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.
181 to 200 of 1,877
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Immunohistochemistry Reveals TRPC Channels in the Human Hearing Organ-A Novel CT-Guided Approach to the Cochlea. | Int J Mol Sci | 2023 | 37298241 | PubTator, text mining | PubMed |
| A single-cell level comparison of human inner ear organoids with the human cochlea and vestibular organs. | Cell Rep | 2023 | 37289589 | PubTator, text mining | PubMed |
| Recent advances in understanding molecular bases of Ménière's disease. | Fac Rev | 2023 | 37284494 | PubTator, text mining | PubMed |
| Identification of genetic alterations in couples and their products of conceptions from recurrent pregnancy loss in North Indian population. | Front Genet | 2023 | 37260775 | PubTator, text mining | PubMed |
| Identification of Rare Variants Involved in High Myopia Unraveled by Whole Genome Sequencing. | Ophthalmol Sci | 2023 | 37250922 | PubTator, text mining | PubMed |
| Accelerated Evolution Analysis Uncovers PKNOX2 as a Key Transcription Factor in the Mammalian Cochlea. | Mol Biol Evol | 2023 | 37247388 | PubTator, text mining | PubMed |
| RNA-Seq Analysis Reveals an Essential Role of the cGMP-PKG-MAPK Pathways in Retinal Degeneration Caused by Cep250 Deficiency. | Int J Mol Sci | 2023 | 37240188 | PubTator, text mining | PubMed |
| Case report: Compound heterozygous nonsense PCDH15 variant and a novel deep-intronic variant in a Chinese child with profound hearing loss. | Mol Genet Genomic Med | 2023 | 37232061 | PubTator, text mining | PubMed |
| Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification. | Front Physiol | 2023 | 37228816 | PubTator, text mining | PubMed |
| Establishment of a novel lysosomal signature for the diagnosis of gastric cancer with in-vitro and in-situ validation. | Front Immunol | 2023 | 37215115 | PubTator, text mining | PubMed |
| The applications of CRISPR/Cas-mediated genome editing in genetic hearing loss. | Cell Biosci | 2023 | 37210555 | PubTator, text mining | PubMed |
| Regulatory T cells in peripheral tissue tolerance and diseases. | Front Immunol | 2023 | 37197653 | PubTator, text mining | PubMed |
| Characteristic of molecular subtype based on lysosome-associated genes reveals clinical prognosis and immune infiltration of gastric cancer. | Front Oncol | 2023 | 37197421 | PubTator, text mining | PubMed |
| The vestibular calyceal junction is dismantled following subchronic streptomycin in rats and sensory epithelium stress in humans. | Arch Toxicol | 2023 | 37195449 | PubTator, text mining | PubMed |
| Familial Whole Exome Sequencing Study of 30 Families With Early-Onset High Myopia. | Invest Ophthalmol Vis Sci | 2023 | 37191617 | PubTator, text mining | PubMed |
| Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families. | Hum Genomics | 2023 | 37189200 | PubTator, text mining | PubMed |
| A nonsense mutation in C8orf37 linked with retinitis pigmentosa, early macular degeneration, cataract, and myopia in an arRP family from North India. | BMC Ophthalmol | 2023 | 37170250 | PubTator, text mining | PubMed |
| Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous families. | BMC Ophthalmol | 2023 | 37165311 | PubTator, text mining | PubMed |
| Interactome-Based Machine Learning Predicts Potential Therapeutics for COVID-19. | ACS Omega | 2023 | 37163139 | PubTator, text mining | PubMed |
| The genetic landscape of inherited retinal dystrophies in Arabs. | BMC Med Genomics | 2023 | 37127645 | 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=10