Gene · 7399
Papers2,630
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1,081 to 1,100 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Human Cytomegalovirus and Autoimmune Diseases: Where Are We? | Viruses | 2021 | 33567734 | PubTator, text mining | PubMed |
| Yap1 Mediates Trametinib Resistance in Head and Neck Squamous Cell Carcinomas. | Clin Cancer Res | 2021 | 33547198 | PubTator, text mining | PubMed |
| Near-infrared fundus autofluorescence alterations correlate with swept-source optical coherence tomography angiography findings in patients with retinitis pigmentosa. | Sci Rep | 2021 | 33542393 | PubTator, text mining | PubMed |
| Roan, ticked and clear coat patterns in the canine are associated with three haplotypes near usherin on CFA38. | Anim Genet | 2021 | 33539602 | PubTator, text mining | PubMed |
| USH2A-Related Retinitis Pigmentosa: Staging of Disease Severity and Morpho-Functional Studies. | Diagnostics (Basel) | 2021 | 33535592 | PubTator, text mining | PubMed |
| Genomic scans for selective sweeps through haplotype homozygosity and allelic fixation in 14 indigenous sheep breeds from Middle East and South Asia. | Sci Rep | 2021 | 33531649 | PubTator, text mining | PubMed |
| A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss. | BMC Med Genomics | 2021 | 33530996 | PubTator, text mining | PubMed |
| Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon. | Mol Genet Genomic Med | 2021 | 33528103 | PubTator, text mining | PubMed |
| A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa. | Commun Biol | 2021 | 33514863 | PubTator, text mining | PubMed |
| Stereochemistry Enhances Potency, Efficacy, and Durability of Malat1 Antisense Oligonucleotides In Vitro and In Vivo in Multiple Species. | Transl Vis Sci Technol | 2021 | 33510962 | PubTator, text mining | PubMed |
| The future of retinal gene therapy: evolving from subretinal to intravitreal vector delivery. | Neural Regen Res | 2021 | 33510064 | PubTator, text mining | PubMed |
| Analysis of Pathogenic Variants Correctable With CRISPR Base Editing Among Patients With Recessive Inherited Retinal Degeneration. | JAMA Ophthalmol | 2021 | 33507217 | PubTator, text mining | PubMed |
| The MHC Class II Transactivator CIITA: Not (Quite) the Odd-One-Out Anymore among NLR Proteins. | Int J Mol Sci | 2021 | 33499042 | PubTator, text mining | PubMed |
| Peripheral Anomalies in USH2A Cause Central Auditory Anomalies in a Mouse Model of Usher Syndrome and CAPD. | Genes (Basel) | 2021 | 33498833 | PubTator, text mining | PubMed |
| Reticular Basement Membrane Thickness Is Associated with Growth- and Fibrosis-Promoting Airway Transcriptome Profile-Study in Asthma Patients. | Int J Mol Sci | 2021 | 33498209 | PubTator, text mining | PubMed |
| X-Linked Retinitis Pigmentosa Caused by Non-Canonical Splice Site Variants in RPGR. | Int J Mol Sci | 2021 | 33467000 | PubTator, text mining | PubMed |
| Prepubertal exposure to high dose of cadmium induces hypothalamic injury through transcriptome profiling alteration and neuronal degeneration in female rats. | Chem Biol Interact | 2021 | 33453195 | PubTator, text mining | PubMed |
| Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications. | Sci Rep | 2021 | 33452396 | PubTator, text mining | PubMed |
| Zebrafish Models of Photoreceptor Dysfunction and Degeneration. | Biomolecules | 2021 | 33435268 | PubTator, text mining | PubMed |
| Ultraviolet radiation drives mutations in a subset of mucosal melanomas. | Nat Commun | 2021 | 33431815 | 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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/7399/papers?page=55