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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.

121 to 140 of 1,877

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TitleJournalYearPMIDFound bySource
Formononetin ameliorates cisplatin-induced hair cell death via activation of the PI3K/AKT-Nrf2 signaling pathway.Heliyon202438192850PubTator, text miningPubMed
Genetic profile of syndromic retinitis pigmentosa in Portugal.Graefes Arch Clin Exp Ophthalmol202438189974PubTator, text miningPubMed
Development and validation of a novel lysosome-related LncRNA signature for predicting prognosis and the immune landscape features in colon cancer.Sci Rep202438182713PubTator, text miningPubMed
Using multi-scale genomics to associate poorly annotated genes with rare diseases.Genome Med202438178268PubTator, text miningPubMed
Genetic correction of induced pluripotent stem cells from a DFNA36 patient results in morphologic and functional recovery of derived hair cell-like cells.Stem Cell Res Ther202438167128PubTator, text miningPubMed
Macrophages reprogramming driven by cancer-associated fibroblasts under FOLFIRINOX treatment correlates with shorter survival in pancreatic cancer.Cell Commun Signal202438167013PubTator, text miningPubMed
The dynamics of actin protrusions can be controlled by tip-localized myosin motors.J Biol Chem202438042485PubTator, text miningPubMed
Natural Multifunctional Silk Microcarriers for Noise-Induced Hearing Loss Therapy.Adv Sci (Weinh)202437984871PubTator, text miningPubMed
Epidemiology and genetics of Meniere's disease.Curr Opin Neurol202437865853PubTator, text miningPubMed
Stem Cell-Based Hair Cell Regeneration and Therapy in the Inner Ear.Neurosci Bull202437787875PubTator, text miningPubMed
Novel cis compound heterozygous variants in MYO6 causes early onset of non-syndromic hearing loss in a Chinese family.Front Genet202338274113PubTator, text miningPubMed
The Potential and Application of iPSCs in Gene and Cell Therapy for Retinopathies and Optic Neuropathies.Acta Naturae202338234607PubTator, text miningPubMed
Identification of a novel compound heterozygous pathogenic variant in MYO7A causing Usher syndrome type IB in a Chinese patient: a case report.J Int Med Res202338141656PubTator, text miningPubMed
Recent Therapeutic Progress and Future Perspectives for the Treatment of Hearing Loss.Biomedicines202338137568PubTator, text miningPubMed
Treatment following Triple-AAV Delivery in Mature Murine Model of Human CDH23-Associated Hearing Loss.Curr Issues Mol Biol202338132436PubTator, text miningPubMed
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders.Audiol Res202338131811PubTator, text miningPubMed
Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss.Genome Med202338111038PubTator, text miningPubMed
A role for mutations in AK9 and other genes affecting ependymal cells in idiopathic normal pressure hydrocephalus.Proc Natl Acad Sci U S A202338100419PubTator, text miningPubMed
The Relevance of Autophagy within Inner Ear in Baseline Conditions and Tinnitus-Related Syndromes.Int J Mol Sci202338068993PubTator, text miningPubMed
Outcomes of cochlear implantation in 75 patients with auditory neuropathy.Front Neurosci202338027523PubTator, 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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