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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.

101 to 120 of 1,877

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TitleJournalYearPMIDFound bySource
Age-related changes in olivocochlear efferent innervation in gerbils.Front Synaptic Neurosci202438887655PubTator, text miningPubMed
Multicentric Longitudinal Prospective Study in a European Cohort of MYO7A Patients: Disease Course and Implications for Gene Therapy.Invest Ophthalmol Vis Sci202438884554PubTator, text miningPubMed
Optical coherence tomography biomarkers in MYO7A-inherited retinal dystrophy: longitudinal study in pediatric patients.Graefes Arch Clin Exp Ophthalmol202438871877PubTator, text miningPubMed
Whole-Exome Sequencing in Turkish Patients with Inherited Retinal Dystrophies Reveals Novel Variants in Ten Genes.Mol Syndromol202438841332PubTator, text miningPubMed
A novel homozygous missense variant identified in the myosin VIIA motor domain of a Moroccan patient with usher syndrome.Mol Biol Rep202438796585PubTator, text miningPubMed
Sensory transduction in auditory hair cells-PIEZOs can't touch this.J Gen Physiol202438727631PubTator, text miningPubMed
The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individuals.medRxiv202438712155PubTator, text miningPubMed
Toxic effect and mechanism of β-cypermethrin and its chiral isomers on HTR-8/SVneo cells.Pestic Biochem Physiol202438685233PubTator, text miningPubMed
Biomolecular Condensates Decipher Molecular Codes of Cell Fate: From Biophysical Fundamentals to Therapeutic Practices.Int J Mol Sci202438612940PubTator, text miningPubMed
Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss.J Clin Med202438610765PubTator, text miningPubMed
The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B.Sci Rep202438594301PubTator, text miningPubMed
Pathophysiology of human hearing loss associated with variants in myosins.Front Physiol202438562617PubTator, text miningPubMed
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades.J Cell Mol Med202438534090PubTator, text miningPubMed
Navigating the Usher Syndrome Genetic Landscape: An Evaluation of the Associations between Specific Genes and Quality Categories of Cochlear Implant Outcomes.Audiol Res202438525684PubTator, text miningPubMed
Precision ophthalmology: a call for Africa not to be left in the dark.Gene Ther202438519591PubTator, text miningPubMed
Retinal Ciliopathies and Potential Gene Therapies: A Focus on Human iPSC-Derived Organoid Models.Int J Mol Sci202438474133PubTator, text miningPubMed
Whole-exome sequencing reveals genetic variants that may play a role in neurocytomas.J Neurooncol202438319496PubTator, text miningPubMed
GelMA/PEDOT:PSS Composite Conductive Hydrogel-Based Generation and Protection of Cochlear Hair Cells through Multiple Signaling Pathways.Biomolecules202438254695PubTator, text miningPubMed
Whole genome sequencing enables new genetic diagnosis for inherited retinal diseases by identifying pathogenic variants.NPJ Genom Med202438245557PubTator, text miningPubMed
MSC-derived exosomes protect auditory hair cells from neomycin-induced damage via autophagy regulation.Biol Res202438217055PubTator, text miningPubMed

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.

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