Gene · 6103
Papers1,847
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
481 to 500 of 1,847
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Genetic Testing of Inherited Retinal Disease in Australian Private Tertiary Ophthalmology Practice. | Clin Ophthalmol | 2022 | 35444405 | PubTator, text mining | PubMed |
| Environmental induced transgenerational inheritance impacts systems epigenetics in disease etiology. | Sci Rep | 2022 | 35440735 | PubTator, text mining | PubMed |
| Mutation Analysis of the RPGR Gene in a Chinese Cohort. | Front Genet | 2022 | 35432464 | PubTator, text mining | PubMed |
| An OTX2 Gene Mutation Causing a More Severe Retinal Phenotype in a Female RPGR Mutation Carrier. | Ophthalmic Surg Lasers Imaging Retina | 2022 | 35417297 | PubTator, text mining | PubMed |
| Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. | Int J Mol Sci | 2022 | 35409265 | PubTator, text mining | PubMed |
| Prevalence and associated relating factors in patients with hereditary retinal dystrophy: a nationwide population-based study in Taiwan. | BMJ Open | 2022 | 35396285 | PubTator, text mining | PubMed |
| Spata7 is required for maintenance of the retinal connecting cilium. | Sci Rep | 2022 | 35368022 | PubTator, text mining | PubMed |
| Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series. | Orphanet J Rare Dis | 2022 | 35365235 | PubTator, text mining | PubMed |
| 3D and organoid culture in research: physiology, hereditary genetic diseases and cancer. | Cell Biosci | 2022 | 35365227 | PubTator, text mining | PubMed |
| Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease. | PLoS Genet | 2022 | 35353811 | PubTator, text mining | PubMed |
| The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification. | Hum Genet | 2022 | 35353227 | PubTator, text mining | PubMed |
| Primary ciliary dyskinesia in Volendam: Diagnostic and phenotypic features in patients with a CCDC114 mutation. | Am J Med Genet C Semin Med Genet | 2022 | 35343062 | PubTator, text mining | PubMed |
| Class A and C GPCR Dimers in Neurodegenerative Diseases. | Curr Neuropharmacol | 2022 | 35339177 | PubTator, text mining | PubMed |
| Antioxidant and lipid supplementation improve the development of photoreceptor outer segments in pluripotent stem cell-derived retinal organoids. | Stem Cell Reports | 2022 | 35334217 | PubTator, text mining | PubMed |
| Human iPSC-Derived Retinal Organoids and Retinal Pigment Epithelium for Novel Intronic RPGR Variant Assessment for Therapy Suitability. | J Pers Med | 2022 | 35330501 | PubTator, text mining | PubMed |
| Ciliated (FOXJ1+) Cells Display Reduced Ferritin Light Chain in the Airways of Idiopathic Pulmonary Fibrosis Patients. | Cells | 2022 | 35326483 | PubTator, text mining | PubMed |
| The Current State of Genetic Testing Platforms for Inherited Retinal Diseases. | Ophthalmol Retina | 2022 | 35307606 | PubTator, text mining | PubMed |
| Deoxynivalenol triggers porcine intestinal tight junction disorder through hijacking SLC5A1 and PGC1α-mediated mitochondrial function. | Food Chem Toxicol | 2022 | 35307453 | PubTator, text mining | PubMed |
| Automated assessment of hyoid movement during normal swallow using ultrasound. | Int J Lang Commun Disord | 2022 | 35285113 | PubTator, text mining | PubMed |
| Understanding the functional role of membrane confinements in TNF-mediated signaling by multiscale simulations. | Commun Biol | 2022 | 35277586 | 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/v1/6103/papers?page=25