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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.

361 to 380 of 1,877

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TitleJournalYearPMIDFound bySource
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss.Cells202235681420PubTator, text miningPubMed
Clinical exome sequencing for inherited retinal degenerations at a tertiary care center.Sci Rep202235672425PubTator, text miningPubMed
The Genomics of Auditory Function and Disease.Annu Rev Genomics Hum Genet202235667089PubTator, text miningPubMed
Engineering of near-PAMless adenine base editor with enhanced editing activity and reduced off-target.Mol Ther Nucleic Acids202235664696PubTator, text miningPubMed
Defective α-tectorin may involve tectorial membrane in familial Meniere disease.Clin Transl Med202235653455PubTator, text miningPubMed
Novel Missense and Splice Site Mutations in USH2A, CDH23, PCDH15, and ADGRV1 Are Associated With Usher Syndrome in Lebanon.Front Genet202235651951PubTator, text miningPubMed
Genetics of Hearing Impairment.Genes (Basel)202235627237PubTator, text miningPubMed
Critical roles of FGF, RA, and WNT signalling in the development of the human otic placode and subsequent lineages in a dish.Regen Ther202235620640PubTator, text miningPubMed
In vitro and in vivo models: What have we learnt about inner ear regeneration and treatment for hearing loss?Mol Cell Neurosci202235577314PubTator, text miningPubMed
Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns.Front Genet202235571039PubTator, text miningPubMed
Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.Orphanet J Rare Dis202235551639PubTator, text miningPubMed
MicroRNA Signature and Cellular Characterization of Undifferentiated and Differentiated House Ear Institute-Organ of Corti 1 (HEI-OC1) Cells.J Assoc Res Otolaryngol202235546217PubTator, text miningPubMed
Identification of heritable rare variants associated with early-stage lung adenocarcinoma risk.Transl Lung Cancer Res202235529798PubTator, text miningPubMed
Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort.Invest Ophthalmol Vis Sci202235481838PubTator, text miningPubMed
Comprehensive Landscape of Prognostic Significance and Immune Characteristics of Myosins in Squamous Cell Carcinoma of the Head and Neck.J Immunol Res202235478939PubTator, text miningPubMed
ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death.J Mol Med (Berl)202235471608PubTator, text miningPubMed
The role of motor proteins in photoreceptor protein transport and visual function.Ophthalmic Genet202235470760PubTator, text miningPubMed
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia.J Lipid Res202235460704PubTator, text miningPubMed
Electrophysiology-Guided Genetic Characterisation Maximises Molecular Diagnosis in an Irish Paediatric Inherited Retinal Degeneration Population.Genes (Basel)202235456422PubTator, text miningPubMed
Genetic Testing for Rare Diseases.Diagnostics (Basel)202235453856PubTator, 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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