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Gene · 5172

Papers3,149

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

TitleJournalYearPMIDFound bySource
A Unique SLC26A4 Mutation Spectrum in a Mongolian Enlarged Vestibular Aqueduct Cohort via Whole-Exome Sequencing: A Preliminary Study.Int J Mol Sci202642353084PubTator, text miningPubMed
Conformational changes underlying electromechanical transduction in prestin resemble a transport transition in pendrin.bioRxiv202642327119PubTator, text miningPubMed
Integrative Bioinformatics Analysis Reveals COL13A1 and COL23A1 as Potential Diagnostic and Prognostic Biomarkers in Thyroid Cancer.Health Sci Rep202642306204PubTator, text miningPubMed
Synergistic oxidation and adsorption of arsenic(III) by epigallocatechin gallate activated iron(III) peroxydisulfate system.Sci Rep202642288697PubTator, text miningPubMed
Low-Dose 125I-Irradiation Enhances PRC1-Targeted NIS-CAR-T Cell Cytotoxicity Against Breast Cancer Cells.Mol Imaging202642282942PubTator, text miningPubMed
Pragmatic Use of Thyroid Autoantibodies in Clinical Practice: An Update.touchREV Endocrinol202642273002PubTator, text miningPubMed
Molecular diagnosis of non-syndromic hearing loss in seven Iranian families using whole-exome sequencing.BMC Med Genomics202642231373PubTator, text miningPubMed
Insights into transcriptomics and metabolic engineering of microalgal systems for enhancing industrial and environmental applications.World J Microbiol Biotechnol202642216982PubTator, text miningPubMed
Expanding the Utility of Exome Sequencing in Preventive and Population Genetics.Am J Med Genet A202642212615PubTator, text miningPubMed
[Application of PCR-MALDI-TOF MS in genetic detection of non-syndromic hearing loss and genotype-audiometric phenotype analysis].Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi202642208963PubTator, text miningPubMed
Green synthesis of N-doped hierarchical porous biochar from Artemisia leaf for enhanced peroxydisulfate activation: Synergistic roles of edge nitrogen and carbonyl group.Environ Res202642203057PubTator, text miningPubMed
Disparities in deafness gene mutations between Han and Li ethnic newborns in Hainan, China: insights from a combined screening program.BMC Med Genomics202642152029PubTator, text miningPubMed
Identification of Novel LOXHD1 Variants in Chinese Patients with Non-Syndromic Hearing Loss.J Otol202642131115PubTator, text miningPubMed
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from Pakistan.Sci Rep202642086625PubTator, text miningPubMed
Association of GJB2 P.V37I With Sudden Sensorineural Hearing Loss and Endoplasmic Reticulum Stress.Otolaryngol Head Neck Surg202642047511PubTator, text miningPubMed
[Primary prevention study of preimplantation genetic testing for GJB2 gene mutation families].Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi202641956763PubTator, text miningPubMed
Genetic landscapes and audiological trajectories in pediatric asymmetric hearing loss and interaural asymmetry.Clin Exp Otorhinolaryngol202641937395PubTator, text miningPubMed
Endogenous promoter G-quadruplexes scaffold apurinic/apyrimidinic endonuclease (APE1) to drive gene expression.Nucleic Acids Res202641925230PubTator, text miningPubMed
Trends and Prospects in Inflammation Resolution in Acute Lung Injury and Acute Respiratory Distress Syndrome: A Bibliometric Quantitative and Visualization Analysis.Mediators Inflamm202641923487PubTator, text miningPubMed
Genomic Biomarkers and Mutational Landscape of Nonsyndromic Hearing Loss (NSHL) in the Singaporean Population: Clinical Translational Implications.Biomolecules202641897287PubTator, 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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