Biol | 2023 | 36649236 | PubTator, text mining | PubMed |
| Characterizing macular edema in retinitis pigmentosa through a combined structural and microvascular optical coherence tomography investigation. | Sci Rep | 2023 | 36646739 | PubTator, text mining | PubMed |
| Ensembles of human myosin-19 bound to calmodulin and regulatory light chain RLC12B drive multimicron transport. | J Biol Chem | 2023 | 36642185 | PubTator, text mining | PubMed |
| Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS. | Genes Genomics | 2023 | 36630074 | PubTator, text mining | PubMed |
| Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel. | Hum Genomics | 2023 | 36597107 | PubTator, text mining | PubMed |
| Mutation-agnostic RNA interference with engineered replacement rescues Tmc1-related hearing loss. | Life Sci Alliance | 2023 | 36574989 | PubTator, text mining | PubMed |
| Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss. | Saudi J Biol Sci | 2023 | 36568409 | PubTator, text mining | PubMed |
| Genetic advances in Meniere Disease. | Mol Biol Rep | 2023 | 36565421 | PubTator, text mining | PubMed |
| Task force Guideline of Brazilian Society of Otology ‒ hearing loss in children - Part I ‒ Evaluation. | Braz J Otorhinolaryngol | 2023 | 36529647 | PubTator, text mining | PubMed |
| New splice site mutations in MYO7A causing Usher syndrome type 1: a study on a Chinese consanguineous family. | Int Ophthalmol | 2023 | 36484953 | PubTator, text mining | PubMed |
| Evaluation of CRISPR/Cas9 exon-skipping vector for choroideremia using human induced pluripotent stem cell-derived RPE. | J Gene Med | 2023 | 36413603 | PubTator, text mining | PubMed |
| Prevalence and associated factors of cystoid macular edema in children with early onset inherited retinal dystrophies. | Eur J Ophthalmol | 2023 | 36317312 | PubTator, text mining | PubMed |
| Retinal organoids provide unique insights into molecular signatures of inherited retinal disease throughout retinogenesis. | J Anat | 2023 | 36177499 | PubTator, text mining | PubMed |
| Expression and subcellular localization of USH1C/harmonin in human retina provides insights into pathomechanisms and therapy. | Hum Mol Genet | 2023 | 35997788 | PubTator, text mining | PubMed |
| Prediction of visual impairment in retinitis pigmentosa using deep learning and multimodal fundus images. | Br J Ophthalmol | 2023 | 35896367 | PubTator, text mining | PubMed |
| Increased mitophagy protects cochlear hair cells from aminoglycoside-induced damage. | Autophagy | 2023 | 35471096 | 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/v1/4647/papers?page=13